[{"versioned_ensembl_gene_id":"ENSG00000283891.1","gene_symbol":"MIR628","gene_name":"microRNA 628 [Source:HGNC Symbol;Acc:HGNC:32884]","synonyms":"MIRN628,hsa-mir-628","biotype":"miRNA","ncbi_id":"693213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55372940,"end":55373034,"strand":-1,"description":"microRNA 628 [Source:HGNC Symbol;Acc:HGNC:32884]"}, {"versioned_ensembl_gene_id":"ENSG00000251931.1","gene_symbol":"RNU6-871P","gene_name":"RNA, U6 small nuclear 871, pseudogene [Source:HGNC Symbol;Acc:HGNC:47834]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479950","summary":null,"start":59450673,"end":59450772,"strand":-1,"description":"RNA, U6 small nuclear 871, pseudogene [Source:HGNC Symbol;Acc:HGNC:47834]"}, {"versioned_ensembl_gene_id":"ENSG00000207766.1","gene_symbol":"MIR626","gene_name":"microRNA 626 [Source:HGNC Symbol;Acc:HGNC:32882]","synonyms":"MIRN626,hsa-mir-626","biotype":"miRNA","ncbi_id":"693211","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41691585,"end":41691678,"strand":1,"description":"microRNA 626 [Source:HGNC Symbol;Acc:HGNC:32882]"}, {"versioned_ensembl_gene_id":"ENSG00000275323.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000276678.1","gene_symbol":"GHRLOS","gene_name":"Ghrelin opposite strand RNA conserved region [Source:RFAM;Acc:RF02126]","synonyms":"NCRNA00068,GHRL-AS1","biotype":"misc_RNA","ncbi_id":"100126793","summary":"This gene is an antisense gene of the ghrelin/obestatin prepropeptide gene. Alternatively spliced transcript variants have been identified and they may function as non-coding regulatory RNAs. [provided by RefSeq, Jan 2013]","start":10287413,"end":10287482,"strand":1,"description":"Ghrelin opposite strand RNA conserved region [Source:RFAM;Acc:RF02126]"}, {"versioned_ensembl_gene_id":"ENSG00000207260.1","gene_symbol":"RNU6-35P","gene_name":"RNA, U6 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:34279]","synonyms":"RNU6-35","biotype":"snRNA","ncbi_id":"100873750","summary":null,"start":109992325,"end":109992431,"strand":1,"description":"RNA, U6 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:34279]"}, {"versioned_ensembl_gene_id":"ENSG00000265993.1","gene_symbol":"MIR5694","gene_name":"microRNA 5694 [Source:HGNC Symbol;Acc:HGNC:43530]","synonyms":"hsa-mir-5694","biotype":"miRNA","ncbi_id":"100847064","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67441855,"end":67441930,"strand":-1,"description":"microRNA 5694 [Source:HGNC Symbol;Acc:HGNC:43530]"}, {"versioned_ensembl_gene_id":"ENSG00000207185.1","gene_symbol":"RNU6-1157P","gene_name":"RNA, U6 small nuclear 1157, pseudogene [Source:HGNC Symbol;Acc:HGNC:48120]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481545","summary":null,"start":118593988,"end":118594093,"strand":1,"description":"RNA, U6 small nuclear 1157, pseudogene [Source:HGNC Symbol;Acc:HGNC:48120]"}, {"versioned_ensembl_gene_id":"ENSG00000283793.1","gene_symbol":"MIR6861","gene_name":"microRNA 6861 [Source:HGNC Symbol;Acc:HGNC:50129]","synonyms":"hsa-mir-6861","biotype":"miRNA","ncbi_id":"102465519","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112163258,"end":112163321,"strand":-1,"description":"microRNA 6861 [Source:HGNC Symbol;Acc:HGNC:50129]"}, {"versioned_ensembl_gene_id":"ENSG00000201545.1","gene_symbol":"RNU4-85P","gene_name":"RNA, U4 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:47021]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479597","summary":null,"start":19996803,"end":19996925,"strand":1,"description":"RNA, U4 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:47021]"}, {"versioned_ensembl_gene_id":"ENSG00000272439.1","gene_symbol":"RNU6-91P","gene_name":"RNA, U6 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:47054]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479606","summary":null,"start":99444306,"end":99444412,"strand":1,"description":"RNA, U6 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:47054]"}, {"versioned_ensembl_gene_id":"ENSG00000241821.3","gene_symbol":"RN7SL170P","gene_name":"RNA, 7SL, cytoplasmic 170, pseudogene [Source:HGNC Symbol;Acc:HGNC:46186]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479283","summary":null,"start":56688401,"end":56688695,"strand":1,"description":"RNA, 7SL, cytoplasmic 170, pseudogene [Source:HGNC Symbol;Acc:HGNC:46186]"}, {"versioned_ensembl_gene_id":"ENSG00000265889.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36285312,"end":36285413,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207194.1","gene_symbol":"RNU6-1026P","gene_name":"RNA, U6 small nuclear 1026, pseudogene [Source:HGNC Symbol;Acc:HGNC:47989]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480631","summary":null,"start":50582404,"end":50582511,"strand":1,"description":"RNA, U6 small nuclear 1026, pseudogene [Source:HGNC Symbol;Acc:HGNC:47989]"}, {"versioned_ensembl_gene_id":"ENSG00000283621.1","gene_symbol":"MIR6759","gene_name":"microRNA 6759 [Source:HGNC Symbol;Acc:HGNC:50063]","synonyms":"hsa-mir-6759","biotype":"miRNA","ncbi_id":"102466729","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57748618,"end":57748682,"strand":-1,"description":"microRNA 6759 [Source:HGNC Symbol;Acc:HGNC:50063]"}, {"versioned_ensembl_gene_id":"ENSG00000264032.1","gene_symbol":"MIR4491","gene_name":"microRNA 4491 [Source:HGNC Symbol;Acc:HGNC:41808]","synonyms":"hsa-mir-4491","biotype":"miRNA","ncbi_id":"100616330","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111347757,"end":111347824,"strand":1,"description":"microRNA 4491 [Source:HGNC Symbol;Acc:HGNC:41808]"}, {"versioned_ensembl_gene_id":"ENSG00000207172.1","gene_symbol":"RNU6-1162P","gene_name":"RNA, U6 small nuclear 1162, pseudogene [Source:HGNC Symbol;Acc:HGNC:48125]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480078","summary":null,"start":63630678,"end":63630781,"strand":1,"description":"RNA, U6 small nuclear 1162, pseudogene [Source:HGNC Symbol;Acc:HGNC:48125]"}, {"versioned_ensembl_gene_id":"ENSG00000206629.1","gene_symbol":"RNU1-63P","gene_name":"RNA, U1 small nuclear 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:48405]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480664","summary":null,"start":67429591,"end":67429754,"strand":-1,"description":"RNA, U1 small nuclear 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:48405]"}, {"versioned_ensembl_gene_id":"ENSG00000283558.1","gene_symbol":"hsa-mir-3158-1","gene_name":"hsa-mir-3158-1 [Source:miRBase;Acc:MI0014186]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":101601417,"end":101601497,"strand":-1,"description":"hsa-mir-3158-1 [Source:miRBase;Acc:MI0014186]"}, {"versioned_ensembl_gene_id":"ENSG00000252735.1","gene_symbol":"RNU6-528P","gene_name":"RNA, U6 small nuclear 528, pseudogene [Source:HGNC Symbol;Acc:HGNC:47491]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479800","summary":null,"start":33338867,"end":33338966,"strand":1,"description":"RNA, U6 small nuclear 528, pseudogene [Source:HGNC Symbol;Acc:HGNC:47491]"}, {"versioned_ensembl_gene_id":"ENSG00000252319.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8720034,"end":8720132,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201912.1","gene_symbol":"RN7SKP189","gene_name":"RNA, 7SK small nuclear pseudogene 189 [Source:HGNC Symbol;Acc:HGNC:45913]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479180","summary":null,"start":145057108,"end":145057437,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 189 [Source:HGNC Symbol;Acc:HGNC:45913]"}, {"versioned_ensembl_gene_id":"ENSG00000274122.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28387160,"end":28387417,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200162.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153607377,"end":153607479,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200163.1","gene_symbol":"SNORD115-18","gene_name":"small nucleolar RNA, C/D box 115-18 [Source:HGNC Symbol;Acc:HGNC:33037]","synonyms":"HBII-52-18","biotype":"snoRNA","ncbi_id":"100033456","summary":null,"start":25203227,"end":25203308,"strand":1,"description":"small nucleolar RNA, C/D box 115-18 [Source:HGNC Symbol;Acc:HGNC:33037]"}, {"versioned_ensembl_gene_id":"ENSG00000276764.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18958147,"end":18958413,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275994.1","gene_symbol":"SNORA24","gene_name":"small nucleolar RNA, H/ACA box 24 [Source:HGNC Symbol;Acc:HGNC:32614]","synonyms":"SNORA24A,ACA24","biotype":"snoRNA","ncbi_id":"677809","summary":null,"start":118279190,"end":118279320,"strand":1,"description":"small nucleolar RNA, H/ACA box 24 [Source:HGNC Symbol;Acc:HGNC:32614]"}, {"versioned_ensembl_gene_id":"ENSG00000277950.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20070716,"end":20070965,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222308.1","gene_symbol":"RNA5SP198","gene_name":"RNA, 5S ribosomal pseudogene 198 [Source:HGNC Symbol;Acc:HGNC:43098]","synonyms":"RN5S198","biotype":"rRNA","ncbi_id":"100873460","summary":null,"start":151875566,"end":151875692,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 198 [Source:HGNC Symbol;Acc:HGNC:43098]"}, {"versioned_ensembl_gene_id":"ENSG00000201965.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38125292,"end":38125394,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252264.1","gene_symbol":"RNU7-153P","gene_name":"RNA, U7 small nuclear 153 pseudogene [Source:HGNC Symbol;Acc:HGNC:45687]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479082","summary":null,"start":14319455,"end":14319516,"strand":1,"description":"RNA, U7 small nuclear 153 pseudogene [Source:HGNC Symbol;Acc:HGNC:45687]"}, {"versioned_ensembl_gene_id":"ENSG00000200121.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":175176493,"end":175176586,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251770.1","gene_symbol":"RNA5SP486","gene_name":"RNA, 5S ribosomal pseudogene 486 [Source:HGNC Symbol;Acc:HGNC:43386]","synonyms":"RN5S486","biotype":"rRNA","ncbi_id":"100873728","summary":null,"start":47873191,"end":47873273,"strand":1,"description":"RNA, 5S ribosomal pseudogene 486 [Source:HGNC Symbol;Acc:HGNC:43386]"}, {"versioned_ensembl_gene_id":"ENSG00000202217.1","gene_symbol":"RN7SKP47","gene_name":"RNA, 7SK small nuclear pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:45771]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481974","summary":null,"start":74799895,"end":74800222,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:45771]"}, {"versioned_ensembl_gene_id":"ENSG00000244748.3","gene_symbol":"RN7SL153P","gene_name":"RNA, 7SL, cytoplasmic 153, pseudogene [Source:HGNC Symbol;Acc:HGNC:46169]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480490","summary":null,"start":72314397,"end":72314688,"strand":-1,"description":"RNA, 7SL, cytoplasmic 153, pseudogene [Source:HGNC Symbol;Acc:HGNC:46169]"}, {"versioned_ensembl_gene_id":"ENSG00000251972.1","gene_symbol":"RNU6-123P","gene_name":"RNA, U6 small nuclear 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:47086]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479620","summary":null,"start":25943044,"end":25943145,"strand":-1,"description":"RNA, U6 small nuclear 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:47086]"}, {"versioned_ensembl_gene_id":"ENSG00000212607.1","gene_symbol":"SNORA3B","gene_name":"small nucleolar RNA, H/ACA box 3B [Source:HGNC Symbol;Acc:HGNC:32638]","synonyms":"ACA3-2,SNORA45B,SNORA45","biotype":"snoRNA","ncbi_id":"677826","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA45, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":8685439,"end":8685569,"strand":1,"description":"small nucleolar RNA, H/ACA box 3B [Source:HGNC Symbol;Acc:HGNC:32638]"}, {"versioned_ensembl_gene_id":"ENSG00000283290.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":24352057,"end":24352157,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207321.1","gene_symbol":"RNU6-160P","gene_name":"RNA, U6 small nuclear 160, pseudogene [Source:HGNC Symbol;Acc:HGNC:47123]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479637","summary":null,"start":153331622,"end":153331728,"strand":1,"description":"RNA, U6 small nuclear 160, pseudogene [Source:HGNC Symbol;Acc:HGNC:47123]"}, {"versioned_ensembl_gene_id":"ENSG00000273541.1","gene_symbol":"DLEU1_2","gene_name":"Deleted in lymphocytic leukemia 1 conserved region 2 [Source:RFAM;Acc:RF02104]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50104833,"end":50105174,"strand":1,"description":"Deleted in lymphocytic leukemia 1 conserved region 2 [Source:RFAM;Acc:RF02104]"}, {"versioned_ensembl_gene_id":"ENSG00000253792.1","gene_symbol":"AC025437.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158173601,"end":158176422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284185.1","gene_symbol":"MIR219A2","gene_name":"microRNA 219a-2 [Source:HGNC Symbol;Acc:HGNC:31598]","synonyms":"MIRN219-2,MIR219-2,hsa-mir-219-2,MIRN219-2,MIR219-2,hsa-mir-219-2","biotype":"miRNA","ncbi_id":"407003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128392618,"end":128392714,"strand":-1,"description":"microRNA 219a-2 [Source:HGNC Symbol;Acc:HGNC:31598]"}, {"versioned_ensembl_gene_id":"ENSG00000263858.1","gene_symbol":"MIR4769","gene_name":"microRNA 4769 [Source:HGNC Symbol;Acc:HGNC:41694]","synonyms":"hsa-mir-4769","biotype":"miRNA","ncbi_id":"100616147","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47587429,"end":47587505,"strand":1,"description":"microRNA 4769 [Source:HGNC Symbol;Acc:HGNC:41694]"}, {"versioned_ensembl_gene_id":"ENSG00000283409.1","gene_symbol":"MIR3662","gene_name":"microRNA 3662 [Source:HGNC Symbol;Acc:HGNC:38983]","synonyms":"hsa-mir-3662","biotype":"miRNA","ncbi_id":"100500880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134979338,"end":134979432,"strand":-1,"description":"microRNA 3662 [Source:HGNC Symbol;Acc:HGNC:38983]"}, {"versioned_ensembl_gene_id":"ENSG00000264357.1","gene_symbol":"MIR4648","gene_name":"microRNA 4648 [Source:HGNC Symbol;Acc:HGNC:41560]","synonyms":"hsa-mir-4648","biotype":"miRNA","ncbi_id":"100616116","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2527074,"end":2527145,"strand":1,"description":"microRNA 4648 [Source:HGNC Symbol;Acc:HGNC:41560]"}, {"versioned_ensembl_gene_id":"ENSG00000264249.1","gene_symbol":"MIR3912","gene_name":"microRNA 3912 [Source:HGNC Symbol;Acc:HGNC:38923]","synonyms":"hsa-mir-3912","biotype":"miRNA","ncbi_id":"100500831","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":171386656,"end":171386760,"strand":-1,"description":"microRNA 3912 [Source:HGNC Symbol;Acc:HGNC:38923]"}, {"versioned_ensembl_gene_id":"ENSG00000239822.3","gene_symbol":"RN7SL754P","gene_name":"RNA, 7SL, cytoplasmic 754, pseudogene [Source:HGNC Symbol;Acc:HGNC:46770]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479497","summary":null,"start":430239,"end":430504,"strand":-1,"description":"RNA, 7SL, cytoplasmic 754, pseudogene [Source:HGNC Symbol;Acc:HGNC:46770]"}, {"versioned_ensembl_gene_id":"ENSG00000274046.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7092616,"end":7092716,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199879.1","gene_symbol":"RNU1-120P","gene_name":"RNA, U1 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:48462]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481627","summary":null,"start":148263476,"end":148263632,"strand":1,"description":"RNA, U1 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:48462]"}, {"versioned_ensembl_gene_id":"ENSG00000221763.1","gene_symbol":"MIR1289-1","gene_name":"microRNA 1289-1 [Source:HGNC Symbol;Acc:HGNC:35281]","synonyms":"MIRN1289-1,hsa-mir-1289-1","biotype":"miRNA","ncbi_id":"100302125","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35453954,"end":35454097,"strand":-1,"description":"microRNA 1289-1 [Source:HGNC Symbol;Acc:HGNC:35281]"}, {"versioned_ensembl_gene_id":"ENSG00000202081.1","gene_symbol":"RNU6-1280P","gene_name":"RNA, U6 small nuclear 1280, pseudogene [Source:HGNC Symbol;Acc:HGNC:48243]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481584","summary":null,"start":85651522,"end":85651628,"strand":-1,"description":"RNA, U6 small nuclear 1280, pseudogene [Source:HGNC Symbol;Acc:HGNC:48243]"}, {"versioned_ensembl_gene_id":"ENSG00000278618.1","gene_symbol":"MIR8069-2","gene_name":"microRNA 8069-2 [Source:HGNC Symbol;Acc:HGNC:50836]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504736","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13724189,"end":13724274,"strand":1,"description":"microRNA 8069-2 [Source:HGNC Symbol;Acc:HGNC:50836]"}, {"versioned_ensembl_gene_id":"ENSG00000264075.1","gene_symbol":"MIR4783","gene_name":"microRNA 4783 [Source:HGNC Symbol;Acc:HGNC:41874]","synonyms":"hsa-mir-4783","biotype":"miRNA","ncbi_id":"100616187","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127423537,"end":127423618,"strand":-1,"description":"microRNA 4783 [Source:HGNC Symbol;Acc:HGNC:41874]"}, {"versioned_ensembl_gene_id":"ENSG00000252076.1","gene_symbol":"RN7SKP196","gene_name":"RNA, 7SK small nuclear pseudogene 196 [Source:HGNC Symbol;Acc:HGNC:45920]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479182","summary":null,"start":58869184,"end":58869528,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 196 [Source:HGNC Symbol;Acc:HGNC:45920]"}, {"versioned_ensembl_gene_id":"ENSG00000263510.1","gene_symbol":"MIR4497","gene_name":"microRNA 4497 [Source:HGNC Symbol;Acc:HGNC:41737]","synonyms":"hsa-mir-4497","biotype":"miRNA","ncbi_id":"100616454","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109833348,"end":109833436,"strand":1,"description":"microRNA 4497 [Source:HGNC Symbol;Acc:HGNC:41737]"}, {"versioned_ensembl_gene_id":"ENSG00000266555.1","gene_symbol":"MIR3145","gene_name":"microRNA 3145 [Source:HGNC Symbol;Acc:HGNC:38327]","synonyms":"hsa-mir-3145","biotype":"miRNA","ncbi_id":"100423001","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":138435213,"end":138435294,"strand":-1,"description":"microRNA 3145 [Source:HGNC Symbol;Acc:HGNC:38327]"}, {"versioned_ensembl_gene_id":"ENSG00000264986.1","gene_symbol":"MIR5092","gene_name":"microRNA 5092 [Source:HGNC Symbol;Acc:HGNC:43467]","synonyms":"hsa-mir-5092","biotype":"miRNA","ncbi_id":"100847039","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":125151465,"end":125151552,"strand":-1,"description":"microRNA 5092 [Source:HGNC Symbol;Acc:HGNC:43467]"}, {"versioned_ensembl_gene_id":"ENSG00000207924.3","gene_symbol":"MIR196A2","gene_name":"microRNA 196a-2 [Source:HGNC Symbol;Acc:HGNC:31568]","synonyms":"MIRN196A2,MIRN196-2,hsa-mir-196a-2,hsa-mir-196-2","biotype":"miRNA","ncbi_id":"406973","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53991738,"end":53991847,"strand":1,"description":"microRNA 196a-2 [Source:HGNC Symbol;Acc:HGNC:31568]"}, {"versioned_ensembl_gene_id":"ENSG00000243015.2","gene_symbol":"RN7SL737P","gene_name":"RNA, 7SL, cytoplasmic 737, pseudogene [Source:HGNC Symbol;Acc:HGNC:46753]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481123","summary":null,"start":93509487,"end":93509768,"strand":1,"description":"RNA, 7SL, cytoplasmic 737, pseudogene [Source:HGNC Symbol;Acc:HGNC:46753]"}, {"versioned_ensembl_gene_id":"ENSG00000202515.1","gene_symbol":"VTRNA1-3","gene_name":"vault RNA 1-3 [Source:HGNC Symbol;Acc:HGNC:12656]","synonyms":"HVG3,hvg-3,vtRNA1-3,VR3,VAULTRC3","biotype":"misc_RNA","ncbi_id":"56662","summary":null,"start":140726158,"end":140726246,"strand":1,"description":"vault RNA 1-3 [Source:HGNC Symbol;Acc:HGNC:12656]"}, {"versioned_ensembl_gene_id":"ENSG00000252305.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":14177131,"end":14177310,"strand":1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000207798.1","gene_symbol":"MIR216A","gene_name":"microRNA 216a [Source:HGNC Symbol;Acc:HGNC:31593]","synonyms":"MIRN216A,MIRN216,hsa-mir-216a,hsa-mir-216","biotype":"miRNA","ncbi_id":"406998","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55988950,"end":55989059,"strand":-1,"description":"microRNA 216a [Source:HGNC Symbol;Acc:HGNC:31593]"}, {"versioned_ensembl_gene_id":"ENSG00000268674.2","gene_symbol":"FAM231D","gene_name":"family with sequence similarity 231 member D [Source:NCBI gene;Acc:644634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644634","summary":null,"start":35407,"end":35916,"strand":1,"description":"family with sequence similarity 231 member D [Source:NCBI gene;Acc:644634]"}, {"versioned_ensembl_gene_id":"ENSG00000264975.1","gene_symbol":"MIR4431","gene_name":"microRNA 4431 [Source:HGNC Symbol;Acc:HGNC:41738]","synonyms":"hsa-mir-4431","biotype":"miRNA","ncbi_id":"100616431","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52702522,"end":52702615,"strand":-1,"description":"microRNA 4431 [Source:HGNC Symbol;Acc:HGNC:41738]"}, {"versioned_ensembl_gene_id":"ENSG00000201216.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":102950467,"end":102950564,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277845.1","gene_symbol":"RN7SKP175","gene_name":"RNA, 7SK small nuclear pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:45899]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479173","summary":null,"start":143542110,"end":143542398,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:45899]"}, {"versioned_ensembl_gene_id":"ENSG00000266663.1","gene_symbol":"MIR3169","gene_name":"microRNA 3169 [Source:HGNC Symbol;Acc:HGNC:38380]","synonyms":"hsa-mir-3169","biotype":"miRNA","ncbi_id":"100422973","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61199798,"end":61199880,"strand":-1,"description":"microRNA 3169 [Source:HGNC Symbol;Acc:HGNC:38380]"}, {"versioned_ensembl_gene_id":"ENSG00000283664.1","gene_symbol":"MIR4679-1","gene_name":"microRNA 4679-1 [Source:HGNC Symbol;Acc:HGNC:41612]","synonyms":"hsa-mir-4679-1","biotype":"miRNA","ncbi_id":"100616128","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89063336,"end":89063410,"strand":1,"description":"microRNA 4679-1 [Source:HGNC Symbol;Acc:HGNC:41612]"}, {"versioned_ensembl_gene_id":"ENSG00000207122.1","gene_symbol":"RNU6-591P","gene_name":"RNA, U6 small nuclear 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:47554]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479827","summary":null,"start":39081180,"end":39081285,"strand":-1,"description":"RNA, U6 small nuclear 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:47554]"}, {"versioned_ensembl_gene_id":"ENSG00000212238.1","gene_symbol":"RNA5SP244","gene_name":"RNA, 5S ribosomal pseudogene 244 [Source:HGNC Symbol;Acc:HGNC:43144]","synonyms":"RN5S244","biotype":"rRNA","ncbi_id":"100885864","summary":null,"start":129756266,"end":129756377,"strand":1,"description":"RNA, 5S ribosomal pseudogene 244 [Source:HGNC Symbol;Acc:HGNC:43144]"}, {"versioned_ensembl_gene_id":"ENSG00000201489.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7537096,"end":7537196,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277994.1","gene_symbol":"HOTAIR_3","gene_name":"HOTAIR conserved region 3 [Source:RFAM;Acc:RF01906]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53965965,"end":53966061,"strand":1,"description":"HOTAIR conserved region 3 [Source:RFAM;Acc:RF01906]"}, {"versioned_ensembl_gene_id":"ENSG00000206917.1","gene_symbol":"RNU1-52P","gene_name":"RNA, U1 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:48394]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480164","summary":null,"start":58677574,"end":58677737,"strand":-1,"description":"RNA, U1 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:48394]"}, {"versioned_ensembl_gene_id":"ENSG00000206722.1","gene_symbol":"RNU6-1074P","gene_name":"RNA, U6 small nuclear 1074, pseudogene [Source:HGNC Symbol;Acc:HGNC:48037]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480635","summary":null,"start":139256657,"end":139256760,"strand":-1,"description":"RNA, U6 small nuclear 1074, pseudogene [Source:HGNC Symbol;Acc:HGNC:48037]"}, {"versioned_ensembl_gene_id":"ENSG00000222950.1","gene_symbol":"RN7SKP262","gene_name":"RNA, 7SK small nuclear pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:45986]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479212","summary":null,"start":25779287,"end":25779569,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:45986]"}, {"versioned_ensembl_gene_id":"ENSG00000244677.3","gene_symbol":"RN7SL706P","gene_name":"RNA, 7SL, cytoplasmic 706, pseudogene [Source:HGNC Symbol;Acc:HGNC:46722]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479480","summary":null,"start":68149617,"end":68149908,"strand":-1,"description":"RNA, 7SL, cytoplasmic 706, pseudogene [Source:HGNC Symbol;Acc:HGNC:46722]"}, {"versioned_ensembl_gene_id":"ENSG00000277922.1","gene_symbol":"FTX_5","gene_name":"FTX transcript, XIST regulator conserved region 5 [Source:RFAM;Acc:RF02122]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74293357,"end":74293574,"strand":1,"description":"FTX transcript, XIST regulator conserved region 5 [Source:RFAM;Acc:RF02122]"}, {"versioned_ensembl_gene_id":"ENSG00000222154.1","gene_symbol":"RN7SKP218","gene_name":"RNA, 7SK small nuclear pseudogene 218 [Source:HGNC Symbol;Acc:HGNC:45942]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480900","summary":null,"start":53490148,"end":53490439,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 218 [Source:HGNC Symbol;Acc:HGNC:45942]"}, {"versioned_ensembl_gene_id":"ENSG00000277752.1","gene_symbol":"DLEU2_5","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 5 [Source:RFAM;Acc:RF02109]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50075570,"end":50075653,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 5 [Source:RFAM;Acc:RF02109]"}, {"versioned_ensembl_gene_id":"ENSG00000276253.1","gene_symbol":"AC243790.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30361040,"end":30361438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221216.1","gene_symbol":"RNU6ATAC27P","gene_name":"RNA, U6atac small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:46926]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481167","summary":null,"start":28481362,"end":28481480,"strand":1,"description":"RNA, U6atac small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:46926]"}, {"versioned_ensembl_gene_id":"ENSG00000200831.1","gene_symbol":"SNORD36B","gene_name":"small nucleolar RNA, C/D box 36B [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000201980.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"E2-1,RNU108,E2,RNE2","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":4756645,"end":4756797,"strand":1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000251756.1","gene_symbol":"RNA5SP385","gene_name":"RNA, 5S ribosomal pseudogene 385 [Source:HGNC Symbol;Acc:HGNC:43285]","synonyms":"RN5S385","biotype":"rRNA","ncbi_id":"100873640","summary":null,"start":51692752,"end":51692861,"strand":1,"description":"RNA, 5S ribosomal pseudogene 385 [Source:HGNC Symbol;Acc:HGNC:43285]"}, {"versioned_ensembl_gene_id":"ENSG00000244307.3","gene_symbol":"RN7SL395P","gene_name":"RNA, 7SL, cytoplasmic 395, pseudogene [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93483936,"end":93484019,"strand":-1,"description":"microRNA 489 [Source:HGNC Symbol;Acc:HGNC:32074]"}, {"versioned_ensembl_gene_id":"ENSG00000198995.3","gene_symbol":"MIR340","gene_name":"microRNA 340 [Source:HGNC Symbol;Acc:HGNC:31777]","synonyms":"MIRN340,hsa-mir-340","biotype":"miRNA","ncbi_id":"442908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":180015303,"end":180015397,"strand":-1,"description":"microRNA 340 [Source:HGNC Symbol;Acc:HGNC:31777]"}, {"versioned_ensembl_gene_id":"ENSG00000201511.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101647421,"end":101647522,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207428.1","gene_symbol":"RNU6-95P","gene_name":"RNA, U6 small nuclear 95, pseudogene [Source:HGNC Symbol;Acc:HGNC:47058]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479608","summary":null,"start":68003895,"end":68004001,"strand":1,"description":"RNA, U6 small nuclear 95, pseudogene [Source:HGNC Symbol;Acc:HGNC:47058]"}, {"versioned_ensembl_gene_id":"ENSG00000216058.1","gene_symbol":"MIR944","gene_name":"microRNA 944 [Source:HGNC Symbol;Acc:HGNC:33690]","synonyms":"MIRN944,hsa-mir-944","biotype":"miRNA","ncbi_id":"100126340","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":189829922,"end":189830009,"strand":1,"description":"microRNA 944 [Source:HGNC Symbol;Acc:HGNC:33690]"}, {"versioned_ensembl_gene_id":"ENSG00000273818.1","gene_symbol":"RN7SL673P","gene_name":"RNA, 7SL, cytoplasmic 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:46689]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480525","summary":null,"start":30091662,"end":30091898,"strand":1,"description":"RNA, 7SL, cytoplasmic 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:46689]"}, {"versioned_ensembl_gene_id":"ENSG00000207041.1","gene_symbol":"RNU6-3P","gene_name":"RNA, U6 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:34275]","synonyms":"U6-3,RNU6-3","biotype":"snRNA","ncbi_id":"106478919","summary":null,"start":141118030,"end":141118136,"strand":-1,"description":"RNA, U6 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:34275]"}, {"versioned_ensembl_gene_id":"ENSG00000201223.1","gene_symbol":"RNU6-1305P","gene_name":"RNA, U6 small nuclear 1305, pseudogene [Source:HGNC Symbol;Acc:HGNC:48268]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481592","summary":null,"start":36155119,"end":36155222,"strand":1,"description":"RNA, U6 small nuclear 1305, pseudogene [Source:HGNC Symbol;Acc:HGNC:48268]"}, {"versioned_ensembl_gene_id":"ENSG00000253287.1","gene_symbol":"AC104012.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71779605,"end":71792875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284448.1","gene_symbol":"MIR6501","gene_name":"microRNA 6501 [Source:HGNC Symbol;Acc:HGNC:50033]","synonyms":"hsa-mir-6501","biotype":"miRNA","ncbi_id":"102465248","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33550662,"end":33550728,"strand":1,"description":"microRNA 6501 [Source:HGNC Symbol;Acc:HGNC:50033]"}, {"versioned_ensembl_gene_id":"ENSG00000199832.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":107202577,"end":107202683,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275458.1","gene_symbol":"MIR6809","gene_name":"microRNA 6809 [Source:HGNC Symbol;Acc:HGNC:49926]","synonyms":"hsa-mir-6809","biotype":"miRNA","ncbi_id":"102465485","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":217900513,"end":217900628,"strand":-1,"description":"microRNA 6809 [Source:HGNC Symbol;Acc:HGNC:49926]"}, {"versioned_ensembl_gene_id":"ENSG00000273752.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54855316,"end":54855422,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000284067.1","gene_symbol":"MIR6837","gene_name":"microRNA 6837 [Source:HGNC Symbol;Acc:HGNC:50125]","synonyms":"hsa-mir-6837","biotype":"miRNA","ncbi_id":"102466985","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44051766,"end":44051829,"strand":1,"description":"microRNA 6837 [Source:HGNC Symbol;Acc:HGNC:50125]"}, {"versioned_ensembl_gene_id":"ENSG00000200455.1","gene_symbol":"RNU6-1112P","gene_name":"RNA, U6 small nuclear 1112, pseudogene [Source:HGNC Symbol;Acc:HGNC:48075]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480055","summary":null,"start":40077884,"end":40077982,"strand":1,"description":"RNA, U6 small nuclear 1112, pseudogene [Source:HGNC Symbol;Acc:HGNC:48075]"}, {"versioned_ensembl_gene_id":"ENSG00000221288.1","gene_symbol":"MIR663B","gene_name":"microRNA 663b [Source:HGNC Symbol;Acc:HGNC:35270]","synonyms":"MIRN663B,hsa-mir-663b","biotype":"miRNA","ncbi_id":"100313824","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132256966,"end":132257080,"strand":-1,"description":"microRNA 663b [Source:HGNC Symbol;Acc:HGNC:35270]"}, {"versioned_ensembl_gene_id":"ENSG00000207645.2","gene_symbol":"MIR512-1","gene_name":"microRNA 512-1 [Source:HGNC Symbol;Acc:HGNC:32090]","synonyms":"hsa-mir-512-1,MIRN512-1","biotype":"miRNA","ncbi_id":"574458","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53666679,"end":53666762,"strand":1,"description":"microRNA 512-1 [Source:HGNC Symbol;Acc:HGNC:32090]"}, {"versioned_ensembl_gene_id":"ENSG00000199047.3","gene_symbol":"MIR378A","gene_name":"microRNA 378a [Source:HGNC Symbol;Acc:HGNC:31871]","synonyms":"hsa-mir-378,MIRN378,MIR378","biotype":"miRNA","ncbi_id":"494327","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149732825,"end":149732890,"strand":1,"description":"microRNA 378a [Source:HGNC Symbol;Acc:HGNC:31871]"}, {"versioned_ensembl_gene_id":"ENSG00000199792.1","gene_symbol":"RNU6-1233P","gene_name":"RNA, U6 small nuclear 1233, pseudogene [Source:HGNC Symbol;Acc:HGNC:48196]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481569","summary":null,"start":175397247,"end":175397348,"strand":-1,"description":"RNA, U6 small nuclear 1233, pseudogene [Source:HGNC Symbol;Acc:HGNC:48196]"}, {"versioned_ensembl_gene_id":"ENSG00000236360.2","gene_symbol":"AL445183.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52993201,"end":52993702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274390.1","gene_symbol":"MIR6885","gene_name":"microRNA 6885 [Source:HGNC Symbol;Acc:HGNC:50221]","synonyms":"hsa-mir-6885","biotype":"miRNA","ncbi_id":"102465533","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6389638,"end":6389703,"strand":-1,"description":"microRNA 6885 [Source:HGNC Symbol;Acc:HGNC:50221]"}, {"versioned_ensembl_gene_id":"ENSG00000238562.1","gene_symbol":"RNU7-159P","gene_name":"RNA, U7 small nuclear 159 pseudogene [Source:HGNC Symbol;Acc:HGNC:45693]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481747","summary":null,"start":102903892,"end":102903953,"strand":-1,"description":"RNA, U7 small nuclear 159 pseudogene [Source:HGNC Symbol;Acc:HGNC:45693]"}, {"versioned_ensembl_gene_id":"ENSG00000264233.1","gene_symbol":"MIR4456","gene_name":"microRNA 4456 [Source:HGNC Symbol;Acc:HGNC:41606]","synonyms":"hsa-mir-4456","biotype":"miRNA","ncbi_id":"100616381","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":535840,"end":535882,"strand":-1,"description":"microRNA 4456 [Source:HGNC Symbol;Acc:HGNC:41606]"}, {"versioned_ensembl_gene_id":"ENSG00000266146.1","gene_symbol":"MIR5190","gene_name":"microRNA 5190 [Source:HGNC Symbol;Acc:HGNC:43549]","synonyms":"hsa-mir-5190","biotype":"miRNA","ncbi_id":"100847080","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13459947,"end":13460026,"strand":1,"description":"microRNA 5190 [Source:HGNC Symbol;Acc:HGNC:43549]"}, {"versioned_ensembl_gene_id":"ENSG00000263955.2","gene_symbol":"RN7SL850P","gene_name":"RNA, 7SL, cytoplasmic 850, pseudogene [Source:HGNC Symbol;Acc:HGNC:46866]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479532","summary":null,"start":4633591,"end":4633881,"strand":-1,"description":"RNA, 7SL, cytoplasmic 850, pseudogene [Source:HGNC Symbol;Acc:HGNC:46866]"}, {"versioned_ensembl_gene_id":"ENSG00000212624.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":51724775,"end":51724896,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000278250.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":120018900,"end":120019261,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283744.1","gene_symbol":"MIR6755","gene_name":"microRNA 6755 [Source:HGNC Symbol;Acc:HGNC:50224]","synonyms":"hsa-mir-6755","biotype":"miRNA","ncbi_id":"102465452","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86278333,"end":86278398,"strand":1,"description":"microRNA 6755 [Source:HGNC Symbol;Acc:HGNC:50224]"}, {"versioned_ensembl_gene_id":"ENSG00000266439.2","gene_symbol":"RN7SL493P","gene_name":"RNA, 7SL, cytoplasmic 493, pseudogene [Source:HGNC Symbol;Acc:HGNC:46509]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479403","summary":null,"start":10221775,"end":10222073,"strand":-1,"description":"RNA, 7SL, cytoplasmic 493, pseudogene [Source:HGNC Symbol;Acc:HGNC:46509]"}, {"versioned_ensembl_gene_id":"ENSG00000263912.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30743271,"end":30743522,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000274284.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38231043,"end":38231144,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000262579.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":69175662,"end":69175768,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000276222.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46226740,"end":46226841,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201415.1","gene_symbol":"RNA5SP204","gene_name":"RNA, 5S ribosomal pseudogene 204 [Source:HGNC Symbol;Acc:HGNC:43104]","synonyms":"RN5S204","biotype":"rRNA","ncbi_id":"100873465","summary":null,"start":17721786,"end":17721903,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 204 [Source:HGNC Symbol;Acc:HGNC:43104]"}, {"versioned_ensembl_gene_id":"ENSG00000263908.1","gene_symbol":"MIR3116-1","gene_name":"microRNA 3116-1 [Source:HGNC Symbol;Acc:HGNC:38200]","synonyms":"hsa-mir-3116-1","biotype":"miRNA","ncbi_id":"100422902","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62078786,"end":62078859,"strand":1,"description":"microRNA 3116-1 [Source:HGNC Symbol;Acc:HGNC:38200]"}, {"versioned_ensembl_gene_id":"ENSG00000266203.1","gene_symbol":"MIR5585","gene_name":"microRNA 5585 [Source:HGNC Symbol;Acc:HGNC:43452]","synonyms":"hsa-mir-5585","biotype":"miRNA","ncbi_id":"100847018","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32086949,"end":32087007,"strand":1,"description":"microRNA 5585 [Source:HGNC Symbol;Acc:HGNC:43452]"}, {"versioned_ensembl_gene_id":"ENSG00000206911.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93827622,"end":93827734,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278124.1","gene_symbol":"RN7SL186P","gene_name":"RNA, 7SL, cytoplasmic 186, pseudogene [Source:HGNC Symbol;Acc:HGNC:46202]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480972","summary":null,"start":22010650,"end":22010946,"strand":1,"description":"RNA, 7SL, cytoplasmic 186, pseudogene [Source:HGNC Symbol;Acc:HGNC:46202]"}, {"versioned_ensembl_gene_id":"ENSG00000199469.1","gene_symbol":"RNU1-62P","gene_name":"RNA, U1 small nuclear 62, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000199934.1","gene_symbol":"SNORD81","gene_name":"Small nucleolar RNA SNORD81 [Source:RFAM;Acc:RF00136]","synonyms":null,"biotype":"snoRNA","ncbi_id":"26769","summary":null,"start":85592280,"end":85592356,"strand":1,"description":"Small nucleolar RNA SNORD81 [Source:RFAM;Acc:RF00136]"}, {"versioned_ensembl_gene_id":"ENSG00000201710.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":100979992,"end":100980066,"strand":1,"description":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]"}, {"versioned_ensembl_gene_id":"ENSG00000243900.3","gene_symbol":"RN7SL320P","gene_name":"RNA, 7SL, cytoplasmic 320, pseudogene [Source:HGNC Symbol;Acc:HGNC:46336]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481010","summary":null,"start":51469753,"end":51470047,"strand":1,"description":"RNA, 7SL, cytoplasmic 320, pseudogene [Source:HGNC Symbol;Acc:HGNC:46336]"}, {"versioned_ensembl_gene_id":"ENSG00000276918.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66374138,"end":66374435,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277653.1","gene_symbol":"CDKN2B-AS","gene_name":"CDKN2B antisense RNA 1 intronic convserved region [Source:RFAM;Acc:RF01909]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22117665,"end":22117814,"strand":1,"description":"CDKN2B antisense RNA 1 intronic convserved region [Source:RFAM;Acc:RF01909]"}, {"versioned_ensembl_gene_id":"ENSG00000251705.1","gene_symbol":"RNA5-8SP6","gene_name":"RNA, 5.8S ribosomal pseudogene 6 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000272075.2","gene_symbol":"RN7SL828P","gene_name":"RNA, 7SL, cytoplasmic 828, pseudogene [Source:HGNC Symbol;Acc:HGNC:46844]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481147","summary":null,"start":118067237,"end":118067539,"strand":1,"description":"RNA, 7SL, cytoplasmic 828, pseudogene [Source:HGNC Symbol;Acc:HGNC:46844]"}, {"versioned_ensembl_gene_id":"ENSG00000277542.1","gene_symbol":"HOXB13-AS1_2","gene_name":"HOXB13 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02133]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48723692,"end":48723772,"strand":1,"description":"HOXB13 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02133]"}, {"versioned_ensembl_gene_id":"ENSG00000278123.1","gene_symbol":"SNORD116-28","gene_name":"small nucleolar RNA, C/D box 116-28 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000244512.3","gene_symbol":"RN7SL28P","gene_name":"RNA, 7SL, cytoplasmic 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46044]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480929","summary":null,"start":184278936,"end":184279233,"strand":1,"description":"RNA, 7SL, cytoplasmic 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46044]"}, {"versioned_ensembl_gene_id":"ENSG00000203573.4","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40585454,"end":40585751,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212579.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 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{"versioned_ensembl_gene_id":"ENSG00000273642.1","gene_symbol":"AC012314.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251859.1","gene_symbol":"RNU6-1288P","gene_name":"RNA, U6 small nuclear 1288, pseudogene [Source:HGNC Symbol;Acc:HGNC:48251]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480128","summary":null,"start":14274622,"end":14274725,"strand":-1,"description":"RNA, U6 small nuclear 1288, pseudogene [Source:HGNC Symbol;Acc:HGNC:48251]"}, {"versioned_ensembl_gene_id":"ENSG00000284317.1","gene_symbol":"MIR7114","gene_name":"microRNA 7114 [Source:HGNC Symbol;Acc:HGNC:50157]","synonyms":"hsa-mir-7114","biotype":"miRNA","ncbi_id":"102466223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":137450026,"end":137450086,"strand":-1,"description":"microRNA 7114 [Source:HGNC Symbol;Acc:HGNC:50157]"}, {"versioned_ensembl_gene_id":"ENSG00000252426.1","gene_symbol":"RNU1-107P","gene_name":"RNA, U1 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48449]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480186","summary":null,"start":25723342,"end":25723495,"strand":1,"description":"RNA, U1 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48449]"}, {"versioned_ensembl_gene_id":"ENSG00000207380.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":5964538,"end":5964650,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201325.1","gene_symbol":"RNA5SP142","gene_name":"RNA, 5S ribosomal pseudogene 142 [Source:HGNC Symbol;Acc:HGNC:43042]","synonyms":"RN5S142","biotype":"rRNA","ncbi_id":"100873409","summary":null,"start":137518134,"end":137518255,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 142 [Source:HGNC Symbol;Acc:HGNC:43042]"}, {"versioned_ensembl_gene_id":"ENSG00000221275.1","gene_symbol":"MIR548I2","gene_name":"microRNA 548i-2 [Source:HGNC Symbol;Acc:HGNC:35353]","synonyms":"MIRN548I2,hsa-mir-548i-2","biotype":"miRNA","ncbi_id":"100302277","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9556168,"end":9556316,"strand":-1,"description":"microRNA 548i-2 [Source:HGNC Symbol;Acc:HGNC:35353]"}, {"versioned_ensembl_gene_id":"ENSG00000252468.1","gene_symbol":"RNU2-57P","gene_name":"RNA, U2 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:48550]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480222","summary":null,"start":5019076,"end":5019266,"strand":1,"description":"RNA, U2 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:48550]"}, {"versioned_ensembl_gene_id":"ENSG00000266780.1","gene_symbol":"MIR4444-2","gene_name":"microRNA 4444-2 [Source:HGNC Symbol;Acc:HGNC:43481]","synonyms":"hsa-mir-4444-2","biotype":"miRNA","ncbi_id":"100846999","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75214476,"end":75214549,"strand":1,"description":"microRNA 4444-2 [Source:HGNC Symbol;Acc:HGNC:43481]"}, {"versioned_ensembl_gene_id":"ENSG00000275708.1","gene_symbol":"MIR3648-1","gene_name":"microRNA 3648-1 [Source:HGNC Symbol;Acc:HGNC:38941]","synonyms":"MIR3648,hsa-mir-3648","biotype":"miRNA","ncbi_id":"100500862","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8208473,"end":8208652,"strand":1,"description":"microRNA 3648-1 [Source:HGNC Symbol;Acc:HGNC:38941]"}, {"versioned_ensembl_gene_id":"ENSG00000199350.1","gene_symbol":"RNA5SP432","gene_name":"RNA, 5S ribosomal pseudogene 432 [Source:HGNC Symbol;Acc:HGNC:43332]","synonyms":"RN5S432","biotype":"rRNA","ncbi_id":"100873682","summary":null,"start":84039918,"end":84040033,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 432 [Source:HGNC Symbol;Acc:HGNC:43332]"}, {"versioned_ensembl_gene_id":"ENSG00000252699.1","gene_symbol":"SNORA21B","gene_name":"small nucleolar RNA, H/ACA box 21B [Source:HGNC Symbol;Acc:HGNC:52195]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617002","summary":null,"start":38851524,"end":38851659,"strand":-1,"description":"small nucleolar RNA, H/ACA box 21B [Source:HGNC Symbol;Acc:HGNC:52195]"}, {"versioned_ensembl_gene_id":"ENSG00000221628.1","gene_symbol":"MIR1302-4","gene_name":"microRNA 1302-4 [Source:HGNC Symbol;Acc:HGNC:35296]","synonyms":"MIRN1302-4,hsa-mir-1302-4","biotype":"miRNA","ncbi_id":"100302130","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207269275,"end":207269424,"strand":-1,"description":"microRNA 1302-4 [Source:HGNC Symbol;Acc:HGNC:35296]"}, {"versioned_ensembl_gene_id":"ENSG00000207513.1","gene_symbol":"RNU1-3","gene_name":"RNA, U1 small nuclear 3 [Source:HGNC Symbol;Acc:HGNC:10130]","synonyms":"HSD4,RNU1G3","biotype":"snRNA","ncbi_id":"26869","summary":null,"start":16666785,"end":16666948,"strand":-1,"description":"RNA, U1 small nuclear 3 [Source:HGNC Symbol;Acc:HGNC:10130]"}, {"versioned_ensembl_gene_id":"ENSG00000207653.1","gene_symbol":"MIR558","gene_name":"microRNA 558 [Source:HGNC Symbol;Acc:HGNC:32814]","synonyms":"MIRN558,hsa-mir-558","biotype":"miRNA","ncbi_id":"693143","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32532153,"end":32532246,"strand":1,"description":"microRNA 558 [Source:HGNC Symbol;Acc:HGNC:32814]"}, {"versioned_ensembl_gene_id":"ENSG00000201377.1","gene_symbol":"RNY4P23","gene_name":"RNA, Ro-associated Y4 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42473]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873801","summary":null,"start":70396279,"end":70396375,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42473]"}, {"versioned_ensembl_gene_id":"ENSG00000277887.1","gene_symbol":"SNORA50C","gene_name":"small nucleolar RNA, H/ACA box 50C [Source:HGNC Symbol;Acc:HGNC:32662]","synonyms":"SNORA76C,SNORA76,ACA62","biotype":"snoRNA","ncbi_id":"677842","summary":null,"start":64146339,"end":64146471,"strand":1,"description":"small nucleolar RNA, H/ACA box 50C [Source:HGNC Symbol;Acc:HGNC:32662]"}, {"versioned_ensembl_gene_id":"ENSG00000221548.1","gene_symbol":"MIR1283-2","gene_name":"microRNA 1283-2 [Source:HGNC Symbol;Acc:HGNC:35361]","synonyms":"MIRN1283-2,hsa-mir-1283-2","biotype":"miRNA","ncbi_id":"100302205","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53758232,"end":53758318,"strand":1,"description":"microRNA 1283-2 [Source:HGNC Symbol;Acc:HGNC:35361]"}, {"versioned_ensembl_gene_id":"ENSG00000284361.1","gene_symbol":"MIR4745","gene_name":"microRNA 4745 [Source:HGNC Symbol;Acc:HGNC:41868]","synonyms":"hsa-mir-4745","biotype":"miRNA","ncbi_id":"100616459","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":804940,"end":805001,"strand":1,"description":"microRNA 4745 [Source:HGNC Symbol;Acc:HGNC:41868]"}, {"versioned_ensembl_gene_id":"ENSG00000207031.1","gene_symbol":"SNORD59A","gene_name":"small nucleolar RNA, C/D box 59A [Source:HGNC Symbol;Acc:HGNC:10210]","synonyms":"U59,RNU59","biotype":"snoRNA","ncbi_id":"26789","summary":null,"start":56645027,"end":56645101,"strand":-1,"description":"small nucleolar RNA, C/D box 59A [Source:HGNC Symbol;Acc:HGNC:10210]"}, {"versioned_ensembl_gene_id":"ENSG00000207378.1","gene_symbol":"RNU6-748P","gene_name":"RNA, U6 small nuclear 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:47711]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481416","summary":null,"start":98462944,"end":98463050,"strand":-1,"description":"RNA, U6 small nuclear 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:47711]"}, {"versioned_ensembl_gene_id":"ENSG00000201287.1","gene_symbol":"RN7SKP171","gene_name":"RNA, 7SK small nuclear pseudogene 171 [Source:HGNC Symbol;Acc:HGNC:45895]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480887","summary":null,"start":37661747,"end":37662049,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 171 [Source:HGNC Symbol;Acc:HGNC:45895]"}, {"versioned_ensembl_gene_id":"ENSG00000274655.1","gene_symbol":"XIST_intron","gene_name":"XIST 3' intron conserved motif [Source:RFAM;Acc:RF02266]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73821657,"end":73821724,"strand":-1,"description":"XIST 3' intron conserved motif [Source:RFAM;Acc:RF02266]"}, {"versioned_ensembl_gene_id":"ENSG00000283172.1","gene_symbol":"hsa-mir-548d-1","gene_name":"hsa-mir-548d-1 [Source:miRBase;Acc:MI0003668]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":123348034,"end":123348130,"strand":-1,"description":"hsa-mir-548d-1 [Source:miRBase;Acc:MI0003668]"}, {"versioned_ensembl_gene_id":"ENSG00000202542.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48325558,"end":48325671,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265635.1","gene_symbol":"MIR3612","gene_name":"microRNA 3612 [Source:HGNC Symbol;Acc:HGNC:38951]","synonyms":"hsa-mir-3612","biotype":"miRNA","ncbi_id":"100500817","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128294092,"end":128294178,"strand":1,"description":"microRNA 3612 [Source:HGNC Symbol;Acc:HGNC:38951]"}, {"versioned_ensembl_gene_id":"ENSG00000253005.1","gene_symbol":"RNU6-176P","gene_name":"RNA, U6 small nuclear 176, pseudogene [Source:HGNC Symbol;Acc:HGNC:47139]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479644","summary":null,"start":28142737,"end":28142841,"strand":-1,"description":"RNA, U6 small nuclear 176, pseudogene [Source:HGNC Symbol;Acc:HGNC:47139]"}, {"versioned_ensembl_gene_id":"ENSG00000276622.1","gene_symbol":"MIR6499","gene_name":"microRNA 6499 [Source:HGNC Symbol;Acc:HGNC:49962]","synonyms":"hsa-mir-6499","biotype":"miRNA","ncbi_id":"102465246","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151522087,"end":151522148,"strand":-1,"description":"microRNA 6499 [Source:HGNC Symbol;Acc:HGNC:49962]"}, {"versioned_ensembl_gene_id":"ENSG00000239041.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":172691299,"end":172691402,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000265345.1","gene_symbol":"MIR5188","gene_name":"microRNA 5188 [Source:HGNC Symbol;Acc:HGNC:43502]","synonyms":"hsa-mir-5188","biotype":"miRNA","ncbi_id":"100847004","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124915547,"end":124915659,"strand":1,"description":"microRNA 5188 [Source:HGNC Symbol;Acc:HGNC:43502]"}, {"versioned_ensembl_gene_id":"ENSG00000276220.1","gene_symbol":"AC012314.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212450.1","gene_symbol":"RNU6-241P","gene_name":"RNA, U6 small nuclear 241, pseudogene [Source:HGNC Symbol;Acc:HGNC:47204]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479674","summary":null,"start":45789585,"end":45789688,"strand":1,"description":"RNA, U6 small nuclear 241, pseudogene [Source:HGNC Symbol;Acc:HGNC:47204]"}, {"versioned_ensembl_gene_id":"ENSG00000276507.1","gene_symbol":"AC068944.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29010619,"end":29011021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265357.1","gene_symbol":"MIR4493","gene_name":"microRNA 4493 [Source:HGNC Symbol;Acc:HGNC:41778]","synonyms":"hsa-mir-4493","biotype":"miRNA","ncbi_id":"100616319","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123381440,"end":123381512,"strand":-1,"description":"microRNA 4493 [Source:HGNC Symbol;Acc:HGNC:41778]"}, {"versioned_ensembl_gene_id":"ENSG00000253065.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":168033091,"end":168033205,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000272036.1","gene_symbol":"MIR139","gene_name":"microRNA 139 [Source:HGNC Symbol;Acc:HGNC:31526]","synonyms":"MIRN139,hsa-mir-139","biotype":"miRNA","ncbi_id":"406931","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72615063,"end":72615130,"strand":-1,"description":"microRNA 139 [Source:HGNC Symbol;Acc:HGNC:31526]"}, {"versioned_ensembl_gene_id":"ENSG00000207133.1","gene_symbol":"SNORD116-7","gene_name":"small nucleolar RNA, C/D box 116-7 [Source:HGNC Symbol;Acc:HGNC:33073]","synonyms":"HBII-85-7","biotype":"snoRNA","ncbi_id":"100033419","summary":null,"start":25067788,"end":25067882,"strand":1,"description":"small nucleolar RNA, C/D box 116-7 [Source:HGNC Symbol;Acc:HGNC:33073]"}, {"versioned_ensembl_gene_id":"ENSG00000223305.1","gene_symbol":"RN7SKP30","gene_name":"RNA, 7SK small nuclear pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:45754]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479108","summary":null,"start":55540502,"end":55540835,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:45754]"}, {"versioned_ensembl_gene_id":"ENSG00000266666.1","gene_symbol":"MIR4325","gene_name":"microRNA 4325 [Source:HGNC Symbol;Acc:HGNC:38304]","synonyms":"hsa-mir-4325","biotype":"miRNA","ncbi_id":"100422883","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57321502,"end":57321591,"strand":-1,"description":"microRNA 4325 [Source:HGNC Symbol;Acc:HGNC:38304]"}, {"versioned_ensembl_gene_id":"ENSG00000264559.1","gene_symbol":"MIR3162","gene_name":"microRNA 3162 [Source:HGNC Symbol;Acc:HGNC:38271]","synonyms":"hsa-mir-3162","biotype":"miRNA","ncbi_id":"100422880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59595077,"end":59595158,"strand":-1,"description":"microRNA 3162 [Source:HGNC Symbol;Acc:HGNC:38271]"}, {"versioned_ensembl_gene_id":"ENSG00000199575.1","gene_symbol":"SNORD114-1","gene_name":"small nucleolar RNA, C/D box 114-1 [Source:HGNC Symbol;Acc:HGNC:32989]","synonyms":"14q(II-1)","biotype":"snoRNA","ncbi_id":"767577","summary":"Small nucleolar RNAs (snoRNAs), like SNORD114-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD114-1 is 1 of 31 tandem SNORD114 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":100949833,"end":100949904,"strand":1,"description":"small nucleolar RNA, C/D box 114-1 [Source:HGNC Symbol;Acc:HGNC:32989]"}, {"versioned_ensembl_gene_id":"ENSG00000261867.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":101205448,"end":101205554,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000212520.1","gene_symbol":"RNU6-1250P","gene_name":"RNA, U6 small nuclear 1250, pseudogene [Source:HGNC Symbol;Acc:HGNC:48213]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481575","summary":null,"start":67808502,"end":67808608,"strand":1,"description":"RNA, U6 small nuclear 1250, pseudogene [Source:HGNC Symbol;Acc:HGNC:48213]"}, {"versioned_ensembl_gene_id":"ENSG00000199065.3","gene_symbol":"MIR101-2","gene_name":"microRNA 101-2 [Source:HGNC Symbol;Acc:HGNC:31489]","synonyms":"hsa-mir-101-2,MIRN101-2","biotype":"miRNA","ncbi_id":"406894","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4850297,"end":4850375,"strand":1,"description":"microRNA 101-2 [Source:HGNC Symbol;Acc:HGNC:31489]"}, {"versioned_ensembl_gene_id":"ENSG00000212133.1","gene_symbol":"RNU6-1168P","gene_name":"RNA, U6 small nuclear 1168, pseudogene [Source:HGNC Symbol;Acc:HGNC:48131]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481548","summary":null,"start":88383494,"end":88383597,"strand":-1,"description":"RNA, U6 small nuclear 1168, pseudogene [Source:HGNC Symbol;Acc:HGNC:48131]"}, {"versioned_ensembl_gene_id":"ENSG00000200427.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85777639,"end":85777755,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265331.1","gene_symbol":"MIR4524B","gene_name":"microRNA 4524b [Source:HGNC Symbol;Acc:HGNC:43520]","synonyms":"hsa-mir-4524b","biotype":"miRNA","ncbi_id":"100847008","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69099542,"end":69099656,"strand":1,"description":"microRNA 4524b [Source:HGNC Symbol;Acc:HGNC:43520]"}, {"versioned_ensembl_gene_id":"ENSG00000277202.1","gene_symbol":"MIR8063","gene_name":"microRNA 8063 [Source:HGNC Symbol;Acc:HGNC:50088]","synonyms":"hsa-mir-8063","biotype":"miRNA","ncbi_id":"102466875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36972821,"end":36972901,"strand":-1,"description":"microRNA 8063 [Source:HGNC Symbol;Acc:HGNC:50088]"}, {"versioned_ensembl_gene_id":"ENSG00000200737.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97421195,"end":97421307,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264500.1","gene_symbol":"MIR3124","gene_name":"microRNA 3124 [Source:HGNC Symbol;Acc:HGNC:38262]","synonyms":"hsa-mir-3124","biotype":"miRNA","ncbi_id":"100422879","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":248826377,"end":248826443,"strand":1,"description":"microRNA 3124 [Source:HGNC Symbol;Acc:HGNC:38262]"}, {"versioned_ensembl_gene_id":"ENSG00000276640.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30136615,"end":30136690,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000241552.3","gene_symbol":"RN7SL58P","gene_name":"RNA, 7SL, cytoplasmic 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:46074]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479245","summary":null,"start":18547312,"end":18547605,"strand":1,"description":"RNA, 7SL, cytoplasmic 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:46074]"}, {"versioned_ensembl_gene_id":"ENSG00000225091.3","gene_symbol":"SNORA71A","gene_name":"small nucleolar RNA, H/ACA box 71A [Source:HGNC Symbol;Acc:HGNC:10232]","synonyms":"U71a,RNU71A","biotype":"snoRNA","ncbi_id":"26777","summary":null,"start":38427309,"end":38427442,"strand":-1,"description":"small nucleolar RNA, H/ACA box 71A [Source:HGNC Symbol;Acc:HGNC:10232]"}, {"versioned_ensembl_gene_id":"ENSG00000265932.1","gene_symbol":"MIR3146","gene_name":"microRNA 3146 [Source:HGNC Symbol;Acc:HGNC:38368]","synonyms":"hsa-mir-3146","biotype":"miRNA","ncbi_id":"100422967","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19705358,"end":19705436,"strand":-1,"description":"microRNA 3146 [Source:HGNC Symbol;Acc:HGNC:38368]"}, {"versioned_ensembl_gene_id":"ENSG00000207607.3","gene_symbol":"MIR200A","gene_name":"microRNA 200a [Source:HGNC Symbol;Acc:HGNC:31578]","synonyms":"MIRN200A,hsa-mir-200a","biotype":"miRNA","ncbi_id":"406983","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1167863,"end":1167952,"strand":1,"description":"microRNA 200a [Source:HGNC Symbol;Acc:HGNC:31578]"}, {"versioned_ensembl_gene_id":"ENSG00000243125.3","gene_symbol":"RN7SL807P","gene_name":"RNA, 7SL, cytoplasmic 807, pseudogene [Source:HGNC Symbol;Acc:HGNC:46823]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481141","summary":null,"start":223248498,"end":223248794,"strand":-1,"description":"RNA, 7SL, cytoplasmic 807, pseudogene [Source:HGNC Symbol;Acc:HGNC:46823]"}, {"versioned_ensembl_gene_id":"ENSG00000223056.1","gene_symbol":"RN7SKP169","gene_name":"RNA, 7SK small nuclear pseudogene 169 [Source:HGNC Symbol;Acc:HGNC:45893]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480886","summary":null,"start":25963983,"end":25964273,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 169 [Source:HGNC Symbol;Acc:HGNC:45893]"}, {"versioned_ensembl_gene_id":"ENSG00000207327.1","gene_symbol":"RNU6-883P","gene_name":"RNA, U6 small nuclear 883, pseudogene [Source:HGNC Symbol;Acc:HGNC:47846]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481921","summary":null,"start":73529051,"end":73529157,"strand":-1,"description":"RNA, U6 small nuclear 883, pseudogene [Source:HGNC Symbol;Acc:HGNC:47846]"}, {"versioned_ensembl_gene_id":"ENSG00000273927.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73039085,"end":73039186,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252491.1","gene_symbol":"RNU1-142P","gene_name":"RNA, U1 small nuclear 142, pseudogene [Source:HGNC Symbol;Acc:HGNC:48484]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480197","summary":null,"start":26790142,"end":26790286,"strand":1,"description":"RNA, U1 small nuclear 142, pseudogene [Source:HGNC Symbol;Acc:HGNC:48484]"}, {"versioned_ensembl_gene_id":"ENSG00000260454.1","gene_symbol":"AL355607.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90997054,"end":91001871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266415.1","gene_symbol":"MIR4636","gene_name":"microRNA 4636 [Source:HGNC Symbol;Acc:HGNC:41798]","synonyms":"hsa-mir-4636","biotype":"miRNA","ncbi_id":"100616326","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9053816,"end":9053895,"strand":-1,"description":"microRNA 4636 [Source:HGNC Symbol;Acc:HGNC:41798]"}, {"versioned_ensembl_gene_id":"ENSG00000279049.1","gene_symbol":"AL353898.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":54099968,"end":54100224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207452.1","gene_symbol":"RNU6-606P","gene_name":"RNA, U6 small nuclear 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:47569]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479834","summary":null,"start":87299687,"end":87299797,"strand":-1,"description":"RNA, U6 small nuclear 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:47569]"}, {"versioned_ensembl_gene_id":"ENSG00000207042.1","gene_symbol":"RNU6-196P","gene_name":"RNA, U6 small nuclear 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:47159]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481238","summary":null,"start":21642294,"end":21642400,"strand":1,"description":"RNA, U6 small nuclear 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:47159]"}, {"versioned_ensembl_gene_id":"ENSG00000278278.1","gene_symbol":"MIR6816","gene_name":"microRNA 6816 [Source:HGNC Symbol;Acc:HGNC:50256]","synonyms":"hsa-mir-6816","biotype":"miRNA","ncbi_id":"102465490","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20114686,"end":20114751,"strand":-1,"description":"microRNA 6816 [Source:HGNC Symbol;Acc:HGNC:50256]"}, {"versioned_ensembl_gene_id":"ENSG00000278469.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3124777,"end":3125063,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266436.1","gene_symbol":"MIR4264","gene_name":"microRNA 4264 [Source:HGNC Symbol;Acc:HGNC:38338]","synonyms":"hsa-mir-4264","biotype":"miRNA","ncbi_id":"100422888","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79649294,"end":79649359,"strand":-1,"description":"microRNA 4264 [Source:HGNC Symbol;Acc:HGNC:38338]"}, {"versioned_ensembl_gene_id":"ENSG00000206716.1","gene_symbol":"RNU6-133P","gene_name":"RNA, U6 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:47096]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481877","summary":null,"start":21214637,"end":21214743,"strand":1,"description":"RNA, U6 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:47096]"}, {"versioned_ensembl_gene_id":"ENSG00000206925.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40342329,"end":40342441,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264049.1","gene_symbol":"MIR4737","gene_name":"microRNA 4737 [Source:HGNC Symbol;Acc:HGNC:41669]","synonyms":"hsa-mir-4737","biotype":"miRNA","ncbi_id":"100616210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60043025,"end":60043105,"strand":-1,"description":"microRNA 4737 [Source:HGNC Symbol;Acc:HGNC:41669]"}, {"versioned_ensembl_gene_id":"ENSG00000251980.1","gene_symbol":"RNU6-436P","gene_name":"RNA, U6 small nuclear 436, pseudogene [Source:HGNC Symbol;Acc:HGNC:47399]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481316","summary":null,"start":157912772,"end":157912885,"strand":1,"description":"RNA, U6 small nuclear 436, pseudogene [Source:HGNC Symbol;Acc:HGNC:47399]"}, {"versioned_ensembl_gene_id":"ENSG00000201078.1","gene_symbol":"RN7SKP214","gene_name":"RNA, 7SK small nuclear pseudogene 214 [Source:HGNC Symbol;Acc:HGNC:45938]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480473","summary":null,"start":37055033,"end":37055347,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 214 [Source:HGNC Symbol;Acc:HGNC:45938]"}, {"versioned_ensembl_gene_id":"ENSG00000274860.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6521131,"end":6521412,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207287.1","gene_symbol":"RNU6-1274P","gene_name":"RNA, U6 small nuclear 1274, pseudogene [Source:HGNC Symbol;Acc:HGNC:48237]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481582","summary":null,"start":96743167,"end":96743273,"strand":1,"description":"RNA, U6 small nuclear 1274, pseudogene [Source:HGNC Symbol;Acc:HGNC:48237]"}, {"versioned_ensembl_gene_id":"ENSG00000202339.1","gene_symbol":"RNU4-45P","gene_name":"RNA, U4 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:46981]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481186","summary":null,"start":22205192,"end":22205332,"strand":1,"description":"RNA, U4 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:46981]"}, {"versioned_ensembl_gene_id":"ENSG00000275901.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":16187313,"end":16187566,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202000.1","gene_symbol":"RNU1-36P","gene_name":"RNA, U1 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48378]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481783","summary":null,"start":88000237,"end":88000401,"strand":1,"description":"RNA, U1 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48378]"}, {"versioned_ensembl_gene_id":"ENSG00000201388.1","gene_symbol":"SNORA68B","gene_name":"small nucleolar RNA, H/ACA box 68B [Source:HGNC Symbol;Acc:HGNC:52213]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616972","summary":null,"start":32608337,"end":32608469,"strand":-1,"description":"small nucleolar RNA, H/ACA box 68B [Source:HGNC Symbol;Acc:HGNC:52213]"}, {"versioned_ensembl_gene_id":"ENSG00000201642.1","gene_symbol":"RNU6-865P","gene_name":"RNA, U6 small nuclear 865, pseudogene [Source:HGNC Symbol;Acc:HGNC:47828]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479948","summary":null,"start":100952627,"end":100952733,"strand":1,"description":"RNA, U6 small nuclear 865, pseudogene [Source:HGNC Symbol;Acc:HGNC:47828]"}, {"versioned_ensembl_gene_id":"ENSG00000207811.3","gene_symbol":"MIR34B","gene_name":"microRNA 34b [Source:HGNC Symbol;Acc:HGNC:31636]","synonyms":"MIRN34B,hsa-mir-34b","biotype":"miRNA","ncbi_id":"407041","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111512938,"end":111513021,"strand":1,"description":"microRNA 34b [Source:HGNC Symbol;Acc:HGNC:31636]"}, {"versioned_ensembl_gene_id":"ENSG00000207759.1","gene_symbol":"MIR181A1","gene_name":"microRNA 181a-1 [Source:HGNC Symbol;Acc:HGNC:31590]","synonyms":"MIRN213,MIRN181A1,hsa-mir-213","biotype":"miRNA","ncbi_id":"406995","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":198859044,"end":198859153,"strand":-1,"description":"microRNA 181a-1 [Source:HGNC Symbol;Acc:HGNC:31590]"}, {"versioned_ensembl_gene_id":"ENSG00000201770.1","gene_symbol":"RNU6-384P","gene_name":"RNA, U6 small nuclear 384, pseudogene [Source:HGNC Symbol;Acc:HGNC:47347]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481299","summary":null,"start":31581089,"end":31581192,"strand":1,"description":"RNA, U6 small nuclear 384, pseudogene [Source:HGNC Symbol;Acc:HGNC:47347]"}, {"versioned_ensembl_gene_id":"ENSG00000252988.1","gene_symbol":"RNU6-111P","gene_name":"RNA, U6 small nuclear 111, pseudogene [Source:HGNC Symbol;Acc:HGNC:47074]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481212","summary":null,"start":73298683,"end":73298787,"strand":1,"description":"RNA, U6 small nuclear 111, pseudogene [Source:HGNC Symbol;Acc:HGNC:47074]"}, {"versioned_ensembl_gene_id":"ENSG00000264419.1","gene_symbol":"MIR548AC","gene_name":"microRNA 548ac [Source:HGNC Symbol;Acc:HGNC:41626]","synonyms":"hsa-mir-548ac","biotype":"miRNA","ncbi_id":"100616384","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116560024,"end":116560111,"strand":-1,"description":"microRNA 548ac [Source:HGNC Symbol;Acc:HGNC:41626]"}, {"versioned_ensembl_gene_id":"ENSG00000212316.1","gene_symbol":"RNU6-1228P","gene_name":"RNA, U6 small nuclear 1228, pseudogene [Source:HGNC Symbol;Acc:HGNC:48191]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480103","summary":null,"start":75198071,"end":75198177,"strand":1,"description":"RNA, U6 small nuclear 1228, pseudogene [Source:HGNC Symbol;Acc:HGNC:48191]"}, {"versioned_ensembl_gene_id":"ENSG00000266263.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30908902,"end":30909204,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000200799.1","gene_symbol":"RNU6-770P","gene_name":"RNA, U6 small nuclear 770, pseudogene [Source:HGNC Symbol;Acc:HGNC:47733]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481423","summary":null,"start":108392073,"end":108392177,"strand":1,"description":"RNA, U6 small nuclear 770, pseudogene [Source:HGNC Symbol;Acc:HGNC:47733]"}, {"versioned_ensembl_gene_id":"ENSG00000277605.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47476822,"end":47477152,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000273875.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000239128.1","gene_symbol":"SNORD13P3","gene_name":"small nucleolar RNA, C/D box 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10112]","synonyms":"U13.4B,U13,RNU13P3","biotype":"snoRNA","ncbi_id":"6078","summary":null,"start":47250523,"end":47250626,"strand":-1,"description":"small nucleolar RNA, C/D box 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10112]"}, {"versioned_ensembl_gene_id":"ENSG00000200225.1","gene_symbol":"RNA5SP382","gene_name":"RNA, 5S ribosomal pseudogene 382 [Source:HGNC Symbol;Acc:HGNC:43282]","synonyms":"RN5S382","biotype":"rRNA","ncbi_id":"100873637","summary":null,"start":20414987,"end":20415098,"strand":1,"description":"RNA, 5S ribosomal pseudogene 382 [Source:HGNC Symbol;Acc:HGNC:43282]"}, {"versioned_ensembl_gene_id":"ENSG00000201201.1","gene_symbol":"RN7SKP118","gene_name":"RNA, 7SK small nuclear pseudogene 118 [Source:HGNC Symbol;Acc:HGNC:45842]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106633802","summary":null,"start":67321658,"end":67321987,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 118 [Source:HGNC Symbol;Acc:HGNC:45842]"}, {"versioned_ensembl_gene_id":"ENSG00000222356.1","gene_symbol":"RNU6-710P","gene_name":"RNA, U6 small nuclear 710, pseudogene [Source:HGNC Symbol;Acc:HGNC:47673]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479880","summary":null,"start":111996635,"end":111996739,"strand":-1,"description":"RNA, U6 small nuclear 710, pseudogene [Source:HGNC Symbol;Acc:HGNC:47673]"}, {"versioned_ensembl_gene_id":"ENSG00000200942.1","gene_symbol":"RNU6-501P","gene_name":"RNA, U6 small nuclear 501, pseudogene [Source:HGNC Symbol;Acc:HGNC:47464]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481339","summary":null,"start":201733406,"end":201733505,"strand":1,"description":"RNA, U6 small nuclear 501, pseudogene [Source:HGNC Symbol;Acc:HGNC:47464]"}, {"versioned_ensembl_gene_id":"ENSG00000278264.1","gene_symbol":"MIR6803","gene_name":"microRNA 6803 [Source:HGNC Symbol;Acc:HGNC:50035]","synonyms":"hsa-mir-6803","biotype":"miRNA","ncbi_id":"102466739","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55245186,"end":55245250,"strand":-1,"description":"microRNA 6803 [Source:HGNC Symbol;Acc:HGNC:50035]"}, {"versioned_ensembl_gene_id":"ENSG00000200257.1","gene_symbol":"RNU6-97P","gene_name":"RNA, U6 small nuclear 97, pseudogene [Source:HGNC Symbol;Acc:HGNC:47060]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480551","summary":null,"start":76752912,"end":76753015,"strand":1,"description":"RNA, U6 small nuclear 97, pseudogene [Source:HGNC Symbol;Acc:HGNC:47060]"}, {"versioned_ensembl_gene_id":"ENSG00000277595.1","gene_symbol":"AC007546.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":110032245,"end":110032803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255348.1","gene_symbol":"AP001775.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134178824,"end":134186166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284542.1","gene_symbol":"MIR3614","gene_name":"microRNA 3614 [Source:HGNC Symbol;Acc:HGNC:38995]","synonyms":"hsa-mir-3614","biotype":"miRNA","ncbi_id":"100500827","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56891270,"end":56891355,"strand":-1,"description":"microRNA 3614 [Source:HGNC Symbol;Acc:HGNC:38995]"}, {"versioned_ensembl_gene_id":"ENSG00000281557.1","gene_symbol":"AL357055.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113013524,"end":113074942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283416.1","gene_symbol":"MIR1910","gene_name":"microRNA 1910 [Source:HGNC Symbol;Acc:HGNC:35394]","synonyms":"MIRN1910,hsa-mir-1910","biotype":"miRNA","ncbi_id":"100302261","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85741621,"end":85741700,"strand":-1,"description":"microRNA 1910 [Source:HGNC Symbol;Acc:HGNC:35394]"}, {"versioned_ensembl_gene_id":"ENSG00000251814.1","gene_symbol":"RN7SKP18","gene_name":"RNA, 7SK small nuclear pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:45742]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480838","summary":null,"start":117299364,"end":117299638,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:45742]"}, {"versioned_ensembl_gene_id":"ENSG00000265855.1","gene_symbol":"MIR4514","gene_name":"microRNA 4514 [Source:HGNC Symbol;Acc:HGNC:41845]","synonyms":"hsa-mir-4514","biotype":"miRNA","ncbi_id":"100616181","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80997417,"end":80997473,"strand":-1,"description":"microRNA 4514 [Source:HGNC Symbol;Acc:HGNC:41845]"}, {"versioned_ensembl_gene_id":"ENSG00000244404.3","gene_symbol":"RN7SL216P","gene_name":"RNA, 7SL, cytoplasmic 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:46232]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480495","summary":null,"start":25020166,"end":25020463,"strand":-1,"description":"RNA, 7SL, cytoplasmic 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:46232]"}, {"versioned_ensembl_gene_id":"ENSG00000207961.3","gene_symbol":"MIR496","gene_name":"microRNA 496 [Source:HGNC Symbol;Acc:HGNC:32086]","synonyms":"MIRN496,hsa-mir-496","biotype":"miRNA","ncbi_id":"574454","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101060573,"end":101060674,"strand":1,"description":"microRNA 496 [Source:HGNC Symbol;Acc:HGNC:32086]"}, {"versioned_ensembl_gene_id":"ENSG00000266611.1","gene_symbol":"MIR4703","gene_name":"microRNA 4703 [Source:HGNC Symbol;Acc:HGNC:41817]","synonyms":"hsa-mir-4703","biotype":"miRNA","ncbi_id":"100616423","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51552589,"end":51552667,"strand":1,"description":"microRNA 4703 [Source:HGNC Symbol;Acc:HGNC:41817]"}, {"versioned_ensembl_gene_id":"ENSG00000266188.1","gene_symbol":"MIR5095","gene_name":"microRNA 5095 [Source:HGNC Symbol;Acc:HGNC:41849]","synonyms":"hsa-mir-5095","biotype":"miRNA","ncbi_id":"100616458","summary":"This record was withdrawn by miRBase.","start":52934930,"end":52935017,"strand":1,"description":"microRNA 5095 [Source:HGNC Symbol;Acc:HGNC:41849]"}, {"versioned_ensembl_gene_id":"ENSG00000200726.1","gene_symbol":"SNORD115-8","gene_name":"small nucleolar RNA, C/D box 115-8 [Source:HGNC Symbol;Acc:HGNC:33027]","synonyms":"HBII-52-8","biotype":"snoRNA","ncbi_id":"100033445","summary":null,"start":25184306,"end":25184387,"strand":1,"description":"small nucleolar RNA, C/D box 115-8 [Source:HGNC Symbol;Acc:HGNC:33027]"}, {"versioned_ensembl_gene_id":"ENSG00000202184.1","gene_symbol":"RNU6-1283P","gene_name":"RNA, U6 small nuclear 1283, pseudogene [Source:HGNC Symbol;Acc:HGNC:48246]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481782","summary":null,"start":246189014,"end":246189118,"strand":-1,"description":"RNA, U6 small nuclear 1283, pseudogene [Source:HGNC Symbol;Acc:HGNC:48246]"}, {"versioned_ensembl_gene_id":"ENSG00000252061.1","gene_symbol":"RNU6-415P","gene_name":"RNA, U6 small nuclear 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:47378]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481309","summary":null,"start":78898840,"end":78898936,"strand":-1,"description":"RNA, U6 small nuclear 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:47378]"}, {"versioned_ensembl_gene_id":"ENSG00000273537.1","gene_symbol":"ZEB2_AS1_3","gene_name":"ZEB2 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF01986]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144520456,"end":144520555,"strand":1,"description":"ZEB2 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF01986]"}, {"versioned_ensembl_gene_id":"ENSG00000201403.1","gene_symbol":"SNORD14B","gene_name":"small nucleolar RNA, C/D box 14B [Source:HGNC Symbol;Acc:HGNC:31803]","synonyms":"U14B,U14,RNU14B","biotype":"snoRNA","ncbi_id":"85388","summary":null,"start":17075779,"end":17075868,"strand":-1,"description":"small nucleolar RNA, C/D box 14B [Source:HGNC Symbol;Acc:HGNC:31803]"}, {"versioned_ensembl_gene_id":"ENSG00000251185.1","gene_symbol":"AC025244.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75269068,"end":75361182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278073.1","gene_symbol":"MIR6726","gene_name":"microRNA 6726 [Source:HGNC Symbol;Acc:HGNC:50009]","synonyms":"hsa-mir-6726","biotype":"miRNA","ncbi_id":"102465434","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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[provided by RefSeq, Sep 2009]","start":118974586,"end":118974670,"strand":1,"description":"microRNA 1244-2 [Source:HGNC Symbol;Acc:HGNC:38321]"}, {"versioned_ensembl_gene_id":"ENSG00000252097.1","gene_symbol":"RNU6-346P","gene_name":"RNA, U6 small nuclear 346, pseudogene [Source:HGNC Symbol;Acc:HGNC:47309]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481768","summary":null,"start":76800664,"end":76800774,"strand":-1,"description":"RNA, U6 small nuclear 346, pseudogene [Source:HGNC Symbol;Acc:HGNC:47309]"}, {"versioned_ensembl_gene_id":"ENSG00000202469.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10061222,"end":10061323,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252390.1","gene_symbol":"RNU5F-4P","gene_name":"RNA, U5F small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42516]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873867","summary":null,"start":31594093,"end":31594206,"strand":-1,"description":"RNA, U5F small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42516]"}, {"versioned_ensembl_gene_id":"ENSG00000272166.1","gene_symbol":"SNORD5","gene_name":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]","synonyms":"mgh28S-2410","biotype":"snoRNA","ncbi_id":"692072","summary":null,"start":25555543,"end":25555606,"strand":-1,"description":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]"}, {"versioned_ensembl_gene_id":"ENSG00000207408.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53324562,"end":53324674,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274713.1","gene_symbol":"MIR7974","gene_name":"microRNA 7974 [Source:HGNC Symbol;Acc:HGNC:49992]","synonyms":"hsa-mir-7974","biotype":"miRNA","ncbi_id":"102465856","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. 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[provided by RefSeq, Sep 2009]","start":11495544,"end":11495622,"strand":-1,"description":"microRNA 7974 [Source:HGNC Symbol;Acc:HGNC:49992]"}, {"versioned_ensembl_gene_id":"ENSG00000252132.1","gene_symbol":"RNU6-795P","gene_name":"RNA, U6 small nuclear 795, pseudogene [Source:HGNC Symbol;Acc:HGNC:47758]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480610","summary":null,"start":38043873,"end":38043975,"strand":-1,"description":"RNA, U6 small nuclear 795, pseudogene [Source:HGNC Symbol;Acc:HGNC:47758]"}, {"versioned_ensembl_gene_id":"ENSG00000200895.1","gene_symbol":"RN7SKP245","gene_name":"RNA, 7SK small nuclear pseudogene 245 [Source:HGNC Symbol;Acc:HGNC:45969]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480909","summary":null,"start":131820334,"end":131820653,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 245 [Source:HGNC Symbol;Acc:HGNC:45969]"}, {"versioned_ensembl_gene_id":"ENSG00000275391.1","gene_symbol":"MIR6770-3","gene_name":"microRNA 6770-3 [Source:HGNC Symbol;Acc:HGNC:50034]","synonyms":"hsa-mir-6770-3","biotype":"miRNA","ncbi_id":"102466259","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18379351,"end":18379410,"strand":-1,"description":"microRNA 6770-3 [Source:HGNC Symbol;Acc:HGNC:50034]"}, {"versioned_ensembl_gene_id":"ENSG00000238326.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56000518,"end":56000621,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000276941.1","gene_symbol":"MIR4509-1","gene_name":"microRNA 4509-1 [Source:HGNC Symbol;Acc:HGNC:41860]","synonyms":"hsa-mir-4509-1","biotype":"miRNA","ncbi_id":"100616223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23197827,"end":23197920,"strand":1,"description":"microRNA 4509-1 [Source:HGNC Symbol;Acc:HGNC:41860]"}, {"versioned_ensembl_gene_id":"ENSG00000200635.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55582733,"end":55582834,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266704.1","gene_symbol":"MIR4498","gene_name":"microRNA 4498 [Source:HGNC Symbol;Acc:HGNC:41838]","synonyms":"hsa-mir-4498","biotype":"miRNA","ncbi_id":"100616179","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":120155434,"end":120155499,"strand":-1,"description":"microRNA 4498 [Source:HGNC Symbol;Acc:HGNC:41838]"}, {"versioned_ensembl_gene_id":"ENSG00000252073.1","gene_symbol":"RNU6-947P","gene_name":"RNA, U6 small nuclear 947, pseudogene [Source:HGNC Symbol;Acc:HGNC:47910]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479985","summary":null,"start":244954858,"end":244954963,"strand":1,"description":"RNA, U6 small nuclear 947, pseudogene [Source:HGNC Symbol;Acc:HGNC:47910]"}, {"versioned_ensembl_gene_id":"ENSG00000265355.1","gene_symbol":"MIR3136","gene_name":"microRNA 3136 [Source:HGNC Symbol;Acc:HGNC:38340]","synonyms":"hsa-mir-3136","biotype":"miRNA","ncbi_id":"100422859","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69048958,"end":69049035,"strand":-1,"description":"microRNA 3136 [Source:HGNC Symbol;Acc:HGNC:38340]"}, {"versioned_ensembl_gene_id":"ENSG00000252292.1","gene_symbol":"RN7SKP238","gene_name":"RNA, 7SK small nuclear pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:45962]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479201","summary":null,"start":85650012,"end":85650260,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:45962]"}, {"versioned_ensembl_gene_id":"ENSG00000221114.1","gene_symbol":"RNU6ATAC30P","gene_name":"RNA, U6atac small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:46929]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481868","summary":null,"start":49684544,"end":49684665,"strand":1,"description":"RNA, U6atac small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:46929]"}, {"versioned_ensembl_gene_id":"ENSG00000273648.1","gene_symbol":"MIR8065","gene_name":"microRNA 8065 [Source:HGNC Symbol;Acc:HGNC:49959]","synonyms":"hsa-mir-8065","biotype":"miRNA","ncbi_id":"102465867","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5632467,"end":5632566,"strand":1,"description":"microRNA 8065 [Source:HGNC Symbol;Acc:HGNC:49959]"}, {"versioned_ensembl_gene_id":"ENSG00000201492.1","gene_symbol":"RNA5SP78","gene_name":"RNA, 5S ribosomal pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:42855]","synonyms":"RN5S78","biotype":"rRNA","ncbi_id":"100873312","summary":null,"start":229549905,"end":229550022,"strand":1,"description":"RNA, 5S ribosomal pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:42855]"}, {"versioned_ensembl_gene_id":"ENSG00000284160.1","gene_symbol":"MIR7706","gene_name":"microRNA 7706 [Source:HGNC Symbol;Acc:HGNC:50110]","synonyms":"hsa-mir-7706","biotype":"miRNA","ncbi_id":"102465803","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85380596,"end":85380662,"strand":1,"description":"microRNA 7706 [Source:HGNC Symbol;Acc:HGNC:50110]"}, {"versioned_ensembl_gene_id":"ENSG00000275372.1","gene_symbol":"ZEB2_AS1_1","gene_name":"ZEB2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF01984]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144518447,"end":144518574,"strand":1,"description":"ZEB2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF01984]"}, {"versioned_ensembl_gene_id":"ENSG00000239105.1","gene_symbol":"RNU7-73P","gene_name":"RNA, U7 small nuclear 73 pseudogene [Source:HGNC Symbol;Acc:HGNC:34169]","synonyms":"U7.73","biotype":"snRNA","ncbi_id":"100151670","summary":null,"start":37573151,"end":37573213,"strand":-1,"description":"RNA, U7 small nuclear 73 pseudogene [Source:HGNC Symbol;Acc:HGNC:34169]"}, {"versioned_ensembl_gene_id":"ENSG00000200914.1","gene_symbol":"RNA5SP435","gene_name":"RNA, 5S ribosomal pseudogene 435 [Source:HGNC Symbol;Acc:HGNC:43335]","synonyms":"RN5S435","biotype":"rRNA","ncbi_id":"106479013","summary":null,"start":6600944,"end":6601051,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 435 [Source:HGNC Symbol;Acc:HGNC:43335]"}, {"versioned_ensembl_gene_id":"ENSG00000239002.3","gene_symbol":"SCARNA10","gene_name":"small Cajal body-specific RNA 10 [Source:HGNC Symbol;Acc:HGNC:32567]","synonyms":"U85","biotype":"snoRNA","ncbi_id":"692148","summary":null,"start":6510222,"end":6510551,"strand":1,"description":"small Cajal body-specific RNA 10 [Source:HGNC Symbol;Acc:HGNC:32567]"}, {"versioned_ensembl_gene_id":"ENSG00000267421.6","gene_symbol":"AC005498.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56536156,"end":56538575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212040.3","gene_symbol":"MIR543","gene_name":"microRNA 543 [Source:HGNC Symbol;Acc:HGNC:33664]","synonyms":"MIRN543,hsa-mir-543","biotype":"miRNA","ncbi_id":"100126335","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101031987,"end":101032064,"strand":1,"description":"microRNA 543 [Source:HGNC Symbol;Acc:HGNC:33664]"}, {"versioned_ensembl_gene_id":"ENSG00000216192.1","gene_symbol":"MIR920","gene_name":"microRNA 920 [Source:HGNC Symbol;Acc:HGNC:33670]","synonyms":"hsa-mir-920,MIRN920","biotype":"miRNA","ncbi_id":"100126320","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24212421,"end":24212495,"strand":1,"description":"microRNA 920 [Source:HGNC Symbol;Acc:HGNC:33670]"}, {"versioned_ensembl_gene_id":"ENSG00000278359.1","gene_symbol":"MIR7155","gene_name":"microRNA 7155 [Source:HGNC Symbol;Acc:HGNC:50005]","synonyms":"hsa-mir-7155","biotype":"miRNA","ncbi_id":"102466815","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64341849,"end":64341904,"strand":-1,"description":"microRNA 7155 [Source:HGNC Symbol;Acc:HGNC:50005]"}, {"versioned_ensembl_gene_id":"ENSG00000240014.3","gene_symbol":"RN7SL254P","gene_name":"RNA, 7SL, cytoplasmic 254, pseudogene [Source:HGNC Symbol;Acc:HGNC:46270]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480991","summary":null,"start":147808926,"end":147809209,"strand":1,"description":"RNA, 7SL, cytoplasmic 254, pseudogene [Source:HGNC Symbol;Acc:HGNC:46270]"}, {"versioned_ensembl_gene_id":"ENSG00000207874.1","gene_symbol":"MIR610","gene_name":"microRNA 610 [Source:HGNC Symbol;Acc:HGNC:32866]","synonyms":"MIRN610,hsa-mir-610","biotype":"miRNA","ncbi_id":"693195","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28056815,"end":28056910,"strand":1,"description":"microRNA 610 [Source:HGNC Symbol;Acc:HGNC:32866]"}, {"versioned_ensembl_gene_id":"ENSG00000200686.1","gene_symbol":"RNY3P3","gene_name":"RNA, Ro-associated Y3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42487]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862669","summary":null,"start":78355227,"end":78355328,"strand":-1,"description":"RNA, Ro-associated Y3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42487]"}, {"versioned_ensembl_gene_id":"ENSG00000281894.2","gene_symbol":"ZKSCAN7","gene_name":"zinc finger with KRAB and SCAN domains 7 [Source:HGNC Symbol;Acc:HGNC:12955]","synonyms":"ZSCAN39,ZNF64,ZNF448,ZNF167,FLJ12738","biotype":"protein_coding","ncbi_id":"55888","summary":null,"start":44555193,"end":44594173,"strand":1,"description":"zinc finger with KRAB and SCAN domains 7 [Source:HGNC Symbol;Acc:HGNC:12955]"}, {"versioned_ensembl_gene_id":"ENSG00000222585.1","gene_symbol":"RNA5SP494","gene_name":"RNA, 5S ribosomal pseudogene 494 [Source:HGNC Symbol;Acc:HGNC:43394]","synonyms":"RN5S494","biotype":"rRNA","ncbi_id":"100873736","summary":null,"start":25715041,"end":25715169,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 494 [Source:HGNC Symbol;Acc:HGNC:43394]"}, {"versioned_ensembl_gene_id":"ENSG00000238490.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108060818,"end":108060930,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201715.1","gene_symbol":"RN7SKP133","gene_name":"RNA, 7SK small nuclear pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:45857]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481812","summary":null,"start":17345616,"end":17345955,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:45857]"}, {"versioned_ensembl_gene_id":"ENSG00000263595.2","gene_symbol":"RN7SL823P","gene_name":"RNA, 7SL, cytoplasmic 823, pseudogene [Source:HGNC Symbol;Acc:HGNC:46839]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479522","summary":null,"start":16910490,"end":16910784,"strand":-1,"description":"RNA, 7SL, cytoplasmic 823, pseudogene [Source:HGNC Symbol;Acc:HGNC:46839]"}, {"versioned_ensembl_gene_id":"ENSG00000283204.1","gene_symbol":"MIR4434","gene_name":"microRNA 4434 [Source:HGNC Symbol;Acc:HGNC:41832]","synonyms":"hsa-mir-4434","biotype":"miRNA","ncbi_id":"100616419","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64525513,"end":64525565,"strand":1,"description":"microRNA 4434 [Source:HGNC Symbol;Acc:HGNC:41832]"}, {"versioned_ensembl_gene_id":"ENSG00000201810.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":180542701,"end":180542836,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000238819.1","gene_symbol":"SNORD11","gene_name":"Small nucleolar RNA SNORD11 [Source:RFAM;Acc:RF01182]","synonyms":"HBII-95","biotype":"snoRNA","ncbi_id":"692058","summary":null,"start":46351662,"end":46351746,"strand":-1,"description":"Small nucleolar RNA SNORD11 [Source:RFAM;Acc:RF01182]"}, {"versioned_ensembl_gene_id":"ENSG00000280683.1","gene_symbol":"AL354704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30388935,"end":30575012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263752.1","gene_symbol":"MIR3133","gene_name":"microRNA 3133 [Source:HGNC Symbol;Acc:HGNC:38305]","synonyms":"hsa-mir-3133","biotype":"miRNA","ncbi_id":"100422942","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":241477905,"end":241477982,"strand":1,"description":"microRNA 3133 [Source:HGNC Symbol;Acc:HGNC:38305]"}, {"versioned_ensembl_gene_id":"ENSG00000266180.1","gene_symbol":"MIR4282","gene_name":"microRNA 4282 [Source:HGNC Symbol;Acc:HGNC:38189]","synonyms":"hsa-mir-4282","biotype":"miRNA","ncbi_id":"100423005","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72967687,"end":72967753,"strand":-1,"description":"microRNA 4282 [Source:HGNC Symbol;Acc:HGNC:38189]"}, {"versioned_ensembl_gene_id":"ENSG00000201843.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133302470,"end":133302563,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240961.3","gene_symbol":"RN7SL415P","gene_name":"RNA, 7SL, cytoplasmic 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:46431]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479375","summary":null,"start":91739609,"end":91739897,"strand":1,"description":"RNA, 7SL, cytoplasmic 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:46431]"}, {"versioned_ensembl_gene_id":"ENSG00000281226.2","gene_symbol":"AL590644.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17189783,"end":17197617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264834.1","gene_symbol":"MIR1273F","gene_name":"microRNA 1273f [Source:HGNC Symbol;Acc:HGNC:41733]","synonyms":"hsa-mir-1273f","biotype":"miRNA","ncbi_id":"100616156","summary":"This record was withdrawn by miRBase.","start":52928674,"end":52928772,"strand":1,"description":"microRNA 1273f [Source:HGNC Symbol;Acc:HGNC:41733]"}, {"versioned_ensembl_gene_id":"ENSG00000253057.1","gene_symbol":"RN7SKP57","gene_name":"RNA, 7SK small nuclear pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:45781]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479120","summary":null,"start":111719769,"end":111720061,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:45781]"}, {"versioned_ensembl_gene_id":"ENSG00000206915.1","gene_symbol":"RNU6-439P","gene_name":"RNA, U6 small nuclear 439, pseudogene [Source:HGNC Symbol;Acc:HGNC:47402]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481317","summary":null,"start":49233794,"end":49233899,"strand":-1,"description":"RNA, U6 small nuclear 439, pseudogene [Source:HGNC Symbol;Acc:HGNC:47402]"}, {"versioned_ensembl_gene_id":"ENSG00000276859.1","gene_symbol":"GNAS-AS1_1","gene_name":"GNAS antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02127]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58842030,"end":58842132,"strand":1,"description":"GNAS antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02127]"}, {"versioned_ensembl_gene_id":"ENSG00000239057.2","gene_symbol":"MIR500B","gene_name":"microRNA 500b [Source:HGNC Symbol;Acc:HGNC:38223]","synonyms":"hsa-mir-500b","biotype":"miRNA","ncbi_id":"100422911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50010672,"end":50010750,"strand":1,"description":"microRNA 500b [Source:HGNC Symbol;Acc:HGNC:38223]"}, {"versioned_ensembl_gene_id":"ENSG00000201263.1","gene_symbol":"SNORD114-6","gene_name":"small nucleolar RNA, C/D box 114-6 [Source:HGNC Symbol;Acc:HGNC:32994]","synonyms":"14q(II-6)","biotype":"snoRNA","ncbi_id":"767582","summary":null,"start":100957166,"end":100957237,"strand":1,"description":"small nucleolar RNA, C/D box 114-6 [Source:HGNC Symbol;Acc:HGNC:32994]"}, {"versioned_ensembl_gene_id":"ENSG00000207268.1","gene_symbol":"SNORA70C","gene_name":"small nucleolar RNA, H/ACA box 70C [Source:HGNC Symbol;Acc:HGNC:33619]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124538","summary":"This gene produces a small nucleolar RNA (snoRNA) that plays a role in post-transcriptional modification. This snoRNA is a type-3 retrotransposed snoRNA, where the ribosomal protein L10 gene on chromosome X is its parental gene, and this, together with part of the parental gene, was subsequently mobilized into an intron of the astrotactin 2 host gene on chromosome 9. This snoRNA contains a H/ACA box, which serves as a guide for the pseudouridylation of selected bases of ribosomal RNA by forming short duplexes with the 18S rRNA U1692, the target for this snoRNA. This gene is specific to human, chimp and orangutan, and is not found in the genomes of rhesus or marmoset. [provided by RefSeq, Jun 2010]","start":117181066,"end":117181200,"strand":-1,"description":"small nucleolar RNA, H/ACA box 70C [Source:HGNC Symbol;Acc:HGNC:33619]"}, {"versioned_ensembl_gene_id":"ENSG00000280781.1","gene_symbol":"EI24P3","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131881","summary":null,"start":44524744,"end":44525805,"strand":-1,"description":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]"}, {"versioned_ensembl_gene_id":"ENSG00000238386.1","gene_symbol":"RNU7-48P","gene_name":"RNA, U7 small nuclear 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:34144]","synonyms":"U7.48","biotype":"snRNA","ncbi_id":"100147835","summary":null,"start":70513294,"end":70513356,"strand":1,"description":"RNA, U7 small nuclear 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:34144]"}, {"versioned_ensembl_gene_id":"ENSG00000201026.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2184710,"end":2184820,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238923.1","gene_symbol":"RNU7-1","gene_name":"RNA, U7 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:34033]","synonyms":"U7.1,RNU7","biotype":"snRNA","ncbi_id":"100147744","summary":null,"start":6943816,"end":6943878,"strand":1,"description":"RNA, U7 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:34033]"}, {"versioned_ensembl_gene_id":"ENSG00000278331.1","gene_symbol":"RNU6-156P","gene_name":"RNA, U6 small nuclear 156, pseudogene [Source:HGNC Symbol;Acc:HGNC:47119]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479635","summary":null,"start":40759600,"end":40759706,"strand":-1,"description":"RNA, U6 small nuclear 156, pseudogene [Source:HGNC Symbol;Acc:HGNC:47119]"}, {"versioned_ensembl_gene_id":"ENSG00000252037.1","gene_symbol":"RNU6-162P","gene_name":"RNA, U6 small nuclear 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:47125]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481226","summary":null,"start":143574746,"end":143574848,"strand":1,"description":"RNA, U6 small nuclear 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:47125]"}, {"versioned_ensembl_gene_id":"ENSG00000274210.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":148522601,"end":148522765,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000252205.1","gene_symbol":"RNU6-764P","gene_name":"RNA, U6 small nuclear 764, pseudogene [Source:HGNC Symbol;Acc:HGNC:47727]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479904","summary":null,"start":152250572,"end":152250676,"strand":-1,"description":"RNA, U6 small nuclear 764, pseudogene [Source:HGNC Symbol;Acc:HGNC:47727]"}, {"versioned_ensembl_gene_id":"ENSG00000278998.1","gene_symbol":"AC099552.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":155222903,"end":155223851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207976.1","gene_symbol":"MIR607","gene_name":"microRNA 607 [Source:HGNC Symbol;Acc:HGNC:32863]","synonyms":"hsa-mir-607,MIRN607","biotype":"miRNA","ncbi_id":"693192","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96828669,"end":96828764,"strand":-1,"description":"microRNA 607 [Source:HGNC Symbol;Acc:HGNC:32863]"}, {"versioned_ensembl_gene_id":"ENSG00000284587.1","gene_symbol":"MIR943","gene_name":"microRNA 943 [Source:HGNC Symbol;Acc:HGNC:33689]","synonyms":"MIRN943,hsa-mir-943","biotype":"miRNA","ncbi_id":"100126332","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1986384,"end":1986477,"strand":-1,"description":"microRNA 943 [Source:HGNC Symbol;Acc:HGNC:33689]"}, {"versioned_ensembl_gene_id":"ENSG00000283634.1","gene_symbol":"MIR3155B","gene_name":"microRNA 3155b [Source:HGNC Symbol;Acc:HGNC:50003]","synonyms":"hsa-mir-3155b","biotype":"miRNA","ncbi_id":"100628560","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6152207,"end":6152262,"strand":-1,"description":"microRNA 3155b [Source:HGNC Symbol;Acc:HGNC:50003]"}, {"versioned_ensembl_gene_id":"ENSG00000264984.1","gene_symbol":"MIR5691","gene_name":"microRNA 5691 [Source:HGNC Symbol;Acc:HGNC:43545]","synonyms":"hsa-mir-5691","biotype":"miRNA","ncbi_id":"100847015","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9090312,"end":9090379,"strand":-1,"description":"microRNA 5691 [Source:HGNC Symbol;Acc:HGNC:43545]"}, {"versioned_ensembl_gene_id":"ENSG00000199038.1","gene_symbol":"MIR210","gene_name":"microRNA 210 [Source:HGNC Symbol;Acc:HGNC:31587]","synonyms":"hsa-mir-210,MIRN210","biotype":"miRNA","ncbi_id":"406992","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":568089,"end":568198,"strand":-1,"description":"microRNA 210 [Source:HGNC Symbol;Acc:HGNC:31587]"}, {"versioned_ensembl_gene_id":"ENSG00000251825.1","gene_symbol":"RN7SKP19","gene_name":"RNA, 7SK small nuclear pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:45743]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479103","summary":null,"start":73191604,"end":73191855,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:45743]"}, {"versioned_ensembl_gene_id":"ENSG00000264192.1","gene_symbol":"RN7SL117P","gene_name":"RNA, 7SL, cytoplasmic 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:46133]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479264","summary":null,"start":21922993,"end":21923288,"strand":1,"description":"RNA, 7SL, cytoplasmic 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:46133]"}, {"versioned_ensembl_gene_id":"ENSG00000207728.1","gene_symbol":"MIR449B","gene_name":"microRNA 449b [Source:HGNC Symbol;Acc:HGNC:32794]","synonyms":"MIRN449B,hsa-mir-449b","biotype":"miRNA","ncbi_id":"693123","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55170646,"end":55170742,"strand":-1,"description":"microRNA 449b [Source:HGNC Symbol;Acc:HGNC:32794]"}, {"versioned_ensembl_gene_id":"ENSG00000239542.3","gene_symbol":"RN7SL399P","gene_name":"RNA, 7SL, cytoplasmic 399, pseudogene [Source:HGNC Symbol;Acc:HGNC:46415]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479370","summary":null,"start":41730127,"end":41730405,"strand":-1,"description":"RNA, 7SL, cytoplasmic 399, pseudogene [Source:HGNC Symbol;Acc:HGNC:46415]"}, {"versioned_ensembl_gene_id":"ENSG00000276669.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86216596,"end":86216878,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000264141.1","gene_symbol":"MIR3928","gene_name":"microRNA 3928 [Source:HGNC Symbol;Acc:HGNC:38933]","synonyms":"hsa-mir-3928","biotype":"miRNA","ncbi_id":"100500901","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31160062,"end":31160119,"strand":-1,"description":"microRNA 3928 [Source:HGNC Symbol;Acc:HGNC:38933]"}, {"versioned_ensembl_gene_id":"ENSG00000207098.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":32841861,"end":32841995,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000206622.1","gene_symbol":"SNORA69","gene_name":"small nucleolar RNA, H/ACA box 69 [Source:HGNC Symbol;Acc:HGNC:10226]","synonyms":"U69,RNU69","biotype":"snoRNA","ncbi_id":"26779","summary":"This gene encodes a member of the family of box ACA small nucleolar RNAs, characterized by a consensus ACA motif positioned 3 nucleotides from the 3' end of the RNAs and a double-hairpin structure. The box ACA small nucleolar RNAs may play a role in rRNA maturation. This gene is co-transcribed with the ribosomal protein L39 gene. [provided by RefSeq, Oct 2009]","start":119787353,"end":119787484,"strand":-1,"description":"small nucleolar RNA, H/ACA box 69 [Source:HGNC Symbol;Acc:HGNC:10226]"}, {"versioned_ensembl_gene_id":"ENSG00000263815.2","gene_symbol":"RN7SL426P","gene_name":"RNA, 7SL, cytoplasmic 426, pseudogene [Source:HGNC Symbol;Acc:HGNC:46442]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481842","summary":null,"start":21229334,"end":21229628,"strand":-1,"description":"RNA, 7SL, cytoplasmic 426, pseudogene [Source:HGNC Symbol;Acc:HGNC:46442]"}, {"versioned_ensembl_gene_id":"ENSG00000252217.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65502741,"end":65502836,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211578.3","gene_symbol":"MIR766","gene_name":"microRNA 766 [Source:HGNC Symbol;Acc:HGNC:33139]","synonyms":"MIRN766,hsa-mir-766","biotype":"miRNA","ncbi_id":"768218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119646738,"end":119646848,"strand":-1,"description":"microRNA 766 [Source:HGNC Symbol;Acc:HGNC:33139]"}, {"versioned_ensembl_gene_id":"ENSG00000207782.3","gene_symbol":"MIR150","gene_name":"microRNA 150 [Source:HGNC Symbol;Acc:HGNC:31537]","synonyms":"hsa-mir-150,MIRN150","biotype":"miRNA","ncbi_id":"406942","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49500785,"end":49500868,"strand":-1,"description":"microRNA 150 [Source:HGNC Symbol;Acc:HGNC:31537]"}, {"versioned_ensembl_gene_id":"ENSG00000207736.1","gene_symbol":"MIR657","gene_name":"microRNA 657 [Source:HGNC Symbol;Acc:HGNC:32913]","synonyms":"MIRN657,hsa-mir-657","biotype":"miRNA","ncbi_id":"724027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81125276,"end":81125373,"strand":-1,"description":"microRNA 657 [Source:HGNC Symbol;Acc:HGNC:32913]"}, {"versioned_ensembl_gene_id":"ENSG00000199295.1","gene_symbol":"RNU6-1312P","gene_name":"RNA, U6 small nuclear 1312, pseudogene [Source:HGNC Symbol;Acc:HGNC:48275]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481594","summary":null,"start":83657735,"end":83657842,"strand":1,"description":"RNA, U6 small nuclear 1312, pseudogene [Source:HGNC Symbol;Acc:HGNC:48275]"}, {"versioned_ensembl_gene_id":"ENSG00000277478.1","gene_symbol":"MIR6165","gene_name":"microRNA 6165 [Source:HGNC Symbol;Acc:HGNC:50197]","synonyms":"hsa-mir-6165","biotype":"miRNA","ncbi_id":"102465141","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49510817,"end":49510900,"strand":1,"description":"microRNA 6165 [Source:HGNC Symbol;Acc:HGNC:50197]"}, {"versioned_ensembl_gene_id":"ENSG00000238759.1","gene_symbol":"RNU7-155P","gene_name":"RNA, U7 small nuclear 155 pseudogene [Source:HGNC Symbol;Acc:HGNC:45689]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480825","summary":null,"start":71298156,"end":71298218,"strand":-1,"description":"RNA, U7 small nuclear 155 pseudogene [Source:HGNC Symbol;Acc:HGNC:45689]"}, {"versioned_ensembl_gene_id":"ENSG00000201957.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":179169083,"end":179169210,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000202331.1","gene_symbol":"RNA5SP167","gene_name":"RNA, 5S ribosomal pseudogene 167 [Source:HGNC Symbol;Acc:HGNC:43067]","synonyms":"RN5S167","biotype":"rRNA","ncbi_id":"100873432","summary":null,"start":149907560,"end":149907675,"strand":1,"description":"RNA, 5S ribosomal pseudogene 167 [Source:HGNC Symbol;Acc:HGNC:43067]"}, {"versioned_ensembl_gene_id":"ENSG00000200832.1","gene_symbol":"SNORD114-4","gene_name":"small nucleolar RNA, C/D box 114-4 [Source:HGNC Symbol;Acc:HGNC:32992]","synonyms":"14q(II-4)","biotype":"snoRNA","ncbi_id":"767580","summary":null,"start":100954374,"end":100954448,"strand":1,"description":"small nucleolar RNA, C/D box 114-4 [Source:HGNC Symbol;Acc:HGNC:32992]"}, {"versioned_ensembl_gene_id":"ENSG00000199753.1","gene_symbol":"SNORD104","gene_name":"small nucleolar RNA, C/D box 104 [Source:HGNC Symbol;Acc:HGNC:32768]","synonyms":"U104","biotype":"snoRNA","ncbi_id":"692227","summary":null,"start":64146083,"end":64146152,"strand":1,"description":"small nucleolar RNA, C/D box 104 [Source:HGNC Symbol;Acc:HGNC:32768]"}, {"versioned_ensembl_gene_id":"ENSG00000200997.1","gene_symbol":"RNU1-85P","gene_name":"RNA, U1 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:48427]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480177","summary":null,"start":58679527,"end":58679690,"strand":-1,"description":"RNA, U1 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:48427]"}, {"versioned_ensembl_gene_id":"ENSG00000206636.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7976259,"end":7976360,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252550.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":105897523,"end":105897643,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000201023.1","gene_symbol":"RNY3P11","gene_name":"RNA, Ro-associated Y3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50887]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481713","summary":null,"start":109305494,"end":109305595,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50887]"}, {"versioned_ensembl_gene_id":"ENSG00000265176.1","gene_symbol":"MIR3202-1","gene_name":"microRNA 3202-1 [Source:HGNC Symbol;Acc:HGNC:38224]","synonyms":"hsa-mir-3202-1","biotype":"miRNA","ncbi_id":"100422987","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153981097,"end":153981177,"strand":1,"description":"microRNA 3202-1 [Source:HGNC Symbol;Acc:HGNC:38224]"}, {"versioned_ensembl_gene_id":"ENSG00000252539.1","gene_symbol":"RNA5SP462","gene_name":"RNA, 5S ribosomal pseudogene 462 [Source:HGNC Symbol;Acc:HGNC:43362]","synonyms":"RN5S462","biotype":"rRNA","ncbi_id":"100873706","summary":null,"start":453134,"end":453245,"strand":1,"description":"RNA, 5S ribosomal pseudogene 462 [Source:HGNC Symbol;Acc:HGNC:43362]"}, {"versioned_ensembl_gene_id":"ENSG00000208032.1","gene_symbol":"MIR548A3","gene_name":"microRNA 548a-3 [Source:HGNC Symbol;Acc:HGNC:32798]","synonyms":"MIRN548A3,hsa-mir-548a-3","biotype":"miRNA","ncbi_id":"693127","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104484369,"end":104484465,"strand":-1,"description":"microRNA 548a-3 [Source:HGNC Symbol;Acc:HGNC:32798]"}, {"versioned_ensembl_gene_id":"ENSG00000265226.1","gene_symbol":"MIR548AI","gene_name":"microRNA 548ai [Source:HGNC Symbol;Acc:HGNC:41854]","synonyms":"hsa-mir-548ai","biotype":"miRNA","ncbi_id":"100616347","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99124609,"end":99124696,"strand":1,"description":"microRNA 548ai [Source:HGNC Symbol;Acc:HGNC:41854]"}, {"versioned_ensembl_gene_id":"ENSG00000200241.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86159956,"end":86160066,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212389.1","gene_symbol":"RNU6-1275P","gene_name":"RNA, U6 small nuclear 1275, pseudogene [Source:HGNC Symbol;Acc:HGNC:48238]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480122","summary":null,"start":147877422,"end":147877528,"strand":1,"description":"RNA, U6 small nuclear 1275, pseudogene [Source:HGNC Symbol;Acc:HGNC:48238]"}, {"versioned_ensembl_gene_id":"ENSG00000283300.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28743208,"end":28743291,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000277506.1","gene_symbol":"RN7SL802P","gene_name":"RNA, 7SL, cytoplasmic 802, pseudogene [Source:HGNC Symbol;Acc:HGNC:46818]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479513","summary":null,"start":101581830,"end":101582128,"strand":1,"description":"RNA, 7SL, cytoplasmic 802, pseudogene [Source:HGNC Symbol;Acc:HGNC:46818]"}, {"versioned_ensembl_gene_id":"ENSG00000241524.3","gene_symbol":"RN7SL632P","gene_name":"RNA, 7SL, cytoplasmic 632, pseudogene [Source:HGNC Symbol;Acc:HGNC:46648]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481095","summary":null,"start":60831664,"end":60831929,"strand":-1,"description":"RNA, 7SL, cytoplasmic 632, pseudogene [Source:HGNC Symbol;Acc:HGNC:46648]"}, {"versioned_ensembl_gene_id":"ENSG00000277553.1","gene_symbol":"HOTTIP_4","gene_name":"HOXA transcript at the distal tip, conserved region 4 [Source:RFAM;Acc:RF02043]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27206139,"end":27206303,"strand":1,"description":"HOXA transcript at the distal tip, conserved region 4 [Source:RFAM;Acc:RF02043]"}, {"versioned_ensembl_gene_id":"ENSG00000198982.4","gene_symbol":"MIR380","gene_name":"microRNA 380 [Source:HGNC Symbol;Acc:HGNC:31873]","synonyms":"MIRN380,hsa-mir-380","biotype":"miRNA","ncbi_id":"494329","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101025017,"end":101025077,"strand":1,"description":"microRNA 380 [Source:HGNC Symbol;Acc:HGNC:31873]"}, {"versioned_ensembl_gene_id":"ENSG00000206835.1","gene_symbol":"RNU1-74P","gene_name":"RNA, U1 small nuclear 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:48416]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480171","summary":null,"start":232832017,"end":232832187,"strand":-1,"description":"RNA, U1 small nuclear 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:48416]"}, {"versioned_ensembl_gene_id":"ENSG00000269889.1","gene_symbol":"AC078802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169769649,"end":169772043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282567.1","gene_symbol":"AC243913.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28716523,"end":28720895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277892.1","gene_symbol":"MIR6746","gene_name":"microRNA 6746 [Source:HGNC Symbol;Acc:HGNC:49925]","synonyms":"hsa-mir-6746","biotype":"miRNA","ncbi_id":"102465446","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61878216,"end":61878278,"strand":-1,"description":"microRNA 6746 [Source:HGNC Symbol;Acc:HGNC:49925]"}, {"versioned_ensembl_gene_id":"ENSG00000206766.1","gene_symbol":"RNU6-435P","gene_name":"RNA, U6 small nuclear 435, pseudogene [Source:HGNC Symbol;Acc:HGNC:47398]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479758","summary":null,"start":24218300,"end":24218404,"strand":1,"description":"RNA, U6 small nuclear 435, pseudogene [Source:HGNC Symbol;Acc:HGNC:47398]"}, {"versioned_ensembl_gene_id":"ENSG00000252766.1","gene_symbol":"RNU6-255P","gene_name":"RNA, U6 small nuclear 255, pseudogene [Source:HGNC Symbol;Acc:HGNC:47218]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481258","summary":null,"start":19018983,"end":19019087,"strand":-1,"description":"RNA, U6 small nuclear 255, pseudogene [Source:HGNC Symbol;Acc:HGNC:47218]"}, {"versioned_ensembl_gene_id":"ENSG00000274711.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130517049,"end":130517312,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000208036.1","gene_symbol":"MIR106B","gene_name":"microRNA 106b [Source:HGNC Symbol;Acc:HGNC:31495]","synonyms":"MIRN106B,hsa-mir-106b","biotype":"miRNA","ncbi_id":"406900","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100093993,"end":100094074,"strand":-1,"description":"microRNA 106b [Source:HGNC Symbol;Acc:HGNC:31495]"}, {"versioned_ensembl_gene_id":"ENSG00000264056.1","gene_symbol":"MIR5685","gene_name":"microRNA 5685 [Source:HGNC Symbol;Acc:HGNC:43543]","synonyms":"hsa-mir-5685","biotype":"miRNA","ncbi_id":"100847075","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53276993,"end":53277071,"strand":1,"description":"microRNA 5685 [Source:HGNC Symbol;Acc:HGNC:43543]"}, {"versioned_ensembl_gene_id":"ENSG00000201423.1","gene_symbol":"RN7SKP246","gene_name":"RNA, 7SK small nuclear pseudogene 246 [Source:HGNC Symbol;Acc:HGNC:45970]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479204","summary":null,"start":144535354,"end":144535670,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 246 [Source:HGNC Symbol;Acc:HGNC:45970]"}, {"versioned_ensembl_gene_id":"ENSG00000206621.1","gene_symbol":"SNORD116-14","gene_name":"small nucleolar RNA, C/D box 116-14 [Source:HGNC Symbol;Acc:HGNC:33080]","synonyms":"HBII-85-14","biotype":"snoRNA","ncbi_id":"100033426","summary":null,"start":25080142,"end":25080233,"strand":1,"description":"small nucleolar RNA, C/D box 116-14 [Source:HGNC Symbol;Acc:HGNC:33080]"}, {"versioned_ensembl_gene_id":"ENSG00000264425.1","gene_symbol":"MIR4653","gene_name":"microRNA 4653 [Source:HGNC Symbol;Acc:HGNC:41562]","synonyms":"hsa-mir-4653","biotype":"miRNA","ncbi_id":"100616117","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101159473,"end":101159555,"strand":1,"description":"microRNA 4653 [Source:HGNC Symbol;Acc:HGNC:41562]"}, {"versioned_ensembl_gene_id":"ENSG00000265422.1","gene_symbol":"MIR4684","gene_name":"microRNA 4684 [Source:HGNC Symbol;Acc:HGNC:41695]","synonyms":"hsa-mir-4684","biotype":"miRNA","ncbi_id":"100616391","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22719517,"end":22719598,"strand":1,"description":"microRNA 4684 [Source:HGNC Symbol;Acc:HGNC:41695]"}, {"versioned_ensembl_gene_id":"ENSG00000283438.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23132730,"end":23133005,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253016.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38274448,"end":38274549,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200385.1","gene_symbol":"SNORA42","gene_name":"Small nucleolar RNA SNORA42/SNORA80 family [Source:RFAM;Acc:RF00406]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":37720425,"end":37720561,"strand":1,"description":"Small nucleolar RNA SNORA42/SNORA80 family [Source:RFAM;Acc:RF00406]"}, {"versioned_ensembl_gene_id":"ENSG00000253080.1","gene_symbol":"RNA5SP373","gene_name":"RNA, 5S ribosomal pseudogene 373 [Source:HGNC Symbol;Acc:HGNC:43273]","synonyms":"RN5S373","biotype":"rRNA","ncbi_id":"100873631","summary":null,"start":111339527,"end":111339621,"strand":1,"description":"RNA, 5S ribosomal pseudogene 373 [Source:HGNC Symbol;Acc:HGNC:43273]"}, {"versioned_ensembl_gene_id":"ENSG00000282422.1","gene_symbol":"AC243913.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28706490,"end":28706648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264014.1","gene_symbol":"MIR4253","gene_name":"microRNA 4253 [Source:HGNC Symbol;Acc:HGNC:38231]","synonyms":"hsa-mir-4253","biotype":"miRNA","ncbi_id":"100422914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22863159,"end":22863226,"strand":-1,"description":"microRNA 4253 [Source:HGNC Symbol;Acc:HGNC:38231]"}, {"versioned_ensembl_gene_id":"ENSG00000274878.1","gene_symbol":"DLEU2_3","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50049591,"end":50049663,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]"}, {"versioned_ensembl_gene_id":"ENSG00000252604.1","gene_symbol":"RNU2-44P","gene_name":"RNA, U2 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:48537]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481648","summary":null,"start":154790291,"end":154790484,"strand":1,"description":"RNA, U2 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:48537]"}, {"versioned_ensembl_gene_id":"ENSG00000207199.1","gene_symbol":"SNORD38","gene_name":"Small nucleolar RNA SNORD38 [Source:RFAM;Acc:RF00212]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":39018615,"end":39018683,"strand":-1,"description":"Small nucleolar RNA SNORD38 [Source:RFAM;Acc:RF00212]"}, {"versioned_ensembl_gene_id":"ENSG00000278108.1","gene_symbol":"MIR6757","gene_name":"microRNA 6757 [Source:HGNC Symbol;Acc:HGNC:50160]","synonyms":"hsa-mir-6757","biotype":"miRNA","ncbi_id":"102466193","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53056944,"end":53057012,"strand":1,"description":"microRNA 6757 [Source:HGNC Symbol;Acc:HGNC:50160]"}, {"versioned_ensembl_gene_id":"ENSG00000273912.1","gene_symbol":"MIR8068","gene_name":"microRNA 8068 [Source:HGNC Symbol;Acc:HGNC:50238]","synonyms":"hsa-mir-8068","biotype":"miRNA","ncbi_id":"102466876","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28477481,"end":28477548,"strand":-1,"description":"microRNA 8068 [Source:HGNC Symbol;Acc:HGNC:50238]"}, {"versioned_ensembl_gene_id":"ENSG00000199700.1","gene_symbol":"RNU6-223P","gene_name":"RNA, U6 small nuclear 223, pseudogene [Source:HGNC Symbol;Acc:HGNC:47186]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481248","summary":null,"start":135960703,"end":135960809,"strand":1,"description":"RNA, U6 small nuclear 223, pseudogene [Source:HGNC Symbol;Acc:HGNC:47186]"}, {"versioned_ensembl_gene_id":"ENSG00000206649.1","gene_symbol":"SNORA20","gene_name":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]","synonyms":"ACA20","biotype":"snoRNA","ncbi_id":"677806","summary":null,"start":80316939,"end":80317069,"strand":-1,"description":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]"}, {"versioned_ensembl_gene_id":"ENSG00000238761.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":112371004,"end":112371107,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000276982.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000207421.1","gene_symbol":"SNORD38B","gene_name":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]","synonyms":"U38B,RNU38B,U38B,RNU38B","biotype":"snoRNA","ncbi_id":"94163","summary":null,"start":44778390,"end":44778456,"strand":1,"description":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]"}, {"versioned_ensembl_gene_id":"ENSG00000242436.3","gene_symbol":"RN7SL789P","gene_name":"RNA, 7SL, cytoplasmic 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:46805]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479508","summary":null,"start":32655016,"end":32655308,"strand":-1,"description":"RNA, 7SL, cytoplasmic 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:46805]"}, {"versioned_ensembl_gene_id":"ENSG00000268991.2","gene_symbol":"FAM231B","gene_name":"family with sequence similarity 231 member B [Source:HGNC Symbol;Acc:HGNC:49506]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100133301","summary":null,"start":16539066,"end":16539575,"strand":1,"description":"family with sequence similarity 231 member B [Source:HGNC Symbol;Acc:HGNC:49506]"}, {"versioned_ensembl_gene_id":"ENSG00000222076.1","gene_symbol":"RNU2-3P","gene_name":"RNA, U2 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:10153]","synonyms":"U2,RNU2P1","biotype":"snRNA","ncbi_id":"26854","summary":null,"start":95745804,"end":95745994,"strand":1,"description":"RNA, U2 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:10153]"}, {"versioned_ensembl_gene_id":"ENSG00000266503.2","gene_symbol":"RN7SL162P","gene_name":"RNA, 7SL, cytoplasmic 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:46178]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481828","summary":null,"start":28642979,"end":28643270,"strand":-1,"description":"RNA, 7SL, cytoplasmic 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:46178]"}, {"versioned_ensembl_gene_id":"ENSG00000265105.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29747821,"end":29747922,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252626.1","gene_symbol":"RNU6-1308P","gene_name":"RNA, U6 small nuclear 1308, pseudogene [Source:HGNC Symbol;Acc:HGNC:48271]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480137","summary":null,"start":107007568,"end":107007670,"strand":1,"description":"RNA, U6 small nuclear 1308, pseudogene [Source:HGNC Symbol;Acc:HGNC:48271]"}, {"versioned_ensembl_gene_id":"ENSG00000202050.1","gene_symbol":"RNU6-391P","gene_name":"RNA, U6 small nuclear 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:47354]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479739","summary":null,"start":24365651,"end":24365754,"strand":1,"description":"RNA, U6 small nuclear 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:47354]"}, {"versioned_ensembl_gene_id":"ENSG00000252332.1","gene_symbol":"RNU6-911P","gene_name":"RNA, U6 small nuclear 911, pseudogene [Source:HGNC Symbol;Acc:HGNC:47874]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479969","summary":null,"start":139448740,"end":139448843,"strand":1,"description":"RNA, U6 small nuclear 911, pseudogene [Source:HGNC Symbol;Acc:HGNC:47874]"}, {"versioned_ensembl_gene_id":"ENSG00000239115.1","gene_symbol":"RNU7-67P","gene_name":"RNA, U7 small nuclear 67 pseudogene [Source:HGNC Symbol;Acc:HGNC:34163]","synonyms":"U7.67","biotype":"snRNA","ncbi_id":"100151665","summary":null,"start":101307367,"end":101307428,"strand":1,"description":"RNA, U7 small nuclear 67 pseudogene [Source:HGNC Symbol;Acc:HGNC:34163]"}, {"versioned_ensembl_gene_id":"ENSG00000212424.1","gene_symbol":"RNU1-119P","gene_name":"RNA, U1 small nuclear 119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48461]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480668","summary":null,"start":44884616,"end":44884780,"strand":1,"description":"RNA, U1 small nuclear 119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48461]"}, {"versioned_ensembl_gene_id":"ENSG00000264102.1","gene_symbol":"MIR4688","gene_name":"microRNA 4688 [Source:HGNC Symbol;Acc:HGNC:41897]","synonyms":"hsa-mir-4688","biotype":"miRNA","ncbi_id":"100616368","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46376402,"end":46376484,"strand":1,"description":"microRNA 4688 [Source:HGNC Symbol;Acc:HGNC:41897]"}, {"versioned_ensembl_gene_id":"ENSG00000202263.1","gene_symbol":"RNA5SP22","gene_name":"RNA, 5S ribosomal pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42590]","synonyms":"RN5S22","biotype":"rRNA","ncbi_id":"100873277","summary":null,"start":78094807,"end":78094915,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42590]"}, {"versioned_ensembl_gene_id":"ENSG00000207146.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108676951,"end":108677057,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221406.1","gene_symbol":"MIR320B2","gene_name":"microRNA 320b-2 [Source:HGNC Symbol;Acc:HGNC:35256]","synonyms":"MIRN320B2,hsa-mir-320b-2","biotype":"miRNA","ncbi_id":"100313769","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":224257004,"end":224257141,"strand":-1,"description":"microRNA 320b-2 [Source:HGNC Symbol;Acc:HGNC:35256]"}, {"versioned_ensembl_gene_id":"ENSG00000200670.1","gene_symbol":"RNU6-912P","gene_name":"RNA, U6 small nuclear 912, pseudogene [Source:HGNC Symbol;Acc:HGNC:47875]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479970","summary":null,"start":65814672,"end":65814775,"strand":1,"description":"RNA, U6 small nuclear 912, pseudogene [Source:HGNC Symbol;Acc:HGNC:47875]"}, {"versioned_ensembl_gene_id":"ENSG00000207077.1","gene_symbol":"RNU6-1119P","gene_name":"RNA, U6 small nuclear 1119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48082]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481533","summary":null,"start":100153672,"end":100153779,"strand":1,"description":"RNA, U6 small nuclear 1119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48082]"}, {"versioned_ensembl_gene_id":"ENSG00000252261.1","gene_symbol":"RNA5SP262","gene_name":"RNA, 5S ribosomal pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:43162]","synonyms":"RN5S262","biotype":"rRNA","ncbi_id":"100873516","summary":null,"start":32192028,"end":32192153,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:43162]"}, {"versioned_ensembl_gene_id":"ENSG00000200064.1","gene_symbol":"RNY4P9","gene_name":"RNA, Ro-associated Y4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:34058]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379300","summary":null,"start":49908634,"end":49908730,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:34058]"}, {"versioned_ensembl_gene_id":"ENSG00000276162.1","gene_symbol":"MIR5739","gene_name":"microRNA 5739 [Source:HGNC Symbol;Acc:HGNC:49977]","synonyms":"hsa-mir-5739","biotype":"miRNA","ncbi_id":"102466081","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28459869,"end":28459948,"strand":1,"description":"microRNA 5739 [Source:HGNC Symbol;Acc:HGNC:49977]"}, {"versioned_ensembl_gene_id":"ENSG00000283385.1","gene_symbol":"MIR4524A","gene_name":"microRNA 4524a [Source:HGNC Symbol;Acc:HGNC:41771]","synonyms":"MIR4524,hsa-mir-4524","biotype":"miRNA","ncbi_id":"100616316","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69099564,"end":69099632,"strand":-1,"description":"microRNA 4524a [Source:HGNC Symbol;Acc:HGNC:41771]"}, {"versioned_ensembl_gene_id":"ENSG00000263918.1","gene_symbol":"MIR3670-1","gene_name":"microRNA 3670-1 [Source:HGNC Symbol;Acc:HGNC:38997]","synonyms":"MIR3670,hsa-mir-3670","biotype":"miRNA","ncbi_id":"100500910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14907717,"end":14907781,"strand":1,"description":"microRNA 3670-1 [Source:HGNC Symbol;Acc:HGNC:38997]"}, {"versioned_ensembl_gene_id":"ENSG00000197889.9","gene_symbol":"MEIG1","gene_name":"meiosis/spermiogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:23429]","synonyms":"SPATA39,bA2K17.3","biotype":"protein_coding","ncbi_id":"644890","summary":null,"start":14959439,"end":14988050,"strand":1,"description":"meiosis/spermiogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:23429]"}, {"versioned_ensembl_gene_id":"ENSG00000179044.15","gene_symbol":"EXOC3L1","gene_name":"exocyst complex component 3 like 1 [Source:HGNC Symbol;Acc:HGNC:27540]","synonyms":"FLJ35587,FLJ35539,EXOC3L","biotype":"protein_coding","ncbi_id":"283849","summary":null,"start":67184366,"end":67190204,"strand":-1,"description":"exocyst complex component 3 like 1 [Source:HGNC Symbol;Acc:HGNC:27540]"}, {"versioned_ensembl_gene_id":"ENSG00000277052.1","gene_symbol":"MIR6763","gene_name":"microRNA 6763 [Source:HGNC Symbol;Acc:HGNC:50139]","synonyms":"hsa-mir-6763","biotype":"miRNA","ncbi_id":"102465975","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132581997,"end":132582061,"strand":1,"description":"microRNA 6763 [Source:HGNC Symbol;Acc:HGNC:50139]"}, {"versioned_ensembl_gene_id":"ENSG00000223321.1","gene_symbol":"RN7SKP293","gene_name":"RNA, 7SK small nuclear pseudogene 293 [Source:HGNC Symbol;Acc:HGNC:46017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480923","summary":null,"start":12406486,"end":12406781,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 293 [Source:HGNC Symbol;Acc:HGNC:46017]"}, {"versioned_ensembl_gene_id":"ENSG00000221333.1","gene_symbol":"MIR548K","gene_name":"microRNA 548k [Source:HGNC Symbol;Acc:HGNC:35285]","synonyms":"MIRN548K,hsa-mir-548k","biotype":"miRNA","ncbi_id":"100313770","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70283955,"end":70284070,"strand":1,"description":"microRNA 548k [Source:HGNC Symbol;Acc:HGNC:35285]"}, {"versioned_ensembl_gene_id":"ENSG00000199373.1","gene_symbol":"RNA5SP453","gene_name":"RNA, 5S ribosomal pseudogene 453 [Source:HGNC Symbol;Acc:HGNC:43353]","synonyms":"RN5S453","biotype":"rRNA","ncbi_id":"100873698","summary":null,"start":32176050,"end":32176168,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 453 [Source:HGNC Symbol;Acc:HGNC:43353]"}, {"versioned_ensembl_gene_id":"ENSG00000273516.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":121008362,"end":121008507,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000238616.1","gene_symbol":"RNU6-300P","gene_name":"RNA, U6 small nuclear 300, pseudogene [Source:HGNC Symbol;Acc:HGNC:47263]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479700","summary":null,"start":151201341,"end":151201444,"strand":1,"description":"RNA, U6 small nuclear 300, pseudogene [Source:HGNC Symbol;Acc:HGNC:47263]"}, {"versioned_ensembl_gene_id":"ENSG00000283276.1","gene_symbol":"ABBA01000935.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91374331,"end":91514157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222810.1","gene_symbol":"RNU2-68P","gene_name":"RNA, U2 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48561]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481962","summary":null,"start":72376979,"end":72377169,"strand":-1,"description":"RNA, U2 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48561]"}, {"versioned_ensembl_gene_id":"ENSG00000200356.1","gene_symbol":"RNU6-833P","gene_name":"RNA, U6 small nuclear 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:47796]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481444","summary":null,"start":73279062,"end":73279168,"strand":1,"description":"RNA, U6 small nuclear 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:47796]"}, {"versioned_ensembl_gene_id":"ENSG00000262354.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69191115,"end":69191215,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221066.1","gene_symbol":"SNORD111","gene_name":"small nucleolar RNA, C/D box 111 [Source:HGNC Symbol;Acc:HGNC:32776]","synonyms":"HBII-82","biotype":"snoRNA","ncbi_id":"692214","summary":null,"start":70538005,"end":70538098,"strand":1,"description":"small nucleolar RNA, C/D box 111 [Source:HGNC Symbol;Acc:HGNC:32776]"}, {"versioned_ensembl_gene_id":"ENSG00000253739.1","gene_symbol":"RNU6-323P","gene_name":"RNA, U6 small nuclear 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:47286]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481281","summary":null,"start":38166012,"end":38166118,"strand":-1,"description":"RNA, U6 small nuclear 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:47286]"}, {"versioned_ensembl_gene_id":"ENSG00000200613.1","gene_symbol":"RNA5SP349","gene_name":"RNA, 5S ribosomal pseudogene 349 [Source:HGNC Symbol;Acc:HGNC:43249]","synonyms":"RN5S349","biotype":"rRNA","ncbi_id":"100873611","summary":null,"start":109120878,"end":109120986,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 349 [Source:HGNC Symbol;Acc:HGNC:43249]"}, {"versioned_ensembl_gene_id":"ENSG00000252238.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":4827001,"end":4827084,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000206903.1","gene_symbol":"SNORA24B","gene_name":"small nucleolar RNA, H/ACA box 24B [Source:HGNC Symbol;Acc:HGNC:52198]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617003","summary":null,"start":65285461,"end":65285591,"strand":-1,"description":"small nucleolar RNA, H/ACA box 24B [Source:HGNC Symbol;Acc:HGNC:52198]"}, {"versioned_ensembl_gene_id":"ENSG00000201277.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":173254190,"end":173254290,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264741.1","gene_symbol":"MIR4505","gene_name":"microRNA 4505 [Source:HGNC Symbol;Acc:HGNC:41743]","synonyms":"hsa-mir-4505","biotype":"miRNA","ncbi_id":"100616158","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":73758747,"end":73758819,"strand":1,"description":"microRNA 4505 [Source:HGNC Symbol;Acc:HGNC:41743]"}, {"versioned_ensembl_gene_id":"ENSG00000221369.1","gene_symbol":"MIR548G","gene_name":"microRNA 548g [Source:HGNC Symbol;Acc:HGNC:35326]","synonyms":"MIRN548G,hsa-mir-548g","biotype":"miRNA","ncbi_id":"100313938","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147344629,"end":147344717,"strand":-1,"description":"microRNA 548g [Source:HGNC Symbol;Acc:HGNC:35326]"}, {"versioned_ensembl_gene_id":"ENSG00000187510.8","gene_symbol":"PLEKHG7","gene_name":"pleckstrin homology and RhoGEF domain containing G7 [Source:HGNC Symbol;Acc:HGNC:33829]","synonyms":"FLJ46688","biotype":"protein_coding","ncbi_id":"440107","summary":null,"start":92721462,"end":92772455,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G7 [Source:HGNC Symbol;Acc:HGNC:33829]"}, {"versioned_ensembl_gene_id":"ENSG00000012983.11","gene_symbol":"MAP4K5","gene_name":"mitogen-activated protein kinase kinase kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6867]","synonyms":"KHS1,KHS,GCKR","biotype":"protein_coding","ncbi_id":"11183","summary":"This gene encodes a member of the serine/threonine protein kinase family, that is highly similar to yeast SPS1/STE20 kinase. Yeast SPS1/STE20 functions near the beginning of the MAP kinase signal cascades that is essential for yeast pheromone response. This kinase was shown to activate Jun kinase in mammalian cells, which suggested a role in stress response. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":50418501,"end":50561126,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6867]"}, {"versioned_ensembl_gene_id":"ENSG00000151748.14","gene_symbol":"SAV1","gene_name":"salvador family WW domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:17795]","synonyms":"WWP4,WW45,salvador","biotype":"protein_coding","ncbi_id":"60485","summary":"WW domain-containing proteins are found in all eukaryotes and play an important role in the regulation of a wide variety of cellular functions such as protein degradation, transcription, and RNA splicing. This gene encodes a protein with two WW domains, a SARAH domain, and a coiled-coil region and is ubiquitously expressed in adult tissues. This protein binds to MST1 (mammalian sterile 20-like kinase 1) and promotes MST1-induced apoptosis. It has also been shown to bind to HAX1 (hematopoietic cell-specific protein 1 (HS1)-associated protein X-1) and to attenuate the anti-apoptotic effects of HAX1. Studies in human and mouse suggest this gene acts as a tumor suppressor. [provided by RefSeq, Aug 2012]","start":50632058,"end":50668331,"strand":-1,"description":"salvador family WW domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:17795]"}, {"versioned_ensembl_gene_id":"ENSG00000237848.1","gene_symbol":"AL606489.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204394541,"end":204394774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261065.1","gene_symbol":"AL592146.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":204131062,"end":204131966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126456.15","gene_symbol":"IRF3","gene_name":"interferon regulatory factor 3 [Source:HGNC Symbol;Acc:HGNC:6118]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3661","summary":"This gene encodes a member of the interferon regulatory transcription factor (IRF) family. The encoded protein is found in an inactive cytoplasmic form that upon serine/threonine phosphorylation forms a complex with CREBBP. This complex translocates to the nucleus and activates the transcription of interferons alpha and beta, as well as other interferon-induced genes. The protein plays an important role in the innate immune response against DNA and RNA viruses. Mutations in this gene are associated with Encephalopathy, acute, infection-induced, herpes-specific, 7. [provided by RefSeq, Sep 2020]","start":49659569,"end":49665875,"strand":-1,"description":"interferon regulatory factor 3 [Source:HGNC Symbol;Acc:HGNC:6118]"}, {"versioned_ensembl_gene_id":"ENSG00000270179.1","gene_symbol":"AP002840.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113368478,"end":113369117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149292.16","gene_symbol":"TTC12","gene_name":"tetratricopeptide repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:23700]","synonyms":"TPARM,FLJ20535,FLJ13859","biotype":"protein_coding","ncbi_id":"54970","summary":null,"start":113314529,"end":113383544,"strand":1,"description":"tetratricopeptide repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:23700]"}, {"versioned_ensembl_gene_id":"ENSG00000141858.11","gene_symbol":"SAMD1","gene_name":"sterile alpha motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17958]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90378","summary":null,"start":14087840,"end":14091036,"strand":-1,"description":"sterile alpha motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17958]"}, {"versioned_ensembl_gene_id":"ENSG00000251678.1","gene_symbol":"AC027343.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7344579,"end":7345921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247732.2","gene_symbol":"AC091951.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7290823,"end":7296345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112941.13","gene_symbol":"PAPD7","gene_name":"poly(A) RNA polymerase D7, non-canonical [Source:HGNC Symbol;Acc:HGNC:16705]","synonyms":"TRF4-1,TRF4,POLS,POLK,LAK-1","biotype":"protein_coding","ncbi_id":"11044","summary":"The protein encoded by this gene is a DNA polymerase that is likely involved in DNA repair. In addition, the encoded protein may be required for sister chromatid adhesion. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jan 2010]","start":6713007,"end":6757048,"strand":1,"description":"poly(A) RNA polymerase D7, non-canonical [Source:HGNC Symbol;Acc:HGNC:16705]"}, {"versioned_ensembl_gene_id":"ENSG00000262099.1","gene_symbol":"AC004148.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5469092,"end":5470360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271963.1","gene_symbol":"AC026786.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133115692,"end":133122340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247970.2","gene_symbol":"AL160313.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99604556,"end":99625740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250842.1","gene_symbol":"AC137770.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145337932,"end":145381670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213326.4","gene_symbol":"RPS7P11","gene_name":"ribosomal protein S7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35841]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644315","summary":null,"start":46721582,"end":46722167,"strand":-1,"description":"ribosomal protein S7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35841]"}, {"versioned_ensembl_gene_id":"ENSG00000262660.1","gene_symbol":"AC139530.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":81703371,"end":81720539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262814.7","gene_symbol":"MRPL12","gene_name":"mitochondrial ribosomal protein L12 [Source:HGNC Symbol;Acc:HGNC:10378]","synonyms":"RPML12,MRPL7/L12,MRPL7","biotype":"protein_coding","ncbi_id":"6182","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein which forms homodimers. In prokaryotic ribosomes, two L7/L12 dimers and one L10 protein form the L8 protein complex. [provided by RefSeq, Jul 2008]","start":81703357,"end":81707526,"strand":1,"description":"mitochondrial ribosomal protein L12 [Source:HGNC Symbol;Acc:HGNC:10378]"}, {"versioned_ensembl_gene_id":"ENSG00000058673.16","gene_symbol":"ZC3H11A","gene_name":"zinc finger CCCH-type containing 11A [Source:HGNC Symbol;Acc:HGNC:29093]","synonyms":"ZC3HDC11A,KIAA0663","biotype":"protein_coding","ncbi_id":"9877","summary":null,"start":203795654,"end":203854999,"strand":1,"description":"zinc finger CCCH-type containing 11A [Source:HGNC Symbol;Acc:HGNC:29093]"}, {"versioned_ensembl_gene_id":"ENSG00000243904.1","gene_symbol":"RPSAP5","gene_name":"ribosomal protein SA pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:20139]","synonyms":"LAMR1P5","biotype":"processed_pseudogene","ncbi_id":"319129","summary":null,"start":103374033,"end":103374916,"strand":-1,"description":"ribosomal protein SA pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:20139]"}, {"versioned_ensembl_gene_id":"ENSG00000266364.1","gene_symbol":"AC087499.8","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20633034,"end":20633259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229402.1","gene_symbol":"AL162151.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99158416,"end":99159669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232573.1","gene_symbol":"RPL3P4","gene_name":"ribosomal protein L3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:19805]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326307","summary":null,"start":98972879,"end":98973301,"strand":-1,"description":"ribosomal protein L3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:19805]"}, {"versioned_ensembl_gene_id":"ENSG00000176605.7","gene_symbol":"C14orf177","gene_name":"chromosome 14 open reading frame 177 [Source:HGNC Symbol;Acc:HGNC:26375]","synonyms":"FLJ25773","biotype":"protein_coding","ncbi_id":"283598","summary":null,"start":98711613,"end":98717761,"strand":1,"description":"chromosome 14 open reading frame 177 [Source:HGNC Symbol;Acc:HGNC:26375]"}, {"versioned_ensembl_gene_id":"ENSG00000231258.2","gene_symbol":"ZSWIM5P2","gene_name":"zinc finger SWIM-type containing 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43769]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132201","summary":null,"start":20583758,"end":20591180,"strand":-1,"description":"zinc finger SWIM-type containing 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43769]"}, {"versioned_ensembl_gene_id":"ENSG00000235323.2","gene_symbol":"COTL1P2","gene_name":"coactosin-like F-actin binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24322]","synonyms":"CLPSMCR","biotype":"processed_pseudogene","ncbi_id":"347720","summary":null,"start":20564538,"end":20564889,"strand":1,"description":"coactosin-like F-actin binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24322]"}, {"versioned_ensembl_gene_id":"ENSG00000259110.1","gene_symbol":"LINC02304","gene_name":"long intergenic non-protein coding RNA 2304 [Source:HGNC Symbol;Acc:HGNC:53223]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370648","summary":null,"start":97154857,"end":97158736,"strand":1,"description":"long intergenic non-protein coding RNA 2304 [Source:HGNC Symbol;Acc:HGNC:53223]"}, {"versioned_ensembl_gene_id":"ENSG00000263946.1","gene_symbol":"AC015818.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20554971,"end":20559410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137726.16","gene_symbol":"FXYD6","gene_name":"FXYD domain containing ion transport regulator 6 [Source:HGNC Symbol;Acc:HGNC:4030]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53826","summary":"This gene encodes a member of the FXYD family of transmembrane proteins. This particular protein encodes phosphohippolin, which likely affects the activity of Na,K-ATPase. Multiple alternatively spliced transcript variants encoding the same protein have been described. Related pseudogenes have been identified on chromosomes 10 and X. Read-through transcripts have been observed between this locus and the downstream sodium/potassium-transporting ATPase subunit gamma (FXYD2, GeneID 486) locus.[provided by RefSeq, Feb 2011]","start":117836976,"end":117877486,"strand":-1,"description":"FXYD domain containing ion transport regulator 6 [Source:HGNC Symbol;Acc:HGNC:4030]"}, {"versioned_ensembl_gene_id":"ENSG00000258401.1","gene_symbol":"AL512361.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49373966,"end":49374383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224025.2","gene_symbol":"AL353616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68609125,"end":68611984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258392.1","gene_symbol":"RPA2P1","gene_name":"replication protein A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19676]","synonyms":"RPA2P","biotype":"processed_pseudogene","ncbi_id":"326628","summary":null,"start":46996454,"end":46997174,"strand":1,"description":"replication protein A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19676]"}, {"versioned_ensembl_gene_id":"ENSG00000105357.15","gene_symbol":"MYH14","gene_name":"myosin heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:23212]","synonyms":"MYH17,MHC16,KIAA2034,FLJ13881,DFNA4","biotype":"protein_coding","ncbi_id":"79784","summary":"This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it should not be confused with the unconventional myosin-14 (MYO14). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene result in one form of autosomal dominant hearing impairment. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":50188186,"end":50310545,"strand":1,"description":"myosin heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:23212]"}, {"versioned_ensembl_gene_id":"ENSG00000267815.1","gene_symbol":"AC008655.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50310022,"end":50310539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133055.8","gene_symbol":"MYBPH","gene_name":"myosin binding protein H [Source:HGNC Symbol;Acc:HGNC:7552]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4608","summary":null,"start":203167811,"end":203175813,"strand":-1,"description":"myosin binding protein H [Source:HGNC Symbol;Acc:HGNC:7552]"}, {"versioned_ensembl_gene_id":"ENSG00000188766.12","gene_symbol":"SPRED3","gene_name":"sprouty related EVH1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:31041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"399473","summary":"This gene encodes a protein with a C-terminal Sprouty-like cysteine-rich domain (SRY) and an N-terminal Ena/Vasodilator-stimulated phosphoprotein (VASP) homology-1 (EVH-1) domain. The encoded protein is a member of a family of proteins that negatively regulates mitogen-activated protein (MAP) kinase signaling, particularly during organogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":38388421,"end":38399587,"strand":1,"description":"sprouty related EVH1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:31041]"}, {"versioned_ensembl_gene_id":"ENSG00000258845.1","gene_symbol":"AL139354.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45567995,"end":45569069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229567.1","gene_symbol":"AL139421.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93278961,"end":93279129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237003.1","gene_symbol":"AC126124.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93190740,"end":93191060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165684.4","gene_symbol":"SNAPC4","gene_name":"small nuclear RNA activating complex polypeptide 4 [Source:HGNC Symbol;Acc:HGNC:11137]","synonyms":"FLJ13451,SNAP190,PTFalpha","biotype":"protein_coding","ncbi_id":"6621","summary":"This gene encodes the largest subunit of the small nuclear RNA-activating protein (SNAP) complex. The encoded protein contains a Myb DNA-binding domain, and is essential for RNA polymerase II and III polymerase transcription from small nuclear RNA promoters. A mutation in this gene is associated with ankylosing spondylitis. [provided by RefSeq, Jul 2016]","start":136375577,"end":136400168,"strand":-1,"description":"small nuclear RNA activating complex polypeptide 4 [Source:HGNC Symbol;Acc:HGNC:11137]"}, {"versioned_ensembl_gene_id":"ENSG00000183475.12","gene_symbol":"ASB7","gene_name":"ankyrin repeat and SOCS box containing 7 [Source:HGNC Symbol;Acc:HGNC:17182]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140460","summary":"The protein encoded by this gene belongs to a family of ankyrin repeat proteins that, along with four other protein families, contains a C-terminal SOCS box motif. Growing evidence suggests that the SOCS box acts as a bridge between specific substrate-binding domains and the more generic proteins that comprise a large family of E3 ubiquitin protein ligases. In this way, SOCS box containing proteins may regulate protein turnover by targeting proteins for polyubiquination and, therefore, for proteasome-mediated degradation. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":100602534,"end":100651705,"strand":1,"description":"ankyrin repeat and SOCS box containing 7 [Source:HGNC Symbol;Acc:HGNC:17182]"}, {"versioned_ensembl_gene_id":"ENSG00000108559.11","gene_symbol":"NUP88","gene_name":"nucleoporin 88 [Source:HGNC Symbol;Acc:HGNC:8067]","synonyms":"MGC8530","biotype":"protein_coding","ncbi_id":"4927","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins, a family of 50 to 100 proteins, are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene belongs to the nucleoporin family and is associated with the oncogenic nucleoporin CAN/Nup214 in a dynamic subcomplex. This protein is also overexpressed in a large number of malignant neoplasms and precancerous dysplasias. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":5360963,"end":5420160,"strand":-1,"description":"nucleoporin 88 [Source:HGNC Symbol;Acc:HGNC:8067]"}, {"versioned_ensembl_gene_id":"ENSG00000231407.5","gene_symbol":"AL354732.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170460453,"end":170532647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233703.1","gene_symbol":"AC027673.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80749632,"end":80751231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153823.18","gene_symbol":"PID1","gene_name":"phosphotyrosine interaction domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26084]","synonyms":"NYGGF4,FLJ20701","biotype":"protein_coding","ncbi_id":"55022","summary":null,"start":228850526,"end":229271285,"strand":-1,"description":"phosphotyrosine interaction domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26084]"}, {"versioned_ensembl_gene_id":"ENSG00000260919.1","gene_symbol":"AC100835.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74613194,"end":74615596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233990.1","gene_symbol":"AL353754.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7833618,"end":7833957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237357.2","gene_symbol":"BX088651.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42566679,"end":42569353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175602.3","gene_symbol":"CCDC85B","gene_name":"coiled-coil domain containing 85B [Source:HGNC Symbol;Acc:HGNC:24926]","synonyms":"DIPA","biotype":"protein_coding","ncbi_id":"11007","summary":"Hepatitis delta virus (HDV) is a pathogenic human virus whose RNA genome and replication cycle resemble those of plant viroids. Delta-interacting protein A (DIPA), a cellular gene product, has been found to have homology to hepatitis delta virus antigen (HDAg). DIPA interacts with the viral antigen, HDAg, and can affect HDV replication in vitro. [provided by RefSeq, Jul 2008]","start":65890112,"end":65891635,"strand":1,"description":"coiled-coil domain containing 85B [Source:HGNC Symbol;Acc:HGNC:24926]"}, {"versioned_ensembl_gene_id":"ENSG00000174059.16","gene_symbol":"CD34","gene_name":"CD34 molecule [Source:HGNC Symbol;Acc:HGNC:1662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"947","summary":"The protein encoded by this gene may play a role in the attachment of stem cells to the bone marrow extracellular matrix or to stromal cells. This single-pass membrane protein is highly glycosylated and phosphorylated by protein kinase C. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":207880972,"end":207911402,"strand":-1,"description":"CD34 molecule [Source:HGNC Symbol;Acc:HGNC:1662]"}, {"versioned_ensembl_gene_id":"ENSG00000238041.3","gene_symbol":"AP004245.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56690465,"end":56690723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225497.5","gene_symbol":"KCNMA1-AS2","gene_name":"KCNMA1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51214]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929310","summary":null,"start":77147652,"end":77150100,"strand":1,"description":"KCNMA1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51214]"}, {"versioned_ensembl_gene_id":"ENSG00000279993.1","gene_symbol":"AC078925.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131025561,"end":131028060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186318.16","gene_symbol":"BACE1","gene_name":"beta-secretase 1 [Source:HGNC Symbol;Acc:HGNC:933]","synonyms":"BACE","biotype":"protein_coding","ncbi_id":"23621","summary":"This gene encodes a member of the peptidase A1 family of aspartic proteases. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protease. This transmembrane protease catalyzes the first step in the formation of amyloid beta peptide from amyloid precursor protein. Amyloid beta peptides are the main constituent of amyloid beta plaques, which accumulate in the brains of human Alzheimer's disease patients. [provided by RefSeq, Nov 2015]","start":117285207,"end":117316259,"strand":-1,"description":"beta-secretase 1 [Source:HGNC Symbol;Acc:HGNC:933]"}, {"versioned_ensembl_gene_id":"ENSG00000210049.1","gene_symbol":"MT-TF","gene_name":"mitochondrially encoded tRNA phenylalanine [Source:HGNC Symbol;Acc:HGNC:7481]","synonyms":"trnF,MTTF","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":577,"end":647,"strand":1,"description":"mitochondrially encoded tRNA phenylalanine [Source:HGNC Symbol;Acc:HGNC:7481]"}, {"versioned_ensembl_gene_id":"ENSG00000211459.2","gene_symbol":"MT-RNR1","gene_name":"mitochondrially encoded 12S RNA [Source:HGNC Symbol;Acc:HGNC:7470]","synonyms":"MTRNR1,12S","biotype":"Mt_rRNA","ncbi_id":null,"summary":null,"start":648,"end":1601,"strand":1,"description":"mitochondrially encoded 12S RNA [Source:HGNC Symbol;Acc:HGNC:7470]"}, {"versioned_ensembl_gene_id":"ENSG00000210077.1","gene_symbol":"MT-TV","gene_name":"mitochondrially encoded tRNA valine [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000198888.2","gene_symbol":"MT-ND1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 [Source:HGNC Symbol;Acc:HGNC:7455]","synonyms":"MTND1,ND1,NAD1","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3307,"end":4262,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 [Source:HGNC Symbol;Acc:HGNC:7455]"}, {"versioned_ensembl_gene_id":"ENSG00000210100.1","gene_symbol":"MT-TI","gene_name":"mitochondrially encoded tRNA isoleucine [Source:HGNC Symbol;Acc:HGNC:7488]","synonyms":"trnI,MTTI","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":4263,"end":4331,"strand":1,"description":"mitochondrially encoded tRNA isoleucine [Source:HGNC Symbol;Acc:HGNC:7488]"}, {"versioned_ensembl_gene_id":"ENSG00000210107.1","gene_symbol":"MT-TQ","gene_name":"mitochondrially encoded tRNA glutamine [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000198804.2","gene_symbol":"MT-CO1","gene_name":"mitochondrially encoded cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:7419]","synonyms":"MTCO1,COX1,COI","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5904,"end":7445,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:7419]"}, {"versioned_ensembl_gene_id":"ENSG00000210151.2","gene_symbol":"MT-TS1","gene_name":"mitochondrially encoded tRNA serine 1 (UCN) [Source:HGNC Symbol;Acc:HGNC:7497]","synonyms":"TRNS1,MTTS1","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":7446,"end":7514,"strand":-1,"description":"mitochondrially encoded tRNA serine 1 (UCN) [Source:HGNC Symbol;Acc:HGNC:7497]"}, {"versioned_ensembl_gene_id":"ENSG00000210154.1","gene_symbol":"MT-TD","gene_name":"mitochondrially encoded tRNA aspartic acid [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000163431.12","gene_symbol":"LMOD1","gene_name":"leiomodin 1 [Source:HGNC Symbol;Acc:HGNC:6647]","synonyms":"D1,64kD,1D","biotype":"protein_coding","ncbi_id":"25802","summary":" The leiomodin 1 protein has a putative membrane-spanning region and 2 types of tandemly repeated blocks. The transcript is expressed in all tissues tested, with the highest levels in thyroid, eye muscle, skeletal muscle, and ovary. Increased expression of leiomodin 1 may be linked to Graves' disease and thyroid-associated ophthalmopathy. [provided by RefSeq, Jul 2008]","start":201896452,"end":201946588,"strand":-1,"description":"leiomodin 1 [Source:HGNC Symbol;Acc:HGNC:6647]"}, {"versioned_ensembl_gene_id":"ENSG00000170549.3","gene_symbol":"IRX1","gene_name":"iroquois homeobox 1 [Source:HGNC Symbol;Acc:HGNC:14358]","synonyms":"IRX-5","biotype":"protein_coding","ncbi_id":"79192","summary":"This gene encodes a member of the Iroquois homeobox protein family. Homeobox genes in this family are involved in pattern formation in the embryo. The gene product has been identified as a tumor suppressor in gastric (PMID: 21602894, 20440264) and head and neck cancers (PMID: 18559491). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Dec 2011]","start":3596054,"end":3601403,"strand":1,"description":"iroquois homeobox 1 [Source:HGNC Symbol;Acc:HGNC:14358]"}, {"versioned_ensembl_gene_id":"ENSG00000228253.1","gene_symbol":"MT-ATP8","gene_name":"mitochondrially encoded ATP synthase 8 [Source:HGNC Symbol;Acc:HGNC:7415]","synonyms":"MTATP8,ATP8,A6L","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8366,"end":8572,"strand":1,"description":"mitochondrially encoded ATP synthase 8 [Source:HGNC Symbol;Acc:HGNC:7415]"}, {"versioned_ensembl_gene_id":"ENSG00000241978.9","gene_symbol":"AKAP2","gene_name":"A-kinase anchoring protein 2 [Source:HGNC Symbol;Acc:HGNC:372]","synonyms":"PRKA2,MISP2,KIAA0920,DKFZp564L0716,AKAP-KL","biotype":"protein_coding","ncbi_id":"11217","summary":null,"start":110048598,"end":110172512,"strand":1,"description":"A-kinase anchoring protein 2 [Source:HGNC Symbol;Acc:HGNC:372]"}, {"versioned_ensembl_gene_id":"ENSG00000259603.1","gene_symbol":"AC016595.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3596211,"end":3600188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198899.2","gene_symbol":"MT-ATP6","gene_name":"mitochondrially encoded ATP synthase 6 [Source:HGNC Symbol;Acc:HGNC:7414]","synonyms":"ATP6,Su6m,RP,MTATP6,ATPase-6","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8527,"end":9207,"strand":1,"description":"mitochondrially encoded ATP synthase 6 [Source:HGNC Symbol;Acc:HGNC:7414]"}, {"versioned_ensembl_gene_id":"ENSG00000258820.5","gene_symbol":"AF111167.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75259411,"end":75271950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272154.4","gene_symbol":"AC244517.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141100242,"end":141174391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235754.7","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"NG20,G3a,ApoM","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31643159,"end":31648952,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000235219.1","gene_symbol":"AC236972.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153203044,"end":153205534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268870.1","gene_symbol":"AC008758.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12391949,"end":12441082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198938.2","gene_symbol":"MT-CO3","gene_name":"mitochondrially encoded cytochrome c oxidase III [Source:HGNC Symbol;Acc:HGNC:7422]","synonyms":"COIII,CO3,MTCO3,COX3","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":9207,"end":9990,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III [Source:HGNC 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core subunit 4L [Source:HGNC Symbol;Acc:HGNC:7460]","synonyms":"ND4L,NAD4L,MTND4L","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10470,"end":10766,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L [Source:HGNC Symbol;Acc:HGNC:7460]"}, {"versioned_ensembl_gene_id":"ENSG00000156575.2","gene_symbol":"PRG3","gene_name":"proteoglycan 3, pro eosinophil major basic protein 2 [Source:HGNC Symbol;Acc:HGNC:9363]","synonyms":"MBPH,MBP2","biotype":"protein_coding","ncbi_id":"10394","summary":null,"start":57376769,"end":57381150,"strand":-1,"description":"proteoglycan 3, pro eosinophil major basic protein 2 [Source:HGNC Symbol;Acc:HGNC:9363]"}, {"versioned_ensembl_gene_id":"ENSG00000117834.12","gene_symbol":"SLC5A9","gene_name":"solute carrier family 5 member 9 [Source:HGNC Symbol;Acc:HGNC:22146]","synonyms":"SGLT4","biotype":"protein_coding","ncbi_id":"200010","summary":null,"start":48222685,"end":48248644,"strand":1,"description":"solute carrier family 5 member 9 [Source:HGNC Symbol;Acc:HGNC:22146]"}, {"versioned_ensembl_gene_id":"ENSG00000198886.2","gene_symbol":"MT-ND4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 [Source:HGNC Symbol;Acc:HGNC:7459]","synonyms":"ND4,NAD4,MTND4,LHON","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10760,"end":12137,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 [Source:HGNC Symbol;Acc:HGNC:7459]"}, {"versioned_ensembl_gene_id":"ENSG00000233452.6","gene_symbol":"STXBP5-AS1","gene_name":"STXBP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44183]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729178","summary":null,"start":146841901,"end":147204614,"strand":-1,"description":"STXBP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44183]"}, {"versioned_ensembl_gene_id":"ENSG00000226752.9","gene_symbol":"PSMD5-AS1","gene_name":"PSMD5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27367]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"253039","summary":null,"start":120824828,"end":120854385,"strand":1,"description":"PSMD5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27367]"}, {"versioned_ensembl_gene_id":"ENSG00000210176.1","gene_symbol":"MT-TH","gene_name":"mitochondrially encoded tRNA histidine [Source:HGNC Symbol;Acc:HGNC:7487]","synonyms":"MTTH,trnH","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":12138,"end":12206,"strand":1,"description":"mitochondrially encoded tRNA histidine [Source:HGNC Symbol;Acc:HGNC:7487]"}, {"versioned_ensembl_gene_id":"ENSG00000170482.16","gene_symbol":"SLC23A1","gene_name":"solute carrier family 23 member 1 [Source:HGNC Symbol;Acc:HGNC:10974]","synonyms":"YSPL3,SVCT1,SLC23A2","biotype":"protein_coding","ncbi_id":"9963","summary":"The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two transporters. The encoded protein is active in bulk vitamin C transport involving epithelial surfaces. Previously, this gene had an official symbol of SLC23A2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":139367196,"end":139384553,"strand":-1,"description":"solute carrier family 23 member 1 [Source:HGNC Symbol;Acc:HGNC:10974]"}, {"versioned_ensembl_gene_id":"ENSG00000210184.1","gene_symbol":"MT-TS2","gene_name":"mitochondrially encoded tRNA serine 2 (AGU/C) [Source:HGNC Symbol;Acc:HGNC:7498]","synonyms":"TRNS2,RP8,MTTS2","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":12207,"end":12265,"strand":1,"description":"mitochondrially encoded tRNA serine 2 (AGU/C) [Source:HGNC Symbol;Acc:HGNC:7498]"}, {"versioned_ensembl_gene_id":"ENSG00000210191.1","gene_symbol":"MT-TL2","gene_name":"mitochondrially encoded tRNA leucine 2 (CUN) [Source:HGNC Symbol;Acc:HGNC:7491]","synonyms":"TRNL2,MTTL2","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":12266,"end":12336,"strand":1,"description":"mitochondrially encoded tRNA leucine 2 (CUN) [Source:HGNC Symbol;Acc:HGNC:7491]"}, {"versioned_ensembl_gene_id":"ENSG00000273010.1","gene_symbol":"AL360270.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110963302,"end":110964649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198786.2","gene_symbol":"MT-ND5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 [Source:HGNC Symbol;Acc:HGNC:7461]","synonyms":"MTND5,ND5,NAD5","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12337,"end":14148,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 [Source:HGNC Symbol;Acc:HGNC:7461]"}, {"versioned_ensembl_gene_id":"ENSG00000228872.2","gene_symbol":"AC096664.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63717122,"end":63717899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259413.2","gene_symbol":"AC011270.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78382573,"end":78383155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278054.1","gene_symbol":"AL591926.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41647825,"end":41648035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275493.1","gene_symbol":"FAM27D1","gene_name":"family with sequence similarity 27 member D1 [Source:HGNC Symbol;Acc:HGNC:32015]","synonyms":"OTTHUMG00000013267","biotype":"processed_pseudogene","ncbi_id":"724094","summary":null,"start":41644430,"end":41644770,"strand":-1,"description":"family with sequence similarity 27 member D1 [Source:HGNC Symbol;Acc:HGNC:32015]"}, {"versioned_ensembl_gene_id":"ENSG00000198695.2","gene_symbol":"MT-ND6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 [Source:HGNC Symbol;Acc:HGNC:7462]","synonyms":"ND6,NAD6,MTND6","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14149,"end":14673,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 [Source:HGNC Symbol;Acc:HGNC:7462]"}, {"versioned_ensembl_gene_id":"ENSG00000099290.15","gene_symbol":"WASHC2A","gene_name":"WASH complex subunit 2A [Source:HGNC Symbol;Acc:HGNC:23416]","synonyms":"FAM21B,FAM21A,bA98I6.1,bA56A21.1,FLJ10824","biotype":"protein_coding","ncbi_id":"387680","summary":null,"start":50067888,"end":50133506,"strand":1,"description":"WASH complex subunit 2A [Source:HGNC Symbol;Acc:HGNC:23416]"}, {"versioned_ensembl_gene_id":"ENSG00000258630.1","gene_symbol":"LINC02292","gene_name":"long intergenic non-protein coding RNA 2292 [Source:HGNC Symbol;Acc:HGNC:53208]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929080","summary":null,"start":95329584,"end":95335504,"strand":1,"description":"long intergenic non-protein coding RNA 2292 [Source:HGNC Symbol;Acc:HGNC:53208]"}, {"versioned_ensembl_gene_id":"ENSG00000210194.1","gene_symbol":"MT-TE","gene_name":"mitochondrially encoded tRNA glutamic acid [Source:HGNC Symbol;Acc:HGNC:7479]","synonyms":"trnE,MTTE","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":14674,"end":14742,"strand":-1,"description":"mitochondrially encoded tRNA glutamic acid [Source:HGNC Symbol;Acc:HGNC:7479]"}, {"versioned_ensembl_gene_id":"ENSG00000224077.1","gene_symbol":"AP000936.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117098987,"end":117108170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198727.2","gene_symbol":"MT-CYB","gene_name":"mitochondrially encoded cytochrome b [Source:HGNC Symbol;Acc:HGNC:7427]","synonyms":"UQCR3,MTCYB,CYTB,COB","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14747,"end":15887,"strand":1,"description":"mitochondrially encoded cytochrome b [Source:HGNC Symbol;Acc:HGNC:7427]"}, {"versioned_ensembl_gene_id":"ENSG00000279983.1","gene_symbol":"AC244517.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":141223372,"end":141245861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280200.1","gene_symbol":"AC073862.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130976786,"end":130978812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143119.12","gene_symbol":"CD53","gene_name":"CD53 molecule [Source:HGNC Symbol;Acc:HGNC:1686]","synonyms":"TSPAN25,MOX44","biotype":"protein_coding","ncbi_id":"963","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins. It contributes to the transduction of CD2-generated signals in T cells and natural killer cells and has been suggested to play a role in growth regulation. Familial deficiency of this gene has been linked to an immunodeficiency associated with recurrent infectious diseases caused by bacteria, fungi and viruses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":110873154,"end":110899928,"strand":1,"description":"CD53 molecule [Source:HGNC Symbol;Acc:HGNC:1686]"}, {"versioned_ensembl_gene_id":"ENSG00000211968.3","gene_symbol":"IGHV1-58","gene_name":"immunoglobulin heavy variable 1-58 [Source:HGNC Symbol;Acc:HGNC:5555]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28464","summary":null,"start":106622357,"end":106622855,"strand":-1,"description":"immunoglobulin heavy variable 1-58 [Source:HGNC Symbol;Acc:HGNC:5555]"}, {"versioned_ensembl_gene_id":"ENSG00000210195.2","gene_symbol":"MT-TT","gene_name":"mitochondrially encoded tRNA threonine [Source:HGNC Symbol;Acc:HGNC:7499]","synonyms":"trnT,MTTT,LIMM","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":15888,"end":15953,"strand":1,"description":"mitochondrially encoded tRNA threonine [Source:HGNC Symbol;Acc:HGNC:7499]"}, {"versioned_ensembl_gene_id":"ENSG00000211966.2","gene_symbol":"IGHV5-51","gene_name":"immunoglobulin heavy variable 5-51 [Source:HGNC Symbol;Acc:HGNC:5659]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28388","summary":null,"start":106578744,"end":106579236,"strand":-1,"description":"immunoglobulin heavy variable 5-51 [Source:HGNC Symbol;Acc:HGNC:5659]"}, {"versioned_ensembl_gene_id":"ENSG00000210196.2","gene_symbol":"MT-TP","gene_name":"mitochondrially encoded tRNA proline [Source:HGNC Symbol;Acc:HGNC:7494]","synonyms":"trnP,MTTP","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":15956,"end":16023,"strand":-1,"description":"mitochondrially encoded tRNA proline [Source:HGNC Symbol;Acc:HGNC:7494]"}, {"versioned_ensembl_gene_id":"ENSG00000256108.1","gene_symbol":"AC135586.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132745156,"end":132745729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170409.7","gene_symbol":"AC091390.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102327256,"end":102329530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260469.2","gene_symbol":"C15orf59-AS1","gene_name":"C15orf59 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51422]","synonyms":"TCONS_00023459","biotype":"lincRNA","ncbi_id":"101929221","summary":null,"start":73752317,"end":73770613,"strand":1,"description":"C15orf59 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51422]"}, {"versioned_ensembl_gene_id":"ENSG00000116962.14","gene_symbol":"NID1","gene_name":"nidogen 1 [Source:HGNC Symbol;Acc:HGNC:7821]","synonyms":"NID,entactin","biotype":"protein_coding","ncbi_id":"4811","summary":"This gene encodes a member of the nidogen family of basement membrane glycoproteins. The protein interacts with several other components of basement membranes, and may play a role in cell interactions with the extracellular matrix. [provided by RefSeq, Jul 2008]","start":235975830,"end":236065162,"strand":-1,"description":"nidogen 1 [Source:HGNC Symbol;Acc:HGNC:7821]"}, {"versioned_ensembl_gene_id":"ENSG00000279096.2","gene_symbol":"AL356289.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48102068,"end":48104736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283562.1","gene_symbol":"IGHVIII-44","gene_name":"immunoglobulin heavy variable (III)-44 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5700]","synonyms":"IGHV(III)-44","biotype":"IG_V_pseudogene","ncbi_id":"28345","summary":null,"start":106478006,"end":106478393,"strand":-1,"description":"immunoglobulin heavy variable (III)-44 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5700]"}, {"versioned_ensembl_gene_id":"ENSG00000260029.2","gene_symbol":"AC007608.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50551824,"end":50553940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106780.8","gene_symbol":"MEGF9","gene_name":"multiple EGF like domains 9 [Source:HGNC Symbol;Acc:HGNC:3234]","synonyms":"EGFL5","biotype":"protein_coding","ncbi_id":"1955","summary":null,"start":120600813,"end":120714470,"strand":-1,"description":"multiple EGF like domains 9 [Source:HGNC Symbol;Acc:HGNC:3234]"}, {"versioned_ensembl_gene_id":"ENSG00000215397.3","gene_symbol":"SCRT2","gene_name":"scratch family transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:15952]","synonyms":"ZNF898B","biotype":"protein_coding","ncbi_id":"85508","summary":null,"start":661596,"end":676179,"strand":-1,"description":"scratch family transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:15952]"}, {"versioned_ensembl_gene_id":"ENSG00000204149.10","gene_symbol":"AGAP6","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 6 [Source:HGNC Symbol;Acc:HGNC:23466]","synonyms":"CTGLF3,bA324H6.1","biotype":"protein_coding","ncbi_id":"414189","summary":null,"start":49982190,"end":50010499,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 6 [Source:HGNC Symbol;Acc:HGNC:23466]"}, {"versioned_ensembl_gene_id":"ENSG00000160185.14","gene_symbol":"UBASH3A","gene_name":"ubiquitin associated and SH3 domain containing A [Source:HGNC Symbol;Acc:HGNC:12462]","synonyms":"TULA,STS-2,CLIP4","biotype":"protein_coding","ncbi_id":"53347","summary":"This gene encodes one of two family members belonging to the T-cell ubiquitin ligand (TULA) family. Both family members can negatively regulate T-cell signaling. This family member can facilitate growth factor withdrawal-induced apoptosis in T cells, which may occur via its interaction with AIF, an apoptosis-inducing factor. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":42403447,"end":42447681,"strand":1,"description":"ubiquitin associated and SH3 domain containing A [Source:HGNC Symbol;Acc:HGNC:12462]"}, {"versioned_ensembl_gene_id":"ENSG00000162076.12","gene_symbol":"FLYWCH2","gene_name":"FLYWCH family member 2 [Source:HGNC Symbol;Acc:HGNC:25178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114984","summary":null,"start":2883186,"end":2899382,"strand":1,"description":"FLYWCH family member 2 [Source:HGNC Symbol;Acc:HGNC:25178]"}, {"versioned_ensembl_gene_id":"ENSG00000227883.1","gene_symbol":"ATP6V0E1P4","gene_name":"ATPase H+ transporting V0 subunit e1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874504","summary":null,"start":47550196,"end":47550753,"strand":1,"description":"ATPase H+ transporting V0 subunit e1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41938]"}, {"versioned_ensembl_gene_id":"ENSG00000229833.9","gene_symbol":"PET100","gene_name":"PET100 homolog [Source:HGNC Symbol;Acc:HGNC:40038]","synonyms":"C19orf79","biotype":"protein_coding","ncbi_id":"100131801","summary":"Mitochondrial complex IV, or cytochrome c oxidase, is a large transmembrane protein complex that is part of the respiratory electron transport chain of mitochondria. The small protein encoded by this gene plays a role in the biogenesis of mitochondrial complex IV. This protein localizes to the inner mitochondrial membrane and is exposed to the intermembrane space. Mutations in this gene are associated with mitochondrial complex IV deficiency. This gene has a pseudogene on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":7629737,"end":7631956,"strand":1,"description":"PET100 homolog [Source:HGNC Symbol;Acc:HGNC:40038]"}, {"versioned_ensembl_gene_id":"ENSG00000205209.7","gene_symbol":"SCGB2B2","gene_name":"secretoglobin family 2B member 2 [Source:HGNC Symbol;Acc:HGNC:27616]","synonyms":"SCGBL,SCGB4A2","biotype":"protein_coding","ncbi_id":"284402","summary":null,"start":34593329,"end":34675699,"strand":-1,"description":"secretoglobin family 2B member 2 [Source:HGNC Symbol;Acc:HGNC:27616]"}, {"versioned_ensembl_gene_id":"ENSG00000205025.8","gene_symbol":"OR5G5P","gene_name":"olfactory receptor family 5 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15289]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56801856,"end":56820422,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15289]"}, {"versioned_ensembl_gene_id":"ENSG00000129951.18","gene_symbol":"PLPPR3","gene_name":"phospholipid phosphatase related 3 [Source:HGNC Symbol;Acc:HGNC:23497]","synonyms":"LPPR3,FLJ11535,PRG2,PRG-2","biotype":"protein_coding","ncbi_id":"79948","summary":"The proteins in the lipid phosphate phosphatase (LPP) family, including PRG2, are integral membrane proteins that modulate bioactive lipid phosphates including phosphatidate, lysophosphatidate, and sphingosine-1-phosphate in the context of cell migration, neurite retraction, and mitogenesis (Brauer et al., 2003 [PubMed 12730698]).[supplied by OMIM, Mar 2008]","start":812488,"end":821977,"strand":-1,"description":"phospholipid phosphatase related 3 [Source:HGNC Symbol;Acc:HGNC:23497]"}, {"versioned_ensembl_gene_id":"ENSG00000117335.19","gene_symbol":"CD46","gene_name":"CD46 molecule [Source:HGNC Symbol;Acc:HGNC:6953]","synonyms":"TRA2.10,TLX,MIC10,MGC26544,MCP","biotype":"protein_coding","ncbi_id":"4179","summary":"The protein encoded by this gene is a type I membrane protein and is a regulatory part of the complement system. The encoded protein has cofactor activity for inactivation of complement components C3b and C4b by serum factor I, which protects the host cell from damage by complement. In addition, the encoded protein can act as a receptor for the Edmonston strain of measles virus, human herpesvirus-6, and type IV pili of pathogenic Neisseria. Finally, the protein encoded by this gene may be involved in the fusion of the spermatozoa with the oocyte during fertilization. Mutations at this locus have been associated with susceptibility to hemolytic uremic syndrome. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2010]","start":207752057,"end":207795513,"strand":1,"description":"CD46 molecule [Source:HGNC Symbol;Acc:HGNC:6953]"}, {"versioned_ensembl_gene_id":"ENSG00000196893.3","gene_symbol":"AC090286.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18951625,"end":18954149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211952.3","gene_symbol":"IGHV4-28","gene_name":"immunoglobulin heavy variable 4-28 [Source:HGNC Symbol;Acc:HGNC:5645]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28400","summary":null,"start":106324254,"end":106324760,"strand":-1,"description":"immunoglobulin heavy variable 4-28 [Source:HGNC Symbol;Acc:HGNC:5645]"}, {"versioned_ensembl_gene_id":"ENSG00000249305.1","gene_symbol":"AC048346.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140619694,"end":140619837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253462.1","gene_symbol":"IGHVIII-26-1","gene_name":"immunoglobulin heavy variable (III)-26-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5698]","synonyms":"IGHV(III)-26-1","biotype":"IG_V_pseudogene","ncbi_id":"28347","summary":null,"start":106309417,"end":106309666,"strand":-1,"description":"immunoglobulin heavy variable (III)-26-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5698]"}, {"versioned_ensembl_gene_id":"ENSG00000255421.1","gene_symbol":"AP002340.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76137315,"end":76137731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113318.9","gene_symbol":"MSH3","gene_name":"mutS homolog 3 [Source:HGNC Symbol;Acc:HGNC:7326]","synonyms":"MRP1,DUP","biotype":"protein_coding","ncbi_id":"4437","summary":"The protein encoded by this gene forms a heterodimer with MSH2 to form MutS beta, part of the post-replicative DNA mismatch repair system. MutS beta initiates mismatch repair by binding to a mismatch and then forming a complex with MutL alpha heterodimer. This gene contains a polymorphic 9 bp tandem repeat sequence in the first exon. The repeat is present 6 times in the reference genome sequence and 3-7 repeats have been reported. Defects in this gene are a cause of susceptibility to endometrial cancer. [provided by RefSeq, Mar 2011]","start":80654648,"end":80876460,"strand":1,"description":"mutS homolog 3 [Source:HGNC Symbol;Acc:HGNC:7326]"}, {"versioned_ensembl_gene_id":"ENSG00000259013.2","gene_symbol":"AL118558.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101969364,"end":101969601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116353.15","gene_symbol":"MECR","gene_name":"mitochondrial trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:19691]","synonyms":"NRBF1,FASN2B,ETR1,CGI-63","biotype":"protein_coding","ncbi_id":"51102","summary":"The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]","start":29192873,"end":29230942,"strand":-1,"description":"mitochondrial trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:19691]"}, {"versioned_ensembl_gene_id":"ENSG00000140459.17","gene_symbol":"CYP11A1","gene_name":"cytochrome P450 family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2590]","synonyms":"P450SCC,CYP11A","biotype":"protein_coding","ncbi_id":"1583","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane and catalyzes the conversion of cholesterol to pregnenolone, the first and rate-limiting step in the synthesis of the steroid hormones. Two transcript variants encoding different isoforms have been found for this gene. The cellular location of the smaller isoform is unclear since it lacks the mitochondrial-targeting transit peptide. [provided by RefSeq, Jul 2008]","start":74337759,"end":74367740,"strand":-1,"description":"cytochrome P450 family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2590]"}, {"versioned_ensembl_gene_id":"ENSG00000183644.13","gene_symbol":"C11orf88","gene_name":"chromosome 11 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:25061]","synonyms":"FLJ46266","biotype":"protein_coding","ncbi_id":"399949","summary":null,"start":111514785,"end":111537031,"strand":1,"description":"chromosome 11 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:25061]"}, {"versioned_ensembl_gene_id":"ENSG00000137707.13","gene_symbol":"BTG4","gene_name":"BTG anti-proliferation factor 4 [Source:HGNC Symbol;Acc:HGNC:13862]","synonyms":"PC3B,APRO3","biotype":"protein_coding","ncbi_id":"54766","summary":"The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein can induce G1 arrest in the cell cycle. [provided by RefSeq, Jul 2008]","start":111467526,"end":111512354,"strand":-1,"description":"BTG anti-proliferation factor 4 [Source:HGNC Symbol;Acc:HGNC:13862]"}, {"versioned_ensembl_gene_id":"ENSG00000178440.5","gene_symbol":"LINC00843","gene_name":"long intergenic non-protein coding RNA 843 [Source:HGNC Symbol;Acc:HGNC:45009]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102902672","summary":null,"start":49972763,"end":49982053,"strand":1,"description":"long intergenic non-protein coding RNA 843 [Source:HGNC Symbol;Acc:HGNC:45009]"}, {"versioned_ensembl_gene_id":"ENSG00000253260.1","gene_symbol":"AC087664.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59561327,"end":59593701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196814.14","gene_symbol":"MVB12B","gene_name":"multivesicular body subunit 12B [Source:HGNC Symbol;Acc:HGNC:23368]","synonyms":"FLJ00001,FAM125B,C9orf28","biotype":"protein_coding","ncbi_id":"89853","summary":"The protein encoded by this gene is a component of the ESCRT-I complex, a heterotetramer, which mediates the sorting of ubiquitinated cargo protein from the plasma membrane to the endosomal vesicle. ESCRT-I complex plays an essential role in HIV budding and endosomal protein sorting. Depletion and overexpression of this and related protein (MVB12A) inhibit HIV-1 infectivity and induce unusual viral assembly defects, indicating a role for MVB12 subunits in regulating ESCRT-mediated virus budding. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":126326849,"end":126507041,"strand":1,"description":"multivesicular body subunit 12B [Source:HGNC Symbol;Acc:HGNC:23368]"}, {"versioned_ensembl_gene_id":"ENSG00000257127.6","gene_symbol":"CLLU1","gene_name":"chronic lymphocytic leukemia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:29841]","synonyms":null,"biotype":"protein_coding","ncbi_id":"574028","summary":"Expression of this gene has been shown to be upregulated in some individuals with chronic lymphocytic leukemia (CLL), and has been used for prognostic and diagnostic purposes. This gene was originally identified as a human-specific putative protein-coding gene due to the presence of a peptide (PAp00140670, HIIYSTFLSK) that could have supported translation at this locus. This peptide is not present in more recent builds of PeptideAtlas, and the presence of a protein product at this locus has not been independently verified. For this reason, this gene is being represented as non-coding. Sequence comparisons to other primates indicates that no other primate is predicted to contain an open reading frame. [provided by RefSeq, Feb 2017]","start":92421531,"end":92431002,"strand":1,"description":"chronic lymphocytic leukemia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:29841]"}, {"versioned_ensembl_gene_id":"ENSG00000249818.1","gene_symbol":"AC097375.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151904932,"end":151928648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158258.16","gene_symbol":"CLSTN2","gene_name":"calsyntenin 2 [Source:HGNC Symbol;Acc:HGNC:17448]","synonyms":"FLJ39113,CSTN2,CS2,CDHR13","biotype":"protein_coding","ncbi_id":"64084","summary":null,"start":139935185,"end":140577397,"strand":1,"description":"calsyntenin 2 [Source:HGNC Symbol;Acc:HGNC:17448]"}, {"versioned_ensembl_gene_id":"ENSG00000232413.1","gene_symbol":"AL589923.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126057580,"end":126159613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254215.1","gene_symbol":"IGHVIII-11-1","gene_name":"immunoglobulin heavy variable (III)-11-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5692]","synonyms":"IGHV(III)-11-1","biotype":"IG_V_pseudogene","ncbi_id":"28352","summary":null,"start":106120207,"end":106120473,"strand":-1,"description":"immunoglobulin heavy variable (III)-11-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5692]"}, {"versioned_ensembl_gene_id":"ENSG00000224044.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464469,"end":29469679,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000265246.1","gene_symbol":"AC129926.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27237859,"end":27241661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124191.17","gene_symbol":"TOX2","gene_name":"TOX high mobility group box family member 2 [Source:HGNC Symbol;Acc:HGNC:16095]","synonyms":"C20orf100,GCX-1,dJ1108D11.2","biotype":"protein_coding","ncbi_id":"84969","summary":null,"start":43914864,"end":44069616,"strand":1,"description":"TOX high mobility group box family member 2 [Source:HGNC Symbol;Acc:HGNC:16095]"}, {"versioned_ensembl_gene_id":"ENSG00000282738.1","gene_symbol":"AC243829.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36161607,"end":36162926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144744.16","gene_symbol":"UBA3","gene_name":"ubiquitin like modifier activating enzyme 3 [Source:HGNC Symbol;Acc:HGNC:12470]","synonyms":"UBE1C,NAE2,hUba3","biotype":"protein_coding","ncbi_id":"9039","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E1 ubiquitin-activating enzyme family. The encoded enzyme associates with AppBp1, an amyloid beta precursor protein binding protein, to form a heterodimer, and then the enzyme complex activates NEDD8, a ubiquitin-like protein, which regulates cell division, signaling and embryogenesis. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":69054730,"end":69080408,"strand":-1,"description":"ubiquitin like modifier activating enzyme 3 [Source:HGNC Symbol;Acc:HGNC:12470]"}, {"versioned_ensembl_gene_id":"ENSG00000167912.5","gene_symbol":"AC090152.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59119040,"end":59121346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198846.5","gene_symbol":"TOX","gene_name":"thymocyte selection associated high mobility group box [Source:HGNC Symbol;Acc:HGNC:18988]","synonyms":"TOX1,KIAA0808","biotype":"protein_coding","ncbi_id":"9760","summary":"The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]","start":58805418,"end":59119208,"strand":-1,"description":"thymocyte selection associated high mobility group box [Source:HGNC Symbol;Acc:HGNC:18988]"}, {"versioned_ensembl_gene_id":"ENSG00000256250.1","gene_symbol":"AC073912.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130810606,"end":130812438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053254.15","gene_symbol":"FOXN3","gene_name":"forkhead box N3 [Source:HGNC Symbol;Acc:HGNC:1928]","synonyms":"CHES1,C14orf116","biotype":"protein_coding","ncbi_id":"1112","summary":"This gene is a member of the forkhead/winged helix transcription factor family. Checkpoints are eukaryotic DNA damage-inducible cell cycle arrests at G1 and G2. Checkpoint suppressor 1 suppresses multiple yeast checkpoint mutations including mec1, rad9, rad53 and dun1 by activating a MEC1-independent checkpoint pathway. Alternative splicing is observed at the locus, resulting in distinct isoforms. [provided by RefSeq, Jul 2008]","start":89124871,"end":89619149,"strand":-1,"description":"forkhead box N3 [Source:HGNC Symbol;Acc:HGNC:1928]"}, {"versioned_ensembl_gene_id":"ENSG00000259073.1","gene_symbol":"FOXN3-AS2","gene_name":"FOXN3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:30119]","synonyms":"PRO1768","biotype":"antisense_RNA","ncbi_id":"29018","summary":null,"start":89576216,"end":89577477,"strand":1,"description":"FOXN3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:30119]"}, {"versioned_ensembl_gene_id":"ENSG00000123643.12","gene_symbol":"SLC36A1","gene_name":"solute carrier family 36 member 1 [Source:HGNC Symbol;Acc:HGNC:18761]","synonyms":"TRAMD3,PAT1,LYAAT-1","biotype":"protein_coding","ncbi_id":"206358","summary":"This gene encodes a member of the eukaryote-specific amino acid/auxin permease (AAAP) 1 transporter family. The encoded protein functions as a proton-dependent, small amino acid transporter. This gene is clustered with related family members on chromosome 5q33.1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":151437046,"end":151492381,"strand":1,"description":"solute carrier family 36 member 1 [Source:HGNC Symbol;Acc:HGNC:18761]"}, {"versioned_ensembl_gene_id":"ENSG00000211933.2","gene_symbol":"IGHV6-1","gene_name":"immunoglobulin heavy variable 6-1 [Source:HGNC Symbol;Acc:HGNC:5662]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28385","summary":null,"start":105939756,"end":105940253,"strand":-1,"description":"immunoglobulin heavy variable 6-1 [Source:HGNC Symbol;Acc:HGNC:5662]"}, {"versioned_ensembl_gene_id":"ENSG00000257065.1","gene_symbol":"AL049844.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":143807092,"end":143844617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000021852.12","gene_symbol":"C8B","gene_name":"complement C8 beta chain [Source:HGNC Symbol;Acc:HGNC:1353]","synonyms":null,"biotype":"protein_coding","ncbi_id":"732","summary":"This gene encodes one of the three subunits of the complement component 8 (C8) protein. C8 is composed of equimolar amounts of alpha, beta and gamma subunits, which are encoded by three separate genes. C8 is one component of the membrane attack complex, which mediates cell lysis, and it initiates membrane penetration of the complex. This protein mediates the interaction of C8 with the C5b-7 membrane attack complex precursor. In humans deficiency of this protein is associated with increased risk of meningococcal infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":56929210,"end":56966140,"strand":-1,"description":"complement C8 beta chain [Source:HGNC Symbol;Acc:HGNC:1353]"}, {"versioned_ensembl_gene_id":"ENSG00000236170.1","gene_symbol":"IGHD1-1","gene_name":"immunoglobulin heavy diversity 1-1 [Source:HGNC Symbol;Acc:HGNC:5482]","synonyms":"IGHD11","biotype":"IG_D_gene","ncbi_id":"28510","summary":null,"start":105919502,"end":105919518,"strand":-1,"description":"immunoglobulin heavy diversity 1-1 [Source:HGNC Symbol;Acc:HGNC:5482]"}, {"versioned_ensembl_gene_id":"ENSG00000226777.7","gene_symbol":"FAM30A","gene_name":"family with sequence similarity 30 member A [Source:HGNC Symbol;Acc:HGNC:19955]","synonyms":"KIAA0125,HSPC053,C14orf110","biotype":"lincRNA","ncbi_id":"9834","summary":null,"start":105917979,"end":105932642,"strand":1,"description":"family with sequence similarity 30 member A [Source:HGNC Symbol;Acc:HGNC:19955]"}, {"versioned_ensembl_gene_id":"ENSG00000255280.1","gene_symbol":"AP001922.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75642600,"end":75642889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270371.1","gene_symbol":"AL122127.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105785505,"end":105785831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254298.1","gene_symbol":"AC008641.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151158106,"end":151158462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244413.1","gene_symbol":"RPL23AP56","gene_name":"ribosomal protein L23a pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35516]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645809","summary":null,"start":134978827,"end":134979279,"strand":-1,"description":"ribosomal protein L23a pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35516]"}, {"versioned_ensembl_gene_id":"ENSG00000236626.1","gene_symbol":"MTND5P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42279]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873353","summary":null,"start":36432882,"end":36434484,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42279]"}, {"versioned_ensembl_gene_id":"ENSG00000187486.5","gene_symbol":"KCNJ11","gene_name":"potassium voltage-gated channel subfamily J member 11 [Source:HGNC Symbol;Acc:HGNC:6257]","synonyms":"Kir6.2,BIR","biotype":"protein_coding","ncbi_id":"3767","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2009]","start":17385859,"end":17389331,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 11 [Source:HGNC Symbol;Acc:HGNC:6257]"}, {"versioned_ensembl_gene_id":"ENSG00000261432.1","gene_symbol":"LINC01613","gene_name":"long intergenic non-protein coding RNA 1613 [Source:HGNC Symbol;Acc:HGNC:51842]","synonyms":"n341773","biotype":"lincRNA","ncbi_id":"106146149","summary":null,"start":119935053,"end":119937832,"strand":1,"description":"long intergenic non-protein coding RNA 1613 [Source:HGNC Symbol;Acc:HGNC:51842]"}, {"versioned_ensembl_gene_id":"ENSG00000278954.1","gene_symbol":"AC130686.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41665566,"end":41668031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268238.1","gene_symbol":"IGFL1P2","gene_name":"IGF like family member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32957]","synonyms":"IGFL-6P","biotype":"unprocessed_pseudogene","ncbi_id":"727704","summary":null,"start":46260420,"end":46260858,"strand":-1,"description":"IGF like family member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32957]"}, {"versioned_ensembl_gene_id":"ENSG00000155087.3","gene_symbol":"ODF1","gene_name":"outer dense fiber of sperm tails 1 [Source:HGNC Symbol;Acc:HGNC:8113]","synonyms":"CT133,RT7,ODFPG,ODF27,HSPB10","biotype":"protein_coding","ncbi_id":"4956","summary":"The outer dense fibers are cytoskeletal structures that surround the axoneme in the middle piece and principal piece of the sperm tail. The fibers function in maintaining the elastic structure and recoil of the sperm tail as well as in protecting the tail from shear forces during epididymal transport and ejaculation. Defects in the outer dense fibers lead to abnormal sperm morphology and infertility. The human outer dense fibers contains at least 10 major proteins and this gene encodes the main protein. [provided by RefSeq, Jul 2008]","start":102551572,"end":102561017,"strand":1,"description":"outer dense fiber of sperm tails 1 [Source:HGNC Symbol;Acc:HGNC:8113]"}, {"versioned_ensembl_gene_id":"ENSG00000249602.1","gene_symbol":"AL589765.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151763384,"end":151769501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203288.3","gene_symbol":"TDRKH-AS1","gene_name":"TDRKH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40578]","synonyms":"RP11-98D18.9","biotype":"antisense_RNA","ncbi_id":"109729141","summary":null,"start":151790804,"end":151794402,"strand":1,"description":"TDRKH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40578]"}, {"versioned_ensembl_gene_id":"ENSG00000100284.20","gene_symbol":"TOM1","gene_name":"target of myb1 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11982]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10043","summary":"This gene was identified as a target of the v-myb oncogene. The encoded protein shares its N-terminal domain in common with proteins associated with vesicular trafficking at the endosome. It is recruited to the endosomes by its interaction with endofin. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":35299275,"end":35347994,"strand":1,"description":"target of myb1 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11982]"}, {"versioned_ensembl_gene_id":"ENSG00000237273.1","gene_symbol":"RSL24D1P8","gene_name":"ribosomal L24 domain containing 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37873]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462809","summary":null,"start":12096424,"end":12096915,"strand":1,"description":"ribosomal L24 domain containing 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37873]"}, {"versioned_ensembl_gene_id":"ENSG00000239269.1","gene_symbol":"RPSAP4","gene_name":"ribosomal protein SA pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:20018]","synonyms":"LAMR1P4","biotype":"processed_pseudogene","ncbi_id":"145259","summary":null,"start":94726288,"end":94727175,"strand":1,"description":"ribosomal protein SA pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:20018]"}, {"versioned_ensembl_gene_id":"ENSG00000268916.6","gene_symbol":"CSAG3","gene_name":"CSAG family member 3 [Source:HGNC Symbol;Acc:HGNC:26237]","synonyms":"CSAG3A","biotype":"protein_coding","ncbi_id":"389903","summary":null,"start":152753921,"end":152760222,"strand":1,"description":"CSAG family member 3 [Source:HGNC Symbol;Acc:HGNC:26237]"}, {"versioned_ensembl_gene_id":"ENSG00000214827.9","gene_symbol":"MTCP1","gene_name":"mature T-cell proliferation 1 [Source:HGNC Symbol;Acc:HGNC:7423]","synonyms":"p8MTCP1,P13MTCP1","biotype":"protein_coding","ncbi_id":"4515","summary":"This gene was identified by involvement in some t(X;14) translocations associated with mature T-cell proliferations. This region has a complex gene structure, with a common promoter and 5' exon spliced to two different sets of 3' exons that encode two different proteins. This gene represents the upstream 13 kDa protein that is a member of the TCL1 family. This protein may be involved in leukemogenesis. [provided by RefSeq, Mar 2009]","start":155061622,"end":155147937,"strand":-1,"description":"mature T-cell proliferation 1 [Source:HGNC Symbol;Acc:HGNC:7423]"}, {"versioned_ensembl_gene_id":"ENSG00000160803.7","gene_symbol":"UBQLN4","gene_name":"ubiquilin 4 [Source:HGNC Symbol;Acc:HGNC:1237]","synonyms":"A1U,UBIN,C1orf6","biotype":"protein_coding","ncbi_id":"56893","summary":null,"start":156035301,"end":156053794,"strand":-1,"description":"ubiquilin 4 [Source:HGNC Symbol;Acc:HGNC:1237]"}, {"versioned_ensembl_gene_id":"ENSG00000186020.12","gene_symbol":"ZNF529","gene_name":"zinc finger protein 529 [Source:HGNC Symbol;Acc:HGNC:29328]","synonyms":"KIAA1615","biotype":"protein_coding","ncbi_id":"57711","summary":null,"start":36534774,"end":36605276,"strand":-1,"description":"zinc finger protein 529 [Source:HGNC Symbol;Acc:HGNC:29328]"}, {"versioned_ensembl_gene_id":"ENSG00000075914.12","gene_symbol":"EXOSC7","gene_name":"exosome component 7 [Source:HGNC Symbol;Acc:HGNC:28112]","synonyms":"hRrp42p,EAP1,Rrp42p,RRP42,p8,KIAA0116","biotype":"protein_coding","ncbi_id":"23016","summary":null,"start":44975241,"end":45036066,"strand":1,"description":"exosome component 7 [Source:HGNC Symbol;Acc:HGNC:28112]"}, {"versioned_ensembl_gene_id":"ENSG00000233646.1","gene_symbol":"OR52T1P","gene_name":"olfactory receptor family 52 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15236]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81244","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5566678,"end":5567616,"strand":-1,"description":"olfactory receptor family 52 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15236]"}, {"versioned_ensembl_gene_id":"ENSG00000268288.1","gene_symbol":"AL589765.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151766486,"end":151767000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258659.6","gene_symbol":"TRIM34","gene_name":"tripartite motif containing 34 [Source:HGNC Symbol;Acc:HGNC:10063]","synonyms":"RNF21","biotype":"protein_coding","ncbi_id":"53840","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, B-box type 1 and B-box type 2 domain, and a coiled-coil region. Expression of this gene is up-regulated by interferon. This gene is mapped to chromosome 11p15, where it resides within a TRIM gene cluster. Alternative splicing results in multiple transcript variants. A read-through transcript from the upstream TRIM6 gene has also been observed, which results in a fusion product from these neighboring family members. [provided by RefSeq, Oct 2010]","start":5619764,"end":5644398,"strand":1,"description":"tripartite motif containing 34 [Source:HGNC Symbol;Acc:HGNC:10063]"}, {"versioned_ensembl_gene_id":"ENSG00000229704.1","gene_symbol":"EIF2S2P2","gene_name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24654]","synonyms":"bcm2636","biotype":"processed_pseudogene","ncbi_id":"347673","summary":null,"start":185245460,"end":185246441,"strand":-1,"description":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24654]"}, {"versioned_ensembl_gene_id":"ENSG00000278339.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755024,"end":54767369,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000239600.1","gene_symbol":"AP000797.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115951105,"end":115951491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167083.6","gene_symbol":"GNGT2","gene_name":"G protein subunit gamma transducin 2 [Source:HGNC Symbol;Acc:HGNC:4412]","synonyms":"GNG9","biotype":"protein_coding","ncbi_id":"2793","summary":"Phototransduction in rod and cone photoreceptors is regulated by groups of signaling proteins. The encoded protein is thought to play a crucial role in cone phototransduction. It belongs to the G protein gamma family and localized specifically in cones. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2010]","start":49202791,"end":49210574,"strand":-1,"description":"G protein subunit gamma transducin 2 [Source:HGNC Symbol;Acc:HGNC:4412]"}, {"versioned_ensembl_gene_id":"ENSG00000162885.12","gene_symbol":"B3GALNT2","gene_name":"beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]","synonyms":"MGC39558","biotype":"protein_coding","ncbi_id":"148789","summary":"This gene encodes a member of the glycosyltransferase 31 family. The encoded protein synthesizes GalNAc:beta-1,3GlcNAc, a novel carbohydrate structure, on N- and O-glycans. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2013]","start":235449923,"end":235504481,"strand":-1,"description":"beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]"}, {"versioned_ensembl_gene_id":"ENSG00000279818.1","gene_symbol":"AP002991.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":115731942,"end":115734742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178243.4","gene_symbol":"C9orf62","gene_name":"chromosome 9 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:28581]","synonyms":"MGC35463","biotype":"lincRNA","ncbi_id":"157927","summary":null,"start":135343249,"end":135346562,"strand":1,"description":"chromosome 9 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:28581]"}, {"versioned_ensembl_gene_id":"ENSG00000146001.5","gene_symbol":"PCDHB18P","gene_name":"protocadherin beta 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:14548]","synonyms":"PCDHB18,PCDH-psi2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54660","summary":null,"start":141234333,"end":141237529,"strand":1,"description":"protocadherin beta 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:14548]"}, {"versioned_ensembl_gene_id":"ENSG00000250719.1","gene_symbol":"AL672043.1","gene_name":"Homo sapiens uncharacterized LOC110117498 (LOC110117498), mRNA. [Source:RefSeq mRNA;Acc:NM_001328655]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46175486,"end":46176478,"strand":-1,"description":"Homo sapiens uncharacterized LOC110117498 (LOC110117498), mRNA. [Source:RefSeq mRNA;Acc:NM_001328655]"}, {"versioned_ensembl_gene_id":"ENSG00000273736.1","gene_symbol":"AC244100.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35963488,"end":35965472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214514.7","gene_symbol":"KRT42P","gene_name":"keratin 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:27581]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284116","summary":null,"start":41626327,"end":41640199,"strand":-1,"description":"keratin 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:27581]"}, {"versioned_ensembl_gene_id":"ENSG00000226957.1","gene_symbol":"AL358075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46046818,"end":46048368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260136.5","gene_symbol":"AC008915.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23452758,"end":23457606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160284.14","gene_symbol":"SPATC1L","gene_name":"spermatogenesis and centriole associated 1 like [Source:HGNC Symbol;Acc:HGNC:1298]","synonyms":"C21orf56","biotype":"protein_coding","ncbi_id":"84221","summary":null,"start":46161148,"end":46184476,"strand":-1,"description":"spermatogenesis and centriole associated 1 like [Source:HGNC Symbol;Acc:HGNC:1298]"}, {"versioned_ensembl_gene_id":"ENSG00000280039.1","gene_symbol":"RN7SKP23","gene_name":"RNA, 7SK small nuclear pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:45747]","synonyms":null,"biotype":"TEC","ncbi_id":"106479105","summary":null,"start":23412380,"end":23416680,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:45747]"}, {"versioned_ensembl_gene_id":"ENSG00000259782.2","gene_symbol":"AC008915.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":23446446,"end":23447282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117461.14","gene_symbol":"PIK3R3","gene_name":"phosphoinositide-3-kinase regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:8981]","synonyms":"p55","biotype":"protein_coding","ncbi_id":"8503","summary":"Phosphatidylinositol 3-kinase (PI3K) phosphorylates phosphatidylinositol and similar compounds, which then serve as second messengers in growth signaling pathways. PI3K is composed of a catalytic and a regulatory subunit. The protein encoded by this gene represents a regulatory subunit of PI3K. The encoded protein contains two SH2 domains through which it binds activated protein tyrosine kinases to regulate their activity. [provided by RefSeq, Jun 2016]","start":46040140,"end":46133036,"strand":-1,"description":"phosphoinositide-3-kinase regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:8981]"}, {"versioned_ensembl_gene_id":"ENSG00000279047.3","gene_symbol":"AC244517.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141046260,"end":141096402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197149.5","gene_symbol":"AC107956.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17228279,"end":17229151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104967.6","gene_symbol":"NOVA2","gene_name":"NOVA alternative splicing regulator 2 [Source:HGNC Symbol;Acc:HGNC:7887]","synonyms":"NOVA3,ANOVA","biotype":"protein_coding","ncbi_id":"4858","summary":null,"start":45933734,"end":45973546,"strand":-1,"description":"NOVA alternative splicing regulator 2 [Source:HGNC Symbol;Acc:HGNC:7887]"}, {"versioned_ensembl_gene_id":"ENSG00000277539.1","gene_symbol":"AC138058.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71276087,"end":71289616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229732.1","gene_symbol":"AC019349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41500983,"end":41502409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223609.7","gene_symbol":"HBD","gene_name":"hemoglobin subunit delta [Source:HGNC Symbol;Acc:HGNC:4829]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3045","summary":"The delta (HBD) and beta (HBB) genes are normally expressed in the adult: two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin. Two alpha chains plus two delta chains constitute HbA-2, which with HbF comprises the remaining 3% of adult hemoglobin. Five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5'-epsilon--Ggamma--Agamma--delta--beta-3'. Mutations in the delta-globin gene are associated with beta-thalassemia. [provided by RefSeq, Jul 2008]","start":5232678,"end":5235370,"strand":-1,"description":"hemoglobin subunit delta [Source:HGNC Symbol;Acc:HGNC:4829]"}, {"versioned_ensembl_gene_id":"ENSG00000099617.3","gene_symbol":"EFNA2","gene_name":"ephrin A2 [Source:HGNC Symbol;Acc:HGNC:3222]","synonyms":"LERK6,EPLG6,ELF-1","biotype":"protein_coding","ncbi_id":"1943","summary":"This gene encodes a member of the ephrin family. The protein is composed of a signal sequence, a receptor-binding region, a spacer region, and a hydrophobic region. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. Posttranslational modifications determine whether this protein localizes to the nucleus or the cytoplasm. [provided by RefSeq, Jul 2008]","start":1286154,"end":1300237,"strand":1,"description":"ephrin A2 [Source:HGNC Symbol;Acc:HGNC:3222]"}, {"versioned_ensembl_gene_id":"ENSG00000229992.1","gene_symbol":"HMGB3P9","gene_name":"high mobility group box 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39301]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873879","summary":null,"start":92647048,"end":92647630,"strand":-1,"description":"high mobility group box 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39301]"}, {"versioned_ensembl_gene_id":"ENSG00000254629.1","gene_symbol":"AP002370.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83789977,"end":83791578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266973.1","gene_symbol":"AC092296.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36378028,"end":36378832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235924.1","gene_symbol":"ZNRF2P3","gene_name":"zinc and ring finger 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45113]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130879","summary":null,"start":79981839,"end":79982212,"strand":1,"description":"zinc and ring finger 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45113]"}, {"versioned_ensembl_gene_id":"ENSG00000276868.1","gene_symbol":"AL353626.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40883634,"end":40883763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249778.1","gene_symbol":"TRMT112P2","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479033","summary":null,"start":80033171,"end":80033302,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44021]"}, {"versioned_ensembl_gene_id":"ENSG00000235220.10","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29720256,"end":29736008,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000240871.5","gene_symbol":"KRTAP4-7","gene_name":"keratin associated protein 4-7 [Source:HGNC Symbol;Acc:HGNC:18898]","synonyms":"KAP4.7","biotype":"protein_coding","ncbi_id":"100132476","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Mar 2009]","start":41084150,"end":41085141,"strand":1,"description":"keratin associated protein 4-7 [Source:HGNC Symbol;Acc:HGNC:18898]"}, {"versioned_ensembl_gene_id":"ENSG00000236838.2","gene_symbol":"AC090617.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2213697,"end":2214414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275386.1","gene_symbol":"AC105081.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":93974671,"end":93974776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255037.1","gene_symbol":"AC136443.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14766402,"end":14770075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198496.10","gene_symbol":"NBR2","gene_name":"neighbor of BRCA1 gene 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20691]","synonyms":"NCRNA00192","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10230","summary":"This gene was identified by its close proximity on chromosome 17 to tumor suppressor gene BRCA1. Experimental evidence indicates that the two genes share a bi-directional promoter. Transcription for either gene is controlled individually by distinct transcriptional repressor factors. A short (112 amino acid) open reading frame is observed which includes a region derived from a LINE1 element. A strong Kozak signal is not observed for the putative ORF and the stop codon is more than 55 nucleotides upstream of the last splice site for the transcript, suggesting that the transcript is subject to nonsense-mediated decay. Therefore, this gene does not appear to encode a protein. Glucose starvation induces the expression of this gene and the long non-coding RNA transcribed by it functions with AMP-activated protein kinase in mediating the energy stress response. [provided by RefSeq, Aug 2016]","start":43125610,"end":43153671,"strand":1,"description":"neighbor of BRCA1 gene 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20691]"}, {"versioned_ensembl_gene_id":"ENSG00000255341.1","gene_symbol":"OR8Q1P","gene_name":"olfactory receptor family 8 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15317]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81163","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124601584,"end":124602238,"strand":1,"description":"olfactory receptor family 8 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15317]"}, {"versioned_ensembl_gene_id":"ENSG00000274473.2","gene_symbol":"SCT","gene_name":"secretin [Source:HGNC Symbol;Acc:HGNC:10607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6343","summary":"This gene encodes a member of the glucagon family of peptides. The encoded preproprotein is secreted by endocrine S cells in the proximal small intestinal mucosa as a prohormone, then proteolytically processed to generate the mature peptide hormone. The release of this active peptide hormone is stimulated by either fatty acids or acidic pH in the duodenum. This hormone stimulates the secretion of bile and bicarbonate in the duodenum, pancreatic and biliary ducts. [provided by RefSeq, Feb 2016]","start":626689,"end":627401,"strand":-1,"description":"secretin [Source:HGNC Symbol;Acc:HGNC:10607]"}, {"versioned_ensembl_gene_id":"ENSG00000223604.1","gene_symbol":"AC007394.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149439897,"end":149440427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175329.12","gene_symbol":"ISX","gene_name":"intestine specific homeobox [Source:HGNC Symbol;Acc:HGNC:28084]","synonyms":"RAXLX","biotype":"protein_coding","ncbi_id":"91464","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the RAXLX homeobox gene family. [provided by RefSeq, Jul 2008]","start":35066136,"end":35087387,"strand":1,"description":"intestine specific homeobox [Source:HGNC Symbol;Acc:HGNC:28084]"}, {"versioned_ensembl_gene_id":"ENSG00000236237.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31656860,"end":31658827,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000253852.1","gene_symbol":"AC011383.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150608428,"end":150615354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165868.13","gene_symbol":"HSPA12A","gene_name":"heat shock protein family A (Hsp70) member 12A [Source:HGNC Symbol;Acc:HGNC:19022]","synonyms":"KIAA0417,FLJ13874","biotype":"protein_coding","ncbi_id":"259217","summary":null,"start":116671192,"end":116849741,"strand":-1,"description":"heat shock protein family A (Hsp70) member 12A [Source:HGNC Symbol;Acc:HGNC:19022]"}, {"versioned_ensembl_gene_id":"ENSG00000237544.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29475501,"end":29476547,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000276896.4","gene_symbol":"GOLGA8F","gene_name":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]","synonyms":"DKFZp434P162","biotype":"protein_coding","ncbi_id":"100132565","summary":null,"start":28378587,"end":28391990,"strand":1,"description":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]"}, {"versioned_ensembl_gene_id":"ENSG00000152422.15","gene_symbol":"XRCC4","gene_name":"X-ray repair cross complementing 4 [Source:HGNC Symbol;Acc:HGNC:12831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7518","summary":"The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternate transcript variants such as NM_022406 are unlikely to be expressed in some individuals due to a polymorphism (rs1805377) in the last splice acceptor site. [provided by RefSeq, Oct 2019]","start":83077498,"end":83353787,"strand":1,"description":"X-ray repair cross complementing 4 [Source:HGNC Symbol;Acc:HGNC:12831]"}, {"versioned_ensembl_gene_id":"ENSG00000259803.6","gene_symbol":"SLC22A31","gene_name":"solute carrier family 22 member 31 [Source:HGNC Symbol;Acc:HGNC:27091]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146429","summary":null,"start":89195761,"end":89201664,"strand":-1,"description":"solute carrier family 22 member 31 [Source:HGNC Symbol;Acc:HGNC:27091]"}, {"versioned_ensembl_gene_id":"ENSG00000280333.1","gene_symbol":"AC090617.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2072823,"end":2072956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248807.1","gene_symbol":"KRTAP9-12P","gene_name":"keratin associated protein 9-12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48873]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287715","summary":null,"start":41212706,"end":41213237,"strand":1,"description":"keratin associated protein 9-12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48873]"}, {"versioned_ensembl_gene_id":"ENSG00000280051.1","gene_symbol":"AC079456.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":129262345,"end":129262824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160325.14","gene_symbol":"CACFD1","gene_name":"calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]","synonyms":"flower,D9S2135,C9orf7","biotype":"protein_coding","ncbi_id":"11094","summary":null,"start":133459965,"end":133470848,"strand":1,"description":"calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]"}, {"versioned_ensembl_gene_id":"ENSG00000256699.1","gene_symbol":"TMEM132D-AS2","gene_name":"TMEM132D antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:53324]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927735","summary":null,"start":129208601,"end":129212662,"strand":1,"description":"TMEM132D antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:53324]"}, {"versioned_ensembl_gene_id":"ENSG00000258673.1","gene_symbol":"LINC01397","gene_name":"long intergenic non-protein coding RNA 1397 [Source:HGNC Symbol;Acc:HGNC:50677]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355139","summary":null,"start":110082688,"end":110109719,"strand":1,"description":"long intergenic non-protein coding RNA 1397 [Source:HGNC Symbol;Acc:HGNC:50677]"}, {"versioned_ensembl_gene_id":"ENSG00000215883.10","gene_symbol":"CYB5RL","gene_name":"cytochrome b5 reductase like [Source:HGNC Symbol;Acc:HGNC:32220]","synonyms":"LOC606495","biotype":"protein_coding","ncbi_id":"606495","summary":null,"start":54169651,"end":54200036,"strand":-1,"description":"cytochrome b5 reductase like [Source:HGNC Symbol;Acc:HGNC:32220]"}, {"versioned_ensembl_gene_id":"ENSG00000135083.14","gene_symbol":"CCNJL","gene_name":"cyclin J like [Source:HGNC Symbol;Acc:HGNC:25876]","synonyms":"FLJ14166","biotype":"protein_coding","ncbi_id":"79616","summary":null,"start":160251652,"end":160345396,"strand":-1,"description":"cyclin J like [Source:HGNC Symbol;Acc:HGNC:25876]"}, {"versioned_ensembl_gene_id":"ENSG00000140691.16","gene_symbol":"ARMC5","gene_name":"armadillo repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:25781]","synonyms":"FLJ13063","biotype":"protein_coding","ncbi_id":"79798","summary":"This gene encodes a member of the ARM (armadillo/beta-catenin-like repeat) superfamily. The ARM repeat is a tandemly repeated sequence motif with approximately 40 amino acid long. This repeat is implicated in mediating protein-protein interactions. The encoded protein contains seven ARM repeats. Mutations in this gene are associated with primary bilateral macronodular adrenal hyperplasia, which is also known as ACTH-independent macronodular adrenal hyperplasia 2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":31458080,"end":31467166,"strand":1,"description":"armadillo repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:25781]"}, {"versioned_ensembl_gene_id":"ENSG00000250821.2","gene_symbol":"EXOC1L","gene_name":"exocyst complex component 1 like [Source:HGNC Symbol;Acc:HGNC:53433]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644145","summary":null,"start":55819819,"end":55837487,"strand":1,"description":"exocyst complex component 1 like [Source:HGNC Symbol;Acc:HGNC:53433]"}, {"versioned_ensembl_gene_id":"ENSG00000256407.2","gene_symbol":"AL357673.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54132686,"end":54200073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242067.1","gene_symbol":"AC091179.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48691116,"end":48691694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171014.2","gene_symbol":"OR4D5","gene_name":"olfactory receptor family 4 subfamily D member 5 [Source:HGNC Symbol;Acc:HGNC:14852]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219875","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123939543,"end":123940637,"strand":1,"description":"olfactory receptor family 4 subfamily D member 5 [Source:HGNC Symbol;Acc:HGNC:14852]"}, {"versioned_ensembl_gene_id":"ENSG00000141298.17","gene_symbol":"SSH2","gene_name":"slingshot protein phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:30580]","synonyms":"KIAA1725","biotype":"protein_coding","ncbi_id":"85464","summary":"This gene encodes a protein tyrosine phosphatase that plays a key role in the regulation of actin filaments. The encoded protein dephosphorylates and activates cofilin, which promotes actin filament depolymerization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":29625938,"end":29930276,"strand":-1,"description":"slingshot protein phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:30580]"}, {"versioned_ensembl_gene_id":"ENSG00000229388.1","gene_symbol":"LINC01715","gene_name":"long intergenic non-protein coding RNA 1715 [Source:HGNC Symbol;Acc:HGNC:52502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378616","summary":null,"start":28643228,"end":28648581,"strand":1,"description":"long intergenic non-protein coding RNA 1715 [Source:HGNC Symbol;Acc:HGNC:52502]"}, {"versioned_ensembl_gene_id":"ENSG00000263063.1","gene_symbol":"AC024361.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82713908,"end":82716255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264985.2","gene_symbol":"AC124804.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73513612,"end":73521407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233271.1","gene_symbol":"AL590440.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54980950,"end":54992274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143001.4","gene_symbol":"TMEM61","gene_name":"transmembrane protein 61 [Source:HGNC Symbol;Acc:HGNC:27296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"199964","summary":null,"start":54980792,"end":54992293,"strand":1,"description":"transmembrane protein 61 [Source:HGNC Symbol;Acc:HGNC:27296]"}, {"versioned_ensembl_gene_id":"ENSG00000231536.1","gene_symbol":"AC226101.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110610916,"end":110612404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216867.2","gene_symbol":"AC226101.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110633947,"end":110634333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242396.1","gene_symbol":"AC096536.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54886875,"end":54888001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226186.1","gene_symbol":"ELOCP21","gene_name":"elongin C pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38157]","synonyms":"TCEB1P21","biotype":"processed_pseudogene","ncbi_id":"100462866","summary":null,"start":70955899,"end":70956234,"strand":-1,"description":"elongin C pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38157]"}, {"versioned_ensembl_gene_id":"ENSG00000235072.2","gene_symbol":"AC012074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25369136,"end":25375845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258881.6","gene_symbol":"AC007040.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":70939318,"end":70995336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255408.3","gene_symbol":"PCDHA3","gene_name":"protocadherin alpha 3 [Source:HGNC Symbol;Acc:HGNC:8669]","synonyms":"PCDH-ALPHA3","biotype":"protein_coding","ncbi_id":"56145","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140801028,"end":141012344,"strand":1,"description":"protocadherin alpha 3 [Source:HGNC Symbol;Acc:HGNC:8669]"}, {"versioned_ensembl_gene_id":"ENSG00000229273.1","gene_symbol":"BX664615.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39809562,"end":39810019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233719.4","gene_symbol":"GOT2P3","gene_name":"glutamic-oxaloacetic transaminase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4436]","synonyms":"GOT2L3P,GOT2L3","biotype":"transcribed_processed_pseudogene","ncbi_id":"644138","summary":null,"start":9641723,"end":9643011,"strand":1,"description":"glutamic-oxaloacetic transaminase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4436]"}, {"versioned_ensembl_gene_id":"ENSG00000273994.1","gene_symbol":"SDR42E1P1","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422340","summary":null,"start":39651901,"end":39652377,"strand":-1,"description":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50378]"}, {"versioned_ensembl_gene_id":"ENSG00000229707.1","gene_symbol":"SKP1P3","gene_name":"S-phase kinase associated protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101119","summary":null,"start":39485379,"end":39485865,"strand":1,"description":"S-phase kinase associated protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50370]"}, {"versioned_ensembl_gene_id":"ENSG00000160323.18","gene_symbol":"ADAMTS13","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]","synonyms":"FLJ42993,VWFCP,DKFZp434C2322,vWF-CP,C9orf8,TTP,MGC118900,MGC118899","biotype":"protein_coding","ncbi_id":"11093","summary":"This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133414358,"end":133459402,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]"}, {"versioned_ensembl_gene_id":"ENSG00000100234.11","gene_symbol":"TIMP3","gene_name":"TIMP metallopeptidase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:11822]","synonyms":"SFD","biotype":"protein_coding","ncbi_id":"7078","summary":"This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix (ECM). Expression of this gene is induced in response to mitogenic stimulation and this netrin domain-containing protein is localized to the ECM. Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy. [provided by RefSeq, Jul 2008]","start":32801701,"end":32863043,"strand":1,"description":"TIMP metallopeptidase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:11822]"}, {"versioned_ensembl_gene_id":"ENSG00000198554.11","gene_symbol":"WDHD1","gene_name":"WD repeat and HMG-box DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:23170]","synonyms":"CHTF4,AND-1,CTF4","biotype":"protein_coding","ncbi_id":"11169","summary":"The protein encoded by this gene contains multiple N-terminal WD40 domains and a C-terminal high mobility group (HMG) box. WD40 domains are found in a variety of eukaryotic proteins and may function as adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54938950,"end":55027105,"strand":-1,"description":"WD repeat and HMG-box DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:23170]"}, {"versioned_ensembl_gene_id":"ENSG00000204444.10","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"NG20,G3a,ApoM","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31652416,"end":31658210,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000254986.7","gene_symbol":"DPP3","gene_name":"dipeptidyl peptidase 3 [Source:HGNC Symbol;Acc:HGNC:3008]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10072","summary":"This gene encodes a protein that is a member of the M49 family of metallopeptidases. This cytoplasmic protein binds a single zinc ion with its zinc-binding motif (HELLGH) and has post-proline dipeptidyl aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. Increased activity of this protein is associated with endometrial and ovarian cancers. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2012]","start":66480013,"end":66509657,"strand":1,"description":"dipeptidyl peptidase 3 [Source:HGNC Symbol;Acc:HGNC:3008]"}, {"versioned_ensembl_gene_id":"ENSG00000189144.13","gene_symbol":"ZNF573","gene_name":"zinc finger protein 573 [Source:HGNC Symbol;Acc:HGNC:26420]","synonyms":"FLJ30921","biotype":"protein_coding","ncbi_id":"126231","summary":null,"start":37735833,"end":37817300,"strand":-1,"description":"zinc finger protein 573 [Source:HGNC Symbol;Acc:HGNC:26420]"}, {"versioned_ensembl_gene_id":"ENSG00000229696.1","gene_symbol":"KARSP1","gene_name":"lysyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39207]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419558","summary":null,"start":41925598,"end":41927349,"strand":1,"description":"lysyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39207]"}, {"versioned_ensembl_gene_id":"ENSG00000137818.11","gene_symbol":"RPLP1","gene_name":"ribosomal protein lateral stalk subunit P1 [Source:HGNC Symbol;Acc:HGNC:10372]","synonyms":"LP1","biotype":"protein_coding","ncbi_id":"6176","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P2. The P1 protein can interact with P0 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Two alternatively spliced transcript variants that encode different proteins have been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":69452784,"end":69456194,"strand":1,"description":"ribosomal protein lateral stalk subunit P1 [Source:HGNC Symbol;Acc:HGNC:10372]"}, {"versioned_ensembl_gene_id":"ENSG00000160447.6","gene_symbol":"PKN3","gene_name":"protein kinase N3 [Source:HGNC Symbol;Acc:HGNC:17999]","synonyms":"UTDP4-1,PKNbeta","biotype":"protein_coding","ncbi_id":"29941","summary":null,"start":128702523,"end":128720918,"strand":1,"description":"protein kinase N3 [Source:HGNC Symbol;Acc:HGNC:17999]"}, {"versioned_ensembl_gene_id":"ENSG00000229954.1","gene_symbol":"MTND2P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23767]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"56168","summary":null,"start":102786813,"end":102788387,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23767]"}, {"versioned_ensembl_gene_id":"ENSG00000224471.2","gene_symbol":"MTCO3P19","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52049]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075156","summary":null,"start":102799563,"end":102799883,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52049]"}, {"versioned_ensembl_gene_id":"ENSG00000158234.12","gene_symbol":"FAIM","gene_name":"Fas apoptotic inhibitory molecule [Source:HGNC Symbol;Acc:HGNC:18703]","synonyms":"FLJ10582,FAIM1","biotype":"protein_coding","ncbi_id":"55179","summary":"The protein encoded by this gene protects against death receptor-triggered apoptosis and regulates B-cell signaling and differentiation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":138608606,"end":138633376,"strand":1,"description":"Fas apoptotic inhibitory molecule [Source:HGNC Symbol;Acc:HGNC:18703]"}, {"versioned_ensembl_gene_id":"ENSG00000185666.14","gene_symbol":"SYN3","gene_name":"synapsin III [Source:HGNC Symbol;Acc:HGNC:11496]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8224","summary":"This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms. [provided by RefSeq, Oct 2008]","start":32512552,"end":33058372,"strand":-1,"description":"synapsin III [Source:HGNC Symbol;Acc:HGNC:11496]"}, {"versioned_ensembl_gene_id":"ENSG00000261379.1","gene_symbol":"AC010735.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":226804036,"end":226805061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087074.7","gene_symbol":"PPP1R15A","gene_name":"protein phosphatase 1 regulatory subunit 15A [Source:HGNC Symbol;Acc:HGNC:14375]","synonyms":"GADD34","biotype":"protein_coding","ncbi_id":"23645","summary":"This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The induction of this gene by ionizing radiation occurs in certain cell lines regardless of p53 status, and its protein response is correlated with apoptosis following ionizing radiation. [provided by RefSeq, Jul 2008]","start":48872392,"end":48876057,"strand":1,"description":"protein phosphatase 1 regulatory subunit 15A [Source:HGNC Symbol;Acc:HGNC:14375]"}, {"versioned_ensembl_gene_id":"ENSG00000256349.1","gene_symbol":"AP002748.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":66509079,"end":66533613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219430.2","gene_symbol":"MBL3P","gene_name":"mannose-binding lectin family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:2221]","synonyms":"MBL,COLEC2","biotype":"unprocessed_pseudogene","ncbi_id":"50639","summary":null,"start":79582298,"end":79584877,"strand":-1,"description":"mannose-binding lectin family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:2221]"}, {"versioned_ensembl_gene_id":"ENSG00000189190.9","gene_symbol":"ZNF600","gene_name":"zinc finger protein 600 [Source:HGNC Symbol;Acc:HGNC:30951]","synonyms":"KR-ZNF1,DKFZp686F06123","biotype":"protein_coding","ncbi_id":"162966","summary":null,"start":52764195,"end":52786791,"strand":-1,"description":"zinc finger protein 600 [Source:HGNC Symbol;Acc:HGNC:30951]"}, {"versioned_ensembl_gene_id":"ENSG00000264734.1","gene_symbol":"AC069061.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26989189,"end":26999941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225401.2","gene_symbol":"TGIF2P1","gene_name":"TGFB induced factor homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33317]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126826","summary":null,"start":244394976,"end":244395660,"strand":-1,"description":"TGFB induced factor homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33317]"}, {"versioned_ensembl_gene_id":"ENSG00000278980.1","gene_symbol":"AP003485.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91208838,"end":91209590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237693.4","gene_symbol":"IRGM","gene_name":"immunity related GTPase M [Source:HGNC Symbol;Acc:HGNC:29597]","synonyms":"IFI1,LRG47,LRG-47,IRGM1","biotype":"protein_coding","ncbi_id":"345611","summary":"This gene encodes a member of the p47 immunity-related GTPase family. The encoded protein may play a role in the innate immune response by regulating autophagy formation in response to intracellular pathogens. Polymorphisms that affect the normal expression of this gene are associated with a susceptibility to Crohn's disease and tuberculosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2016]","start":150846523,"end":150900736,"strand":1,"description":"immunity related GTPase M [Source:HGNC Symbol;Acc:HGNC:29597]"}, {"versioned_ensembl_gene_id":"ENSG00000229960.1","gene_symbol":"AL590483.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":244068820,"end":244093026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254677.1","gene_symbol":"OSBPL9P2","gene_name":"oxysterol binding protein like 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48732]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130038","summary":null,"start":91114724,"end":91115951,"strand":-1,"description":"oxysterol binding protein like 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48732]"}, {"versioned_ensembl_gene_id":"ENSG00000279015.1","gene_symbol":"AC016717.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":225761559,"end":225762112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099821.13","gene_symbol":"POLRMT","gene_name":"RNA polymerase mitochondrial [Source:HGNC Symbol;Acc:HGNC:9200]","synonyms":"MTRPOL,MTRNAP,h-mtRPOL,APOLMT","biotype":"protein_coding","ncbi_id":"5442","summary":"This gene encodes a mitochondrial DNA-directed RNA polymerase. The gene product is responsible for mitochondrial gene expression as well as for providing RNA primers for initiation of replication of the mitochondrial genome. Although this polypeptide has the same function as the three nuclear DNA-directed RNA polymerases, it is more closely related to RNA polymerases of phage and mitochondrial polymerases of lower eukaryotes. [provided by RefSeq, Jul 2008]","start":617224,"end":633604,"strand":-1,"description":"RNA polymerase mitochondrial [Source:HGNC Symbol;Acc:HGNC:9200]"}, {"versioned_ensembl_gene_id":"ENSG00000118496.4","gene_symbol":"FBXO30","gene_name":"F-box protein 30 [Source:HGNC Symbol;Acc:HGNC:15600]","synonyms":"Fbx30,MGC21674","biotype":"protein_coding","ncbi_id":"84085","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it is upregulated in nasopharyngeal carcinoma. [provided by RefSeq, Jul 2008]","start":145793502,"end":145814753,"strand":-1,"description":"F-box protein 30 [Source:HGNC Symbol;Acc:HGNC:15600]"}, {"versioned_ensembl_gene_id":"ENSG00000185651.14","gene_symbol":"UBE2L3","gene_name":"ubiquitin conjugating enzyme E2 L3 [Source:HGNC Symbol;Acc:HGNC:12488]","synonyms":"UBCH7","biotype":"protein_coding","ncbi_id":"7332","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-conjugating enzymes (E2s) and ubiquitin-protein ligases (E3s). This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is demonstrated to participate in the ubiquitination of p53, c-Fos, and the NF-kB precursor p105 in vitro. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":21549447,"end":21624034,"strand":1,"description":"ubiquitin conjugating enzyme E2 L3 [Source:HGNC Symbol;Acc:HGNC:12488]"}, {"versioned_ensembl_gene_id":"ENSG00000183246.6","gene_symbol":"RIMBP3C","gene_name":"RIMS binding protein 3C [Source:HGNC Symbol;Acc:HGNC:33892]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150221","summary":null,"start":21545357,"end":21551461,"strand":-1,"description":"RIMS binding protein 3C [Source:HGNC Symbol;Acc:HGNC:33892]"}, {"versioned_ensembl_gene_id":"ENSG00000260000.2","gene_symbol":"AL133338.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100881471,"end":100882987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279798.1","gene_symbol":"AC018659.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":97563257,"end":97563971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276039.1","gene_symbol":"AL353770.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66962271,"end":66962348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088367.21","gene_symbol":"EPB41L1","gene_name":"erythrocyte membrane protein band 4.1 like 1 [Source:HGNC Symbol;Acc:HGNC:3378]","synonyms":"KIAA0338,4.1N","biotype":"protein_coding","ncbi_id":"2036","summary":"Erythrocyte membrane protein band 4.1 (EPB41) is a multifunctional protein that mediates interactions between the erythrocyte cytoskeleton and the overlying plasma membrane. The encoded protein binds and stabilizes D2 and D3 dopamine receptors at the neuronal plasma membrane. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]","start":36091504,"end":36232799,"strand":1,"description":"erythrocyte membrane protein band 4.1 like 1 [Source:HGNC Symbol;Acc:HGNC:3378]"}, {"versioned_ensembl_gene_id":"ENSG00000263588.1","gene_symbol":"AC091043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22088060,"end":22098780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255360.1","gene_symbol":"AP004607.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89955146,"end":89957165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090581.9","gene_symbol":"GNPTG","gene_name":"N-acetylglucosamine-1-phosphate transferase gamma subunit [Source:HGNC Symbol;Acc:HGNC:23026]","synonyms":"GNPTAG,CAB56184,c316G12.3,C16orf27","biotype":"protein_coding","ncbi_id":"84572","summary":"This gene encodes the gamma sunbunit of the N-acetylglucosamine-1-phosphotransferase complex. This hexameric complex, composed of alpha, beta and gamma subunits, catalyzes the first step in synthesis of a mannose 6-phosphate lysosomal recognition marker. This enzyme complex is necessary for targeting of lysosomal hydrolases to the lysosome. Mutations in the gene encoding the gamma subunit have been associated with mucolipidosis IIIC, also known as mucolipidosis III gamma.[provided by RefSeq, Feb 2010]","start":1351923,"end":1364113,"strand":1,"description":"N-acetylglucosamine-1-phosphate transferase gamma subunit [Source:HGNC Symbol;Acc:HGNC:23026]"}, {"versioned_ensembl_gene_id":"ENSG00000206480.11","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30717229,"end":30732250,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000267992.1","gene_symbol":"AC010605.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39030436,"end":39031323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070669.16","gene_symbol":"ASNS","gene_name":"asparagine synthetase (glutamine-hydrolyzing) [Source:HGNC Symbol;Acc:HGNC:753]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440","summary":"The protein encoded by this gene is involved in the synthesis of asparagine. This gene complements a mutation in the temperature-sensitive hamster mutant ts11, which blocks progression through the G1 phase of the cell cycle at nonpermissive temperature. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]","start":97852118,"end":97872542,"strand":-1,"description":"asparagine synthetase (glutamine-hydrolyzing) [Source:HGNC Symbol;Acc:HGNC:753]"}, {"versioned_ensembl_gene_id":"ENSG00000236822.1","gene_symbol":"AL589674.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142088233,"end":142089219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271402.1","gene_symbol":"IGKV2OR2-2","gene_name":"immunoglobulin kappa variable 2/OR2-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5808]","synonyms":"IGKV2/OR2-2","biotype":"IG_V_pseudogene","ncbi_id":"28859","summary":null,"start":97050729,"end":97051028,"strand":1,"description":"immunoglobulin kappa variable 2/OR2-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5808]"}, {"versioned_ensembl_gene_id":"ENSG00000184677.16","gene_symbol":"ZBTB40","gene_name":"zinc finger and BTB domain containing 40 [Source:HGNC Symbol;Acc:HGNC:29045]","synonyms":"ZNF923,KIAA0478","biotype":"protein_coding","ncbi_id":"9923","summary":null,"start":22451851,"end":22531157,"strand":1,"description":"zinc finger and BTB domain containing 40 [Source:HGNC Symbol;Acc:HGNC:29045]"}, {"versioned_ensembl_gene_id":"ENSG00000236394.2","gene_symbol":"AL807752.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137052662,"end":137053375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278634.4","gene_symbol":"LILRA2","gene_name":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]","synonyms":"LIR7,LIR-7,ILT1,CD85h","biotype":"protein_coding","ncbi_id":"11027","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014]","start":54503437,"end":54518077,"strand":1,"description":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]"}, {"versioned_ensembl_gene_id":"ENSG00000242019.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736536,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000220695.1","gene_symbol":"Z86062.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100530276,"end":100531052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258983.2","gene_symbol":"AL162171.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88499334,"end":88515502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239429.1","gene_symbol":"AF274854.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151611664,"end":151671196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235035.1","gene_symbol":"AC005234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70687142,"end":70691824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281335.1","gene_symbol":"MIF-AS1","gene_name":"MIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27669]","synonyms":"LOC284889,MIF-AS","biotype":"antisense_RNA","ncbi_id":"284889","summary":null,"start":23894426,"end":23898930,"strand":-1,"description":"MIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27669]"}, {"versioned_ensembl_gene_id":"ENSG00000223548.1","gene_symbol":"AC034228.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132003592,"end":132007022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099822.2","gene_symbol":"HCN2","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 [Source:HGNC Symbol;Acc:HGNC:4846]","synonyms":"HAC-1,BCNG2,BCNG-2","biotype":"protein_coding","ncbi_id":"610","summary":"The protein encoded by this gene is a hyperpolarization-activated cation channel involved in the generation of native pacemaker activity in the heart and in the brain. The encoded protein is activated by cAMP and can produce a fast, large current. Defects in this gene were noted as a possible cause of some forms of epilepsy. [provided by RefSeq, Jan 2017]","start":589893,"end":617159,"strand":1,"description":"hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 [Source:HGNC Symbol;Acc:HGNC:4846]"}, {"versioned_ensembl_gene_id":"ENSG00000281287.1","gene_symbol":"AP000350.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23862188,"end":23895223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111199.10","gene_symbol":"TRPV4","gene_name":"transient receptor potential cation channel subfamily V member 4 [Source:HGNC Symbol;Acc:HGNC:18083]","synonyms":"TRP12,OTRPC4,CMT2C,VROAC,VRL-2,VR-OAC","biotype":"protein_coding","ncbi_id":"59341","summary":"This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]","start":109783085,"end":109833401,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 4 [Source:HGNC Symbol;Acc:HGNC:18083]"}, {"versioned_ensembl_gene_id":"ENSG00000196653.11","gene_symbol":"ZNF502","gene_name":"zinc finger protein 502 [Source:HGNC Symbol;Acc:HGNC:23718]","synonyms":"FLJ14855,FLJ12515","biotype":"protein_coding","ncbi_id":"91392","summary":null,"start":44712643,"end":44723831,"strand":1,"description":"zinc finger protein 502 [Source:HGNC Symbol;Acc:HGNC:23718]"}, {"versioned_ensembl_gene_id":"ENSG00000260790.1","gene_symbol":"AC092338.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22374859,"end":22378180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228790.1","gene_symbol":"AC245128.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105550.8","gene_symbol":"FGF21","gene_name":"fibroblast growth factor 21 [Source:HGNC Symbol;Acc:HGNC:3678]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26291","summary":"Theis gene encodes a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. This protein is a secreted endocrine factor that functions as a major metabolic regulator. The encoded protein stimulates the uptake of glucose in adipose tissue. [provided by RefSeq, Mar 2016]","start":48755559,"end":48758330,"strand":1,"description":"fibroblast growth factor 21 [Source:HGNC Symbol;Acc:HGNC:3678]"}, {"versioned_ensembl_gene_id":"ENSG00000211878.1","gene_symbol":"TRAJ11","gene_name":"T-cell receptor alpha joining 11 [Source:HGNC Symbol;Acc:HGNC:12039]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28744","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22532502,"end":22532561,"strand":1,"description":"T-cell receptor alpha joining 11 [Source:HGNC Symbol;Acc:HGNC:12039]"}, {"versioned_ensembl_gene_id":"ENSG00000282952.1","gene_symbol":"AL583852.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78538391,"end":78551719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174951.10","gene_symbol":"FUT1","gene_name":"fucosyltransferase 1 (H blood group) [Source:HGNC Symbol;Acc:HGNC:4012]","synonyms":"HSC,H","biotype":"protein_coding","ncbi_id":"2523","summary":"This gene encodes a Golgi stack membrane protein that is involved in the creation of a precursor of the H antigen, which is required for the final step in the synthesis of soluble A and B antigens. This is one of two genes encoding the galactoside 2-L-fucosyltransferase enzyme. Mutations in this gene are a cause of the H-Bombay blood group. [provided by RefSeq, Aug 2016]","start":48748011,"end":48755390,"strand":-1,"description":"fucosyltransferase 1 (H blood group) [Source:HGNC Symbol;Acc:HGNC:4012]"}, {"versioned_ensembl_gene_id":"ENSG00000070778.12","gene_symbol":"PTPN21","gene_name":"protein tyrosine phosphatase, non-receptor type 21 [Source:HGNC Symbol;Acc:HGNC:9651]","synonyms":"PTPRL10,PTPD1","biotype":"protein_coding","ncbi_id":"11099","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N-terminal domain, similar to cytoskeletal- associated proteins including band 4.1, ezrin, merlin, and radixin. This PTP was shown to specially interact with BMX/ETK, a member of Tec tyrosine kinase family characterized by a multimodular structures including PH, SH3, and SH2 domains. The interaction of this PTP with BMX kinase was found to increase the activation of STAT3, but not STAT2 kinase. Studies of the similar gene in mice suggested the possible roles of this PTP in liver regeneration and spermatogenesis. [provided by RefSeq, Jul 2008]","start":88465778,"end":88554733,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 21 [Source:HGNC Symbol;Acc:HGNC:9651]"}, {"versioned_ensembl_gene_id":"ENSG00000230229.1","gene_symbol":"AC010163.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78352597,"end":78356100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282863.1","gene_symbol":"AC012560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78179174,"end":78675109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081019.13","gene_symbol":"RSBN1","gene_name":"round spermatid basic protein 1 [Source:HGNC Symbol;Acc:HGNC:25642]","synonyms":"ROSBIN,FLJ11220","biotype":"protein_coding","ncbi_id":"54665","summary":null,"start":113761832,"end":113812476,"strand":-1,"description":"round spermatid basic protein 1 [Source:HGNC Symbol;Acc:HGNC:25642]"}, {"versioned_ensembl_gene_id":"ENSG00000137700.17","gene_symbol":"SLC37A4","gene_name":"solute carrier family 37 member 4 [Source:HGNC Symbol;Acc:HGNC:4061]","synonyms":"G6PT1,GSD1d,GSD1c,GSD1b,G6PT3,G6PT2","biotype":"protein_coding","ncbi_id":"2542","summary":"This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants.[provided by RefSeq, Aug 2009]","start":119024114,"end":119030906,"strand":-1,"description":"solute carrier family 37 member 4 [Source:HGNC Symbol;Acc:HGNC:4061]"}, {"versioned_ensembl_gene_id":"ENSG00000278220.2","gene_symbol":"CLN8","gene_name":"CLN8, transmembrane ER and ERGIC protein [Source:HGNC Symbol;Acc:HGNC:2079]","synonyms":"FLJ39417,EPMR,C8orf61","biotype":"protein_coding","ncbi_id":"2055","summary":"This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with a disorder characterized by progressive epilepsy with cognitive disabilities (EPMR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain. [provided by RefSeq, Jul 2017]","start":1755340,"end":1786132,"strand":1,"description":"CLN8, transmembrane ER and ERGIC protein [Source:HGNC Symbol;Acc:HGNC:2079]"}, {"versioned_ensembl_gene_id":"ENSG00000148346.11","gene_symbol":"LCN2","gene_name":"lipocalin 2 [Source:HGNC Symbol;Acc:HGNC:6526]","synonyms":"NGAL,24p3","biotype":"protein_coding","ncbi_id":"3934","summary":"This gene encodes a protein that belongs to the lipocalin family. Members of this family transport small hydrophobic molecules such as lipids, steroid hormones and retinoids. The protein encoded by this gene is a neutrophil gelatinase-associated lipocalin and plays a role in innate immunity by limiting bacterial growth as a result of sequestering iron-containing siderophores. The presence of this protein in blood and urine is an early biomarker of acute kidney injury. This protein is thought to be be involved in multiple cellular processes, including maintenance of skin homeostasis, and suppression of invasiveness and metastasis. Mice lacking this gene are more susceptible to bacterial infection than wild type mice. [provided by RefSeq, Sep 2015]","start":128149071,"end":128153455,"strand":1,"description":"lipocalin 2 [Source:HGNC Symbol;Acc:HGNC:6526]"}, {"versioned_ensembl_gene_id":"ENSG00000243478.9","gene_symbol":"AOX2P","gene_name":"aldehyde oxidase 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:18450]","synonyms":"AOX2,AOH2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"344454","summary":null,"start":200738608,"end":200794239,"strand":1,"description":"aldehyde oxidase 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:18450]"}, {"versioned_ensembl_gene_id":"ENSG00000138326.18","gene_symbol":"RPS24","gene_name":"ribosomal protein S24 [Source:HGNC Symbol;Acc:HGNC:10411]","synonyms":"S24","biotype":"protein_coding","ncbi_id":"6229","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S24E family of ribosomal proteins. It is located in the cytoplasm. Multiple transcript variants encoding different isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Mutations in this gene result in Diamond-Blackfan anemia. [provided by RefSeq, Nov 2008]","start":78033760,"end":78056812,"strand":1,"description":"ribosomal protein S24 [Source:HGNC Symbol;Acc:HGNC:10411]"}, {"versioned_ensembl_gene_id":"ENSG00000265217.1","gene_symbol":"AC090358.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65606090,"end":65652053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272343.1","gene_symbol":"AC107952.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56222688,"end":56223173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264232.1","gene_symbol":"LINC01916","gene_name":"long intergenic non-protein coding RNA 1916 [Source:HGNC Symbol;Acc:HGNC:52735]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985128","summary":null,"start":65424013,"end":65447512,"strand":1,"description":"long intergenic non-protein coding RNA 1916 [Source:HGNC Symbol;Acc:HGNC:52735]"}, {"versioned_ensembl_gene_id":"ENSG00000235990.2","gene_symbol":"RPL23AP20","gene_name":"ribosomal protein L23a pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36622]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645962","summary":null,"start":241916123,"end":241916543,"strand":1,"description":"ribosomal protein L23a pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36622]"}, {"versioned_ensembl_gene_id":"ENSG00000280201.1","gene_symbol":"AP003400.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89576913,"end":89577652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074603.18","gene_symbol":"DPP8","gene_name":"dipeptidyl peptidase 8 [Source:HGNC Symbol;Acc:HGNC:16490]","synonyms":"DP8,MSTP141,MGC26191,FLJ20283,FLJ14920,DPRP1","biotype":"protein_coding","ncbi_id":"54878","summary":"This gene encodes a member of the peptidase S9B family, a small family of dipeptidyl peptidases that are able to cleave peptide substrates at a prolyl bond. The encoded protein shares similarity with dipeptidyl peptidase IV in that it is ubiquitously expressed, and hydrolyzes the same substrates. These similarities suggest that, like dipeptidyl peptidase IV, this protein may play a role in T-cell activation and immune function. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":65442463,"end":65517704,"strand":-1,"description":"dipeptidyl peptidase 8 [Source:HGNC Symbol;Acc:HGNC:16490]"}, {"versioned_ensembl_gene_id":"ENSG00000185963.13","gene_symbol":"BICD2","gene_name":"BICD cargo adaptor 2 [Source:HGNC Symbol;Acc:HGNC:17208]","synonyms":"KIAA0699","biotype":"protein_coding","ncbi_id":"23299","summary":"This gene is one of two human homologs of Drosophila bicaudal-D and a member of the Bicoid family. It has been implicated in dynein-mediated, minus end-directed motility along microtubules. It has also been reported to be a phosphorylation target of NIMA related kinase 8. Two alternative splice variants have been described. [provided by RefSeq, Jul 2008]","start":92711363,"end":92764812,"strand":-1,"description":"BICD cargo adaptor 2 [Source:HGNC Symbol;Acc:HGNC:17208]"}, {"versioned_ensembl_gene_id":"ENSG00000273622.1","gene_symbol":"CDC42EP5","gene_name":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]","synonyms":"CEP5,Borg3","biotype":"protein_coding","ncbi_id":"148170","summary":"Cell division control protein 42 (CDC42), a small Rho GTPase, regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins. The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins. Borg family proteins contain a CRIB (Cdc42/Rac interactive-binding) domain. They bind to CDC42 and regulate its function negatively. The encoded protein may inhibit c-Jun N-terminal kinase (JNK) independently of CDC42 binding. The protein may also play a role in septin organization and inducing pseudopodia formation in fibroblasts [provided by RefSeq, Jul 2013]","start":54395351,"end":54403578,"strand":-1,"description":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]"}, {"versioned_ensembl_gene_id":"ENSG00000232197.1","gene_symbol":"AL596442.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170162517,"end":170163027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164430.15","gene_symbol":"MB21D1","gene_name":"Mab-21 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21367]","synonyms":"cGAS,C6orf150","biotype":"protein_coding","ncbi_id":"115004","summary":null,"start":73413515,"end":73452276,"strand":-1,"description":"Mab-21 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21367]"}, {"versioned_ensembl_gene_id":"ENSG00000212916.4","gene_symbol":"MAP10","gene_name":"microtubule associated protein 10 [Source:HGNC Symbol;Acc:HGNC:29265]","synonyms":"MTR120,KIAA1383","biotype":"protein_coding","ncbi_id":"54627","summary":null,"start":232804892,"end":232808407,"strand":1,"description":"microtubule associated protein 10 [Source:HGNC Symbol;Acc:HGNC:29265]"}, {"versioned_ensembl_gene_id":"ENSG00000073584.18","gene_symbol":"SMARCE1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [Source:HGNC Symbol;Acc:HGNC:11109]","synonyms":"BAF57","biotype":"protein_coding","ncbi_id":"6605","summary":"The protein encoded by this gene is part of the large ATP-dependent chromatin remodeling complex SWI/SNF, which is required for transcriptional activation of genes normally repressed by chromatin. The encoded protein, either alone or when in the SWI/SNF complex, can bind to 4-way junction DNA, which is thought to mimic the topology of DNA as it enters or exits the nucleosome. The protein contains a DNA-binding HMG domain, but disruption of this domain does not abolish the DNA-binding or nucleosome-displacement activities of the SWI/SNF complex. Unlike most of the SWI/SNF complex proteins, this protein has no yeast counterpart. [provided by RefSeq, Jul 2008]","start":40624962,"end":40648508,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [Source:HGNC Symbol;Acc:HGNC:11109]"}, {"versioned_ensembl_gene_id":"ENSG00000264058.1","gene_symbol":"AC073508.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":40628797,"end":40665141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225427.1","gene_symbol":"LINC00331","gene_name":"long intergenic non-protein coding RNA 331 [Source:HGNC Symbol;Acc:HGNC:42048]","synonyms":"NCRNA00331","biotype":"lincRNA","ncbi_id":"100874126","summary":null,"start":78787319,"end":78792307,"strand":-1,"description":"long intergenic non-protein coding RNA 331 [Source:HGNC Symbol;Acc:HGNC:42048]"}, {"versioned_ensembl_gene_id":"ENSG00000228616.1","gene_symbol":"AF274858.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153610694,"end":153612925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232850.3","gene_symbol":"PTGES2-AS1","gene_name":"PTGES2 antisense RNA 1 (head to head) [Source:NCBI gene;Acc:389791]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389791","summary":null,"start":128128529,"end":128130628,"strand":1,"description":"PTGES2 antisense RNA 1 (head to head) [Source:NCBI gene;Acc:389791]"}, {"versioned_ensembl_gene_id":"ENSG00000221910.2","gene_symbol":"OR2F2","gene_name":"olfactory receptor family 2 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:8247]","synonyms":"OR7-1","biotype":"protein_coding","ncbi_id":"135948","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143935166,"end":143936279,"strand":1,"description":"olfactory receptor family 2 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:8247]"}, {"versioned_ensembl_gene_id":"ENSG00000258930.1","gene_symbol":"AC005230.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":71031686,"end":71031970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132275.10","gene_symbol":"RRP8","gene_name":"ribosomal RNA processing 8 [Source:HGNC Symbol;Acc:HGNC:29030]","synonyms":"NML,KIAA0409","biotype":"protein_coding","ncbi_id":"23378","summary":null,"start":6595075,"end":6603620,"strand":-1,"description":"ribosomal RNA processing 8 [Source:HGNC Symbol;Acc:HGNC:29030]"}, {"versioned_ensembl_gene_id":"ENSG00000128581.15","gene_symbol":"IFT22","gene_name":"intraflagellar transport 22 [Source:HGNC Symbol;Acc:HGNC:21895]","synonyms":"RABL5,FLJ14117,FLJ13225,DKFZp761N0823","biotype":"protein_coding","ncbi_id":"64792","summary":null,"start":101313367,"end":101321823,"strand":-1,"description":"intraflagellar transport 22 [Source:HGNC Symbol;Acc:HGNC:21895]"}, {"versioned_ensembl_gene_id":"ENSG00000185433.8","gene_symbol":"LINC00158","gene_name":"long intergenic non-protein coding RNA 158 [Source:HGNC Symbol;Acc:HGNC:1283]","synonyms":"NCRNA00158,C21orf42","biotype":"lincRNA","ncbi_id":"54072","summary":null,"start":25385820,"end":25431701,"strand":-1,"description":"long intergenic non-protein coding RNA 158 [Source:HGNC Symbol;Acc:HGNC:1283]"}, {"versioned_ensembl_gene_id":"ENSG00000054983.16","gene_symbol":"GALC","gene_name":"galactosylceramidase [Source:HGNC Symbol;Acc:HGNC:4115]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2581","summary":"This gene encodes a lysosomal protein which hydrolyzes the galactose ester bonds of galactosylceramide, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride. Mutations in this gene have been associated with Krabbe disease, also known as globoid cell leukodystrophy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":87837820,"end":87993665,"strand":-1,"description":"galactosylceramidase [Source:HGNC Symbol;Acc:HGNC:4115]"}, {"versioned_ensembl_gene_id":"ENSG00000167106.11","gene_symbol":"FAM102A","gene_name":"family with sequence similarity 102 member A [Source:HGNC Symbol;Acc:HGNC:31419]","synonyms":"SYM-3A,Eeig1,C9orf132,bA203J24.7","biotype":"protein_coding","ncbi_id":"399665","summary":null,"start":127940579,"end":127980513,"strand":-1,"description":"family with sequence similarity 102 member A [Source:HGNC Symbol;Acc:HGNC:31419]"}, {"versioned_ensembl_gene_id":"ENSG00000238114.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31571300,"end":31573267,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000258505.1","gene_symbol":"AL442163.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":42608868,"end":42609577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255075.1","gene_symbol":"CENPUP1","gene_name":"centromere protein U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130384","summary":null,"start":13756027,"end":13757560,"strand":1,"description":"centromere protein U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49889]"}, {"versioned_ensembl_gene_id":"ENSG00000148296.6","gene_symbol":"SURF6","gene_name":"surfeit 6 [Source:HGNC Symbol;Acc:HGNC:11478]","synonyms":"RRP14,FLJ30322","biotype":"protein_coding","ncbi_id":"6838","summary":"This gene encodes a conserved protein that is localized to the nucleolus. The encoded protein may function as a nucleolar-matrix protein with nucleic acid-binding properties. There is a pseudogene for this gene on chromosome Y. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133328774,"end":133336398,"strand":-1,"description":"surfeit 6 [Source:HGNC Symbol;Acc:HGNC:11478]"}, {"versioned_ensembl_gene_id":"ENSG00000226717.2","gene_symbol":"PTPRD-AS2","gene_name":"PTPRD antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:49754]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929428","summary":null,"start":10613202,"end":10620420,"strand":1,"description":"PTPRD antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:49754]"}, {"versioned_ensembl_gene_id":"ENSG00000231701.1","gene_symbol":"BMS1P13","gene_name":"BMS1, ribosome biogenesis factor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49158]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644716","summary":null,"start":65828120,"end":65831696,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49158]"}, {"versioned_ensembl_gene_id":"ENSG00000249987.1","gene_symbol":"RPS4XP20","gene_name":"ribosomal protein S4X pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36437]","synonyms":"RPS4P20","biotype":"processed_pseudogene","ncbi_id":"100271386","summary":null,"start":34022656,"end":34023427,"strand":-1,"description":"ribosomal protein S4X pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36437]"}, {"versioned_ensembl_gene_id":"ENSG00000133275.15","gene_symbol":"CSNK1G2","gene_name":"casein kinase 1 gamma 2 [Source:HGNC Symbol;Acc:HGNC:2455]","synonyms":"CK1g2","biotype":"protein_coding","ncbi_id":"1455","summary":null,"start":1941149,"end":1981338,"strand":1,"description":"casein kinase 1 gamma 2 [Source:HGNC Symbol;Acc:HGNC:2455]"}, {"versioned_ensembl_gene_id":"ENSG00000176318.8","gene_symbol":"FOXN3P1","gene_name":"forkhead box N3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43882]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643976","summary":null,"start":102546734,"end":102548213,"strand":-1,"description":"forkhead box N3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43882]"}, {"versioned_ensembl_gene_id":"ENSG00000218510.7","gene_symbol":"LINC00339","gene_name":"long intergenic non-protein coding RNA 339 [Source:HGNC Symbol;Acc:HGNC:25011]","synonyms":"NCRNA00339,HSPC157","biotype":"transcribed_processed_pseudogene","ncbi_id":"29092","summary":null,"start":22024558,"end":22031223,"strand":1,"description":"long intergenic non-protein coding RNA 339 [Source:HGNC Symbol;Acc:HGNC:25011]"}, {"versioned_ensembl_gene_id":"ENSG00000107807.12","gene_symbol":"TLX1","gene_name":"T-cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5056]","synonyms":"TCL3,HOX11","biotype":"protein_coding","ncbi_id":"3195","summary":"This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily of homeobox genes. The encoded protein is required for normal development of the spleen during embryogenesis. This protein is also involved in specification of neuronal cell fates. Ectopic expression of this gene due to chromosomal translocations is associated with certain T-cell acute lymphoblastic leukemias. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":101130505,"end":101137789,"strand":1,"description":"T-cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5056]"}, {"versioned_ensembl_gene_id":"ENSG00000228169.3","gene_symbol":"PPIAP19","gene_name":"peptidylprolyl isomerase A pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:31663]","synonyms":"bA108K1.2","biotype":"processed_pseudogene","ncbi_id":"390006","summary":null,"start":114690143,"end":114690634,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:31663]"}, {"versioned_ensembl_gene_id":"ENSG00000240388.2","gene_symbol":"AC008799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91354478,"end":91354934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277447.1","gene_symbol":"AP005431.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3025069,"end":3025387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204414.12","gene_symbol":"CSHL1","gene_name":"chorionic somatomammotropin hormone like 1 [Source:HGNC Symbol;Acc:HGNC:2442]","synonyms":"MGC149868,hCS-L,CSL,CSHP1,CS-5","biotype":"protein_coding","ncbi_id":"1444","summary":"The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. This particular family member is expressed in placental villi, although it was originally thought to be a pseudogene. In fact, alternative splicing suggests that the majority of the transcripts would be unable to express a secreted protein. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":63909597,"end":63918838,"strand":-1,"description":"chorionic somatomammotropin hormone like 1 [Source:HGNC Symbol;Acc:HGNC:2442]"}, {"versioned_ensembl_gene_id":"ENSG00000108352.11","gene_symbol":"RAPGEFL1","gene_name":"Rap guanine nucleotide exchange factor like 1 [Source:HGNC Symbol;Acc:HGNC:17428]","synonyms":"Link-GEFII","biotype":"protein_coding","ncbi_id":"51195","summary":null,"start":40177010,"end":40195656,"strand":1,"description":"Rap guanine nucleotide exchange factor like 1 [Source:HGNC Symbol;Acc:HGNC:17428]"}, {"versioned_ensembl_gene_id":"ENSG00000282240.1","gene_symbol":"TRBV6-4","gene_name":"T-cell receptor beta variable 6-4 [Source:HGNC Symbol;Acc:HGNC:12229]","synonyms":"TRBV64,TCRBV6S4,TCRBV13S5","biotype":"TR_V_gene","ncbi_id":"28603","summary":null,"start":142402503,"end":142402958,"strand":1,"description":"T-cell receptor beta variable 6-4 [Source:HGNC Symbol;Acc:HGNC:12229]"}, {"versioned_ensembl_gene_id":"ENSG00000134202.10","gene_symbol":"GSTM3","gene_name":"glutathione S-transferase mu 3 [Source:HGNC Symbol;Acc:HGNC:4635]","synonyms":"GST5","biotype":"protein_coding","ncbi_id":"2947","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Mutations of this class mu gene have been linked with a slight increase in a number of cancers, likely due to exposure with environmental toxins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":109733932,"end":109741038,"strand":-1,"description":"glutathione S-transferase mu 3 [Source:HGNC Symbol;Acc:HGNC:4635]"}, {"versioned_ensembl_gene_id":"ENSG00000241720.2","gene_symbol":"AL158847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109725820,"end":109775252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251093.1","gene_symbol":"AC093281.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91226475,"end":91227071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276327.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"EB6ActI,CD158H,EB6ActII,CD158H,EB6ActII,EB6ActI","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54905478,"end":54919948,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000275937.1","gene_symbol":"GU182339.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54770973,"end":54780252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137168.7","gene_symbol":"PPIL1","gene_name":"peptidylprolyl isomerase like 1 [Source:HGNC Symbol;Acc:HGNC:9260]","synonyms":"CYPL1","biotype":"protein_coding","ncbi_id":"51645","summary":"This gene is a member of the cyclophilin family of peptidylprolyl isomerases (PPIases). The cyclophilins are a highly conserved, ubiquitous family, members of which play an important role in protein folding, immunosuppression by cyclosporin A, and infection of HIV-1 virions. Based on similarity to other PPIases, this protein could accelerate the folding of proteins and might catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. [provided by RefSeq, Jul 2008]","start":36854827,"end":36875024,"strand":-1,"description":"peptidylprolyl isomerase like 1 [Source:HGNC Symbol;Acc:HGNC:9260]"}, {"versioned_ensembl_gene_id":"ENSG00000278306.1","gene_symbol":"KIR2DS3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]","synonyms":"nkat7","biotype":"protein_coding","ncbi_id":"3808","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54782354,"end":54796789,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]"}, {"versioned_ensembl_gene_id":"ENSG00000206287.5","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33137310,"end":33141537,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000232379.1","gene_symbol":"AL390879.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136947748,"end":136948133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143164.15","gene_symbol":"DCAF6","gene_name":"DDB1 and CUL4 associated factor 6 [Source:HGNC Symbol;Acc:HGNC:30002]","synonyms":"PC326,IQWD1","biotype":"protein_coding","ncbi_id":"55827","summary":"The protein encoded by this gene is a ligand-dependent coactivator of nuclear receptors, including nuclear receptor subfamily 3 group C member 1 (NR3C1), glucocorticoid receptor (GR), and androgen receptor (AR). The encoded protein and DNA damage binding protein 2 (DDB2) may act as tumor promoters and tumor suppressors, respectively, by regulating the level of androgen receptor in prostate tissues. In addition, this protein can act with glucocorticoid receptor to promote human papillomavirus gene expression. [provided by RefSeq, Mar 2017]","start":167935783,"end":168075843,"strand":1,"description":"DDB1 and CUL4 associated factor 6 [Source:HGNC Symbol;Acc:HGNC:30002]"}, {"versioned_ensembl_gene_id":"ENSG00000253629.1","gene_symbol":"AP000426.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101686547,"end":101689093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251199.5","gene_symbol":"AC109830.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134255173,"end":134327473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211820.1","gene_symbol":"TRAV41","gene_name":"T-cell receptor alpha variable 41 [Source:HGNC Symbol;Acc:HGNC:12142]","synonyms":"TCRAV41S1,TCRAV19S1","biotype":"TR_V_gene","ncbi_id":"28640","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22320188,"end":22320691,"strand":1,"description":"T-cell receptor alpha variable 41 [Source:HGNC Symbol;Acc:HGNC:12142]"}, {"versioned_ensembl_gene_id":"ENSG00000189238.5","gene_symbol":"LINC00943","gene_name":"long intergenic non-protein coding RNA 943 [Source:HGNC Symbol;Acc:HGNC:48639]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507206","summary":null,"start":126726270,"end":126746252,"strand":1,"description":"long intergenic non-protein coding RNA 943 [Source:HGNC Symbol;Acc:HGNC:48639]"}, {"versioned_ensembl_gene_id":"ENSG00000280013.1","gene_symbol":"CU639417.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6008604,"end":6008810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237405.10","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32188640,"end":32191996,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000237283.1","gene_symbol":"AL691515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188705623,"end":188710880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150732.8","gene_symbol":"AL136372.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188067298,"end":188067525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279784.1","gene_symbol":"FP236315.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5705345,"end":5707160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211817.2","gene_symbol":"TRAV38-2DV8","gene_name":"T-cell receptor alpha variable 38-2/delta variable 8 [Source:HGNC Symbol;Acc:HGNC:12138]","synonyms":"TRAV382DV8,TRAV38-2/DV8,TCRAV14S1,hADV38S2","biotype":"TR_V_gene","ncbi_id":"28643","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22281105,"end":22281748,"strand":1,"description":"T-cell receptor alpha variable 38-2/delta variable 8 [Source:HGNC Symbol;Acc:HGNC:12138]"}, {"versioned_ensembl_gene_id":"ENSG00000238285.1","gene_symbol":"MRPL50P2","gene_name":"mitochondrial ribosomal protein L50 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359749","summary":null,"start":203315390,"end":203315871,"strand":-1,"description":"mitochondrial ribosomal protein L50 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29720]"}, {"versioned_ensembl_gene_id":"ENSG00000233620.5","gene_symbol":"AC093581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216072465,"end":216086917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139899.10","gene_symbol":"CBLN3","gene_name":"cerebellin 3 precursor [Source:HGNC Symbol;Acc:HGNC:20146]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643866","summary":"Members of the precerebellin family, such as CBLN3, contain a cerebellin motif (see CBLN1; MIM 600432) and a C-terminal C1q signature domain (see MIM 120550) that mediates trimeric assembly of atypical collagen complexes. However, precerebellins do not contain a collagen motif, suggesting that they are not conventional components of the extracellular matrix (Pang et al., 2000 [PubMed 10964938]).[supplied by OMIM, Aug 2009]","start":24426532,"end":24430954,"strand":-1,"description":"cerebellin 3 precursor [Source:HGNC Symbol;Acc:HGNC:20146]"}, {"versioned_ensembl_gene_id":"ENSG00000276450.1","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54905329,"end":54909244,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000229852.2","gene_symbol":"AC019205.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73263215,"end":73301401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116793.15","gene_symbol":"PHTF1","gene_name":"putative homeodomain transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:8939]","synonyms":"PHTF","biotype":"protein_coding","ncbi_id":"10745","summary":null,"start":113696831,"end":113759489,"strand":-1,"description":"putative homeodomain transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:8939]"}, {"versioned_ensembl_gene_id":"ENSG00000105501.12","gene_symbol":"SIGLEC5","gene_name":"sialic acid binding Ig like lectin 5 [Source:HGNC Symbol;Acc:HGNC:10874]","synonyms":"OB-BP2,CD33L2,CD170,SIGLEC-5","biotype":"protein_coding","ncbi_id":"8778","summary":"This gene encodes a member of the sialic acid-binding immunoglobulin-like lectin (Siglec) family. These cell surface lectins are characterized by structural motifs in the immunoglobulin (Ig)-like domains and sialic acid recognition sites in the first Ig V set domain. The encoded protein is a member of the CD33-related subset of Siglecs and inhibits the activation of several cell types including monocytes, macrophages and neutrophils. Binding of group B Streptococcus (GBS) to the encoded protein plays a role in GBS immune evasion. [provided by RefSeq, Feb 2012]","start":51611927,"end":51645545,"strand":-1,"description":"sialic acid binding Ig like lectin 5 [Source:HGNC Symbol;Acc:HGNC:10874]"}, {"versioned_ensembl_gene_id":"ENSG00000108602.17","gene_symbol":"ALDH3A1","gene_name":"aldehyde dehydrogenase 3 family member A1 [Source:HGNC Symbol;Acc:HGNC:405]","synonyms":"ALDH3","biotype":"protein_coding","ncbi_id":"218","summary":"Aldehyde dehydrogenases oxidize various aldehydes to the corresponding acids. They are involved in the detoxification of alcohol-derived acetaldehyde and in the metabolism of corticosteroids, biogenic amines, neurotransmitters, and lipid peroxidation. The enzyme encoded by this gene forms a cytoplasmic homodimer that preferentially oxidizes aromatic and medium-chain (6 carbons or more) saturated and unsaturated aldehyde substrates. It is thought to promote resistance to UV and 4-hydroxy-2-nonenal-induced oxidative damage in the cornea. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2008]","start":19737984,"end":19748943,"strand":-1,"description":"aldehyde dehydrogenase 3 family member A1 [Source:HGNC Symbol;Acc:HGNC:405]"}, {"versioned_ensembl_gene_id":"ENSG00000276293.4","gene_symbol":"PIP4K2B","gene_name":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]","synonyms":"PIP5KIIbeta,PIP5KIIB,PIP5K2B","biotype":"protein_coding","ncbi_id":"8396","summary":"The protein encoded by this gene catalyzes the phosphorylation of phosphatidylinositol-5-phosphate on the fourth hydroxyl of the myo-inositol ring to form phosphatidylinositol-5,4-bisphosphate. This gene is a member of the phosphatidylinositol-5-phosphate 4-kinase family. The encoded protein sequence does not show similarity to other kinases, but the protein does exhibit kinase activity. Additionally, the encoded protein interacts with p55 TNF receptor. [provided by RefSeq, Jul 2008]","start":38765689,"end":38800126,"strand":-1,"description":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]"}, {"versioned_ensembl_gene_id":"ENSG00000282477.1","gene_symbol":"AC100803.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141443230,"end":141443856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244071.1","gene_symbol":"RPL9P33","gene_name":"ribosomal protein L9 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36273]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271229","summary":null,"start":51621136,"end":51621701,"strand":1,"description":"ribosomal protein L9 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36273]"}, {"versioned_ensembl_gene_id":"ENSG00000232145.1","gene_symbol":"AC099548.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143796295,"end":143796720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241136.1","gene_symbol":"PAICSP6","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780812","summary":null,"start":143782667,"end":143784284,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38099]"}, {"versioned_ensembl_gene_id":"ENSG00000196735.11","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32628179,"end":32647062,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000251497.2","gene_symbol":"PITPNM2-AS1","gene_name":"PITPNM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53391]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507091","summary":null,"start":123081384,"end":123084744,"strand":1,"description":"PITPNM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53391]"}, {"versioned_ensembl_gene_id":"ENSG00000250057.1","gene_symbol":"AC114781.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83233512,"end":83247213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167716.18","gene_symbol":"WDR81","gene_name":"WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]","synonyms":"FLJ33817,CAMRQ2,SORF-2,PPP1R166","biotype":"protein_coding","ncbi_id":"124997","summary":"This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":1716523,"end":1738599,"strand":1,"description":"WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]"}, {"versioned_ensembl_gene_id":"ENSG00000279568.1","gene_symbol":"AC093525.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2575628,"end":2577373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153885.14","gene_symbol":"KCTD15","gene_name":"potassium channel tetramerization domain containing 15 [Source:HGNC Symbol;Acc:HGNC:23297]","synonyms":"MGC25497","biotype":"protein_coding","ncbi_id":"79047","summary":null,"start":33795933,"end":33815763,"strand":1,"description":"potassium channel tetramerization domain containing 15 [Source:HGNC Symbol;Acc:HGNC:23297]"}, {"versioned_ensembl_gene_id":"ENSG00000229524.10","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31626429,"end":31640114,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000277238.2","gene_symbol":"TAS2R10","gene_name":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]","synonyms":"TRB2,T2R10","biotype":"protein_coding","ncbi_id":"50839","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10825317,"end":10826358,"strand":-1,"description":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]"}, {"versioned_ensembl_gene_id":"ENSG00000270132.1","gene_symbol":"WISP1-OT1","gene_name":"WISP1 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49126]","synonyms":"WISP1-UT1","biotype":"sense_intronic","ncbi_id":"106144543","summary":null,"start":133229056,"end":133229697,"strand":1,"description":"WISP1 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49126]"}, {"versioned_ensembl_gene_id":"ENSG00000165775.17","gene_symbol":"FUNDC2","gene_name":"FUN14 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24925]","synonyms":"HCBP6,DC44","biotype":"protein_coding","ncbi_id":"65991","summary":null,"start":155025980,"end":155060303,"strand":1,"description":"FUN14 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24925]"}, {"versioned_ensembl_gene_id":"ENSG00000064225.12","gene_symbol":"ST3GAL6","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:18080]","synonyms":"ST3GALVI,SIAT10","biotype":"protein_coding","ncbi_id":"10402","summary":"The protein encoded by this gene is a member of the sialyltransferase family. Members of this family are enzymes that transfer sialic acid from the activated cytidine 5'-monophospho-N-acetylneuraminic acid to terminal positions on sialylated glycolipids (gangliosides) or to the N- or O-linked sugar chains of glycoproteins. This protein has high specificity for neolactotetraosylceramide and neolactohexaosylceramide as glycolipid substrates and may contribute to the formation of selectin ligands and sialyl Lewis X, a carbohydrate important for cell-to-cell recognition and a blood group antigen. [provided by RefSeq, Apr 2016]","start":98732236,"end":98821201,"strand":1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:18080]"}, {"versioned_ensembl_gene_id":"ENSG00000099804.8","gene_symbol":"CDC34","gene_name":"cell division cycle 34 [Source:HGNC Symbol;Acc:HGNC:1734]","synonyms":"UBE2R1,UBC3,E2-CDC34","biotype":"protein_coding","ncbi_id":"997","summary":"The protein encoded by this gene is a member of the ubiquitin-conjugating enzyme family. Ubiquitin-conjugating enzyme catalyzes the covalent attachment of ubiquitin to other proteins. This protein is a part of the large multiprotein complex, which is required for ubiquitin-mediated degradation of cell cycle G1 regulators, and for the initiation of DNA replication. [provided by RefSeq, Jul 2008]","start":531712,"end":542092,"strand":1,"description":"cell division cycle 34 [Source:HGNC Symbol;Acc:HGNC:1734]"}, {"versioned_ensembl_gene_id":"ENSG00000064270.12","gene_symbol":"ATP2C2","gene_name":"ATPase secretory pathway Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:29103]","synonyms":"SPCA2,KIAA0703","biotype":"protein_coding","ncbi_id":"9914","summary":null,"start":84368527,"end":84464187,"strand":1,"description":"ATPase secretory pathway Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:29103]"}, {"versioned_ensembl_gene_id":"ENSG00000067842.17","gene_symbol":"ATP2B3","gene_name":"ATPase plasma membrane Ca2+ transporting 3 [Source:HGNC Symbol;Acc:HGNC:816]","synonyms":"SCAX1,PMCA3,CLA2,CFAP39","biotype":"protein_coding","ncbi_id":"492","summary":"The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 3. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":153517676,"end":153582939,"strand":1,"description":"ATPase plasma membrane Ca2+ transporting 3 [Source:HGNC Symbol;Acc:HGNC:816]"}, {"versioned_ensembl_gene_id":"ENSG00000270276.2","gene_symbol":"HIST2H4B","gene_name":"histone cluster 2 H4 family member b [Source:HGNC Symbol;Acc:HGNC:29607]","synonyms":"H4/o","biotype":"protein_coding","ncbi_id":"554313","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-dependent histone that is a member of the histone H4 family. Some transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the telomeric copy. [provided by RefSeq, May 2020]","start":149854045,"end":149861210,"strand":-1,"description":"histone cluster 2 H4 family member b [Source:HGNC Symbol;Acc:HGNC:29607]"}, {"versioned_ensembl_gene_id":"ENSG00000268892.1","gene_symbol":"AC010620.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21221645,"end":21222746,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117016.9","gene_symbol":"RIMS3","gene_name":"regulating synaptic membrane exocytosis 3 [Source:HGNC Symbol;Acc:HGNC:21292]","synonyms":"RIM3,NIM3","biotype":"protein_coding","ncbi_id":"9783","summary":null,"start":40620679,"end":40665657,"strand":-1,"description":"regulating synaptic membrane exocytosis 3 [Source:HGNC Symbol;Acc:HGNC:21292]"}, {"versioned_ensembl_gene_id":"ENSG00000236786.1","gene_symbol":"TSPY15P","gene_name":"testis specific protein, Y-linked 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:37474]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642631","summary":null,"start":9548108,"end":9550681,"strand":1,"description":"testis specific protein, Y-linked 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:37474]"}, {"versioned_ensembl_gene_id":"ENSG00000146063.19","gene_symbol":"TRIM41","gene_name":"tripartite motif containing 41 [Source:HGNC Symbol;Acc:HGNC:19013]","synonyms":"RINCK,MGC1127","biotype":"protein_coding","ncbi_id":"90933","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM family is characterized by a signature motif composed of a RING finger, one or more B-box domains, and a coiled-coil region. This encoded protein may play a role in protein kinase C signaling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":181222499,"end":181235809,"strand":1,"description":"tripartite motif containing 41 [Source:HGNC Symbol;Acc:HGNC:19013]"}, {"versioned_ensembl_gene_id":"ENSG00000254579.1","gene_symbol":"AC013488.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40445304,"end":40447141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278698.1","gene_symbol":"AL162574.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106773623,"end":106774279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137502.9","gene_symbol":"RAB30","gene_name":"RAB30, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9770]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27314","summary":null,"start":82973133,"end":83071923,"strand":-1,"description":"RAB30, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9770]"}, {"versioned_ensembl_gene_id":"ENSG00000266916.5","gene_symbol":"ZNF793-AS1","gene_name":"ZNF793 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51303]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927720","summary":null,"start":37497159,"end":37507046,"strand":-1,"description":"ZNF793 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51303]"}, {"versioned_ensembl_gene_id":"ENSG00000259067.1","gene_symbol":"AL583810.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104904342,"end":104905204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261219.1","gene_symbol":"AC090651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57720295,"end":57720928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261270.1","gene_symbol":"AC012181.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56940278,"end":56941342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224216.1","gene_symbol":"AC234781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155334858,"end":155351957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261114.1","gene_symbol":"AC012181.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56941028,"end":56941726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225108.1","gene_symbol":"ZBTB45P1","gene_name":"zinc finger and BTB domain containing 45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49227]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645129","summary":null,"start":109986939,"end":109988394,"strand":-1,"description":"zinc finger and BTB domain containing 45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49227]"}, {"versioned_ensembl_gene_id":"ENSG00000104635.13","gene_symbol":"SLC39A14","gene_name":"solute carrier family 39 member 14 [Source:HGNC Symbol;Acc:HGNC:20858]","synonyms":"ZIP14,NET34,KIAA0062","biotype":"protein_coding","ncbi_id":"23516","summary":"This gene encodes a member of the the SLC39A family of divalent metal transporters that mediates the cellular uptake of manganese, zinc, iron, and cadmium. The encoded protein contains eight transmembrane domains, a histidine-rich motif, and a metalloprotease motif, and is expressed on the plasma membrane and the endocytic vesicle membrane. It is an important transporter of nontransferrin-bound iron and a critical regulator of manganese homeostasis. Naturally occurring mutations in this gene are associated with neurodegeneration with brain iron accumulation and early-onset parkinsonism-dystonia with hypermanganesemia. [provided by RefSeq, May 2017]","start":22367249,"end":22434129,"strand":1,"description":"solute carrier family 39 member 14 [Source:HGNC Symbol;Acc:HGNC:20858]"}, {"versioned_ensembl_gene_id":"ENSG00000196301.3","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206E,HLA-DRB1L,D6S206,HLA-DR1BL","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32459821,"end":32473500,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000144792.9","gene_symbol":"ZNF660","gene_name":"zinc finger protein 660 [Source:HGNC Symbol;Acc:HGNC:26720]","synonyms":"FLJ36870","biotype":"protein_coding","ncbi_id":"285349","summary":"This gene encodes a protein that contains multiple C2H2 zinc finger domains, and is located in a cluster of zinc-finger encoding genes on chromosome 3. Naturally-occurring readthrough transcription is observed between this gene and the downstream zinc finger protein 197 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017]","start":44578223,"end":44599694,"strand":1,"description":"zinc finger protein 660 [Source:HGNC Symbol;Acc:HGNC:26720]"}, {"versioned_ensembl_gene_id":"ENSG00000265751.1","gene_symbol":"AC015878.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21380286,"end":21451017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251051.1","gene_symbol":"ELL2P2","gene_name":"elongation factor for RNA polymerase II 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421143","summary":null,"start":132367786,"end":132368479,"strand":-1,"description":"elongation factor for RNA polymerase II 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39344]"}, {"versioned_ensembl_gene_id":"ENSG00000109610.5","gene_symbol":"SOD3","gene_name":"superoxide dismutase 3 [Source:HGNC Symbol;Acc:HGNC:11181]","synonyms":"EC-SOD","biotype":"protein_coding","ncbi_id":"6649","summary":"This gene encodes a member of the superoxide dismutase (SOD) protein family. SODs are antioxidant enzymes that catalyze the conversion of superoxide radicals into hydrogen peroxide and oxygen, which may protect the brain, lungs, and other tissues from oxidative stress. Proteolytic processing of the encoded protein results in the formation of two distinct homotetramers that differ in their ability to interact with the extracellular matrix (ECM). Homotetramers consisting of the intact protein, or type C subunit, exhibit high affinity for heparin and are anchored to the ECM. Homotetramers consisting of a proteolytically cleaved form of the protein, or type A subunit, exhibit low affinity for heparin and do not interact with the ECM. A mutation in this gene may be associated with increased heart disease risk. [provided by RefSeq, Oct 2015]","start":24789912,"end":24800842,"strand":1,"description":"superoxide dismutase 3 [Source:HGNC Symbol;Acc:HGNC:11181]"}, {"versioned_ensembl_gene_id":"ENSG00000254081.1","gene_symbol":"LINC01299","gene_name":"long intergenic non-protein coding RNA 1299 [Source:HGNC Symbol;Acc:HGNC:27839]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286186","summary":null,"start":65527008,"end":65562780,"strand":-1,"description":"long intergenic non-protein coding RNA 1299 [Source:HGNC Symbol;Acc:HGNC:27839]"}, {"versioned_ensembl_gene_id":"ENSG00000243007.1","gene_symbol":"RPL12P35","gene_name":"ribosomal protein L12 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400389","summary":null,"start":72379215,"end":72379710,"strand":-1,"description":"ribosomal protein L12 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35969]"}, {"versioned_ensembl_gene_id":"ENSG00000137819.13","gene_symbol":"PAQR5","gene_name":"progestin and adipoQ receptor family member 5 [Source:HGNC Symbol;Acc:HGNC:29645]","synonyms":"MPRG,FLJ20190","biotype":"protein_coding","ncbi_id":"54852","summary":null,"start":69298947,"end":69407780,"strand":1,"description":"progestin and adipoQ receptor family member 5 [Source:HGNC Symbol;Acc:HGNC:29645]"}, {"versioned_ensembl_gene_id":"ENSG00000279659.1","gene_symbol":"AL451064.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79573877,"end":79575530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253470.1","gene_symbol":"AC016074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125749055,"end":125750241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271356.1","gene_symbol":"AC073091.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76260755,"end":76261661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079950.13","gene_symbol":"STX7","gene_name":"syntaxin 7 [Source:HGNC Symbol;Acc:HGNC:11442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8417","summary":"The protein encoded by this gene is a syntaxin family membrane receptor involved in vesicle transport. The encoded protein binds alpha-SNAP, an important regulator of transport vesicle fusion. Along with syntaxin 13, this protein plays a role in the ordered fusion of endosomes and lysosomes with the phagosome. [provided by RefSeq, May 2016]","start":132445867,"end":132513198,"strand":-1,"description":"syntaxin 7 [Source:HGNC Symbol;Acc:HGNC:11442]"}, {"versioned_ensembl_gene_id":"ENSG00000143320.8","gene_symbol":"CRABP2","gene_name":"cellular retinoic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2339]","synonyms":"CRABP-II","biotype":"protein_coding","ncbi_id":"1382","summary":"This gene encodes a member of the retinoic acid (RA, a form of vitamin A) binding protein family and lipocalin/cytosolic fatty-acid binding protein family. The protein is a cytosol-to-nuclear shuttling protein, which facilitates RA binding to its cognate receptor complex and transfer to the nucleus. It is involved in the retinoid signaling pathway, and is associated with increased circulating low-density lipoprotein cholesterol. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2010]","start":156699606,"end":156705816,"strand":-1,"description":"cellular retinoic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2339]"}, {"versioned_ensembl_gene_id":"ENSG00000225107.1","gene_symbol":"AC092484.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145569294,"end":145588024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280094.2","gene_symbol":"OR1B1","gene_name":"olfactory receptor family 1 subfamily B member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8181]","synonyms":"OR9-B","biotype":"polymorphic_pseudogene","ncbi_id":"347169","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":122628579,"end":122629573,"strand":-1,"description":"olfactory receptor family 1 subfamily B member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8181]"}, {"versioned_ensembl_gene_id":"ENSG00000140939.14","gene_symbol":"NOL3","gene_name":"nucleolar protein 3 [Source:HGNC Symbol;Acc:HGNC:7869]","synonyms":"NOP30,MYP,CARD2,ARC","biotype":"protein_coding","ncbi_id":"8996","summary":"This gene encodes an anti-apoptotic protein that has been shown to down-regulate the enzyme activities of caspase 2, caspase 8 and tumor protein p53. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":67170154,"end":67175735,"strand":1,"description":"nucleolar protein 3 [Source:HGNC Symbol;Acc:HGNC:7869]"}, {"versioned_ensembl_gene_id":"ENSG00000139537.10","gene_symbol":"CCDC65","gene_name":"coiled-coil domain containing 65 [Source:HGNC Symbol;Acc:HGNC:29937]","synonyms":"NYD-SP28,FLJ35732,FAP250,DRC2,CILD27,CFAP250","biotype":"protein_coding","ncbi_id":"85478","summary":"This gene encodes a sperm tail protein that is highly expressed in adult testis, spermatocytes and spermatids. The protein plays a critical role in the assembly of the nexin-dynein regulatory complex. Mutations in this gene result in primary ciliary dyskinesia. [provided by RefSeq, Nov 2013]","start":48904110,"end":48931840,"strand":1,"description":"coiled-coil domain containing 65 [Source:HGNC Symbol;Acc:HGNC:29937]"}, {"versioned_ensembl_gene_id":"ENSG00000226347.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"dJ80I19.4,OR6-8,hs6M1-6","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173273,"end":29174544,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000134287.9","gene_symbol":"ARF3","gene_name":"ADP ribosylation factor 3 [Source:HGNC Symbol;Acc:HGNC:654]","synonyms":null,"biotype":"protein_coding","ncbi_id":"377","summary":"ADP-ribosylation factor 3 (ARF3) is a member of the human ARF gene family. These genes encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of phospholipase D. The gene products include 6 ARF proteins and 11 ARF-like proteins and constitute 1 family of the RAS superfamily. The ARF proteins are categorized as class I (ARF1, ARF2,and ARF3), class II (ARF4 and ARF5) and class III (ARF6) and members of each class share a common gene organization. The ARF3 gene contains five exons and four introns. [provided by RefSeq, Jul 2008]","start":48935723,"end":48957551,"strand":-1,"description":"ADP ribosylation factor 3 [Source:HGNC Symbol;Acc:HGNC:654]"}, {"versioned_ensembl_gene_id":"ENSG00000284721.1","gene_symbol":"AL662907.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33194788,"end":33200353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233880.1","gene_symbol":"AL161722.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35761499,"end":35762479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215351.3","gene_symbol":"PPIAP1","gene_name":"peptidylprolyl isomerase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9254]","synonyms":"PPIAP","biotype":"processed_pseudogene","ncbi_id":"100288185","summary":null,"start":20828127,"end":20828622,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9254]"}, {"versioned_ensembl_gene_id":"ENSG00000145975.14","gene_symbol":"FAM217A","gene_name":"family with sequence similarity 217 member A [Source:HGNC Symbol;Acc:HGNC:21362]","synonyms":"MGC43581,C6orf146","biotype":"protein_coding","ncbi_id":"222826","summary":null,"start":4049434,"end":4087344,"strand":-1,"description":"family with sequence similarity 217 member A [Source:HGNC Symbol;Acc:HGNC:21362]"}, {"versioned_ensembl_gene_id":"ENSG00000218748.1","gene_symbol":"DBIP1","gene_name":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2692]","synonyms":"DBIL2","biotype":"processed_pseudogene","ncbi_id":"1624","summary":null,"start":79436908,"end":79437167,"strand":-1,"description":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2692]"}, {"versioned_ensembl_gene_id":"ENSG00000254325.2","gene_symbol":"AC018607.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55893595,"end":55895739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176219.3","gene_symbol":"OR11H6","gene_name":"olfactory receptor family 11 subfamily H member 6 [Source:HGNC Symbol;Acc:HGNC:15349]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122748","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20223710,"end":20224702,"strand":1,"description":"olfactory receptor family 11 subfamily H member 6 [Source:HGNC Symbol;Acc:HGNC:15349]"}, {"versioned_ensembl_gene_id":"ENSG00000227689.1","gene_symbol":"SRP68P2","gene_name":"signal recognition particle 68 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30426]","synonyms":"SRPSMCR","biotype":"processed_pseudogene","ncbi_id":"252840","summary":null,"start":18527557,"end":18528461,"strand":1,"description":"signal recognition particle 68 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30426]"}, {"versioned_ensembl_gene_id":"ENSG00000224455.9","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"ARE1,SACM2L","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33420661,"end":33442416,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000006125.17","gene_symbol":"AP2B1","gene_name":"adaptor related protein complex 2 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:563]","synonyms":"CLAPB1,ADTB2","biotype":"protein_coding","ncbi_id":"163","summary":"The protein encoded by this gene is one of two large chain components of the assembly protein complex 2, which serves to link clathrin to receptors in coated vesicles. The encoded protein is found on the cytoplasmic face of coated vesicles in the plasma membrane. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":35578046,"end":35726409,"strand":1,"description":"adaptor related protein complex 2 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:563]"}, {"versioned_ensembl_gene_id":"ENSG00000225393.1","gene_symbol":"BX571846.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155468286,"end":155487046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226225.6","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"D6S218E,KE-3,S18,HKE3,KE3","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33442379,"end":33446883,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000111077.17","gene_symbol":"TNS2","gene_name":"tensin 2 [Source:HGNC Symbol;Acc:HGNC:19737]","synonyms":"TENC1,KIAA1075,C1-TEN","biotype":"protein_coding","ncbi_id":"23371","summary":"The protein encoded by this gene belongs to the tensin family. Tensin is a focal adhesion molecule that binds to actin filaments and participates in signaling pathways. This protein plays a role in regulating cell migration. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":53046969,"end":53064372,"strand":1,"description":"tensin 2 [Source:HGNC Symbol;Acc:HGNC:19737]"}, {"versioned_ensembl_gene_id":"ENSG00000139737.21","gene_symbol":"SLAIN1","gene_name":"SLAIN motif family member 1 [Source:HGNC Symbol;Acc:HGNC:26387]","synonyms":"FLJ30046,C13orf32","biotype":"protein_coding","ncbi_id":"122060","summary":null,"start":77697854,"end":77764242,"strand":1,"description":"SLAIN motif family member 1 [Source:HGNC Symbol;Acc:HGNC:26387]"}, {"versioned_ensembl_gene_id":"ENSG00000277987.1","gene_symbol":"LINC02351","gene_name":"long intergenic non-protein coding RNA 2351 [Source:HGNC Symbol;Acc:HGNC:53273]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371011","summary":null,"start":98324273,"end":98327494,"strand":-1,"description":"long intergenic non-protein coding RNA 2351 [Source:HGNC Symbol;Acc:HGNC:53273]"}, {"versioned_ensembl_gene_id":"ENSG00000233955.1","gene_symbol":"AHCYP3","gene_name":"adenosylhomocysteinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44995]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402093","summary":null,"start":104395002,"end":104396280,"strand":-1,"description":"adenosylhomocysteinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44995]"}, {"versioned_ensembl_gene_id":"ENSG00000169410.9","gene_symbol":"PTPN9","gene_name":"protein tyrosine phosphatase, non-receptor type 9 [Source:HGNC Symbol;Acc:HGNC:9661]","synonyms":"MEG2","biotype":"protein_coding","ncbi_id":"5780","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N-terminal domain that shares a significant similarity with yeast SEC14, which is a protein that has phosphatidylinositol transfer activity and is required for protein secretion through the Golgi complex in yeast. This PTP was found to be activated by polyphosphoinositide, and is thought to be involved in signaling events regulating phagocytosis. [provided by RefSeq, Jul 2008]","start":75463251,"end":75579289,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 9 [Source:HGNC Symbol;Acc:HGNC:9661]"}, {"versioned_ensembl_gene_id":"ENSG00000181698.4","gene_symbol":"OR5T1","gene_name":"olfactory receptor family 5 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14821]","synonyms":"OR5T1P","biotype":"protein_coding","ncbi_id":"390155","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56274154,"end":56276819,"strand":1,"description":"olfactory receptor family 5 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14821]"}, {"versioned_ensembl_gene_id":"ENSG00000143977.13","gene_symbol":"SNRPG","gene_name":"small nuclear ribonucleoprotein polypeptide G [Source:HGNC Symbol;Acc:HGNC:11163]","synonyms":"Sm-G","biotype":"protein_coding","ncbi_id":"6637","summary":"The protein encoded by this gene is a component of the U1, U2, U4, and U5 small nuclear ribonucleoprotein complexes, precursors of the spliceosome. The encoded protein may also be a part of the U7 small nuclear ribonucleoprotein complex, which participates in the processing of the 3' end of histone transcripts. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":70281362,"end":70293771,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G [Source:HGNC Symbol;Acc:HGNC:11163]"}, {"versioned_ensembl_gene_id":"ENSG00000107643.15","gene_symbol":"MAPK8","gene_name":"mitogen-activated protein kinase 8 [Source:HGNC Symbol;Acc:HGNC:6881]","synonyms":"JNK1,JNK,SAPK1,PRKM8","biotype":"protein_coding","ncbi_id":"5599","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is activated by various cell stimuli, and targets specific transcription factors, and thus mediates immediate-early gene expression in response to cell stimuli. The activation of this kinase by tumor-necrosis factor alpha (TNF-alpha) is found to be required for TNF-alpha induced apoptosis. This kinase is also involved in UV radiation induced apoptosis, which is thought to be related to cytochrom c-mediated cell death pathway. Studies of the mouse counterpart of this gene suggested that this kinase play a key role in T cell proliferation, apoptosis and differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Apr 2016]","start":48306639,"end":48439360,"strand":1,"description":"mitogen-activated protein kinase 8 [Source:HGNC Symbol;Acc:HGNC:6881]"}, {"versioned_ensembl_gene_id":"ENSG00000267592.1","gene_symbol":"AC004134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35596904,"end":35597128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259424.1","gene_symbol":"AC118658.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98646951,"end":98647371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182022.17","gene_symbol":"CHST15","gene_name":"carbohydrate sulfotransferase 15 [Source:HGNC Symbol;Acc:HGNC:18137]","synonyms":"KIAA0598,GALNAC4S-6ST,BRAG","biotype":"protein_coding","ncbi_id":"51363","summary":"Chondroitin sulfate (CS) is a glycosaminoglycan which is an important structural component of the extracellular matrix and which links to proteins to form proteoglycans. Chondroitin sulfate E (CS-E) is an isomer of chondroitin sulfate in which the C-4 and C-6 hydroxyl groups are sulfated. This gene encodes a type II transmembrane glycoprotein that acts as a sulfotransferase to transfer sulfate to the C-6 hydroxal group of chondroitin sulfate. This gene has also been identified as being co-expressed with RAG1 in B-cells and as potentially acting as a B-cell surface signaling receptor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012]","start":124007666,"end":124093607,"strand":-1,"description":"carbohydrate sulfotransferase 15 [Source:HGNC Symbol;Acc:HGNC:18137]"}, {"versioned_ensembl_gene_id":"ENSG00000124490.13","gene_symbol":"CRISP2","gene_name":"cysteine rich secretory protein 2 [Source:HGNC Symbol;Acc:HGNC:12024]","synonyms":"TPX1,GAPDL5,CT36,CRISP-2","biotype":"protein_coding","ncbi_id":"7180","summary":null,"start":49692358,"end":49713590,"strand":-1,"description":"cysteine rich secretory protein 2 [Source:HGNC Symbol;Acc:HGNC:12024]"}, {"versioned_ensembl_gene_id":"ENSG00000215547.1","gene_symbol":"DEFB115","gene_name":"defensin beta 115 [Source:HGNC Symbol;Acc:HGNC:18096]","synonyms":"DEFB-15","biotype":"protein_coding","ncbi_id":"245929","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. [provided by RefSeq, Oct 2014]","start":31257664,"end":31259632,"strand":1,"description":"defensin beta 115 [Source:HGNC Symbol;Acc:HGNC:18096]"}, {"versioned_ensembl_gene_id":"ENSG00000260269.5","gene_symbol":"AC105036.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":75527150,"end":75601205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232334.1","gene_symbol":"AL683842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124004304,"end":124004828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277112.3","gene_symbol":"ANKRD20A21P","gene_name":"ankyrin repeat domain 20 family member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:52329]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"102723552","summary":null,"start":30656033,"end":30723932,"strand":-1,"description":"ankyrin repeat domain 20 family member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:52329]"}, {"versioned_ensembl_gene_id":"ENSG00000267477.1","gene_symbol":"AC008481.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":11466240,"end":11505698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270894.1","gene_symbol":"AC015849.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":35818399,"end":35823713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213438.2","gene_symbol":"YBX2P1","gene_name":"Y-box binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100124332","summary":null,"start":123991910,"end":123992669,"strand":1,"description":"Y-box binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49498]"}, {"versioned_ensembl_gene_id":"ENSG00000254508.5","gene_symbol":"FBXO3-AS1","gene_name":"FBXO3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51147]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928440","summary":null,"start":33774699,"end":33775670,"strand":1,"description":"FBXO3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51147]"}, {"versioned_ensembl_gene_id":"ENSG00000110921.13","gene_symbol":"MVK","gene_name":"mevalonate kinase [Source:HGNC Symbol;Acc:HGNC:7530]","synonyms":"MK,LRBP","biotype":"protein_coding","ncbi_id":"4598","summary":"This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":109573255,"end":109598117,"strand":1,"description":"mevalonate kinase [Source:HGNC Symbol;Acc:HGNC:7530]"}, {"versioned_ensembl_gene_id":"ENSG00000266806.1","gene_symbol":"AC087575.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22331597,"end":22332410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214244.4","gene_symbol":"SETP21","gene_name":"SET pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100856878","summary":null,"start":60459848,"end":60460739,"strand":-1,"description":"SET pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42940]"}, {"versioned_ensembl_gene_id":"ENSG00000213303.3","gene_symbol":"AC008481.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11523436,"end":11523831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282568.1","gene_symbol":"TRBV2","gene_name":"T-cell receptor beta variable 2 [Source:HGNC Symbol;Acc:HGNC:12195]","synonyms":"TCRBV2S1,TCRBV22S1A2N1T","biotype":"TR_V_gene","ncbi_id":"28620","summary":null,"start":142300947,"end":142301455,"strand":1,"description":"T-cell receptor beta variable 2 [Source:HGNC Symbol;Acc:HGNC:12195]"}, {"versioned_ensembl_gene_id":"ENSG00000278991.1","gene_symbol":"AC090181.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77063397,"end":77064910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259652.1","gene_symbol":"AC090181.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77043680,"end":77045160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280071.3","gene_symbol":"FP565260.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5079294,"end":5128425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237515.8","gene_symbol":"SHISA9","gene_name":"shisa family member 9 [Source:HGNC Symbol;Acc:HGNC:37231]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729993","summary":null,"start":12901620,"end":13240413,"strand":1,"description":"shisa family member 9 [Source:HGNC Symbol;Acc:HGNC:37231]"}, {"versioned_ensembl_gene_id":"ENSG00000155961.4","gene_symbol":"RAB39B","gene_name":"RAB39B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16499]","synonyms":"MRX72","biotype":"protein_coding","ncbi_id":"116442","summary":"This gene encodes a member of the Rab family of proteins. Rab proteins are small GTPases that are involved in vesicular trafficking. Mutations in this gene are associated with X-linked cognitive disability. [provided by RefSeq, Aug 2013]","start":155258241,"end":155264589,"strand":-1,"description":"RAB39B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16499]"}, {"versioned_ensembl_gene_id":"ENSG00000254658.3","gene_symbol":"OR8J2","gene_name":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15311]","synonyms":"OR8J2P","biotype":"polymorphic_pseudogene","ncbi_id":"81169","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":56208985,"end":56215222,"strand":-1,"description":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15311]"}, {"versioned_ensembl_gene_id":"ENSG00000118292.8","gene_symbol":"C1orf54","gene_name":"chromosome 1 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26258]","synonyms":"FLJ23221","biotype":"protein_coding","ncbi_id":"79630","summary":null,"start":150268200,"end":150280916,"strand":1,"description":"chromosome 1 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26258]"}, {"versioned_ensembl_gene_id":"ENSG00000255025.1","gene_symbol":"AF228730.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7238286,"end":7238631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238200.1","gene_symbol":"MGAT2P2","gene_name":"MGAT2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51243]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422589","summary":null,"start":135751119,"end":135752583,"strand":1,"description":"MGAT2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51243]"}, {"versioned_ensembl_gene_id":"ENSG00000236844.1","gene_symbol":"AC069213.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195554610,"end":195555083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181718.6","gene_symbol":"OR5T2","gene_name":"olfactory receptor family 5 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:15296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219464","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56231282,"end":56234255,"strand":-1,"description":"olfactory receptor family 5 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:15296]"}, {"versioned_ensembl_gene_id":"ENSG00000228929.1","gene_symbol":"RPS13P2","gene_name":"ribosomal protein S13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729236","summary":null,"start":52772194,"end":52772648,"strand":-1,"description":"ribosomal protein S13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36364]"}, {"versioned_ensembl_gene_id":"ENSG00000269096.6","gene_symbol":"CT45A3","gene_name":"cancer/testis antigen family 45 member A3 [Source:HGNC Symbol;Acc:HGNC:33268]","synonyms":"CT45A4,CT45.4,CT45.3,CT45-4,CT45-3","biotype":"protein_coding","ncbi_id":"441519","summary":null,"start":135759846,"end":135768191,"strand":-1,"description":"cancer/testis antigen family 45 member A3 [Source:HGNC Symbol;Acc:HGNC:33268]"}, {"versioned_ensembl_gene_id":"ENSG00000225008.1","gene_symbol":"AC234781.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155290360,"end":155291353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231319.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR6-4,OR2B3P","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086272,"end":29087278,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000228986.1","gene_symbol":"AC234781.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155292169,"end":155293432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247345.2","gene_symbol":"AC092343.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59039761,"end":59063503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230491.1","gene_symbol":"AC234781.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155310247,"end":155310490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155962.12","gene_symbol":"CLIC2","gene_name":"chloride intracellular channel 2 [Source:HGNC Symbol;Acc:HGNC:2063]","synonyms":"XAP121","biotype":"protein_coding","ncbi_id":"1193","summary":"This gene encodes a chloride intracellular channel protein. Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. This protein plays a role in inhibiting the function of ryanodine receptor 2. A mutation in this gene is the cause of an X-linked form of cognitive disability. [provided by RefSeq, Jul 2017]","start":155276211,"end":155334657,"strand":-1,"description":"chloride intracellular channel 2 [Source:HGNC Symbol;Acc:HGNC:2063]"}, {"versioned_ensembl_gene_id":"ENSG00000262116.1","gene_symbol":"AC009134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13197606,"end":13204907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152931.7","gene_symbol":"PART1","gene_name":"prostate androgen-regulated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17263]","synonyms":"NCRNA00206,DKFZP586D0823","biotype":"lincRNA","ncbi_id":"25859","summary":"This gene is induced by androgen in prostate adenocarcinoma cells. Multiple alternatively transcript variants have been described for this gene, none of which are predicted to encode a protein product. [provided by RefSeq, Sep 2009]","start":60487713,"end":60547657,"strand":1,"description":"prostate androgen-regulated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17263]"}, {"versioned_ensembl_gene_id":"ENSG00000161914.9","gene_symbol":"ZNF653","gene_name":"zinc finger protein 653 [Source:HGNC Symbol;Acc:HGNC:25196]","synonyms":"Zip67","biotype":"protein_coding","ncbi_id":"115950","summary":null,"start":11483427,"end":11505923,"strand":-1,"description":"zinc finger protein 653 [Source:HGNC Symbol;Acc:HGNC:25196]"}, {"versioned_ensembl_gene_id":"ENSG00000279137.1","gene_symbol":"AL356309.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126518840,"end":126520773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226078.1","gene_symbol":"AL356309.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126527618,"end":126530343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230227.4","gene_symbol":"SIAH1P1","gene_name":"siah E3 ubiquitin protein ligase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30966]","synonyms":"SIAH1L","biotype":"processed_pseudogene","ncbi_id":"340571","summary":null,"start":35626142,"end":35627064,"strand":1,"description":"siah E3 ubiquitin protein ligase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30966]"}, {"versioned_ensembl_gene_id":"ENSG00000212330.1","gene_symbol":"RNU6-244P","gene_name":"RNA, U6 small nuclear 244, pseudogene [Source:HGNC Symbol;Acc:HGNC:47207]","synonyms":null,"biotype":"snRNA","ncbi_id":"106866981","summary":null,"start":102501676,"end":102501779,"strand":1,"description":"RNA, U6 small nuclear 244, pseudogene [Source:HGNC Symbol;Acc:HGNC:47207]"}, {"versioned_ensembl_gene_id":"ENSG00000207171.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":168471409,"end":168471539,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000264960.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32579248,"end":32579395,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000212442.1","gene_symbol":"RNU6-243P","gene_name":"RNA, U6 small nuclear 243, pseudogene [Source:HGNC Symbol;Acc:HGNC:47206]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479675","summary":null,"start":35256840,"end":35256946,"strand":-1,"description":"RNA, U6 small nuclear 243, pseudogene [Source:HGNC Symbol;Acc:HGNC:47206]"}, {"versioned_ensembl_gene_id":"ENSG00000278144.1","gene_symbol":"NEAT1_1","gene_name":"Nuclear enriched abundant transcript 1 conserved region 1 [Source:RFAM;Acc:RF01955]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65423273,"end":65423392,"strand":1,"description":"Nuclear enriched abundant transcript 1 conserved region 1 [Source:RFAM;Acc:RF01955]"}, {"versioned_ensembl_gene_id":"ENSG00000283926.1","gene_symbol":"MIR192","gene_name":"microRNA 192 [Source:HGNC Symbol;Acc:HGNC:31562]","synonyms":"MIRN192,hsa-mir-192","biotype":"miRNA","ncbi_id":"406967","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64891137,"end":64891246,"strand":-1,"description":"microRNA 192 [Source:HGNC Symbol;Acc:HGNC:31562]"}, {"versioned_ensembl_gene_id":"ENSG00000207940.1","gene_symbol":"MIR567","gene_name":"microRNA 567 [Source:HGNC Symbol;Acc:HGNC:32823]","synonyms":"MIRN567,hsa-mir-567","biotype":"miRNA","ncbi_id":"693152","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112112801,"end":112112898,"strand":1,"description":"microRNA 567 [Source:HGNC Symbol;Acc:HGNC:32823]"}, {"versioned_ensembl_gene_id":"ENSG00000221502.1","gene_symbol":"MIR1245A","gene_name":"microRNA 1245a [Source:HGNC Symbol;Acc:HGNC:35311]","synonyms":"MIR1245,hsa-mir-1245,MIRN1245","biotype":"miRNA","ncbi_id":"100302219","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188978092,"end":188978161,"strand":1,"description":"microRNA 1245a [Source:HGNC Symbol;Acc:HGNC:35311]"}, {"versioned_ensembl_gene_id":"ENSG00000215952.1","gene_symbol":"MIR921","gene_name":"microRNA 921 [Source:HGNC Symbol;Acc:HGNC:33671]","synonyms":"MIRN921,hsa-mir-921","biotype":"miRNA","ncbi_id":"100126349","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":166154743,"end":166154798,"strand":-1,"description":"microRNA 921 [Source:HGNC Symbol;Acc:HGNC:33671]"}, {"versioned_ensembl_gene_id":"ENSG00000278549.1","gene_symbol":"MIR6736","gene_name":"microRNA 6736 [Source:HGNC Symbol;Acc:HGNC:50072]","synonyms":"hsa-mir-6736","biotype":"miRNA","ncbi_id":"102466191","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145850587,"end":145850645,"strand":-1,"description":"microRNA 6736 [Source:HGNC Symbol;Acc:HGNC:50072]"}, {"versioned_ensembl_gene_id":"ENSG00000252303.2","gene_symbol":"RNU6-280P","gene_name":"RNA, U6 small nuclear 280, pseudogene [Source:HGNC Symbol;Acc:HGNC:47243]","synonyms":"RNU6-1221P","biotype":"snRNA","ncbi_id":"106481886","summary":null,"start":67546651,"end":67546754,"strand":1,"description":"RNA, U6 small nuclear 280, pseudogene [Source:HGNC Symbol;Acc:HGNC:47243]"}, {"versioned_ensembl_gene_id":"ENSG00000223190.1","gene_symbol":"RN7SKP100","gene_name":"RNA, 7SK small nuclear pseudogene 100 [Source:HGNC Symbol;Acc:HGNC:45824]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479139","summary":null,"start":43063326,"end":43063609,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 100 [Source:HGNC Symbol;Acc:HGNC:45824]"}, {"versioned_ensembl_gene_id":"ENSG00000274208.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":189720125,"end":189720300,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000221698.1","gene_symbol":"MIR548H3","gene_name":"microRNA 548h-3 [Source:HGNC Symbol;Acc:HGNC:35344]","synonyms":"MIRN548H3,hsa-mir-548h-3","biotype":"miRNA","ncbi_id":"100302287","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13543529,"end":13543646,"strand":-1,"description":"microRNA 548h-3 [Source:HGNC Symbol;Acc:HGNC:35344]"}, {"versioned_ensembl_gene_id":"ENSG00000266886.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31360234,"end":31360340,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000239471.3","gene_symbol":"RN7SL584P","gene_name":"RNA, 7SL, cytoplasmic 584, pseudogene [Source:HGNC Symbol;Acc:HGNC:46600]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480519","summary":null,"start":20095733,"end":20096029,"strand":-1,"description":"RNA, 7SL, cytoplasmic 584, pseudogene [Source:HGNC Symbol;Acc:HGNC:46600]"}, {"versioned_ensembl_gene_id":"ENSG00000206939.1","gene_symbol":"RNU6-281P","gene_name":"RNA, U6 small nuclear 281, pseudogene [Source:HGNC 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processing and modification. snoRNAs of the box C/D class, like SNORD83B, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]","start":39313819,"end":39313911,"strand":-1,"description":"small nucleolar RNA, C/D box 83B [Source:HGNC Symbol;Acc:HGNC:17132]"}, {"versioned_ensembl_gene_id":"ENSG00000252595.1","gene_symbol":"RN7SKP82","gene_name":"RNA, 7SK small nuclear pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:45806]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480462","summary":null,"start":42892396,"end":42892618,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:45806]"}, {"versioned_ensembl_gene_id":"ENSG00000278007.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":4127492,"end":4127732,"strand":1,"description":"Metazoan signal recognition 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{"versioned_ensembl_gene_id":"ENSG00000212135.1","gene_symbol":"SNORD67","gene_name":"small nucleolar RNA, C/D box 67 [Source:HGNC Symbol;Acc:HGNC:32728]","synonyms":"HBII-166","biotype":"snoRNA","ncbi_id":"692108","summary":null,"start":46762389,"end":46762499,"strand":-1,"description":"small nucleolar RNA, C/D box 67 [Source:HGNC Symbol;Acc:HGNC:32728]"}, {"versioned_ensembl_gene_id":"ENSG00000207187.1","gene_symbol":"SNORA10B","gene_name":"small nucleolar RNA, H/ACA box 10B [Source:HGNC Symbol;Acc:HGNC:52188]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616960","summary":null,"start":30187434,"end":30187566,"strand":1,"description":"small nucleolar RNA, H/ACA box 10B [Source:HGNC Symbol;Acc:HGNC:52188]"}, {"versioned_ensembl_gene_id":"ENSG00000200827.1","gene_symbol":"RNU6-324P","gene_name":"RNA, U6 small nuclear 324, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000212260.1","gene_symbol":"RNU6-724P","gene_name":"RNA, U6 small nuclear 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:47687]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479887","summary":null,"start":69530613,"end":69530717,"strand":-1,"description":"RNA, U6 small nuclear 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:47687]"}, {"versioned_ensembl_gene_id":"ENSG00000242020.3","gene_symbol":"RN7SL68P","gene_name":"RNA, 7SL, cytoplasmic 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:46084]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080632","summary":null,"start":141479316,"end":141479625,"strand":1,"description":"RNA, 7SL, cytoplasmic 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:46084]"}, {"versioned_ensembl_gene_id":"ENSG00000200487.1","gene_symbol":"RNA5SP322","gene_name":"RNA, 5S ribosomal pseudogene 322 [Source:HGNC 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Box H/ACA snoRNAs, such as SNORA5C, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":45104906,"end":45105042,"strand":-1,"description":"small nucleolar RNA, H/ACA box 5C [Source:HGNC Symbol;Acc:HGNC:32590]"}, {"versioned_ensembl_gene_id":"ENSG00000202141.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":183022859,"end":183022971,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265733.1","gene_symbol":"SNORA74C-1","gene_name":"small nucleolar RNA, H/ACA box 74C-1 [Source:HGNC Symbol;Acc:HGNC:52217]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616974","summary":null,"start":45984610,"end":45984810,"strand":1,"description":"small nucleolar RNA, H/ACA box 74C-1 [Source:HGNC Symbol;Acc:HGNC:52217]"}, 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{"versioned_ensembl_gene_id":"ENSG00000223142.1","gene_symbol":"RN7SKP252","gene_name":"RNA, 7SK small nuclear pseudogene 252 [Source:HGNC Symbol;Acc:HGNC:45976]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479207","summary":null,"start":49738677,"end":49739003,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 252 [Source:HGNC Symbol;Acc:HGNC:45976]"}, {"versioned_ensembl_gene_id":"ENSG00000200674.1","gene_symbol":"RN7SKP160","gene_name":"RNA, 7SK small nuclear pseudogene 160 [Source:HGNC Symbol;Acc:HGNC:45884]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479166","summary":null,"start":173791548,"end":173791887,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 160 [Source:HGNC Symbol;Acc:HGNC:45884]"}, {"versioned_ensembl_gene_id":"ENSG00000206613.1","gene_symbol":"RNU6-1336P","gene_name":"RNA, U6 small nuclear 1336, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000283694.1","gene_symbol":"MIR3202-2","gene_name":"microRNA 3202-2 [Source:HGNC Symbol;Acc:HGNC:38228]","synonyms":"hsa-mir-3202-2","biotype":"miRNA","ncbi_id":"100422877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153981098,"end":153981176,"strand":-1,"description":"microRNA 3202-2 [Source:HGNC Symbol;Acc:HGNC:38228]"}, {"versioned_ensembl_gene_id":"ENSG00000252171.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45047103,"end":45047215,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000271886.1","gene_symbol":"MIR98","gene_name":"microRNA 98 [Source:HGNC Symbol;Acc:HGNC:31649]","synonyms":"MIRN98,hsa-mir-98","biotype":"miRNA","ncbi_id":"407054","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53556223,"end":53556341,"strand":-1,"description":"microRNA 98 [Source:HGNC Symbol;Acc:HGNC:31649]"}, {"versioned_ensembl_gene_id":"ENSG00000199960.1","gene_symbol":"SNORD115-14","gene_name":"small nucleolar RNA, C/D box 115-14 [Source:HGNC Symbol;Acc:HGNC:33033]","synonyms":"HBII-52-14","biotype":"snoRNA","ncbi_id":"100033451","summary":null,"start":25194921,"end":25195001,"strand":1,"description":"small nucleolar RNA, C/D box 115-14 [Source:HGNC Symbol;Acc:HGNC:33033]"}, {"versioned_ensembl_gene_id":"ENSG00000252903.2","gene_symbol":"RNU6-894P","gene_name":"RNA, U6 small nuclear 894, pseudogene [Source:HGNC Symbol;Acc:HGNC:47857]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481461","summary":null,"start":31348192,"end":31348296,"strand":1,"description":"RNA, U6 small nuclear 894, pseudogene [Source:HGNC Symbol;Acc:HGNC:47857]"}, {"versioned_ensembl_gene_id":"ENSG00000241152.3","gene_symbol":"RN7SL720P","gene_name":"RNA, 7SL, cytoplasmic 720, pseudogene [Source:HGNC Symbol;Acc:HGNC:46736]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480528","summary":null,"start":17053901,"end":17054204,"strand":1,"description":"RNA, 7SL, cytoplasmic 720, pseudogene [Source:HGNC Symbol;Acc:HGNC:46736]"}, {"versioned_ensembl_gene_id":"ENSG00000207804.1","gene_symbol":"MIR599","gene_name":"microRNA 599 [Source:HGNC Symbol;Acc:HGNC:32855]","synonyms":"hsa-mir-599,MIRN599","biotype":"miRNA","ncbi_id":"693184","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99536636,"end":99536730,"strand":-1,"description":"microRNA 599 [Source:HGNC Symbol;Acc:HGNC:32855]"}, {"versioned_ensembl_gene_id":"ENSG00000206654.1","gene_symbol":"RNU6-608P","gene_name":"RNA, U6 small nuclear 608, pseudogene [Source:HGNC Symbol;Acc:HGNC:47571]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481373","summary":null,"start":39120940,"end":39121043,"strand":-1,"description":"RNA, U6 small nuclear 608, pseudogene [Source:HGNC Symbol;Acc:HGNC:47571]"}, {"versioned_ensembl_gene_id":"ENSG00000252657.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":29777619,"end":29777744,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000275362.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18615581,"end":18615900,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252436.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62726636,"end":62726740,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264706.2","gene_symbol":"RN7SL217P","gene_name":"RNA, 7SL, cytoplasmic 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:46233]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479301","summary":null,"start":49863375,"end":49863660,"strand":-1,"description":"RNA, 7SL, cytoplasmic 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:46233]"}, {"versioned_ensembl_gene_id":"ENSG00000212336.1","gene_symbol":"RNA5SP210","gene_name":"RNA, 5S ribosomal pseudogene 210 [Source:HGNC Symbol;Acc:HGNC:43110]","synonyms":"RN5S210","biotype":"rRNA","ncbi_id":"100873470","summary":null,"start":81622200,"end":81622319,"strand":1,"description":"RNA, 5S ribosomal pseudogene 210 [Source:HGNC Symbol;Acc:HGNC:43110]"}, {"versioned_ensembl_gene_id":"ENSG00000251929.1","gene_symbol":"RNU6-189P","gene_name":"RNA, U6 small nuclear 189, pseudogene [Source:HGNC Symbol;Acc:HGNC:47152]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479650","summary":null,"start":49901850,"end":49901950,"strand":-1,"description":"RNA, U6 small nuclear 189, pseudogene [Source:HGNC Symbol;Acc:HGNC:47152]"}, {"versioned_ensembl_gene_id":"ENSG00000278048.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43251829,"end":43252019,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000200118.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":170244782,"end":170244881,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284266.1","gene_symbol":"MIR4534","gene_name":"microRNA 4534 [Source:HGNC Symbol;Acc:HGNC:41692]","synonyms":"hsa-mir-4534","biotype":"miRNA","ncbi_id":"100616146","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37988794,"end":37988853,"strand":1,"description":"microRNA 4534 [Source:HGNC Symbol;Acc:HGNC:41692]"}, {"versioned_ensembl_gene_id":"ENSG00000199398.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":160008445,"end":160008546,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200026.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":38147428,"end":38147561,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000284256.1","gene_symbol":"MIR5004","gene_name":"microRNA 5004 [Source:HGNC Symbol;Acc:HGNC:43532]","synonyms":"hsa-mir-5004","biotype":"miRNA","ncbi_id":"100847012","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33438331,"end":33438437,"strand":1,"description":"microRNA 5004 [Source:HGNC Symbol;Acc:HGNC:43532]"}, {"versioned_ensembl_gene_id":"ENSG00000240803.3","gene_symbol":"RN7SL231P","gene_name":"RNA, 7SL, cytoplasmic 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:46247]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480984","summary":null,"start":14213052,"end":14213323,"strand":1,"description":"RNA, 7SL, cytoplasmic 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:46247]"}, {"versioned_ensembl_gene_id":"ENSG00000284325.1","gene_symbol":"MIR3655","gene_name":"microRNA 3655 [Source:HGNC Symbol;Acc:HGNC:38960]","synonyms":"hsa-mir-3655","biotype":"miRNA","ncbi_id":"100500820","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140647844,"end":140647926,"strand":1,"description":"microRNA 3655 [Source:HGNC Symbol;Acc:HGNC:38960]"}, {"versioned_ensembl_gene_id":"ENSG00000200545.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":19598247,"end":19598463,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000206764.1","gene_symbol":"RNU6-152P","gene_name":"RNA, U6 small nuclear 152, pseudogene [Source:HGNC Symbol;Acc:HGNC:47115]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481223","summary":null,"start":182327068,"end":182327174,"strand":1,"description":"RNA, U6 small nuclear 152, pseudogene [Source:HGNC Symbol;Acc:HGNC:47115]"}, {"versioned_ensembl_gene_id":"ENSG00000264999.1","gene_symbol":"MIR5089","gene_name":"microRNA 5089 [Source:HGNC Symbol;Acc:HGNC:43536]","synonyms":"hsa-mir-5089","biotype":"miRNA","ncbi_id":"100847067","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46973017,"end":46973100,"strand":1,"description":"microRNA 5089 [Source:HGNC Symbol;Acc:HGNC:43536]"}, {"versioned_ensembl_gene_id":"ENSG00000284082.1","gene_symbol":"MIR7109","gene_name":"microRNA 7109 [Source:HGNC Symbol;Acc:HGNC:50122]","synonyms":"hsa-mir-7109","biotype":"miRNA","ncbi_id":"102465666","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31621467,"end":31621531,"strand":-1,"description":"microRNA 7109 [Source:HGNC Symbol;Acc:HGNC:50122]"}, {"versioned_ensembl_gene_id":"ENSG00000277864.1","gene_symbol":"SCARNA15","gene_name":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]","synonyms":"ACA45,ACA45","biotype":"scaRNA","ncbi_id":"677778","summary":null,"start":82755945,"end":82756071,"strand":1,"description":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]"}, {"versioned_ensembl_gene_id":"ENSG00000238498.1","gene_symbol":"SNORD13P1","gene_name":"small nucleolar RNA, C/D box 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10110]","synonyms":"U13.32A,U13,RNU13P1","biotype":"snoRNA","ncbi_id":"6076","summary":null,"start":42076058,"end":42076161,"strand":-1,"description":"small nucleolar RNA, C/D box 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10110]"}, {"versioned_ensembl_gene_id":"ENSG00000207318.1","gene_symbol":"RNU6-1184P","gene_name":"RNA, U6 small nuclear 1184, pseudogene [Source:HGNC Symbol;Acc:HGNC:48147]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481553","summary":null,"start":147831770,"end":147831877,"strand":1,"description":"RNA, U6 small nuclear 1184, pseudogene [Source:HGNC Symbol;Acc:HGNC:48147]"}, {"versioned_ensembl_gene_id":"ENSG00000223019.1","gene_symbol":"RNA5SP306","gene_name":"RNA, 5S ribosomal pseudogene 306 [Source:HGNC Symbol;Acc:HGNC:43206]","synonyms":"RN5S306","biotype":"rRNA","ncbi_id":"100873580","summary":null,"start":25813811,"end":25813917,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 306 [Source:HGNC Symbol;Acc:HGNC:43206]"}, {"versioned_ensembl_gene_id":"ENSG00000238749.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61883640,"end":61883751,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283301.1","gene_symbol":"MIR4520-2","gene_name":"microRNA 4520-2 [Source:HGNC Symbol;Acc:HGNC:41839]","synonyms":"MIR4520B,hsa-mir-4520b","biotype":"miRNA","ncbi_id":"100616466","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6655449,"end":6655502,"strand":1,"description":"microRNA 4520-2 [Source:HGNC Symbol;Acc:HGNC:41839]"}, {"versioned_ensembl_gene_id":"ENSG00000253000.1","gene_symbol":"RNU1-45P","gene_name":"RNA, U1 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:48387]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481610","summary":null,"start":178116721,"end":178116861,"strand":-1,"description":"RNA, U1 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:48387]"}, {"versioned_ensembl_gene_id":"ENSG00000264796.1","gene_symbol":"MIR5009","gene_name":"microRNA 5009 [Source:HGNC Symbol;Acc:HGNC:43458]","synonyms":"hsa-mir-5009","biotype":"miRNA","ncbi_id":"100846993","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89883931,"end":89884030,"strand":-1,"description":"microRNA 5009 [Source:HGNC Symbol;Acc:HGNC:43458]"}, {"versioned_ensembl_gene_id":"ENSG00000207094.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"RNU67,U67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":88449092,"end":88449231,"strand":-1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000265003.1","gene_symbol":"MIR4780","gene_name":"microRNA 4780 [Source:HGNC Symbol;Acc:HGNC:41552]","synonyms":"hsa-mir-4780","biotype":"miRNA","ncbi_id":"100616447","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88082519,"end":88082599,"strand":-1,"description":"microRNA 4780 [Source:HGNC Symbol;Acc:HGNC:41552]"}, {"versioned_ensembl_gene_id":"ENSG00000278236.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87184849,"end":87185020,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000207579.1","gene_symbol":"MIR662","gene_name":"microRNA 662 [Source:HGNC Symbol;Acc:HGNC:32918]","synonyms":"MIRN662,hsa-mir-662","biotype":"miRNA","ncbi_id":"724032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":770183,"end":770277,"strand":1,"description":"microRNA 662 [Source:HGNC Symbol;Acc:HGNC:32918]"}, {"versioned_ensembl_gene_id":"ENSG00000252254.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8328067,"end":8328179,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201044.1","gene_symbol":"RNU6-268P","gene_name":"RNA, U6 small nuclear 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:47231]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479685","summary":null,"start":230752141,"end":230752247,"strand":1,"description":"RNA, U6 small nuclear 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:47231]"}, {"versioned_ensembl_gene_id":"ENSG00000283881.1","gene_symbol":"MIR3916","gene_name":"microRNA 3916 [Source:HGNC Symbol;Acc:HGNC:38912]","synonyms":"hsa-mir-3916","biotype":"miRNA","ncbi_id":"100500849","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":247201967,"end":247202060,"strand":-1,"description":"microRNA 3916 [Source:HGNC Symbol;Acc:HGNC:38912]"}, {"versioned_ensembl_gene_id":"ENSG00000201733.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":66432763,"end":66432902,"strand":1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000239005.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":139436368,"end":139436494,"strand":-1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000243505.3","gene_symbol":"RN7SL240P","gene_name":"RNA, 7SL, cytoplasmic 240, pseudogene [Source:HGNC Symbol;Acc:HGNC:46256]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479310","summary":null,"start":29721399,"end":29721684,"strand":-1,"description":"RNA, 7SL, cytoplasmic 240, pseudogene [Source:HGNC Symbol;Acc:HGNC:46256]"}, {"versioned_ensembl_gene_id":"ENSG00000252661.1","gene_symbol":"RNU6-782P","gene_name":"RNA, U6 small nuclear 782, pseudogene [Source:HGNC Symbol;Acc:HGNC:47745]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481917","summary":null,"start":15145215,"end":15145318,"strand":1,"description":"RNA, U6 small nuclear 782, pseudogene [Source:HGNC Symbol;Acc:HGNC:47745]"}, {"versioned_ensembl_gene_id":"ENSG00000252684.1","gene_symbol":"RNU6ATAC36P","gene_name":"RNA, U6atac small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46935]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480543","summary":null,"start":76948791,"end":76948870,"strand":1,"description":"RNA, U6atac small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46935]"}, {"versioned_ensembl_gene_id":"ENSG00000283789.1","gene_symbol":"MIR7846","gene_name":"microRNA 7846 [Source:HGNC Symbol;Acc:HGNC:50029]","synonyms":"hsa-mir-7846","biotype":"miRNA","ncbi_id":"102465836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12166943,"end":12167038,"strand":1,"description":"microRNA 7846 [Source:HGNC Symbol;Acc:HGNC:50029]"}, {"versioned_ensembl_gene_id":"ENSG00000202151.1","gene_symbol":"RNY4P28","gene_name":"RNA, Ro-associated Y4 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42496]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873822","summary":null,"start":60187738,"end":60187830,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42496]"}, {"versioned_ensembl_gene_id":"ENSG00000277311.1","gene_symbol":"Six3os1_2","gene_name":"Six3os1 conserved region 2 [Source:RFAM;Acc:RF02247]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44934055,"end":44934271,"strand":1,"description":"Six3os1 conserved region 2 [Source:RFAM;Acc:RF02247]"}, {"versioned_ensembl_gene_id":"ENSG00000201113.1","gene_symbol":"RNU6-647P","gene_name":"RNA, U6 small nuclear 647, pseudogene [Source:HGNC Symbol;Acc:HGNC:47610]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480598","summary":null,"start":32214456,"end":32214562,"strand":-1,"description":"RNA, U6 small nuclear 647, pseudogene [Source:HGNC Symbol;Acc:HGNC:47610]"}, {"versioned_ensembl_gene_id":"ENSG00000239899.3","gene_symbol":"RN7SL674P","gene_name":"RNA, 7SL, cytoplasmic 674, pseudogene [Source:HGNC Symbol;Acc:HGNC:46690]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479468","summary":null,"start":11584773,"end":11585047,"strand":1,"description":"RNA, 7SL, cytoplasmic 674, pseudogene [Source:HGNC Symbol;Acc:HGNC:46690]"}, {"versioned_ensembl_gene_id":"ENSG00000251971.1","gene_symbol":"RNU6-1333P","gene_name":"RNA, U6 small nuclear 1333, pseudogene [Source:HGNC Symbol;Acc:HGNC:48296]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481601","summary":null,"start":238028971,"end":238029063,"strand":-1,"description":"RNA, U6 small nuclear 1333, pseudogene [Source:HGNC Symbol;Acc:HGNC:48296]"}, {"versioned_ensembl_gene_id":"ENSG00000201444.1","gene_symbol":"RNU6-1082P","gene_name":"RNA, U6 small nuclear 1082, pseudogene [Source:HGNC Symbol;Acc:HGNC:48045]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480041","summary":null,"start":117707996,"end":117708102,"strand":-1,"description":"RNA, U6 small nuclear 1082, pseudogene [Source:HGNC Symbol;Acc:HGNC:48045]"}, {"versioned_ensembl_gene_id":"ENSG00000275021.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868796,"end":54868902,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000238724.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":114527129,"end":114527232,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000242565.3","gene_symbol":"RN7SL372P","gene_name":"RNA, 7SL, cytoplasmic 372, pseudogene [Source:HGNC Symbol;Acc:HGNC:46388]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479358","summary":null,"start":153704088,"end":153704385,"strand":1,"description":"RNA, 7SL, cytoplasmic 372, pseudogene [Source:HGNC Symbol;Acc:HGNC:46388]"}, {"versioned_ensembl_gene_id":"ENSG00000212270.1","gene_symbol":"SNORD37","gene_name":"Small nucleolar RNA SNORD37 [Source:RFAM;Acc:RF00440]","synonyms":"U37,RNU37","biotype":"snoRNA","ncbi_id":"26812","summary":null,"start":25806648,"end":25806712,"strand":-1,"description":"Small nucleolar RNA SNORD37 [Source:RFAM;Acc:RF00440]"}, {"versioned_ensembl_gene_id":"ENSG00000239142.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":5093408,"end":5093543,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000274078.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34,SEN34L,SEN34L,LENG5,LENG5,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000276442.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":144265217,"end":144265326,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000252845.1","gene_symbol":"RNA5SP101","gene_name":"RNA, 5S ribosomal pseudogene 101 [Source:HGNC Symbol;Acc:HGNC:42899]","synonyms":"RN5S101","biotype":"rRNA","ncbi_id":"100873372","summary":null,"start":96956708,"end":96956815,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 101 [Source:HGNC Symbol;Acc:HGNC:42899]"}, {"versioned_ensembl_gene_id":"ENSG00000277591.1","gene_symbol":"RN7SL575P","gene_name":"RNA, 7SL, cytoplasmic 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:46591]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479432","summary":null,"start":95003545,"end":95003843,"strand":-1,"description":"RNA, 7SL, cytoplasmic 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:46591]"}, {"versioned_ensembl_gene_id":"ENSG00000239690.3","gene_symbol":"RN7SL668P","gene_name":"RNA, 7SL, cytoplasmic 668, pseudogene [Source:HGNC Symbol;Acc:HGNC:46684]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479466","summary":null,"start":234904186,"end":234904488,"strand":1,"description":"RNA, 7SL, cytoplasmic 668, pseudogene [Source:HGNC Symbol;Acc:HGNC:46684]"}, {"versioned_ensembl_gene_id":"ENSG00000207155.1","gene_symbol":"RNY1P14","gene_name":"RNA, Ro-associated Y1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:50877]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480311","summary":null,"start":140700835,"end":140700942,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:50877]"}, {"versioned_ensembl_gene_id":"ENSG00000238950.1","gene_symbol":"RNU7-173P","gene_name":"RNA, U7 small nuclear 173 pseudogene [Source:HGNC Symbol;Acc:HGNC:45707]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479090","summary":null,"start":47826969,"end":47827044,"strand":-1,"description":"RNA, U7 small nuclear 173 pseudogene [Source:HGNC Symbol;Acc:HGNC:45707]"}, {"versioned_ensembl_gene_id":"ENSG00000242818.3","gene_symbol":"RN7SL846P","gene_name":"RNA, 7SL, cytoplasmic 846, pseudogene [Source:HGNC Symbol;Acc:HGNC:46862]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479530","summary":null,"start":119768247,"end":119768538,"strand":1,"description":"RNA, 7SL, cytoplasmic 846, pseudogene [Source:HGNC Symbol;Acc:HGNC:46862]"}, {"versioned_ensembl_gene_id":"ENSG00000240940.3","gene_symbol":"RN7SL591P","gene_name":"RNA, 7SL, cytoplasmic 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:46607]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481084","summary":null,"start":62350006,"end":62350297,"strand":1,"description":"RNA, 7SL, cytoplasmic 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:46607]"}, {"versioned_ensembl_gene_id":"ENSG00000251778.1","gene_symbol":"SNORA3","gene_name":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":41882205,"end":41882300,"strand":1,"description":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]"}, {"versioned_ensembl_gene_id":"ENSG00000283931.1","gene_symbol":"MIR18B","gene_name":"microRNA 18b [Source:HGNC Symbol;Acc:HGNC:32025]","synonyms":"MIRN18B,hsa-mir-18b","biotype":"miRNA","ncbi_id":"574033","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134170041,"end":134170111,"strand":-1,"description":"microRNA 18b [Source:HGNC Symbol;Acc:HGNC:32025]"}, {"versioned_ensembl_gene_id":"ENSG00000202334.1","gene_symbol":"RNA5SP238","gene_name":"RNA, 5S ribosomal pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:43138]","synonyms":"RN5S238","biotype":"rRNA","ncbi_id":"100873496","summary":null,"start":114613787,"end":114613906,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:43138]"}, {"versioned_ensembl_gene_id":"ENSG00000253437.1","gene_symbol":"RNU6-988P","gene_name":"RNA, U6 small nuclear 988, pseudogene [Source:HGNC Symbol;Acc:HGNC:47951]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480003","summary":null,"start":38122374,"end":38122480,"strand":1,"description":"RNA, U6 small nuclear 988, pseudogene [Source:HGNC Symbol;Acc:HGNC:47951]"}, {"versioned_ensembl_gene_id":"ENSG00000266017.1","gene_symbol":"MIR4477B","gene_name":"microRNA 4477b [Source:HGNC Symbol;Acc:HGNC:41898]","synonyms":"hsa-mir-4477b","biotype":"miRNA","ncbi_id":"100616194","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63819574,"end":63819654,"strand":1,"description":"microRNA 4477b [Source:HGNC Symbol;Acc:HGNC:41898]"}, {"versioned_ensembl_gene_id":"ENSG00000201775.1","gene_symbol":"RNU6-1325P","gene_name":"RNA, U6 small nuclear 1325, pseudogene [Source:HGNC Symbol;Acc:HGNC:48288]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480145","summary":null,"start":59834063,"end":59834167,"strand":1,"description":"RNA, U6 small nuclear 1325, pseudogene [Source:HGNC Symbol;Acc:HGNC:48288]"}, {"versioned_ensembl_gene_id":"ENSG00000275889.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54264566,"end":54264668,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000263533.1","gene_symbol":"MIR4463","gene_name":"microRNA 4463 [Source:HGNC Symbol;Acc:HGNC:41665]","synonyms":"hsa-mir-4463","biotype":"miRNA","ncbi_id":"100616389","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75428407,"end":75428473,"strand":1,"description":"microRNA 4463 [Source:HGNC Symbol;Acc:HGNC:41665]"}, {"versioned_ensembl_gene_id":"ENSG00000284469.1","gene_symbol":"MIR6721","gene_name":"microRNA 6721 [Source:HGNC Symbol;Acc:HGNC:50049]","synonyms":"hsa-mir-6721","biotype":"miRNA","ncbi_id":"102466190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32170030,"end":32170116,"strand":-1,"description":"microRNA 6721 [Source:HGNC Symbol;Acc:HGNC:50049]"}, {"versioned_ensembl_gene_id":"ENSG00000265846.1","gene_symbol":"MIR4276","gene_name":"microRNA 4276 [Source:HGNC Symbol;Acc:HGNC:38232]","synonyms":"hsa-mir-4276","biotype":"miRNA","ncbi_id":"100423042","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":174423795,"end":174423864,"strand":1,"description":"microRNA 4276 [Source:HGNC Symbol;Acc:HGNC:38232]"}, {"versioned_ensembl_gene_id":"ENSG00000207399.1","gene_symbol":"RNU6-1011P","gene_name":"RNA, U6 small nuclear 1011, pseudogene [Source:HGNC Symbol;Acc:HGNC:47974]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480011","summary":null,"start":103384961,"end":103385067,"strand":1,"description":"RNA, U6 small nuclear 1011, pseudogene [Source:HGNC Symbol;Acc:HGNC:47974]"}, {"versioned_ensembl_gene_id":"ENSG00000266518.1","gene_symbol":"MIR4268","gene_name":"microRNA 4268 [Source:HGNC Symbol;Acc:HGNC:38352]","synonyms":"hsa-mir-4268","biotype":"miRNA","ncbi_id":"100422959","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":219906502,"end":219906565,"strand":-1,"description":"microRNA 4268 [Source:HGNC Symbol;Acc:HGNC:38352]"}, {"versioned_ensembl_gene_id":"ENSG00000239183.1","gene_symbol":"SNORA84","gene_name":"small nucleolar RNA, H/ACA box 84 [Source:HGNC Symbol;Acc:HGNC:33615]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124534","summary":null,"start":92292461,"end":92292593,"strand":-1,"description":"small nucleolar RNA, H/ACA box 84 [Source:HGNC Symbol;Acc:HGNC:33615]"}, {"versioned_ensembl_gene_id":"ENSG00000222397.1","gene_symbol":"RN7SKP229","gene_name":"RNA, 7SK small nuclear pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:45953]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480904","summary":null,"start":181839473,"end":181839774,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:45953]"}, {"versioned_ensembl_gene_id":"ENSG00000212190.1","gene_symbol":"RNU6-298P","gene_name":"RNA, U6 small nuclear 298, pseudogene [Source:HGNC Symbol;Acc:HGNC:47261]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481273","summary":null,"start":30861843,"end":30861938,"strand":1,"description":"RNA, U6 small nuclear 298, pseudogene [Source:HGNC Symbol;Acc:HGNC:47261]"}, {"versioned_ensembl_gene_id":"ENSG00000206717.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34821445,"end":34821542,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201943.1","gene_symbol":"SNORD115-10","gene_name":"small nucleolar RNA, C/D box 115-10 [Source:HGNC Symbol;Acc:HGNC:33029]","synonyms":"HBII-52-10","biotype":"snoRNA","ncbi_id":"100033447","summary":null,"start":25187536,"end":25187616,"strand":1,"description":"small nucleolar RNA, C/D box 115-10 [Source:HGNC Symbol;Acc:HGNC:33029]"}, {"versioned_ensembl_gene_id":"ENSG00000264557.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32429038,"end":32429144,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000267611.1","gene_symbol":"AC008521.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33051515,"end":33051701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259655.1","gene_symbol":"AC090825.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":99791127,"end":99792847,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263872.1","gene_symbol":"MIR4528","gene_name":"microRNA 4528 [Source:HGNC Symbol;Acc:HGNC:41547]","synonyms":"hsa-mir-4528","biotype":"miRNA","ncbi_id":"100616232","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53237101,"end":53237190,"strand":1,"description":"microRNA 4528 [Source:HGNC Symbol;Acc:HGNC:41547]"}, {"versioned_ensembl_gene_id":"ENSG00000251815.1","gene_symbol":"SNORD116-26","gene_name":"small nucleolar RNA, C/D box 116-26 [Source:HGNC Symbol;Acc:HGNC:33092]","synonyms":"HBII-85-26","biotype":"snoRNA","ncbi_id":"100033438","summary":null,"start":25099499,"end":25099594,"strand":1,"description":"small nucleolar RNA, C/D box 116-26 [Source:HGNC Symbol;Acc:HGNC:33092]"}, {"versioned_ensembl_gene_id":"ENSG00000251794.1","gene_symbol":"RNU6-237P","gene_name":"RNA, U6 small nuclear 237, pseudogene [Source:HGNC Symbol;Acc:HGNC:47200]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479672","summary":null,"start":74456541,"end":74456611,"strand":1,"description":"RNA, U6 small nuclear 237, pseudogene [Source:HGNC Symbol;Acc:HGNC:47200]"}, {"versioned_ensembl_gene_id":"ENSG00000284541.1","gene_symbol":"MIR4517","gene_name":"microRNA 4517 [Source:HGNC Symbol;Acc:HGNC:41878]","synonyms":"hsa-mir-4517","biotype":"miRNA","ncbi_id":"100616487","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28958583,"end":28958661,"strand":1,"description":"microRNA 4517 [Source:HGNC Symbol;Acc:HGNC:41878]"}, {"versioned_ensembl_gene_id":"ENSG00000263735.1","gene_symbol":"MIR4662B","gene_name":"microRNA 4662b [Source:HGNC Symbol;Acc:HGNC:41607]","synonyms":"hsa-mir-4662b","biotype":"miRNA","ncbi_id":"100616255","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124821978,"end":124822058,"strand":-1,"description":"microRNA 4662b [Source:HGNC Symbol;Acc:HGNC:41607]"}, {"versioned_ensembl_gene_id":"ENSG00000202341.1","gene_symbol":"RNU6-1051P","gene_name":"RNA, U6 small nuclear 1051, pseudogene [Source:HGNC Symbol;Acc:HGNC:48014]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481932","summary":null,"start":237015204,"end":237015305,"strand":-1,"description":"RNA, U6 small nuclear 1051, pseudogene [Source:HGNC Symbol;Acc:HGNC:48014]"}, {"versioned_ensembl_gene_id":"ENSG00000207639.1","gene_symbol":"MIR193B","gene_name":"microRNA 193b [Source:HGNC Symbol;Acc:HGNC:32087]","synonyms":"MIRN193B,hsa-mir-193b","biotype":"miRNA","ncbi_id":"574455","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14303967,"end":14304049,"strand":1,"description":"microRNA 193b [Source:HGNC Symbol;Acc:HGNC:32087]"}, {"versioned_ensembl_gene_id":"ENSG00000201998.1","gene_symbol":"SNORA23","gene_name":"small nucleolar RNA, H/ACA box 23 [Source:HGNC Symbol;Acc:HGNC:32613]","synonyms":"ACA23","biotype":"snoRNA","ncbi_id":"677808","summary":null,"start":9428773,"end":9428954,"strand":1,"description":"small nucleolar RNA, H/ACA box 23 [Source:HGNC Symbol;Acc:HGNC:32613]"}, {"versioned_ensembl_gene_id":"ENSG00000212017.2","gene_symbol":"MIR548U","gene_name":"microRNA 548u [Source:HGNC Symbol;Acc:HGNC:38316]","synonyms":"hsa-mir-548u","biotype":"miRNA","ncbi_id":"100422884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57390132,"end":57390212,"strand":1,"description":"microRNA 548u [Source:HGNC Symbol;Acc:HGNC:38316]"}, {"versioned_ensembl_gene_id":"ENSG00000252848.1","gene_symbol":"RNA5SP230","gene_name":"RNA, 5S ribosomal pseudogene 230 [Source:HGNC Symbol;Acc:HGNC:43130]","synonyms":"RN5S230","biotype":"rRNA","ncbi_id":"100873488","summary":null,"start":44125752,"end":44125873,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 230 [Source:HGNC Symbol;Acc:HGNC:43130]"}, {"versioned_ensembl_gene_id":"ENSG00000252747.1","gene_symbol":"RNA5SP364","gene_name":"RNA, 5S ribosomal pseudogene 364 [Source:HGNC Symbol;Acc:HGNC:43264]","synonyms":"RN5S364","biotype":"rRNA","ncbi_id":"100873623","summary":null,"start":88051701,"end":88051778,"strand":1,"description":"RNA, 5S ribosomal pseudogene 364 [Source:HGNC Symbol;Acc:HGNC:43264]"}, {"versioned_ensembl_gene_id":"ENSG00000206614.1","gene_symbol":"RNU6-477P","gene_name":"RNA, U6 small nuclear 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:47440]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481330","summary":null,"start":169552449,"end":169552555,"strand":1,"description":"RNA, U6 small nuclear 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:47440]"}, {"versioned_ensembl_gene_id":"ENSG00000199219.1","gene_symbol":"RNU6-500P","gene_name":"RNA, U6 small nuclear 500, pseudogene [Source:HGNC Symbol;Acc:HGNC:47463]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479788","summary":null,"start":173362134,"end":173362240,"strand":-1,"description":"RNA, U6 small nuclear 500, pseudogene [Source:HGNC Symbol;Acc:HGNC:47463]"}, {"versioned_ensembl_gene_id":"ENSG00000199396.1","gene_symbol":"RNA5S5","gene_name":"RNA, 5S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:34366]","synonyms":"RN5S5","biotype":"rRNA","ncbi_id":"100169756","summary":null,"start":228619232,"end":228619350,"strand":-1,"description":"RNA, 5S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:34366]"}, {"versioned_ensembl_gene_id":"ENSG00000265064.1","gene_symbol":"MIR4692","gene_name":"microRNA 4692 [Source:HGNC Symbol;Acc:HGNC:41856]","synonyms":"hsa-mir-4692","biotype":"miRNA","ncbi_id":"100616410","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72783530,"end":72783592,"strand":1,"description":"microRNA 4692 [Source:HGNC Symbol;Acc:HGNC:41856]"}, {"versioned_ensembl_gene_id":"ENSG00000264633.1","gene_symbol":"MIR4271","gene_name":"microRNA 4271 [Source:HGNC Symbol;Acc:HGNC:38332]","synonyms":"hsa-mir-4271","biotype":"miRNA","ncbi_id":"100422952","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49274120,"end":49274186,"strand":1,"description":"microRNA 4271 [Source:HGNC Symbol;Acc:HGNC:38332]"}, {"versioned_ensembl_gene_id":"ENSG00000242065.3","gene_symbol":"RN7SL291P","gene_name":"RNA, 7SL, cytoplasmic 291, pseudogene [Source:HGNC Symbol;Acc:HGNC:46307]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479328","summary":null,"start":44772773,"end":44773061,"strand":-1,"description":"RNA, 7SL, cytoplasmic 291, pseudogene [Source:HGNC Symbol;Acc:HGNC:46307]"}, {"versioned_ensembl_gene_id":"ENSG00000253032.1","gene_symbol":"RNU6-299P","gene_name":"RNA, U6 small nuclear 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:47262]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480389","summary":null,"start":56125671,"end":56125770,"strand":1,"description":"RNA, U6 small nuclear 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:47262]"}, {"versioned_ensembl_gene_id":"ENSG00000221043.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":149695748,"end":149695959,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000274396.1","gene_symbol":"HOTAIRM1_4","gene_name":"HOX antisense intergenic RNA myeloid 1 conserved region 4 [Source:RFAM;Acc:RF01978]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27099856,"end":27099957,"strand":1,"description":"HOX antisense intergenic RNA myeloid 1 conserved region 4 [Source:RFAM;Acc:RF01978]"}, {"versioned_ensembl_gene_id":"ENSG00000207979.1","gene_symbol":"MIR527","gene_name":"microRNA 527 [Source:HGNC Symbol;Acc:HGNC:32129]","synonyms":"MIRN527,hsa-mir-527","biotype":"miRNA","ncbi_id":"574497","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53754018,"end":53754102,"strand":1,"description":"microRNA 527 [Source:HGNC Symbol;Acc:HGNC:32129]"}, {"versioned_ensembl_gene_id":"ENSG00000266564.1","gene_symbol":"MIR4418","gene_name":"microRNA 4418 [Source:HGNC Symbol;Acc:HGNC:41789]","synonyms":"hsa-mir-4418","biotype":"miRNA","ncbi_id":"100616433","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22266239,"end":22266300,"strand":1,"description":"microRNA 4418 [Source:HGNC Symbol;Acc:HGNC:41789]"}, {"versioned_ensembl_gene_id":"ENSG00000283540.1","gene_symbol":"MIR520F","gene_name":"microRNA 520f [Source:HGNC Symbol;Acc:HGNC:32096]","synonyms":"MIRN520F,hsa-mir-520f","biotype":"miRNA","ncbi_id":"574464","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53682159,"end":53682245,"strand":1,"description":"microRNA 520f [Source:HGNC Symbol;Acc:HGNC:32096]"}, {"versioned_ensembl_gene_id":"ENSG00000252635.1","gene_symbol":"RNU2-56P","gene_name":"RNA, U2 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:48549]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480221","summary":null,"start":18265690,"end":18265879,"strand":-1,"description":"RNA, U2 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:48549]"}, {"versioned_ensembl_gene_id":"ENSG00000200823.1","gene_symbol":"SNORD114-2","gene_name":"small nucleolar RNA, C/D box 114-2 [Source:HGNC Symbol;Acc:HGNC:32990]","synonyms":"14q(II-2)","biotype":"snoRNA","ncbi_id":"767578","summary":null,"start":100951856,"end":100951933,"strand":1,"description":"small nucleolar RNA, C/D box 114-2 [Source:HGNC Symbol;Acc:HGNC:32990]"}, {"versioned_ensembl_gene_id":"ENSG00000212333.1","gene_symbol":"RNA5SP213","gene_name":"RNA, 5S ribosomal pseudogene 213 [Source:HGNC Symbol;Acc:HGNC:43113]","synonyms":"RN5S213","biotype":"rRNA","ncbi_id":"100873473","summary":null,"start":114220681,"end":114220786,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 213 [Source:HGNC Symbol;Acc:HGNC:43113]"}, {"versioned_ensembl_gene_id":"ENSG00000222890.1","gene_symbol":"RNU6-1068P","gene_name":"RNA, U6 small nuclear 1068, pseudogene [Source:HGNC Symbol;Acc:HGNC:48031]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481933","summary":null,"start":101411357,"end":101411459,"strand":1,"description":"RNA, U6 small nuclear 1068, pseudogene [Source:HGNC Symbol;Acc:HGNC:48031]"}, {"versioned_ensembl_gene_id":"ENSG00000202332.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75431990,"end":75432087,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000272979.1","gene_symbol":"AC093388.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":190454092,"end":190454521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265879.1","gene_symbol":"MIR4748","gene_name":"microRNA 4748 [Source:HGNC Symbol;Acc:HGNC:41557]","synonyms":"hsa-mir-4748","biotype":"miRNA","ncbi_id":"100616425","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10780254,"end":10780335,"strand":1,"description":"microRNA 4748 [Source:HGNC Symbol;Acc:HGNC:41557]"}, {"versioned_ensembl_gene_id":"ENSG00000263849.1","gene_symbol":"MIR4744","gene_name":"microRNA 4744 [Source:HGNC Symbol;Acc:HGNC:41866]","synonyms":"hsa-mir-4744","biotype":"miRNA","ncbi_id":"100616420","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49049687,"end":49049768,"strand":-1,"description":"microRNA 4744 [Source:HGNC Symbol;Acc:HGNC:41866]"}, {"versioned_ensembl_gene_id":"ENSG00000251706.1","gene_symbol":"RNU7-61P","gene_name":"RNA, U7 small nuclear 61 pseudogene [Source:HGNC Symbol;Acc:HGNC:34157]","synonyms":"U7.61","biotype":"snRNA","ncbi_id":"100151656","summary":null,"start":30483135,"end":30483195,"strand":-1,"description":"RNA, U7 small nuclear 61 pseudogene [Source:HGNC Symbol;Acc:HGNC:34157]"}, {"versioned_ensembl_gene_id":"ENSG00000199368.1","gene_symbol":"RNU6-1084P","gene_name":"RNA, U6 small nuclear 1084, pseudogene [Source:HGNC Symbol;Acc:HGNC:48047]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480042","summary":null,"start":11392411,"end":11392517,"strand":-1,"description":"RNA, U6 small nuclear 1084, pseudogene [Source:HGNC Symbol;Acc:HGNC:48047]"}, {"versioned_ensembl_gene_id":"ENSG00000284586.1","gene_symbol":"MIR92B","gene_name":"microRNA 92b [Source:HGNC Symbol;Acc:HGNC:32920]","synonyms":"MIRN92B,hsa-mir-92b","biotype":"miRNA","ncbi_id":"693235","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155195177,"end":155195272,"strand":1,"description":"microRNA 92b [Source:HGNC Symbol;Acc:HGNC:32920]"}, {"versioned_ensembl_gene_id":"ENSG00000275257.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28845055,"end":28845291,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284596.1","gene_symbol":"MIR4467","gene_name":"microRNA 4467 [Source:HGNC Symbol;Acc:HGNC:41896]","synonyms":"hsa-mir-4467","biotype":"miRNA","ncbi_id":"100616367","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102471469,"end":102471531,"strand":1,"description":"microRNA 4467 [Source:HGNC Symbol;Acc:HGNC:41896]"}, {"versioned_ensembl_gene_id":"ENSG00000265596.1","gene_symbol":"MIR3659","gene_name":"microRNA 3659 [Source:HGNC Symbol;Acc:HGNC:38882]","synonyms":"hsa-mir-3659","biotype":"miRNA","ncbi_id":"100500801","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38089231,"end":38089329,"strand":1,"description":"microRNA 3659 [Source:HGNC Symbol;Acc:HGNC:38882]"}, {"versioned_ensembl_gene_id":"ENSG00000212302.1","gene_symbol":"SNORD41","gene_name":"Small nucleolar RNA SNORD41 [Source:RFAM;Acc:RF00588]","synonyms":"U41,RNU41","biotype":"snoRNA","ncbi_id":"26810","summary":null,"start":22756761,"end":22756829,"strand":-1,"description":"Small nucleolar RNA SNORD41 [Source:RFAM;Acc:RF00588]"}, {"versioned_ensembl_gene_id":"ENSG00000206875.1","gene_symbol":"RNU6-761P","gene_name":"RNA, U6 small nuclear 761, pseudogene [Source:HGNC Symbol;Acc:HGNC:47724]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480607","summary":null,"start":42018408,"end":42018514,"strand":-1,"description":"RNA, U6 small nuclear 761, pseudogene [Source:HGNC Symbol;Acc:HGNC:47724]"}, {"versioned_ensembl_gene_id":"ENSG00000221400.2","gene_symbol":"SNORD3J","gene_name":"small nucleolar RNA, C/D box 3J [Source:HGNC Symbol;Acc:HGNC:52243]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616985","summary":null,"start":43417249,"end":43417438,"strand":-1,"description":"small nucleolar RNA, C/D box 3J [Source:HGNC Symbol;Acc:HGNC:52243]"}, {"versioned_ensembl_gene_id":"ENSG00000274934.1","gene_symbol":"SMAD5-AS1_4","gene_name":"SMAD5 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02176]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":136134082,"end":136134248,"strand":1,"description":"SMAD5 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02176]"}, {"versioned_ensembl_gene_id":"ENSG00000201182.1","gene_symbol":"RNU6-670P","gene_name":"RNA, U6 small nuclear 670, pseudogene [Source:HGNC Symbol;Acc:HGNC:47633]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479863","summary":null,"start":10037552,"end":10037655,"strand":1,"description":"RNA, U6 small nuclear 670, pseudogene [Source:HGNC Symbol;Acc:HGNC:47633]"}, {"versioned_ensembl_gene_id":"ENSG00000202089.1","gene_symbol":"RNU6-1306P","gene_name":"RNA, U6 small nuclear 1306, pseudogene [Source:HGNC Symbol;Acc:HGNC:48269]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480136","summary":null,"start":63882587,"end":63882685,"strand":-1,"description":"RNA, U6 small nuclear 1306, pseudogene [Source:HGNC Symbol;Acc:HGNC:48269]"}, {"versioned_ensembl_gene_id":"ENSG00000222225.1","gene_symbol":"RNU6-447P","gene_name":"RNA, U6 small nuclear 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:47410]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481320","summary":null,"start":152999,"end":153102,"strand":-1,"description":"RNA, U6 small nuclear 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:47410]"}, {"versioned_ensembl_gene_id":"ENSG00000239221.3","gene_symbol":"RN7SL442P","gene_name":"RNA, 7SL, cytoplasmic 442, pseudogene [Source:HGNC Symbol;Acc:HGNC:46458]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481043","summary":null,"start":16191832,"end":16192151,"strand":1,"description":"RNA, 7SL, cytoplasmic 442, pseudogene [Source:HGNC Symbol;Acc:HGNC:46458]"}, {"versioned_ensembl_gene_id":"ENSG00000274514.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12576961,"end":12577237,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252219.2","gene_symbol":"MIR892C","gene_name":"microRNA 892c [Source:HGNC Symbol;Acc:HGNC:50194]","synonyms":"hsa-mir-892c","biotype":"miRNA","ncbi_id":"102466721","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145992750,"end":145992826,"strand":-1,"description":"microRNA 892c [Source:HGNC Symbol;Acc:HGNC:50194]"}, {"versioned_ensembl_gene_id":"ENSG00000241248.3","gene_symbol":"RN7SL727P","gene_name":"RNA, 7SL, cytoplasmic 727, pseudogene [Source:HGNC Symbol;Acc:HGNC:46743]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481121","summary":null,"start":140085855,"end":140086150,"strand":1,"description":"RNA, 7SL, cytoplasmic 727, pseudogene [Source:HGNC Symbol;Acc:HGNC:46743]"}, {"versioned_ensembl_gene_id":"ENSG00000252797.1","gene_symbol":"RN7SKP272","gene_name":"RNA, 7SK small nuclear pseudogene 272 [Source:HGNC Symbol;Acc:HGNC:45996]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479217","summary":null,"start":89987713,"end":89987944,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 272 [Source:HGNC Symbol;Acc:HGNC:45996]"}, {"versioned_ensembl_gene_id":"ENSG00000277411.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":15522195,"end":15522300,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000264136.1","gene_symbol":"MIR3689D2","gene_name":"microRNA 3689d-2 [Source:HGNC Symbol;Acc:HGNC:41846]","synonyms":"hsa-mir-3689d-2","biotype":"miRNA","ncbi_id":"100616344","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134850277,"end":134850356,"strand":-1,"description":"microRNA 3689d-2 [Source:HGNC Symbol;Acc:HGNC:41846]"}, {"versioned_ensembl_gene_id":"ENSG00000201255.1","gene_symbol":"RNU6-990P","gene_name":"RNA, U6 small nuclear 990, pseudogene [Source:HGNC Symbol;Acc:HGNC:47953]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480627","summary":null,"start":30360463,"end":30360566,"strand":1,"description":"RNA, U6 small nuclear 990, pseudogene [Source:HGNC Symbol;Acc:HGNC:47953]"}, {"versioned_ensembl_gene_id":"ENSG00000266583.1","gene_symbol":"MIR4478","gene_name":"microRNA 4478 [Source:HGNC Symbol;Acc:HGNC:41759]","synonyms":"hsa-mir-4478","biotype":"miRNA","ncbi_id":"100616312","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":122120082,"end":122120167,"strand":-1,"description":"microRNA 4478 [Source:HGNC Symbol;Acc:HGNC:41759]"}, {"versioned_ensembl_gene_id":"ENSG00000202198.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52995620,"end":52995950,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000200656.1","gene_symbol":"SNORA5B","gene_name":"small nucleolar RNA, H/ACA box 5B [Source:HGNC Symbol;Acc:HGNC:32589]","synonyms":"ACA5b","biotype":"snoRNA","ncbi_id":"677795","summary":null,"start":45105968,"end":45106099,"strand":-1,"description":"small nucleolar RNA, H/ACA box 5B [Source:HGNC Symbol;Acc:HGNC:32589]"}, {"versioned_ensembl_gene_id":"ENSG00000263740.2","gene_symbol":"RN7SL4P","gene_name":"RNA, 7SL, cytoplasmic 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10039]","synonyms":"RN7SLP1,RN7SL427P,7L28","biotype":"misc_RNA","ncbi_id":"6030","summary":null,"start":15738515,"end":15738809,"strand":1,"description":"RNA, 7SL, cytoplasmic 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10039]"}, {"versioned_ensembl_gene_id":"ENSG00000200883.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9249649,"end":9249746,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265306.1","gene_symbol":"MIR3195","gene_name":"microRNA 3195 [Source:HGNC Symbol;Acc:HGNC:38250]","synonyms":"hsa-mir-3195","biotype":"miRNA","ncbi_id":"100422838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62064802,"end":62064885,"strand":1,"description":"microRNA 3195 [Source:HGNC Symbol;Acc:HGNC:38250]"}, {"versioned_ensembl_gene_id":"ENSG00000252705.1","gene_symbol":"RNU6-175P","gene_name":"RNA, U6 small nuclear 175, pseudogene [Source:HGNC Symbol;Acc:HGNC:47138]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480558","summary":null,"start":132406752,"end":132406858,"strand":-1,"description":"RNA, U6 small nuclear 175, pseudogene [Source:HGNC Symbol;Acc:HGNC:47138]"}, {"versioned_ensembl_gene_id":"ENSG00000276027.1","gene_symbol":"RNU12","gene_name":"RNA, U12 small nuclear [Source:HGNC Symbol;Acc:HGNC:19380]","synonyms":"RNU12P,RNU12-1","biotype":"snRNA","ncbi_id":"267010","summary":null,"start":42615244,"end":42615393,"strand":1,"description":"RNA, U12 small nuclear [Source:HGNC Symbol;Acc:HGNC:19380]"}, {"versioned_ensembl_gene_id":"ENSG00000201000.1","gene_symbol":"RNA5SP516","gene_name":"RNA, 5S ribosomal pseudogene 516 [Source:HGNC Symbol;Acc:HGNC:43416]","synonyms":"RN5S516","biotype":"rRNA","ncbi_id":"100873567","summary":null,"start":142411053,"end":142411171,"strand":1,"description":"RNA, 5S ribosomal pseudogene 516 [Source:HGNC Symbol;Acc:HGNC:43416]"}, {"versioned_ensembl_gene_id":"ENSG00000200120.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49137762,"end":49137863,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264119.1","gene_symbol":"MIR4795","gene_name":"microRNA 4795 [Source:HGNC Symbol;Acc:HGNC:41757]","synonyms":"hsa-mir-4795","biotype":"miRNA","ncbi_id":"100616161","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87226189,"end":87226277,"strand":-1,"description":"microRNA 4795 [Source:HGNC Symbol;Acc:HGNC:41757]"}, {"versioned_ensembl_gene_id":"ENSG00000222533.1","gene_symbol":"RNU6-705P","gene_name":"RNA, U6 small nuclear 705, pseudogene [Source:HGNC Symbol;Acc:HGNC:47668]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481403","summary":null,"start":181301967,"end":181302070,"strand":1,"description":"RNA, U6 small nuclear 705, pseudogene [Source:HGNC Symbol;Acc:HGNC:47668]"}, {"versioned_ensembl_gene_id":"ENSG00000239007.1","gene_symbol":"RNU7-95P","gene_name":"RNA, U7 small nuclear 95 pseudogene [Source:HGNC Symbol;Acc:HGNC:45629]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479062","summary":null,"start":53688749,"end":53688812,"strand":-1,"description":"RNA, U7 small nuclear 95 pseudogene [Source:HGNC Symbol;Acc:HGNC:45629]"}, {"versioned_ensembl_gene_id":"ENSG00000199327.1","gene_symbol":"RNU6-230P","gene_name":"RNA, U6 small nuclear 230, pseudogene [Source:HGNC Symbol;Acc:HGNC:47193]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479669","summary":null,"start":125119097,"end":125119200,"strand":-1,"description":"RNA, U6 small nuclear 230, pseudogene [Source:HGNC Symbol;Acc:HGNC:47193]"}, {"versioned_ensembl_gene_id":"ENSG00000222148.1","gene_symbol":"RNY4P30","gene_name":"RNA, Ro-associated Y4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42498]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862673","summary":null,"start":49889634,"end":49889728,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42498]"}, {"versioned_ensembl_gene_id":"ENSG00000273519.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54813162,"end":54813268,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000222314.1","gene_symbol":"RNU6-1118P","gene_name":"RNA, U6 small nuclear 1118, pseudogene [Source:HGNC Symbol;Acc:HGNC:48081]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480058","summary":null,"start":38423625,"end":38423728,"strand":1,"description":"RNA, U6 small nuclear 1118, pseudogene [Source:HGNC Symbol;Acc:HGNC:48081]"}, {"versioned_ensembl_gene_id":"ENSG00000284442.1","gene_symbol":"MIR2110","gene_name":"microRNA 2110 [Source:HGNC Symbol;Acc:HGNC:37071]","synonyms":"hsa-mir-2110","biotype":"miRNA","ncbi_id":"100302224","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114174105,"end":114174179,"strand":-1,"description":"microRNA 2110 [Source:HGNC Symbol;Acc:HGNC:37071]"}, {"versioned_ensembl_gene_id":"ENSG00000283497.1","gene_symbol":"MIR3160-2","gene_name":"microRNA 3160-2 [Source:HGNC Symbol;Acc:HGNC:38192]","synonyms":"hsa-mir-3160-2","biotype":"miRNA","ncbi_id":"100422825","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46451807,"end":46451887,"strand":1,"description":"microRNA 3160-2 [Source:HGNC Symbol;Acc:HGNC:38192]"}, {"versioned_ensembl_gene_id":"ENSG00000272232.2","gene_symbol":"RN7SL726P","gene_name":"RNA, 7SL, cytoplasmic 726, pseudogene [Source:HGNC Symbol;Acc:HGNC:46742]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479488","summary":null,"start":70579163,"end":70579461,"strand":-1,"description":"RNA, 7SL, cytoplasmic 726, pseudogene [Source:HGNC Symbol;Acc:HGNC:46742]"}, {"versioned_ensembl_gene_id":"ENSG00000221031.1","gene_symbol":"CoTC_ribozyme","gene_name":"Beta-globin co-transcriptional cleavage ribozyme [Source:RFAM;Acc:RF00621]","synonyms":null,"biotype":"ribozyme","ncbi_id":null,"summary":null,"start":5224448,"end":5224639,"strand":-1,"description":"Beta-globin co-transcriptional cleavage ribozyme [Source:RFAM;Acc:RF00621]"}, {"versioned_ensembl_gene_id":"ENSG00000251947.1","gene_symbol":"RN7SKP164","gene_name":"RNA, 7SK small nuclear 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{"versioned_ensembl_gene_id":"ENSG00000251891.1","gene_symbol":"RNU7-79P","gene_name":"RNA, U7 small nuclear 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:34175]","synonyms":"U7.79","biotype":"snRNA","ncbi_id":"100151676","summary":null,"start":85389823,"end":85389884,"strand":-1,"description":"RNA, U7 small nuclear 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:34175]"}, {"versioned_ensembl_gene_id":"ENSG00000222412.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31756042,"end":31756136,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207086.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9615267,"end":9615373,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252516.1","gene_symbol":"RNA5SP82","gene_name":"RNA, 5S ribosomal pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:42859]","synonyms":"RN5S82","biotype":"rRNA","ncbi_id":"100873316","summary":null,"start":247204570,"end":247204661,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:42859]"}, {"versioned_ensembl_gene_id":"ENSG00000202430.1","gene_symbol":"RNA5SP88","gene_name":"RNA, 5S ribosomal pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:42886]","synonyms":"RN5S88","biotype":"rRNA","ncbi_id":"100873321","summary":null,"start":24564630,"end":24564738,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:42886]"}, {"versioned_ensembl_gene_id":"ENSG00000240606.3","gene_symbol":"RN7SL564P","gene_name":"RNA, 7SL, cytoplasmic 564, pseudogene [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111771061,"end":111771134,"strand":-1,"description":"microRNA 4771-2 [Source:HGNC Symbol;Acc:HGNC:41774]"}, {"versioned_ensembl_gene_id":"ENSG00000278159.1","gene_symbol":"MIR8062","gene_name":"microRNA 8062 [Source:HGNC Symbol;Acc:HGNC:49975]","synonyms":"hsa-mir-8062","biotype":"miRNA","ncbi_id":"102465865","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7371608,"end":7371692,"strand":1,"description":"microRNA 8062 [Source:HGNC Symbol;Acc:HGNC:49975]"}, {"versioned_ensembl_gene_id":"ENSG00000264692.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31392641,"end":31392739,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275726.1","gene_symbol":"MIR6088","gene_name":"microRNA 6088 [Source:HGNC Symbol;Acc:HGNC:50164]","synonyms":"hsa-mir-6088","biotype":"miRNA","ncbi_id":"102464836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45436654,"end":45436704,"strand":1,"description":"microRNA 6088 [Source:HGNC Symbol;Acc:HGNC:50164]"}, {"versioned_ensembl_gene_id":"ENSG00000278598.1","gene_symbol":"MIR6775","gene_name":"microRNA 6775 [Source:HGNC Symbol;Acc:HGNC:50100]","synonyms":"hsa-mir-6775","biotype":"miRNA","ncbi_id":"102465464","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87834592,"end":87834660,"strand":-1,"description":"microRNA 6775 [Source:HGNC Symbol;Acc:HGNC:50100]"}, {"versioned_ensembl_gene_id":"ENSG00000284038.1","gene_symbol":"MIR10A","gene_name":"microRNA 10a [Source:HGNC Symbol;Acc:HGNC:31497]","synonyms":"MIRN10A,hsa-mir-10a","biotype":"miRNA","ncbi_id":"406902","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48579838,"end":48579947,"strand":-1,"description":"microRNA 10a [Source:HGNC Symbol;Acc:HGNC:31497]"}, {"versioned_ensembl_gene_id":"ENSG00000266758.1","gene_symbol":"MIR3680-2","gene_name":"microRNA 3680-2 [Source:HGNC Symbol;Acc:HGNC:43472]","synonyms":"hsa-mir-3680-2","biotype":"miRNA","ncbi_id":"100847041","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29599179,"end":29599265,"strand":-1,"description":"microRNA 3680-2 [Source:HGNC Symbol;Acc:HGNC:43472]"}, {"versioned_ensembl_gene_id":"ENSG00000264963.2","gene_symbol":"RN7SL440P","gene_name":"RNA, 7SL, cytoplasmic 440, pseudogene [Source:HGNC Symbol;Acc:HGNC:46456]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481042","summary":null,"start":94150738,"end":94151080,"strand":1,"description":"RNA, 7SL, cytoplasmic 440, pseudogene [Source:HGNC Symbol;Acc:HGNC:46456]"}, {"versioned_ensembl_gene_id":"ENSG00000284644.1","gene_symbol":"AC074386.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144251264,"end":144355707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207269.1","gene_symbol":"RN7SKP62","gene_name":"RNA, 7SK small nuclear pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:45786]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480460","summary":null,"start":100733058,"end":100733386,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:45786]"}, {"versioned_ensembl_gene_id":"ENSG00000283170.1","gene_symbol":"MIR382","gene_name":"microRNA 382 [Source:HGNC Symbol;Acc:HGNC:31875]","synonyms":"MIRN382,hsa-mir-382","biotype":"miRNA","ncbi_id":"494331","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101054306,"end":101054381,"strand":1,"description":"microRNA 382 [Source:HGNC Symbol;Acc:HGNC:31875]"}, {"versioned_ensembl_gene_id":"ENSG00000200296.1","gene_symbol":"RNU1-83P","gene_name":"RNA, U1 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:48425]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480176","summary":null,"start":62850738,"end":62850901,"strand":-1,"description":"RNA, U1 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:48425]"}, {"versioned_ensembl_gene_id":"ENSG00000201900.1","gene_symbol":"RNY1P13","gene_name":"RNA, Ro-associated Y1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50876]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480310","summary":null,"start":114727720,"end":114727824,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50876]"}, {"versioned_ensembl_gene_id":"ENSG00000206898.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":10296047,"end":10296180,"strand":-1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000263439.1","gene_symbol":"MIR4753","gene_name":"microRNA 4753 [Source:HGNC Symbol;Acc:HGNC:41527]","synonyms":"hsa-mir-4753","biotype":"miRNA","ncbi_id":"100616224","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":235190034,"end":235190116,"strand":-1,"description":"microRNA 4753 [Source:HGNC Symbol;Acc:HGNC:41527]"}, {"versioned_ensembl_gene_id":"ENSG00000284214.1","gene_symbol":"MIR29C","gene_name":"microRNA 29c [Source:HGNC Symbol;Acc:HGNC:31621]","synonyms":"MIRN29C,hsa-mir-29c","biotype":"miRNA","ncbi_id":"407026","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207801852,"end":207801939,"strand":-1,"description":"microRNA 29c [Source:HGNC Symbol;Acc:HGNC:31621]"}, {"versioned_ensembl_gene_id":"ENSG00000252929.1","gene_symbol":"RNU6-218P","gene_name":"RNA, U6 small nuclear 218, pseudogene [Source:HGNC Symbol;Acc:HGNC:47181]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479663","summary":null,"start":6057500,"end":6057604,"strand":1,"description":"RNA, U6 small nuclear 218, pseudogene [Source:HGNC Symbol;Acc:HGNC:47181]"}, {"versioned_ensembl_gene_id":"ENSG00000238949.1","gene_symbol":"RNU7-66P","gene_name":"RNA, U7 small nuclear 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:34162]","synonyms":"U7.66","biotype":"snRNA","ncbi_id":"100151664","summary":null,"start":66728843,"end":66728904,"strand":-1,"description":"RNA, U7 small nuclear 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:34162]"}, {"versioned_ensembl_gene_id":"ENSG00000206924.1","gene_symbol":"RNU6-689P","gene_name":"RNA, U6 small nuclear 689, pseudogene [Source:HGNC Symbol;Acc:HGNC:47652]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479870","summary":null,"start":75020761,"end":75020867,"strand":1,"description":"RNA, U6 small nuclear 689, pseudogene [Source:HGNC Symbol;Acc:HGNC:47652]"}, {"versioned_ensembl_gene_id":"ENSG00000238357.1","gene_symbol":"RNU7-148P","gene_name":"RNA, U7 small nuclear 148 pseudogene [Source:HGNC Symbol;Acc:HGNC:45682]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480823","summary":null,"start":167631480,"end":167631541,"strand":-1,"description":"RNA, U7 small nuclear 148 pseudogene [Source:HGNC Symbol;Acc:HGNC:45682]"}, {"versioned_ensembl_gene_id":"ENSG00000252129.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15574019,"end":15574198,"strand":1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000266300.1","gene_symbol":"SNORD52","gene_name":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]","synonyms":"RNU52,U52,RNU52,U52","biotype":"snoRNA","ncbi_id":"26797","summary":null,"start":31904099,"end":31904165,"strand":1,"description":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]"}, {"versioned_ensembl_gene_id":"ENSG00000207183.1","gene_symbol":"RNU6-843P","gene_name":"RNA, U6 small nuclear 843, pseudogene [Source:HGNC Symbol;Acc:HGNC:47806]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480614","summary":null,"start":12411398,"end":12411501,"strand":-1,"description":"RNA, U6 small nuclear 843, pseudogene [Source:HGNC Symbol;Acc:HGNC:47806]"}, {"versioned_ensembl_gene_id":"ENSG00000277046.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23170674,"end":23170963,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238730.1","gene_symbol":"RNU7-164P","gene_name":"RNA, U7 small nuclear 164 pseudogene [Source:HGNC Symbol;Acc:HGNC:45698]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479086","summary":null,"start":40535502,"end":40535563,"strand":-1,"description":"RNA, U7 small nuclear 164 pseudogene [Source:HGNC Symbol;Acc:HGNC:45698]"}, {"versioned_ensembl_gene_id":"ENSG00000244197.3","gene_symbol":"RN7SL766P","gene_name":"RNA, 7SL, cytoplasmic 766, pseudogene [Source:HGNC Symbol;Acc:HGNC:46782]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479501","summary":null,"start":21790537,"end":21790845,"strand":1,"description":"RNA, 7SL, cytoplasmic 766, pseudogene [Source:HGNC Symbol;Acc:HGNC:46782]"}, {"versioned_ensembl_gene_id":"ENSG00000200343.1","gene_symbol":"RNA5S8","gene_name":"RNA, 5S ribosomal 8 [Source:HGNC Symbol;Acc:HGNC:34369]","synonyms":"RN5S8","biotype":"rRNA","ncbi_id":"100169759","summary":null,"start":228625909,"end":228626027,"strand":-1,"description":"RNA, 5S ribosomal 8 [Source:HGNC Symbol;Acc:HGNC:34369]"}, {"versioned_ensembl_gene_id":"ENSG00000274012.1","gene_symbol":"RN7SL2","gene_name":"RNA, 7SL, cytoplasmic 2 [Source:HGNC Symbol;Acc:HGNC:23134]","synonyms":"RNSRP2,7SL1c,7L30.1","biotype":"misc_RNA","ncbi_id":"378706","summary":"The signal recognition particle (SRP) is a cytoplasmic ribonucleoprotein complex that mediates cotranslational insertion of secretory proteins into the lumen of the endoplasmic reticulum. The SRP consists of 6 polypeptides (e.g., SRP19; MIM 182175) and a 7SL RNA molecule, such as RN7SL2, that is partially homologous to Alu DNA (Ullu and Weiner, 1984 [PubMed 6084597]).[supplied by OMIM, Jul 2008]","start":49862550,"end":49862849,"strand":-1,"description":"RNA, 7SL, cytoplasmic 2 [Source:HGNC Symbol;Acc:HGNC:23134]"}, {"versioned_ensembl_gene_id":"ENSG00000202239.1","gene_symbol":"RNU6-396P","gene_name":"RNA, U6 small nuclear 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:47359]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481303","summary":null,"start":46525618,"end":46525722,"strand":1,"description":"RNA, U6 small nuclear 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:47359]"}, {"versioned_ensembl_gene_id":"ENSG00000277418.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":48316669,"end":48316770,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000273511.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000201687.1","gene_symbol":"RNU6-1107P","gene_name":"RNA, U6 small nuclear 1107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48070]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481529","summary":null,"start":113859346,"end":113859449,"strand":1,"description":"RNA, U6 small nuclear 1107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48070]"}, {"versioned_ensembl_gene_id":"ENSG00000207134.1","gene_symbol":"RNU6-106P","gene_name":"RNA, U6 small nuclear 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:47069]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479613","summary":null,"start":155358712,"end":155358818,"strand":-1,"description":"RNA, U6 small nuclear 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:47069]"}, {"versioned_ensembl_gene_id":"ENSG00000199711.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99936610,"end":99936711,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207034.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2778941,"end":2779057,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242175.3","gene_symbol":"RN7SL127P","gene_name":"RNA, 7SL, cytoplasmic 127, pseudogene [Source:HGNC Symbol;Acc:HGNC:46143]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480956","summary":null,"start":78898855,"end":78899154,"strand":1,"description":"RNA, 7SL, cytoplasmic 127, pseudogene [Source:HGNC Symbol;Acc:HGNC:46143]"}, {"versioned_ensembl_gene_id":"ENSG00000223282.1","gene_symbol":"RN7SKP165","gene_name":"RNA, 7SK small nuclear pseudogene 165 [Source:HGNC Symbol;Acc:HGNC:45889]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480367","summary":null,"start":226445937,"end":226446292,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 165 [Source:HGNC Symbol;Acc:HGNC:45889]"}, {"versioned_ensembl_gene_id":"ENSG00000252178.1","gene_symbol":"RNU7-69P","gene_name":"RNA, U7 small nuclear 69 pseudogene [Source:HGNC Symbol;Acc:HGNC:34165]","synonyms":"U7.69","biotype":"snRNA","ncbi_id":"100151666","summary":null,"start":123772078,"end":123772139,"strand":-1,"description":"RNA, U7 small nuclear 69 pseudogene [Source:HGNC Symbol;Acc:HGNC:34165]"}, {"versioned_ensembl_gene_id":"ENSG00000201602.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":248594925,"end":248595033,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238423.1","gene_symbol":"SNORD42B","gene_name":"small nucleolar RNA, C/D box 42B [Source:HGNC Symbol;Acc:HGNC:10181]","synonyms":"U42B,RNU42B","biotype":"snoRNA","ncbi_id":"26808","summary":null,"start":28720550,"end":28720616,"strand":1,"description":"small nucleolar RNA, C/D box 42B [Source:HGNC Symbol;Acc:HGNC:10181]"}, {"versioned_ensembl_gene_id":"ENSG00000280632.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133302618,"end":133302711,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207251.1","gene_symbol":"RNU6-342P","gene_name":"RNA, U6 small nuclear 342, pseudogene [Source:HGNC Symbol;Acc:HGNC:47305]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479718","summary":null,"start":27265580,"end":27265683,"strand":-1,"description":"RNA, U6 small nuclear 342, 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{"versioned_ensembl_gene_id":"ENSG00000251811.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43472477,"end":43472596,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212257.1","gene_symbol":"RNU6-1176P","gene_name":"RNA, U6 small nuclear 1176, pseudogene [Source:HGNC Symbol;Acc:HGNC:48139]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481551","summary":null,"start":65022968,"end":65023074,"strand":-1,"description":"RNA, U6 small nuclear 1176, pseudogene [Source:HGNC Symbol;Acc:HGNC:48139]"}, {"versioned_ensembl_gene_id":"ENSG00000206982.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128584390,"end":128584491,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276565.1","gene_symbol":"AP006285.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1586202,"end":1591699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252717.1","gene_symbol":"RNU6-352P","gene_name":"RNA, U6 small nuclear 352, pseudogene [Source:HGNC Symbol;Acc:HGNC:47315]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480573","summary":null,"start":101859851,"end":101859957,"strand":1,"description":"RNA, U6 small nuclear 352, pseudogene [Source:HGNC Symbol;Acc:HGNC:47315]"}, {"versioned_ensembl_gene_id":"ENSG00000199515.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41065554,"end":41065646,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199556.1","gene_symbol":"RNA5SP361","gene_name":"RNA, 5S ribosomal pseudogene 361 [Source:HGNC Symbol;Acc:HGNC:43261]","synonyms":"RN5S361","biotype":"rRNA","ncbi_id":"100873620","summary":null,"start":45117771,"end":45117888,"strand":1,"description":"RNA, 5S ribosomal pseudogene 361 [Source:HGNC Symbol;Acc:HGNC:43261]"}, {"versioned_ensembl_gene_id":"ENSG00000207100.1","gene_symbol":"SNORA8","gene_name":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]","synonyms":"ACA8","biotype":"snoRNA","ncbi_id":"654320","summary":null,"start":133152754,"end":133152892,"strand":1,"description":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]"}, {"versioned_ensembl_gene_id":"ENSG00000206700.1","gene_symbol":"RNU6-723P","gene_name":"RNA, U6 small nuclear 723, pseudogene [Source:HGNC Symbol;Acc:HGNC:47686]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479886","summary":null,"start":48344209,"end":48344315,"strand":1,"description":"RNA, U6 small nuclear 723, pseudogene [Source:HGNC Symbol;Acc:HGNC:47686]"}, {"versioned_ensembl_gene_id":"ENSG00000252386.1","gene_symbol":"RNU6-1018P","gene_name":"RNA, U6 small nuclear 1018, pseudogene [Source:HGNC Symbol;Acc:HGNC:47981]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481502","summary":null,"start":41684986,"end":41685091,"strand":-1,"description":"RNA, U6 small nuclear 1018, pseudogene [Source:HGNC Symbol;Acc:HGNC:47981]"}, {"versioned_ensembl_gene_id":"ENSG00000275776.1","gene_symbol":"RN7SL185P","gene_name":"RNA, 7SL, cytoplasmic 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:46201]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479289","summary":null,"start":32394365,"end":32394613,"strand":-1,"description":"RNA, 7SL, cytoplasmic 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:46201]"}, {"versioned_ensembl_gene_id":"ENSG00000201925.1","gene_symbol":"RNA5S15","gene_name":"RNA, 5S ribosomal 15 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000207136.1","gene_symbol":"RNU6-769P","gene_name":"RNA, U6 small nuclear 769, pseudogene [Source:HGNC Symbol;Acc:HGNC:47732]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479906","summary":null,"start":50633273,"end":50633376,"strand":1,"description":"RNA, U6 small nuclear 769, pseudogene [Source:HGNC Symbol;Acc:HGNC:47732]"}, {"versioned_ensembl_gene_id":"ENSG00000275823.1","gene_symbol":"DLEU2_3","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63549294,"end":63549366,"strand":-1,"description":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]"}, {"versioned_ensembl_gene_id":"ENSG00000240647.3","gene_symbol":"RN7SL305P","gene_name":"RNA, 7SL, cytoplasmic 305, pseudogene [Source:HGNC 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[Source:HGNC Symbol;Acc:HGNC:46928]"}, {"versioned_ensembl_gene_id":"ENSG00000199490.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49920597,"end":49920694,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223238.1","gene_symbol":"RNA5SP294","gene_name":"RNA, 5S ribosomal pseudogene 294 [Source:HGNC Symbol;Acc:HGNC:43194]","synonyms":"RN5S294","biotype":"rRNA","ncbi_id":"100873547","summary":null,"start":111411644,"end":111411742,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 294 [Source:HGNC Symbol;Acc:HGNC:43194]"}, {"versioned_ensembl_gene_id":"ENSG00000206728.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23273807,"end":23273910,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263723.1","gene_symbol":"SNORD39","gene_name":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":237869904,"end":237869982,"strand":1,"description":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]"}, {"versioned_ensembl_gene_id":"ENSG00000276516.1","gene_symbol":"RN7SL284P","gene_name":"RNA, 7SL, cytoplasmic 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:46300]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480999","summary":null,"start":77912271,"end":77912545,"strand":-1,"description":"RNA, 7SL, cytoplasmic 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:46300]"}, {"versioned_ensembl_gene_id":"ENSG00000252047.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":103434994,"end":103435092,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239367.2","gene_symbol":"RN7SL477P","gene_name":"RNA, 7SL, cytoplasmic 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:46493]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479397","summary":null,"start":1570575,"end":1570860,"strand":-1,"description":"RNA, 7SL, cytoplasmic 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:46493]"}, {"versioned_ensembl_gene_id":"ENSG00000222546.1","gene_symbol":"RNA5SP251","gene_name":"RNA, 5S ribosomal pseudogene 251 [Source:HGNC Symbol;Acc:HGNC:43151]","synonyms":"RN5S251","biotype":"rRNA","ncbi_id":"100873507","summary":null,"start":3700492,"end":3700628,"strand":1,"description":"RNA, 5S ribosomal pseudogene 251 [Source:HGNC Symbol;Acc:HGNC:43151]"}, {"versioned_ensembl_gene_id":"ENSG00000283188.1","gene_symbol":"MIR2052","gene_name":"microRNA 2052 [Source:HGNC Symbol;Acc:HGNC:37068]","synonyms":"hsa-mir-2052","biotype":"miRNA","ncbi_id":"100302260","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74705693,"end":74705747,"strand":1,"description":"microRNA 2052 [Source:HGNC Symbol;Acc:HGNC:37068]"}, {"versioned_ensembl_gene_id":"ENSG00000207081.1","gene_symbol":"RNU6-616P","gene_name":"RNA, U6 small nuclear 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:47579]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479838","summary":null,"start":134918310,"end":134918416,"strand":-1,"description":"RNA, U6 small nuclear 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:47579]"}, {"versioned_ensembl_gene_id":"ENSG00000272015.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"E2-1,RNU108,E2,RNE2","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":38894785,"end":38894867,"strand":1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000227482.1","gene_symbol":"AL157702.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113650956,"end":113682855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263649.1","gene_symbol":"MIR3135B","gene_name":"microRNA 3135b [Source:HGNC Symbol;Acc:HGNC:41783]","synonyms":"hsa-mir-3135b","biotype":"miRNA","ncbi_id":"100616218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32749912,"end":32749979,"strand":-1,"description":"microRNA 3135b [Source:HGNC Symbol;Acc:HGNC:41783]"}, {"versioned_ensembl_gene_id":"ENSG00000240877.3","gene_symbol":"RN7SL521P","gene_name":"RNA, 7SL, cytoplasmic 521, pseudogene [Source:HGNC Symbol;Acc:HGNC:46537]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479413","summary":null,"start":149125690,"end":149125986,"strand":-1,"description":"RNA, 7SL, cytoplasmic 521, pseudogene [Source:HGNC Symbol;Acc:HGNC:46537]"}, {"versioned_ensembl_gene_id":"ENSG00000207049.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":236153071,"end":236153172,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284286.1","gene_symbol":"MIR718","gene_name":"microRNA 718 [Source:HGNC Symbol;Acc:HGNC:37317]","synonyms":"hsa-mir-718","biotype":"miRNA","ncbi_id":"100313781","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154019920,"end":154019989,"strand":-1,"description":"microRNA 718 [Source:HGNC Symbol;Acc:HGNC:37317]"}, {"versioned_ensembl_gene_id":"ENSG00000202354.1","gene_symbol":"RNY3","gene_name":"RNA, Ro-associated Y3 [Source:HGNC Symbol;Acc:HGNC:10243]","synonyms":"hY3","biotype":"misc_RNA","ncbi_id":"6085","summary":null,"start":148983755,"end":148983856,"strand":1,"description":"RNA, Ro-associated Y3 [Source:HGNC Symbol;Acc:HGNC:10243]"}, {"versioned_ensembl_gene_id":"ENSG00000208018.1","gene_symbol":"MIR645","gene_name":"microRNA 645 [Source:HGNC Symbol;Acc:HGNC:32901]","synonyms":"MIRN645,hsa-mir-645","biotype":"miRNA","ncbi_id":"693230","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50585786,"end":50585879,"strand":1,"description":"microRNA 645 [Source:HGNC Symbol;Acc:HGNC:32901]"}, {"versioned_ensembl_gene_id":"ENSG00000263403.1","gene_symbol":"MIR4673","gene_name":"microRNA 4673 [Source:HGNC Symbol;Acc:HGNC:41574]","synonyms":"hsa-mir-4673","biotype":"miRNA","ncbi_id":"100616242","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136519568,"end":136519626,"strand":-1,"description":"microRNA 4673 [Source:HGNC Symbol;Acc:HGNC:41574]"}, {"versioned_ensembl_gene_id":"ENSG00000283734.1","gene_symbol":"MIR4785","gene_name":"microRNA 4785 [Source:HGNC Symbol;Acc:HGNC:41889]","synonyms":"hsa-mir-4785","biotype":"miRNA","ncbi_id":"100616364","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160407810,"end":160407882,"strand":-1,"description":"microRNA 4785 [Source:HGNC Symbol;Acc:HGNC:41889]"}, {"versioned_ensembl_gene_id":"ENSG00000269782.1","gene_symbol":"MIR1470","gene_name":"microRNA 1470 [Source:HGNC Symbol;Acc:HGNC:35379]","synonyms":"MIRN1470,hsa-mir-1470","biotype":"miRNA","ncbi_id":"100302127","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15449548,"end":15449608,"strand":1,"description":"microRNA 1470 [Source:HGNC Symbol;Acc:HGNC:35379]"}, {"versioned_ensembl_gene_id":"ENSG00000252927.1","gene_symbol":"RNA5SP404","gene_name":"RNA, 5S ribosomal pseudogene 404 [Source:HGNC Symbol;Acc:HGNC:43304]","synonyms":"RN5S404","biotype":"rRNA","ncbi_id":"100873656","summary":null,"start":9600097,"end":9600228,"strand":1,"description":"RNA, 5S ribosomal pseudogene 404 [Source:HGNC Symbol;Acc:HGNC:43304]"}, {"versioned_ensembl_gene_id":"ENSG00000251352.1","gene_symbol":"AC122714.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180671892,"end":180672598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278412.1","gene_symbol":"MIR6854","gene_name":"microRNA 6854 [Source:HGNC Symbol;Acc:HGNC:50084]","synonyms":"hsa-mir-6854","biotype":"miRNA","ncbi_id":"102465514","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98229149,"end":98229217,"strand":-1,"description":"microRNA 6854 [Source:HGNC Symbol;Acc:HGNC:50084]"}, {"versioned_ensembl_gene_id":"ENSG00000266530.1","gene_symbol":"MIR4318","gene_name":"microRNA 4318 [Source:HGNC Symbol;Acc:HGNC:38333]","synonyms":"hsa-mir-4318","biotype":"miRNA","ncbi_id":"100422857","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37657135,"end":37657215,"strand":1,"description":"microRNA 4318 [Source:HGNC Symbol;Acc:HGNC:38333]"}, {"versioned_ensembl_gene_id":"ENSG00000251745.1","gene_symbol":"RNU7-124P","gene_name":"RNA, U7 small nuclear 124 pseudogene [Source:HGNC Symbol;Acc:HGNC:45658]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479072","summary":null,"start":37936707,"end":37936768,"strand":-1,"description":"RNA, U7 small nuclear 124 pseudogene [Source:HGNC Symbol;Acc:HGNC:45658]"}, {"versioned_ensembl_gene_id":"ENSG00000266324.1","gene_symbol":"MIR4663","gene_name":"microRNA 4663 [Source:HGNC Symbol;Acc:HGNC:41623]","synonyms":"hsa-mir-4663","biotype":"miRNA","ncbi_id":"100616260","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123215788,"end":123215863,"strand":-1,"description":"microRNA 4663 [Source:HGNC Symbol;Acc:HGNC:41623]"}, {"versioned_ensembl_gene_id":"ENSG00000207351.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":184086791,"end":184086903,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276326.1","gene_symbol":"MIR2909","gene_name":"microRNA 2909 [Source:HGNC Symbol;Acc:HGNC:38372]","synonyms":"hsa-mir-2909","biotype":"miRNA","ncbi_id":"100422969","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37033745,"end":37033813,"strand":1,"description":"microRNA 2909 [Source:HGNC Symbol;Acc:HGNC:38372]"}, {"versioned_ensembl_gene_id":"ENSG00000265375.1","gene_symbol":"MIR4679-2","gene_name":"microRNA 4679-2 [Source:HGNC Symbol;Acc:HGNC:41890]","synonyms":"hsa-mir-4679-2","biotype":"miRNA","ncbi_id":"100616192","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89063335,"end":89063411,"strand":-1,"description":"microRNA 4679-2 [Source:HGNC Symbol;Acc:HGNC:41890]"}, {"versioned_ensembl_gene_id":"ENSG00000208037.1","gene_symbol":"MIR320A","gene_name":"microRNA 320a [Source:HGNC Symbol;Acc:HGNC:31632]","synonyms":"hsa-mir-320,MIRN320A,MIRN320","biotype":"miRNA","ncbi_id":"407037","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22244962,"end":22245043,"strand":-1,"description":"microRNA 320a [Source:HGNC Symbol;Acc:HGNC:31632]"}, {"versioned_ensembl_gene_id":"ENSG00000277617.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32269338,"end":32269597,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212595.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":151026295,"end":151026406,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000199220.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":114657949,"end":114658062,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263894.1","gene_symbol":"MIR3925","gene_name":"microRNA 3925 [Source:HGNC Symbol;Acc:HGNC:38996]","synonyms":"hsa-mir-3925","biotype":"miRNA","ncbi_id":"100500885","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36622436,"end":36622512,"strand":-1,"description":"microRNA 3925 [Source:HGNC Symbol;Acc:HGNC:38996]"}, {"versioned_ensembl_gene_id":"ENSG00000239250.3","gene_symbol":"RN7SL271P","gene_name":"RNA, 7SL, cytoplasmic 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:46287]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479321","summary":null,"start":71827177,"end":71827471,"strand":1,"description":"RNA, 7SL, cytoplasmic 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:46287]"}, {"versioned_ensembl_gene_id":"ENSG00000252252.1","gene_symbol":"RNU6-687P","gene_name":"RNA, U6 small nuclear 687, pseudogene [Source:HGNC Symbol;Acc:HGNC:47650]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479869","summary":null,"start":54452423,"end":54452511,"strand":-1,"description":"RNA, U6 small nuclear 687, pseudogene [Source:HGNC Symbol;Acc:HGNC:47650]"}, {"versioned_ensembl_gene_id":"ENSG00000278401.1","gene_symbol":"AP000351.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24022930,"end":24023387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200875.1","gene_symbol":"RNU6-340P","gene_name":"RNA, U6 small nuclear 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:47303]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479717","summary":null,"start":2649761,"end":2649867,"strand":-1,"description":"RNA, U6 small nuclear 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:47303]"}, {"versioned_ensembl_gene_id":"ENSG00000266478.1","gene_symbol":"MIR5197","gene_name":"microRNA 5197 [Source:HGNC Symbol;Acc:HGNC:43450]","synonyms":"hsa-mir-5197","biotype":"miRNA","ncbi_id":"100846991","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143679860,"end":143679971,"strand":1,"description":"microRNA 5197 [Source:HGNC Symbol;Acc:HGNC:43450]"}, {"versioned_ensembl_gene_id":"ENSG00000278774.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43273101,"end":43273292,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000207956.1","gene_symbol":"MIR579","gene_name":"microRNA 579 [Source:HGNC Symbol;Acc:HGNC:32835]","synonyms":"MIRN579,hsa-mir-579","biotype":"miRNA","ncbi_id":"693164","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32394378,"end":32394475,"strand":-1,"description":"microRNA 579 [Source:HGNC Symbol;Acc:HGNC:32835]"}, {"versioned_ensembl_gene_id":"ENSG00000252230.1","gene_symbol":"SNORD111","gene_name":"Small nucleolar RNA SNORD111 [Source:RFAM;Acc:RF00611]","synonyms":"HBII-82","biotype":"snoRNA","ncbi_id":"692214","summary":null,"start":34637696,"end":34637781,"strand":-1,"description":"Small nucleolar RNA SNORD111 [Source:RFAM;Acc:RF00611]"}, {"versioned_ensembl_gene_id":"ENSG00000251900.1","gene_symbol":"VTRNA2-2P","gene_name":"vault RNA 2-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:46889]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479538","summary":null,"start":65555432,"end":65555534,"strand":-1,"description":"vault RNA 2-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:46889]"}, {"versioned_ensembl_gene_id":"ENSG00000277209.1","gene_symbol":"RPPH1","gene_name":"ribonuclease P RNA component H1 [Source:HGNC Symbol;Acc:HGNC:19273]","synonyms":"RPPH1-1,H1RNA","biotype":"ribozyme","ncbi_id":"85495","summary":"H1RNA is the RNA component of the RNase P ribonucleoprotein, an endoribonuclease that cleaves tRNA precursor molecules to form the mature 5-prime termini of their tRNA sequences (Baer et al., 1989 [PubMed 2308839]).[supplied by OMIM, Mar 2008]","start":20343075,"end":20343407,"strand":-1,"description":"ribonuclease P RNA component H1 [Source:HGNC Symbol;Acc:HGNC:19273]"}, {"versioned_ensembl_gene_id":"ENSG00000283990.1","gene_symbol":"MIRLET7A3","gene_name":"microRNA let-7a-3 [Source:HGNC Symbol;Acc:HGNC:31478]","synonyms":"MIRNLET7A3,hsa-let-7a-3","biotype":"miRNA","ncbi_id":"406883","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46112749,"end":46112822,"strand":1,"description":"microRNA let-7a-3 [Source:HGNC Symbol;Acc:HGNC:31478]"}, {"versioned_ensembl_gene_id":"ENSG00000251940.1","gene_symbol":"SNORA15","gene_name":"Small nucleolar RNA SNORA15 [Source:RFAM;Acc:RF00398]","synonyms":"SNORA15A,ACA15","biotype":"snoRNA","ncbi_id":"677803","summary":null,"start":19249873,"end":19249966,"strand":1,"description":"Small nucleolar RNA SNORA15 [Source:RFAM;Acc:RF00398]"}, {"versioned_ensembl_gene_id":"ENSG00000266317.2","gene_symbol":"RN7SL703P","gene_name":"RNA, 7SL, cytoplasmic 703, pseudogene [Source:HGNC Symbol;Acc:HGNC:46719]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479479","summary":null,"start":181813401,"end":181813702,"strand":1,"description":"RNA, 7SL, cytoplasmic 703, pseudogene [Source:HGNC Symbol;Acc:HGNC:46719]"}, {"versioned_ensembl_gene_id":"ENSG00000207328.1","gene_symbol":"RNU6-636P","gene_name":"RNA, U6 small nuclear 636, pseudogene [Source:HGNC Symbol;Acc:HGNC:47599]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480597","summary":null,"start":37203610,"end":37203716,"strand":1,"description":"RNA, U6 small nuclear 636, pseudogene [Source:HGNC Symbol;Acc:HGNC:47599]"}, {"versioned_ensembl_gene_id":"ENSG00000200563.1","gene_symbol":"RNU6-640P","gene_name":"RNA, U6 small nuclear 640, pseudogene [Source:HGNC Symbol;Acc:HGNC:47603]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479850","summary":null,"start":86515204,"end":86515308,"strand":-1,"description":"RNA, U6 small nuclear 640, pseudogene [Source:HGNC Symbol;Acc:HGNC:47603]"}, {"versioned_ensembl_gene_id":"ENSG00000239096.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":179614775,"end":179614878,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000202056.1","gene_symbol":"RNA5SP19","gene_name":"RNA, 5S ribosomal pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42587]","synonyms":"RN5S19","biotype":"rRNA","ncbi_id":"100873274","summary":null,"start":228555793,"end":228555901,"strand":1,"description":"RNA, 5S ribosomal pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42587]"}, {"versioned_ensembl_gene_id":"ENSG00000265007.1","gene_symbol":"MIR4327","gene_name":"microRNA 4327 [Source:HGNC Symbol;Acc:HGNC:38355]","synonyms":"hsa-mir-4327","biotype":"miRNA","ncbi_id":"100422891","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30375294,"end":30375378,"strand":-1,"description":"microRNA 4327 [Source:HGNC Symbol;Acc:HGNC:38355]"}, {"versioned_ensembl_gene_id":"ENSG00000241997.3","gene_symbol":"RN7SL323P","gene_name":"RNA, 7SL, cytoplasmic 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:46339]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479341","summary":null,"start":56022019,"end":56022313,"strand":-1,"description":"RNA, 7SL, cytoplasmic 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:46339]"}, {"versioned_ensembl_gene_id":"ENSG00000275108.1","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":98987387,"end":98987449,"strand":1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000212517.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":5121417,"end":5121539,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000284125.1","gene_symbol":"MIR1825","gene_name":"microRNA 1825 [Source:HGNC Symbol;Acc:HGNC:35389]","synonyms":"MIRN1825,hsa-mir-1825","biotype":"miRNA","ncbi_id":"100302183","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32237795,"end":32237847,"strand":1,"description":"microRNA 1825 [Source:HGNC Symbol;Acc:HGNC:35389]"}, {"versioned_ensembl_gene_id":"ENSG00000265093.2","gene_symbol":"RN7SL246P","gene_name":"RNA, 7SL, cytoplasmic 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:46262]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480989","summary":null,"start":45874035,"end":45874330,"strand":1,"description":"RNA, 7SL, cytoplasmic 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:46262]"}, {"versioned_ensembl_gene_id":"ENSG00000283222.1","gene_symbol":"MIR4433A","gene_name":"microRNA 4433a [Source:HGNC Symbol;Acc:HGNC:41634]","synonyms":"MIR4433,hsa-mir-4433","biotype":"miRNA","ncbi_id":"100616265","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64340759,"end":64340839,"strand":1,"description":"microRNA 4433a [Source:HGNC Symbol;Acc:HGNC:41634]"}, {"versioned_ensembl_gene_id":"ENSG00000201013.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":233379843,"end":233379955,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283978.1","gene_symbol":"MIR365B","gene_name":"microRNA 365b [Source:HGNC Symbol;Acc:HGNC:33693]","synonyms":"MIRN365-2,MIR365-2,hsa-mir-365-2","biotype":"miRNA","ncbi_id":"100126356","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31575411,"end":31575521,"strand":1,"description":"microRNA 365b [Source:HGNC Symbol;Acc:HGNC:33693]"}, {"versioned_ensembl_gene_id":"ENSG00000202313.1","gene_symbol":"RNU1-64P","gene_name":"RNA, U1 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:48406]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480168","summary":null,"start":11503509,"end":11503671,"strand":-1,"description":"RNA, U1 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:48406]"}, {"versioned_ensembl_gene_id":"ENSG00000239080.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":136134317,"end":136134420,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000200208.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23457584,"end":23457685,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274300.1","gene_symbol":"MIR6864","gene_name":"microRNA 6864 [Source:HGNC Symbol;Acc:HGNC:50226]","synonyms":"hsa-mir-6864","biotype":"miRNA","ncbi_id":"102465521","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4969702,"end":4969771,"strand":-1,"description":"microRNA 6864 [Source:HGNC Symbol;Acc:HGNC:50226]"}, {"versioned_ensembl_gene_id":"ENSG00000207419.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"RNU67,U67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":11709819,"end":11709960,"strand":1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000199200.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34201979,"end":34202074,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278523.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61928634,"end":61928704,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266643.1","gene_symbol":"MIR3677","gene_name":"microRNA 3677 [Source:HGNC Symbol;Acc:HGNC:38932]","synonyms":"hsa-mir-3677","biotype":"miRNA","ncbi_id":"100500812","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2270713,"end":2270772,"strand":1,"description":"microRNA 3677 [Source:HGNC Symbol;Acc:HGNC:38932]"}, {"versioned_ensembl_gene_id":"ENSG00000239030.1","gene_symbol":"RNU6-956P","gene_name":"RNA, U6 small nuclear 956, pseudogene [Source:HGNC Symbol;Acc:HGNC:47919]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480404","summary":null,"start":94712409,"end":94712511,"strand":1,"description":"RNA, U6 small nuclear 956, pseudogene [Source:HGNC Symbol;Acc:HGNC:47919]"}, {"versioned_ensembl_gene_id":"ENSG00000268154.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":154950210,"end":154950492,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000198984.1","gene_symbol":"MIR345","gene_name":"microRNA 345 [Source:HGNC Symbol;Acc:HGNC:31779]","synonyms":"MIRN345,hsa-mir-345","biotype":"miRNA","ncbi_id":"442910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100307859,"end":100307956,"strand":1,"description":"microRNA 345 [Source:HGNC Symbol;Acc:HGNC:31779]"}, {"versioned_ensembl_gene_id":"ENSG00000222987.1","gene_symbol":"RN7SKP68","gene_name":"RNA, 7SK small nuclear pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:45792]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480854","summary":null,"start":102302504,"end":102302810,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:45792]"}, {"versioned_ensembl_gene_id":"ENSG00000266531.1","gene_symbol":"MIR4706","gene_name":"microRNA 4706 [Source:HGNC Symbol;Acc:HGNC:41576]","synonyms":"hsa-mir-4706","biotype":"miRNA","ncbi_id":"100616490","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65044688,"end":65044769,"strand":1,"description":"microRNA 4706 [Source:HGNC Symbol;Acc:HGNC:41576]"}, {"versioned_ensembl_gene_id":"ENSG00000272393.1","gene_symbol":"RNU6-92P","gene_name":"RNA, U6 small nuclear 92, pseudogene [Source:HGNC Symbol;Acc:HGNC:47055]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479607","summary":null,"start":133082829,"end":133082932,"strand":1,"description":"RNA, U6 small nuclear 92, pseudogene [Source:HGNC Symbol;Acc:HGNC:47055]"}, {"versioned_ensembl_gene_id":"ENSG00000201451.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133337728,"end":133337824,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277488.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":37940704,"end":37940790,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000276528.1","gene_symbol":"HOTAIRM1_1","gene_name":"HOX antisense intergenic RNA myeloid 1 conserved region 1 [Source:RFAM;Acc:RF01975]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27096124,"end":27096248,"strand":1,"description":"HOX antisense intergenic RNA myeloid 1 conserved region 1 [Source:RFAM;Acc:RF01975]"}, {"versioned_ensembl_gene_id":"ENSG00000274824.1","gene_symbol":"MIR7152","gene_name":"microRNA 7152 [Source:HGNC Symbol;Acc:HGNC:50257]","synonyms":"hsa-mir-7152","biotype":"miRNA","ncbi_id":"102465689","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71790747,"end":71790800,"strand":1,"description":"microRNA 7152 [Source:HGNC Symbol;Acc:HGNC:50257]"}, {"versioned_ensembl_gene_id":"ENSG00000200424.1","gene_symbol":"RNU6-1155P","gene_name":"RNA, U6 small nuclear 1155, pseudogene [Source:HGNC Symbol;Acc:HGNC:48118]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481544","summary":null,"start":58744251,"end":58744357,"strand":-1,"description":"RNA, U6 small nuclear 1155, pseudogene [Source:HGNC Symbol;Acc:HGNC:48118]"}, {"versioned_ensembl_gene_id":"ENSG00000240936.3","gene_symbol":"RN7SL554P","gene_name":"RNA, 7SL, cytoplasmic 554, pseudogene [Source:HGNC Symbol;Acc:HGNC:46570]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479423","summary":null,"start":6938606,"end":6938897,"strand":-1,"description":"RNA, 7SL, cytoplasmic 554, pseudogene [Source:HGNC Symbol;Acc:HGNC:46570]"}, {"versioned_ensembl_gene_id":"ENSG00000206726.1","gene_symbol":"RNU6-259P","gene_name":"RNA, U6 small nuclear 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:47222]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481260","summary":null,"start":124989219,"end":124989325,"strand":1,"description":"RNA, U6 small nuclear 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:47222]"}, {"versioned_ensembl_gene_id":"ENSG00000252580.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":26796173,"end":26796304,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000252337.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":106546665,"end":106546803,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000223026.1","gene_symbol":"RN7SKP247","gene_name":"RNA, 7SK small nuclear pseudogene 247 [Source:HGNC Symbol;Acc:HGNC:45971]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479205","summary":null,"start":81251789,"end":81252096,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 247 [Source:HGNC Symbol;Acc:HGNC:45971]"}, {"versioned_ensembl_gene_id":"ENSG00000200579.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38014568,"end":38014669,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200974.1","gene_symbol":"RNU4-87P","gene_name":"RNA, U4 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:47023]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479598","summary":null,"start":165252580,"end":165252661,"strand":1,"description":"RNA, U4 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:47023]"}, {"versioned_ensembl_gene_id":"ENSG00000264470.1","gene_symbol":"MIR4794","gene_name":"microRNA 4794 [Source:HGNC Symbol;Acc:HGNC:41829]","synonyms":"hsa-mir-4794","biotype":"miRNA","ncbi_id":"100616338","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64579847,"end":64579923,"strand":1,"description":"microRNA 4794 [Source:HGNC Symbol;Acc:HGNC:41829]"}, {"versioned_ensembl_gene_id":"ENSG00000212521.1","gene_symbol":"RNU6-918P","gene_name":"RNA, U6 small nuclear 918, pseudogene [Source:HGNC Symbol;Acc:HGNC:47881]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481469","summary":null,"start":98032230,"end":98032335,"strand":1,"description":"RNA, U6 small nuclear 918, pseudogene [Source:HGNC Symbol;Acc:HGNC:47881]"}, {"versioned_ensembl_gene_id":"ENSG00000241588.3","gene_symbol":"RN7SL484P","gene_name":"RNA, 7SL, cytoplasmic 484, pseudogene [Source:HGNC Symbol;Acc:HGNC:46500]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479400","summary":null,"start":99791209,"end":99791410,"strand":1,"description":"RNA, 7SL, cytoplasmic 484, pseudogene [Source:HGNC Symbol;Acc:HGNC:46500]"}, {"versioned_ensembl_gene_id":"ENSG00000264036.2","gene_symbol":"RN7SL198P","gene_name":"RNA, 7SL, cytoplasmic 198, pseudogene [Source:HGNC Symbol;Acc:HGNC:46214]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479294","summary":null,"start":12328132,"end":12328389,"strand":-1,"description":"RNA, 7SL, cytoplasmic 198, pseudogene [Source:HGNC Symbol;Acc:HGNC:46214]"}, {"versioned_ensembl_gene_id":"ENSG00000274836.1","gene_symbol":"SMCR2_2","gene_name":"Smith-Magenis syndrome chromosome region, candidate 2 conserved region 2 [Source:RFAM;Acc:RF02178]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17676211,"end":17676371,"strand":1,"description":"Smith-Magenis syndrome chromosome region, candidate 2 conserved region 2 [Source:RFAM;Acc:RF02178]"}, {"versioned_ensembl_gene_id":"ENSG00000279336.1","gene_symbol":"AL353662.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":34201273,"end":34201515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222952.1","gene_symbol":"RNA5SP41","gene_name":"RNA, 5S ribosomal pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:42817]","synonyms":"RN5S41","biotype":"rRNA","ncbi_id":"100873280","summary":null,"start":13623184,"end":13623284,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:42817]"}, {"versioned_ensembl_gene_id":"ENSG00000266295.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31526642,"end":31526717,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000199094.3","gene_symbol":"MIR30C2","gene_name":"microRNA 30c-2 [Source:HGNC Symbol;Acc:HGNC:31627]","synonyms":"MIRN30C2,hsa-mir-30c-2","biotype":"miRNA","ncbi_id":"407032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71376960,"end":71377031,"strand":-1,"description":"microRNA 30c-2 [Source:HGNC Symbol;Acc:HGNC:31627]"}, {"versioned_ensembl_gene_id":"ENSG00000276770.1","gene_symbol":"MIR6780B","gene_name":"microRNA 6780b [Source:HGNC Symbol;Acc:HGNC:50237]","synonyms":"hsa-mir-6780b","biotype":"miRNA","ncbi_id":"102466746","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43434542,"end":43434620,"strand":1,"description":"microRNA 6780b [Source:HGNC Symbol;Acc:HGNC:50237]"}, {"versioned_ensembl_gene_id":"ENSG00000201665.1","gene_symbol":"RN7SKP6","gene_name":"RNA, 7SK small nuclear pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42624]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873850","summary":null,"start":56885284,"end":56885602,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42624]"}, {"versioned_ensembl_gene_id":"ENSG00000264342.3","gene_symbol":"MIR3660","gene_name":"microRNA 3660 [Source:HGNC Symbol;Acc:HGNC:38985]","synonyms":"hsa-mir-3660","biotype":"miRNA","ncbi_id":"100500825","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90016621,"end":90016720,"strand":-1,"description":"microRNA 3660 [Source:HGNC Symbol;Acc:HGNC:38985]"}, {"versioned_ensembl_gene_id":"ENSG00000207056.1","gene_symbol":"RNU1-8P","gene_name":"RNA, U1 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48307]","synonyms":"RNU1-8","biotype":"snRNA","ncbi_id":"106481604","summary":null,"start":7219360,"end":7219524,"strand":1,"description":"RNA, U1 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48307]"}, {"versioned_ensembl_gene_id":"ENSG00000283971.1","gene_symbol":"MIR4442","gene_name":"microRNA 4442 [Source:HGNC Symbol;Acc:HGNC:41718]","synonyms":"hsa-mir-4442","biotype":"miRNA","ncbi_id":"100616477","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25664873,"end":25664939,"strand":-1,"description":"microRNA 4442 [Source:HGNC Symbol;Acc:HGNC:41718]"}, {"versioned_ensembl_gene_id":"ENSG00000207627.1","gene_symbol":"MIR581","gene_name":"microRNA 581 [Source:HGNC Symbol;Acc:HGNC:32837]","synonyms":"MIRN581,hsa-mir-581","biotype":"miRNA","ncbi_id":"693166","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53951504,"end":53951599,"strand":-1,"description":"microRNA 581 [Source:HGNC Symbol;Acc:HGNC:32837]"}, {"versioned_ensembl_gene_id":"ENSG00000271898.1","gene_symbol":"MIR4791","gene_name":"microRNA 4791 [Source:HGNC Symbol;Acc:HGNC:41704]","synonyms":"hsa-mir-4791","biotype":"miRNA","ncbi_id":"100616291","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19314848,"end":19314931,"strand":-1,"description":"microRNA 4791 [Source:HGNC Symbol;Acc:HGNC:41704]"}, {"versioned_ensembl_gene_id":"ENSG00000273571.1","gene_symbol":"ST7-OT4_2","gene_name":"ST7 overlapping transcript 4 conserved region 2 [Source:RFAM;Acc:RF02188]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116954983,"end":116955154,"strand":1,"description":"ST7 overlapping transcript 4 conserved region 2 [Source:RFAM;Acc:RF02188]"}, {"versioned_ensembl_gene_id":"ENSG00000223324.1","gene_symbol":"RN7SKP273","gene_name":"RNA, 7SK small nuclear pseudogene 273 [Source:HGNC Symbol;Acc:HGNC:45997]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481821","summary":null,"start":111683111,"end":111683424,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 273 [Source:HGNC Symbol;Acc:HGNC:45997]"}, {"versioned_ensembl_gene_id":"ENSG00000283880.1","gene_symbol":"MIR7704","gene_name":"microRNA 7704 [Source:HGNC Symbol;Acc:HGNC:50089]","synonyms":"hsa-mir-7704","biotype":"miRNA","ncbi_id":"102465802","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176188843,"end":176188901,"strand":1,"description":"microRNA 7704 [Source:HGNC Symbol;Acc:HGNC:50089]"}, {"versioned_ensembl_gene_id":"ENSG00000275107.1","gene_symbol":"MIR6782","gene_name":"microRNA 6782 [Source:HGNC Symbol;Acc:HGNC:50270]","synonyms":"hsa-mir-6782","biotype":"miRNA","ncbi_id":"102465469","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44207771,"end":44207839,"strand":-1,"description":"microRNA 6782 [Source:HGNC Symbol;Acc:HGNC:50270]"}, {"versioned_ensembl_gene_id":"ENSG00000206857.1","gene_symbol":"RNU6-214P","gene_name":"RNA, U6 small nuclear 214, pseudogene [Source:HGNC Symbol;Acc:HGNC:47177]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479661","summary":null,"start":120526294,"end":120526400,"strand":-1,"description":"RNA, U6 small nuclear 214, pseudogene [Source:HGNC Symbol;Acc:HGNC:47177]"}, {"versioned_ensembl_gene_id":"ENSG00000284152.1","gene_symbol":"MIR6758","gene_name":"microRNA 6758 [Source:HGNC Symbol;Acc:HGNC:50038]","synonyms":"hsa-mir-6758","biotype":"miRNA","ncbi_id":"102465454","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57512688,"end":57512750,"strand":1,"description":"microRNA 6758 [Source:HGNC Symbol;Acc:HGNC:50038]"}, {"versioned_ensembl_gene_id":"ENSG00000283340.1","gene_symbol":"MIR3119-2","gene_name":"microRNA 3119-2 [Source:HGNC Symbol;Acc:HGNC:38315]","synonyms":"hsa-mir-3119-2","biotype":"miRNA","ncbi_id":"100423010","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":170151378,"end":170151462,"strand":-1,"description":"microRNA 3119-2 [Source:HGNC Symbol;Acc:HGNC:38315]"}, {"versioned_ensembl_gene_id":"ENSG00000212538.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":163923670,"end":163923873,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000266458.1","gene_symbol":"MIR4259","gene_name":"microRNA 4259 [Source:HGNC Symbol;Acc:HGNC:38309]","synonyms":"hsa-mir-4259","biotype":"miRNA","ncbi_id":"100422852","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":159899979,"end":159900079,"strand":-1,"description":"microRNA 4259 [Source:HGNC Symbol;Acc:HGNC:38309]"}, {"versioned_ensembl_gene_id":"ENSG00000238926.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72284945,"end":72285045,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000271841.1","gene_symbol":"RNU7-10P","gene_name":"RNA, U7 small nuclear 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:34106]","synonyms":"U7.10","biotype":"snRNA","ncbi_id":"100147758","summary":null,"start":17664963,"end":17665025,"strand":1,"description":"RNA, U7 small nuclear 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:34106]"}, {"versioned_ensembl_gene_id":"ENSG00000263987.1","gene_symbol":"MIR5698","gene_name":"microRNA 5698 [Source:HGNC Symbol;Acc:HGNC:43487]","synonyms":"hsa-mir-5698","biotype":"miRNA","ncbi_id":"100847024","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154104521,"end":154104592,"strand":-1,"description":"microRNA 5698 [Source:HGNC Symbol;Acc:HGNC:43487]"}, {"versioned_ensembl_gene_id":"ENSG00000263671.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30795686,"end":30795937,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275968.1","gene_symbol":"DAOA-AS1_1","gene_name":"DAOA antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02090]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105459815,"end":105460015,"strand":1,"description":"DAOA antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02090]"}, {"versioned_ensembl_gene_id":"ENSG00000207991.1","gene_symbol":"MIR601","gene_name":"microRNA 601 [Source:HGNC Symbol;Acc:HGNC:32857]","synonyms":"MIRN601,hsa-mir-601","biotype":"miRNA","ncbi_id":"693186","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123402525,"end":123402603,"strand":-1,"description":"microRNA 601 [Source:HGNC Symbol;Acc:HGNC:32857]"}, {"versioned_ensembl_gene_id":"ENSG00000279413.1","gene_symbol":"AC112497.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":15702602,"end":15703243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222112.1","gene_symbol":"RN7SKP16","gene_name":"RNA, 7SK small nuclear pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:45740]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480837","summary":null,"start":33336566,"end":33336864,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:45740]"}, {"versioned_ensembl_gene_id":"ENSG00000221616.1","gene_symbol":"MIR548H4","gene_name":"microRNA 548h-4 [Source:HGNC Symbol;Acc:HGNC:35345]","synonyms":"MIRN548H4,hsa-mir-548h-4","biotype":"miRNA","ncbi_id":"100313884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27048853,"end":27048963,"strand":-1,"description":"microRNA 548h-4 [Source:HGNC Symbol;Acc:HGNC:35345]"}, {"versioned_ensembl_gene_id":"ENSG00000266240.1","gene_symbol":"MIR5091","gene_name":"microRNA 5091 [Source:HGNC Symbol;Acc:HGNC:43478]","synonyms":"hsa-mir-5091","biotype":"miRNA","ncbi_id":"100847023","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13627865,"end":13627957,"strand":1,"description":"microRNA 5091 [Source:HGNC Symbol;Acc:HGNC:43478]"}, {"versioned_ensembl_gene_id":"ENSG00000275231.1","gene_symbol":"RMST_4","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 4 [Source:RFAM;Acc:RF01965]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97493897,"end":97494003,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 4 [Source:RFAM;Acc:RF01965]"}, {"versioned_ensembl_gene_id":"ENSG00000252902.1","gene_symbol":"RNA5SP342","gene_name":"RNA, 5S ribosomal pseudogene 342 [Source:HGNC Symbol;Acc:HGNC:43242]","synonyms":"RN5S342","biotype":"rRNA","ncbi_id":"106479008","summary":null,"start":71845196,"end":71845245,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 342 [Source:HGNC Symbol;Acc:HGNC:43242]"}, {"versioned_ensembl_gene_id":"ENSG00000202534.1","gene_symbol":"RNU6-1329P","gene_name":"RNA, U6 small nuclear 1329, pseudogene [Source:HGNC Symbol;Acc:HGNC:48292]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481600","summary":null,"start":92952639,"end":92952745,"strand":1,"description":"RNA, U6 small nuclear 1329, pseudogene [Source:HGNC Symbol;Acc:HGNC:48292]"}, {"versioned_ensembl_gene_id":"ENSG00000238723.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46215070,"end":46215171,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280864.1","gene_symbol":"AC255560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72505075,"end":72550889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284074.1","gene_symbol":"MIR4758","gene_name":"microRNA 4758 [Source:HGNC Symbol;Acc:HGNC:41836]","synonyms":"hsa-mir-4758","biotype":"miRNA","ncbi_id":"100616340","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62332487,"end":62332557,"strand":-1,"description":"microRNA 4758 [Source:HGNC Symbol;Acc:HGNC:41836]"}, {"versioned_ensembl_gene_id":"ENSG00000263750.1","gene_symbol":"MIR548AV","gene_name":"microRNA 548av [Source:HGNC Symbol;Acc:HGNC:43537]","synonyms":"hsa-mir-548av","biotype":"miRNA","ncbi_id":"100847083","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72853321,"end":72853382,"strand":-1,"description":"microRNA 548av [Source:HGNC Symbol;Acc:HGNC:43537]"}, {"versioned_ensembl_gene_id":"ENSG00000200521.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":157768013,"end":157768113,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252943.1","gene_symbol":"RNU6-264P","gene_name":"RNA, U6 small nuclear 264, pseudogene [Source:HGNC Symbol;Acc:HGNC:47227]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481262","summary":null,"start":19073843,"end":19073946,"strand":1,"description":"RNA, U6 small nuclear 264, pseudogene [Source:HGNC Symbol;Acc:HGNC:47227]"}, {"versioned_ensembl_gene_id":"ENSG00000274838.1","gene_symbol":"MIR6788","gene_name":"microRNA 6788 [Source:HGNC Symbol;Acc:HGNC:50078]","synonyms":"hsa-mir-6788","biotype":"miRNA","ncbi_id":"102466735","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10759584,"end":10759649,"strand":-1,"description":"microRNA 6788 [Source:HGNC Symbol;Acc:HGNC:50078]"}, {"versioned_ensembl_gene_id":"ENSG00000243027.3","gene_symbol":"RN7SL354P","gene_name":"RNA, 7SL, cytoplasmic 354, pseudogene [Source:HGNC Symbol;Acc:HGNC:46370]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481838","summary":null,"start":50688900,"end":50689193,"strand":1,"description":"RNA, 7SL, cytoplasmic 354, pseudogene [Source:HGNC Symbol;Acc:HGNC:46370]"}, {"versioned_ensembl_gene_id":"ENSG00000199053.3","gene_symbol":"MIR324","gene_name":"microRNA 324 [Source:HGNC Symbol;Acc:HGNC:31767]","synonyms":"MIRN324,hsa-mir-324","biotype":"miRNA","ncbi_id":"442898","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7223297,"end":7223379,"strand":-1,"description":"microRNA 324 [Source:HGNC Symbol;Acc:HGNC:31767]"}, {"versioned_ensembl_gene_id":"ENSG00000201384.1","gene_symbol":"SNORA32","gene_name":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]","synonyms":"ACA32","biotype":"snoRNA","ncbi_id":"692063","summary":null,"start":77201026,"end":77201140,"strand":-1,"description":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]"}, {"versioned_ensembl_gene_id":"ENSG00000278233.1","gene_symbol":"RNA5-8SN5","gene_name":"RNA, 5.8S ribosomal N5 [Source:HGNC Symbol;Acc:HGNC:53533]","synonyms":null,"biotype":"rRNA","ncbi_id":"100008587","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. This gene is a representative copy of the 5.8S ribosomal RNA whose chromosomal location is unknown. [provided by RefSeq, Mar 2017]","start":8212572,"end":8212724,"strand":1,"description":"RNA, 5.8S ribosomal N5 [Source:HGNC Symbol;Acc:HGNC:53533]"}, {"versioned_ensembl_gene_id":"ENSG00000207004.1","gene_symbol":"RNU6-301P","gene_name":"RNA, U6 small nuclear 301, pseudogene [Source:HGNC Symbol;Acc:HGNC:47264]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481274","summary":null,"start":51724103,"end":51724209,"strand":1,"description":"RNA, U6 small nuclear 301, pseudogene [Source:HGNC Symbol;Acc:HGNC:47264]"}, {"versioned_ensembl_gene_id":"ENSG00000207749.4","gene_symbol":"MIR299","gene_name":"microRNA 299 [Source:HGNC Symbol;Acc:HGNC:31618]","synonyms":"hsa-mir-299,MIRN299","biotype":"miRNA","ncbi_id":"407023","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101023794,"end":101023856,"strand":1,"description":"microRNA 299 [Source:HGNC Symbol;Acc:HGNC:31618]"}, {"versioned_ensembl_gene_id":"ENSG00000202046.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":120192245,"end":120192357,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000259543.1","gene_symbol":"AC060809.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81427448,"end":81755217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199082.1","gene_symbol":"MIR342","gene_name":"microRNA 342 [Source:HGNC Symbol;Acc:HGNC:31778]","synonyms":"MIRN342,hsa-mir-342","biotype":"miRNA","ncbi_id":"442909","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100109655,"end":100109753,"strand":1,"description":"microRNA 342 [Source:HGNC Symbol;Acc:HGNC:31778]"}, {"versioned_ensembl_gene_id":"ENSG00000252485.1","gene_symbol":"Vault","gene_name":"Vault RNA [Source:RFAM;Acc:RF00006]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206007880,"end":206007974,"strand":-1,"description":"Vault RNA [Source:RFAM;Acc:RF00006]"}, {"versioned_ensembl_gene_id":"ENSG00000199453.1","gene_symbol":"SNORD115-12","gene_name":"small nucleolar RNA, C/D box 115-12 [Source:HGNC Symbol;Acc:HGNC:33031]","synonyms":"HBII-52-12","biotype":"snoRNA","ncbi_id":"100033449","summary":null,"start":25191416,"end":25191497,"strand":1,"description":"small nucleolar RNA, C/D box 115-12 [Source:HGNC Symbol;Acc:HGNC:33031]"}, {"versioned_ensembl_gene_id":"ENSG00000283126.1","gene_symbol":"MIR1297","gene_name":"microRNA 1297 [Source:HGNC Symbol;Acc:HGNC:35289]","synonyms":"hsa-mir-1297,MIRN1297","biotype":"miRNA","ncbi_id":"100302187","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8388362,"end":8388453,"strand":1,"description":"microRNA 6724-3 [Source:HGNC Symbol;Acc:HGNC:50842]"}, {"versioned_ensembl_gene_id":"ENSG00000265595.1","gene_symbol":"MIR4756","gene_name":"microRNA 4756 [Source:HGNC Symbol;Acc:HGNC:41529]","synonyms":"hsa-mir-4756","biotype":"miRNA","ncbi_id":"100616225","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54068408,"end":54068485,"strand":-1,"description":"microRNA 4756 [Source:HGNC Symbol;Acc:HGNC:41529]"}, {"versioned_ensembl_gene_id":"ENSG00000251724.1","gene_symbol":"RNU7-175P","gene_name":"RNA, U7 small nuclear 175 pseudogene [Source:HGNC Symbol;Acc:HGNC:45709]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479091","summary":null,"start":75538598,"end":75538658,"strand":-1,"description":"RNA, U7 small nuclear 175 pseudogene [Source:HGNC Symbol;Acc:HGNC:45709]"}, {"versioned_ensembl_gene_id":"ENSG00000263529.2","gene_symbol":"RN7SL122P","gene_name":"RNA, 7SL, cytoplasmic 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:46138]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480954","summary":null,"start":32457835,"end":32458135,"strand":1,"description":"RNA, 7SL, cytoplasmic 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:46138]"}, {"versioned_ensembl_gene_id":"ENSG00000252777.1","gene_symbol":"SCARNA24","gene_name":"Small Cajal body specific RNA 24 [Source:RFAM;Acc:RF00422]","synonyms":null,"biotype":"scaRNA","ncbi_id":null,"summary":null,"start":28689665,"end":28689794,"strand":1,"description":"Small Cajal body specific RNA 24 [Source:RFAM;Acc:RF00422]"}, {"versioned_ensembl_gene_id":"ENSG00000283455.1","gene_symbol":"MIR523","gene_name":"microRNA 523 [Source:HGNC Symbol;Acc:HGNC:32103]","synonyms":"MIRN523,hsa-mir-523","biotype":"miRNA","ncbi_id":"574471","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53698385,"end":53698471,"strand":1,"description":"microRNA 523 [Source:HGNC Symbol;Acc:HGNC:32103]"}, {"versioned_ensembl_gene_id":"ENSG00000239910.3","gene_symbol":"RN7SL530P","gene_name":"RNA, 7SL, cytoplasmic 530, pseudogene [Source:HGNC Symbol;Acc:HGNC:46546]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481067","summary":null,"start":74174456,"end":74174753,"strand":1,"description":"RNA, 7SL, cytoplasmic 530, pseudogene [Source:HGNC Symbol;Acc:HGNC:46546]"}, {"versioned_ensembl_gene_id":"ENSG00000251996.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7341531,"end":7341642,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283502.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":47781379,"end":47781465,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000215930.1","gene_symbol":"MIR942","gene_name":"microRNA 942 [Source:HGNC Symbol;Acc:HGNC:33688]","synonyms":"MIRN942,hsa-mir-942","biotype":"miRNA","ncbi_id":"100126331","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":117094643,"end":117094728,"strand":1,"description":"microRNA 942 [Source:HGNC Symbol;Acc:HGNC:33688]"}, {"versioned_ensembl_gene_id":"ENSG00000207754.3","gene_symbol":"MIR487B","gene_name":"microRNA 487b [Source:HGNC Symbol;Acc:HGNC:32533]","synonyms":"MIRN487B,hsa-mir-487b","biotype":"miRNA","ncbi_id":"664616","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101046455,"end":101046538,"strand":1,"description":"microRNA 487b [Source:HGNC Symbol;Acc:HGNC:32533]"}, {"versioned_ensembl_gene_id":"ENSG00000281696.1","gene_symbol":"MIR664A","gene_name":"microRNA 664a [Source:HGNC Symbol;Acc:HGNC:35370]","synonyms":"MIRN664,MIR664,hsa-mir-664","biotype":"miRNA","ncbi_id":"100302234","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":220200538,"end":220200619,"strand":-1,"description":"microRNA 664a [Source:HGNC Symbol;Acc:HGNC:35370]"}, {"versioned_ensembl_gene_id":"ENSG00000275878.1","gene_symbol":"RN7SL43P","gene_name":"RNA, 7SL, cytoplasmic 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:46059]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479241","summary":null,"start":66980120,"end":66980410,"strand":1,"description":"RNA, 7SL, cytoplasmic 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:46059]"}, {"versioned_ensembl_gene_id":"ENSG00000200885.1","gene_symbol":"RNU1-146P","gene_name":"RNA, U1 small nuclear 146, pseudogene [Source:HGNC Symbol;Acc:HGNC:48488]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480198","summary":null,"start":19724435,"end":19724599,"strand":1,"description":"RNA, U1 small nuclear 146, pseudogene [Source:HGNC Symbol;Acc:HGNC:48488]"}, {"versioned_ensembl_gene_id":"ENSG00000274409.1","gene_symbol":"DLX6-AS1_1","gene_name":"Embryonic ventral forebrain RNA 1 conserved region 1 [Source:RFAM;Acc:RF01887]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96965302,"end":96965481,"strand":1,"description":"Embryonic ventral forebrain RNA 1 conserved region 1 [Source:RFAM;Acc:RF01887]"}, {"versioned_ensembl_gene_id":"ENSG00000200403.1","gene_symbol":"RNU6-1099P","gene_name":"RNA, U6 small nuclear 1099, pseudogene [Source:HGNC Symbol;Acc:HGNC:48062]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481526","summary":null,"start":19305076,"end":19305182,"strand":-1,"description":"RNA, U6 small nuclear 1099, pseudogene [Source:HGNC Symbol;Acc:HGNC:48062]"}, {"versioned_ensembl_gene_id":"ENSG00000199337.1","gene_symbol":"RNA5S3","gene_name":"RNA, 5S ribosomal 3 [Source:HGNC Symbol;Acc:HGNC:34364]","synonyms":"RN5S3","biotype":"rRNA","ncbi_id":"100169754","summary":null,"start":228614750,"end":228614868,"strand":-1,"description":"RNA, 5S ribosomal 3 [Source:HGNC Symbol;Acc:HGNC:34364]"}, {"versioned_ensembl_gene_id":"ENSG00000273744.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":106271634,"end":106271720,"strand":1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000274799.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":148389748,"end":148390029,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207109.1","gene_symbol":"SNORD38C","gene_name":"small nucleolar RNA, C/D box 38C [Source:HGNC Symbol;Acc:HGNC:52227]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617024","summary":null,"start":53333060,"end":53333128,"strand":-1,"description":"small nucleolar RNA, C/D box 38C [Source:HGNC Symbol;Acc:HGNC:52227]"}, {"versioned_ensembl_gene_id":"ENSG00000206847.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":129030459,"end":129030572,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252065.1","gene_symbol":"RNU6-864P","gene_name":"RNA, U6 small nuclear 864, pseudogene [Source:HGNC Symbol;Acc:HGNC:47827]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481776","summary":null,"start":28982303,"end":28982410,"strand":-1,"description":"RNA, U6 small nuclear 864, pseudogene [Source:HGNC Symbol;Acc:HGNC:47827]"}, {"versioned_ensembl_gene_id":"ENSG00000274055.1","gene_symbol":"CDKN2B-AS_3","gene_name":"CDKN2B antisense RNA 1 convserved region 3 [Source:RFAM;Acc:RF02045]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22046758,"end":22046901,"strand":1,"description":"CDKN2B antisense RNA 1 convserved region 3 [Source:RFAM;Acc:RF02045]"}, {"versioned_ensembl_gene_id":"ENSG00000272160.1","gene_symbol":"RNU4-5P","gene_name":"RNA, U4 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10198]","synonyms":"U4/6,U4,RNU4P5","biotype":"snRNA","ncbi_id":"26839","summary":null,"start":109869858,"end":109869992,"strand":1,"description":"RNA, U4 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10198]"}, {"versioned_ensembl_gene_id":"ENSG00000209482.1","gene_symbol":"SNORD83A","gene_name":"small nucleolar RNA, C/D box 83A [Source:HGNC Symbol;Acc:HGNC:17131]","synonyms":"U83A,RNU83A","biotype":"snoRNA","ncbi_id":"116937","summary":"Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD83A, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD83A, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]","start":39315213,"end":39315307,"strand":-1,"description":"small nucleolar RNA, C/D box 83A [Source:HGNC Symbol;Acc:HGNC:17131]"}, {"versioned_ensembl_gene_id":"ENSG00000206758.1","gene_symbol":"RNU6-317P","gene_name":"RNA, U6 small nuclear 317, pseudogene [Source:HGNC Symbol;Acc:HGNC:47280]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479708","summary":null,"start":48793152,"end":48793258,"strand":-1,"description":"RNA, U6 small nuclear 317, pseudogene [Source:HGNC Symbol;Acc:HGNC:47280]"}, {"versioned_ensembl_gene_id":"ENSG00000264271.2","gene_symbol":"RN7SL488P","gene_name":"RNA, 7SL, cytoplasmic 488, pseudogene [Source:HGNC Symbol;Acc:HGNC:46504]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479401","summary":null,"start":63529613,"end":63529898,"strand":-1,"description":"RNA, 7SL, cytoplasmic 488, pseudogene [Source:HGNC Symbol;Acc:HGNC:46504]"}, {"versioned_ensembl_gene_id":"ENSG00000238391.1","gene_symbol":"RNA5SP233","gene_name":"RNA, 5S ribosomal pseudogene 233 [Source:HGNC Symbol;Acc:HGNC:43133]","synonyms":"RN5S233","biotype":"rRNA","ncbi_id":"100873491","summary":null,"start":74487428,"end":74487540,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 233 [Source:HGNC Symbol;Acc:HGNC:43133]"}, {"versioned_ensembl_gene_id":"ENSG00000201348.1","gene_symbol":"RNU105B","gene_name":"RNA, U105B small nucleolar [Source:HGNC Symbol;Acc:HGNC:10103]","synonyms":"E1-2","biotype":"snoRNA","ncbi_id":"26767","summary":null,"start":8831186,"end":8831393,"strand":1,"description":"RNA, U105B small nucleolar [Source:HGNC Symbol;Acc:HGNC:10103]"}, {"versioned_ensembl_gene_id":"ENSG00000244139.3","gene_symbol":"RN7SL397P","gene_name":"RNA, 7SL, cytoplasmic 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:46413]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479369","summary":null,"start":120121909,"end":120122206,"strand":1,"description":"RNA, 7SL, cytoplasmic 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:46413]"}, {"versioned_ensembl_gene_id":"ENSG00000222123.1","gene_symbol":"RNA5SP390","gene_name":"RNA, 5S ribosomal pseudogene 390 [Source:HGNC Symbol;Acc:HGNC:43290]","synonyms":"RN5S390","biotype":"rRNA","ncbi_id":"100873643","summary":null,"start":25738508,"end":25738620,"strand":1,"description":"RNA, 5S ribosomal pseudogene 390 [Source:HGNC Symbol;Acc:HGNC:43290]"}, {"versioned_ensembl_gene_id":"ENSG00000281614.2","gene_symbol":"INPP5D","gene_name":"inositol polyphosphate-5-phosphatase D [Source:HGNC Symbol;Acc:HGNC:6079]","synonyms":"SHIP,hp51CN,SHIP1","biotype":"protein_coding","ncbi_id":"3635","summary":"This gene is a member of the inositol polyphosphate-5-phosphatase (INPP5) family and encodes a protein with an N-terminal SH2 domain, an inositol phosphatase domain, and two C-terminal protein interaction domains. Expression of this protein is restricted to hematopoietic cells where its movement from the cytosol to the plasma membrane is mediated by tyrosine phosphorylation. At the plasma membrane, the protein hydrolyzes the 5' phosphate from phosphatidylinositol (3,4,5)-trisphosphate and inositol-1,3,4,5-tetrakisphosphate, thereby affecting multiple signaling pathways. The protein is also partly localized to the nucleus, where it may be involved in nuclear inositol phosphate signaling processes. Overall, the protein functions as a negative regulator of myeloid cell proliferation and survival. Mutations in this gene are associated with defects and cancers of the immune system. Deficiencies in the encoded protein, SHIP1, have been associated with Inflammatory Bowel Disease types such as Crohn's Disease and Ulcerative Colitis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":233059967,"end":233207903,"strand":1,"description":"inositol polyphosphate-5-phosphatase D [Source:HGNC Symbol;Acc:HGNC:6079]"}, {"versioned_ensembl_gene_id":"ENSG00000274380.1","gene_symbol":"MIR6801","gene_name":"microRNA 6801 [Source:HGNC Symbol;Acc:HGNC:50178]","synonyms":"hsa-mir-6801","biotype":"miRNA","ncbi_id":"102466984","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52222020,"end":52222098,"strand":1,"description":"microRNA 6801 [Source:HGNC Symbol;Acc:HGNC:50178]"}, {"versioned_ensembl_gene_id":"ENSG00000202479.1","gene_symbol":"SNORD14","gene_name":"Small nucleolar RNA SNORD14 [Source:RFAM;Acc:RF00016]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":24969388,"end":24969477,"strand":-1,"description":"Small nucleolar RNA SNORD14 [Source:RFAM;Acc:RF00016]"}, {"versioned_ensembl_gene_id":"ENSG00000265154.1","gene_symbol":"MIR151B","gene_name":"microRNA 151b [Source:HGNC Symbol;Acc:HGNC:41588]","synonyms":"hsa-mir-151b","biotype":"miRNA","ncbi_id":"100616247","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100109419,"end":100109514,"strand":-1,"description":"microRNA 151b [Source:HGNC Symbol;Acc:HGNC:41588]"}, {"versioned_ensembl_gene_id":"ENSG00000252964.1","gene_symbol":"RNA5SP400","gene_name":"RNA, 5S ribosomal pseudogene 400 [Source:HGNC Symbol;Acc:HGNC:43300]","synonyms":"RN5S400","biotype":"rRNA","ncbi_id":"100873653","summary":null,"start":86138269,"end":86138379,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 400 [Source:HGNC Symbol;Acc:HGNC:43300]"}, {"versioned_ensembl_gene_id":"ENSG00000252537.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":16005808,"end":16005923,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000206592.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":79220942,"end":79221073,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000238443.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133238455,"end":133238549,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252487.1","gene_symbol":"RNY4P20","gene_name":"RNA, Ro-associated Y4 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:34070]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379378","summary":null,"start":151298841,"end":151298933,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:34070]"}, {"versioned_ensembl_gene_id":"ENSG00000252342.1","gene_symbol":"RNA5SP164","gene_name":"RNA, 5S ribosomal pseudogene 164 [Source:HGNC Symbol;Acc:HGNC:43064]","synonyms":"RN5S164","biotype":"rRNA","ncbi_id":"100873429","summary":null,"start":93820171,"end":93820280,"strand":1,"description":"RNA, 5S ribosomal pseudogene 164 [Source:HGNC Symbol;Acc:HGNC:43064]"}, {"versioned_ensembl_gene_id":"ENSG00000201624.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33982465,"end":33982566,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252944.1","gene_symbol":"RNU6-897P","gene_name":"RNA, U6 small nuclear 897, pseudogene [Source:HGNC Symbol;Acc:HGNC:47860]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479963","summary":null,"start":104766822,"end":104766926,"strand":1,"description":"RNA, U6 small nuclear 897, pseudogene [Source:HGNC Symbol;Acc:HGNC:47860]"}, {"versioned_ensembl_gene_id":"ENSG00000264997.1","gene_symbol":"SNORD39","gene_name":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":109263494,"end":109263564,"strand":-1,"description":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]"}, {"versioned_ensembl_gene_id":"ENSG00000233737.3","gene_symbol":"AP003072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93221486,"end":93221630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207975.1","gene_symbol":"MIR181B1","gene_name":"microRNA 181b-1 [Source:HGNC Symbol;Acc:HGNC:31550]","synonyms":"MIRN181B1,hsa-mir-181b-1","biotype":"miRNA","ncbi_id":"406955","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12719132,"end":12719190,"strand":1,"description":"microRNA 5692a-2 [Source:HGNC Symbol;Acc:HGNC:43466]"}, {"versioned_ensembl_gene_id":"ENSG00000201782.1","gene_symbol":"RN7SKP226","gene_name":"RNA, 7SK small nuclear pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:45950]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480903","summary":null,"start":128220504,"end":128220803,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:45950]"}, {"versioned_ensembl_gene_id":"ENSG00000199878.1","gene_symbol":"RN7SKP149","gene_name":"RNA, 7SK small nuclear pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:45873]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479161","summary":null,"start":143197248,"end":143197591,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:45873]"}, {"versioned_ensembl_gene_id":"ENSG00000201600.1","gene_symbol":"RN7SKP124","gene_name":"RNA, 7SK small nuclear pseudogene 124 [Source:HGNC Symbol;Acc:HGNC:45848]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480871","summary":null,"start":139584105,"end":139584445,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 124 [Source:HGNC Symbol;Acc:HGNC:45848]"}, {"versioned_ensembl_gene_id":"ENSG00000252977.1","gene_symbol":"RNA5SP70","gene_name":"RNA, 5S ribosomal pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:42847]","synonyms":"RN5S70","biotype":"rRNA","ncbi_id":"106480436","summary":null,"start":181771566,"end":181771644,"strand":1,"description":"RNA, 5S ribosomal pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:42847]"}, {"versioned_ensembl_gene_id":"ENSG00000207022.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":92846059,"end":92846182,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000276575.1","gene_symbol":"MIR6895","gene_name":"microRNA 6895 [Source:HGNC Symbol;Acc:HGNC:50210]","synonyms":"hsa-mir-6895","biotype":"miRNA","ncbi_id":"102465539","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53195411,"end":53195488,"strand":-1,"description":"microRNA 6895 [Source:HGNC Symbol;Acc:HGNC:50210]"}, {"versioned_ensembl_gene_id":"ENSG00000207716.1","gene_symbol":"MIR572","gene_name":"microRNA 572 [Source:HGNC Symbol;Acc:HGNC:32828]","synonyms":"MIRN572,hsa-mir-572","biotype":"miRNA","ncbi_id":"693157","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11368827,"end":11368921,"strand":1,"description":"microRNA 572 [Source:HGNC Symbol;Acc:HGNC:32828]"}, {"versioned_ensembl_gene_id":"ENSG00000264814.1","gene_symbol":"MIR1273C","gene_name":"microRNA 1273c [Source:HGNC Symbol;Acc:HGNC:38173]","synonyms":"hsa-mir-1273c","biotype":"miRNA","ncbi_id":"100422821","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154853360,"end":154853436,"strand":1,"description":"microRNA 1273c [Source:HGNC Symbol;Acc:HGNC:38173]"}, {"versioned_ensembl_gene_id":"ENSG00000252692.1","gene_symbol":"SNORD60","gene_name":"Small nucleolar RNA SNORD60 [Source:RFAM;Acc:RF00271]","synonyms":"U60,RNU60","biotype":"snoRNA","ncbi_id":"26788","summary":null,"start":206080239,"end":206080324,"strand":1,"description":"Small nucleolar RNA SNORD60 [Source:RFAM;Acc:RF00271]"}, {"versioned_ensembl_gene_id":"ENSG00000200839.1","gene_symbol":"RNA5SP48","gene_name":"RNA, 5S ribosomal pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:42824]","synonyms":"RN5S48","biotype":"rRNA","ncbi_id":"100873287","summary":null,"start":51973410,"end":51973535,"strand":1,"description":"RNA, 5S ribosomal pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:42824]"}, {"versioned_ensembl_gene_id":"ENSG00000242170.3","gene_symbol":"RN7SL329P","gene_name":"RNA, 7SL, cytoplasmic 329, pseudogene [Source:HGNC Symbol;Acc:HGNC:46345]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479343","summary":null,"start":125270604,"end":125270902,"strand":1,"description":"RNA, 7SL, cytoplasmic 329, pseudogene [Source:HGNC Symbol;Acc:HGNC:46345]"}, {"versioned_ensembl_gene_id":"ENSG00000263669.2","gene_symbol":"RN7SL470P","gene_name":"RNA, 7SL, cytoplasmic 470, pseudogene [Source:HGNC Symbol;Acc:HGNC:46486]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479394","summary":null,"start":70075014,"end":70075272,"strand":-1,"description":"RNA, 7SL, cytoplasmic 470, pseudogene [Source:HGNC Symbol;Acc:HGNC:46486]"}, {"versioned_ensembl_gene_id":"ENSG00000199322.1","gene_symbol":"RNA5SP183","gene_name":"RNA, 5S ribosomal pseudogene 183 [Source:HGNC Symbol;Acc:HGNC:43083]","synonyms":"RN5S183","biotype":"rRNA","ncbi_id":"100873445","summary":null,"start":55777469,"end":55777587,"strand":1,"description":"RNA, 5S ribosomal pseudogene 183 [Source:HGNC Symbol;Acc:HGNC:43083]"}, {"versioned_ensembl_gene_id":"ENSG00000212365.1","gene_symbol":"RNA5SP332","gene_name":"RNA, 5S ribosomal pseudogene 332 [Source:HGNC Symbol;Acc:HGNC:43232]","synonyms":"RN5S332","biotype":"rRNA","ncbi_id":"100873598","summary":null,"start":14134986,"end":14135100,"strand":1,"description":"RNA, 5S ribosomal pseudogene 332 [Source:HGNC Symbol;Acc:HGNC:43232]"}, {"versioned_ensembl_gene_id":"ENSG00000244710.3","gene_symbol":"RN7SL47P","gene_name":"RNA, 7SL, cytoplasmic 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:46063]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479242","summary":null,"start":106283413,"end":106283711,"strand":-1,"description":"RNA, 7SL, cytoplasmic 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:46063]"}, {"versioned_ensembl_gene_id":"ENSG00000238880.1","gene_symbol":"RNU7-59P","gene_name":"RNA, U7 small nuclear 59 pseudogene [Source:HGNC Symbol;Acc:HGNC:34155]","synonyms":"U7.59","biotype":"snRNA","ncbi_id":"100151654","summary":null,"start":77566934,"end":77566994,"strand":-1,"description":"RNA, U7 small nuclear 59 pseudogene [Source:HGNC Symbol;Acc:HGNC:34155]"}, {"versioned_ensembl_gene_id":"ENSG00000278340.1","gene_symbol":"MIR6862-2","gene_name":"microRNA 6862-2 [Source:HGNC Symbol;Acc:HGNC:50192]","synonyms":"hsa-mir-6862-2","biotype":"miRNA","ncbi_id":"102465907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28724252,"end":28724321,"strand":1,"description":"microRNA 6862-2 [Source:HGNC Symbol;Acc:HGNC:50192]"}, {"versioned_ensembl_gene_id":"ENSG00000200314.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":106454828,"end":106454929,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264530.2","gene_symbol":"RN7SL25P","gene_name":"RNA, 7SL, cytoplasmic 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:46041]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479233","summary":null,"start":6542094,"end":6542353,"strand":1,"description":"RNA, 7SL, cytoplasmic 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:46041]"}, {"versioned_ensembl_gene_id":"ENSG00000201493.1","gene_symbol":"RNU1-141P","gene_name":"RNA, U1 small nuclear 141, pseudogene [Source:HGNC Symbol;Acc:HGNC:48483]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481633","summary":null,"start":218129795,"end":218129952,"strand":1,"description":"RNA, U1 small nuclear 141, pseudogene [Source:HGNC Symbol;Acc:HGNC:48483]"}, {"versioned_ensembl_gene_id":"ENSG00000252443.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"RNU108,E2,RNE2,E2-1","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":69785994,"end":69786113,"strand":-1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000241542.3","gene_symbol":"RN7SL369P","gene_name":"RNA, 7SL, cytoplasmic 369, pseudogene [Source:HGNC Symbol;Acc:HGNC:46385]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480694","summary":null,"start":67705954,"end":67706252,"strand":1,"description":"RNA, 7SL, cytoplasmic 369, pseudogene [Source:HGNC Symbol;Acc:HGNC:46385]"}, {"versioned_ensembl_gene_id":"ENSG00000212348.1","gene_symbol":"RNU6-1300P","gene_name":"RNA, U6 small nuclear 1300, pseudogene [Source:HGNC Symbol;Acc:HGNC:48263]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480134","summary":null,"start":74048677,"end":74048784,"strand":1,"description":"RNA, U6 small nuclear 1300, pseudogene [Source:HGNC Symbol;Acc:HGNC:48263]"}, {"versioned_ensembl_gene_id":"ENSG00000207935.3","gene_symbol":"MIR204","gene_name":"microRNA 204 [Source:HGNC Symbol;Acc:HGNC:31582]","synonyms":"MIRN204,hsa-mir-204","biotype":"miRNA","ncbi_id":"406987","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70809975,"end":70810084,"strand":-1,"description":"microRNA 204 [Source:HGNC Symbol;Acc:HGNC:31582]"}, {"versioned_ensembl_gene_id":"ENSG00000221269.1","gene_symbol":"MIR1302-8","gene_name":"microRNA 1302-8 [Source:HGNC Symbol;Acc:HGNC:35300]","synonyms":"MIRN1302-8,hsa-mir-1302-8","biotype":"miRNA","ncbi_id":"100302223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97363554,"end":97363681,"strand":-1,"description":"microRNA 1302-8 [Source:HGNC Symbol;Acc:HGNC:35300]"}, {"versioned_ensembl_gene_id":"ENSG00000207116.1","gene_symbol":"RNU6-31P","gene_name":"RNA, U6 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:34250]","synonyms":"RNU6-31","biotype":"snRNA","ncbi_id":"100873740","summary":null,"start":200830009,"end":200830116,"strand":1,"description":"RNA, U6 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:34250]"}, {"versioned_ensembl_gene_id":"ENSG00000238721.1","gene_symbol":"RNU7-194P","gene_name":"RNA, U7 small nuclear 194 pseudogene [Source:HGNC Symbol;Acc:HGNC:45728]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480834","summary":null,"start":150209706,"end":150209768,"strand":1,"description":"RNA, U7 small nuclear 194 pseudogene [Source:HGNC Symbol;Acc:HGNC:45728]"}, {"versioned_ensembl_gene_id":"ENSG00000207165.1","gene_symbol":"SNORA70","gene_name":"small nucleolar RNA, H/ACA box 70 [Source:HGNC Symbol;Acc:HGNC:10231]","synonyms":"RNU70,U70,DXS648E","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":154400281,"end":154400415,"strand":1,"description":"small nucleolar RNA, H/ACA box 70 [Source:HGNC Symbol;Acc:HGNC:10231]"}, {"versioned_ensembl_gene_id":"ENSG00000222859.1","gene_symbol":"RN7SKP136","gene_name":"RNA, 7SK small nuclear pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:45860]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479155","summary":null,"start":177181442,"end":177181741,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:45860]"}, {"versioned_ensembl_gene_id":"ENSG00000272055.1","gene_symbol":"RNU6-6P","gene_name":"RNA, U6 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:10228]","synonyms":"U6-6,RNU6B,RNU6-6","biotype":"snRNA","ncbi_id":"26826","summary":null,"start":13217269,"end":13217375,"strand":1,"description":"RNA, U6 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:10228]"}, {"versioned_ensembl_gene_id":"ENSG00000207138.1","gene_symbol":"RNU6-869P","gene_name":"RNA, U6 small nuclear 869, pseudogene [Source:HGNC Symbol;Acc:HGNC:47832]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480616","summary":null,"start":126504763,"end":126504869,"strand":1,"description":"RNA, U6 small nuclear 869, pseudogene [Source:HGNC Symbol;Acc:HGNC:47832]"}, {"versioned_ensembl_gene_id":"ENSG00000278712.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34,SEN34L,SEN34L,LENG5,LENG5,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000199400.1","gene_symbol":"RNY4P19","gene_name":"RNA, Ro-associated Y4 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:34069]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100169834","summary":null,"start":230058229,"end":230058324,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:34069]"}, {"versioned_ensembl_gene_id":"ENSG00000251759.1","gene_symbol":"RN7SKP298","gene_name":"RNA, 7SK small nuclear pseudogene 298 [Source:HGNC Symbol;Acc:HGNC:46022]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479228","summary":null,"start":166670029,"end":166670122,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 298 [Source:HGNC Symbol;Acc:HGNC:46022]"}, {"versioned_ensembl_gene_id":"ENSG00000251991.1","gene_symbol":"RNU7-49P","gene_name":"RNA, U7 small nuclear 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:34145]","synonyms":"U7.49","biotype":"snRNA","ncbi_id":"100147836","summary":null,"start":14478892,"end":14478953,"strand":1,"description":"RNA, U7 small nuclear 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:34145]"}, {"versioned_ensembl_gene_id":"ENSG00000277188.1","gene_symbol":"NCRUPAR_1","gene_name":"Non-protein coding RNA, upstream of F2R/PAR1 conserved region 1 [Source:RFAM;Acc:RF02154]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76712195,"end":76712327,"strand":1,"description":"Non-protein coding RNA, upstream of F2R/PAR1 conserved region 1 [Source:RFAM;Acc:RF02154]"}, {"versioned_ensembl_gene_id":"ENSG00000264879.2","gene_symbol":"RN7SL690P","gene_name":"RNA, 7SL, cytoplasmic 690, pseudogene [Source:HGNC Symbol;Acc:HGNC:46706]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479475","summary":null,"start":20316755,"end":20316994,"strand":1,"description":"RNA, 7SL, cytoplasmic 690, pseudogene [Source:HGNC Symbol;Acc:HGNC:46706]"}, {"versioned_ensembl_gene_id":"ENSG00000207705.2","gene_symbol":"MIR129-1","gene_name":"microRNA 129-1 [Source:HGNC Symbol;Acc:HGNC:31512]","synonyms":"MIRN129-1,hsa-mir-129-1","biotype":"miRNA","ncbi_id":"406917","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128207872,"end":128207943,"strand":1,"description":"microRNA 129-1 [Source:HGNC Symbol;Acc:HGNC:31512]"}, {"versioned_ensembl_gene_id":"ENSG00000201856.1","gene_symbol":"RNA5SP331","gene_name":"RNA, 5S ribosomal pseudogene 331 [Source:HGNC Symbol;Acc:HGNC:43231]","synonyms":"RN5S331","biotype":"rRNA","ncbi_id":"100873597","summary":null,"start":13907484,"end":13907590,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 331 [Source:HGNC Symbol;Acc:HGNC:43231]"}, {"versioned_ensembl_gene_id":"ENSG00000200238.1","gene_symbol":"RNA5SP133","gene_name":"RNA, 5S ribosomal pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:43033]","synonyms":"RN5S133","biotype":"rRNA","ncbi_id":"100873402","summary":null,"start":56185104,"end":56185222,"strand":1,"description":"RNA, 5S ribosomal pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:43033]"}, {"versioned_ensembl_gene_id":"ENSG00000201311.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":82307067,"end":82307168,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240905.3","gene_symbol":"RN7SL798P","gene_name":"RNA, 7SL, cytoplasmic 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:46814]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480533","summary":null,"start":55980240,"end":55980540,"strand":-1,"description":"RNA, 7SL, cytoplasmic 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:46814]"}, {"versioned_ensembl_gene_id":"ENSG00000271150.1","gene_symbol":"AC008745.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47794650,"end":47794920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274705.2","gene_symbol":"MIR486-1","gene_name":"microRNA 486-1 [Source:HGNC Symbol;Acc:HGNC:32342]","synonyms":"MIRN486,MIR486,hsa-mir-486","biotype":"miRNA","ncbi_id":"619554","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41660441,"end":41660508,"strand":-1,"description":"microRNA 486-1 [Source:HGNC Symbol;Acc:HGNC:32342]"}, {"versioned_ensembl_gene_id":"ENSG00000266320.1","gene_symbol":"MIR3909","gene_name":"microRNA 3909 [Source:HGNC Symbol;Acc:HGNC:38987]","synonyms":"hsa-mir-3909","biotype":"miRNA","ncbi_id":"100500826","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35335640,"end":35335758,"strand":1,"description":"microRNA 3909 [Source:HGNC Symbol;Acc:HGNC:38987]"}, {"versioned_ensembl_gene_id":"ENSG00000262104.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":78544095,"end":78544188,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284407.1","gene_symbol":"MIR5001","gene_name":"microRNA 5001 [Source:HGNC Symbol;Acc:HGNC:43462]","synonyms":"hsa-mir-5001","biotype":"miRNA","ncbi_id":"100847037","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":232550474,"end":232550573,"strand":-1,"description":"microRNA 5001 [Source:HGNC Symbol;Acc:HGNC:43462]"}, {"versioned_ensembl_gene_id":"ENSG00000201822.1","gene_symbol":"RNA5SP149","gene_name":"RNA, 5S ribosomal pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:43049]","synonyms":"RN5S149","biotype":"rRNA","ncbi_id":"106480437","summary":null,"start":180161886,"end":180161977,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:43049]"}, {"versioned_ensembl_gene_id":"ENSG00000277904.1","gene_symbol":"MIR7850","gene_name":"microRNA 7850 [Source:HGNC Symbol;Acc:HGNC:50118]","synonyms":"hsa-mir-7850","biotype":"miRNA","ncbi_id":"102465838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2630715,"end":2630793,"strand":1,"description":"microRNA 7850 [Source:HGNC Symbol;Acc:HGNC:50118]"}, {"versioned_ensembl_gene_id":"ENSG00000208002.1","gene_symbol":"MIR643","gene_name":"microRNA 643 [Source:HGNC Symbol;Acc:HGNC:32899]","synonyms":"MIRN643,hsa-mir-643","biotype":"miRNA","ncbi_id":"693228","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52281797,"end":52281893,"strand":1,"description":"microRNA 643 [Source:HGNC Symbol;Acc:HGNC:32899]"}, {"versioned_ensembl_gene_id":"ENSG00000244296.3","gene_symbol":"RN7SL168P","gene_name":"RNA, 7SL, cytoplasmic 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:46184]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480491","summary":null,"start":19365766,"end":19366044,"strand":1,"description":"RNA, 7SL, cytoplasmic 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:46184]"}, {"versioned_ensembl_gene_id":"ENSG00000276281.1","gene_symbol":"RN7SL126P","gene_name":"RNA, 7SL, cytoplasmic 126, pseudogene [Source:HGNC Symbol;Acc:HGNC:46142]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479268","summary":null,"start":85567662,"end":85567960,"strand":-1,"description":"RNA, 7SL, cytoplasmic 126, pseudogene [Source:HGNC Symbol;Acc:HGNC:46142]"}, {"versioned_ensembl_gene_id":"ENSG00000201428.1","gene_symbol":"RN7SKP71","gene_name":"RNA, 7SK small nuclear pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:45795]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479126","summary":null,"start":112267077,"end":112267394,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:45795]"}, {"versioned_ensembl_gene_id":"ENSG00000207390.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44697333,"end":44697430,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206747.1","gene_symbol":"RNU6-245P","gene_name":"RNA, U6 small nuclear 245, pseudogene [Source:HGNC Symbol;Acc:HGNC:47208]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481255","summary":null,"start":68539443,"end":68539549,"strand":-1,"description":"RNA, U6 small nuclear 245, pseudogene [Source:HGNC Symbol;Acc:HGNC:47208]"}, {"versioned_ensembl_gene_id":"ENSG00000199237.1","gene_symbol":"RNU6-834P","gene_name":"RNA, U6 small nuclear 834, pseudogene [Source:HGNC Symbol;Acc:HGNC:47797]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479935","summary":null,"start":49593104,"end":49593213,"strand":1,"description":"RNA, U6 small nuclear 834, pseudogene [Source:HGNC Symbol;Acc:HGNC:47797]"}, {"versioned_ensembl_gene_id":"ENSG00000238962.1","gene_symbol":"RNU7-176P","gene_name":"RNA, U7 small nuclear 176 pseudogene [Source:HGNC Symbol;Acc:HGNC:45710]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481803","summary":null,"start":10815485,"end":10815546,"strand":-1,"description":"RNA, U7 small nuclear 176 pseudogene [Source:HGNC Symbol;Acc:HGNC:45710]"}, {"versioned_ensembl_gene_id":"ENSG00000242080.1","gene_symbol":"AC008571.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152495718,"end":152496017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284219.1","gene_symbol":"MIR202","gene_name":"microRNA 202 [Source:HGNC Symbol;Acc:HGNC:32080]","synonyms":"MIRN202,hsa-mir-202","biotype":"miRNA","ncbi_id":"574448","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133247511,"end":133247620,"strand":-1,"description":"microRNA 202 [Source:HGNC Symbol;Acc:HGNC:32080]"}, {"versioned_ensembl_gene_id":"ENSG00000251964.2","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":14643787,"end":14643848,"strand":1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000252752.1","gene_symbol":"RNU6-210P","gene_name":"RNA, U6 small nuclear 210, pseudogene [Source:HGNC Symbol;Acc:HGNC:47173]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479659","summary":null,"start":93010257,"end":93010351,"strand":1,"description":"RNA, U6 small nuclear 210, pseudogene [Source:HGNC Symbol;Acc:HGNC:47173]"}, {"versioned_ensembl_gene_id":"ENSG00000274819.1","gene_symbol":"RMST_7","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 7 [Source:RFAM;Acc:RF01968]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97532691,"end":97532958,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 7 [Source:RFAM;Acc:RF01968]"}, {"versioned_ensembl_gene_id":"ENSG00000199605.1","gene_symbol":"RNY4P24","gene_name":"RNA, Ro-associated Y4 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42474]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862664","summary":null,"start":52400004,"end":52400099,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42474]"}, {"versioned_ensembl_gene_id":"ENSG00000278802.1","gene_symbol":"RMST_8","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 8 [Source:RFAM;Acc:RF01969]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97560557,"end":97560721,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 8 [Source:RFAM;Acc:RF01969]"}, {"versioned_ensembl_gene_id":"ENSG00000251943.1","gene_symbol":"RNU6-693P","gene_name":"RNA, U6 small nuclear 693, pseudogene [Source:HGNC Symbol;Acc:HGNC:47656]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481399","summary":null,"start":172613428,"end":172613534,"strand":-1,"description":"RNA, U6 small nuclear 693, pseudogene [Source:HGNC Symbol;Acc:HGNC:47656]"}, {"versioned_ensembl_gene_id":"ENSG00000277776.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NALP7,PAN7,PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54931214,"end":54955210,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000206781.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64445130,"end":64445243,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000271922.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":154329716,"end":154329819,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000275337.1","gene_symbol":"RN7SL680P","gene_name":"RNA, 7SL, cytoplasmic 680, pseudogene [Source:HGNC Symbol;Acc:HGNC:46696]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480380","summary":null,"start":39349094,"end":39349392,"strand":-1,"description":"RNA, 7SL, cytoplasmic 680, pseudogene [Source:HGNC Symbol;Acc:HGNC:46696]"}, {"versioned_ensembl_gene_id":"ENSG00000253093.1","gene_symbol":"RNA5SP179","gene_name":"RNA, 5S ribosomal pseudogene 179 [Source:HGNC Symbol;Acc:HGNC:43079]","synonyms":"RN5S179","biotype":"rRNA","ncbi_id":"100873441","summary":null,"start":16853994,"end":16854114,"strand":1,"description":"RNA, 5S ribosomal pseudogene 179 [Source:HGNC Symbol;Acc:HGNC:43079]"}, {"versioned_ensembl_gene_id":"ENSG00000239607.3","gene_symbol":"RN7SL573P","gene_name":"RNA, 7SL, cytoplasmic 573, pseudogene [Source:HGNC Symbol;Acc:HGNC:46589]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481078","summary":null,"start":75041740,"end":75042015,"strand":1,"description":"RNA, 7SL, cytoplasmic 573, pseudogene [Source:HGNC Symbol;Acc:HGNC:46589]"}, {"versioned_ensembl_gene_id":"ENSG00000206853.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":59137372,"end":59137502,"strand":-1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000273566.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":21455236,"end":21455515,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200283.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28972414,"end":28972521,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199585.1","gene_symbol":"RNA5SP119","gene_name":"RNA, 5S ribosomal pseudogene 119 [Source:HGNC Symbol;Acc:HGNC:42917]","synonyms":"RN5S119","biotype":"rRNA","ncbi_id":"100873389","summary":null,"start":211535653,"end":211535769,"strand":1,"description":"RNA, 5S ribosomal pseudogene 119 [Source:HGNC Symbol;Acc:HGNC:42917]"}, {"versioned_ensembl_gene_id":"ENSG00000222449.1","gene_symbol":"RNU6-1140P","gene_name":"RNA, U6 small nuclear 1140, pseudogene [Source:HGNC Symbol;Acc:HGNC:48103]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480068","summary":null,"start":237563165,"end":237563270,"strand":1,"description":"RNA, U6 small nuclear 1140, pseudogene [Source:HGNC Symbol;Acc:HGNC:48103]"}, {"versioned_ensembl_gene_id":"ENSG00000241082.3","gene_symbol":"RN7SL259P","gene_name":"RNA, 7SL, cytoplasmic 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:46275]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480992","summary":null,"start":62935982,"end":62936234,"strand":-1,"description":"RNA, 7SL, cytoplasmic 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:46275]"}, {"versioned_ensembl_gene_id":"ENSG00000284575.1","gene_symbol":"MIR4793","gene_name":"microRNA 4793 [Source:HGNC Symbol;Acc:HGNC:41538]","synonyms":"hsa-mir-4793","biotype":"miRNA","ncbi_id":"100616112","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48644194,"end":48644280,"strand":-1,"description":"microRNA 4793 [Source:HGNC Symbol;Acc:HGNC:41538]"}, {"versioned_ensembl_gene_id":"ENSG00000239856.3","gene_symbol":"RN7SL225P","gene_name":"RNA, 7SL, cytoplasmic 225, pseudogene [Source:HGNC Symbol;Acc:HGNC:46241]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479304","summary":null,"start":86324012,"end":86324309,"strand":-1,"description":"RNA, 7SL, cytoplasmic 225, pseudogene [Source:HGNC Symbol;Acc:HGNC:46241]"}, {"versioned_ensembl_gene_id":"ENSG00000240327.3","gene_symbol":"RN7SL93P","gene_name":"RNA, 7SL, cytoplasmic 93, pseudogene [Source:HGNC Symbol;Acc:HGNC:46109]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480947","summary":null,"start":113976341,"end":113976633,"strand":-1,"description":"RNA, 7SL, cytoplasmic 93, pseudogene [Source:HGNC Symbol;Acc:HGNC:46109]"}, {"versioned_ensembl_gene_id":"ENSG00000222222.1","gene_symbol":"RNU2-17P","gene_name":"RNA, U2 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48510]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480204","summary":null,"start":150236967,"end":150237156,"strand":1,"description":"RNA, U2 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48510]"}, {"versioned_ensembl_gene_id":"ENSG00000206730.1","gene_symbol":"RNU6-468P","gene_name":"RNA, U6 small nuclear 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:47431]","synonyms":null,"biotype":"snRNA","ncbi_id":"106865374","summary":null,"start":17578631,"end":17578739,"strand":1,"description":"RNA, U6 small nuclear 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:47431]"}, {"versioned_ensembl_gene_id":"ENSG00000275067.1","gene_symbol":"MIR6825","gene_name":"microRNA 6825 [Source:HGNC Symbol;Acc:HGNC:50208]","synonyms":"hsa-mir-6825","biotype":"miRNA","ncbi_id":"102466199","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127575266,"end":127575331,"strand":-1,"description":"microRNA 6825 [Source:HGNC Symbol;Acc:HGNC:50208]"}, {"versioned_ensembl_gene_id":"ENSG00000274816.1","gene_symbol":"MIR6772","gene_name":"microRNA 6772 [Source:HGNC Symbol;Acc:HGNC:50064]","synonyms":"hsa-mir-6772","biotype":"miRNA","ncbi_id":"102465463","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57772289,"end":57772352,"strand":-1,"description":"microRNA 6772 [Source:HGNC Symbol;Acc:HGNC:50064]"}, {"versioned_ensembl_gene_id":"ENSG00000266107.1","gene_symbol":"MIR4525","gene_name":"microRNA 4525 [Source:HGNC Symbol;Acc:HGNC:41903]","synonyms":"hsa-mir-4525","biotype":"miRNA","ncbi_id":"100616196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82668233,"end":82668307,"strand":-1,"description":"microRNA 4525 [Source:HGNC Symbol;Acc:HGNC:41903]"}, {"versioned_ensembl_gene_id":"ENSG00000238830.1","gene_symbol":"RNU7-46P","gene_name":"RNA, U7 small nuclear 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:34142]","synonyms":"U7.46","biotype":"snRNA","ncbi_id":"100147833","summary":null,"start":98840675,"end":98840736,"strand":-1,"description":"RNA, U7 small nuclear 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:34142]"}, {"versioned_ensembl_gene_id":"ENSG00000207456.1","gene_symbol":"RNU6-997P","gene_name":"RNA, U6 small nuclear 997, pseudogene [Source:HGNC Symbol;Acc:HGNC:47960]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480007","summary":null,"start":53570374,"end":53570480,"strand":-1,"description":"RNA, U6 small nuclear 997, pseudogene [Source:HGNC Symbol;Acc:HGNC:47960]"}, {"versioned_ensembl_gene_id":"ENSG00000244256.3","gene_symbol":"RN7SL130P","gene_name":"RNA, 7SL, cytoplasmic 130, pseudogene [Source:HGNC Symbol;Acc:HGNC:46146]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479269","summary":null,"start":63655743,"end":63656047,"strand":1,"description":"RNA, 7SL, cytoplasmic 130, pseudogene [Source:HGNC Symbol;Acc:HGNC:46146]"}, {"versioned_ensembl_gene_id":"ENSG00000202206.1","gene_symbol":"RNU6-169P","gene_name":"RNA, U6 small nuclear 169, pseudogene [Source:HGNC Symbol;Acc:HGNC:47132]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481229","summary":null,"start":195514036,"end":195514142,"strand":1,"description":"RNA, U6 small nuclear 169, pseudogene [Source:HGNC Symbol;Acc:HGNC:47132]"}, {"versioned_ensembl_gene_id":"ENSG00000265145.1","gene_symbol":"SNORD53","gene_name":"small nucleolar RNA, C/D box 53 [Source:HGNC Symbol;Acc:HGNC:10203]","synonyms":"U53,SNORD53A,RNU53","biotype":"snoRNA","ncbi_id":"26796","summary":null,"start":28927067,"end":28927144,"strand":1,"description":"small nucleolar RNA, C/D box 53 [Source:HGNC Symbol;Acc:HGNC:10203]"}, {"versioned_ensembl_gene_id":"ENSG00000200331.1","gene_symbol":"RNU6-183P","gene_name":"RNA, U6 small nuclear 183, pseudogene [Source:HGNC Symbol;Acc:HGNC:47146]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481234","summary":null,"start":78314916,"end":78315025,"strand":-1,"description":"RNA, U6 small nuclear 183, pseudogene [Source:HGNC Symbol;Acc:HGNC:47146]"}, {"versioned_ensembl_gene_id":"ENSG00000200711.1","gene_symbol":"RNA5SP28","gene_name":"RNA, 5S ribosomal pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42604]","synonyms":"RN5S28","biotype":"rRNA","ncbi_id":"100873360","summary":null,"start":50812988,"end":50813106,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42604]"}, {"versioned_ensembl_gene_id":"ENSG00000265368.1","gene_symbol":"MIR4476","gene_name":"microRNA 4476 [Source:HGNC Symbol;Acc:HGNC:41793]","synonyms":"hsa-mir-4476","biotype":"miRNA","ncbi_id":"100616456","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36893462,"end":36893531,"strand":-1,"description":"microRNA 4476 [Source:HGNC Symbol;Acc:HGNC:41793]"}, {"versioned_ensembl_gene_id":"ENSG00000215939.3","gene_symbol":"MIR873","gene_name":"microRNA 873 [Source:HGNC Symbol;Acc:HGNC:33663]","synonyms":"MIRN873,hsa-mir-873","biotype":"miRNA","ncbi_id":"100126316","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28888879,"end":28888955,"strand":-1,"description":"microRNA 873 [Source:HGNC Symbol;Acc:HGNC:33663]"}, {"versioned_ensembl_gene_id":"ENSG00000274051.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76721216,"end":76721396,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000212551.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":32081764,"end":32081973,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000250751.1","gene_symbol":"AC015795.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49708334,"end":49720060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206804.1","gene_symbol":"RNU6-1293P","gene_name":"RNA, U6 small nuclear 1293, pseudogene [Source:HGNC Symbol;Acc:HGNC:48256]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480130","summary":null,"start":64880369,"end":64880475,"strand":-1,"description":"RNA, U6 small nuclear 1293, pseudogene [Source:HGNC Symbol;Acc:HGNC:48256]"}, {"versioned_ensembl_gene_id":"ENSG00000283506.1","gene_symbol":"MIR7157","gene_name":"microRNA 7157 [Source:HGNC Symbol;Acc:HGNC:50010]","synonyms":"hsa-mir-7157","biotype":"miRNA","ncbi_id":"102465692","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140586626,"end":140586685,"strand":-1,"description":"microRNA 7157 [Source:HGNC Symbol;Acc:HGNC:50010]"}, {"versioned_ensembl_gene_id":"ENSG00000251870.1","gene_symbol":"RNU2-69P","gene_name":"RNA, U2 small nuclear 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:48562]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481656","summary":null,"start":58926197,"end":58926296,"strand":-1,"description":"RNA, U2 small nuclear 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:48562]"}, {"versioned_ensembl_gene_id":"ENSG00000265134.1","gene_symbol":"MIR3190","gene_name":"microRNA 3190 [Source:HGNC Symbol;Acc:HGNC:38190]","synonyms":"hsa-mir-3190","biotype":"miRNA","ncbi_id":"100422899","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47226942,"end":47227021,"strand":1,"description":"microRNA 3190 [Source:HGNC Symbol;Acc:HGNC:38190]"}, {"versioned_ensembl_gene_id":"ENSG00000252716.1","gene_symbol":"RN7SKP260","gene_name":"RNA, 7SK small nuclear pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:45984]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479211","summary":null,"start":206260066,"end":206260214,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:45984]"}, {"versioned_ensembl_gene_id":"ENSG00000199870.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75353885,"end":75353986,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239744.3","gene_symbol":"RN7SL63P","gene_name":"RNA, 7SL, cytoplasmic 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:46079]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480939","summary":null,"start":30555601,"end":30555904,"strand":-1,"description":"RNA, 7SL, cytoplasmic 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:46079]"}, {"versioned_ensembl_gene_id":"ENSG00000274544.1","gene_symbol":"SNORD28","gene_name":"small nucleolar RNA, C/D box 28 [Source:HGNC Symbol;Acc:HGNC:10150]","synonyms":"U28,SNORD28A,RNU28","biotype":"snoRNA","ncbi_id":"9300","summary":null,"start":62854621,"end":62854695,"strand":-1,"description":"small nucleolar RNA, C/D box 28 [Source:HGNC Symbol;Acc:HGNC:10150]"}, {"versioned_ensembl_gene_id":"ENSG00000275287.5","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":388100,"end":388389,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200146.1","gene_symbol":"RNU6-544P","gene_name":"RNA, U6 small nuclear 544, pseudogene [Source:HGNC Symbol;Acc:HGNC:47507]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481353","summary":null,"start":80527960,"end":80528066,"strand":1,"description":"RNA, U6 small nuclear 544, pseudogene [Source:HGNC Symbol;Acc:HGNC:47507]"}, {"versioned_ensembl_gene_id":"ENSG00000275359.1","gene_symbol":"ST7-AS1_1","gene_name":"ST7 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02179]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116952698,"end":116952813,"strand":1,"description":"ST7 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02179]"}, {"versioned_ensembl_gene_id":"ENSG00000277912.1","gene_symbol":"MIR8089","gene_name":"microRNA 8089 [Source:HGNC Symbol;Acc:HGNC:50196]","synonyms":"hsa-mir-8089","biotype":"miRNA","ncbi_id":"102465882","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":181043403,"end":181043484,"strand":-1,"description":"microRNA 8089 [Source:HGNC Symbol;Acc:HGNC:50196]"}, {"versioned_ensembl_gene_id":"ENSG00000265699.1","gene_symbol":"MIR548AE2","gene_name":"microRNA 548ae-2 [Source:HGNC Symbol;Acc:HGNC:41831]","synonyms":"hsa-mir-548ae-2","biotype":"miRNA","ncbi_id":"100616339","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58530043,"end":58530109,"strand":-1,"description":"microRNA 548ae-2 [Source:HGNC Symbol;Acc:HGNC:41831]"}, {"versioned_ensembl_gene_id":"ENSG00000264024.2","gene_symbol":"MIR4507","gene_name":"microRNA 4507 [Source:HGNC Symbol;Acc:HGNC:41642]","synonyms":"hsa-mir-4507","biotype":"miRNA","ncbi_id":"100616135","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105858124,"end":105858175,"strand":-1,"description":"microRNA 4507 [Source:HGNC Symbol;Acc:HGNC:41642]"}, {"versioned_ensembl_gene_id":"ENSG00000249881.1","gene_symbol":"AC008696.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":143605628,"end":143828772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252867.1","gene_symbol":"RNU6-909P","gene_name":"RNA, U6 small nuclear 909, pseudogene [Source:HGNC Symbol;Acc:HGNC:47872]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481466","summary":null,"start":28624657,"end":28624763,"strand":1,"description":"RNA, U6 small nuclear 909, pseudogene [Source:HGNC Symbol;Acc:HGNC:47872]"}, {"versioned_ensembl_gene_id":"ENSG00000264602.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30922178,"end":30922269,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222266.1","gene_symbol":"RNU6-757P","gene_name":"RNA, U6 small nuclear 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:47720]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479901","summary":null,"start":134715483,"end":134715582,"strand":1,"description":"RNA, U6 small nuclear 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:47720]"}, {"versioned_ensembl_gene_id":"ENSG00000275881.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62393607,"end":62393880,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266890.1","gene_symbol":"MIR4634","gene_name":"microRNA 4634 [Source:HGNC Symbol;Acc:HGNC:41559]","synonyms":"hsa-mir-4634","biotype":"miRNA","ncbi_id":"100616202","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":174751734,"end":174751787,"strand":1,"description":"microRNA 4634 [Source:HGNC Symbol;Acc:HGNC:41559]"}, {"versioned_ensembl_gene_id":"ENSG00000207207.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85434507,"end":85434619,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263390.1","gene_symbol":"hsa-mir-3119-1","gene_name":"hsa-mir-3119-1 [Source:miRBase;Acc:MI0014134]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":170151378,"end":170151462,"strand":1,"description":"hsa-mir-3119-1 [Source:miRBase;Acc:MI0014134]"}, {"versioned_ensembl_gene_id":"ENSG00000252919.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49592236,"end":49592337,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277217.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":129170092,"end":129170238,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000253056.1","gene_symbol":"RNU7-128P","gene_name":"RNA, U7 small nuclear 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:45662]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480819","summary":null,"start":48180328,"end":48180389,"strand":1,"description":"RNA, U7 small nuclear 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:45662]"}, {"versioned_ensembl_gene_id":"ENSG00000277515.1","gene_symbol":"RN7SL495P","gene_name":"RNA, 7SL, cytoplasmic 495, pseudogene [Source:HGNC Symbol;Acc:HGNC:46511]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479404","summary":null,"start":22609141,"end":22609377,"strand":-1,"description":"RNA, 7SL, cytoplasmic 495, pseudogene [Source:HGNC Symbol;Acc:HGNC:46511]"}, {"versioned_ensembl_gene_id":"ENSG00000265013.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29582051,"end":29582134,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000277980.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30825003,"end":30825096,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200090.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47726894,"end":47726992,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199751.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":71491066,"end":71491167,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221081.1","gene_symbol":"MIR320D2","gene_name":"microRNA 320d-2 [Source:HGNC Symbol;Acc:HGNC:35388]","synonyms":"MIRN320D2,hsa-mir-320d-2","biotype":"miRNA","ncbi_id":"100302169","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140926172,"end":140926219,"strand":-1,"description":"microRNA 320d-2 [Source:HGNC Symbol;Acc:HGNC:35388]"}, {"versioned_ensembl_gene_id":"ENSG00000284231.1","gene_symbol":"MIR424","gene_name":"microRNA 424 [Source:HGNC Symbol;Acc:HGNC:31881]","synonyms":"MIRN424,hsa-mir-424","biotype":"miRNA","ncbi_id":"494336","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134546614,"end":134546711,"strand":-1,"description":"microRNA 424 [Source:HGNC Symbol;Acc:HGNC:31881]"}, {"versioned_ensembl_gene_id":"ENSG00000239517.1","gene_symbol":"AC116337.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74931662,"end":74931817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249343.1","gene_symbol":"LINC01333","gene_name":"long intergenic non-protein coding RNA 1333 [Source:HGNC Symbol;Acc:HGNC:50539]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929082","summary":null,"start":74322486,"end":74328297,"strand":1,"description":"long intergenic non-protein coding RNA 1333 [Source:HGNC Symbol;Acc:HGNC:50539]"}, {"versioned_ensembl_gene_id":"ENSG00000280924.1","gene_symbol":"LINC00628","gene_name":"long intergenic non-protein coding RNA 628 [Source:HGNC Symbol;Acc:HGNC:27008]","synonyms":null,"biotype":"lincRNA","ncbi_id":"127841","summary":null,"start":204368431,"end":204369719,"strand":-1,"description":"long intergenic non-protein coding RNA 628 [Source:HGNC Symbol;Acc:HGNC:27008]"}, {"versioned_ensembl_gene_id":"ENSG00000268364.1","gene_symbol":"SMC5-AS1","gene_name":"SMC5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48718]","synonyms":"MAMDC2-AS2","biotype":"antisense_RNA","ncbi_id":"100507299","summary":null,"start":70193997,"end":70258866,"strand":-1,"description":"SMC5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48718]"}, {"versioned_ensembl_gene_id":"ENSG00000165525.17","gene_symbol":"NEMF","gene_name":"nuclear export mediator factor [Source:HGNC Symbol;Acc:HGNC:10663]","synonyms":"SDCCAG1,NY-CO-1,FLJ10051","biotype":"protein_coding","ncbi_id":"9147","summary":"This gene encodes a component of the ribosome quality control complex. The encoded protein facilitates the recognition and ubiquitination of stalled 60S subunits by the ubiquitin ligase listerin. A similar protein in fly functions as a tumor suppressor. [provided by RefSeq, Jul 2016]","start":49782083,"end":49853203,"strand":-1,"description":"nuclear export mediator factor [Source:HGNC Symbol;Acc:HGNC:10663]"}, {"versioned_ensembl_gene_id":"ENSG00000165516.10","gene_symbol":"KLHDC2","gene_name":"kelch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20231]","synonyms":"LCP,HCLP-1","biotype":"protein_coding","ncbi_id":"23588","summary":null,"start":49767608,"end":49786385,"strand":1,"description":"kelch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20231]"}, {"versioned_ensembl_gene_id":"ENSG00000258560.1","gene_symbol":"AL157912.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100052803,"end":100074878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266497.1","gene_symbol":"AC138645.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46503946,"end":46509339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176087.14","gene_symbol":"SLC35A4","gene_name":"solute carrier family 35 member A4 [Source:HGNC Symbol;Acc:HGNC:20753]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113829","summary":null,"start":140564456,"end":140569103,"strand":1,"description":"solute carrier family 35 member A4 [Source:HGNC Symbol;Acc:HGNC:20753]"}, {"versioned_ensembl_gene_id":"ENSG00000113108.19","gene_symbol":"APBB3","gene_name":"amyloid beta precursor protein binding family B member 3 [Source:HGNC Symbol;Acc:HGNC:20708]","synonyms":"FE65L2","biotype":"protein_coding","ncbi_id":"10307","summary":"The protein encoded by this gene is a member of the APBB protein family. It is found in the cytoplasm and binds to the intracellular domain of the Alzheimer's disease beta-amyloid precursor protein (APP) as well as to other APP-like proteins. It is thought that the protein encoded by this gene may modulate the internalization of APP. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":140558268,"end":140564781,"strand":-1,"description":"amyloid beta precursor protein binding family B member 3 [Source:HGNC Symbol;Acc:HGNC:20708]"}, {"versioned_ensembl_gene_id":"ENSG00000271198.1","gene_symbol":"VDAC3P1","gene_name":"voltage dependent anion channel 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20722]","synonyms":"VDAC3P","biotype":"processed_pseudogene","ncbi_id":"341965","summary":null,"start":99964529,"end":99965378,"strand":1,"description":"voltage dependent anion channel 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20722]"}, {"versioned_ensembl_gene_id":"ENSG00000267750.5","gene_symbol":"RUNDC3A-AS1","gene_name":"RUNDC3A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51344]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926996","summary":null,"start":44299574,"end":44315315,"strand":-1,"description":"RUNDC3A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51344]"}, {"versioned_ensembl_gene_id":"ENSG00000162736.15","gene_symbol":"NCSTN","gene_name":"nicastrin [Source:HGNC Symbol;Acc:HGNC:17091]","synonyms":"KIAA0253,APH2","biotype":"protein_coding","ncbi_id":"23385","summary":"This gene encodes a type I transmembrane glycoprotein that is an integral component of the multimeric gamma-secretase complex. The encoded protein cleaves integral membrane proteins, including Notch receptors and beta-amyloid precursor protein, and may be a stabilizing cofactor required for gamma-secretase complex assembly. The cleavage of beta-amyloid precursor protein yields amyloid beta peptide, the main component of the neuritic plaque and the hallmark lesion in the brains of patients with Alzheimer's disease; however, the nature of the encoded protein's role in Alzheimer's disease is not known for certain. Mutations in this gene are associated with familial acne inversa. A pseudogene of this gene is present on chromosome 21. Alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Feb 2014]","start":160343272,"end":160358952,"strand":1,"description":"nicastrin [Source:HGNC Symbol;Acc:HGNC:17091]"}, {"versioned_ensembl_gene_id":"ENSG00000258297.1","gene_symbol":"AP001157.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66666036,"end":66668374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182004.12","gene_symbol":"SNRPE","gene_name":"small nuclear ribonucleoprotein polypeptide E [Source:HGNC Symbol;Acc:HGNC:11161]","synonyms":"Sm-E","biotype":"protein_coding","ncbi_id":"6635","summary":"The protein encoded by this gene is a core component of U small nuclear ribonucleoproteins, which are key components of the pre-mRNA processing spliceosome. The encoded protein plays a role in the 3' end processing of histone transcripts. This protein is one of the targets in the autoimmune disease systemic lupus erythematosus, and mutations in this gene have been associated with hypotrichosis. Several pseudogenes of this gene have been identified. [provided by RefSeq, Jun 2016]","start":203861603,"end":203870550,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide E [Source:HGNC Symbol;Acc:HGNC:11161]"}, {"versioned_ensembl_gene_id":"ENSG00000229832.1","gene_symbol":"AL360091.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":212357418,"end":212358353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173933.19","gene_symbol":"RBM4","gene_name":"RNA binding motif protein 4 [Source:HGNC Symbol;Acc:HGNC:9901]","synonyms":"ZCCHC21,RBM4A,LARK,ZCRB3A","biotype":"protein_coding","ncbi_id":"5936","summary":null,"start":66638617,"end":66666682,"strand":1,"description":"RNA binding motif protein 4 [Source:HGNC Symbol;Acc:HGNC:9901]"}, {"versioned_ensembl_gene_id":"ENSG00000251556.1","gene_symbol":"AC091887.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146099406,"end":146120412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141522.11","gene_symbol":"ARHGDIA","gene_name":"Rho GDP dissociation inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:678]","synonyms":"RHOGDI,GDIA1","biotype":"protein_coding","ncbi_id":"396","summary":"This gene encodes a protein that plays a key role in the regulation of signaling through Rho GTPases. The encoded protein inhibits the disassociation of Rho family members from GDP (guanine diphosphate), thereby maintaining these factors in an inactive state. Activity of this protein is important in a variety of cellular processes, and expression of this gene may be altered in tumors. Mutations in this gene have been found in individuals with nephrotic syndrome, type 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":81867721,"end":81871406,"strand":-1,"description":"Rho GDP dissociation inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:678]"}, {"versioned_ensembl_gene_id":"ENSG00000248125.1","gene_symbol":"AC008700.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145429868,"end":145451099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119139.17","gene_symbol":"TJP2","gene_name":"tight junction protein 2 [Source:HGNC Symbol;Acc:HGNC:11828]","synonyms":"ZO2,ZO-2,X104,DFNA51","biotype":"protein_coding","ncbi_id":"9414","summary":"This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":69121264,"end":69255208,"strand":1,"description":"tight junction protein 2 [Source:HGNC Symbol;Acc:HGNC:11828]"}, {"versioned_ensembl_gene_id":"ENSG00000258750.2","gene_symbol":"AL358335.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48398310,"end":48399375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250692.1","gene_symbol":"AC008667.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139848290,"end":139856389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259117.1","gene_symbol":"AL121576.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47801926,"end":47802201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259129.5","gene_symbol":"LINC00648","gene_name":"long intergenic non-protein coding RNA 648 [Source:HGNC Symbol;Acc:HGNC:44302]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506433","summary":null,"start":47764954,"end":47795092,"strand":-1,"description":"long intergenic non-protein coding RNA 648 [Source:HGNC Symbol;Acc:HGNC:44302]"}, {"versioned_ensembl_gene_id":"ENSG00000162735.18","gene_symbol":"PEX19","gene_name":"peroxisomal biogenesis factor 19 [Source:HGNC Symbol;Acc:HGNC:9713]","synonyms":"PXMP1,PXF,PMPI,PMP1,HK33,D1S2223E","biotype":"protein_coding","ncbi_id":"5824","summary":"This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":160276812,"end":160286348,"strand":-1,"description":"peroxisomal biogenesis factor 19 [Source:HGNC Symbol;Acc:HGNC:9713]"}, {"versioned_ensembl_gene_id":"ENSG00000232002.1","gene_symbol":"LINC01880","gene_name":"long intergenic non-protein coding RNA 1880 [Source:HGNC Symbol;Acc:HGNC:52699]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373979","summary":null,"start":242047695,"end":242084138,"strand":-1,"description":"long intergenic non-protein coding RNA 1880 [Source:HGNC Symbol;Acc:HGNC:52699]"}, {"versioned_ensembl_gene_id":"ENSG00000220537.1","gene_symbol":"AL121977.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82263996,"end":82264974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247828.7","gene_symbol":"TMEM161B-AS1","gene_name":"TMEM161B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43839]","synonyms":"linc-POLR3G-8","biotype":"antisense_RNA","ncbi_id":"100505894","summary":null,"start":88268895,"end":88436685,"strand":1,"description":"TMEM161B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43839]"}, {"versioned_ensembl_gene_id":"ENSG00000214401.4","gene_symbol":"KANSL1-AS1","gene_name":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644246","summary":null,"start":46193576,"end":46196723,"strand":1,"description":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]"}, {"versioned_ensembl_gene_id":"ENSG00000262372.1","gene_symbol":"CR936218.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46035313,"end":46035770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262772.1","gene_symbol":"LINC01977","gene_name":"long intergenic non-protein coding RNA 1977 [Source:HGNC Symbol;Acc:HGNC:52804]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371919","summary":null,"start":79823452,"end":79827704,"strand":1,"description":"long intergenic non-protein coding RNA 1977 [Source:HGNC Symbol;Acc:HGNC:52804]"}, {"versioned_ensembl_gene_id":"ENSG00000259717.1","gene_symbol":"LINC00677","gene_name":"long intergenic non-protein coding RNA 677 [Source:HGNC Symbol;Acc:HGNC:20121]","synonyms":"C14orf74","biotype":"lincRNA","ncbi_id":"105370683","summary":null,"start":103120847,"end":103123007,"strand":-1,"description":"long intergenic non-protein coding RNA 677 [Source:HGNC Symbol;Acc:HGNC:20121]"}, {"versioned_ensembl_gene_id":"ENSG00000273645.2","gene_symbol":"KBTBD11","gene_name":"kelch repeat and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:29104]","synonyms":"KLHDC7C,KIAA0711","biotype":"protein_coding","ncbi_id":"9920","summary":null,"start":1973878,"end":2006936,"strand":1,"description":"kelch repeat and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:29104]"}, {"versioned_ensembl_gene_id":"ENSG00000139970.16","gene_symbol":"RTN1","gene_name":"reticulon 1 [Source:HGNC Symbol;Acc:HGNC:10467]","synonyms":"NSP","biotype":"protein_coding","ncbi_id":"6252","summary":"This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. This gene is considered to be a specific marker for neurological diseases and cancer, and is a potential molecular target for therapy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2011]","start":59595976,"end":59870966,"strand":-1,"description":"reticulon 1 [Source:HGNC Symbol;Acc:HGNC:10467]"}, {"versioned_ensembl_gene_id":"ENSG00000225014.1","gene_symbol":"KCTD9P1","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21428]","synonyms":"HsT38306","biotype":"transcribed_processed_pseudogene","ncbi_id":"100422273","summary":null,"start":20111824,"end":20112990,"strand":1,"description":"potassium channel tetramerization domain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21428]"}, {"versioned_ensembl_gene_id":"ENSG00000283769.1","gene_symbol":"CR392000.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136263925,"end":136267237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064195.7","gene_symbol":"DLX3","gene_name":"distal-less homeobox 3 [Source:HGNC Symbol;Acc:HGNC:2916]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1747","summary":"Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism. [provided by RefSeq, Jul 2008]","start":49990005,"end":49995224,"strand":-1,"description":"distal-less homeobox 3 [Source:HGNC Symbol;Acc:HGNC:2916]"}, {"versioned_ensembl_gene_id":"ENSG00000227455.2","gene_symbol":"AL450345.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164827750,"end":164831630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156453.13","gene_symbol":"PCDH1","gene_name":"protocadherin 1 [Source:HGNC Symbol;Acc:HGNC:8655]","synonyms":"pc42","biotype":"protein_coding","ncbi_id":"5097","summary":"This gene belongs to the protocadherin subfamily within the cadherin superfamily. The encoded protein is a membrane protein found at cell-cell boundaries. It is involved in neural cell adhesion, suggesting a possible role in neuronal development. The protein includes an extracelllular region, containing 7 cadherin-like domains, a transmembrane region and a C-terminal cytoplasmic region. Cells expressing the protein showed cell aggregation activity. Alternative splicing occurs in this gene. [provided by RefSeq, Jul 2008]","start":141853111,"end":141879246,"strand":-1,"description":"protocadherin 1 [Source:HGNC Symbol;Acc:HGNC:8655]"}, {"versioned_ensembl_gene_id":"ENSG00000250882.1","gene_symbol":"AC010261.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112173570,"end":112175548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239481.1","gene_symbol":"RPS3AP41","gene_name":"ribosomal protein S3a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:37000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271595","summary":null,"start":71669520,"end":71670297,"strand":1,"description":"ribosomal protein S3a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:37000]"}, {"versioned_ensembl_gene_id":"ENSG00000254892.1","gene_symbol":"AP003396.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119403963,"end":119404227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254740.2","gene_symbol":"AP003396.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119372706,"end":119381613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108219.14","gene_symbol":"TSPAN14","gene_name":"tetraspanin 14 [Source:HGNC Symbol;Acc:HGNC:23303]","synonyms":"TM4SF14,MGC11352,DC-TM4F2","biotype":"protein_coding","ncbi_id":"81619","summary":null,"start":80454166,"end":80533123,"strand":1,"description":"tetraspanin 14 [Source:HGNC Symbol;Acc:HGNC:23303]"}, {"versioned_ensembl_gene_id":"ENSG00000100767.15","gene_symbol":"PAPLN","gene_name":"papilin, proteoglycan like sulfated glycoprotein [Source:HGNC Symbol;Acc:HGNC:19262]","synonyms":"MGC50452","biotype":"protein_coding","ncbi_id":"89932","summary":null,"start":73237497,"end":73274640,"strand":1,"description":"papilin, proteoglycan like sulfated glycoprotein [Source:HGNC Symbol;Acc:HGNC:19262]"}, {"versioned_ensembl_gene_id":"ENSG00000258944.1","gene_symbol":"AC004846.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73272182,"end":73274081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217195.1","gene_symbol":"AL513475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144706733,"end":144707047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055208.18","gene_symbol":"TAB2","gene_name":"TGF-beta activated kinase 1/MAP3K7 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17075]","synonyms":"MAP3K7IP2,KIAA0733","biotype":"protein_coding","ncbi_id":"23118","summary":"The protein encoded by this gene is an activator of MAP3K7/TAK1, which is required for for the IL-1 induced activation of nuclear factor kappaB and MAPK8/JNK. This protein forms a kinase complex with TRAF6, MAP3K7 and TAB1, and it thus serves as an adaptor that links MAP3K7 and TRAF6. This protein, along with TAB1 and MAP3K7, also participates in the signal transduction induced by TNFSF11/RANKl through the activation of the receptor activator of NF-kappaB (TNFRSF11A/RANK), which may regulate the development and function of osteoclasts. Studies of the related mouse protein indicate that it functions to protect against liver damage caused by chemical stressors. Mutations in this gene cause congenital heart defects, multiple types, 2 (CHTD2). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":149218641,"end":149411613,"strand":1,"description":"TGF-beta activated kinase 1/MAP3K7 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17075]"}, {"versioned_ensembl_gene_id":"ENSG00000149150.8","gene_symbol":"SLC43A1","gene_name":"solute carrier family 43 member 1 [Source:HGNC Symbol;Acc:HGNC:9225]","synonyms":"POV1,PB39,R00504","biotype":"protein_coding","ncbi_id":"8501","summary":"SLC43A1 belongs to the system L family of plasma membrane carrier proteins that transports large neutral amino acids (Babu et al., 2003 [PubMed 12930836]).[supplied by OMIM, Mar 2008]","start":57484534,"end":57515786,"strand":-1,"description":"solute carrier family 43 member 1 [Source:HGNC Symbol;Acc:HGNC:9225]"}, {"versioned_ensembl_gene_id":"ENSG00000071246.10","gene_symbol":"VASH1","gene_name":"vasohibin 1 [Source:HGNC Symbol;Acc:HGNC:19964]","synonyms":"KIAA1036","biotype":"protein_coding","ncbi_id":"22846","summary":null,"start":76762189,"end":76783015,"strand":1,"description":"vasohibin 1 [Source:HGNC Symbol;Acc:HGNC:19964]"}, {"versioned_ensembl_gene_id":"ENSG00000258610.1","gene_symbol":"AF111169.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76778952,"end":76782249,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230666.5","gene_symbol":"CEACAM22P","gene_name":"carcinoembryonic antigen related cell adhesion molecule 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:38029]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388550","summary":null,"start":44537058,"end":44620821,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:38029]"}, {"versioned_ensembl_gene_id":"ENSG00000040933.15","gene_symbol":"INPP4A","gene_name":"inositol polyphosphate-4-phosphatase type I A [Source:HGNC Symbol;Acc:HGNC:6074]","synonyms":"INPP4","biotype":"protein_coding","ncbi_id":"3631","summary":"This gene encodes an Mg++ independent enzyme that hydrolyzes the 4-position phosphate from the inositol ring of phosphatidylinositol 3,4-bisphosphate, inositol 1,3,4-trisphosphate, and inositol 3,4-bisphosphate. Multiple transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Aug 2008]","start":98444854,"end":98594390,"strand":1,"description":"inositol polyphosphate-4-phosphatase type I A [Source:HGNC Symbol;Acc:HGNC:6074]"}, {"versioned_ensembl_gene_id":"ENSG00000250921.1","gene_symbol":"LINC02063","gene_name":"long intergenic non-protein coding RNA 2063 [Source:HGNC Symbol;Acc:HGNC:52908]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374627","summary":null,"start":4135682,"end":4143648,"strand":1,"description":"long intergenic non-protein coding RNA 2063 [Source:HGNC Symbol;Acc:HGNC:52908]"}, {"versioned_ensembl_gene_id":"ENSG00000260763.1","gene_symbol":"AC106799.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4436850,"end":4440259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254417.1","gene_symbol":"ANO1-AS2","gene_name":"ANO1 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:33275]","synonyms":"NCRNA00224,C11orf78","biotype":"antisense_RNA","ncbi_id":"100009613","summary":null,"start":70072434,"end":70075433,"strand":-1,"description":"ANO1 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:33275]"}, {"versioned_ensembl_gene_id":"ENSG00000228982.1","gene_symbol":"AL627095.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":247085389,"end":247086067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261382.1","gene_symbol":"AC091962.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153901459,"end":153903223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135740.16","gene_symbol":"SLC9A5","gene_name":"solute carrier family 9 member A5 [Source:HGNC Symbol;Acc:HGNC:11078]","synonyms":"NHE5","biotype":"protein_coding","ncbi_id":"6553","summary":null,"start":67237683,"end":67272190,"strand":1,"description":"solute carrier family 9 member A5 [Source:HGNC Symbol;Acc:HGNC:11078]"}, {"versioned_ensembl_gene_id":"ENSG00000105605.7","gene_symbol":"CACNG7","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 7 [Source:HGNC Symbol;Acc:HGNC:13626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59284","summary":"The protein encoded by this gene is a type II transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type I TARP and a calcium channel gamma subunit. [provided by RefSeq, Dec 2010]","start":53909335,"end":53943941,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 7 [Source:HGNC Symbol;Acc:HGNC:13626]"}, {"versioned_ensembl_gene_id":"ENSG00000235397.1","gene_symbol":"EPN2-AS1","gene_name":"EPN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40849]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874018","summary":null,"start":19296596,"end":19306261,"strand":-1,"description":"EPN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40849]"}, {"versioned_ensembl_gene_id":"ENSG00000234575.1","gene_symbol":"CTSLP8","gene_name":"cathepsin L pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39084]","synonyms":"CTSL1P8","biotype":"unprocessed_pseudogene","ncbi_id":"1518","summary":null,"start":87844152,"end":87847314,"strand":1,"description":"cathepsin L pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39084]"}, {"versioned_ensembl_gene_id":"ENSG00000260482.3","gene_symbol":"AC008870.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":23670011,"end":23675499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249478.1","gene_symbol":"AC010307.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133243764,"end":133248781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226089.2","gene_symbol":"AL122017.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":81527102,"end":81534915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250409.1","gene_symbol":"AC010608.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133387773,"end":133388549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112297.14","gene_symbol":"CRYBG1","gene_name":"crystallin beta-gamma domain containing 1 [Source:HGNC Symbol;Acc:HGNC:356]","synonyms":"ST4,AIM1","biotype":"protein_coding","ncbi_id":"202","summary":null,"start":106360808,"end":106571978,"strand":1,"description":"crystallin beta-gamma domain containing 1 [Source:HGNC Symbol;Acc:HGNC:356]"}, {"versioned_ensembl_gene_id":"ENSG00000166847.9","gene_symbol":"DCTN5","gene_name":"dynactin subunit 5 [Source:HGNC Symbol;Acc:HGNC:24594]","synonyms":"p25,MGC3248","biotype":"protein_coding","ncbi_id":"84516","summary":"This gene encodes a subunit of dynactin, a component of the cytoplasmic dynein motor machinery involved in minus-end-directed transport. The encoded protein is a component of the pointed-end subcomplex and is thought to bind membranous cargo. A pseudogene of this gene is located on the long arm of chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":23641392,"end":23677455,"strand":1,"description":"dynactin subunit 5 [Source:HGNC Symbol;Acc:HGNC:24594]"}, {"versioned_ensembl_gene_id":"ENSG00000269590.1","gene_symbol":"AC010422.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12664828,"end":12669397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162373.12","gene_symbol":"BEND5","gene_name":"BEN domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25668]","synonyms":"FLJ11588,C1orf165","biotype":"protein_coding","ncbi_id":"79656","summary":null,"start":48727523,"end":48776969,"strand":-1,"description":"BEN domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25668]"}, {"versioned_ensembl_gene_id":"ENSG00000183605.16","gene_symbol":"SFXN4","gene_name":"sideroflexin 4 [Source:HGNC Symbol;Acc:HGNC:16088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119559","summary":"This gene encodes a member of the sideroflexin family. The encoded protein is a transmembrane protein of the inner mitochondrial membrane, and is required for mitochondrial respiratory homeostasis and erythropoiesis. Mutations in this gene are associated with mitochondriopathy and macrocytic anemia. Alternatively spliced transcript variants have been found in this gene. [provided by RefSeq, Jan 2014]","start":119140767,"end":119165667,"strand":-1,"description":"sideroflexin 4 [Source:HGNC Symbol;Acc:HGNC:16088]"}, {"versioned_ensembl_gene_id":"ENSG00000229846.1","gene_symbol":"AC092264.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49048316,"end":49187585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281856.1","gene_symbol":"AC106017.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19219143,"end":19222527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204650.14","gene_symbol":"LINC02210","gene_name":"long intergenic non-protein coding RNA 2210 [Source:HGNC Symbol;Acc:HGNC:26327]","synonyms":"CRHR1-IT1,C17orf69,CRHR1-IT1,C17orf69,FLJ25168","biotype":"transcribed_unitary_pseudogene","ncbi_id":"147081","summary":null,"start":45620328,"end":45655156,"strand":1,"description":"long intergenic non-protein coding RNA 2210 [Source:HGNC Symbol;Acc:HGNC:26327]"}, {"versioned_ensembl_gene_id":"ENSG00000263715.7","gene_symbol":"LINC02210-CRHR1","gene_name":"LINC02210-CRHR1 readthrough [Source:HGNC Symbol;Acc:HGNC:51483]","synonyms":null,"biotype":"protein_coding","ncbi_id":"104909134","summary":"This locus represents naturally occurring readthrough transcription between neighboring genes CRHR1-IT1, CRHR1 intronic transcript 1 (Gene ID: 147081) and CRHR1, corticotropin releasing hormone receptor 1 (Gene ID: 1394) on chromosome 17. The readthrough transcript encodes a protein that shares sequence identity with the product of the CRHR1 gene. [provided by RefSeq, Dec 2016]","start":45620344,"end":45835826,"strand":1,"description":"LINC02210-CRHR1 readthrough [Source:HGNC Symbol;Acc:HGNC:51483]"}, {"versioned_ensembl_gene_id":"ENSG00000102595.19","gene_symbol":"UGGT2","gene_name":"UDP-glucose glycoprotein glucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15664]","synonyms":"UGCGL2,MGC87276,MGC150689,MGC117360,HUGT2,FLJ11485,FLJ10873","biotype":"protein_coding","ncbi_id":"55757","summary":"UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the endoplasmic reticulum (ER) that selectively reglucosylates unfolded glycoproteins, thus providing quality control for protein transport out of the ER.[supplied by OMIM, Oct 2009]","start":95801580,"end":96053482,"strand":-1,"description":"UDP-glucose glycoprotein glucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15664]"}, {"versioned_ensembl_gene_id":"ENSG00000265547.1","gene_symbol":"AC217774.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45731703,"end":45732977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185294.6","gene_symbol":"SPPL2C","gene_name":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]","synonyms":"IMP5,IMP5","biotype":"protein_coding","ncbi_id":"162540","summary":null,"start":45844835,"end":45847072,"strand":1,"description":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]"}, {"versioned_ensembl_gene_id":"ENSG00000215796.3","gene_symbol":"AL512637.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247042791,"end":247044021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186280.6","gene_symbol":"KDM4D","gene_name":"lysine demethylase 4D [Source:HGNC Symbol;Acc:HGNC:25498]","synonyms":"JMJD2D,FLJ10251","biotype":"protein_coding","ncbi_id":"55693","summary":null,"start":94973681,"end":94999518,"strand":1,"description":"lysine demethylase 4D [Source:HGNC Symbol;Acc:HGNC:25498]"}, {"versioned_ensembl_gene_id":"ENSG00000105369.9","gene_symbol":"CD79A","gene_name":"CD79a molecule [Source:HGNC Symbol;Acc:HGNC:1698]","synonyms":"MB-1,IGA","biotype":"protein_coding","ncbi_id":"973","summary":"The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-alpha protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":41877120,"end":41881372,"strand":1,"description":"CD79a molecule [Source:HGNC Symbol;Acc:HGNC:1698]"}, {"versioned_ensembl_gene_id":"ENSG00000262870.1","gene_symbol":"CYCSP40","gene_name":"cytochrome c, somatic pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:24414]","synonyms":"HC7,HCP40","biotype":"processed_pseudogene","ncbi_id":"360185","summary":null,"start":77198950,"end":77199543,"strand":-1,"description":"cytochrome c, somatic pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:24414]"}, {"versioned_ensembl_gene_id":"ENSG00000219361.1","gene_symbol":"RPSAP72","gene_name":"ribosomal protein SA pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:51925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075112","summary":null,"start":80470071,"end":80470428,"strand":-1,"description":"ribosomal protein SA pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:51925]"}, {"versioned_ensembl_gene_id":"ENSG00000260645.1","gene_symbol":"AL359715.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80466958,"end":80469080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000066739.11","gene_symbol":"ATG2B","gene_name":"autophagy related 2B [Source:HGNC Symbol;Acc:HGNC:20187]","synonyms":"FLJ10242,C14orf103","biotype":"protein_coding","ncbi_id":"55102","summary":"This gene encodes a protein required for autophagy. The encoded protein is involved in autophagosome formation. A germline duplication of a region that includes this gene is associated with predisposition to myeloid malignancies. [provided by RefSeq, Jul 2016]","start":96279202,"end":96363870,"strand":-1,"description":"autophagy related 2B [Source:HGNC Symbol;Acc:HGNC:20187]"}, {"versioned_ensembl_gene_id":"ENSG00000067829.18","gene_symbol":"IDH3G","gene_name":"isocitrate dehydrogenase 3 (NAD(+)) gamma [Source:HGNC Symbol;Acc:HGNC:5386]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3421","summary":"Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. NAD(+)-dependent isocitrate dehydrogenases catalyze the allosterically regulated rate-limiting step of the tricarboxylic acid cycle. Each isozyme is a heterotetramer that is composed of two alpha subunits, one beta subunit, and one gamma subunit. The protein encoded by this gene is the gamma subunit of one isozyme of NAD(+)-dependent isocitrate dehydrogenase. This gene is a candidate gene for periventricular heterotopia. Several alternatively spliced transcript variants of this gene have been described, but only some of their full length natures have been determined. [provided by RefSeq, Jul 2008]","start":153785766,"end":153794523,"strand":-1,"description":"isocitrate dehydrogenase 3 (NAD(+)) gamma [Source:HGNC Symbol;Acc:HGNC:5386]"}, {"versioned_ensembl_gene_id":"ENSG00000180879.13","gene_symbol":"SSR4","gene_name":"signal sequence receptor subunit 4 [Source:HGNC Symbol;Acc:HGNC:11326]","synonyms":"TRAPD","biotype":"protein_coding","ncbi_id":"6748","summary":"This gene encodes the delta subunit of the translocon-associated protein complex which is involved in translocating proteins across the endoplasmic reticulum membrane. The encoded protein is located in the Xq28 region and is arranged in a compact head-to-head manner with the isocitrate dehydrogenase 3 (NAD+) gamma gene and both genes are driven by a CpG-embedded bidirectional promoter. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]","start":153793516,"end":153798505,"strand":1,"description":"signal sequence receptor subunit 4 [Source:HGNC Symbol;Acc:HGNC:11326]"}, {"versioned_ensembl_gene_id":"ENSG00000271833.1","gene_symbol":"AL445222.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":127366770,"end":127367397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269502.5","gene_symbol":"DMRTC1","gene_name":"DMRT like family C1 [Source:HGNC Symbol;Acc:HGNC:13910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63947","summary":null,"start":72872025,"end":72943814,"strand":-1,"description":"DMRT like family C1 [Source:HGNC Symbol;Acc:HGNC:13910]"}, {"versioned_ensembl_gene_id":"ENSG00000112309.10","gene_symbol":"B3GAT2","gene_name":"beta-1,3-glucuronyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:922]","synonyms":"GlcAT-S","biotype":"protein_coding","ncbi_id":"135152","summary":"The product of this gene is a transmembrane protein belonging to the glucuronyltransferase family, and catalyzes the transfer of a beta-1,3 linked glucuronic acid to a terminal galactose in different glycoproteins or glycolipids containing a Gal-beta-1-4GlcNAc or Gal-beta-1-3GlcNAc residue. The encoded protein is involved in the synthesis of the human natural killer-1 (HNK-1) carbohydrate epitope, a sulfated trisaccharide implicated in cellular migration and adhesion in the nervous system. [provided by RefSeq, Jul 2008]","start":70856679,"end":70957038,"strand":-1,"description":"beta-1,3-glucuronyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:922]"}, {"versioned_ensembl_gene_id":"ENSG00000258793.1","gene_symbol":"AL355102.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96259411,"end":96268624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120318.15","gene_symbol":"ARAP3","gene_name":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:24097]","synonyms":"FLJ21065,DRAG1,CENTD3","biotype":"protein_coding","ncbi_id":"64411","summary":"This gene encodes a phosphoinositide binding protein containing ARF-GAP, RHO-GAP, RAS-associating, and pleckstrin homology domains. The ARF-GAP and RHO-GAP domains cooperate in mediating rearrangements in the cell cytoskeleton and cell shape. It is a specific PtdIns(3,4,5)P3/PtdIns(3,4)P2-stimulated Arf6-GAP protein. An alternatively spliced transcript has been found for this gene, but its biological validity has not been determined. [provided by RefSeq, Sep 2015]","start":141653401,"end":141682221,"strand":-1,"description":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:24097]"}, {"versioned_ensembl_gene_id":"ENSG00000258402.1","gene_symbol":"AC016526.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76280943,"end":76310066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267535.1","gene_symbol":"LINC00868","gene_name":"long intergenic non-protein coding RNA 868 [Source:HGNC Symbol;Acc:HGNC:27562]","synonyms":"C17orf52","biotype":"lincRNA","ncbi_id":"283994","summary":null,"start":76850176,"end":76861836,"strand":1,"description":"long intergenic non-protein coding RNA 868 [Source:HGNC Symbol;Acc:HGNC:27562]"}, {"versioned_ensembl_gene_id":"ENSG00000267198.1","gene_symbol":"AC091132.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45545804,"end":45563230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086848.14","gene_symbol":"ALG9","gene_name":"ALG9, alpha-1,2-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:15672]","synonyms":"DIBD1","biotype":"protein_coding","ncbi_id":"79796","summary":"This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":111782195,"end":111871581,"strand":-1,"description":"ALG9, alpha-1,2-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:15672]"}, {"versioned_ensembl_gene_id":"ENSG00000237124.1","gene_symbol":"MTND2P11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42112]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873222","summary":null,"start":109300186,"end":109301172,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42112]"}, {"versioned_ensembl_gene_id":"ENSG00000279737.1","gene_symbol":"AC112204.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35895689,"end":35896020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262292.2","gene_symbol":"AC007952.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19160789,"end":19162274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283122.1","gene_symbol":"HYMAI","gene_name":"hydatidiform mole associated and imprinted (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:5326]","synonyms":"NCRNA00020","biotype":"non_coding","ncbi_id":"57061","summary":"This gene, which encodes a non-protein coding transcript, exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island, and is expressed only from the paternal allele. It is believed to be one of the causative genes for transient neonatal diabetes mellitus (TNDM), which is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal insulin secretion. [provided by RefSeq, Oct 2010]","start":144004916,"end":144008262,"strand":-1,"description":"hydatidiform mole associated and imprinted (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:5326]"}, {"versioned_ensembl_gene_id":"ENSG00000244717.1","gene_symbol":"AC145146.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69469883,"end":69470136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147642.16","gene_symbol":"SYBU","gene_name":"syntabulin [Source:HGNC Symbol;Acc:HGNC:26011]","synonyms":"SNPHL,OCSYN,KIAA1472,GOLSYN,FLJ20366","biotype":"protein_coding","ncbi_id":"55638","summary":"Syntabulin/GOLSYN is part of a kinesin motor-adaptor complex that is critical for the anterograde axonal transport of active zone components and contributes to activity-dependent presynaptic assembly during neuronal development (Cai et al., 2007 [PubMed 17611281]).[supplied by OMIM, Mar 2008]","start":109573978,"end":109691791,"strand":-1,"description":"syntabulin [Source:HGNC Symbol;Acc:HGNC:26011]"}, {"versioned_ensembl_gene_id":"ENSG00000254052.1","gene_symbol":"IGHVIII-67-4","gene_name":"immunoglobulin heavy variable (III)-67-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5707]","synonyms":"IGHV(III)-67-4","biotype":"IG_V_pseudogene","ncbi_id":"28340","summary":null,"start":106695102,"end":106695397,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5707]"}, {"versioned_ensembl_gene_id":"ENSG00000254036.1","gene_symbol":"IGHVIII-67-2","gene_name":"immunoglobulin heavy variable (III)-67-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5705]","synonyms":"IGHV(III)-67-2","biotype":"IG_V_pseudogene","ncbi_id":"28342","summary":null,"start":106687113,"end":106687200,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5705]"}, {"versioned_ensembl_gene_id":"ENSG00000228830.1","gene_symbol":"AL160408.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234607008,"end":234609483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253820.1","gene_symbol":"IGHVII-67-1","gene_name":"immunoglobulin heavy variable (II)-67-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5689]","synonyms":"IGHV(II)-67-1","biotype":"IG_V_pseudogene","ncbi_id":"28358","summary":null,"start":106686517,"end":106686562,"strand":-1,"description":"immunoglobulin heavy variable (II)-67-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5689]"}, {"versioned_ensembl_gene_id":"ENSG00000165629.19","gene_symbol":"ATP5C1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:833]","synonyms":"ATP5CL1,ATP5C","biotype":"protein_coding","ncbi_id":"509","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the gamma subunit of the catalytic core. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene also has a pseudogene on chromosome 14. [provided by RefSeq, Jul 2008]","start":7788129,"end":7807815,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:833]"}, {"versioned_ensembl_gene_id":"ENSG00000123977.9","gene_symbol":"DAW1","gene_name":"dynein assembly factor with WD repeats 1 [Source:HGNC Symbol;Acc:HGNC:26383]","synonyms":"WDR69,ODA16,FLJ25955","biotype":"protein_coding","ncbi_id":"164781","summary":null,"start":227871054,"end":227924344,"strand":1,"description":"dynein assembly factor with WD repeats 1 [Source:HGNC Symbol;Acc:HGNC:26383]"}, {"versioned_ensembl_gene_id":"ENSG00000149577.15","gene_symbol":"SIDT2","gene_name":"SID1 transmembrane family member 2 [Source:HGNC Symbol;Acc:HGNC:24272]","synonyms":"CGI-40","biotype":"protein_coding","ncbi_id":"51092","summary":null,"start":117178733,"end":117197445,"strand":1,"description":"SID1 transmembrane family member 2 [Source:HGNC Symbol;Acc:HGNC:24272]"}, {"versioned_ensembl_gene_id":"ENSG00000214255.5","gene_symbol":"AC091305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70430231,"end":70431125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232249.1","gene_symbol":"AC152007.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153355733,"end":153355956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197561.6","gene_symbol":"ELANE","gene_name":"elastase, neutrophil expressed [Source:HGNC Symbol;Acc:HGNC:3309]","synonyms":"ELA2,NE,HNE,HLE","biotype":"protein_coding","ncbi_id":"1991","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode structurally similar proteins. The encoded preproprotein is proteolytically processed to generate the active protease. Following activation, this protease hydrolyzes proteins within specialized neutrophil lysosomes, called azurophil granules, as well as proteins of the extracellular matrix. The enzyme may play a role in degenerative and inflammatory diseases through proteolysis of collagen-IV and elastin. This protein also degrades the outer membrane protein A (OmpA) of E. coli as well as the virulence factors of such bacteria as Shigella, Salmonella and Yersinia. Mutations in this gene are associated with cyclic neutropenia and severe congenital neutropenia (SCN). This gene is present in a gene cluster on chromosome 19. [provided by RefSeq, Jan 2016]","start":851014,"end":856247,"strand":1,"description":"elastase, neutrophil expressed [Source:HGNC Symbol;Acc:HGNC:3309]"}, {"versioned_ensembl_gene_id":"ENSG00000166189.7","gene_symbol":"HPS6","gene_name":"HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 [Source:HGNC Symbol;Acc:HGNC:18817]","synonyms":"FLJ22501,BLOC2S3","biotype":"protein_coding","ncbi_id":"79803","summary":"This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008]","start":102065390,"end":102068038,"strand":1,"description":"HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 [Source:HGNC Symbol;Acc:HGNC:18817]"}, {"versioned_ensembl_gene_id":"ENSG00000225110.2","gene_symbol":"PNMA6F","gene_name":"paraneoplastic Ma antigen family member 6F [Source:HGNC Symbol;Acc:HGNC:53119]","synonyms":"PNMA6BL","biotype":"protein_coding","ncbi_id":"105373377","summary":null,"start":153317681,"end":153321822,"strand":-1,"description":"paraneoplastic Ma antigen family member 6F [Source:HGNC Symbol;Acc:HGNC:53119]"}, {"versioned_ensembl_gene_id":"ENSG00000249348.1","gene_symbol":"UGDH-AS1","gene_name":"UGDH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40601]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885776","summary":null,"start":39528019,"end":39594707,"strand":1,"description":"UGDH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40601]"}, {"versioned_ensembl_gene_id":"ENSG00000235686.1","gene_symbol":"PPIAP20","gene_name":"peptidylprolyl isomerase A pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38037]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100500737","summary":null,"start":12508129,"end":12508263,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38037]"}, {"versioned_ensembl_gene_id":"ENSG00000269693.1","gene_symbol":"AC010422.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12525720,"end":12580975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188831.4","gene_symbol":"DPPA3P2","gene_name":"developmental pluripotency associated 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20417]","synonyms":"STELLAR","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400206","summary":null,"start":36371165,"end":36372383,"strand":1,"description":"developmental pluripotency associated 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20417]"}, {"versioned_ensembl_gene_id":"ENSG00000185009.12","gene_symbol":"AP3M1","gene_name":"adaptor related protein complex 3 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:569]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26985","summary":"The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane, and it may directly function in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":74120255,"end":74151063,"strand":-1,"description":"adaptor related protein complex 3 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:569]"}, {"versioned_ensembl_gene_id":"ENSG00000225761.1","gene_symbol":"AL596247.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":74005137,"end":74027915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172893.15","gene_symbol":"DHCR7","gene_name":"7-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:HGNC:2860]","synonyms":"SLOS","biotype":"protein_coding","ncbi_id":"1717","summary":"This gene encodes an enzyme that removes the C(7-8) double bond in the B ring of sterols and catalyzes the conversion of 7-dehydrocholesterol to cholesterol. This gene is ubiquitously expressed and its transmembrane protein localizes to the endoplasmic reticulum membrane and nuclear outer membrane. Mutations in this gene cause Smith-Lemli-Opitz syndrome (SLOS); a syndrome that is metabolically characterized by reduced serum cholesterol levels and elevated serum 7-dehydrocholesterol levels and phenotypically characterized by cognitive disability, facial dysmorphism, syndactyly of second and third toes, and holoprosencephaly in severe cases to minimal physical abnormalities and near-normal intelligence in mild cases. Alternative splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Aug 2009]","start":71428193,"end":71452868,"strand":-1,"description":"7-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:HGNC:2860]"}, {"versioned_ensembl_gene_id":"ENSG00000252767.1","gene_symbol":"RNU6-250P","gene_name":"RNA, U6 small nuclear 250, pseudogene [Source:HGNC Symbol;Acc:HGNC:47213]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479678","summary":null,"start":40407853,"end":40407955,"strand":1,"description":"RNA, U6 small nuclear 250, pseudogene [Source:HGNC Symbol;Acc:HGNC:47213]"}, {"versioned_ensembl_gene_id":"ENSG00000200391.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43863893,"end":43864005,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221340.1","gene_symbol":"RNU6ATAC18P","gene_name":"RNA, U6atac small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46917]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479551","summary":null,"start":12569972,"end":12570072,"strand":-1,"description":"RNA, U6atac small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46917]"}, {"versioned_ensembl_gene_id":"ENSG00000255114.1","gene_symbol":"AP003392.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119044188,"end":119045493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106665.15","gene_symbol":"CLIP2","gene_name":"CAP-Gly domain containing linker protein 2 [Source:HGNC Symbol;Acc:HGNC:2586]","synonyms":"CYLN2,CLIP-115,CLIP,WSCR4,WSCR3,WBSCR4,WBSCR3,KIAA0291","biotype":"protein_coding","ncbi_id":"7461","summary":"The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]","start":74289475,"end":74405943,"strand":1,"description":"CAP-Gly domain containing linker protein 2 [Source:HGNC Symbol;Acc:HGNC:2586]"}, {"versioned_ensembl_gene_id":"ENSG00000077585.13","gene_symbol":"GPR137B","gene_name":"G protein-coupled receptor 137B [Source:HGNC Symbol;Acc:HGNC:11862]","synonyms":"TM7SF1","biotype":"protein_coding","ncbi_id":"7107","summary":null,"start":236142505,"end":236221865,"strand":1,"description":"G protein-coupled receptor 137B [Source:HGNC Symbol;Acc:HGNC:11862]"}, {"versioned_ensembl_gene_id":"ENSG00000263394.1","gene_symbol":"AC007952.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19091069,"end":19091825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159917.15","gene_symbol":"ZNF235","gene_name":"zinc finger protein 235 [Source:HGNC Symbol;Acc:HGNC:12866]","synonyms":"ZNF270,ZFP93,HZF6,ANF270","biotype":"protein_coding","ncbi_id":"9310","summary":"This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein is a member of the Kruppel family of zinc finger proteins, and contains Kruppel-associated box (KRAB) A and B domains and 15 tandemly arrayed C2H2-type zinc fingers. It is an ortholog of the mouse Zfp93 protein. This gene is located in a cluster of zinc finger genes on 19q13.2. [provided by RefSeq, Jul 2008]","start":44228729,"end":44305046,"strand":-1,"description":"zinc finger protein 235 [Source:HGNC Symbol;Acc:HGNC:12866]"}, {"versioned_ensembl_gene_id":"ENSG00000270679.1","gene_symbol":"AC138473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44290081,"end":44290911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225236.1","gene_symbol":"AP000936.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117117794,"end":117119181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239486.1","gene_symbol":"AC091390.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102380465,"end":102382737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276832.1","gene_symbol":"AL354718.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41341000,"end":41342041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198883.11","gene_symbol":"PNMA5","gene_name":"paraneoplastic Ma antigen family member 5 [Source:HGNC Symbol;Acc:HGNC:18743]","synonyms":"KIAA1934","biotype":"protein_coding","ncbi_id":"114824","summary":"This gene encodes a member of the paraneoplastic Ma antigen protein family. These proteins have been implicated in the development of paraneoplastic disorders resulting from an immune response directed against them. Paraneoplastic disorders are the result of an abnormal immune response to a tumor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2011]","start":152988824,"end":152994127,"strand":-1,"description":"paraneoplastic Ma antigen family member 5 [Source:HGNC Symbol;Acc:HGNC:18743]"}, {"versioned_ensembl_gene_id":"ENSG00000149557.12","gene_symbol":"FEZ1","gene_name":"fasciculation and elongation protein zeta 1 [Source:HGNC Symbol;Acc:HGNC:3659]","synonyms":"UNC-76","biotype":"protein_coding","ncbi_id":"9638","summary":"This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal bundling and elongation within axon bundles. Expression of this gene in C. elegans unc-76 mutants can restore to the mutants partial locomotion and axonal fasciculation, suggesting that it also functions in axonal outgrowth. The N-terminal half of the gene product is highly acidic. Alternatively spliced transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]","start":125445745,"end":125496317,"strand":-1,"description":"fasciculation and elongation protein zeta 1 [Source:HGNC Symbol;Acc:HGNC:3659]"}, {"versioned_ensembl_gene_id":"ENSG00000233011.1","gene_symbol":"SLC9A3P1","gene_name":"solute carrier family 9 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11074]","synonyms":"NHE3P,SLC9A3P4,SLC9A3P","biotype":"processed_pseudogene","ncbi_id":"6551","summary":null,"start":50150603,"end":50152287,"strand":1,"description":"solute carrier family 9 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11074]"}, {"versioned_ensembl_gene_id":"ENSG00000176894.9","gene_symbol":"PXMP2","gene_name":"peroxisomal membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:9716]","synonyms":"PMP22","biotype":"protein_coding","ncbi_id":"5827","summary":null,"start":132687606,"end":132704991,"strand":1,"description":"peroxisomal membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:9716]"}, {"versioned_ensembl_gene_id":"ENSG00000283464.1","gene_symbol":"AC244452.4","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106481424,"end":106481706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275765.5","gene_symbol":"AC091982.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151770242,"end":151771508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253921.1","gene_symbol":"AC091982.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151753992,"end":151767247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242042.1","gene_symbol":"LINC01743","gene_name":"long intergenic non-protein coding RNA 1743 [Source:HGNC Symbol;Acc:HGNC:52531]","synonyms":null,"biotype":"lincRNA","ncbi_id":"255654","summary":null,"start":246516039,"end":246524287,"strand":-1,"description":"long intergenic non-protein coding RNA 1743 [Source:HGNC Symbol;Acc:HGNC:52531]"}, {"versioned_ensembl_gene_id":"ENSG00000198700.9","gene_symbol":"IPO9","gene_name":"importin 9 [Source:HGNC Symbol;Acc:HGNC:19425]","synonyms":"Imp9,FLJ10402","biotype":"protein_coding","ncbi_id":"55705","summary":null,"start":201829141,"end":201884294,"strand":1,"description":"importin 9 [Source:HGNC Symbol;Acc:HGNC:19425]"}, {"versioned_ensembl_gene_id":"ENSG00000268423.4","gene_symbol":"AC093503.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46547056,"end":46600861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271043.2","gene_symbol":"MTRNR2L2","gene_name":"MT-RNR2-like 2 [Source:HGNC Symbol;Acc:HGNC:37156]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462981","summary":null,"start":80650000,"end":80650086,"strand":-1,"description":"MT-RNR2-like 2 [Source:HGNC Symbol;Acc:HGNC:37156]"}, {"versioned_ensembl_gene_id":"ENSG00000251396.6","gene_symbol":"LINC01301","gene_name":"long intergenic non-protein coding RNA 1301 [Source:HGNC Symbol;Acc:HGNC:50464]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505532","summary":null,"start":60384588,"end":60516795,"strand":-1,"description":"long intergenic non-protein coding RNA 1301 [Source:HGNC Symbol;Acc:HGNC:50464]"}, {"versioned_ensembl_gene_id":"ENSG00000214215.3","gene_symbol":"C12orf74","gene_name":"chromosome 12 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27887]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338809","summary":null,"start":92702843,"end":92708549,"strand":1,"description":"chromosome 12 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27887]"}, {"versioned_ensembl_gene_id":"ENSG00000258262.1","gene_symbol":"AC063949.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92530460,"end":92531324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049541.10","gene_symbol":"RFC2","gene_name":"replication factor C subunit 2 [Source:HGNC Symbol;Acc:HGNC:9970]","synonyms":"RFC40,A1","biotype":"protein_coding","ncbi_id":"5982","summary":"This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2. [provided by RefSeq, Jul 2013]","start":74231499,"end":74254458,"strand":-1,"description":"replication factor C subunit 2 [Source:HGNC Symbol;Acc:HGNC:9970]"}, {"versioned_ensembl_gene_id":"ENSG00000279665.1","gene_symbol":"AC012100.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50742702,"end":50743276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259773.1","gene_symbol":"AC012100.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50746709,"end":50749829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250433.1","gene_symbol":"CLSTN2-AS1","gene_name":"CLSTN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49095]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927808","summary":null,"start":140505611,"end":140508789,"strand":-1,"description":"CLSTN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49095]"}, {"versioned_ensembl_gene_id":"ENSG00000147383.10","gene_symbol":"NSDHL","gene_name":"NAD(P) dependent steroid dehydrogenase-like [Source:HGNC Symbol;Acc:HGNC:13398]","synonyms":"XAP104,SDR31E1,H105e3","biotype":"protein_coding","ncbi_id":"50814","summary":"The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]","start":152830967,"end":152869729,"strand":1,"description":"NAD(P) dependent steroid dehydrogenase-like [Source:HGNC Symbol;Acc:HGNC:13398]"}, {"versioned_ensembl_gene_id":"ENSG00000226773.1","gene_symbol":"AL663109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92203148,"end":92203991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278474.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4a,CD158K,cl-5,nkat4b,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54880532,"end":54897308,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000231810.1","gene_symbol":"RPL36AP35","gene_name":"ribosomal protein L36a pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35639]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271610","summary":null,"start":108821697,"end":108822004,"strand":1,"description":"ribosomal protein L36a pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35639]"}, {"versioned_ensembl_gene_id":"ENSG00000229052.2","gene_symbol":"AL449283.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":92930696,"end":92934098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253158.1","gene_symbol":"IGKV3-31","gene_name":"immunoglobulin kappa variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5819]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28910","summary":null,"start":89252211,"end":89252736,"strand":-1,"description":"immunoglobulin kappa variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5819]"}, {"versioned_ensembl_gene_id":"ENSG00000230546.1","gene_symbol":"AL445193.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58084419,"end":58084559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271584.2","gene_symbol":"LINC02550","gene_name":"long intergenic non-protein coding RNA 2550 [Source:HGNC Symbol;Acc:HGNC:53585]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369490","summary":null,"start":111091932,"end":111179641,"strand":-1,"description":"long intergenic non-protein coding RNA 2550 [Source:HGNC Symbol;Acc:HGNC:53585]"}, {"versioned_ensembl_gene_id":"ENSG00000271390.1","gene_symbol":"AP003973.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111089870,"end":111090368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277852.1","gene_symbol":"AC244255.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89203509,"end":89203906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211907.1","gene_symbol":"IGHD1-26","gene_name":"immunoglobulin heavy diversity 1-26 [Source:HGNC Symbol;Acc:HGNC:5485]","synonyms":"IGHD126","biotype":"IG_D_gene","ncbi_id":"28506","summary":null,"start":105881034,"end":105881053,"strand":-1,"description":"immunoglobulin heavy diversity 1-26 [Source:HGNC Symbol;Acc:HGNC:5485]"}, {"versioned_ensembl_gene_id":"ENSG00000242472.1","gene_symbol":"IGHJ5","gene_name":"immunoglobulin heavy joining 5 [Source:HGNC Symbol;Acc:HGNC:5539]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28476","summary":null,"start":105863814,"end":105863862,"strand":-1,"description":"immunoglobulin heavy joining 5 [Source:HGNC Symbol;Acc:HGNC:5539]"}, {"versioned_ensembl_gene_id":"ENSG00000237111.1","gene_symbol":"IGHJ3P","gene_name":"immunoglobulin heavy joining 3P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5537]","synonyms":"Jpsi3","biotype":"IG_J_pseudogene","ncbi_id":"28478","summary":null,"start":105863416,"end":105863465,"strand":-1,"description":"immunoglobulin heavy joining 3P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5537]"}, {"versioned_ensembl_gene_id":"ENSG00000130653.15","gene_symbol":"PNPLA7","gene_name":"patatin like phospholipase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:24768]","synonyms":"RP11-48C7.2,NTEL1,NTE-R1,FLJ44279,FLJ43070,FLJ31318,C9orf111","biotype":"protein_coding","ncbi_id":"375775","summary":"Human patatin-like phospholipases, such as PNPLA7, have been implicated in regulation of adipocyte differentiation and have been induced by metabolic stimuli (Wilson et al., 2006 [PubMed 16799181]).[supplied by OMIM, Jun 2008]","start":137459953,"end":137550534,"strand":-1,"description":"patatin like phospholipase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:24768]"}, {"versioned_ensembl_gene_id":"ENSG00000211900.2","gene_symbol":"IGHJ6","gene_name":"immunoglobulin heavy joining 6 [Source:HGNC Symbol;Acc:HGNC:5540]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28475","summary":null,"start":105863198,"end":105863258,"strand":-1,"description":"immunoglobulin heavy joining 6 [Source:HGNC Symbol;Acc:HGNC:5540]"}, {"versioned_ensembl_gene_id":"ENSG00000249497.1","gene_symbol":"LINC02075","gene_name":"long intergenic non-protein coding RNA 2075 [Source:HGNC Symbol;Acc:HGNC:52921]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927207","summary":null,"start":49457861,"end":49461749,"strand":-1,"description":"long intergenic non-protein coding RNA 2075 [Source:HGNC Symbol;Acc:HGNC:52921]"}, {"versioned_ensembl_gene_id":"ENSG00000250186.3","gene_symbol":"AC091180.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49404081,"end":49405197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237210.1","gene_symbol":"AC073324.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55244247,"end":55245681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256797.1","gene_symbol":"KLRF2","gene_name":"killer cell lectin like receptor F2 [Source:HGNC Symbol;Acc:HGNC:37646]","synonyms":"NKp65","biotype":"protein_coding","ncbi_id":"100431172","summary":null,"start":9881489,"end":9895833,"strand":1,"description":"killer cell lectin like receptor F2 [Source:HGNC Symbol;Acc:HGNC:37646]"}, {"versioned_ensembl_gene_id":"ENSG00000248966.1","gene_symbol":"BCLAF1P1","gene_name":"BCL2 associated transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728366","summary":null,"start":110948029,"end":110950780,"strand":-1,"description":"BCL2 associated transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51329]"}, {"versioned_ensembl_gene_id":"ENSG00000237189.1","gene_symbol":"AL138900.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157287703,"end":157288053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274363.1","gene_symbol":"AC087742.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4267691,"end":4268430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219736.1","gene_symbol":"AL356473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74849077,"end":74850484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254221.2","gene_symbol":"PCDHGB1","gene_name":"protocadherin gamma subfamily B, 1 [Source:HGNC Symbol;Acc:HGNC:8708]","synonyms":"PCDH-GAMMA-B1","biotype":"protein_coding","ncbi_id":"56104","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141350102,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 1 [Source:HGNC Symbol;Acc:HGNC:8708]"}, {"versioned_ensembl_gene_id":"ENSG00000199899.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":113156763,"end":113156861,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252391.1","gene_symbol":"RNU6-638P","gene_name":"RNA, U6 small nuclear 638, pseudogene [Source:HGNC Symbol;Acc:HGNC:47601]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481383","summary":null,"start":78696694,"end":78696797,"strand":-1,"description":"RNA, U6 small nuclear 638, pseudogene [Source:HGNC Symbol;Acc:HGNC:47601]"}, {"versioned_ensembl_gene_id":"ENSG00000273701.1","gene_symbol":"PART1_1","gene_name":"Prostate androgen-regulated transcript 1 conserved region 1 [Source:RFAM;Acc:RF02159]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":60487713,"end":60487929,"strand":1,"description":"Prostate androgen-regulated transcript 1 conserved region 1 [Source:RFAM;Acc:RF02159]"}, {"versioned_ensembl_gene_id":"ENSG00000223078.1","gene_symbol":"RNU2-55P","gene_name":"RNA, U2 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:48548]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481961","summary":null,"start":23281736,"end":23281909,"strand":-1,"description":"RNA, U2 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:48548]"}, {"versioned_ensembl_gene_id":"ENSG00000274017.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49196784,"end":49197062,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000197406.7","gene_symbol":"DIO3","gene_name":"iodothyronine deiodinase 3 [Source:HGNC Symbol;Acc:HGNC:2885]","synonyms":"TXDI3","biotype":"protein_coding","ncbi_id":"1735","summary":"The protein encoded by this intronless gene belongs to the iodothyronine deiodinase family. It catalyzes the inactivation of thyroid hormone by inner ring deiodination of the prohormone thyroxine (T4) and the bioactive hormone 3,3',5-triiodothyronine (T3) to inactive metabolites, 3,3',5'-triiodothyronine (RT3) and 3,3'-diiodothyronine (T2), respectively. This enzyme is highly expressed in pregnant uterus, placenta, fetal and neonatal tissues, and thought to prevent premature exposure of developing fetal tissues to adult levels of thyroid hormones. It regulates circulating fetal thyroid hormone concentrations, and thus plays a critical role in mammalian development. Knockout mice lacking this gene exhibit abnormalities related to development and reproduction, and increased activity of this enzyme in infants with hemangiomas causes severe hypothyroidism. This protein is a selenoprotein, containing the rare selenocysteine (Sec) amino acid at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. [provided by RefSeq, May 2016]","start":101561351,"end":101563452,"strand":1,"description":"iodothyronine deiodinase 3 [Source:HGNC Symbol;Acc:HGNC:2885]"}, {"versioned_ensembl_gene_id":"ENSG00000261868.1","gene_symbol":"MFSD1P1","gene_name":"major facilitator superfamily domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100313532","summary":null,"start":4301372,"end":4302698,"strand":1,"description":"major facilitator superfamily domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50625]"}, {"versioned_ensembl_gene_id":"ENSG00000132388.12","gene_symbol":"UBE2G1","gene_name":"ubiquitin conjugating enzyme E2 G1 [Source:HGNC Symbol;Acc:HGNC:12482]","synonyms":"UBE2G,UBC7","biotype":"protein_coding","ncbi_id":"7326","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family and catalyzes the covalent attachment of ubiquitin to other proteins. The protein may be involved in degradation of muscle-specific proteins. [provided by RefSeq, Jul 2008]","start":4269259,"end":4366628,"strand":-1,"description":"ubiquitin conjugating enzyme E2 G1 [Source:HGNC Symbol;Acc:HGNC:12482]"}, {"versioned_ensembl_gene_id":"ENSG00000258919.1","gene_symbol":"AL049836.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101628984,"end":101632530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232482.2","gene_symbol":"AL357134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23410832,"end":23412146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258512.1","gene_symbol":"LINC00239","gene_name":"long intergenic non-protein coding RNA 239 [Source:HGNC Symbol;Acc:HGNC:20119]","synonyms":"NCRNA00239,C14orf72","biotype":"lincRNA","ncbi_id":"145200","summary":null,"start":101730437,"end":101732522,"strand":1,"description":"long intergenic non-protein coding RNA 239 [Source:HGNC Symbol;Acc:HGNC:20119]"}, {"versioned_ensembl_gene_id":"ENSG00000254157.1","gene_symbol":"IGKV2-18","gene_name":"immunoglobulin kappa variable 2-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5778]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28926","summary":null,"start":89128724,"end":89129483,"strand":-1,"description":"immunoglobulin kappa variable 2-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5778]"}, {"versioned_ensembl_gene_id":"ENSG00000258404.1","gene_symbol":"LINC02320","gene_name":"long intergenic non-protein coding RNA 2320 [Source:HGNC Symbol;Acc:HGNC:53239]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370676","summary":null,"start":101634454,"end":101731108,"strand":-1,"description":"long intergenic non-protein coding RNA 2320 [Source:HGNC Symbol;Acc:HGNC:53239]"}, {"versioned_ensembl_gene_id":"ENSG00000204219.9","gene_symbol":"TCEA3","gene_name":"transcription elongation factor A3 [Source:HGNC Symbol;Acc:HGNC:11615]","synonyms":"TFIIS.H","biotype":"protein_coding","ncbi_id":"6920","summary":null,"start":23381061,"end":23424740,"strand":-1,"description":"transcription elongation factor A3 [Source:HGNC Symbol;Acc:HGNC:11615]"}, {"versioned_ensembl_gene_id":"ENSG00000241494.1","gene_symbol":"AL355032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101677943,"end":101678380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223353.2","gene_symbol":"AL589763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":245123471,"end":245124450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167085.11","gene_symbol":"PHB","gene_name":"prohibitin [Source:HGNC Symbol;Acc:HGNC:8912]","synonyms":"PHB1","biotype":"protein_coding","ncbi_id":"5245","summary":"This gene is evolutionarily conserved, and its product is proposed to play a role in human cellular senescence and tumor suppression. Antiproliferative activity is reported to be localized to the 3' UTR, which is proposed to function as a trans-acting regulatory RNA. Several pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":49404049,"end":49414905,"strand":-1,"description":"prohibitin [Source:HGNC Symbol;Acc:HGNC:8912]"}, {"versioned_ensembl_gene_id":"ENSG00000136099.13","gene_symbol":"PCDH8","gene_name":"protocadherin 8 [Source:HGNC Symbol;Acc:HGNC:8660]","synonyms":"ARCADLIN,PAPC","biotype":"protein_coding","ncbi_id":"5100","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The gene encodes an integral membrane protein that is thought to function in cell adhesion in a CNS-specific manner. Unlike classical cadherins, which are generally encoded by 15-17 exons, this gene includes only 3 exons. Notable is the large first exon encoding the extracellular region, including 6 cadherin domains and a transmembrane region. Alternative splicing yields isoforms with unique cytoplasmic tails. [provided by RefSeq, Jul 2008]","start":52842889,"end":52848641,"strand":-1,"description":"protocadherin 8 [Source:HGNC Symbol;Acc:HGNC:8660]"}, {"versioned_ensembl_gene_id":"ENSG00000253026.1","gene_symbol":"RNU6-464P","gene_name":"RNA, U6 small nuclear 464, pseudogene [Source:HGNC Symbol;Acc:HGNC:47427]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479771","summary":null,"start":53153795,"end":53153898,"strand":-1,"description":"RNA, U6 small nuclear 464, pseudogene [Source:HGNC Symbol;Acc:HGNC:47427]"}, {"versioned_ensembl_gene_id":"ENSG00000252010.1","gene_symbol":"SCARNA5","gene_name":"small Cajal body-specific RNA 5 [Source:HGNC Symbol;Acc:HGNC:32561]","synonyms":"U87","biotype":"scaRNA","ncbi_id":"677775","summary":null,"start":233275727,"end":233276002,"strand":1,"description":"small Cajal body-specific RNA 5 [Source:HGNC Symbol;Acc:HGNC:32561]"}, {"versioned_ensembl_gene_id":"ENSG00000252894.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130914340,"end":130914452,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201208.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":113178423,"end":113178519,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223298.1","gene_symbol":"RNY3P8","gene_name":"RNA, Ro-associated Y3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42492]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106478985","summary":null,"start":95310830,"end":95310955,"strand":-1,"description":"RNA, Ro-associated Y3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42492]"}, {"versioned_ensembl_gene_id":"ENSG00000266151.1","gene_symbol":"MIR3646","gene_name":"microRNA 3646 [Source:HGNC Symbol;Acc:HGNC:38935]","synonyms":"hsa-mir-3646","biotype":"miRNA","ncbi_id":"100500813","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44408120,"end":44408203,"strand":1,"description":"microRNA 3646 [Source:HGNC Symbol;Acc:HGNC:38935]"}, {"versioned_ensembl_gene_id":"ENSG00000201218.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7102573,"end":7102681,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252042.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75145670,"end":75145762,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278794.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1101007,"end":1101273,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000263816.1","gene_symbol":"MIR548AW","gene_name":"microRNA 548aw [Source:HGNC Symbol;Acc:HGNC:43454]","synonyms":"hsa-mir-548aw","biotype":"miRNA","ncbi_id":"100846992","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132945707,"end":132945771,"strand":1,"description":"microRNA 548aw [Source:HGNC Symbol;Acc:HGNC:43454]"}, {"versioned_ensembl_gene_id":"ENSG00000263558.2","gene_symbol":"RN7SL716P","gene_name":"RNA, 7SL, cytoplasmic 716, pseudogene [Source:HGNC Symbol;Acc:HGNC:46732]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479484","summary":null,"start":59059226,"end":59059493,"strand":1,"description":"RNA, 7SL, cytoplasmic 716, pseudogene [Source:HGNC Symbol;Acc:HGNC:46732]"}, {"versioned_ensembl_gene_id":"ENSG00000274632.1","gene_symbol":"RN7SL719P","gene_name":"RNA, 7SL, cytoplasmic 719, pseudogene [Source:HGNC Symbol;Acc:HGNC:46735]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481119","summary":null,"start":28703554,"end":28703790,"strand":-1,"description":"RNA, 7SL, cytoplasmic 719, pseudogene [Source:HGNC Symbol;Acc:HGNC:46735]"}, {"versioned_ensembl_gene_id":"ENSG00000266150.1","gene_symbol":"MIR4711","gene_name":"microRNA 4711 [Source:HGNC Symbol;Acc:HGNC:41847]","synonyms":"hsa-mir-4711","biotype":"miRNA","ncbi_id":"100616409","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59733227,"end":59733296,"strand":-1,"description":"microRNA 4711 [Source:HGNC Symbol;Acc:HGNC:41847]"}, {"versioned_ensembl_gene_id":"ENSG00000207608.3","gene_symbol":"MIR127","gene_name":"microRNA 127 [Source:HGNC Symbol;Acc:HGNC:31509]","synonyms":"MIRN127,hsa-mir-127","biotype":"miRNA","ncbi_id":"406914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100882979,"end":100883075,"strand":1,"description":"microRNA 127 [Source:HGNC Symbol;Acc:HGNC:31509]"}, {"versioned_ensembl_gene_id":"ENSG00000275625.1","gene_symbol":"FTX_4","gene_name":"FTX transcript, XIST regulator conserved region 4 [Source:RFAM;Acc:RF02123]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74281703,"end":74281849,"strand":1,"description":"FTX transcript, XIST regulator conserved region 4 [Source:RFAM;Acc:RF02123]"}, {"versioned_ensembl_gene_id":"ENSG00000283475.1","gene_symbol":"MIR1244-4","gene_name":"microRNA 1244-4 [Source:HGNC Symbol;Acc:HGNC:50831]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504734","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12111952,"end":12112036,"strand":1,"description":"microRNA 1244-4 [Source:HGNC Symbol;Acc:HGNC:50831]"}, {"versioned_ensembl_gene_id":"ENSG00000212264.1","gene_symbol":"SNORD65C","gene_name":"small nucleolar RNA, C/D box 65C [Source:HGNC Symbol;Acc:HGNC:52232]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616981","summary":null,"start":23396446,"end":23396516,"strand":1,"description":"small nucleolar RNA, C/D box 65C [Source:HGNC Symbol;Acc:HGNC:52232]"}, {"versioned_ensembl_gene_id":"ENSG00000201809.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":73764279,"end":73764413,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000278483.1","gene_symbol":"MIR8087","gene_name":"microRNA 8087 [Source:HGNC Symbol;Acc:HGNC:50059]","synonyms":"hsa-mir-8087","biotype":"miRNA","ncbi_id":"102465881","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27514970,"end":27515047,"strand":-1,"description":"microRNA 8087 [Source:HGNC Symbol;Acc:HGNC:50059]"}, {"versioned_ensembl_gene_id":"ENSG00000244391.3","gene_symbol":"RN7SL330P","gene_name":"RNA, 7SL, cytoplasmic 330, pseudogene [Source:HGNC Symbol;Acc:HGNC:46346]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481013","summary":null,"start":94361220,"end":94361526,"strand":1,"description":"RNA, 7SL, cytoplasmic 330, pseudogene [Source:HGNC Symbol;Acc:HGNC:46346]"}, {"versioned_ensembl_gene_id":"ENSG00000222832.1","gene_symbol":"RNA5SP120","gene_name":"RNA, 5S ribosomal pseudogene 120 [Source:HGNC Symbol;Acc:HGNC:42918]","synonyms":"RN5S120","biotype":"rRNA","ncbi_id":"100873390","summary":null,"start":216793489,"end":216793600,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 120 [Source:HGNC Symbol;Acc:HGNC:42918]"}, {"versioned_ensembl_gene_id":"ENSG00000252368.1","gene_symbol":"RNA5SP43","gene_name":"RNA, 5S ribosomal pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:42819]","synonyms":"RN5S43","biotype":"rRNA","ncbi_id":"100873282","summary":null,"start":37264677,"end":37264786,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:42819]"}, {"versioned_ensembl_gene_id":"ENSG00000275656.1","gene_symbol":"RFPL3-AS1_1","gene_name":"RFPL3 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02171]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32188400,"end":32188487,"strand":-1,"description":"RFPL3 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02171]"}, {"versioned_ensembl_gene_id":"ENSG00000266782.1","gene_symbol":"MIR3663","gene_name":"microRNA 3663 [Source:HGNC Symbol;Acc:HGNC:38958]","synonyms":"hsa-mir-3663","biotype":"miRNA","ncbi_id":"100500893","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":117167678,"end":117167774,"strand":-1,"description":"microRNA 3663 [Source:HGNC Symbol;Acc:HGNC:38958]"}, {"versioned_ensembl_gene_id":"ENSG00000273981.1","gene_symbol":"RN7SL106P","gene_name":"RNA, 7SL, cytoplasmic 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:46122]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479261","summary":null,"start":23165897,"end":23166186,"strand":1,"description":"RNA, 7SL, cytoplasmic 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:46122]"}, {"versioned_ensembl_gene_id":"ENSG00000222281.1","gene_symbol":"RN7SKP111","gene_name":"RNA, 7SK small nuclear pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:45835]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479144","summary":null,"start":11818821,"end":11819091,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:45835]"}, {"versioned_ensembl_gene_id":"ENSG00000283938.1","gene_symbol":"MIR3917","gene_name":"microRNA 3917 [Source:HGNC Symbol;Acc:HGNC:38911]","synonyms":"hsa-mir-3917","biotype":"miRNA","ncbi_id":"100500808","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25906362,"end":25906454,"strand":-1,"description":"microRNA 3917 [Source:HGNC Symbol;Acc:HGNC:38911]"}, {"versioned_ensembl_gene_id":"ENSG00000266477.2","gene_symbol":"RN7SL616P","gene_name":"RNA, 7SL, cytoplasmic 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:46632]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481090","summary":null,"start":69478997,"end":69479265,"strand":-1,"description":"RNA, 7SL, cytoplasmic 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:46632]"}, {"versioned_ensembl_gene_id":"ENSG00000241413.3","gene_symbol":"RN7SL441P","gene_name":"RNA, 7SL, cytoplasmic 441, pseudogene [Source:HGNC Symbol;Acc:HGNC:46457]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479383","summary":null,"start":109866214,"end":109866509,"strand":-1,"description":"RNA, 7SL, cytoplasmic 441, pseudogene [Source:HGNC Symbol;Acc:HGNC:46457]"}, {"versioned_ensembl_gene_id":"ENSG00000222224.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28927243,"end":28927340,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206719.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":113950886,"end":113950998,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252401.1","gene_symbol":"RNU4ATAC6P","gene_name":"RNA, U4atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46892]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479540","summary":null,"start":28652630,"end":28652755,"strand":1,"description":"RNA, U4atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46892]"}, {"versioned_ensembl_gene_id":"ENSG00000201613.1","gene_symbol":"RNU6-200P","gene_name":"RNA, U6 small nuclear 200, pseudogene [Source:HGNC Symbol;Acc:HGNC:47163]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479655","summary":null,"start":126590287,"end":126590393,"strand":-1,"description":"RNA, U6 small nuclear 200, pseudogene [Source:HGNC Symbol;Acc:HGNC:47163]"}, {"versioned_ensembl_gene_id":"ENSG00000265894.2","gene_symbol":"RN7SL357P","gene_name":"RNA, 7SL, cytoplasmic 357, pseudogene [Source:HGNC Symbol;Acc:HGNC:46373]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481021","summary":null,"start":56805834,"end":56806131,"strand":1,"description":"RNA, 7SL, cytoplasmic 357, pseudogene [Source:HGNC Symbol;Acc:HGNC:46373]"}, {"versioned_ensembl_gene_id":"ENSG00000264423.2","gene_symbol":"RN7SL718P","gene_name":"RNA, 7SL, cytoplasmic 718, pseudogene [Source:HGNC Symbol;Acc:HGNC:46734]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479485","summary":null,"start":41190927,"end":41191229,"strand":-1,"description":"RNA, 7SL, cytoplasmic 718, pseudogene [Source:HGNC Symbol;Acc:HGNC:46734]"}, {"versioned_ensembl_gene_id":"ENSG00000277474.1","gene_symbol":"MIR6894","gene_name":"microRNA 6894 [Source:HGNC Symbol;Acc:HGNC:49938]","synonyms":"hsa-mir-6894","biotype":"miRNA","ncbi_id":"102466759","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53198889,"end":53198945,"strand":-1,"description":"microRNA 6894 [Source:HGNC Symbol;Acc:HGNC:49938]"}, {"versioned_ensembl_gene_id":"ENSG00000272412.2","gene_symbol":"RN7SL778P","gene_name":"RNA, 7SL, cytoplasmic 778, pseudogene [Source:HGNC Symbol;Acc:HGNC:46794]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479504","summary":null,"start":130310180,"end":130310476,"strand":1,"description":"RNA, 7SL, cytoplasmic 778, pseudogene [Source:HGNC Symbol;Acc:HGNC:46794]"}, {"versioned_ensembl_gene_id":"ENSG00000207291.1","gene_symbol":"RNU6-30P","gene_name":"RNA, U6 small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:34274]","synonyms":"RNU6-30","biotype":"snRNA","ncbi_id":"100873747","summary":null,"start":101634006,"end":101634112,"strand":-1,"description":"RNA, U6 small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:34274]"}, {"versioned_ensembl_gene_id":"ENSG00000208033.1","gene_symbol":"MIR609","gene_name":"microRNA 609 [Source:HGNC Symbol;Acc:HGNC:32865]","synonyms":"MIRN609,hsa-mir-609","biotype":"miRNA","ncbi_id":"693194","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104218789,"end":104218883,"strand":-1,"description":"microRNA 609 [Source:HGNC Symbol;Acc:HGNC:32865]"}, {"versioned_ensembl_gene_id":"ENSG00000201407.1","gene_symbol":"SNORA68","gene_name":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]","synonyms":"RNU68,U68,SNORA68A","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":24133186,"end":24133317,"strand":1,"description":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]"}, {"versioned_ensembl_gene_id":"ENSG00000274428.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":146409903,"end":146410062,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000201339.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93967926,"end":93968020,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263989.2","gene_symbol":"RN7SL615P","gene_name":"RNA, 7SL, cytoplasmic 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:46631]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479446","summary":null,"start":41290280,"end":41290577,"strand":-1,"description":"RNA, 7SL, cytoplasmic 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:46631]"}, {"versioned_ensembl_gene_id":"ENSG00000200033.1","gene_symbol":"RNU6-403P","gene_name":"RNA, U6 small nuclear 403, pseudogene [Source:HGNC Symbol;Acc:HGNC:47366]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480578","summary":null,"start":221837334,"end":221837437,"strand":-1,"description":"RNA, U6 small nuclear 403, pseudogene [Source:HGNC Symbol;Acc:HGNC:47366]"}, {"versioned_ensembl_gene_id":"ENSG00000264833.1","gene_symbol":"RN7SL468P","gene_name":"RNA, 7SL, cytoplasmic 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:46484]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481050","summary":null,"start":119169822,"end":119170115,"strand":1,"description":"RNA, 7SL, cytoplasmic 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:46484]"}, {"versioned_ensembl_gene_id":"ENSG00000200629.1","gene_symbol":"RNY1P11","gene_name":"RNA, Ro-associated Y1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50874]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481710","summary":null,"start":129164849,"end":129164961,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50874]"}, {"versioned_ensembl_gene_id":"ENSG00000276168.1","gene_symbol":"RN7SL1","gene_name":"RNA, 7SL, cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:10038]","synonyms":"7SL,7L1a,RNSRP1,RN7SL","biotype":"misc_RNA","ncbi_id":"6029","summary":"The signal recognition particle (SRP) is a cytoplasmic ribonucleoprotein complex that mediates cotranslational insertion of secretory proteins into the lumen of the endoplasmic reticulum. The SRP consists of 6 polypeptides (e.g., SRP19; MIM 182175) and a 7SL RNA molecule, such as RN7SL1, that is partially homologous to Alu DNA (Ullu and Weiner, 1984 [PubMed 6084597]).[supplied by OMIM, Jul 2008]","start":49586580,"end":49586878,"strand":1,"description":"RNA, 7SL, cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:10038]"}, {"versioned_ensembl_gene_id":"ENSG00000206862.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":118569405,"end":118569515,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200485.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33196547,"end":33196637,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200906.1","gene_symbol":"RNU6-854P","gene_name":"RNA, U6 small nuclear 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{"versioned_ensembl_gene_id":"ENSG00000222581.1","gene_symbol":"RNU2-47P","gene_name":"RNA, U2 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:48540]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480672","summary":null,"start":12300266,"end":12300451,"strand":-1,"description":"RNA, U2 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:48540]"}, {"versioned_ensembl_gene_id":"ENSG00000202150.1","gene_symbol":"RNU6-407P","gene_name":"RNA, U6 small nuclear 407, pseudogene [Source:HGNC Symbol;Acc:HGNC:47370]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479745","summary":null,"start":35030317,"end":35030420,"strand":-1,"description":"RNA, U6 small nuclear 407, pseudogene [Source:HGNC Symbol;Acc:HGNC:47370]"}, {"versioned_ensembl_gene_id":"ENSG00000243437.3","gene_symbol":"RN7SL370P","gene_name":"RNA, 7SL, cytoplasmic 370, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000207088.1","gene_symbol":"SNORA7B","gene_name":"small nucleolar RNA, H/ACA box 7B [Source:HGNC Symbol;Acc:HGNC:32593]","synonyms":"ACA7B","biotype":"snoRNA","ncbi_id":"677797","summary":null,"start":129397210,"end":129397348,"strand":-1,"description":"small nucleolar RNA, H/ACA box 7B [Source:HGNC Symbol;Acc:HGNC:32593]"}, {"versioned_ensembl_gene_id":"ENSG00000273532.1","gene_symbol":"H19_1","gene_name":"H19 conserved region 1 [Source:RFAM;Acc:RF01972]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51722,"end":51792,"strand":1,"description":"H19 conserved region 1 [Source:RFAM;Acc:RF01972]"}, {"versioned_ensembl_gene_id":"ENSG00000252416.1","gene_symbol":"RNU6-885P","gene_name":"RNA, U6 small nuclear 885, pseudogene [Source:HGNC Symbol;Acc:HGNC:47848]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481458","summary":null,"start":42832447,"end":42832550,"strand":-1,"description":"RNA, U6 small nuclear 885, pseudogene [Source:HGNC Symbol;Acc:HGNC:47848]"}, {"versioned_ensembl_gene_id":"ENSG00000200153.1","gene_symbol":"RNU6-23P","gene_name":"RNA, U6 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:34267]","synonyms":"RNU6-23","biotype":"snRNA","ncbi_id":"100873755","summary":null,"start":70445293,"end":70445399,"strand":-1,"description":"RNA, U6 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:34267]"}, {"versioned_ensembl_gene_id":"ENSG00000239958.3","gene_symbol":"RN7SL51P","gene_name":"RNA, 7SL, cytoplasmic 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:46067]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480936","summary":null,"start":62262387,"end":62262671,"strand":-1,"description":"RNA, 7SL, cytoplasmic 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:46067]"}, {"versioned_ensembl_gene_id":"ENSG00000202410.1","gene_symbol":"Y_RNA","gene_name":"Y RNA 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{"versioned_ensembl_gene_id":"ENSG00000201821.1","gene_symbol":"RNU4-9P","gene_name":"RNA, U4 small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42507]","synonyms":null,"biotype":"snRNA","ncbi_id":"100862675","summary":null,"start":21038529,"end":21038667,"strand":-1,"description":"RNA, U4 small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42507]"}, {"versioned_ensembl_gene_id":"ENSG00000277582.1","gene_symbol":"RN7SL428P","gene_name":"RNA, 7SL, cytoplasmic 428, pseudogene [Source:HGNC Symbol;Acc:HGNC:46444]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479379","summary":null,"start":85210053,"end":85210299,"strand":-1,"description":"RNA, 7SL, cytoplasmic 428, pseudogene [Source:HGNC Symbol;Acc:HGNC:46444]"}, {"versioned_ensembl_gene_id":"ENSG00000199476.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48288587,"end":48288694,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206763.1","gene_symbol":"RNU6-10P","gene_name":"RNA, U6 small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34254]","synonyms":"RNU6-10","biotype":"snRNA","ncbi_id":"100873745","summary":null,"start":92701708,"end":92701814,"strand":-1,"description":"RNA, U6 small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34254]"}, {"versioned_ensembl_gene_id":"ENSG00000207871.2","gene_symbol":"MIR513B","gene_name":"microRNA 513b [Source:HGNC Symbol;Acc:HGNC:33935]","synonyms":"MIRN513B,hsa-mir-513b","biotype":"miRNA","ncbi_id":"100313822","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147199044,"end":147199127,"strand":-1,"description":"microRNA 513b [Source:HGNC Symbol;Acc:HGNC:33935]"}, {"versioned_ensembl_gene_id":"ENSG00000251874.1","gene_symbol":"RNU6-615P","gene_name":"RNA, U6 small nuclear 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:47578]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480595","summary":null,"start":83003412,"end":83003517,"strand":1,"description":"RNA, U6 small nuclear 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:47578]"}, {"versioned_ensembl_gene_id":"ENSG00000201800.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":125516979,"end":125517086,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276158.2","gene_symbol":"MIR1264","gene_name":"microRNA 1264 [Source:HGNC Symbol;Acc:HGNC:35246]","synonyms":"hsa-mir-1264,MIRN1264","biotype":"miRNA","ncbi_id":"100302251","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114652655,"end":114652723,"strand":1,"description":"microRNA 1264 [Source:HGNC Symbol;Acc:HGNC:35246]"}, {"versioned_ensembl_gene_id":"ENSG00000251886.1","gene_symbol":"RNU6-120P","gene_name":"RNA, U6 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:47083]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479619","summary":null,"start":21120404,"end":21120506,"strand":-1,"description":"RNA, U6 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:47083]"}, {"versioned_ensembl_gene_id":"ENSG00000207290.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128371099,"end":128371212,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199523.1","gene_symbol":"RNA5SP226","gene_name":"RNA, 5S ribosomal pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:43126]","synonyms":"RN5S226","biotype":"rRNA","ncbi_id":"106479000","summary":null,"start":165409562,"end":165409676,"strand":1,"description":"RNA, 5S ribosomal pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:43126]"}, {"versioned_ensembl_gene_id":"ENSG00000201142.1","gene_symbol":"RNVU1-8","gene_name":"RNA, variant U1 small nuclear 8 [Source:HGNC Symbol;Acc:HGNC:48315]","synonyms":"vU1.8,RNU1-145","biotype":"snRNA","ncbi_id":"101447996","summary":null,"start":147079746,"end":147079870,"strand":1,"description":"RNA, variant U1 small nuclear 8 [Source:HGNC Symbol;Acc:HGNC:48315]"}, {"versioned_ensembl_gene_id":"ENSG00000283461.1","gene_symbol":"hsa-mir-550a-2","gene_name":"hsa-mir-550a-2 [Source:miRBase;Acc:MI0003601]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":32732981,"end":32733077,"strand":-1,"description":"hsa-mir-550a-2 [Source:miRBase;Acc:MI0003601]"}, {"versioned_ensembl_gene_id":"ENSG00000207203.1","gene_symbol":"RNU6-71P","gene_name":"RNA, U6 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:42561]","synonyms":"RNU6-71","biotype":"snRNA","ncbi_id":"100873774","summary":null,"start":36267168,"end":36267274,"strand":1,"description":"RNA, U6 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:42561]"}, {"versioned_ensembl_gene_id":"ENSG00000266776.1","gene_symbol":"MIR4646","gene_name":"microRNA 4646 [Source:HGNC Symbol;Acc:HGNC:41543]","synonyms":"hsa-mir-4646","biotype":"miRNA","ncbi_id":"100616230","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31701029,"end":31701091,"strand":-1,"description":"microRNA 4646 [Source:HGNC Symbol;Acc:HGNC:41543]"}, {"versioned_ensembl_gene_id":"ENSG00000212247.1","gene_symbol":"RNU6-278P","gene_name":"RNA, U6 small nuclear 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:47241]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481767","summary":null,"start":13973316,"end":13973424,"strand":-1,"description":"RNA, U6 small nuclear 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:47241]"}, {"versioned_ensembl_gene_id":"ENSG00000206600.1","gene_symbol":"RNU6-25P","gene_name":"RNA, U6 small nuclear 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:34251]","synonyms":"RNU6-25","biotype":"snRNA","ncbi_id":"106480704","summary":null,"start":195214787,"end":195214893,"strand":1,"description":"RNA, U6 small nuclear 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:34251]"}, {"versioned_ensembl_gene_id":"ENSG00000252169.1","gene_symbol":"RNA5SP200","gene_name":"RNA, 5S ribosomal pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:43100]","synonyms":"RN5S200","biotype":"rRNA","ncbi_id":"100873461","summary":null,"start":173292517,"end":173292619,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:43100]"}, {"versioned_ensembl_gene_id":"ENSG00000263981.1","gene_symbol":"MIR5705","gene_name":"microRNA 5705 [Source:HGNC Symbol;Acc:HGNC:43504]","synonyms":"hsa-mir-5705","biotype":"miRNA","ncbi_id":"100847027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87300495,"end":87300583,"strand":-1,"description":"microRNA 5705 [Source:HGNC Symbol;Acc:HGNC:43504]"}, {"versioned_ensembl_gene_id":"ENSG00000199466.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":124766196,"end":124766297,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265648.2","gene_symbol":"RN7SL279P","gene_name":"RNA, 7SL, cytoplasmic 279, pseudogene [Source:HGNC Symbol;Acc:HGNC:46295]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480998","summary":null,"start":70276069,"end":70276352,"strand":1,"description":"RNA, 7SL, cytoplasmic 279, pseudogene [Source:HGNC Symbol;Acc:HGNC:46295]"}, {"versioned_ensembl_gene_id":"ENSG00000207434.1","gene_symbol":"RNU6-1072P","gene_name":"RNA, U6 small nuclear 1072, pseudogene [Source:HGNC Symbol;Acc:HGNC:48035]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480037","summary":null,"start":12922554,"end":12922660,"strand":1,"description":"RNA, U6 small nuclear 1072, pseudogene [Source:HGNC Symbol;Acc:HGNC:48035]"}, {"versioned_ensembl_gene_id":"ENSG00000239932.3","gene_symbol":"RN7SL606P","gene_name":"RNA, 7SL, cytoplasmic 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:46622]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479443","summary":null,"start":60696313,"end":60696605,"strand":1,"description":"RNA, 7SL, cytoplasmic 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:46622]"}, {"versioned_ensembl_gene_id":"ENSG00000222778.1","gene_symbol":"RNA5SP144","gene_name":"RNA, 5S ribosomal pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:43044]","synonyms":"RN5S144","biotype":"rRNA","ncbi_id":"100873411","summary":null,"start":144186905,"end":144187020,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:43044]"}, {"versioned_ensembl_gene_id":"ENSG00000280751.1","gene_symbol":"AKR7A2P1","gene_name":"aldo-keto reductase family 7 member A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24062]","synonyms":"AFARP1","biotype":"processed_pseudogene","ncbi_id":"246182","summary":null,"start":112923423,"end":112924337,"strand":1,"description":"aldo-keto reductase family 7 member A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24062]"}, {"versioned_ensembl_gene_id":"ENSG00000266754.2","gene_symbol":"RN7SL524P","gene_name":"RNA, 7SL, cytoplasmic 524, pseudogene [Source:HGNC Symbol;Acc:HGNC:46540]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481066","summary":null,"start":103974515,"end":103974814,"strand":-1,"description":"RNA, 7SL, cytoplasmic 524, pseudogene [Source:HGNC Symbol;Acc:HGNC:46540]"}, {"versioned_ensembl_gene_id":"ENSG00000202019.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31230071,"end":31230172,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201289.1","gene_symbol":"RN7SKP76","gene_name":"RNA, 7SK small nuclear pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:45800]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481808","summary":null,"start":61743154,"end":61743476,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:45800]"}, {"versioned_ensembl_gene_id":"ENSG00000251914.1","gene_symbol":"RNU7-200P","gene_name":"RNA, U7 small nuclear 200 pseudogene [Source:HGNC Symbol;Acc:HGNC:45734]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480835","summary":null,"start":20841241,"end":20841302,"strand":1,"description":"RNA, U7 small nuclear 200 pseudogene [Source:HGNC Symbol;Acc:HGNC:45734]"}, {"versioned_ensembl_gene_id":"ENSG00000224278.1","gene_symbol":"AL592447.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188242139,"end":188242678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275652.1","gene_symbol":"MIR6796","gene_name":"microRNA 6796 [Source:HGNC Symbol;Acc:HGNC:50186]","synonyms":"hsa-mir-6796","biotype":"miRNA","ncbi_id":"102465477","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40369846,"end":40369907,"strand":1,"description":"microRNA 6796 [Source:HGNC Symbol;Acc:HGNC:50186]"}, {"versioned_ensembl_gene_id":"ENSG00000252225.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36440880,"end":36440970,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252569.1","gene_symbol":"RNU6-1153P","gene_name":"RNA, U6 small nuclear 1153, pseudogene [Source:HGNC Symbol;Acc:HGNC:48116]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480643","summary":null,"start":53443228,"end":53443332,"strand":-1,"description":"RNA, U6 small nuclear 1153, pseudogene [Source:HGNC Symbol;Acc:HGNC:48116]"}, {"versioned_ensembl_gene_id":"ENSG00000212464.1","gene_symbol":"SNORA12","gene_name":"small nucleolar RNA, H/ACA box 12 [Source:HGNC Symbol;Acc:HGNC:32600]","synonyms":"U108","biotype":"snoRNA","ncbi_id":"677800","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA12, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":100237156,"end":100237302,"strand":-1,"description":"small nucleolar RNA, H/ACA box 12 [Source:HGNC Symbol;Acc:HGNC:32600]"}, {"versioned_ensembl_gene_id":"ENSG00000199168.3","gene_symbol":"MIR374A","gene_name":"microRNA 374a [Source:HGNC Symbol;Acc:HGNC:31788]","synonyms":"MIRN374A,MIRN374,hsa-mir-374a,hsa-mir-374","biotype":"miRNA","ncbi_id":"442919","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74287286,"end":74287357,"strand":-1,"description":"microRNA 374a [Source:HGNC Symbol;Acc:HGNC:31788]"}, {"versioned_ensembl_gene_id":"ENSG00000284190.1","gene_symbol":"MIR21","gene_name":"microRNA 21 [Source:HGNC Symbol;Acc:HGNC:31586]","synonyms":"MIRN21,MIR-21,hsa-mir-21","biotype":"miRNA","ncbi_id":"406991","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59841266,"end":59841337,"strand":1,"description":"microRNA 21 [Source:HGNC Symbol;Acc:HGNC:31586]"}, {"versioned_ensembl_gene_id":"ENSG00000199949.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86275429,"end":86275523,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278526.1","gene_symbol":"ST7-OT3_2","gene_name":"ST7 overlapping transcript 3 conserved region 2 [Source:RFAM;Acc:RF02184]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117190133,"end":117190269,"strand":1,"description":"ST7 overlapping transcript 3 conserved region 2 [Source:RFAM;Acc:RF02184]"}, {"versioned_ensembl_gene_id":"ENSG00000283770.1","gene_symbol":"MIR6849","gene_name":"microRNA 6849 [Source:HGNC Symbol;Acc:HGNC:49991]","synonyms":"hsa-mir-6849","biotype":"miRNA","ncbi_id":"102466749","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144400277,"end":144400345,"strand":-1,"description":"microRNA 6849 [Source:HGNC Symbol;Acc:HGNC:49991]"}, {"versioned_ensembl_gene_id":"ENSG00000222509.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":170783167,"end":170783271,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211997.1","gene_symbol":"MIR708","gene_name":"microRNA 708 [Source:HGNC Symbol;Acc:HGNC:33654]","synonyms":"MIRN708,hsa-mir-708","biotype":"miRNA","ncbi_id":"100126333","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79402022,"end":79402109,"strand":-1,"description":"microRNA 708 [Source:HGNC Symbol;Acc:HGNC:33654]"}, {"versioned_ensembl_gene_id":"ENSG00000200029.1","gene_symbol":"RNU6-642P","gene_name":"RNA, U6 small nuclear 642, pseudogene [Source:HGNC Symbol;Acc:HGNC:47605]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481384","summary":null,"start":218916184,"end":218916287,"strand":-1,"description":"RNA, U6 small nuclear 642, pseudogene [Source:HGNC Symbol;Acc:HGNC:47605]"}, {"versioned_ensembl_gene_id":"ENSG00000207467.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48809911,"end":48810016,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221611.1","gene_symbol":"SNORD88","gene_name":"Small nucleolar RNA SNORD88 [Source:RFAM;Acc:RF00604]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":12972053,"end":12972143,"strand":1,"description":"Small nucleolar RNA SNORD88 [Source:RFAM;Acc:RF00604]"}, {"versioned_ensembl_gene_id":"ENSG00000269859.1","gene_symbol":"AC008735.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55475983,"end":55476482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284047.1","gene_symbol":"MIR6836","gene_name":"microRNA 6836 [Source:HGNC Symbol;Acc:HGNC:50067]","synonyms":"hsa-mir-6836","biotype":"miRNA","ncbi_id":"102465503","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2257515,"end":2257577,"strand":-1,"description":"microRNA 6836 [Source:HGNC Symbol;Acc:HGNC:50067]"}, {"versioned_ensembl_gene_id":"ENSG00000252489.1","gene_symbol":"RNU6-197P","gene_name":"RNA, U6 small nuclear 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:47160]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479654","summary":null,"start":56288485,"end":56288584,"strand":-1,"description":"RNA, U6 small nuclear 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:47160]"}, {"versioned_ensembl_gene_id":"ENSG00000200164.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69191123,"end":69191223,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265806.1","gene_symbol":"MIR4292","gene_name":"microRNA 4292 [Source:HGNC Symbol;Acc:HGNC:38348]","synonyms":"hsa-mir-4292","biotype":"miRNA","ncbi_id":"100422860","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136830957,"end":136831023,"strand":1,"description":"microRNA 4292 [Source:HGNC Symbol;Acc:HGNC:38348]"}, {"versioned_ensembl_gene_id":"ENSG00000221563.1","gene_symbol":"MIR1269A","gene_name":"microRNA 1269a [Source:HGNC Symbol;Acc:HGNC:35337]","synonyms":"MIRN1269,MIR1269,hsa-mir-1269","biotype":"miRNA","ncbi_id":"100302177","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66276824,"end":66276928,"strand":1,"description":"microRNA 1269a [Source:HGNC Symbol;Acc:HGNC:35337]"}, {"versioned_ensembl_gene_id":"ENSG00000263670.1","gene_symbol":"MIR4457","gene_name":"microRNA 4457 [Source:HGNC Symbol;Acc:HGNC:41554]","synonyms":"hsa-mir-4457","biotype":"miRNA","ncbi_id":"100616235","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1309310,"end":1309377,"strand":-1,"description":"microRNA 4457 [Source:HGNC Symbol;Acc:HGNC:41554]"}, {"versioned_ensembl_gene_id":"ENSG00000266690.1","gene_symbol":"MIR4274","gene_name":"microRNA 4274 [Source:HGNC Symbol;Acc:HGNC:38194]","synonyms":"hsa-mir-4274","biotype":"miRNA","ncbi_id":"100422826","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7460028,"end":7460118,"strand":1,"description":"microRNA 4274 [Source:HGNC Symbol;Acc:HGNC:38194]"}, {"versioned_ensembl_gene_id":"ENSG00000252639.1","gene_symbol":"RNU2-24P","gene_name":"RNA, U2 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:48517]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480207","summary":null,"start":27193358,"end":27193500,"strand":-1,"description":"RNA, U2 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:48517]"}, {"versioned_ensembl_gene_id":"ENSG00000265328.1","gene_symbol":"MIR548AB","gene_name":"microRNA 548ab [Source:HGNC Symbol;Acc:HGNC:41825]","synonyms":"hsa-mir-548ab","biotype":"miRNA","ncbi_id":"100616336","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":103524033,"end":103524116,"strand":-1,"description":"microRNA 548ab [Source:HGNC Symbol;Acc:HGNC:41825]"}, {"versioned_ensembl_gene_id":"ENSG00000212214.1","gene_symbol":"SNORA48B","gene_name":"small nucleolar RNA, H/ACA box 48B [Source:HGNC Symbol;Acc:HGNC:52207]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616969","summary":null,"start":3532117,"end":3532251,"strand":-1,"description":"small nucleolar RNA, H/ACA box 48B [Source:HGNC Symbol;Acc:HGNC:52207]"}, {"versioned_ensembl_gene_id":"ENSG00000279214.1","gene_symbol":"AL109659.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48262230,"end":48263179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198987.1","gene_symbol":"MIR16-2","gene_name":"microRNA 16-2 [Source:HGNC Symbol;Acc:HGNC:31546]","synonyms":"MIRN16-2,hsa-mir-16-2","biotype":"miRNA","ncbi_id":"406951","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160404745,"end":160404825,"strand":1,"description":"microRNA 16-2 [Source:HGNC Symbol;Acc:HGNC:31546]"}, {"versioned_ensembl_gene_id":"ENSG00000265253.1","gene_symbol":"MIR4446","gene_name":"microRNA 4446 [Source:HGNC Symbol;Acc:HGNC:41700]","synonyms":"hsa-mir-4446","biotype":"miRNA","ncbi_id":"100616476","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113594876,"end":113594942,"strand":1,"description":"microRNA 4446 [Source:HGNC Symbol;Acc:HGNC:41700]"}, {"versioned_ensembl_gene_id":"ENSG00000264013.1","gene_symbol":"MIR3938","gene_name":"microRNA 3938 [Source:HGNC Symbol;Acc:HGNC:38972]","synonyms":"hsa-mir-3938","biotype":"miRNA","ncbi_id":"100500875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55852492,"end":55852594,"strand":-1,"description":"microRNA 3938 [Source:HGNC Symbol;Acc:HGNC:38972]"}, {"versioned_ensembl_gene_id":"ENSG00000284364.1","gene_symbol":"MIR6824","gene_name":"microRNA 6824 [Source:HGNC Symbol;Acc:HGNC:49946]","synonyms":"hsa-mir-6824","biotype":"miRNA","ncbi_id":"102465495","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48633636,"end":48633698,"strand":-1,"description":"microRNA 6824 [Source:HGNC Symbol;Acc:HGNC:49946]"}, {"versioned_ensembl_gene_id":"ENSG00000284092.1","gene_symbol":"MIR5703","gene_name":"microRNA 5703 [Source:HGNC Symbol;Acc:HGNC:43475]","synonyms":"hsa-mir-5703","biotype":"miRNA","ncbi_id":"100847081","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":227472132,"end":227472187,"strand":1,"description":"microRNA 5703 [Source:HGNC Symbol;Acc:HGNC:43475]"}, {"versioned_ensembl_gene_id":"ENSG00000264139.1","gene_symbol":"MIR3667","gene_name":"microRNA 3667 [Source:HGNC Symbol;Acc:HGNC:38990]","synonyms":"hsa-mir-3667","biotype":"miRNA","ncbi_id":"100500882","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49543393,"end":49543466,"strand":-1,"description":"microRNA 3667 [Source:HGNC Symbol;Acc:HGNC:38990]"}, {"versioned_ensembl_gene_id":"ENSG00000274385.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":30713240,"end":30713346,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200963.1","gene_symbol":"RNU6-289P","gene_name":"RNA, U6 small nuclear 289, pseudogene [Source:HGNC Symbol;Acc:HGNC:47252]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479695","summary":null,"start":111331412,"end":111331518,"strand":1,"description":"RNA, U6 small nuclear 289, pseudogene [Source:HGNC Symbol;Acc:HGNC:47252]"}, {"versioned_ensembl_gene_id":"ENSG00000252035.1","gene_symbol":"RNU6-397P","gene_name":"RNA, U6 small nuclear 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:47360]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479741","summary":null,"start":14487776,"end":14487879,"strand":-1,"description":"RNA, U6 small nuclear 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:47360]"}, {"versioned_ensembl_gene_id":"ENSG00000252568.1","gene_symbol":"RNU7-28P","gene_name":"RNA, U7 small nuclear 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:34124]","synonyms":"U7.28","biotype":"snRNA","ncbi_id":"100147815","summary":null,"start":9843815,"end":9843876,"strand":-1,"description":"RNA, U7 small nuclear 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:34124]"}, {"versioned_ensembl_gene_id":"ENSG00000266705.1","gene_symbol":"MIR4437","gene_name":"microRNA 4437 [Source:HGNC Symbol;Acc:HGNC:41715]","synonyms":"hsa-mir-4437","biotype":"miRNA","ncbi_id":"100616213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":181305593,"end":181305652,"strand":-1,"description":"microRNA 4437 [Source:HGNC Symbol;Acc:HGNC:41715]"}, {"versioned_ensembl_gene_id":"ENSG00000242614.3","gene_symbol":"RN7SL164P","gene_name":"RNA, 7SL, cytoplasmic 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:46180]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480965","summary":null,"start":96169545,"end":96169847,"strand":1,"description":"RNA, 7SL, cytoplasmic 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:46180]"}, {"versioned_ensembl_gene_id":"ENSG00000252136.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":105105987,"end":105106094,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000265499.1","gene_symbol":"MIR3156-2","gene_name":"microRNA 3156-2 [Source:HGNC Symbol;Acc:HGNC:38213]","synonyms":"hsa-mir-3156-2","biotype":"miRNA","ncbi_id":"100422907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14830166,"end":14830242,"strand":1,"description":"microRNA 3156-2 [Source:HGNC Symbol;Acc:HGNC:38213]"}, {"versioned_ensembl_gene_id":"ENSG00000207649.3","gene_symbol":"MIR138-2","gene_name":"microRNA 138-2 [Source:HGNC Symbol;Acc:HGNC:31525]","synonyms":"MIRN138-2,hsa-mir-138-2","biotype":"miRNA","ncbi_id":"406930","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56858518,"end":56858601,"strand":1,"description":"microRNA 138-2 [Source:HGNC Symbol;Acc:HGNC:31525]"}, {"versioned_ensembl_gene_id":"ENSG00000284186.1","gene_symbol":"MIR3615","gene_name":"microRNA 3615 [Source:HGNC Symbol;Acc:HGNC:38905]","synonyms":"hsa-mir-3615","biotype":"miRNA","ncbi_id":"100500847","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74748613,"end":74748699,"strand":1,"description":"microRNA 3615 [Source:HGNC Symbol;Acc:HGNC:38905]"}, {"versioned_ensembl_gene_id":"ENSG00000207606.1","gene_symbol":"MIR554","gene_name":"microRNA 554 [Source:HGNC Symbol;Acc:HGNC:32810]","synonyms":"MIRN554,hsa-mir-554","biotype":"miRNA","ncbi_id":"693139","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151545796,"end":151545891,"strand":1,"description":"microRNA 554 [Source:HGNC Symbol;Acc:HGNC:32810]"}, {"versioned_ensembl_gene_id":"ENSG00000198974.3","gene_symbol":"MIR30E","gene_name":"microRNA 30e [Source:HGNC Symbol;Acc:HGNC:31629]","synonyms":"MIRN30E,hsa-mir-30e","biotype":"miRNA","ncbi_id":"407034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40754355,"end":40754446,"strand":1,"description":"microRNA 30e [Source:HGNC Symbol;Acc:HGNC:31629]"}, {"versioned_ensembl_gene_id":"ENSG00000200413.1","gene_symbol":"SNORD114-26","gene_name":"small nucleolar RNA, C/D box 114-26 [Source:HGNC Symbol;Acc:HGNC:33014]","synonyms":"14q(II-26)","biotype":"snoRNA","ncbi_id":"767606","summary":null,"start":100987046,"end":100987117,"strand":1,"description":"small nucleolar RNA, C/D box 114-26 [Source:HGNC Symbol;Acc:HGNC:33014]"}, {"versioned_ensembl_gene_id":"ENSG00000252357.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":173808489,"end":173808622,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280280.1","gene_symbol":"AC006435.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2460183,"end":2460294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263652.1","gene_symbol":"MIR548AX","gene_name":"microRNA 548ax [Source:HGNC Symbol;Acc:HGNC:43528]","synonyms":"hsa-mir-548ax","biotype":"miRNA","ncbi_id":"100847063","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11318614,"end":11318686,"strand":-1,"description":"microRNA 548ax [Source:HGNC Symbol;Acc:HGNC:43528]"}, {"versioned_ensembl_gene_id":"ENSG00000277264.1","gene_symbol":"MIR6833","gene_name":"microRNA 6833 [Source:HGNC Symbol;Acc:HGNC:50245]","synonyms":"hsa-mir-6833","biotype":"miRNA","ncbi_id":"102465500","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32179816,"end":32179876,"strand":1,"description":"microRNA 6833 [Source:HGNC Symbol;Acc:HGNC:50245]"}, {"versioned_ensembl_gene_id":"ENSG00000277179.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NALP7,PAN7,PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54929128,"end":54953124,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000264661.3","gene_symbol":"MIR3200","gene_name":"microRNA 3200 [Source:HGNC Symbol;Acc:HGNC:38227]","synonyms":"hsa-mir-3200","biotype":"miRNA","ncbi_id":"100422912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30731557,"end":30731641,"strand":1,"description":"microRNA 3200 [Source:HGNC Symbol;Acc:HGNC:38227]"}, {"versioned_ensembl_gene_id":"ENSG00000283894.1","gene_symbol":"MIR1324","gene_name":"microRNA 1324 [Source:HGNC Symbol;Acc:HGNC:35377]","synonyms":"MIRN1324,hsa-mir-1324","biotype":"miRNA","ncbi_id":"100302212","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75630763,"end":75630858,"strand":1,"description":"microRNA 1324 [Source:HGNC Symbol;Acc:HGNC:35377]"}, {"versioned_ensembl_gene_id":"ENSG00000265301.1","gene_symbol":"MIR548AD","gene_name":"microRNA 548ad [Source:HGNC Symbol;Acc:HGNC:41683]","synonyms":"hsa-mir-548ad","biotype":"miRNA","ncbi_id":"100616475","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35471405,"end":35471486,"strand":1,"description":"microRNA 548ad [Source:HGNC Symbol;Acc:HGNC:41683]"}, {"versioned_ensembl_gene_id":"ENSG00000275950.1","gene_symbol":"MIR6724-1","gene_name":"microRNA 6724-1 [Source:HGNC Symbol;Acc:HGNC:50837]","synonyms":null,"biotype":"miRNA","ncbi_id":"102465433","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8205315,"end":8205406,"strand":1,"description":"microRNA 6724-1 [Source:HGNC Symbol;Acc:HGNC:50837]"}, {"versioned_ensembl_gene_id":"ENSG00000264405.1","gene_symbol":"MIR3913-1","gene_name":"microRNA 3913-1 [Source:HGNC Symbol;Acc:HGNC:38884]","synonyms":"hsa-mir-3913-1","biotype":"miRNA","ncbi_id":"100500903","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69584722,"end":69584823,"strand":-1,"description":"microRNA 3913-1 [Source:HGNC Symbol;Acc:HGNC:38884]"}, {"versioned_ensembl_gene_id":"ENSG00000265526.1","gene_symbol":"MIR4304","gene_name":"microRNA 4304 [Source:HGNC Symbol;Acc:HGNC:38276]","synonyms":"hsa-mir-4304","biotype":"miRNA","ncbi_id":"100422931","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123010667,"end":123010728,"strand":-1,"description":"microRNA 4304 [Source:HGNC Symbol;Acc:HGNC:38276]"}, {"versioned_ensembl_gene_id":"ENSG00000185222.8","gene_symbol":"TCEAL9","gene_name":"transcription elongation factor A like 9 [Source:HGNC Symbol;Acc:HGNC:30084]","synonyms":"WEX6,WBP5,DKFZp313K1940","biotype":"protein_coding","ncbi_id":"51186","summary":"The globular WW domain is composed of 38 to 40 semiconserved amino acids shared by proteins of diverse functions including structural, regulatory, and signaling proteins. The domain is involved in mediating protein-protein interactions through the binding of polyproline ligands. This gene encodes a WW domain binding protein. This gene also encodes a domain with similarity to the transcription elongation factor A, SII-related family. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008]","start":103356452,"end":103358451,"strand":1,"description":"transcription elongation factor A like 9 [Source:HGNC Symbol;Acc:HGNC:30084]"}, {"versioned_ensembl_gene_id":"ENSG00000199584.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127619336,"end":127619447,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252470.1","gene_symbol":"RNU6-551P","gene_name":"RNA, U6 small nuclear 551, pseudogene [Source:HGNC Symbol;Acc:HGNC:47514]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479811","summary":null,"start":107435118,"end":107435220,"strand":1,"description":"RNA, U6 small nuclear 551, pseudogene [Source:HGNC Symbol;Acc:HGNC:47514]"}, {"versioned_ensembl_gene_id":"ENSG00000277599.1","gene_symbol":"NEAT1_3","gene_name":"Nuclear enriched abundant transcript 1 conserved region 3 [Source:RFAM;Acc:RF01957]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65423960,"end":65424118,"strand":1,"description":"Nuclear enriched abundant transcript 1 conserved region 3 [Source:RFAM;Acc:RF01957]"}, {"versioned_ensembl_gene_id":"ENSG00000283489.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":132525809,"end":132525887,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000240299.3","gene_symbol":"RN7SL187P","gene_name":"RNA, 7SL, cytoplasmic 187, pseudogene [Source:HGNC Symbol;Acc:HGNC:46203]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481829","summary":null,"start":121494519,"end":121494821,"strand":1,"description":"RNA, 7SL, cytoplasmic 187, pseudogene [Source:HGNC Symbol;Acc:HGNC:46203]"}, {"versioned_ensembl_gene_id":"ENSG00000252173.1","gene_symbol":"RNU6-109P","gene_name":"RNA, U6 small nuclear 109, pseudogene [Source:HGNC Symbol;Acc:HGNC:47072]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481211","summary":null,"start":16248935,"end":16249041,"strand":1,"description":"RNA, U6 small nuclear 109, pseudogene [Source:HGNC Symbol;Acc:HGNC:47072]"}, {"versioned_ensembl_gene_id":"ENSG00000199687.1","gene_symbol":"RNU1-38P","gene_name":"RNA, U1 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:48380]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481608","summary":null,"start":85728194,"end":85728337,"strand":-1,"description":"RNA, U1 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:48380]"}, {"versioned_ensembl_gene_id":"ENSG00000201245.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"ACA25,SNORA25A","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":99783857,"end":99783983,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000207005.1","gene_symbol":"RNU1-2","gene_name":"RNA, U1 small nuclear 2 [Source:HGNC Symbol;Acc:HGNC:10123]","synonyms":"RNU1C2,RNU1C1,U1C21,U1C1","biotype":"snRNA","ncbi_id":"26870","summary":null,"start":16895980,"end":16896143,"strand":1,"description":"RNA, U1 small nuclear 2 [Source:HGNC Symbol;Acc:HGNC:10123]"}, {"versioned_ensembl_gene_id":"ENSG00000212338.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"U67,RNU67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":179196473,"end":179196579,"strand":1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000200350.1","gene_symbol":"RNU6-1285P","gene_name":"RNA, U6 small nuclear 1285, pseudogene [Source:HGNC Symbol;Acc:HGNC:48248]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481948","summary":null,"start":154543933,"end":154544037,"strand":-1,"description":"RNA, U6 small nuclear 1285, pseudogene [Source:HGNC Symbol;Acc:HGNC:48248]"}, {"versioned_ensembl_gene_id":"ENSG00000201207.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31663288,"end":31663401,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000243365.3","gene_symbol":"RN7SL278P","gene_name":"RNA, 7SL, cytoplasmic 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:46294]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479324","summary":null,"start":76976915,"end":76977210,"strand":-1,"description":"RNA, 7SL, cytoplasmic 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:46294]"}, {"versioned_ensembl_gene_id":"ENSG00000212479.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29180425,"end":29180639,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000252837.1","gene_symbol":"RN7SKP99","gene_name":"RNA, 7SK small nuclear pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:45823]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479138","summary":null,"start":57837354,"end":57837660,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:45823]"}, {"versioned_ensembl_gene_id":"ENSG00000275420.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69478716,"end":69478984,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000223086.1","gene_symbol":"RNA5SP155","gene_name":"RNA, 5S ribosomal pseudogene 155 [Source:HGNC Symbol;Acc:HGNC:43055]","synonyms":"RN5S155","biotype":"rRNA","ncbi_id":"100873421","summary":null,"start":10115756,"end":10115884,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 155 [Source:HGNC Symbol;Acc:HGNC:43055]"}, {"versioned_ensembl_gene_id":"ENSG00000274873.1","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160649,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000273770.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":78544095,"end":78544188,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201370.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":16623004,"end":16623095,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200057.1","gene_symbol":"RN7SKP63","gene_name":"RNA, 7SK small nuclear pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:45787]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479123","summary":null,"start":21389191,"end":21389491,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:45787]"}, {"versioned_ensembl_gene_id":"ENSG00000276902.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6365955,"end":6366055,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275319.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18524620,"end":18524935,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252191.1","gene_symbol":"RNU6-751P","gene_name":"RNA, U6 small nuclear 751, pseudogene [Source:HGNC Symbol;Acc:HGNC:47714]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479898","summary":null,"start":53749851,"end":53749951,"strand":-1,"description":"RNA, U6 small nuclear 751, pseudogene [Source:HGNC Symbol;Acc:HGNC:47714]"}, {"versioned_ensembl_gene_id":"ENSG00000277400.1","gene_symbol":"AC145212.2","gene_name":"MaFF-interacting protein [Source:UniProtKB/Swiss-Prot;Acc:Q8WZ33]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53590,"end":115018,"strand":-1,"description":"MaFF-interacting protein [Source:UniProtKB/Swiss-Prot;Acc:Q8WZ33]"}, {"versioned_ensembl_gene_id":"ENSG00000251764.1","gene_symbol":"RNA5SP446","gene_name":"RNA, 5S ribosomal pseudogene 446 [Source:HGNC Symbol;Acc:HGNC:43346]","synonyms":"RN5S446","biotype":"rRNA","ncbi_id":"100873692","summary":null,"start":66895491,"end":66895572,"strand":1,"description":"RNA, 5S ribosomal pseudogene 446 [Source:HGNC Symbol;Acc:HGNC:43346]"}, {"versioned_ensembl_gene_id":"ENSG00000264322.2","gene_symbol":"RN7SL448P","gene_name":"RNA, 7SL, cytoplasmic 448, pseudogene [Source:HGNC 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are present in the nucleoplasm. This RNA is processed from an intron of the prohibitin 2 host gene. It includes both an H/ACA box and a C/D box, and is thought to guide the pseudouridylation of residue U46 in the U5 small nuclear RNA. [provided by RefSeq, Jun 2010]","start":6967337,"end":6967606,"strand":-1,"description":"small Cajal body-specific RNA 12 [Source:HGNC Symbol;Acc:HGNC:32569]"}, {"versioned_ensembl_gene_id":"ENSG00000264275.1","gene_symbol":"RN7SL753P","gene_name":"RNA, 7SL, cytoplasmic 753, pseudogene [Source:HGNC Symbol;Acc:HGNC:46769]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479496","summary":null,"start":202333439,"end":202333728,"strand":1,"description":"RNA, 7SL, cytoplasmic 753, pseudogene [Source:HGNC Symbol;Acc:HGNC:46769]"}, {"versioned_ensembl_gene_id":"ENSG00000252464.1","gene_symbol":"RN7SKP70","gene_name":"RNA, 7SK small nuclear pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:45794]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107057644","summary":null,"start":178619728,"end":178619998,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:45794]"}, {"versioned_ensembl_gene_id":"ENSG00000251830.1","gene_symbol":"SNORD46","gene_name":"Small 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{"versioned_ensembl_gene_id":"ENSG00000200708.1","gene_symbol":"RN7SKP93","gene_name":"RNA, 7SK small nuclear pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:45817]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479136","summary":null,"start":133596091,"end":133596399,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:45817]"}, {"versioned_ensembl_gene_id":"ENSG00000239545.3","gene_symbol":"RN7SL822P","gene_name":"RNA, 7SL, cytoplasmic 822, pseudogene [Source:HGNC Symbol;Acc:HGNC:46838]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479521","summary":null,"start":55215624,"end":55215919,"strand":-1,"description":"RNA, 7SL, cytoplasmic 822, pseudogene [Source:HGNC Symbol;Acc:HGNC:46838]"}, {"versioned_ensembl_gene_id":"ENSG00000244091.1","gene_symbol":"RN7SL483P","gene_name":"RNA, 7SL, cytoplasmic 483, pseudogene [Source:HGNC 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[provided by RefSeq, Sep 2009]","start":140732564,"end":140732653,"strand":-1,"description":"microRNA 151a [Source:HGNC Symbol;Acc:HGNC:31762]"}, {"versioned_ensembl_gene_id":"ENSG00000283522.1","gene_symbol":"MIR3150A","gene_name":"microRNA 3150a [Source:HGNC Symbol;Acc:HGNC:38362]","synonyms":"MIR3150,hsa-mir-3150a,hsa-mir-3150","biotype":"miRNA","ncbi_id":"100422964","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95072914,"end":95072993,"strand":1,"description":"microRNA 3150a [Source:HGNC Symbol;Acc:HGNC:38362]"}, {"versioned_ensembl_gene_id":"ENSG00000222881.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40391232,"end":40391338,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265520.1","gene_symbol":"MIR548V","gene_name":"microRNA 548v [Source:HGNC Symbol;Acc:HGNC:38302]","synonyms":"hsa-mir-548v","biotype":"miRNA","ncbi_id":"100422850","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17681578,"end":17681657,"strand":-1,"description":"microRNA 548v [Source:HGNC Symbol;Acc:HGNC:38302]"}, {"versioned_ensembl_gene_id":"ENSG00000222764.1","gene_symbol":"RN7SKP106","gene_name":"RNA, 7SK small nuclear pseudogene 106 [Source:HGNC Symbol;Acc:HGNC:45830]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479142","summary":null,"start":141486141,"end":141486412,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 106 [Source:HGNC Symbol;Acc:HGNC:45830]"}, {"versioned_ensembl_gene_id":"ENSG00000264732.1","gene_symbol":"MIR4638","gene_name":"microRNA 4638 [Source:HGNC Symbol;Acc:HGNC:41841]","synonyms":"hsa-mir-4638","biotype":"miRNA","ncbi_id":"100616342","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":181222566,"end":181222633,"strand":-1,"description":"microRNA 4638 [Source:HGNC Symbol;Acc:HGNC:41841]"}, {"versioned_ensembl_gene_id":"ENSG00000201240.1","gene_symbol":"SNORD114-9","gene_name":"small nucleolar RNA, C/D box 114-9 [Source:HGNC Symbol;Acc:HGNC:32997]","synonyms":"14q(II-9)","biotype":"snoRNA","ncbi_id":"767585","summary":null,"start":100966029,"end":100966100,"strand":1,"description":"small nucleolar RNA, C/D box 114-9 [Source:HGNC Symbol;Acc:HGNC:32997]"}, {"versioned_ensembl_gene_id":"ENSG00000266698.1","gene_symbol":"MIR3945","gene_name":"microRNA 3945 [Source:HGNC Symbol;Acc:HGNC:38954]","synonyms":"hsa-mir-3945","biotype":"miRNA","ncbi_id":"100500818","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":184851013,"end":184851110,"strand":-1,"description":"microRNA 3945 [Source:HGNC Symbol;Acc:HGNC:38954]"}, {"versioned_ensembl_gene_id":"ENSG00000264494.1","gene_symbol":"MIR4650-2","gene_name":"microRNA 4650-2 [Source:HGNC Symbol;Acc:HGNC:41810]","synonyms":"hsa-mir-4650-2","biotype":"miRNA","ncbi_id":"100616331","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72697903,"end":72697978,"strand":1,"description":"microRNA 4650-2 [Source:HGNC Symbol;Acc:HGNC:41810]"}, {"versioned_ensembl_gene_id":"ENSG00000283275.1","gene_symbol":"MIR4275","gene_name":"microRNA 4275 [Source:HGNC Symbol;Acc:HGNC:38293]","synonyms":"hsa-mir-4275","biotype":"miRNA","ncbi_id":"100422937","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28819582,"end":28819668,"strand":1,"description":"microRNA 4275 [Source:HGNC Symbol;Acc:HGNC:38293]"}, {"versioned_ensembl_gene_id":"ENSG00000201314.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":145958128,"end":145958240,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201649.1","gene_symbol":"RNY4P34","gene_name":"RNA, Ro-associated Y4 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:50882]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481712","summary":null,"start":200373175,"end":200373269,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:50882]"}, {"versioned_ensembl_gene_id":"ENSG00000200288.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":177624282,"end":177624409,"strand":-1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000283733.1","gene_symbol":"MIR146A","gene_name":"microRNA 146a [Source:HGNC Symbol;Acc:HGNC:31533]","synonyms":"MIRN146A,MIRN146,hsa-mir-146a,hsa-mir-146","biotype":"miRNA","ncbi_id":"406938","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. Some of the targets of the encoded miRNA are the transcripts for tumor necrosis factor, interleukin 1 receptor-associated kinase 1, interleukin 1-beta, TNF receptor-associated factor 6, and complement factor H. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2015]","start":160485352,"end":160485450,"strand":1,"description":"microRNA 146a [Source:HGNC Symbol;Acc:HGNC:31533]"}, {"versioned_ensembl_gene_id":"ENSG00000273709.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43241180,"end":43241370,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000275523.1","gene_symbol":"MIR6508","gene_name":"microRNA 6508 [Source:HGNC Symbol;Acc:HGNC:50217]","synonyms":"hsa-mir-6508","biotype":"miRNA","ncbi_id":"102466972","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39447010,"end":39447069,"strand":1,"description":"microRNA 6508 [Source:HGNC Symbol;Acc:HGNC:50217]"}, {"versioned_ensembl_gene_id":"ENSG00000277671.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8250060,"end":8250149,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000252139.1","gene_symbol":"SCARNA18","gene_name":"small Cajal body-specific RNA 18 [Source:RFAM;Acc:RF00283]","synonyms":"U109,SCARNA18A","biotype":"scaRNA","ncbi_id":"677765","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":49814361,"end":49814443,"strand":1,"description":"small Cajal body-specific RNA 18 [Source:RFAM;Acc:RF00283]"}, {"versioned_ensembl_gene_id":"ENSG00000222378.1","gene_symbol":"RNA5SP44","gene_name":"RNA, 5S ribosomal pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:42820]","synonyms":"RN5S44","biotype":"rRNA","ncbi_id":"100873283","summary":null,"start":39154164,"end":39154296,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:42820]"}, {"versioned_ensembl_gene_id":"ENSG00000212205.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":211803017,"end":211803104,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265321.1","gene_symbol":"MIR4263","gene_name":"microRNA 4263 [Source:HGNC Symbol;Acc:HGNC:38365]","synonyms":"hsa-mir-4263","biotype":"miRNA","ncbi_id":"100422965","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27996367,"end":27996449,"strand":1,"description":"microRNA 4263 [Source:HGNC Symbol;Acc:HGNC:38365]"}, {"versioned_ensembl_gene_id":"ENSG00000199788.1","gene_symbol":"RNY3P2","gene_name":"RNA, Ro-associated Y3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42486]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862668","summary":null,"start":49095391,"end":49095492,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42486]"}, {"versioned_ensembl_gene_id":"ENSG00000199143.1","gene_symbol":"MIR373","gene_name":"microRNA 373 [Source:HGNC Symbol;Acc:HGNC:31787]","synonyms":"MIRN373,hsa-mir-373","biotype":"miRNA","ncbi_id":"442918","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53788705,"end":53788773,"strand":1,"description":"microRNA 373 [Source:HGNC Symbol;Acc:HGNC:31787]"}, {"versioned_ensembl_gene_id":"ENSG00000284031.1","gene_symbol":"MIR4761","gene_name":"microRNA 4761 [Source:HGNC Symbol;Acc:HGNC:41591]","synonyms":"hsa-mir-4761","biotype":"miRNA","ncbi_id":"100616414","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19963753,"end":19963834,"strand":1,"description":"microRNA 4761 [Source:HGNC Symbol;Acc:HGNC:41591]"}, {"versioned_ensembl_gene_id":"ENSG00000266649.1","gene_symbol":"MIR3126","gene_name":"microRNA 3126 [Source:HGNC Symbol;Acc:HGNC:38225]","synonyms":"hsa-mir-3126","biotype":"miRNA","ncbi_id":"100423030","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69103682,"end":69103755,"strand":1,"description":"microRNA 3126 [Source:HGNC Symbol;Acc:HGNC:38225]"}, {"versioned_ensembl_gene_id":"ENSG00000222293.1","gene_symbol":"RNU2-36P","gene_name":"RNA, U2 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48529]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481645","summary":null,"start":86422938,"end":86423128,"strand":-1,"description":"RNA, U2 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48529]"}, {"versioned_ensembl_gene_id":"ENSG00000207511.1","gene_symbol":"RNU6-443P","gene_name":"RNA, U6 small nuclear 443, pseudogene [Source:HGNC Symbol;Acc:HGNC:47406]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481318","summary":null,"start":13279125,"end":13279231,"strand":-1,"description":"RNA, U6 small nuclear 443, pseudogene [Source:HGNC Symbol;Acc:HGNC:47406]"}, {"versioned_ensembl_gene_id":"ENSG00000264113.2","gene_symbol":"RN7SL784P","gene_name":"RNA, 7SL, cytoplasmic 784, pseudogene [Source:HGNC Symbol;Acc:HGNC:46800]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481134","summary":null,"start":4882975,"end":4883316,"strand":1,"description":"RNA, 7SL, cytoplasmic 784, pseudogene [Source:HGNC Symbol;Acc:HGNC:46800]"}, {"versioned_ensembl_gene_id":"ENSG00000207761.3","gene_symbol":"MIR329-1","gene_name":"microRNA 329-1 [Source:HGNC Symbol;Acc:HGNC:32050]","synonyms":"MIRN329-1,hsa-mir-329-1","biotype":"miRNA","ncbi_id":"574408","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101026785,"end":101026864,"strand":1,"description":"microRNA 329-1 [Source:HGNC Symbol;Acc:HGNC:32050]"}, {"versioned_ensembl_gene_id":"ENSG00000284269.1","gene_symbol":"MIR7855","gene_name":"microRNA 7855 [Source:HGNC Symbol;Acc:HGNC:50244]","synonyms":"hsa-mir-7855","biotype":"miRNA","ncbi_id":"102465841","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64785626,"end":64785686,"strand":-1,"description":"microRNA 7855 [Source:HGNC Symbol;Acc:HGNC:50244]"}, {"versioned_ensembl_gene_id":"ENSG00000283785.1","gene_symbol":"MIR15A","gene_name":"microRNA 15a [Source:HGNC Symbol;Acc:HGNC:31543]","synonyms":"MIRN15A,hsa-mir-15a","biotype":"miRNA","ncbi_id":"406948","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50049119,"end":50049201,"strand":-1,"description":"microRNA 15a [Source:HGNC Symbol;Acc:HGNC:31543]"}, {"versioned_ensembl_gene_id":"ENSG00000201523.1","gene_symbol":"RNA5SP205","gene_name":"RNA, 5S ribosomal pseudogene 205 [Source:HGNC Symbol;Acc:HGNC:43105]","synonyms":"RN5S205","biotype":"rRNA","ncbi_id":"100873466","summary":null,"start":19438283,"end":19438418,"strand":1,"description":"RNA, 5S ribosomal pseudogene 205 [Source:HGNC Symbol;Acc:HGNC:43105]"}, {"versioned_ensembl_gene_id":"ENSG00000238964.1","gene_symbol":"RNU7-125P","gene_name":"RNA, U7 small nuclear 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:45659]","synonyms":"RNU7-135P","biotype":"snRNA","ncbi_id":"106480818","summary":null,"start":14643788,"end":14643849,"strand":1,"description":"RNA, U7 small nuclear 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:45659]"}, {"versioned_ensembl_gene_id":"ENSG00000221540.1","gene_symbol":"MIR1180","gene_name":"microRNA 1180 [Source:HGNC Symbol;Acc:HGNC:35261]","synonyms":"hsa-mir-1180,MIRN1180","biotype":"miRNA","ncbi_id":"100302256","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19344506,"end":19344574,"strand":-1,"description":"microRNA 1180 [Source:HGNC Symbol;Acc:HGNC:35261]"}, {"versioned_ensembl_gene_id":"ENSG00000199409.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":150098406,"end":150098506,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264906.1","gene_symbol":"MIR4494","gene_name":"microRNA 4494 [Source:HGNC Symbol;Acc:HGNC:41731]","synonyms":"hsa-mir-4494","biotype":"miRNA","ncbi_id":"100616478","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47364186,"end":47364269,"strand":-1,"description":"microRNA 4494 [Source:HGNC Symbol;Acc:HGNC:41731]"}, {"versioned_ensembl_gene_id":"ENSG00000207375.1","gene_symbol":"SNORD116-23","gene_name":"small nucleolar RNA, C/D box 116-23 [Source:HGNC Symbol;Acc:HGNC:33089]","synonyms":"HBII-85-23","biotype":"snoRNA","ncbi_id":"100033434","summary":null,"start":25091786,"end":25091877,"strand":1,"description":"small nucleolar RNA, C/D box 116-23 [Source:HGNC Symbol;Acc:HGNC:33089]"}, {"versioned_ensembl_gene_id":"ENSG00000200361.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":106688678,"end":106688779,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277243.1","gene_symbol":"MIR3118-3","gene_name":"microRNA 3118-3 [Source:HGNC Symbol;Acc:HGNC:38274]","synonyms":"hsa-mir-3118-3","biotype":"miRNA","ncbi_id":"100422844","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21406385,"end":21406459,"strand":1,"description":"microRNA 3118-3 [Source:HGNC Symbol;Acc:HGNC:38274]"}, {"versioned_ensembl_gene_id":"ENSG00000202257.1","gene_symbol":"RNA5S16","gene_name":"RNA, 5S ribosomal 16 [Source:HGNC Symbol;Acc:HGNC:34377]","synonyms":"RN5S16","biotype":"rRNA","ncbi_id":"100169767","summary":null,"start":228643809,"end":228643927,"strand":-1,"description":"RNA, 5S ribosomal 16 [Source:HGNC Symbol;Acc:HGNC:34377]"}, {"versioned_ensembl_gene_id":"ENSG00000265719.1","gene_symbol":"MIR4681","gene_name":"microRNA 4681 [Source:HGNC Symbol;Acc:HGNC:41753]","synonyms":"hsa-mir-4681","biotype":"miRNA","ncbi_id":"100616398","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119377972,"end":119378043,"strand":1,"description":"microRNA 4681 [Source:HGNC Symbol;Acc:HGNC:41753]"}, {"versioned_ensembl_gene_id":"ENSG00000277634.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49839401,"end":49839493,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207242.1","gene_symbol":"RNU6-1065P","gene_name":"RNA, U6 small nuclear 1065, pseudogene [Source:HGNC Symbol;Acc:HGNC:48028]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480034","summary":null,"start":10857899,"end":10858004,"strand":-1,"description":"RNA, U6 small nuclear 1065, pseudogene [Source:HGNC Symbol;Acc:HGNC:48028]"}, {"versioned_ensembl_gene_id":"ENSG00000274196.4","gene_symbol":"FAM197Y4","gene_name":"family with sequence similarity 197 Y-linked member 4 [Source:HGNC Symbol;Acc:HGNC:37466]","synonyms":"FAM197Y4P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100289188","summary":null,"start":9479053,"end":9486239,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 4 [Source:HGNC Symbol;Acc:HGNC:37466]"}, {"versioned_ensembl_gene_id":"ENSG00000242206.2","gene_symbol":"AP004217.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118761856,"end":118762201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273997.1","gene_symbol":"AL355365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147406531,"end":147406824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274056.1","gene_symbol":"MIR6507","gene_name":"microRNA 6507 [Source:HGNC Symbol;Acc:HGNC:50199]","synonyms":"hsa-mir-6507","biotype":"miRNA","ncbi_id":"102465253","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98924499,"end":98924568,"strand":-1,"description":"microRNA 6507 [Source:HGNC Symbol;Acc:HGNC:50199]"}, {"versioned_ensembl_gene_id":"ENSG00000284122.1","gene_symbol":"MIR6717","gene_name":"microRNA 6717 [Source:HGNC Symbol;Acc:HGNC:50000]","synonyms":"hsa-mir-6717","biotype":"miRNA","ncbi_id":"102465428","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21023314,"end":21023386,"strand":-1,"description":"microRNA 6717 [Source:HGNC Symbol;Acc:HGNC:50000]"}, {"versioned_ensembl_gene_id":"ENSG00000274202.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":93197,"end":93309,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000278281.1","gene_symbol":"MIR7856","gene_name":"microRNA 7856 [Source:HGNC Symbol;Acc:HGNC:50268]","synonyms":"hsa-mir-7856","biotype":"miRNA","ncbi_id":"102465842","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86357632,"end":86357687,"strand":-1,"description":"microRNA 7856 [Source:HGNC Symbol;Acc:HGNC:50268]"}, {"versioned_ensembl_gene_id":"ENSG00000284425.1","gene_symbol":"MIR8072","gene_name":"microRNA 8072 [Source:HGNC Symbol;Acc:HGNC:50174]","synonyms":"hsa-mir-8072","biotype":"miRNA","ncbi_id":"102466877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123364764,"end":123364843,"strand":-1,"description":"microRNA 8072 [Source:HGNC Symbol;Acc:HGNC:50174]"}, {"versioned_ensembl_gene_id":"ENSG00000207402.1","gene_symbol":"RNU6-959P","gene_name":"RNA, U6 small nuclear 959, pseudogene [Source:HGNC Symbol;Acc:HGNC:47922]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479990","summary":null,"start":191121950,"end":191122056,"strand":1,"description":"RNA, U6 small nuclear 959, pseudogene [Source:HGNC Symbol;Acc:HGNC:47922]"}, {"versioned_ensembl_gene_id":"ENSG00000278715.1","gene_symbol":"SNORD116-20","gene_name":"small nucleolar RNA, C/D box 116-20 [Source:HGNC Symbol;Acc:HGNC:33086]","synonyms":"HBII-85-20","biotype":"snoRNA","ncbi_id":"100033431","summary":null,"start":25087662,"end":25087753,"strand":1,"description":"small nucleolar RNA, C/D box 116-20 [Source:HGNC Symbol;Acc:HGNC:33086]"}, {"versioned_ensembl_gene_id":"ENSG00000263426.2","gene_symbol":"RN7SL471P","gene_name":"RNA, 7SL, cytoplasmic 471, pseudogene [Source:HGNC Symbol;Acc:HGNC:46487]","synonyms":"RN7SL257P","biotype":"misc_RNA","ncbi_id":"106481051","summary":null,"start":28977475,"end":28977773,"strand":1,"description":"RNA, 7SL, cytoplasmic 471, pseudogene [Source:HGNC Symbol;Acc:HGNC:46487]"}, {"versioned_ensembl_gene_id":"ENSG00000207108.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185630428,"end":185630528,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252863.1","gene_symbol":"RNU6-1183P","gene_name":"RNA, U6 small nuclear 1183, pseudogene [Source:HGNC Symbol;Acc:HGNC:48146]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481941","summary":null,"start":101871742,"end":101871801,"strand":-1,"description":"RNA, U6 small nuclear 1183, pseudogene [Source:HGNC Symbol;Acc:HGNC:48146]"}, {"versioned_ensembl_gene_id":"ENSG00000222741.1","gene_symbol":"RNA5SP229","gene_name":"RNA, 5S ribosomal pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:43129]","synonyms":"RN5S229","biotype":"rRNA","ncbi_id":"100873487","summary":null,"start":33177740,"end":33177838,"strand":1,"description":"RNA, 5S ribosomal pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:43129]"}, {"versioned_ensembl_gene_id":"ENSG00000278115.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32682415,"end":32682705,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200422.1","gene_symbol":"SNORD45","gene_name":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":87146733,"end":87146804,"strand":1,"description":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]"}, {"versioned_ensembl_gene_id":"ENSG00000264218.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29747847,"end":29747948,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202093.1","gene_symbol":"SNORD58C","gene_name":"small nucleolar RNA, C/D box 58C [Source:HGNC Symbol;Acc:HGNC:33613]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124516","summary":null,"start":49489245,"end":49489308,"strand":-1,"description":"small nucleolar RNA, C/D box 58C [Source:HGNC Symbol;Acc:HGNC:33613]"}, {"versioned_ensembl_gene_id":"ENSG00000277233.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48429269,"end":48429554,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222515.1","gene_symbol":"RN7SKP240","gene_name":"RNA, 7SK small nuclear pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:45964]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479202","summary":null,"start":22085544,"end":22085918,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:45964]"}, {"versioned_ensembl_gene_id":"ENSG00000223274.6","gene_symbol":"RNA5SP498","gene_name":"RNA, 5S ribosomal pseudogene 498 [Source:HGNC Symbol;Acc:HGNC:43398]","synonyms":"RN5S498","biotype":"rRNA","ncbi_id":"106480770","summary":null,"start":1300256,"end":1300375,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 498 [Source:HGNC Symbol;Acc:HGNC:43398]"}, {"versioned_ensembl_gene_id":"ENSG00000159712.10","gene_symbol":"ANKRD18CP","gene_name":"ankyrin repeat domain 18C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43601]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101926917","summary":null,"start":97156570,"end":97221235,"strand":-1,"description":"ankyrin repeat domain 18C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43601]"}, {"versioned_ensembl_gene_id":"ENSG00000263972.1","gene_symbol":"MIR1587","gene_name":"microRNA 1587 [Source:HGNC Symbol;Acc:HGNC:41596]","synonyms":"hsa-mir-1587","biotype":"miRNA","ncbi_id":"100616251","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39837561,"end":39837613,"strand":1,"description":"microRNA 1587 [Source:HGNC Symbol;Acc:HGNC:41596]"}, {"versioned_ensembl_gene_id":"ENSG00000278704.1","gene_symbol":"BX004987.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56140,"end":58376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284176.1","gene_symbol":"MIR5090","gene_name":"microRNA 5090 [Source:HGNC Symbol;Acc:HGNC:43547]","synonyms":"hsa-mir-5090","biotype":"miRNA","ncbi_id":"100847073","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102465742,"end":102465826,"strand":1,"description":"microRNA 5090 [Source:HGNC Symbol;Acc:HGNC:43547]"}, {"versioned_ensembl_gene_id":"ENSG00000200620.1","gene_symbol":"SNORA7","gene_name":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15716208,"end":15716346,"strand":1,"description":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]"}, {"versioned_ensembl_gene_id":"ENSG00000201596.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185634073,"end":185634182,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221039.3","gene_symbol":"MIR1286","gene_name":"microRNA 1286 [Source:HGNC Symbol;Acc:HGNC:35279]","synonyms":"MIRN1286,hsa-mir-1286","biotype":"miRNA","ncbi_id":"100302118","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20249134,"end":20249211,"strand":-1,"description":"microRNA 1286 [Source:HGNC Symbol;Acc:HGNC:35279]"}, {"versioned_ensembl_gene_id":"ENSG00000222852.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":180909838,"end":180909927,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207150.1","gene_symbol":"RNU6-185P","gene_name":"RNA, U6 small nuclear 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:47148]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481235","summary":null,"start":87474183,"end":87474289,"strand":-1,"description":"RNA, U6 small nuclear 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:47148]"}, {"versioned_ensembl_gene_id":"ENSG00000275745.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66550457,"end":66550567,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284453.1","gene_symbol":"MIR1-2","gene_name":"microRNA 1-2 [Source:HGNC Symbol;Acc:HGNC:31500]","synonyms":"MIRN1-2,hsa-mir-1-2","biotype":"miRNA","ncbi_id":"406905","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21829004,"end":21829088,"strand":-1,"description":"microRNA 1-2 [Source:HGNC Symbol;Acc:HGNC:31500]"}, {"versioned_ensembl_gene_id":"ENSG00000283774.1","gene_symbol":"MIR632","gene_name":"microRNA 632 [Source:HGNC Symbol;Acc:HGNC:32888]","synonyms":"MIRN632,hsa-mir-632","biotype":"miRNA","ncbi_id":"693217","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32350109,"end":32350202,"strand":1,"description":"microRNA 632 [Source:HGNC Symbol;Acc:HGNC:32888]"}, {"versioned_ensembl_gene_id":"ENSG00000264092.2","gene_symbol":"RN7SL474P","gene_name":"RNA, 7SL, cytoplasmic 474, pseudogene [Source:HGNC Symbol;Acc:HGNC:46490]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481052","summary":null,"start":16863196,"end":16863496,"strand":-1,"description":"RNA, 7SL, cytoplasmic 474, pseudogene [Source:HGNC Symbol;Acc:HGNC:46490]"}, {"versioned_ensembl_gene_id":"ENSG00000242707.3","gene_symbol":"RN7SL362P","gene_name":"RNA, 7SL, cytoplasmic 362, pseudogene [Source:HGNC Symbol;Acc:HGNC:46378]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481022","summary":null,"start":13715102,"end":13715368,"strand":-1,"description":"RNA, 7SL, cytoplasmic 362, pseudogene [Source:HGNC Symbol;Acc:HGNC:46378]"}, {"versioned_ensembl_gene_id":"ENSG00000221245.1","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"SNORA11A,U107","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":119569699,"end":119569825,"strand":1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000280049.1","gene_symbol":"AC079597.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87041916,"end":87042423,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280009.1","gene_symbol":"AC020923.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86305233,"end":86306149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266426.1","gene_symbol":"MIR4719","gene_name":"microRNA 4719 [Source:HGNC Symbol;Acc:HGNC:41807]","synonyms":"hsa-mir-4719","biotype":"miRNA","ncbi_id":"100616172","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76868936,"end":76869019,"strand":1,"description":"microRNA 4719 [Source:HGNC Symbol;Acc:HGNC:41807]"}, {"versioned_ensembl_gene_id":"ENSG00000238500.1","gene_symbol":"RNU7-87P","gene_name":"RNA, U7 small nuclear 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:42616]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873842","summary":null,"start":66630715,"end":66630776,"strand":-1,"description":"RNA, U7 small nuclear 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:42616]"}, {"versioned_ensembl_gene_id":"ENSG00000201622.1","gene_symbol":"RNU6-621P","gene_name":"RNA, U6 small nuclear 621, pseudogene [Source:HGNC Symbol;Acc:HGNC:47584]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481907","summary":null,"start":197994601,"end":197994709,"strand":1,"description":"RNA, U6 small nuclear 621, pseudogene [Source:HGNC Symbol;Acc:HGNC:47584]"}, {"versioned_ensembl_gene_id":"ENSG00000201826.1","gene_symbol":"RNU6-867P","gene_name":"RNA, U6 small nuclear 867, pseudogene [Source:HGNC Symbol;Acc:HGNC:47830]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479949","summary":null,"start":76244968,"end":76245074,"strand":1,"description":"RNA, U6 small nuclear 867, pseudogene [Source:HGNC Symbol;Acc:HGNC:47830]"}, {"versioned_ensembl_gene_id":"ENSG00000264773.1","gene_symbol":"MIR4420","gene_name":"microRNA 4420 [Source:HGNC Symbol;Acc:HGNC:41772]","synonyms":"hsa-mir-4420","biotype":"miRNA","ncbi_id":"100616164","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30739156,"end":30739232,"strand":-1,"description":"microRNA 4420 [Source:HGNC Symbol;Acc:HGNC:41772]"}, {"versioned_ensembl_gene_id":"ENSG00000277119.1","gene_symbol":"WT1-AS_8","gene_name":"WT1 antisense RNA conserved region 8 [Source:RFAM;Acc:RF02210]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32440109,"end":32440383,"strand":1,"description":"WT1 antisense RNA conserved region 8 [Source:RFAM;Acc:RF02210]"}, {"versioned_ensembl_gene_id":"ENSG00000240481.3","gene_symbol":"RN7SL38P","gene_name":"RNA, 7SL, cytoplasmic 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46054]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480932","summary":null,"start":24706788,"end":24707083,"strand":1,"description":"RNA, 7SL, cytoplasmic 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46054]"}, {"versioned_ensembl_gene_id":"ENSG00000201518.1","gene_symbol":"RNA5SP513","gene_name":"RNA, 5S ribosomal pseudogene 513 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000201032.1","gene_symbol":"RNU6-704P","gene_name":"RNA, U6 small nuclear 704, pseudogene [Source:HGNC Symbol;Acc:HGNC:47667]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479877","summary":null,"start":200933345,"end":200933447,"strand":-1,"description":"RNA, U6 small nuclear 704, pseudogene [Source:HGNC Symbol;Acc:HGNC:47667]"}, {"versioned_ensembl_gene_id":"ENSG00000212276.1","gene_symbol":"RNA5SP292","gene_name":"RNA, 5S ribosomal pseudogene 292 [Source:HGNC Symbol;Acc:HGNC:43192]","synonyms":"RN5S292","biotype":"rRNA","ncbi_id":"100873545","summary":null,"start":106843749,"end":106843866,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 292 [Source:HGNC Symbol;Acc:HGNC:43192]"}, {"versioned_ensembl_gene_id":"ENSG00000221500.1","gene_symbol":"SNORD100","gene_name":"small nucleolar RNA, C/D box 100 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000276363.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000253089.1","gene_symbol":"RNU1-104P","gene_name":"RNA, U1 small nuclear 104, pseudogene [Source:HGNC Symbol;Acc:HGNC:48446]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480184","summary":null,"start":127321355,"end":127321529,"strand":1,"description":"RNA, U1 small nuclear 104, pseudogene [Source:HGNC Symbol;Acc:HGNC:48446]"}, {"versioned_ensembl_gene_id":"ENSG00000239040.1","gene_symbol":"Y_RNA","gene_name":"Y RNA 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polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145994784,"end":145994860,"strand":-1,"description":"microRNA 888 [Source:HGNC Symbol;Acc:HGNC:33648]"}, {"versioned_ensembl_gene_id":"ENSG00000208013.3","gene_symbol":"MIR652","gene_name":"microRNA 652 [Source:HGNC Symbol;Acc:HGNC:32908]","synonyms":"MIRN652,hsa-mir-652","biotype":"miRNA","ncbi_id":"724022","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110055329,"end":110055426,"strand":1,"description":"microRNA 652 [Source:HGNC Symbol;Acc:HGNC:32908]"}, {"versioned_ensembl_gene_id":"ENSG00000207169.1","gene_symbol":"RNU6-24P","gene_name":"RNA, U6 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:34268]","synonyms":"RNU6-24","biotype":"snRNA","ncbi_id":"106480707","summary":null,"start":76337316,"end":76337422,"strand":1,"description":"RNA, U6 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:34268]"}, {"versioned_ensembl_gene_id":"ENSG00000277888.1","gene_symbol":"MIR6846","gene_name":"microRNA 6846 [Source:HGNC Symbol;Acc:HGNC:50026]","synonyms":"hsa-mir-6846","biotype":"miRNA","ncbi_id":"102465509","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144057321,"end":144057380,"strand":-1,"description":"microRNA 6846 [Source:HGNC Symbol;Acc:HGNC:50026]"}, {"versioned_ensembl_gene_id":"ENSG00000221436.1","gene_symbol":"MIR548F3","gene_name":"microRNA 548f-3 [Source:HGNC Symbol;Acc:HGNC:35307]","synonyms":"MIRN548F3,hsa-mir-548f-3","biotype":"miRNA","ncbi_id":"100302159","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110513829,"end":110513915,"strand":-1,"description":"microRNA 548f-3 [Source:HGNC Symbol;Acc:HGNC:35307]"}, {"versioned_ensembl_gene_id":"ENSG00000222714.1","gene_symbol":"RN7SKP38","gene_name":"RNA, 7SK small nuclear pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45762]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479112","summary":null,"start":218500729,"end":218501037,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45762]"}, {"versioned_ensembl_gene_id":"ENSG00000201003.1","gene_symbol":"SNORA58","gene_name":"Small nucleolar RNA SNORA58 [Source:RFAM;Acc:RF00418]","synonyms":"SNORA58B,ACA58","biotype":"snoRNA","ncbi_id":"677836","summary":null,"start":53771018,"end":53771153,"strand":-1,"description":"Small nucleolar RNA SNORA58 [Source:RFAM;Acc:RF00418]"}, {"versioned_ensembl_gene_id":"ENSG00000284421.1","gene_symbol":"MIR7110","gene_name":"microRNA 7110 [Source:HGNC Symbol;Acc:HGNC:50024]","synonyms":"hsa-mir-7110","biotype":"miRNA","ncbi_id":"102465667","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123161794,"end":123161879,"strand":1,"description":"microRNA 7110 [Source:HGNC Symbol;Acc:HGNC:50024]"}, {"versioned_ensembl_gene_id":"ENSG00000252942.1","gene_symbol":"RNA5SP290","gene_name":"RNA, 5S ribosomal pseudogene 290 [Source:HGNC Symbol;Acc:HGNC:43190]","synonyms":"RN5S290","biotype":"rRNA","ncbi_id":"100873543","summary":null,"start":99145840,"end":99145966,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 290 [Source:HGNC Symbol;Acc:HGNC:43190]"}, {"versioned_ensembl_gene_id":"ENSG00000240663.3","gene_symbol":"RN7SL310P","gene_name":"RNA, 7SL, cytoplasmic 310, pseudogene [Source:HGNC Symbol;Acc:HGNC:46326]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479336","summary":null,"start":50206998,"end":50207278,"strand":-1,"description":"RNA, 7SL, cytoplasmic 310, pseudogene [Source:HGNC Symbol;Acc:HGNC:46326]"}, {"versioned_ensembl_gene_id":"ENSG00000253023.1","gene_symbol":"RNU7-156P","gene_name":"RNA, U7 small nuclear 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:45690]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479083","summary":null,"start":143542514,"end":143542587,"strand":-1,"description":"RNA, U7 small nuclear 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:45690]"}, {"versioned_ensembl_gene_id":"ENSG00000278775.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8433085,"end":8433174,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000252890.1","gene_symbol":"RNU6-699P","gene_name":"RNA, U6 small nuclear 699, pseudogene [Source:HGNC Symbol;Acc:HGNC:47662]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479875","summary":null,"start":66897262,"end":66897371,"strand":1,"description":"RNA, U6 small nuclear 699, pseudogene [Source:HGNC Symbol;Acc:HGNC:47662]"}, {"versioned_ensembl_gene_id":"ENSG00000199728.1","gene_symbol":"RNU6-655P","gene_name":"RNA, U6 small nuclear 655, pseudogene [Source:HGNC Symbol;Acc:HGNC:47618]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479856","summary":null,"start":78036739,"end":78036845,"strand":1,"description":"RNA, U6 small nuclear 655, pseudogene [Source:HGNC Symbol;Acc:HGNC:47618]"}, {"versioned_ensembl_gene_id":"ENSG00000265193.1","gene_symbol":"MIR3923","gene_name":"microRNA 3923 [Source:HGNC Symbol;Acc:HGNC:38978]","synonyms":"hsa-mir-3923","biotype":"miRNA","ncbi_id":"100500877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79507887,"end":79507969,"strand":1,"description":"microRNA 3923 [Source:HGNC Symbol;Acc:HGNC:38978]"}, {"versioned_ensembl_gene_id":"ENSG00000278714.1","gene_symbol":"AL929561.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29063984,"end":29076511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266653.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32145516,"end":32145636,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000200665.1","gene_symbol":"RNU6-1188P","gene_name":"RNA, U6 small nuclear 1188, pseudogene [Source:HGNC Symbol;Acc:HGNC:48151]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480408","summary":null,"start":116082570,"end":116082676,"strand":1,"description":"RNA, U6 small nuclear 1188, pseudogene [Source:HGNC Symbol;Acc:HGNC:48151]"}, {"versioned_ensembl_gene_id":"ENSG00000200259.1","gene_symbol":"SNORD35A","gene_name":"small nucleolar RNA, C/D box 35A [Source:HGNC Symbol;Acc:HGNC:10162]","synonyms":"RNU35,U35,RNU35A","biotype":"snoRNA","ncbi_id":"26816","summary":null,"start":49491175,"end":49491260,"strand":1,"description":"small nucleolar RNA, C/D box 35A [Source:HGNC Symbol;Acc:HGNC:10162]"}, {"versioned_ensembl_gene_id":"ENSG00000207997.1","gene_symbol":"MIR644A","gene_name":"microRNA 644a [Source:HGNC Symbol;Acc:HGNC:32900]","synonyms":"MIRN644,MIR644,hsa-mir-644","biotype":"miRNA","ncbi_id":"693229","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34466325,"end":34466418,"strand":1,"description":"microRNA 644a [Source:HGNC Symbol;Acc:HGNC:32900]"}, {"versioned_ensembl_gene_id":"ENSG00000201321.1","gene_symbol":"RNA5S9","gene_name":"RNA, 5S ribosomal 9 [Source:HGNC Symbol;Acc:HGNC:34370]","synonyms":"RN5S9","biotype":"rRNA","ncbi_id":"100169760","summary":null,"start":228628148,"end":228628266,"strand":-1,"description":"RNA, 5S ribosomal 9 [Source:HGNC Symbol;Acc:HGNC:34370]"}, {"versioned_ensembl_gene_id":"ENSG00000274721.1","gene_symbol":"SPRY4-IT1_2","gene_name":"SPRY4-IT1 conserved region 2 [Source:RFAM;Acc:RF02039]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":142318047,"end":142318167,"strand":1,"description":"SPRY4-IT1 conserved region 2 [Source:RFAM;Acc:RF02039]"}, {"versioned_ensembl_gene_id":"ENSG00000252423.1","gene_symbol":"RNU6-229P","gene_name":"RNA, U6 small nuclear 229, pseudogene [Source:HGNC Symbol;Acc:HGNC:47192]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481250","summary":null,"start":69401202,"end":69401303,"strand":-1,"description":"RNA, U6 small nuclear 229, pseudogene [Source:HGNC Symbol;Acc:HGNC:47192]"}, {"versioned_ensembl_gene_id":"ENSG00000263776.1","gene_symbol":"SNORA4","gene_name":"small nucleolar RNA, H/ACA box 4 [Source:HGNC Symbol;Acc:HGNC:32587]","synonyms":"ACA4","biotype":"snoRNA","ncbi_id":"619568","summary":null,"start":186787612,"end":186787749,"strand":1,"description":"small nucleolar RNA, H/ACA box 4 [Source:HGNC Symbol;Acc:HGNC:32587]"}, {"versioned_ensembl_gene_id":"ENSG00000284362.1","gene_symbol":"MIR519A2","gene_name":"microRNA 519a-2 [Source:HGNC Symbol;Acc:HGNC:32132]","synonyms":"MIRN519A2,MIRN519A-2,hsa-mir-519a-2","biotype":"miRNA","ncbi_id":"574500","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53762344,"end":53762430,"strand":1,"description":"microRNA 519a-2 [Source:HGNC Symbol;Acc:HGNC:32132]"}, {"versioned_ensembl_gene_id":"ENSG00000200222.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":64071807,"end":64072019,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000239175.1","gene_symbol":"RNU6-1218P","gene_name":"RNA, U6 small nuclear 1218, pseudogene [Source:HGNC Symbol;Acc:HGNC:48181]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480099","summary":null,"start":30043801,"end":30043908,"strand":-1,"description":"RNA, U6 small nuclear 1218, pseudogene [Source:HGNC Symbol;Acc:HGNC:48181]"}, {"versioned_ensembl_gene_id":"ENSG00000276263.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"amida,amida,FB1,FB1,INO80F,INO80F","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000199764.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":115207894,"end":115207996,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238653.1","gene_symbol":"RNU7-62P","gene_name":"RNA, U7 small nuclear 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:34158]","synonyms":"U7.62","biotype":"snRNA","ncbi_id":"100151657","summary":null,"start":64384398,"end":64384459,"strand":-1,"description":"RNA, U7 small nuclear 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:34158]"}, {"versioned_ensembl_gene_id":"ENSG00000276641.1","gene_symbol":"MIR6769A","gene_name":"microRNA 6769a [Source:HGNC Symbol;Acc:HGNC:50079]","synonyms":"hsa-mir-6769a","biotype":"miRNA","ncbi_id":"102466731","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4671318,"end":4671390,"strand":1,"description":"microRNA 6769a [Source:HGNC Symbol;Acc:HGNC:50079]"}, {"versioned_ensembl_gene_id":"ENSG00000222608.1","gene_symbol":"RNA5SP504","gene_name":"RNA, 5S ribosomal pseudogene 504 [Source:HGNC Symbol;Acc:HGNC:43404]","synonyms":"RN5S504","biotype":"rRNA","ncbi_id":"100873555","summary":null,"start":52665231,"end":52665347,"strand":1,"description":"RNA, 5S ribosomal pseudogene 504 [Source:HGNC Symbol;Acc:HGNC:43404]"}, {"versioned_ensembl_gene_id":"ENSG00000223037.1","gene_symbol":"RNU6-284P","gene_name":"RNA, U6 small nuclear 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:47247]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481268","summary":null,"start":164620732,"end":164620837,"strand":1,"description":"RNA, U6 small nuclear 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:47247]"}, {"versioned_ensembl_gene_id":"ENSG00000259722.2","gene_symbol":"AC087465.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77204578,"end":77205100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276878.1","gene_symbol":"MIR6074","gene_name":"microRNA 6074 [Source:HGNC Symbol;Acc:HGNC:50060]","synonyms":"hsa-mir-6074","biotype":"miRNA","ncbi_id":"102464827","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66023620,"end":66023726,"strand":-1,"description":"microRNA 6074 [Source:HGNC Symbol;Acc:HGNC:50060]"}, {"versioned_ensembl_gene_id":"ENSG00000251774.1","gene_symbol":"RNU6-377P","gene_name":"RNA, U6 small nuclear 377, pseudogene [Source:HGNC Symbol;Acc:HGNC:47340]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479733","summary":null,"start":12514706,"end":12514807,"strand":1,"description":"RNA, U6 small nuclear 377, pseudogene [Source:HGNC Symbol;Acc:HGNC:47340]"}, {"versioned_ensembl_gene_id":"ENSG00000200814.1","gene_symbol":"RNU6-595P","gene_name":"RNA, U6 small nuclear 595, pseudogene [Source:HGNC Symbol;Acc:HGNC:47558]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479829","summary":null,"start":62334091,"end":62334197,"strand":-1,"description":"RNA, U6 small nuclear 595, pseudogene [Source:HGNC Symbol;Acc:HGNC:47558]"}, {"versioned_ensembl_gene_id":"ENSG00000200830.1","gene_symbol":"RN7SKP134","gene_name":"RNA, 7SK small nuclear pseudogene 134 [Source:HGNC Symbol;Acc:HGNC:45858]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479154","summary":null,"start":14553702,"end":14553970,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 134 [Source:HGNC Symbol;Acc:HGNC:45858]"}, {"versioned_ensembl_gene_id":"ENSG00000263628.1","gene_symbol":"MIR3155A","gene_name":"microRNA 3155a [Source:HGNC Symbol;Acc:HGNC:38245]","synonyms":"MIR3155,hsa-mir-3155","biotype":"miRNA","ncbi_id":"100422989","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6152196,"end":6152277,"strand":1,"description":"microRNA 3155a [Source:HGNC Symbol;Acc:HGNC:38245]"}, {"versioned_ensembl_gene_id":"ENSG00000252627.1","gene_symbol":"RNU6-122P","gene_name":"RNA, U6 small nuclear 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:47085]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481876","summary":null,"start":123874459,"end":123874565,"strand":1,"description":"RNA, U6 small nuclear 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:47085]"}, {"versioned_ensembl_gene_id":"ENSG00000222869.1","gene_symbol":"RNU6-565P","gene_name":"RNA, U6 small nuclear 565, pseudogene [Source:HGNC Symbol;Acc:HGNC:47528]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481360","summary":null,"start":37351143,"end":37351242,"strand":1,"description":"RNA, U6 small nuclear 565, pseudogene [Source:HGNC Symbol;Acc:HGNC:47528]"}, {"versioned_ensembl_gene_id":"ENSG00000242348.3","gene_symbol":"RN7SL561P","gene_name":"RNA, 7SL, cytoplasmic 561, pseudogene [Source:HGNC Symbol;Acc:HGNC:46577]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481075","summary":null,"start":1666360,"end":1666640,"strand":1,"description":"RNA, 7SL, cytoplasmic 561, pseudogene [Source:HGNC Symbol;Acc:HGNC:46577]"}, {"versioned_ensembl_gene_id":"ENSG00000222520.1","gene_symbol":"RNA5SP451","gene_name":"RNA, 5S ribosomal pseudogene 451 [Source:HGNC Symbol;Acc:HGNC:43351]","synonyms":"RN5S451","biotype":"rRNA","ncbi_id":"100873696","summary":null,"start":21928985,"end":21929094,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 451 [Source:HGNC Symbol;Acc:HGNC:43351]"}, {"versioned_ensembl_gene_id":"ENSG00000283666.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":29510635,"end":29510737,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000277809.1","gene_symbol":"Six3os1_4","gene_name":"Six3os1 conserved region 4 [Source:RFAM;Acc:RF02249]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44935585,"end":44935908,"strand":1,"description":"Six3os1 conserved region 4 [Source:RFAM;Acc:RF02249]"}, {"versioned_ensembl_gene_id":"ENSG00000263598.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28915807,"end":28915906,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000276096.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":4756338,"end":4756633,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000278284.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":54782118,"end":54801011,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000202382.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85367585,"end":85367686,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276260.1","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160649,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000263358.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31527123,"end":31527198,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000251720.1","gene_symbol":"RNU7-123P","gene_name":"RNA, U7 small nuclear 123 pseudogene [Source:HGNC Symbol;Acc:HGNC:45657]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479071","summary":null,"start":63536711,"end":63536770,"strand":-1,"description":"RNA, U7 small nuclear 123 pseudogene [Source:HGNC Symbol;Acc:HGNC:45657]"}, {"versioned_ensembl_gene_id":"ENSG00000283081.1","gene_symbol":"AL590644.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17193232,"end":17201733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239003.1","gene_symbol":"RNU7-88P","gene_name":"RNA, U7 small nuclear 88 pseudogene [Source:HGNC Symbol;Acc:HGNC:42617]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873843","summary":null,"start":59480070,"end":59480132,"strand":1,"description":"RNA, U7 small nuclear 88 pseudogene [Source:HGNC Symbol;Acc:HGNC:42617]"}, {"versioned_ensembl_gene_id":"ENSG00000207466.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38950825,"end":38950925,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199938.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38565950,"end":38566055,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284547.1","gene_symbol":"MIR2861","gene_name":"microRNA 2861 [Source:HGNC Symbol;Acc:HGNC:38221]","synonyms":"hsa-mir-2861","biotype":"miRNA","ncbi_id":"100422910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of target mRNAs. This microRNA may play a role in osteoblast differentiation and a mutation in this gene is associated with osteoporosis. Altered expression of this microRNA has been observed in human cancers, with reduced expression seen in cervical cancer, while expression in papillary thyroid carcinoma (PTC) is increased. [provided by RefSeq, Mar 2017]","start":127785918,"end":127786007,"strand":1,"description":"microRNA 2861 [Source:HGNC Symbol;Acc:HGNC:38221]"}, {"versioned_ensembl_gene_id":"ENSG00000277677.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51858070,"end":51858352,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000258452.1","gene_symbol":"AC022404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80822524,"end":80822796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237174.7","gene_symbol":"AL445465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75357214,"end":75399300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283278.1","gene_symbol":"MIR3914-2","gene_name":"microRNA 3914-2 [Source:HGNC Symbol;Acc:HGNC:38975]","synonyms":"hsa-mir-3914-2","biotype":"miRNA","ncbi_id":"100500920","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71307674,"end":71307768,"strand":1,"description":"microRNA 3914-2 [Source:HGNC Symbol;Acc:HGNC:38975]"}, {"versioned_ensembl_gene_id":"ENSG00000212615.1","gene_symbol":"SNORD58","gene_name":"Small nucleolar RNA SNORD58 [Source:RFAM;Acc:RF00151]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":45088243,"end":45088308,"strand":1,"description":"Small nucleolar RNA SNORD58 [Source:RFAM;Acc:RF00151]"}, {"versioned_ensembl_gene_id":"ENSG00000201470.1","gene_symbol":"RNY4P7","gene_name":"RNA, Ro-associated Y4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:34056]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100169850","summary":null,"start":127798903,"end":127798998,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:34056]"}, {"versioned_ensembl_gene_id":"ENSG00000202100.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32463374,"end":32463482,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222276.1","gene_symbol":"RNU2-33P","gene_name":"RNA, U2 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:48526]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480211","summary":null,"start":96384624,"end":96384815,"strand":1,"description":"RNA, U2 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:48526]"}, {"versioned_ensembl_gene_id":"ENSG00000221042.1","gene_symbol":"CPEB3_ribozyme","gene_name":"Mammalian CPEB3 ribozyme [Source:RFAM;Acc:RF00622]","synonyms":null,"biotype":"ribozyme","ncbi_id":null,"summary":null,"start":92204229,"end":92204306,"strand":-1,"description":"Mammalian CPEB3 ribozyme [Source:RFAM;Acc:RF00622]"}, {"versioned_ensembl_gene_id":"ENSG00000274894.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"PRP31,PRP31,hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000199785.1","gene_symbol":"SNORA52","gene_name":"small nucleolar RNA, H/ACA box 52 [Source:HGNC Symbol;Acc:HGNC:32645]","synonyms":"ACA52","biotype":"snoRNA","ncbi_id":"619565","summary":null,"start":811681,"end":811814,"strand":1,"description":"small nucleolar RNA, H/ACA box 52 [Source:HGNC Symbol;Acc:HGNC:32645]"}, {"versioned_ensembl_gene_id":"ENSG00000206727.1","gene_symbol":"SNORD116-9","gene_name":"small nucleolar RNA, C/D box 116-9 [Source:HGNC Symbol;Acc:HGNC:33075]","synonyms":"HBII-85-9","biotype":"snoRNA","ncbi_id":"100033421","summary":null,"start":25073107,"end":25073201,"strand":1,"description":"small nucleolar RNA, C/D box 116-9 [Source:HGNC Symbol;Acc:HGNC:33075]"}, {"versioned_ensembl_gene_id":"ENSG00000276123.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":194658376,"end":194658675,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207365.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93021606,"end":93021712,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276161.1","gene_symbol":"SNORA17B","gene_name":"small nucleolar RNA, H/ACA box 17B [Source:HGNC Symbol;Acc:HGNC:32636]","synonyms":"SNORA43,ACA43,SNORA43,ACA43","biotype":"snoRNA","ncbi_id":"677824","summary":null,"start":136726105,"end":136726234,"strand":-1,"description":"small nucleolar RNA, H/ACA box 17B [Source:HGNC Symbol;Acc:HGNC:32636]"}, {"versioned_ensembl_gene_id":"ENSG00000283665.1","gene_symbol":"MIR3974","gene_name":"microRNA 3974 [Source:HGNC Symbol;Acc:HGNC:41672]","synonyms":"hsa-mir-3974","biotype":"miRNA","ncbi_id":"100616279","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17673299,"end":17673394,"strand":1,"description":"microRNA 3974 [Source:HGNC Symbol;Acc:HGNC:41672]"}, {"versioned_ensembl_gene_id":"ENSG00000221650.1","gene_symbol":"MIR1267","gene_name":"microRNA 1267 [Source:HGNC Symbol;Acc:HGNC:35335]","synonyms":"hsa-mir-1267,MIRN1267","biotype":"miRNA","ncbi_id":"100302286","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":107531171,"end":107531248,"strand":-1,"description":"microRNA 1267 [Source:HGNC Symbol;Acc:HGNC:35335]"}, {"versioned_ensembl_gene_id":"ENSG00000199913.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73095357,"end":73095458,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000198997.2","gene_symbol":"MIR107","gene_name":"microRNA 107 [Source:HGNC Symbol;Acc:HGNC:31496]","synonyms":"MIRN107,hsa-mir-107","biotype":"miRNA","ncbi_id":"406901","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89592747,"end":89592827,"strand":-1,"description":"microRNA 107 [Source:HGNC Symbol;Acc:HGNC:31496]"}, {"versioned_ensembl_gene_id":"ENSG00000201365.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66653469,"end":66653576,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206900.1","gene_symbol":"RNU6-98P","gene_name":"RNA, U6 small nuclear 98, pseudogene [Source:HGNC Symbol;Acc:HGNC:47061]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479609","summary":null,"start":132580117,"end":132580223,"strand":-1,"description":"RNA, U6 small nuclear 98, pseudogene [Source:HGNC Symbol;Acc:HGNC:47061]"}, {"versioned_ensembl_gene_id":"ENSG00000262000.1","gene_symbol":"AC120024.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80515215,"end":80515389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263476.1","gene_symbol":"MIR3156-1","gene_name":"microRNA 3156-1 [Source:HGNC Symbol;Acc:HGNC:38241]","synonyms":"hsa-mir-3156-1","biotype":"miRNA","ncbi_id":"100422988","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45164014,"end":45164088,"strand":1,"description":"microRNA 3156-1 [Source:HGNC Symbol;Acc:HGNC:38241]"}, {"versioned_ensembl_gene_id":"ENSG00000200972.1","gene_symbol":"RNU5A-8P","gene_name":"RNA, U5A small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42530]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873838","summary":null,"start":210374154,"end":210374267,"strand":-1,"description":"RNA, U5A small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42530]"}, {"versioned_ensembl_gene_id":"ENSG00000212475.1","gene_symbol":"RNU6-400P","gene_name":"RNA, U6 small nuclear 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:47363]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481304","summary":null,"start":33576095,"end":33576200,"strand":1,"description":"RNA, U6 small nuclear 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:47363]"}, {"versioned_ensembl_gene_id":"ENSG00000201690.1","gene_symbol":"RNY1P2","gene_name":"RNA, Ro-associated Y1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42479]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862666","summary":null,"start":102016953,"end":102017069,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42479]"}, {"versioned_ensembl_gene_id":"ENSG00000212565.1","gene_symbol":"SNORA68","gene_name":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]","synonyms":"RNU68,U68,SNORA68A","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":48880840,"end":48880967,"strand":1,"description":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]"}, {"versioned_ensembl_gene_id":"ENSG00000252719.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":139909904,"end":139910034,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000223271.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66348276,"end":66348375,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277167.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30763377,"end":30763613,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222329.1","gene_symbol":"RNU6-1076P","gene_name":"RNA, U6 small nuclear 1076, pseudogene [Source:HGNC Symbol;Acc:HGNC:48039]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480038","summary":null,"start":223158,"end":223261,"strand":-1,"description":"RNA, U6 small nuclear 1076, pseudogene [Source:HGNC Symbol;Acc:HGNC:48039]"}, {"versioned_ensembl_gene_id":"ENSG00000252952.1","gene_symbol":"RNU6-58P","gene_name":"RNA, U6 small nuclear 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:42548]","synonyms":"RNU6-58","biotype":"snRNA","ncbi_id":"100873766","summary":null,"start":23217432,"end":23217534,"strand":-1,"description":"RNA, U6 small nuclear 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:42548]"}, {"versioned_ensembl_gene_id":"ENSG00000200855.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108084913,"end":108085014,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201992.1","gene_symbol":"SNORD115-35","gene_name":"small nucleolar RNA, C/D box 115-35 [Source:HGNC Symbol;Acc:HGNC:33054]","synonyms":"HBII-52-35","biotype":"snoRNA","ncbi_id":"100033809","summary":null,"start":25234247,"end":25234328,"strand":1,"description":"small nucleolar RNA, C/D box 115-35 [Source:HGNC Symbol;Acc:HGNC:33054]"}, {"versioned_ensembl_gene_id":"ENSG00000277139.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":69530371,"end":69530475,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000222895.1","gene_symbol":"RNU6-1133P","gene_name":"RNA, U6 small nuclear 1133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48096]","synonyms":"RNU6-186P","biotype":"snRNA","ncbi_id":"106481537","summary":null,"start":31083010,"end":31083109,"strand":1,"description":"RNA, U6 small nuclear 1133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48096]"}, {"versioned_ensembl_gene_id":"ENSG00000202195.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52297995,"end":52298096,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280505.1","gene_symbol":"AC097369.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72583719,"end":72583884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284459.1","gene_symbol":"MIR24-1","gene_name":"microRNA 24-1 [Source:HGNC Symbol;Acc:HGNC:31607]","synonyms":"MIRN24-1,hsa-mir-24-1","biotype":"miRNA","ncbi_id":"407012","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95086021,"end":95086088,"strand":1,"description":"microRNA 24-1 [Source:HGNC Symbol;Acc:HGNC:31607]"}, {"versioned_ensembl_gene_id":"ENSG00000207698.1","gene_symbol":"MIR32","gene_name":"microRNA 32 [Source:HGNC Symbol;Acc:HGNC:31631]","synonyms":"MIRN32,hsa-mir-32","biotype":"miRNA","ncbi_id":"407036","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109046229,"end":109046298,"strand":-1,"description":"microRNA 32 [Source:HGNC Symbol;Acc:HGNC:31631]"}, {"versioned_ensembl_gene_id":"ENSG00000216064.1","gene_symbol":"MIR891B","gene_name":"microRNA 891b [Source:HGNC Symbol;Acc:HGNC:33645]","synonyms":"MIRN891B,hsa-mir-891b","biotype":"miRNA","ncbi_id":"100126304","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":146001053,"end":146001131,"strand":-1,"description":"microRNA 891b [Source:HGNC Symbol;Acc:HGNC:33645]"}, {"versioned_ensembl_gene_id":"ENSG00000225944.1","gene_symbol":"RIOK3P1","gene_name":"RIO kinase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122145","summary":null,"start":74828553,"end":74830080,"strand":1,"description":"RIO kinase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39714]"}, {"versioned_ensembl_gene_id":"ENSG00000265669.1","gene_symbol":"MIR548AJ1","gene_name":"microRNA 548aj-1 [Source:HGNC Symbol;Acc:HGNC:41884]","synonyms":"hsa-mir-548aj-1","biotype":"miRNA","ncbi_id":"100616191","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132115192,"end":132115263,"strand":-1,"description":"microRNA 548aj-1 [Source:HGNC Symbol;Acc:HGNC:41884]"}, {"versioned_ensembl_gene_id":"ENSG00000265657.1","gene_symbol":"MIR3151","gene_name":"microRNA 3151 [Source:HGNC Symbol;Acc:HGNC:38266]","synonyms":"hsa-mir-3151","biotype":"miRNA","ncbi_id":"100422992","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":103154614,"end":103154689,"strand":1,"description":"microRNA 3151 [Source:HGNC Symbol;Acc:HGNC:38266]"}, {"versioned_ensembl_gene_id":"ENSG00000276824.1","gene_symbol":"MIR7159","gene_name":"microRNA 7159 [Source:HGNC Symbol;Acc:HGNC:49978]","synonyms":"hsa-mir-7159","biotype":"miRNA","ncbi_id":"102466816","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33899135,"end":33899200,"strand":1,"description":"microRNA 7159 [Source:HGNC Symbol;Acc:HGNC:49978]"}, {"versioned_ensembl_gene_id":"ENSG00000221398.1","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"U107,SNORA11A","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":34456110,"end":34456237,"strand":-1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000212490.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":52748137,"end":52748259,"strand":1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000238685.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":12297197,"end":12297323,"strand":-1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000223092.1","gene_symbol":"RNA5SP115","gene_name":"RNA, 5S ribosomal pseudogene 115 [Source:HGNC Symbol;Acc:HGNC:42913]","synonyms":"RN5S115","biotype":"rRNA","ncbi_id":"100873385","summary":null,"start":200849038,"end":200849144,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 115 [Source:HGNC Symbol;Acc:HGNC:42913]"}, {"versioned_ensembl_gene_id":"ENSG00000252328.1","gene_symbol":"Vault","gene_name":"Vault RNA [Source:RFAM;Acc:RF00006]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":35097560,"end":35097657,"strand":-1,"description":"Vault RNA [Source:RFAM;Acc:RF00006]"}, {"versioned_ensembl_gene_id":"ENSG00000277250.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128673681,"end":128674021,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238778.1","gene_symbol":"RNU7-80P","gene_name":"RNA, U7 small nuclear 80 pseudogene [Source:HGNC Symbol;Acc:HGNC:34176]","synonyms":"U7.80","biotype":"snRNA","ncbi_id":"100151677","summary":null,"start":67772593,"end":67772653,"strand":-1,"description":"RNA, U7 small nuclear 80 pseudogene [Source:HGNC Symbol;Acc:HGNC:34176]"}, {"versioned_ensembl_gene_id":"ENSG00000283225.1","gene_symbol":"MIR3199-2","gene_name":"microRNA 3199-2 [Source:HGNC Symbol;Acc:HGNC:38205]","synonyms":"hsa-mir-3199-2","biotype":"miRNA","ncbi_id":"100422998","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27920526,"end":27920611,"strand":1,"description":"microRNA 3199-2 [Source:HGNC Symbol;Acc:HGNC:38205]"}, {"versioned_ensembl_gene_id":"ENSG00000284175.1","gene_symbol":"MIR4763","gene_name":"microRNA 4763 [Source:HGNC Symbol;Acc:HGNC:41677]","synonyms":"hsa-mir-4763","biotype":"miRNA","ncbi_id":"100616143","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46113566,"end":46113657,"strand":1,"description":"microRNA 4763 [Source:HGNC Symbol;Acc:HGNC:41677]"}, {"versioned_ensembl_gene_id":"ENSG00000224943.1","gene_symbol":"AL663023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159466321,"end":159483376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228210.1","gene_symbol":"AL121916.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4590993,"end":4591300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251799.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":56818218,"end":56818314,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264802.1","gene_symbol":"MIR5191","gene_name":"microRNA 5191 [Source:HGNC Symbol;Acc:HGNC:43497]","synonyms":"hsa-mir-5191","biotype":"miRNA","ncbi_id":"100847050","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":201719508,"end":201719627,"strand":1,"description":"microRNA 5191 [Source:HGNC Symbol;Acc:HGNC:43497]"}, {"versioned_ensembl_gene_id":"ENSG00000207708.1","gene_symbol":"MIR141","gene_name":"microRNA 141 [Source:HGNC Symbol;Acc:HGNC:31528]","synonyms":"MIRN141,hsa-mir-141","biotype":"miRNA","ncbi_id":"406933","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6964097,"end":6964191,"strand":1,"description":"microRNA 141 [Source:HGNC Symbol;Acc:HGNC:31528]"}, {"versioned_ensembl_gene_id":"ENSG00000200075.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"ACA25,SNORA25A","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":129868590,"end":129868716,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000244618.3","gene_symbol":"RN7SL334P","gene_name":"RNA, 7SL, cytoplasmic 334, pseudogene [Source:HGNC Symbol;Acc:HGNC:46350]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480502","summary":null,"start":25031009,"end":25031287,"strand":-1,"description":"RNA, 7SL, cytoplasmic 334, pseudogene [Source:HGNC Symbol;Acc:HGNC:46350]"}, {"versioned_ensembl_gene_id":"ENSG00000200867.1","gene_symbol":"RN7SKP36","gene_name":"RNA, 7SK small nuclear pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:45760]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480458","summary":null,"start":7112088,"end":7112399,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:45760]"}, {"versioned_ensembl_gene_id":"ENSG00000221464.1","gene_symbol":"MIR1271","gene_name":"microRNA 1271 [Source:HGNC Symbol;Acc:HGNC:35252]","synonyms":"MIRN1271,hsa-mir-1271","biotype":"miRNA","ncbi_id":"100302203","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176367946,"end":176368031,"strand":1,"description":"microRNA 1271 [Source:HGNC Symbol;Acc:HGNC:35252]"}, {"versioned_ensembl_gene_id":"ENSG00000265691.1","gene_symbol":"MIR4460","gene_name":"microRNA 4460 [Source:HGNC Symbol;Acc:HGNC:41795]","synonyms":"hsa-mir-4460","biotype":"miRNA","ncbi_id":"100616325","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129397062,"end":129397147,"strand":-1,"description":"microRNA 4460 [Source:HGNC Symbol;Acc:HGNC:41795]"}, {"versioned_ensembl_gene_id":"ENSG00000284182.1","gene_symbol":"MIR143","gene_name":"microRNA 143 [Source:HGNC Symbol;Acc:HGNC:31530]","synonyms":"MIRN143,hsa-mir-143","biotype":"miRNA","ncbi_id":"406935","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149428918,"end":149429023,"strand":1,"description":"microRNA 143 [Source:HGNC Symbol;Acc:HGNC:31530]"}, {"versioned_ensembl_gene_id":"ENSG00000207039.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153785720,"end":153785821,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199520.1","gene_symbol":"RNU6-386P","gene_name":"RNA, U6 small nuclear 386, pseudogene [Source:HGNC Symbol;Acc:HGNC:47349]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481300","summary":null,"start":77092057,"end":77092163,"strand":1,"description":"RNA, U6 small nuclear 386, pseudogene [Source:HGNC Symbol;Acc:HGNC:47349]"}, {"versioned_ensembl_gene_id":"ENSG00000202438.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130573996,"end":130574112,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207090.1","gene_symbol":"RNU6-517P","gene_name":"RNA, U6 small nuclear 517, pseudogene [Source:HGNC Symbol;Acc:HGNC:47480]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479795","summary":null,"start":121194948,"end":121195057,"strand":-1,"description":"RNA, U6 small nuclear 517, pseudogene [Source:HGNC Symbol;Acc:HGNC:47480]"}, {"versioned_ensembl_gene_id":"ENSG00000201999.1","gene_symbol":"RNA5SP428","gene_name":"RNA, 5S ribosomal pseudogene 428 [Source:HGNC Symbol;Acc:HGNC:43328]","synonyms":"RN5S428","biotype":"rRNA","ncbi_id":"100873679","summary":null,"start":66301809,"end":66301940,"strand":1,"description":"RNA, 5S ribosomal pseudogene 428 [Source:HGNC Symbol;Acc:HGNC:43328]"}, {"versioned_ensembl_gene_id":"ENSG00000253676.1","gene_symbol":"TAGLN2P1","gene_name":"transgelin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418887","summary":null,"start":106697427,"end":106698013,"strand":-1,"description":"transgelin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21739]"}, {"versioned_ensembl_gene_id":"ENSG00000238282.1","gene_symbol":"AL121781.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4475638,"end":4525200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279706.1","gene_symbol":"AL353608.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68250469,"end":68251656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284010.1","gene_symbol":"MIR675","gene_name":"microRNA 675 [Source:HGNC Symbol;Acc:HGNC:33351]","synonyms":"MIRN675,hsa-mir-675","biotype":"miRNA","ncbi_id":"100033819","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1996759,"end":1996831,"strand":-1,"description":"microRNA 675 [Source:HGNC Symbol;Acc:HGNC:33351]"}, {"versioned_ensembl_gene_id":"ENSG00000281393.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133337876,"end":133337972,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202609.4","gene_symbol":"MIR488","gene_name":"microRNA 488 [Source:HGNC Symbol;Acc:HGNC:32073]","synonyms":"MIRN488,hsa-mir-488","biotype":"miRNA","ncbi_id":"574441","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":177029363,"end":177029445,"strand":-1,"description":"microRNA 488 [Source:HGNC Symbol;Acc:HGNC:32073]"}, {"versioned_ensembl_gene_id":"ENSG00000221669.1","gene_symbol":"MIR548N","gene_name":"microRNA 548n [Source:HGNC Symbol;Acc:HGNC:35330]","synonyms":"MIRN548N,hsa-mir-548n","biotype":"miRNA","ncbi_id":"100302152","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34940760,"end":34940834,"strand":-1,"description":"microRNA 548n [Source:HGNC Symbol;Acc:HGNC:35330]"}, {"versioned_ensembl_gene_id":"ENSG00000283921.1","gene_symbol":"MIR1302-9","gene_name":"microRNA 1302-9 [Source:HGNC Symbol;Acc:HGNC:38218]","synonyms":"hsa-mir-1302-9","biotype":"miRNA","ncbi_id":"100422831","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30144,"end":30281,"strand":1,"description":"microRNA 1302-9 [Source:HGNC Symbol;Acc:HGNC:38218]"}, {"versioned_ensembl_gene_id":"ENSG00000198983.1","gene_symbol":"MIR449A","gene_name":"microRNA 449a [Source:HGNC Symbol;Acc:HGNC:27645]","synonyms":"MIRN449A,MIRN449,hsa-mir-449a,hsa-mir-449","biotype":"miRNA","ncbi_id":"554213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55170532,"end":55170622,"strand":-1,"description":"microRNA 449a [Source:HGNC Symbol;Acc:HGNC:27645]"}, {"versioned_ensembl_gene_id":"ENSG00000277073.1","gene_symbol":"MIR6131","gene_name":"microRNA 6131 [Source:HGNC Symbol;Acc:HGNC:49929]","synonyms":"hsa-mir-6131","biotype":"miRNA","ncbi_id":"102465138","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10478037,"end":10478145,"strand":1,"description":"microRNA 6131 [Source:HGNC Symbol;Acc:HGNC:49929]"}, {"versioned_ensembl_gene_id":"ENSG00000174231.16","gene_symbol":"PRPF8","gene_name":"pre-mRNA processing factor 8 [Source:HGNC Symbol;Acc:HGNC:17340]","synonyms":"RP13,PRPC8,Prp8,hPrp8,SNRNP220","biotype":"protein_coding","ncbi_id":"10594","summary":"Pre-mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a component of both U2- and U12-dependent spliceosomes, and found to be essential for the catalytic step II in pre-mRNA splicing process. It contains several WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp8 protein. This gene is a candidate gene for autosomal dominant retinitis pigmentosa. [provided by RefSeq, Jul 2008]","start":1650629,"end":1684882,"strand":-1,"description":"pre-mRNA processing factor 8 [Source:HGNC Symbol;Acc:HGNC:17340]"}, {"versioned_ensembl_gene_id":"ENSG00000284561.1","gene_symbol":"MIR4788","gene_name":"microRNA 4788 [Source:HGNC Symbol;Acc:HGNC:41676]","synonyms":"hsa-mir-4788","biotype":"miRNA","ncbi_id":"100616281","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134437827,"end":134437906,"strand":1,"description":"microRNA 4788 [Source:HGNC Symbol;Acc:HGNC:41676]"}, {"versioned_ensembl_gene_id":"ENSG00000207650.1","gene_symbol":"MIR570","gene_name":"microRNA 570 [Source:HGNC Symbol;Acc:HGNC:32826]","synonyms":"MIRN570,hsa-mir-570","biotype":"miRNA","ncbi_id":"693155","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":195699401,"end":195699497,"strand":1,"description":"microRNA 570 [Source:HGNC Symbol;Acc:HGNC:32826]"}, {"versioned_ensembl_gene_id":"ENSG00000283203.1","gene_symbol":"MIR1246","gene_name":"microRNA 1246 [Source:HGNC Symbol;Acc:HGNC:35312]","synonyms":"MIRN1246,hsa-mir-1246","biotype":"miRNA","ncbi_id":"100302142","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176600980,"end":176601052,"strand":-1,"description":"microRNA 1246 [Source:HGNC Symbol;Acc:HGNC:35312]"}, {"versioned_ensembl_gene_id":"ENSG00000201421.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185251313,"end":185251411,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238943.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8592476,"end":8592585,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275068.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":64082429,"end":64082534,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201371.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27722284,"end":27722392,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252945.1","gene_symbol":"snoU83B","gene_name":"Small nucleolar RNA U83B [Source:RFAM;Acc:RF00593]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":50844625,"end":50844712,"strand":1,"description":"Small nucleolar RNA U83B [Source:RFAM;Acc:RF00593]"}, {"versioned_ensembl_gene_id":"ENSG00000216056.1","gene_symbol":"MIR891A","gene_name":"microRNA 891a [Source:HGNC Symbol;Acc:HGNC:33635]","synonyms":"MIRN891A,hsa-mir-891a","biotype":"miRNA","ncbi_id":"100126341","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":146027794,"end":146027872,"strand":-1,"description":"microRNA 891a [Source:HGNC Symbol;Acc:HGNC:33635]"}, {"versioned_ensembl_gene_id":"ENSG00000252431.1","gene_symbol":"RNU6-1247P","gene_name":"RNA, U6 small nuclear 1247, pseudogene [Source:HGNC Symbol;Acc:HGNC:48210]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481574","summary":null,"start":151280515,"end":151280612,"strand":-1,"description":"RNA, U6 small nuclear 1247, pseudogene [Source:HGNC Symbol;Acc:HGNC:48210]"}, {"versioned_ensembl_gene_id":"ENSG00000283941.1","gene_symbol":"MIR600","gene_name":"microRNA 600 [Source:HGNC Symbol;Acc:HGNC:32856]","synonyms":"MIRN600,hsa-mir-600","biotype":"miRNA","ncbi_id":"693185","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123111546,"end":123111643,"strand":-1,"description":"microRNA 600 [Source:HGNC Symbol;Acc:HGNC:32856]"}, {"versioned_ensembl_gene_id":"ENSG00000137752.23","gene_symbol":"CASP1","gene_name":"caspase 1 [Source:HGNC Symbol;Acc:HGNC:1499]","synonyms":"IL1BC,ICE","biotype":"protein_coding","ncbi_id":"834","summary":"This gene encodes a protein which is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce 2 subunits, large and small, that dimerize to form the active enzyme. This gene was identified by its ability to proteolytically cleave and activate the inactive precursor of interleukin-1, a cytokine involved in the processes such as inflammation, septic shock, and wound healing. This gene has been shown to induce cell apoptosis and may function in various developmental stages. Studies of a similar gene in mouse suggest a role in the pathogenesis of Huntington disease. Alternative splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2012]","start":105025443,"end":105035250,"strand":-1,"description":"caspase 1 [Source:HGNC Symbol;Acc:HGNC:1499]"}, {"versioned_ensembl_gene_id":"ENSG00000207651.1","gene_symbol":"MIR28","gene_name":"microRNA 28 [Source:HGNC Symbol;Acc:HGNC:31615]","synonyms":"MIRN28,hsa-mir-28","biotype":"miRNA","ncbi_id":"407020","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188688781,"end":188688866,"strand":1,"description":"microRNA 28 [Source:HGNC Symbol;Acc:HGNC:31615]"}, {"versioned_ensembl_gene_id":"ENSG00000265141.2","gene_symbol":"RN7SL451P","gene_name":"RNA, 7SL, cytoplasmic 451, pseudogene [Source:HGNC Symbol;Acc:HGNC:46467]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480377","summary":null,"start":8979576,"end":8979874,"strand":-1,"description":"RNA, 7SL, cytoplasmic 451, pseudogene [Source:HGNC Symbol;Acc:HGNC:46467]"}, {"versioned_ensembl_gene_id":"ENSG00000200842.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62036833,"end":62036945,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222067.1","gene_symbol":"RNU4-86P","gene_name":"RNA, U4 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:47022]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481199","summary":null,"start":126214260,"end":126214478,"strand":-1,"description":"RNA, U4 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:47022]"}, {"versioned_ensembl_gene_id":"ENSG00000212306.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100638363,"end":100638457,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201584.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":121040610,"end":121040710,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201315.1","gene_symbol":"RN7SKP227","gene_name":"RNA, 7SK small nuclear pseudogene 227 [Source:HGNC Symbol;Acc:HGNC:45951]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481818","summary":null,"start":36685040,"end":36685369,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 227 [Source:HGNC Symbol;Acc:HGNC:45951]"}, {"versioned_ensembl_gene_id":"ENSG00000201394.1","gene_symbol":"RNA5SP140","gene_name":"RNA, 5S ribosomal pseudogene 140 [Source:HGNC Symbol;Acc:HGNC:43040]","synonyms":"RN5S140","biotype":"rRNA","ncbi_id":"106478996","summary":null,"start":133710076,"end":133710167,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 140 [Source:HGNC Symbol;Acc:HGNC:43040]"}, {"versioned_ensembl_gene_id":"ENSG00000276311.1","gene_symbol":"MIR6511A3","gene_name":"microRNA 6511a-3 [Source:HGNC Symbol;Acc:HGNC:50265]","synonyms":"hsa-mir-6511a-3","biotype":"miRNA","ncbi_id":"102465683","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16368876,"end":16368942,"strand":1,"description":"microRNA 6511a-3 [Source:HGNC Symbol;Acc:HGNC:50265]"}, {"versioned_ensembl_gene_id":"ENSG00000206891.1","gene_symbol":"RNU6-217P","gene_name":"RNA, U6 small nuclear 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:47180]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481246","summary":null,"start":77811741,"end":77811844,"strand":-1,"description":"RNA, U6 small nuclear 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:47180]"}, {"versioned_ensembl_gene_id":"ENSG00000276639.1","gene_symbol":"MIR7154","gene_name":"microRNA 7154 [Source:HGNC Symbol;Acc:HGNC:49972]","synonyms":"hsa-mir-7154","biotype":"miRNA","ncbi_id":"102465691","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45691704,"end":45691776,"strand":-1,"description":"microRNA 7154 [Source:HGNC Symbol;Acc:HGNC:49972]"}, {"versioned_ensembl_gene_id":"ENSG00000222268.1","gene_symbol":"RNA5SP425","gene_name":"RNA, 5S ribosomal pseudogene 425 [Source:HGNC Symbol;Acc:HGNC:43325]","synonyms":"RN5S425","biotype":"rRNA","ncbi_id":"100873676","summary":null,"start":47505432,"end":47505543,"strand":1,"description":"RNA, 5S ribosomal pseudogene 425 [Source:HGNC Symbol;Acc:HGNC:43325]"}, {"versioned_ensembl_gene_id":"ENSG00000207516.1","gene_symbol":"SNORA41B","gene_name":"small nucleolar RNA, H/ACA box 41B [Source:HGNC Symbol;Acc:HGNC:52206]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617005","summary":null,"start":45537250,"end":45537377,"strand":1,"description":"small nucleolar RNA, H/ACA box 41B [Source:HGNC Symbol;Acc:HGNC:52206]"}, {"versioned_ensembl_gene_id":"ENSG00000200495.1","gene_symbol":"RNU6-1205P","gene_name":"RNA, U6 small nuclear 1205, pseudogene [Source:HGNC Symbol;Acc:HGNC:48168]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480093","summary":null,"start":248912690,"end":248912795,"strand":-1,"description":"RNA, U6 small nuclear 1205, pseudogene [Source:HGNC Symbol;Acc:HGNC:48168]"}, {"versioned_ensembl_gene_id":"ENSG00000271907.1","gene_symbol":"SNORA35B","gene_name":"small nucleolar RNA, H/ACA box 35B [Source:HGNC Symbol;Acc:HGNC:52202]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617004","summary":null,"start":115126316,"end":115126444,"strand":-1,"description":"small nucleolar RNA, H/ACA box 35B [Source:HGNC Symbol;Acc:HGNC:52202]"}, {"versioned_ensembl_gene_id":"ENSG00000155959.10","gene_symbol":"VBP1","gene_name":"VHL binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12662]","synonyms":"PFDN3,PFD3","biotype":"protein_coding","ncbi_id":"7411","summary":"The protein encoded by this gene interacts with the Von Hippel-Lindau protein to form an intracellular complex. The encoded protein functions as a chaperone protein, and may play a role in the transport of the Von Hippel-Lindau protein from the perinuclear granules to the nucleus or cytoplasm. Alternative splicing and the use of alternate transcription start sites results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Jan 2015]","start":155197007,"end":155239817,"strand":1,"description":"VHL binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12662]"}, {"versioned_ensembl_gene_id":"ENSG00000283036.2","gene_symbol":"LINC01988","gene_name":"long intergenic non-protein coding RNA 1988 [Source:HGNC Symbol;Acc:HGNC:52820]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506319","summary":null,"start":44424134,"end":44429529,"strand":1,"description":"long intergenic non-protein coding RNA 1988 [Source:HGNC Symbol;Acc:HGNC:52820]"}, {"versioned_ensembl_gene_id":"ENSG00000133983.14","gene_symbol":"COX16","gene_name":"COX16, cytochrome c oxidase assembly homolog [Source:HGNC Symbol;Acc:HGNC:20213]","synonyms":"HSPC203,C14orf112","biotype":"protein_coding","ncbi_id":"51241","summary":null,"start":70325081,"end":70359731,"strand":-1,"description":"COX16, cytochrome c oxidase assembly homolog [Source:HGNC Symbol;Acc:HGNC:20213]"}, {"versioned_ensembl_gene_id":"ENSG00000144668.11","gene_symbol":"ITGA9","gene_name":"integrin subunit alpha 9 [Source:HGNC Symbol;Acc:HGNC:6145]","synonyms":"RLC,ITGA4L,ALPHA-RLC","biotype":"protein_coding","ncbi_id":"3680","summary":"This gene encodes an alpha integrin. Integrins are heterodimeric integral membrane glycoproteins composed of an alpha chain and a beta chain that mediate cell-cell and cell-matrix adhesion. The protein encoded by this gene, when bound to the beta 1 chain, forms an integrin that is a receptor for VCAM1, cytotactin and osteopontin. Expression of this gene has been found to be upregulated in small cell lung cancers. [provided by RefSeq, Jul 2008]","start":37452115,"end":37823514,"strand":1,"description":"integrin subunit alpha 9 [Source:HGNC Symbol;Acc:HGNC:6145]"}, {"versioned_ensembl_gene_id":"ENSG00000127241.16","gene_symbol":"MASP1","gene_name":"mannan binding lectin serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:6901]","synonyms":"PRSS5,MASP,CRARF","biotype":"protein_coding","ncbi_id":"5648","summary":"This gene encodes a serine protease that functions as a component of the lectin pathway of complement activation. The complement pathway plays an essential role in the innate and adaptive immune response. The encoded protein is synthesized as a zymogen and is activated when it complexes with the pathogen recognition molecules of lectin pathway, the mannose-binding lectin and the ficolins. This protein is not directly involved in complement activation but may play a role as an amplifier of complement activation by cleaving complement C2 or by activating another complement serine protease, MASP-2. The encoded protein is also able to cleave fibrinogen and factor XIII and may may be involved in coagulation. A splice variant of this gene which lacks the serine protease domain functions as an inhibitor of the complement pathway. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]","start":187217285,"end":187292022,"strand":-1,"description":"mannan binding lectin serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:6901]"}, {"versioned_ensembl_gene_id":"ENSG00000165458.13","gene_symbol":"INPPL1","gene_name":"inositol polyphosphate phosphatase like 1 [Source:HGNC Symbol;Acc:HGNC:6080]","synonyms":"SHIP2","biotype":"protein_coding","ncbi_id":"3636","summary":"The protein encoded by this gene is an SH2-containing 5'-inositol phosphatase that is involved in the regulation of insulin function. The encoded protein also plays a role in the regulation of epidermal growth factor receptor turnover and actin remodelling. Additionally, this gene supports metastatic growth in breast cancer and is a valuable biomarker for breast cancer. [provided by RefSeq, Jan 2009]","start":72223701,"end":72239105,"strand":1,"description":"inositol polyphosphate phosphatase like 1 [Source:HGNC Symbol;Acc:HGNC:6080]"}, {"versioned_ensembl_gene_id":"ENSG00000230660.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"Em:AB014087.1,FLJ31598,FLJ25550","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30335445,"end":30371782,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000227519.1","gene_symbol":"AL008719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31963357,"end":31970400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276885.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832710,"end":54847746,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000277691.4","gene_symbol":"GU182338.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54786460,"end":54798282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170827.9","gene_symbol":"CELP","gene_name":"carboxyl ester lipase pseudogene [Source:HGNC Symbol;Acc:HGNC:1849]","synonyms":"CELL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1057","summary":null,"start":133079900,"end":133087355,"strand":1,"description":"carboxyl ester lipase pseudogene [Source:HGNC Symbol;Acc:HGNC:1849]"}, {"versioned_ensembl_gene_id":"ENSG00000228663.1","gene_symbol":"PSMD10P1","gene_name":"proteasome 26S subunit, non-ATPase, 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16602]","synonyms":"PSMD10P,dJ914P20.4","biotype":"processed_pseudogene","ncbi_id":"170541","summary":null,"start":50913731,"end":50914411,"strand":1,"description":"proteasome 26S subunit, non-ATPase, 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16602]"}, {"versioned_ensembl_gene_id":"ENSG00000182050.13","gene_symbol":"MGAT4C","gene_name":"MGAT4 family member C [Source:HGNC Symbol;Acc:HGNC:30871]","synonyms":"HGNT-IV-H","biotype":"protein_coding","ncbi_id":"25834","summary":null,"start":85955666,"end":86838904,"strand":-1,"description":"MGAT4 family member C [Source:HGNC Symbol;Acc:HGNC:30871]"}, {"versioned_ensembl_gene_id":"ENSG00000218596.2","gene_symbol":"AL162578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156976294,"end":156977072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120805.13","gene_symbol":"ARL1","gene_name":"ADP ribosylation factor like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:692]","synonyms":"ARFL1","biotype":"protein_coding","ncbi_id":"400","summary":"The protein encoded by this gene belongs to the ARL (ADP-ribosylation factor-like) family of proteins, which are structurally related to ADP-ribosylation factors (ARFs). ARFs, described as activators of cholera toxin (CT) ADP-ribosyltransferase activity, regulate intracellular vesicular membrane trafficking, and stimulate a phospholipase D (PLD) isoform. Although, ARL proteins were initially thought not to activate CT or PLD, later work showed that they are weak stimulators of PLD and CT in a phospholipid dependent manner. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":101393120,"end":101407820,"strand":-1,"description":"ADP ribosylation factor like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:692]"}, {"versioned_ensembl_gene_id":"ENSG00000116703.13","gene_symbol":"PDC","gene_name":"phosducin [Source:HGNC Symbol;Acc:HGNC:8759]","synonyms":"MEKA","biotype":"protein_coding","ncbi_id":"5132","summary":"This gene encodes a phosphoprotein, which is located in the outer and inner segments of the rod cells in the retina. This protein may participate in the regulation of visual phototransduction or in the integration of photoreceptor metabolism. It modulates the phototransduction cascade by interacting with the beta and gamma subunits of the retinal G-protein transducin. This gene is a potential candidate gene for retinitis pigmentosa and Usher syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":186443566,"end":186461122,"strand":-1,"description":"phosducin [Source:HGNC Symbol;Acc:HGNC:8759]"}, {"versioned_ensembl_gene_id":"ENSG00000205403.12","gene_symbol":"CFI","gene_name":"complement factor I [Source:HGNC Symbol;Acc:HGNC:5394]","synonyms":"FI,C3b-INA,KAF,IF","biotype":"protein_coding","ncbi_id":"3426","summary":"This gene encodes a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immune deposits and age-related macular degeneration are other conditions associated with mutations of this gene. [provided by RefSeq, Dec 2015]","start":109740694,"end":109802179,"strand":-1,"description":"complement factor I [Source:HGNC Symbol;Acc:HGNC:5394]"}, {"versioned_ensembl_gene_id":"ENSG00000183379.8","gene_symbol":"SYNDIG1L","gene_name":"synapse differentiation inducing 1 like [Source:HGNC Symbol;Acc:HGNC:32388]","synonyms":"TMEM90A,IFITMD4,capucin","biotype":"protein_coding","ncbi_id":"646658","summary":null,"start":74405893,"end":74426102,"strand":-1,"description":"synapse differentiation inducing 1 like [Source:HGNC Symbol;Acc:HGNC:32388]"}, {"versioned_ensembl_gene_id":"ENSG00000255382.1","gene_symbol":"AP001646.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82791662,"end":82817146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218520.5","gene_symbol":"AL450346.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63229087,"end":63230110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233217.2","gene_symbol":"MROH3P","gene_name":"maestro heat like repeat family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:33122]","synonyms":"C1orf81","biotype":"transcribed_unitary_pseudogene","ncbi_id":"647215","summary":null,"start":200917460,"end":200966668,"strand":1,"description":"maestro heat like repeat family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:33122]"}, {"versioned_ensembl_gene_id":"ENSG00000257108.1","gene_symbol":"NHLRC4","gene_name":"NHL repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:26700]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283948","summary":null,"start":566996,"end":569495,"strand":1,"description":"NHL repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:26700]"}, {"versioned_ensembl_gene_id":"ENSG00000198909.7","gene_symbol":"MAP3K3","gene_name":"mitogen-activated protein kinase kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6855]","synonyms":"MEKK3,MAPKKK3","biotype":"protein_coding","ncbi_id":"4215","summary":"This gene product is a 626-amino acid polypeptide that is 96.5% identical to mouse Mekk3. Its catalytic domain is closely related to those of several other kinases, including mouse Mekk2, tobacco NPK, and yeast Ste11. Northern blot analysis revealed a 4.6-kb transcript that appears to be ubiquitously expressed. This protein directly regulates the stress-activated protein kinase (SAPK) and extracellular signal-regulated protein kinase (ERK) pathways by activating SEK and MEK1/2 respectively; it does not regulate the p38 pathway. In cotransfection assays, it enhanced transcription from a nuclear factor kappa-B (NFKB)-dependent reporter gene, consistent with a role in the SAPK pathway. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":63622415,"end":63696303,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6855]"}, {"versioned_ensembl_gene_id":"ENSG00000162066.14","gene_symbol":"AMDHD2","gene_name":"amidohydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24262]","synonyms":"CGI-14","biotype":"protein_coding","ncbi_id":"51005","summary":null,"start":2520357,"end":2531422,"strand":1,"description":"amidohydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24262]"}, {"versioned_ensembl_gene_id":"ENSG00000229235.1","gene_symbol":"RPL37P18","gene_name":"ribosomal protein L37 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271342","summary":null,"start":34663859,"end":34664101,"strand":-1,"description":"ribosomal protein L37 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35919]"}, {"versioned_ensembl_gene_id":"ENSG00000168495.12","gene_symbol":"POLR3D","gene_name":"RNA polymerase III subunit D [Source:HGNC Symbol;Acc:HGNC:1080]","synonyms":"TSBN51,RPC4,BN51T","biotype":"protein_coding","ncbi_id":"661","summary":"This gene complements a temperature-sensitive mutant isolated from the BHK-21 Syrian hamster cell line. It leads to a block in progression through the G1 phase of the cell cycle at nonpermissive temperatures. [provided by RefSeq, Jul 2008]","start":22245104,"end":22254600,"strand":1,"description":"RNA polymerase III subunit D [Source:HGNC Symbol;Acc:HGNC:1080]"}, {"versioned_ensembl_gene_id":"ENSG00000253894.1","gene_symbol":"AC011124.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63465849,"end":63475482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283005.1","gene_symbol":"CDC27P3","gene_name":"cell division cycle 27 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51754]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723416","summary":null,"start":29746181,"end":29748090,"strand":1,"description":"cell division cycle 27 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51754]"}, {"versioned_ensembl_gene_id":"ENSG00000246366.6","gene_symbol":"LACTB2-AS1","gene_name":"LACTB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27841]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"286190","summary":null,"start":70608577,"end":70663279,"strand":1,"description":"LACTB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27841]"}, {"versioned_ensembl_gene_id":"ENSG00000225487.2","gene_symbol":"AL390119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164921318,"end":164921629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233194.1","gene_symbol":"AL805913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33008496,"end":33008905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168994.13","gene_symbol":"PXDC1","gene_name":"PX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21361]","synonyms":"C6orf145","biotype":"protein_coding","ncbi_id":"221749","summary":null,"start":3722614,"end":3752026,"strand":-1,"description":"PX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21361]"}, {"versioned_ensembl_gene_id":"ENSG00000263635.1","gene_symbol":"AP005242.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15075445,"end":15122767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239305.6","gene_symbol":"RNF103","gene_name":"ring finger protein 103 [Source:HGNC Symbol;Acc:HGNC:12859]","synonyms":"ZFP103,KF1,hkf-1","biotype":"protein_coding","ncbi_id":"7844","summary":"The protein encoded by this gene contains a RING-H2 finger, a motif known to be involved in protein-protein and protein-DNA interactions. This gene is highly expressed in normal cerebellum, but not in the cerebral cortex. The expression of the rat counterpart in the frontal cortex and hippocampus was shown to be induced by elctroconvulsive treatment (ECT) as well as chronic antidepressant treatment, suggesting that this gene may be a molecular target for ECT and antidepressants. The protein is a ubiquitin ligase that functions in the endoplasmic reticulum-associated degradation pathway. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream CHMP3 (charged multivesicular body protein 3) gene. [provided by RefSeq, Oct 2011]","start":86603393,"end":86623866,"strand":-1,"description":"ring finger protein 103 [Source:HGNC Symbol;Acc:HGNC:12859]"}, {"versioned_ensembl_gene_id":"ENSG00000156206.13","gene_symbol":"CFAP161","gene_name":"cilia and flagella associated protein 161 [Source:HGNC Symbol;Acc:HGNC:26782]","synonyms":"FLJ38615,C15orf26","biotype":"protein_coding","ncbi_id":"161502","summary":null,"start":81007033,"end":81149175,"strand":1,"description":"cilia and flagella associated protein 161 [Source:HGNC Symbol;Acc:HGNC:26782]"}, {"versioned_ensembl_gene_id":"ENSG00000268083.5","gene_symbol":"AC008982.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38817471,"end":38840178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279834.1","gene_symbol":"AC068870.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81060953,"end":81063488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259461.1","gene_symbol":"ANP32BP3","gene_name":"acidic nuclear phosphoprotein 32 family member B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44089]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652899","summary":null,"start":81117635,"end":81118340,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44089]"}, {"versioned_ensembl_gene_id":"ENSG00000153561.12","gene_symbol":"RMND5A","gene_name":"required for meiotic nuclear division 5 homolog A [Source:HGNC Symbol;Acc:HGNC:25850]","synonyms":"GID2A,GID2,FLJ13910,RMD5,p44CTLH","biotype":"protein_coding","ncbi_id":"64795","summary":null,"start":86720173,"end":86778041,"strand":1,"description":"required for meiotic nuclear division 5 homolog A [Source:HGNC Symbol;Acc:HGNC:25850]"}, {"versioned_ensembl_gene_id":"ENSG00000184616.8","gene_symbol":"SPDYE12P","gene_name":"speedy/RINGO cell cycle regulator family member E12, pseudogene [Source:HGNC Symbol;Acc:HGNC:51508]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100101268","summary":null,"start":74906673,"end":74913256,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E12, pseudogene [Source:HGNC Symbol;Acc:HGNC:51508]"}, {"versioned_ensembl_gene_id":"ENSG00000069020.18","gene_symbol":"MAST4","gene_name":"microtubule associated serine/threonine kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:19037]","synonyms":"KIAA0303","biotype":"protein_coding","ncbi_id":"375449","summary":"This gene encodes a member of the microtubule-associated serine/threonine protein kinases. The proteins in this family contain a domain that gives the kinase the ability to determine its own scaffold to control the effects of their kinase activities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":66596361,"end":67169595,"strand":1,"description":"microtubule associated serine/threonine kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:19037]"}, {"versioned_ensembl_gene_id":"ENSG00000279341.1","gene_symbol":"AP000756.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87718667,"end":87721233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229666.1","gene_symbol":"MAST4-AS1","gene_name":"MAST4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40865]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928794","summary":null,"start":67001383,"end":67003953,"strand":-1,"description":"MAST4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40865]"}, {"versioned_ensembl_gene_id":"ENSG00000235273.1","gene_symbol":"CR753509.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29224018,"end":29267104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230015.3","gene_symbol":"AL365184.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":240739419,"end":240739853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224990.1","gene_symbol":"CR753509.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29229272,"end":29230202,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234872.2","gene_symbol":"AL358176.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240654241,"end":240654625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266614.1","gene_symbol":"AC103808.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76259166,"end":76260114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229441.1","gene_symbol":"CR933537.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215281,"end":29216224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118200.14","gene_symbol":"CAMSAP2","gene_name":"calmodulin regulated spectrin associated protein family member 2 [Source:HGNC Symbol;Acc:HGNC:29188]","synonyms":"KIAA1078,CAMSAP1L1","biotype":"protein_coding","ncbi_id":"23271","summary":null,"start":200739558,"end":200860704,"strand":1,"description":"calmodulin regulated spectrin associated protein family member 2 [Source:HGNC Symbol;Acc:HGNC:29188]"}, {"versioned_ensembl_gene_id":"ENSG00000274930.1","gene_symbol":"AC105227.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50318420,"end":50319024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100523.14","gene_symbol":"DDHD1","gene_name":"DDHD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19714]","synonyms":"SPG28,PA-PLA1,KIAA1705","biotype":"protein_coding","ncbi_id":"80821","summary":"This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":53036745,"end":53153282,"strand":-1,"description":"DDHD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19714]"}, {"versioned_ensembl_gene_id":"ENSG00000228337.1","gene_symbol":"AC096920.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50685551,"end":50685791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236545.1","gene_symbol":"AP001619.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41870633,"end":41872054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179562.2","gene_symbol":"GCC1","gene_name":"GRIP and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19095]","synonyms":"GCC1P,FLJ22035,MGC20706,GCC88","biotype":"protein_coding","ncbi_id":"79571","summary":"The protein encoded by this gene is a peripheral membrane protein. It is sensitive to brefeldin A. This encoded protein contains a GRIP domain which is thought to be used in targeting. It may play a role in the organization of trans-Golgi network subcompartment involved with membrane transport. [provided by RefSeq, Jul 2008]","start":127580618,"end":127593611,"strand":-1,"description":"GRIP and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19095]"}, {"versioned_ensembl_gene_id":"ENSG00000268756.1","gene_symbol":"AC104534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38820166,"end":38823223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188636.3","gene_symbol":"RTL6","gene_name":"retrotransposon Gag like 6 [Source:HGNC Symbol;Acc:HGNC:13343]","synonyms":"SIRH3,Mart6,Mar6,LDOC1L,DKFZp761O17121,dJ1033E15.2","biotype":"protein_coding","ncbi_id":"84247","summary":null,"start":44492572,"end":44498298,"strand":-1,"description":"retrotransposon Gag like 6 [Source:HGNC Symbol;Acc:HGNC:13343]"}, {"versioned_ensembl_gene_id":"ENSG00000141295.13","gene_symbol":"SCRN2","gene_name":"secernin 2 [Source:HGNC Symbol;Acc:HGNC:30381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90507","summary":null,"start":47837692,"end":47841333,"strand":-1,"description":"secernin 2 [Source:HGNC Symbol;Acc:HGNC:30381]"}, {"versioned_ensembl_gene_id":"ENSG00000184588.17","gene_symbol":"PDE4B","gene_name":"phosphodiesterase 4B [Source:HGNC Symbol;Acc:HGNC:8781]","synonyms":"DPDE4","biotype":"protein_coding","ncbi_id":"5142","summary":"This gene is a member of the type IV, cyclic AMP (cAMP)-specific, cyclic nucleotide phosphodiesterase (PDE) family. The encoded protein regulates the cellular concentrations of cyclic nucleotides and thereby play a role in signal transduction. Altered activity of this protein has been associated with schizophrenia and bipolar affective disorder. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":65792514,"end":66374579,"strand":1,"description":"phosphodiesterase 4B [Source:HGNC Symbol;Acc:HGNC:8781]"}, {"versioned_ensembl_gene_id":"ENSG00000235505.7","gene_symbol":"AP002004.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":104901549,"end":104919073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101405.3","gene_symbol":"OXT","gene_name":"oxytocin/neurophysin I prepropeptide [Source:HGNC Symbol;Acc:HGNC:8528]","synonyms":"OXT-NPI,OT-NPI,OT","biotype":"protein_coding","ncbi_id":"5020","summary":"This gene encodes a precursor protein that is processed to produce oxytocin and neurophysin I. Oxytocin is a posterior pituitary hormone which is synthesized as an inactive precursor in the hypothalamus along with its carrier protein neurophysin I. Together with neurophysin, it is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis, where it is either stored or secreted into the bloodstream. The precursor seems to be activated while it is being transported along the axon to the posterior pituitary. This hormone contracts smooth muscle during parturition and lactation. It is also involved in cognition, tolerance, adaptation and complex sexual and maternal behaviour, as well as in the regulation of water excretion and cardiovascular functions. [provided by RefSeq, Dec 2013]","start":3071620,"end":3072517,"strand":1,"description":"oxytocin/neurophysin I prepropeptide [Source:HGNC Symbol;Acc:HGNC:8528]"}, {"versioned_ensembl_gene_id":"ENSG00000140406.3","gene_symbol":"TLNRD1","gene_name":"talin rod domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13519]","synonyms":"MGC99595,MESDC1","biotype":"protein_coding","ncbi_id":"59274","summary":"This gene encodes a protein that is regulated by micro RNA MiR-574-3, and is thought to have an oncogenic function in human bladder cancer. A similar gene in mouse is located in a chromosomal region critical for differentiation of mesoderm, which affects embryo patterning and the formation of heart, muscle, blood, skeleton and the urogenital system. The mouse gene is expressed in early development, and in the adult. [provided by RefSeq, Nov 2016]","start":81000944,"end":81005788,"strand":1,"description":"talin rod domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13519]"}, {"versioned_ensembl_gene_id":"ENSG00000249667.1","gene_symbol":"LINC01259","gene_name":"long intergenic non-protein coding RNA 1259 [Source:HGNC Symbol;Acc:HGNC:49899]","synonyms":"TCONS_00007515","biotype":"lincRNA","ncbi_id":"106144599","summary":null,"start":38509767,"end":38518056,"strand":1,"description":"long intergenic non-protein coding RNA 1259 [Source:HGNC Symbol;Acc:HGNC:49899]"}, {"versioned_ensembl_gene_id":"ENSG00000249534.1","gene_symbol":"LINC01258","gene_name":"long intergenic non-protein coding RNA 1258 [Source:HGNC Symbol;Acc:HGNC:49898]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928776","summary":null,"start":38420662,"end":38523180,"strand":-1,"description":"long intergenic non-protein coding RNA 1258 [Source:HGNC Symbol;Acc:HGNC:49898]"}, {"versioned_ensembl_gene_id":"ENSG00000228818.1","gene_symbol":"AL359918.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240142670,"end":240145389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213839.4","gene_symbol":"TMX2P1","gene_name":"thioredoxin related transmembrane protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100233198","summary":null,"start":37885683,"end":37886390,"strand":1,"description":"thioredoxin related transmembrane protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49916]"}, {"versioned_ensembl_gene_id":"ENSG00000279528.1","gene_symbol":"AC115618.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48580741,"end":48581165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183814.15","gene_symbol":"LIN9","gene_name":"lin-9 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:30830]","synonyms":"TGS","biotype":"protein_coding","ncbi_id":"286826","summary":"This gene encodes a tumor suppressor protein that inhibits DNA synthesis and oncogenic transformation through association with the retinoblastoma 1 protein. The encoded protein also interacts with a complex of other cell cycle regulators to repress cell cycle-dependent gene expression in non-dividing cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":226231149,"end":226309869,"strand":-1,"description":"lin-9 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:30830]"}, {"versioned_ensembl_gene_id":"ENSG00000235629.1","gene_symbol":"AC090952.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14648194,"end":14649432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006534.15","gene_symbol":"ALDH3B1","gene_name":"aldehyde dehydrogenase 3 family member B1 [Source:HGNC Symbol;Acc:HGNC:410]","synonyms":"ALDH7","biotype":"protein_coding","ncbi_id":"221","summary":"This gene encodes a member of the aldehyde dehydrogenase protein family. Aldehyde dehydrogenases are a family of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The encoded protein is able to oxidize long-chain fatty aldehydes in vitro, and may play a role in protection from oxidative stress. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":68008578,"end":68029282,"strand":1,"description":"aldehyde dehydrogenase 3 family member B1 [Source:HGNC Symbol;Acc:HGNC:410]"}, {"versioned_ensembl_gene_id":"ENSG00000136891.13","gene_symbol":"TEX10","gene_name":"testis expressed 10 [Source:HGNC Symbol;Acc:HGNC:25988]","synonyms":"Ipi1,FLJ20287,bA208F1.2","biotype":"protein_coding","ncbi_id":"54881","summary":null,"start":100302077,"end":100352939,"strand":-1,"description":"testis expressed 10 [Source:HGNC Symbol;Acc:HGNC:25988]"}, {"versioned_ensembl_gene_id":"ENSG00000271657.1","gene_symbol":"AC018462.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62168862,"end":62171163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232636.2","gene_symbol":"AL360267.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87427200,"end":87447235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255019.1","gene_symbol":"OR5D15P","gene_name":"olfactory receptor family 5 subfamily D member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:15282]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81198","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55786964,"end":55787905,"strand":1,"description":"olfactory receptor family 5 subfamily D member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:15282]"}, {"versioned_ensembl_gene_id":"ENSG00000180610.10","gene_symbol":"ZBTB12BP","gene_name":"zinc finger and BTB domain containing 12B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37702]","synonyms":"ZNF920,ZBTB12P1,ZBTB12B","biotype":"processed_pseudogene","ncbi_id":"100499252","summary":null,"start":39770081,"end":39771371,"strand":-1,"description":"zinc finger and BTB domain containing 12B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37702]"}, {"versioned_ensembl_gene_id":"ENSG00000227680.1","gene_symbol":"AC108051.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102987323,"end":102988565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232041.1","gene_symbol":"PSMD10P3","gene_name":"proteasome 26S subunit, non-ATPase, 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30152]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338091","summary":null,"start":73036401,"end":73036848,"strand":1,"description":"proteasome 26S subunit, non-ATPase, 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30152]"}, {"versioned_ensembl_gene_id":"ENSG00000107338.9","gene_symbol":"SHB","gene_name":"SH2 domain containing adaptor protein B [Source:HGNC Symbol;Acc:HGNC:10838]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6461","summary":null,"start":37919134,"end":38069211,"strand":-1,"description":"SH2 domain containing adaptor protein B [Source:HGNC Symbol;Acc:HGNC:10838]"}, {"versioned_ensembl_gene_id":"ENSG00000234491.1","gene_symbol":"HNRNPA1P51","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729366","summary":null,"start":206419292,"end":206420238,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48781]"}, {"versioned_ensembl_gene_id":"ENSG00000117480.15","gene_symbol":"FAAH","gene_name":"fatty acid amide hydrolase [Source:HGNC Symbol;Acc:HGNC:3553]","synonyms":"FAAH-1","biotype":"protein_coding","ncbi_id":"2166","summary":"This gene encodes a protein that is responsible for the hydrolysis of a number of primary and secondary fatty acid amides, including the neuromodulatory compounds anandamide and oleamide. [provided by RefSeq, Jul 2008]","start":46394265,"end":46413848,"strand":1,"description":"fatty acid amide hydrolase [Source:HGNC Symbol;Acc:HGNC:3553]"}, {"versioned_ensembl_gene_id":"ENSG00000219074.1","gene_symbol":"SOD1P1","gene_name":"superoxide dismutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479055","summary":null,"start":53196720,"end":53197159,"strand":-1,"description":"superoxide dismutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45134]"}, {"versioned_ensembl_gene_id":"ENSG00000196104.10","gene_symbol":"SPOCK3","gene_name":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 3 [Source:HGNC Symbol;Acc:HGNC:13565]","synonyms":"testican-3","biotype":"protein_coding","ncbi_id":"50859","summary":"This gene encodes a member of a novel family of calcium-binding proteoglycan proteins that contain thyroglobulin type-1 and Kazal-like domains. The encoded protein and may play a role in adult T-cell leukemia by inhibiting the activity of membrane-type matrix metalloproteinases. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":166733384,"end":167234796,"strand":-1,"description":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 3 [Source:HGNC Symbol;Acc:HGNC:13565]"}, {"versioned_ensembl_gene_id":"ENSG00000277072.4","gene_symbol":"STAG3L2","gene_name":"stromal antigen 3-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33886]","synonyms":"STAG3L2P,MGC131759","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442582","summary":null,"start":74882163,"end":74890610,"strand":-1,"description":"stromal antigen 3-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33886]"}, {"versioned_ensembl_gene_id":"ENSG00000266460.1","gene_symbol":"AC021506.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75844925,"end":75868252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263821.1","gene_symbol":"AP005121.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14978739,"end":14979839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196597.11","gene_symbol":"ZNF782","gene_name":"zinc finger protein 782 [Source:HGNC Symbol;Acc:HGNC:33110]","synonyms":"FLJ16636","biotype":"protein_coding","ncbi_id":"158431","summary":null,"start":96816472,"end":96875623,"strand":-1,"description":"zinc finger protein 782 [Source:HGNC Symbol;Acc:HGNC:33110]"}, {"versioned_ensembl_gene_id":"ENSG00000059758.7","gene_symbol":"CDK17","gene_name":"cyclin dependent kinase 17 [Source:HGNC Symbol;Acc:HGNC:8750]","synonyms":"PCTK2,PCTAIRE2","biotype":"protein_coding","ncbi_id":"5128","summary":"The protein encoded by this gene belongs to the cdc2/cdkx subfamily of the ser/thr family of protein kinases. It has similarity to a rat protein that is thought to play a role in terminally differentiated neurons. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Jul 2010]","start":96278261,"end":96400560,"strand":-1,"description":"cyclin dependent kinase 17 [Source:HGNC Symbol;Acc:HGNC:8750]"}, {"versioned_ensembl_gene_id":"ENSG00000115902.10","gene_symbol":"SLC1A4","gene_name":"solute carrier family 1 member 4 [Source:HGNC Symbol;Acc:HGNC:10942]","synonyms":"SATT,ASCT1","biotype":"protein_coding","ncbi_id":"6509","summary":"The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]","start":64988477,"end":65023865,"strand":1,"description":"solute carrier family 1 member 4 [Source:HGNC Symbol;Acc:HGNC:10942]"}, {"versioned_ensembl_gene_id":"ENSG00000257169.1","gene_symbol":"AC125612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96386818,"end":96387194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261745.2","gene_symbol":"AL512347.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":53125644,"end":53126146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273521.1","gene_symbol":"AL162274.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131980240,"end":131981337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116918.13","gene_symbol":"TSNAX","gene_name":"translin associated factor X [Source:HGNC Symbol;Acc:HGNC:12380]","synonyms":"TRAX","biotype":"protein_coding","ncbi_id":"7257","summary":"This gene encodes a protein which specifically interacts with translin, a DNA-binding protein that binds consensus sequences at breakpoint junctions of chromosomal translocations. The encoded protein contains bipartite nuclear targeting sequences that may provide nuclear transport for translin, which lacks any nuclear targeting motifs. [provided by RefSeq, Jul 2008]","start":231528653,"end":231566524,"strand":1,"description":"translin associated factor X [Source:HGNC Symbol;Acc:HGNC:12380]"}, {"versioned_ensembl_gene_id":"ENSG00000077514.8","gene_symbol":"POLD3","gene_name":"DNA polymerase delta 3, accessory subunit [Source:HGNC Symbol;Acc:HGNC:20932]","synonyms":"P66,KIAA0039,PPP1R128,P68","biotype":"protein_coding","ncbi_id":"10714","summary":"This gene encodes the 66-kDa subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. The encoded protein plays a role in regulating the activity of DNA polymerase delta through interactions with other subunits and the processivity cofactor proliferating cell nuclear antigen (PCNA). Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012]","start":74493851,"end":74669117,"strand":1,"description":"DNA polymerase delta 3, accessory subunit [Source:HGNC Symbol;Acc:HGNC:20932]"}, {"versioned_ensembl_gene_id":"ENSG00000254201.1","gene_symbol":"AC068880.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19246350,"end":19249240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236026.1","gene_symbol":"AC009237.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95606924,"end":95607152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271003.1","gene_symbol":"AC009237.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95607073,"end":95616592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254762.1","gene_symbol":"AP001107.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66267635,"end":66268129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103888.16","gene_symbol":"CEMIP","gene_name":"cell migration inducing hyaluronan binding protein [Source:HGNC Symbol;Acc:HGNC:29213]","synonyms":"TMEM2L,KIAA1199,IR2155535,HYBID","biotype":"protein_coding","ncbi_id":"57214","summary":null,"start":80779343,"end":80951776,"strand":1,"description":"cell migration inducing hyaluronan binding protein [Source:HGNC Symbol;Acc:HGNC:29213]"}, {"versioned_ensembl_gene_id":"ENSG00000250337.5","gene_symbol":"LINC01021","gene_name":"long intergenic non-protein coding RNA 1021 [Source:HGNC Symbol;Acc:HGNC:48995]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643401","summary":null,"start":27472292,"end":27496401,"strand":1,"description":"long intergenic non-protein coding RNA 1021 [Source:HGNC Symbol;Acc:HGNC:48995]"}, {"versioned_ensembl_gene_id":"ENSG00000226803.7","gene_symbol":"AL136311.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57114894,"end":57174236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206292.13","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-DNA,HLA-D0-alpha,HLA-DZA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":32932859,"end":32938293,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000134258.16","gene_symbol":"VTCN1","gene_name":"V-set domain containing T-cell activation inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28873]","synonyms":"FLJ22418,B7X,B7S1,B7H4,B7-H4","biotype":"protein_coding","ncbi_id":"79679","summary":"This gene encodes a protein belonging to the B7 costimulatory protein family. Proteins in this family are present on the surface of antigen-presenting cells and interact with ligand bound to receptors on the surface of T cells. Studies have shown that high levels of the encoded protein has been correlated with tumor progression. A pseudogene of this gene is located on chromosome 20. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":117143587,"end":117210960,"strand":-1,"description":"V-set domain containing T-cell activation inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28873]"}, {"versioned_ensembl_gene_id":"ENSG00000230847.4","gene_symbol":"AC044797.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71074225,"end":71093193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269681.1","gene_symbol":"AC063977.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51155288,"end":51155624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260121.1","gene_symbol":"AC138028.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88718615,"end":88720459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248228.1","gene_symbol":"SLIT2-IT1","gene_name":"SLIT2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41383]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100505893","summary":null,"start":20392189,"end":20394856,"strand":1,"description":"SLIT2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41383]"}, {"versioned_ensembl_gene_id":"ENSG00000176769.9","gene_symbol":"TCERG1L","gene_name":"transcription elongation regulator 1 like [Source:HGNC Symbol;Acc:HGNC:23533]","synonyms":"FLJ38950","biotype":"protein_coding","ncbi_id":"256536","summary":null,"start":131092391,"end":131311721,"strand":-1,"description":"transcription elongation regulator 1 like [Source:HGNC Symbol;Acc:HGNC:23533]"}, {"versioned_ensembl_gene_id":"ENSG00000273791.1","gene_symbol":"AC007204.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19908268,"end":19909146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164621.5","gene_symbol":"SMAD5-AS1","gene_name":"SMAD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30586]","synonyms":"DAMS,SMAD5OS","biotype":"antisense_RNA","ncbi_id":"9597","summary":null,"start":136129507,"end":136134890,"strand":-1,"description":"SMAD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30586]"}, {"versioned_ensembl_gene_id":"ENSG00000240770.5","gene_symbol":"C21orf91-OT1","gene_name":"C21orf91 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:16729]","synonyms":"NCRNA00285,D21S2089E","biotype":"lincRNA","ncbi_id":"246312","summary":null,"start":17763315,"end":17792523,"strand":-1,"description":"C21orf91 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:16729]"}, {"versioned_ensembl_gene_id":"ENSG00000112182.14","gene_symbol":"BACH2","gene_name":"BTB domain and CNC homolog 2 [Source:HGNC Symbol;Acc:HGNC:14078]","synonyms":"BTBD25","biotype":"protein_coding","ncbi_id":"60468","summary":null,"start":89926529,"end":90296908,"strand":-1,"description":"BTB domain and CNC homolog 2 [Source:HGNC Symbol;Acc:HGNC:14078]"}, {"versioned_ensembl_gene_id":"ENSG00000255107.1","gene_symbol":"AC079089.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69859264,"end":69860540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144837.8","gene_symbol":"PLA1A","gene_name":"phospholipase A1 member A [Source:HGNC Symbol;Acc:HGNC:17661]","synonyms":"ps-PLA1","biotype":"protein_coding","ncbi_id":"51365","summary":"The protein encoded by this gene is a phospholipase that hydrolyzes fatty acids at the sn-1 position of phosphatidylserine and 1-acyl-2-lysophosphatidylserine. This secreted protein hydrolyzes phosphatidylserine in liposomes. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]","start":119597842,"end":119629811,"strand":1,"description":"phospholipase A1 member A [Source:HGNC Symbol;Acc:HGNC:17661]"}, {"versioned_ensembl_gene_id":"ENSG00000272164.1","gene_symbol":"AC005972.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63004672,"end":63005152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065882.15","gene_symbol":"TBC1D1","gene_name":"TBC1 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:11578]","synonyms":"TBC1,TBC,KIAA1108","biotype":"protein_coding","ncbi_id":"23216","summary":"TBC1D1 is the founding member of a family of proteins sharing a 180- to 200-amino acid TBC domain presumed to have a role in regulating cell growth and differentiation. These proteins share significant homology with TRE2 (USP6; MIM 604334), yeast Bub2, and CDC16 (MIM 603461) (White et al., 2000 [PubMed 10965142]).[supplied by OMIM, Mar 2008]","start":37891087,"end":38139175,"strand":1,"description":"TBC1 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:11578]"}, {"versioned_ensembl_gene_id":"ENSG00000265262.1","gene_symbol":"TRMT112P3","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44022]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729667","summary":null,"start":62950831,"end":62951188,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44022]"}, {"versioned_ensembl_gene_id":"ENSG00000120158.11","gene_symbol":"RCL1","gene_name":"RNA terminal phosphate cyclase like 1 [Source:HGNC Symbol;Acc:HGNC:17687]","synonyms":"RPCL1,RNAC","biotype":"protein_coding","ncbi_id":"10171","summary":null,"start":4792869,"end":4885917,"strand":1,"description":"RNA terminal phosphate cyclase like 1 [Source:HGNC Symbol;Acc:HGNC:17687]"}, {"versioned_ensembl_gene_id":"ENSG00000228289.1","gene_symbol":"AL355862.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163769339,"end":163769691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219240.2","gene_symbol":"AL353692.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89886156,"end":89887848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265702.1","gene_symbol":"AC005821.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62699244,"end":62737922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146374.13","gene_symbol":"RSPO3","gene_name":"R-spondin 3 [Source:HGNC Symbol;Acc:HGNC:20866]","synonyms":"THSD2,FLJ14440","biotype":"protein_coding","ncbi_id":"84870","summary":"This gene belongs to the R-spondin family. The encoded protein plays a role in the regulation of Wnt (wingless-type MMTV integration site family)/beta-catenin and Wnt/planar cell polarity (PCP) signaling pathways, which are involved in development, cell growth and disease pathogenesis. Genome-wide association studies suggest a correlation of this gene with bone mineral density and risk of fracture. This gene may be involved in tumor development. [provided by RefSeq, Jul 2013]","start":127118604,"end":127197765,"strand":1,"description":"R-spondin 3 [Source:HGNC Symbol;Acc:HGNC:20866]"}, {"versioned_ensembl_gene_id":"ENSG00000145147.19","gene_symbol":"SLIT2","gene_name":"slit guidance ligand 2 [Source:HGNC Symbol;Acc:HGNC:11086]","synonyms":"Slit-2,SLIL3","biotype":"protein_coding","ncbi_id":"9353","summary":"This gene encodes a member of the slit family of secreted glycoproteins, which are ligands for the Robo family of immunoglobulin receptors. Slit proteins play highly conserved roles in axon guidance and neuronal migration and may also have functions during other cell migration processes including leukocyte migration. Members of the slit family are characterized by an N-terminal signal peptide, four leucine-rich repeats, nine epidermal growth factor repeats, and a C-terminal cysteine knot. Proteolytic processing of this protein gives rise to an N-terminal fragment that contains the four leucine-rich repeats and five epidermal growth factor repeats and a C-terminal fragment that contains four epidermal growth factor repeats and the cysteine knot. Both full length and cleaved proteins are secreted extracellularly and can function in axon repulsion as well as other specific processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":20253260,"end":20620561,"strand":1,"description":"slit guidance ligand 2 [Source:HGNC Symbol;Acc:HGNC:11086]"}, {"versioned_ensembl_gene_id":"ENSG00000248475.5","gene_symbol":"AC016642.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58741581,"end":58817099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148483.8","gene_symbol":"TMEM236","gene_name":"transmembrane protein 236 [Source:HGNC Symbol;Acc:HGNC:23473]","synonyms":"FAM23B,FAM23A,bA16O1.2,bA162I21.2","biotype":"protein_coding","ncbi_id":"653567","summary":null,"start":17752252,"end":17800868,"strand":1,"description":"transmembrane protein 236 [Source:HGNC Symbol;Acc:HGNC:23473]"}, {"versioned_ensembl_gene_id":"ENSG00000255147.1","gene_symbol":"AP003385.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67749043,"end":67756968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279567.1","gene_symbol":"AC005703.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15365323,"end":15365877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253997.1","gene_symbol":"AC090142.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104990308,"end":104990692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233043.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"processed_transcript","ncbi_id":"414768","summary":null,"start":33298642,"end":33301626,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000116690.12","gene_symbol":"PRG4","gene_name":"proteoglycan 4 [Source:HGNC Symbol;Acc:HGNC:9364]","synonyms":"SZP,MSF,JCAP,HAPO,CACP,FLJ32635,bG174L6.2","biotype":"protein_coding","ncbi_id":"10216","summary":"The protein encoded by this gene is a large proteoglycan that is synthesized by chondrocytes located at the surface of articular cartilage and by some synovial lining cells. This protein contains both chondroitin sulfate and keratan sulfate glycosaminoglycans. It functions as a boundary lubricant at the cartilage surface and contributes to the elastic absorption and energy dissipation of synovial fluid. Mutations in this gene result in camptodactyly-arthropathy-coxa vara-pericarditis syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":186296279,"end":186314562,"strand":1,"description":"proteoglycan 4 [Source:HGNC Symbol;Acc:HGNC:9364]"}, {"versioned_ensembl_gene_id":"ENSG00000243171.1","gene_symbol":"AC041039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105287830,"end":105288365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167759.12","gene_symbol":"KLK13","gene_name":"kallikrein related peptidase 13 [Source:HGNC Symbol;Acc:HGNC:6361]","synonyms":"KLK-L4","biotype":"protein_coding","ncbi_id":"26085","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Expression of this gene is regulated by steroid hormones and may be useful as a marker for breast cancer. [provided by RefSeq, Jan 2017]","start":51056206,"end":51065114,"strand":-1,"description":"kallikrein related peptidase 13 [Source:HGNC Symbol;Acc:HGNC:6361]"}, {"versioned_ensembl_gene_id":"ENSG00000281008.1","gene_symbol":"AC004808.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78134079,"end":78134851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249863.2","gene_symbol":"AC021106.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37868292,"end":37869978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277351.1","gene_symbol":"AC013553.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65049188,"end":65049802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278763.1","gene_symbol":"FAM27B","gene_name":"family with sequence similarity 27 member B [Source:HGNC Symbol;Acc:HGNC:23667]","synonyms":"FAM27A2,bA12A20.3","biotype":"processed_pseudogene","ncbi_id":"100133121","summary":null,"start":67725690,"end":67725902,"strand":-1,"description":"family with sequence similarity 27 member B [Source:HGNC Symbol;Acc:HGNC:23667]"}, {"versioned_ensembl_gene_id":"ENSG00000225177.5","gene_symbol":"AL590617.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138692548,"end":138697288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115685.14","gene_symbol":"PPP1R7","gene_name":"protein phosphatase 1 regulatory subunit 7 [Source:HGNC Symbol;Acc:HGNC:9295]","synonyms":"sds22","biotype":"protein_coding","ncbi_id":"5510","summary":"This gene encodes a protein subunit that regulates the activity of the serine/threonine phosphatase, protein phosphatase-1. The encoded protein is required for completion of the mitotic cycle and for targeting protein phosphatase-1 to mitotic kinetochores. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":241149576,"end":241183652,"strand":1,"description":"protein phosphatase 1 regulatory subunit 7 [Source:HGNC Symbol;Acc:HGNC:9295]"}, {"versioned_ensembl_gene_id":"ENSG00000088543.14","gene_symbol":"C3orf18","gene_name":"chromosome 3 open reading frame 18 [Source:HGNC Symbol;Acc:HGNC:24837]","synonyms":"G20","biotype":"protein_coding","ncbi_id":"51161","summary":null,"start":50558025,"end":50571027,"strand":-1,"description":"chromosome 3 open reading frame 18 [Source:HGNC Symbol;Acc:HGNC:24837]"}, {"versioned_ensembl_gene_id":"ENSG00000243709.1","gene_symbol":"LEFTY1","gene_name":"left-right determination factor 1 [Source:HGNC Symbol;Acc:HGNC:6552]","synonyms":"LEFTYB,LEFTB","biotype":"protein_coding","ncbi_id":"10637","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which plays a role in left-right asymmetry determination of organ systems during development. This gene is closely linked to both a related family member and a related pseudogene. [provided by RefSeq, Aug 2016]","start":225886282,"end":225911382,"strand":-1,"description":"left-right determination factor 1 [Source:HGNC Symbol;Acc:HGNC:6552]"}, {"versioned_ensembl_gene_id":"ENSG00000185246.17","gene_symbol":"PRPF39","gene_name":"pre-mRNA processing factor 39 [Source:HGNC Symbol;Acc:HGNC:20314]","synonyms":"FLJ20666,FLJ11128","biotype":"protein_coding","ncbi_id":"55015","summary":null,"start":45084099,"end":45116282,"strand":1,"description":"pre-mRNA processing factor 39 [Source:HGNC Symbol;Acc:HGNC:20314]"}, {"versioned_ensembl_gene_id":"ENSG00000250536.1","gene_symbol":"ABHD17AP3","gene_name":"abhydrolase domain containing 17A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34041]","synonyms":"FAM108A4P,FAM108A4","biotype":"unprocessed_pseudogene","ncbi_id":"648359","summary":null,"start":214605470,"end":214608840,"strand":-1,"description":"abhydrolase domain containing 17A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34041]"}, {"versioned_ensembl_gene_id":"ENSG00000236065.2","gene_symbol":"AL020995.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32987075,"end":33032469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130958.11","gene_symbol":"SLC35D2","gene_name":"solute carrier family 35 member D2 [Source:HGNC Symbol;Acc:HGNC:20799]","synonyms":"UGTrel8,SQV7L","biotype":"protein_coding","ncbi_id":"11046","summary":"Nucleotide sugars, which are synthesized in the cytosol or the nucleus, are high-energy donor substrates for glycosyltransferases located in the lumen of the endoplasmic reticulum and Golgi apparatus. Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters, such as SLC35D2 (Suda et al., 2004 [PubMed 15082721]).[supplied by OMIM, Mar 2008]","start":96320706,"end":96383710,"strand":-1,"description":"solute carrier family 35 member D2 [Source:HGNC Symbol;Acc:HGNC:20799]"}, {"versioned_ensembl_gene_id":"ENSG00000127022.14","gene_symbol":"CANX","gene_name":"calnexin [Source:HGNC Symbol;Acc:HGNC:1473]","synonyms":"P90,IP90,CNX","biotype":"protein_coding","ncbi_id":"821","summary":"This gene encodes a member of the calnexin family of molecular chaperones. The encoded protein is a calcium-binding, endoplasmic reticulum (ER)-associated protein that interacts transiently with newly synthesized N-linked glycoproteins, facilitating protein folding and assembly. It may also play a central role in the quality control of protein folding by retaining incorrectly folded protein subunits within the ER for degradation. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2018]","start":179678628,"end":179730925,"strand":1,"description":"calnexin [Source:HGNC Symbol;Acc:HGNC:1473]"}, {"versioned_ensembl_gene_id":"ENSG00000140943.16","gene_symbol":"MBTPS1","gene_name":"membrane bound transcription factor peptidase, site 1 [Source:HGNC Symbol;Acc:HGNC:15456]","synonyms":"SKI-1,S1P,PCSK8,KIAA0091","biotype":"protein_coding","ncbi_id":"8720","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the cis/medial-Golgi where a second autocatalytic event takes place and the catalytic activity is acquired. It encodes a type 1 membrane bound protease which is ubiquitously expressed and regulates cholesterol or lipid homeostasis via cleavage of substrates at non-basic residues. Mutations in this gene may be associated with lysosomal dysfunction. [provided by RefSeq, Feb 2014]","start":84053761,"end":84116906,"strand":-1,"description":"membrane bound transcription factor peptidase, site 1 [Source:HGNC Symbol;Acc:HGNC:15456]"}, {"versioned_ensembl_gene_id":"ENSG00000206379.12","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30717966,"end":30732991,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000267693.1","gene_symbol":"AC011477.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19768731,"end":19768989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226025.9","gene_symbol":"LGALS17A","gene_name":"galectin 14 pseudogene [Source:NCBI gene;Acc:400696]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400696","summary":null,"start":39679374,"end":39686373,"strand":1,"description":"galectin 14 pseudogene [Source:NCBI gene;Acc:400696]"}, {"versioned_ensembl_gene_id":"ENSG00000112200.16","gene_symbol":"ZNF451","gene_name":"zinc finger protein 451 [Source:HGNC Symbol;Acc:HGNC:21091]","synonyms":"KIAA1702,KIAA0576,dJ417I1.1,COASTER","biotype":"protein_coding","ncbi_id":"26036","summary":null,"start":57086844,"end":57170307,"strand":1,"description":"zinc finger protein 451 [Source:HGNC Symbol;Acc:HGNC:21091]"}, {"versioned_ensembl_gene_id":"ENSG00000183765.20","gene_symbol":"CHEK2","gene_name":"checkpoint kinase 2 [Source:HGNC Symbol;Acc:HGNC:16627]","synonyms":"RAD53,PP1425,HuCds1,CHK2,CDS1,bA444G7","biotype":"protein_coding","ncbi_id":"11200","summary":"In response to DNA damage and replication blocks, cell cycle progression is halted through the control of critical cell cycle regulators. The protein encoded by this gene is a cell cycle checkpoint regulator and putative tumor suppressor. It contains a forkhead-associated protein interaction domain essential for activation in response to DNA damage and is rapidly phosphorylated in response to replication blocks and DNA damage. When activated, the encoded protein is known to inhibit CDC25C phosphatase, preventing entry into mitosis, and has been shown to stabilize the tumor suppressor protein p53, leading to cell cycle arrest in G1. In addition, this protein interacts with and phosphorylates BRCA1, allowing BRCA1 to restore survival after DNA damage. Mutations in this gene have been linked with Li-Fraumeni syndrome, a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53. Also, mutations in this gene are thought to confer a predisposition to sarcomas, breast cancer, and brain tumors. This nuclear protein is a member of the CDS1 subfamily of serine/threonine protein kinases. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":28687743,"end":28742422,"strand":-1,"description":"checkpoint kinase 2 [Source:HGNC Symbol;Acc:HGNC:16627]"}, {"versioned_ensembl_gene_id":"ENSG00000134744.13","gene_symbol":"ZCCHC11","gene_name":"zinc finger CCHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:28981]","synonyms":"KIAA0191,TUT4,PAPD3","biotype":"protein_coding","ncbi_id":"23318","summary":"ZCCHC11 is an RNA uridyltransferase (EC 2.7.7.52) that uses UTP to add uridines to the 3-prime end of substrate RNA molecules (Jones et al., 2009 [PubMed 19701194]).[supplied by OMIM, Jan 2011]","start":52408282,"end":52553487,"strand":-1,"description":"zinc finger CCHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:28981]"}, {"versioned_ensembl_gene_id":"ENSG00000115042.9","gene_symbol":"FAHD2A","gene_name":"fumarylacetoacetate hydrolase domain containing 2A [Source:HGNC Symbol;Acc:HGNC:24252]","synonyms":"CGI-105","biotype":"protein_coding","ncbi_id":"51011","summary":null,"start":95402721,"end":95416616,"strand":1,"description":"fumarylacetoacetate hydrolase domain containing 2A [Source:HGNC Symbol;Acc:HGNC:24252]"}, {"versioned_ensembl_gene_id":"ENSG00000273063.1","gene_symbol":"AC007250.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58241349,"end":58241686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273851.1","gene_symbol":"AC027088.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":69022230,"end":69024176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227432.1","gene_symbol":"AC053503.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219482073,"end":219516877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133030.20","gene_symbol":"MPRIP","gene_name":"myosin phosphatase Rho interacting protein [Source:HGNC Symbol;Acc:HGNC:30321]","synonyms":"RHOIP3,p116Rip,M-RIP","biotype":"protein_coding","ncbi_id":"23164","summary":null,"start":17042545,"end":17217679,"strand":1,"description":"myosin phosphatase Rho interacting protein [Source:HGNC Symbol;Acc:HGNC:30321]"}, {"versioned_ensembl_gene_id":"ENSG00000251323.2","gene_symbol":"AP003086.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78423982,"end":78429836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119705.9","gene_symbol":"SLIRP","gene_name":"SRA stem-loop interacting RNA binding protein [Source:HGNC Symbol;Acc:HGNC:20495]","synonyms":"C14orf156,DC50","biotype":"protein_coding","ncbi_id":"81892","summary":"Steroid receptor RNA activator (SRA, or SRA1; MIM 603819) is a complex RNA molecule containing multiple stable stem-loop structures that functions in coactivation of nuclear receptors. SLIRP interacts with stem-loop structure-7 of SRA (STR7) and modulates nuclear receptor transactivation (Hatchell et al., 2006 [PubMed 16762838]).[supplied by OMIM, Mar 2008]","start":77708071,"end":77761104,"strand":1,"description":"SRA stem-loop interacting RNA binding protein [Source:HGNC Symbol;Acc:HGNC:20495]"}, {"versioned_ensembl_gene_id":"ENSG00000232259.1","gene_symbol":"AL158166.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127929376,"end":127934517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189233.11","gene_symbol":"NUGGC","gene_name":"nuclear GTPase, germinal center associated [Source:HGNC Symbol;Acc:HGNC:33550]","synonyms":"SLIP-GC,HMFN0672,C8orf80","biotype":"protein_coding","ncbi_id":"389643","summary":null,"start":28021964,"end":28083871,"strand":-1,"description":"nuclear GTPase, germinal center associated [Source:HGNC Symbol;Acc:HGNC:33550]"}, {"versioned_ensembl_gene_id":"ENSG00000278563.2","gene_symbol":"MGAM2","gene_name":"maltase-glucoamylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:28101]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93432","summary":null,"start":142111749,"end":142222324,"strand":1,"description":"maltase-glucoamylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:28101]"}, {"versioned_ensembl_gene_id":"ENSG00000131944.9","gene_symbol":"FAAP24","gene_name":"Fanconi anemia core complex associated protein 24 [Source:HGNC Symbol;Acc:HGNC:28467]","synonyms":"C19orf40,MGC32020,FLJ46828","biotype":"protein_coding","ncbi_id":"91442","summary":"FAAP24 is a component of the Fanconi anemia (FA) core complex (see MIM 227650), which plays a crucial role in DNA damage response (Ciccia et al., 2007 [PubMed 17289582]).[supplied by OMIM, Mar 2008]","start":32972209,"end":32978222,"strand":1,"description":"Fanconi anemia core complex associated protein 24 [Source:HGNC Symbol;Acc:HGNC:28467]"}, {"versioned_ensembl_gene_id":"ENSG00000278133.1","gene_symbol":"AC135050.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31122235,"end":31124064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227650.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31598491,"end":31598764,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000275610.1","gene_symbol":"DUX4L21","gene_name":"double homeobox 4 like 21 [Source:HGNC Symbol;Acc:HGNC:50802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723518","summary":null,"start":133680369,"end":133681637,"strand":1,"description":"double homeobox 4 like 21 [Source:HGNC Symbol;Acc:HGNC:50802]"}, {"versioned_ensembl_gene_id":"ENSG00000213079.9","gene_symbol":"SCAF8","gene_name":"SR-related CTD associated factor 8 [Source:HGNC Symbol;Acc:HGNC:20959]","synonyms":"RBM16,KIAA1116","biotype":"protein_coding","ncbi_id":"22828","summary":null,"start":154733325,"end":154834244,"strand":1,"description":"SR-related CTD associated factor 8 [Source:HGNC Symbol;Acc:HGNC:20959]"}, {"versioned_ensembl_gene_id":"ENSG00000253744.1","gene_symbol":"AC025442.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66144156,"end":66144795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248802.1","gene_symbol":"AC078850.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128582999,"end":128601407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166260.11","gene_symbol":"COX11","gene_name":"COX11, cytochrome c oxidase copper chaperone [Source:HGNC Symbol;Acc:HGNC:2261]","synonyms":"COX11P","biotype":"protein_coding","ncbi_id":"1353","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be a heme A biosynthetic enzyme involved in COX formation, according to the yeast mutant studies. However, the studies in Rhodobacter sphaeroides suggest that this gene is not required for heme A biosynthesis, but required for stable formation of the Cu(B) and magnesium centers of COX. This human protein is predicted to contain a transmembrane domain localized in the mitochondrial inner membrane. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene has been found on chromosome 6. [provided by RefSeq, Jun 2009]","start":54951902,"end":54968785,"strand":-1,"description":"COX11, cytochrome c oxidase copper chaperone [Source:HGNC Symbol;Acc:HGNC:2261]"}, {"versioned_ensembl_gene_id":"ENSG00000267277.1","gene_symbol":"AC024575.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11368123,"end":11374935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273055.1","gene_symbol":"AC005046.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107942116,"end":107942740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172867.3","gene_symbol":"KRT2","gene_name":"keratin 2 [Source:HGNC Symbol;Acc:HGNC:6439]","synonyms":"KRTE,KRT2A","biotype":"protein_coding","ncbi_id":"3849","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is expressed largely in the upper spinous layer of epidermal keratinocytes and mutations in this gene have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52644558,"end":52652164,"strand":-1,"description":"keratin 2 [Source:HGNC Symbol;Acc:HGNC:6439]"}, {"versioned_ensembl_gene_id":"ENSG00000127445.13","gene_symbol":"PIN1","gene_name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1 [Source:HGNC Symbol;Acc:HGNC:8988]","synonyms":"dod","biotype":"protein_coding","ncbi_id":"5300","summary":"Peptidyl-prolyl cis/trans isomerases (PPIases) catalyze the cis/trans isomerization of peptidyl-prolyl peptide bonds. This gene encodes one of the PPIases, which specifically binds to phosphorylated ser/thr-pro motifs to catalytically regulate the post-phosphorylation conformation of its substrates. The conformational regulation catalyzed by this PPIase has a profound impact on key proteins involved in the regulation of cell growth, genotoxic and other stress responses, the immune response, induction and maintenance of pluripotency, germ cell development, neuronal differentiation, and survival. This enzyme also plays a key role in the pathogenesis of Alzheimer's disease and many cancers. Multiple alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jun 2011]","start":9835257,"end":9849682,"strand":1,"description":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1 [Source:HGNC Symbol;Acc:HGNC:8988]"}, {"versioned_ensembl_gene_id":"ENSG00000245928.2","gene_symbol":"AC112719.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75980790,"end":76005942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236889.1","gene_symbol":"AC244035.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206175060,"end":206177246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248929.1","gene_symbol":"HIGD1AP3","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42998]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100859920","summary":null,"start":174632932,"end":174633209,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42998]"}, {"versioned_ensembl_gene_id":"ENSG00000138744.14","gene_symbol":"NAAA","gene_name":"N-acylethanolamine acid amidase [Source:HGNC Symbol;Acc:HGNC:736]","synonyms":"ASAHL","biotype":"protein_coding","ncbi_id":"27163","summary":"This gene encodes an N-acylethanolamine-hydrolyzing enzyme which is highly similar to acid ceramidase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75913657,"end":75941051,"strand":-1,"description":"N-acylethanolamine acid amidase [Source:HGNC Symbol;Acc:HGNC:736]"}, {"versioned_ensembl_gene_id":"ENSG00000253474.1","gene_symbol":"AC022568.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49168539,"end":49228925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279649.1","gene_symbol":"AC020978.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68290087,"end":68292790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109944.10","gene_symbol":"C11orf63","gene_name":"chromosome 11 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:26288]","synonyms":"Jhy,FLJ23554","biotype":"protein_coding","ncbi_id":"79864","summary":null,"start":122882528,"end":122959798,"strand":1,"description":"chromosome 11 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:26288]"}, {"versioned_ensembl_gene_id":"ENSG00000137692.11","gene_symbol":"DCUN1D5","gene_name":"defective in cullin neddylation 1 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28409]","synonyms":"MGC2714,FLJ32431","biotype":"protein_coding","ncbi_id":"84259","summary":null,"start":103062076,"end":103092215,"strand":-1,"description":"defective in cullin neddylation 1 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28409]"}, {"versioned_ensembl_gene_id":"ENSG00000275173.1","gene_symbol":"AC243571.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37798894,"end":37802788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105355.8","gene_symbol":"PLIN3","gene_name":"perilipin 3 [Source:HGNC Symbol;Acc:HGNC:16893]","synonyms":"TIP47,PP17,M6PRBP1","biotype":"protein_coding","ncbi_id":"10226","summary":"Mannose 6-phophate receptors (MPRs) deliver lysosomal hydrolase from the Golgi to endosomes and then return to the Golgi complex. The protein encoded by this gene interacts with the cytoplasmic domains of both cation-independent and cation-dependent MPRs, and is required for endosome-to-Golgi transport. This protein also binds directly to the GTPase RAB9 (RAB9A), a member of the RAS oncogene family. The interaction with RAB9 has been shown to increase the affinity of this protein for its cargo. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2009]","start":4838341,"end":4867768,"strand":-1,"description":"perilipin 3 [Source:HGNC Symbol;Acc:HGNC:16893]"}, {"versioned_ensembl_gene_id":"ENSG00000267484.1","gene_symbol":"AC027319.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4838332,"end":4838907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171574.17","gene_symbol":"ZNF584","gene_name":"zinc finger protein 584 [Source:HGNC Symbol;Acc:HGNC:27318]","synonyms":"FLJ39899","biotype":"protein_coding","ncbi_id":"201514","summary":null,"start":58401504,"end":58418327,"strand":1,"description":"zinc finger protein 584 [Source:HGNC Symbol;Acc:HGNC:27318]"}, {"versioned_ensembl_gene_id":"ENSG00000261683.1","gene_symbol":"LINC00838","gene_name":"long intergenic non-protein coding RNA 838 [Source:HGNC Symbol;Acc:HGNC:44963]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505583","summary":null,"start":33759713,"end":33772658,"strand":-1,"description":"long intergenic non-protein coding RNA 838 [Source:HGNC Symbol;Acc:HGNC:44963]"}, {"versioned_ensembl_gene_id":"ENSG00000254505.9","gene_symbol":"CHMP4A","gene_name":"charged multivesicular body protein 4A [Source:HGNC Symbol;Acc:HGNC:20274]","synonyms":"HSPC134,C14orf123,VPS32A","biotype":"protein_coding","ncbi_id":"29082","summary":"CHMP4A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]","start":24209583,"end":24213869,"strand":-1,"description":"charged multivesicular body protein 4A [Source:HGNC Symbol;Acc:HGNC:20274]"}, {"versioned_ensembl_gene_id":"ENSG00000154639.18","gene_symbol":"CXADR","gene_name":"CXADR, Ig-like cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:2559]","synonyms":"CAR","biotype":"protein_coding","ncbi_id":"1525","summary":"The protein encoded by this gene is a type I membrane receptor for group B coxsackieviruses and subgroup C adenoviruses. Several transcript variants encoding different isoforms have been found for this gene. Pseudogenes of this gene are found on chromosomes 15, 18, and 21. [provided by RefSeq, May 2011]","start":17512382,"end":17593579,"strand":1,"description":"CXADR, Ig-like cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:2559]"}, {"versioned_ensembl_gene_id":"ENSG00000221990.4","gene_symbol":"EXOC3-AS1","gene_name":"EXOC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25175]","synonyms":"C5orf55","biotype":"antisense_RNA","ncbi_id":"116349","summary":null,"start":441498,"end":443160,"strand":-1,"description":"EXOC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25175]"}, {"versioned_ensembl_gene_id":"ENSG00000104970.10","gene_symbol":"KIR3DX1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]","synonyms":"LENG12,FLJ00060","biotype":"protein_coding","ncbi_id":"90011","summary":null,"start":54532692,"end":54545771,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]"}, {"versioned_ensembl_gene_id":"ENSG00000134183.11","gene_symbol":"GNAT2","gene_name":"G protein subunit alpha transducin 2 [Source:HGNC Symbol;Acc:HGNC:4394]","synonyms":"ACHM4","biotype":"protein_coding","ncbi_id":"2780","summary":"Transducin is a 3-subunit guanine nucleotide-binding protein (G protein) which stimulates the coupling of rhodopsin and cGMP-phoshodiesterase during visual impulses. The transducin alpha subunits in rods and cones are encoded by separate genes. This gene encodes the alpha subunit in cones. [provided by RefSeq, Jul 2008]","start":109603267,"end":109619929,"strand":-1,"description":"G protein subunit alpha transducin 2 [Source:HGNC Symbol;Acc:HGNC:4394]"}, {"versioned_ensembl_gene_id":"ENSG00000188242.4","gene_symbol":"PP7080","gene_name":"uncharacterized LOC25845 [Source:NCBI gene;Acc:25845]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"25845","summary":null,"start":466124,"end":473098,"strand":-1,"description":"uncharacterized LOC25845 [Source:NCBI gene;Acc:25845]"}, {"versioned_ensembl_gene_id":"ENSG00000168014.16","gene_symbol":"C2CD3","gene_name":"C2 calcium dependent domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24564]","synonyms":"DKFZP586P0123","biotype":"protein_coding","ncbi_id":"26005","summary":"This gene encodes a protein that functions as a regulator of centriole elongation. Studies of the orthologous mouse protein show that it promotes centriolar distal appendage assembly and is also required for the recruitment of other ciliogenic proteins, including intraflagellar transport proteins. Mutations in this gene cause orofaciodigital syndrome XIV (OFD14), a ciliopathy resulting in malformations of the oral cavity, face and digits. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":74012714,"end":74171210,"strand":-1,"description":"C2 calcium dependent domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24564]"}, {"versioned_ensembl_gene_id":"ENSG00000244251.1","gene_symbol":"AC013356.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40480752,"end":40481315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224762.1","gene_symbol":"CR769776.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64473040,"end":64473826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267248.1","gene_symbol":"AC025048.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":60126535,"end":60135644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178732.5","gene_symbol":"GP5","gene_name":"glycoprotein V platelet [Source:HGNC Symbol;Acc:HGNC:4443]","synonyms":"CD42d","biotype":"protein_coding","ncbi_id":"2814","summary":"Human platelet glycoprotein V (GP5) is a part of the Ib-V-IX system of surface glycoproteins that constitute the receptor for von Willebrand factor (VWF; MIM 613160) and mediate the adhesion of platelets to injured vascular surfaces in the arterial circulation, a critical initiating event in hemostasis. The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX (GP9; MIM 173515) and GP5. Mutations in GP1BA, GP1BB, and GP9 have been shown to cause Bernard-Soulier syndrome (MIM 231200), a bleeding disorder (review by Lopez et al., 1998 [PubMed 9616133]).[supplied by OMIM, Nov 2010]","start":194394821,"end":194398354,"strand":-1,"description":"glycoprotein V platelet [Source:HGNC Symbol;Acc:HGNC:4443]"}, {"versioned_ensembl_gene_id":"ENSG00000250080.1","gene_symbol":"AC011416.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127170535,"end":127172266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177932.6","gene_symbol":"ZNF354C","gene_name":"zinc finger protein 354C [Source:HGNC Symbol;Acc:HGNC:16736]","synonyms":"KID3","biotype":"protein_coding","ncbi_id":"30832","summary":null,"start":179060415,"end":179083537,"strand":1,"description":"zinc finger protein 354C [Source:HGNC Symbol;Acc:HGNC:16736]"}, {"versioned_ensembl_gene_id":"ENSG00000253911.1","gene_symbol":"AP003467.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98603253,"end":98606340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253468.1","gene_symbol":"AP003355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98412882,"end":98413784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184925.11","gene_symbol":"LCN12","gene_name":"lipocalin 12 [Source:HGNC Symbol;Acc:HGNC:28733]","synonyms":"MGC48935","biotype":"protein_coding","ncbi_id":"286256","summary":"Members of the lipocalin family, such as LCN12, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al., 2004 [PubMed 15363845]).[supplied by OMIM, Aug 2009]","start":136949551,"end":136955497,"strand":1,"description":"lipocalin 12 [Source:HGNC Symbol;Acc:HGNC:28733]"}, {"versioned_ensembl_gene_id":"ENSG00000273047.1","gene_symbol":"AL121845.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63738270,"end":63740398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257296.1","gene_symbol":"AC093027.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84671598,"end":84672026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213228.5","gene_symbol":"RPL12P38","gene_name":"ribosomal protein L12 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36838]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"645688","summary":null,"start":60433678,"end":60435996,"strand":-1,"description":"ribosomal protein L12 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36838]"}, {"versioned_ensembl_gene_id":"ENSG00000197253.13","gene_symbol":"TPSB2","gene_name":"tryptase beta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14120]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64499","summary":"Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. These genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. The alleles of this gene exhibit an unusual amount of sequence variation, such that the alleles were once thought to represent two separate genes, beta II and beta III. Beta tryptases appear to be the main isoenzymes expressed in mast cells, whereas in basophils, alpha-tryptases predominate. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. [provided by RefSeq, Jul 2008]","start":1227272,"end":1230184,"strand":-1,"description":"tryptase beta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14120]"}, {"versioned_ensembl_gene_id":"ENSG00000232886.1","gene_symbol":"AF212831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16862875,"end":16873691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266489.1","gene_symbol":"AC007922.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24516883,"end":24518006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278801.3","gene_symbol":"IGHD","gene_name":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]","synonyms":"MGC29633,FLJ46727,FLJ00382","biotype":"IG_C_gene","ncbi_id":"3495","summary":null,"start":105837536,"end":105846448,"strand":-1,"description":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]"}, {"versioned_ensembl_gene_id":"ENSG00000233287.1","gene_symbol":"AC009362.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131242590,"end":131242995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249990.1","gene_symbol":"MTCO2P24","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52153]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075193","summary":null,"start":98409675,"end":98410100,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52153]"}, {"versioned_ensembl_gene_id":"ENSG00000160051.11","gene_symbol":"IQCC","gene_name":"IQ motif containing C [Source:HGNC Symbol;Acc:HGNC:25545]","synonyms":"FLJ10547","biotype":"protein_coding","ncbi_id":"55721","summary":null,"start":32205661,"end":32208687,"strand":1,"description":"IQ motif containing C [Source:HGNC Symbol;Acc:HGNC:25545]"}, {"versioned_ensembl_gene_id":"ENSG00000172014.12","gene_symbol":"ANKRD20A4","gene_name":"ankyrin repeat domain 20 family member A4 [Source:HGNC Symbol;Acc:HGNC:31982]","synonyms":"OTTHUMG00000066855","biotype":"protein_coding","ncbi_id":"728747","summary":null,"start":64369394,"end":64413142,"strand":1,"description":"ankyrin repeat domain 20 family member A4 [Source:HGNC Symbol;Acc:HGNC:31982]"}, {"versioned_ensembl_gene_id":"ENSG00000231721.6","gene_symbol":"LINC-PINT","gene_name":"long intergenic non-protein coding RNA, p53 induced transcript [Source:HGNC Symbol;Acc:HGNC:26885]","synonyms":"PINT,MKLN1-AS1,LincRNA-Pint,FLJ43663","biotype":"antisense_RNA","ncbi_id":"378805","summary":null,"start":130941760,"end":131110176,"strand":-1,"description":"long intergenic non-protein coding RNA, p53 induced transcript [Source:HGNC Symbol;Acc:HGNC:26885]"}, {"versioned_ensembl_gene_id":"ENSG00000223752.8","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"Em:AB023049.7,MEC17,C6orf134,FLJ13158","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30616685,"end":30636664,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000106688.11","gene_symbol":"SLC1A1","gene_name":"solute carrier family 1 member 1 [Source:HGNC Symbol;Acc:HGNC:10939]","synonyms":"EAAT3,EAAC1","biotype":"protein_coding","ncbi_id":"6505","summary":"This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]","start":4490444,"end":4587469,"strand":1,"description":"solute carrier family 1 member 1 [Source:HGNC Symbol;Acc:HGNC:10939]"}, {"versioned_ensembl_gene_id":"ENSG00000271328.1","gene_symbol":"B3GNTL1P2","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51318]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480419","summary":null,"start":47368943,"end":47369230,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51318]"}, {"versioned_ensembl_gene_id":"ENSG00000102271.13","gene_symbol":"KLHL4","gene_name":"kelch like family member 4 [Source:HGNC Symbol;Acc:HGNC:6355]","synonyms":"KIAA1687,KHL4,DKELCHL","biotype":"protein_coding","ncbi_id":"56062","summary":"This gene encodes a member of the kelch family of proteins, which are characterized by kelch repeat motifs and a POZ/BTB protein-binding domain. It is thought that kelch repeats are actin binding domains. However, the specific function of this protein has not been determined. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":87517749,"end":87670050,"strand":1,"description":"kelch like family member 4 [Source:HGNC Symbol;Acc:HGNC:6355]"}, {"versioned_ensembl_gene_id":"ENSG00000151322.18","gene_symbol":"NPAS3","gene_name":"neuronal PAS domain protein 3 [Source:HGNC Symbol;Acc:HGNC:19311]","synonyms":"PASD6,MOP6,bHLHe12","biotype":"protein_coding","ncbi_id":"64067","summary":"This gene encodes a member of the basic helix-loop-helix and PAS domain-containing family of transcription factors. The encoded protein is localized to the nucleus and may regulate genes involved in neurogenesis. Chromosomal abnormalities that affect the coding potential of this gene are associated with schizophrenia and cognitive disability. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":32934933,"end":33804176,"strand":1,"description":"neuronal PAS domain protein 3 [Source:HGNC Symbol;Acc:HGNC:19311]"}, {"versioned_ensembl_gene_id":"ENSG00000261292.2","gene_symbol":"AC110491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97759523,"end":97761532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250331.1","gene_symbol":"LINC01340","gene_name":"long intergenic non-protein coding RNA 1340 [Source:HGNC Symbol;Acc:HGNC:50550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546227","summary":null,"start":97504696,"end":97671046,"strand":1,"description":"long intergenic non-protein coding RNA 1340 [Source:HGNC Symbol;Acc:HGNC:50550]"}, {"versioned_ensembl_gene_id":"ENSG00000250125.1","gene_symbol":"LINC02232","gene_name":"long intergenic non-protein coding RNA 2232 [Source:HGNC Symbol;Acc:HGNC:53103]","synonyms":"RP11-707A18.1","biotype":"lincRNA","ncbi_id":"401134","summary":null,"start":64914281,"end":65004500,"strand":-1,"description":"long intergenic non-protein coding RNA 2232 [Source:HGNC Symbol;Acc:HGNC:53103]"}, {"versioned_ensembl_gene_id":"ENSG00000244669.1","gene_symbol":"AC104689.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64767130,"end":64767897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248328.1","gene_symbol":"MTCO3P28","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:52131]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075184","summary":null,"start":64611374,"end":64611888,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:52131]"}, {"versioned_ensembl_gene_id":"ENSG00000132376.19","gene_symbol":"INPP5K","gene_name":"inositol polyphosphate-5-phosphatase K [Source:HGNC Symbol;Acc:HGNC:33882]","synonyms":"SKIP","biotype":"protein_coding","ncbi_id":"51763","summary":"This gene encodes a protein with 5-phosphatase activity toward polyphosphate inositol. The protein localizes to the cytosol in regions lacking actin stress fibers. It is thought that this protein may negatively regulate the actin cytoskeleton. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]","start":1494571,"end":1516888,"strand":-1,"description":"inositol polyphosphate-5-phosphatase K [Source:HGNC Symbol;Acc:HGNC:33882]"}, {"versioned_ensembl_gene_id":"ENSG00000115091.11","gene_symbol":"ACTR3","gene_name":"ARP3 actin related protein 3 homolog [Source:HGNC Symbol;Acc:HGNC:170]","synonyms":"ARP3","biotype":"protein_coding","ncbi_id":"10096","summary":"The specific function of this gene has not yet been determined; however, the protein it encodes is known to be a major constituent of the ARP2/3 complex. This complex is located at the cell surface and is essential to cell shape and motility through lamellipodial actin assembly and protrusion. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Mar 2013]","start":113889960,"end":113962596,"strand":1,"description":"ARP3 actin related protein 3 homolog [Source:HGNC Symbol;Acc:HGNC:170]"}, {"versioned_ensembl_gene_id":"ENSG00000180155.19","gene_symbol":"LYNX1","gene_name":"Ly6/neurotoxin 1 [Source:HGNC Symbol;Acc:HGNC:29604]","synonyms":"SLURP2,SLURP2","biotype":"protein_coding","ncbi_id":"66004","summary":"This gene encodes a GPI-anchored, cell membrane bound member of the Ly6/uPAR (LU) superfamily of proteins containing the unique three-finger LU domain. This protein interacts with nicotinic acetylcholine receptors (nAChRs), and is thought to function as a modulator of nAChR activity to prevent excessive excitation. Alternatively spliced transcript variants have been found for this gene. Read-through transcription between this gene and the neighboring downstream gene (SLURP2) generates naturally-occurring transcripts (LYNX1-SLURP2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Sep 2017]","start":142771197,"end":142777810,"strand":-1,"description":"Ly6/neurotoxin 1 [Source:HGNC Symbol;Acc:HGNC:29604]"}, {"versioned_ensembl_gene_id":"ENSG00000253196.1","gene_symbol":"AC083841.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142763116,"end":142766427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169180.11","gene_symbol":"XPO6","gene_name":"exportin 6 [Source:HGNC Symbol;Acc:HGNC:19733]","synonyms":"RANBP20,KIAA0370,FLJ22519","biotype":"protein_coding","ncbi_id":"23214","summary":"The protein encoded by this gene is a member of the importin-beta family. Members of this family are regulated by the GTPase Ran to mediate transport of cargo across the nuclear envelope. This protein has been shown to mediate nuclear export of profilin-actin complexes. A pseudogene of this gene is located on the long arm of chromosome 14. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":28097979,"end":28211920,"strand":-1,"description":"exportin 6 [Source:HGNC Symbol;Acc:HGNC:19733]"}, {"versioned_ensembl_gene_id":"ENSG00000271626.1","gene_symbol":"AC104763.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60315834,"end":60316215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116984.12","gene_symbol":"MTR","gene_name":"5-methyltetrahydrofolate-homocysteine methyltransferase [Source:HGNC Symbol;Acc:HGNC:7468]","synonyms":"cblG","biotype":"protein_coding","ncbi_id":"4548","summary":"This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":236795281,"end":236903981,"strand":1,"description":"5-methyltetrahydrofolate-homocysteine methyltransferase [Source:HGNC Symbol;Acc:HGNC:7468]"}, {"versioned_ensembl_gene_id":"ENSG00000230533.2","gene_symbol":"AL357060.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137673378,"end":137763984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116786.11","gene_symbol":"PLEKHM2","gene_name":"pleckstrin homology and RUN domain containing M2 [Source:HGNC Symbol;Acc:HGNC:29131]","synonyms":"KIAA0842","biotype":"protein_coding","ncbi_id":"23207","summary":"This gene encodes a protein that binds the plus-end directed microtubule motor protein kinesin, together with the lysosomal GTPase Arl8, and is required for lysosomes to distribute away from the microtubule-organizing center. The encoded protein belongs to the multisubunit BLOC-one-related complex that regulates lysosome positioning. It binds a Salmonella effector protein called Salmonella induced filament A and is a critical host determinant in Salmonella pathogenesis. It has a domain architecture consisting of an N-terminal RPIP8, UNC-14, and NESCA (RUN) domain that binds kinesin-1 as well as the lysosomal GTPase Arl8, and a C-terminal pleckstrin homology domain that binds the Salmonella induced filament A effector protein. Naturally occurring mutations in this gene lead to abnormal localization of lysosomes, impaired autophagy flux and are associated with recessive dilated cardiomyopathy and left ventricular noncompaction. [provided by RefSeq, Feb 2017]","start":15684332,"end":15734769,"strand":1,"description":"pleckstrin homology and RUN domain containing M2 [Source:HGNC Symbol;Acc:HGNC:29131]"}, {"versioned_ensembl_gene_id":"ENSG00000143815.14","gene_symbol":"LBR","gene_name":"lamin B receptor [Source:HGNC Symbol;Acc:HGNC:6518]","synonyms":"TDRD18,DHCR14B","biotype":"protein_coding","ncbi_id":"3930","summary":"The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":225401502,"end":225428925,"strand":-1,"description":"lamin B receptor [Source:HGNC Symbol;Acc:HGNC:6518]"}, {"versioned_ensembl_gene_id":"ENSG00000281649.1","gene_symbol":"EBLN3P","gene_name":"endogenous Bornavirus-like nucleoprotein 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:50682]","synonyms":"LOC100506710,EBLN3","biotype":"lincRNA","ncbi_id":"100506710","summary":null,"start":37079857,"end":37090507,"strand":1,"description":"endogenous Bornavirus-like nucleoprotein 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:50682]"}, {"versioned_ensembl_gene_id":"ENSG00000229996.1","gene_symbol":"AC093585.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241010045,"end":241010744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277532.1","gene_symbol":"AC025048.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60124110,"end":60125474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274220.1","gene_symbol":"AC009163.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75433836,"end":75436392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111144.9","gene_symbol":"LTA4H","gene_name":"leukotriene A4 hydrolase [Source:HGNC Symbol;Acc:HGNC:6710]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4048","summary":"The protein encoded by this gene is an enzyme that contains both hydrolase and aminopeptidase activities. The hydrolase activity is used in the final step of the biosynthesis of leukotriene B4, a proinflammatory mediator. The aminopeptidase activity has been shown to degrade proline-glycine-proline (PGP), a neutrophil chemoattractant and biomarker for chronic obstructive pulmonary disease (COPD). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":96000828,"end":96043520,"strand":-1,"description":"leukotriene A4 hydrolase [Source:HGNC Symbol;Acc:HGNC:6710]"}, {"versioned_ensembl_gene_id":"ENSG00000257715.1","gene_symbol":"AC007298.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96025323,"end":96027971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166889.13","gene_symbol":"PATL1","gene_name":"PAT1 homolog 1, processing body mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:26721]","synonyms":"Pat1b,FLJ36874","biotype":"protein_coding","ncbi_id":"219988","summary":null,"start":59636716,"end":59668980,"strand":-1,"description":"PAT1 homolog 1, processing body mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:26721]"}, {"versioned_ensembl_gene_id":"ENSG00000134684.10","gene_symbol":"YARS","gene_name":"tyrosyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12840]","synonyms":"YTS,YRS,tyrRS","biotype":"protein_coding","ncbi_id":"8565","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Tyrosyl-tRNA synthetase belongs to the class I tRNA synthetase family. Cytokine activities have also been observed for the human tyrosyl-tRNA synthetase, after it is split into two parts, an N-terminal fragment that harbors the catalytic site and a C-terminal fragment found only in the mammalian enzyme. The N-terminal fragment is an interleukin-8-like cytokine, whereas the released C-terminal fragment is an EMAP II-like cytokine. [provided by RefSeq, Jul 2008]","start":32775237,"end":32818153,"strand":-1,"description":"tyrosyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12840]"}, {"versioned_ensembl_gene_id":"ENSG00000071564.14","gene_symbol":"TCF3","gene_name":"transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:11633]","synonyms":"VDIR,MGC129648,MGC129647,ITF1,E47,E2A,bHLHb21","biotype":"protein_coding","ncbi_id":"6929","summary":"This gene encodes a member of the E protein (class I) family of helix-loop-helix transcription factors. E proteins activate transcription by binding to regulatory E-box sequences on target genes as heterodimers or homodimers, and are inhibited by heterodimerization with inhibitor of DNA-binding (class IV) helix-loop-helix proteins. E proteins play a critical role in lymphopoiesis, and the encoded protein is required for B and T lymphocyte development. Deletion of this gene or diminished activity of the encoded protein may play a role in lymphoid malignancies. This gene is also involved in several chromosomal translocations that are associated with lymphoid malignancies including pre-B-cell acute lymphoblastic leukemia (t(1;19), with PBX1), childhood leukemia (t(19;19), with TFPT) and acute leukemia (t(12;19), with ZNF384). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Sep 2011]","start":1609290,"end":1652605,"strand":-1,"description":"transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:11633]"}, {"versioned_ensembl_gene_id":"ENSG00000227306.1","gene_symbol":"AP006285.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1688297,"end":1689056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107537.13","gene_symbol":"PHYH","gene_name":"phytanoyl-CoA 2-hydroxylase [Source:HGNC Symbol;Acc:HGNC:8940]","synonyms":"RD,PHYH1,PAHX","biotype":"protein_coding","ncbi_id":"5264","summary":"This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":13277796,"end":13302412,"strand":-1,"description":"phytanoyl-CoA 2-hydroxylase [Source:HGNC Symbol;Acc:HGNC:8940]"}, {"versioned_ensembl_gene_id":"ENSG00000258957.1","gene_symbol":"AL359317.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69183020,"end":69214092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136286.14","gene_symbol":"MYO1G","gene_name":"myosin IG [Source:HGNC Symbol;Acc:HGNC:13880]","synonyms":"HA-2","biotype":"protein_coding","ncbi_id":"64005","summary":"MYO1G is a plasma membrane-associated class I myosin (see MIM 601478) that is abundant in T and B lymphocytes and mast cells (Pierce et al., 2001 [PubMed 11544309]; Patino-Lopez et al., 2010 [PubMed 20071333]).[supplied by OMIM, Jun 2010]","start":44962662,"end":44979098,"strand":-1,"description":"myosin IG [Source:HGNC Symbol;Acc:HGNC:13880]"}, {"versioned_ensembl_gene_id":"ENSG00000166670.9","gene_symbol":"MMP10","gene_name":"matrix metallopeptidase 10 [Source:HGNC Symbol;Acc:HGNC:7156]","synonyms":"STMY2","biotype":"protein_coding","ncbi_id":"4319","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down fibronectin, laminin, elastin, proteoglycan core protein, gelatins, and several types of collagen. The gene is part of a cluster of MMP genes on chromosome 11. [provided by RefSeq, Jan 2016]","start":102770503,"end":102780628,"strand":-1,"description":"matrix metallopeptidase 10 [Source:HGNC Symbol;Acc:HGNC:7156]"}, {"versioned_ensembl_gene_id":"ENSG00000113100.9","gene_symbol":"CDH9","gene_name":"cadherin 9 [Source:HGNC Symbol;Acc:HGNC:1768]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1007","summary":"This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. The extracellular domain consists of 5 subdomains, each containing a cadherin motif, and appears to determine the specificity of the protein's homophilic cell adhesion activity. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. [provided by RefSeq, Jul 2008]","start":26880600,"end":27121150,"strand":-1,"description":"cadherin 9 [Source:HGNC Symbol;Acc:HGNC:1768]"}, {"versioned_ensembl_gene_id":"ENSG00000183798.4","gene_symbol":"EMILIN3","gene_name":"elastin microfibril interfacer 3 [Source:HGNC Symbol;Acc:HGNC:16123]","synonyms":"EMILIN5,dJ620E11.4,C20orf130","biotype":"protein_coding","ncbi_id":"90187","summary":null,"start":41359966,"end":41366827,"strand":-1,"description":"elastin microfibril interfacer 3 [Source:HGNC Symbol;Acc:HGNC:16123]"}, {"versioned_ensembl_gene_id":"ENSG00000225360.1","gene_symbol":"AL772155.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63729702,"end":63730173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253140.1","gene_symbol":"AC026904.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48515852,"end":48517089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257529.5","gene_symbol":"RPL36A-HNRNPH2","gene_name":"RPL36A-HNRNPH2 readthrough [Source:HGNC Symbol;Acc:HGNC:48349]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529097","summary":"This locus represents naturally occurring read-through transcription between the neighboring ribosomal protein L36a and heterogeneous nuclear ribonucleoprotein H2 (H') genes on chromosome X. The read-through transcript produces a protein with similarity to the protein encoded by the upstream locus, ribosomal protein L36a. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jan 2011]","start":101391011,"end":101412297,"strand":1,"description":"RPL36A-HNRNPH2 readthrough [Source:HGNC Symbol;Acc:HGNC:48349]"}, {"versioned_ensembl_gene_id":"ENSG00000226343.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32770986,"end":32771923,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000268049.1","gene_symbol":"AC012313.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58357999,"end":58359603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261460.1","gene_symbol":"AC009690.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72278867,"end":72351794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254770.1","gene_symbol":"OR4D7P","gene_name":"olfactory receptor family 4 subfamily D member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15176]","synonyms":"OST724","biotype":"unprocessed_pseudogene","ncbi_id":"81304","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59531754,"end":59532695,"strand":1,"description":"olfactory receptor family 4 subfamily D member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15176]"}, {"versioned_ensembl_gene_id":"ENSG00000228674.4","gene_symbol":"AC011483.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50927079,"end":50927571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228763.1","gene_symbol":"LIMS1-AS1","gene_name":"LIMS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40342]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106182118","summary":null,"start":108676795,"end":108678601,"strand":-1,"description":"LIMS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40342]"}, {"versioned_ensembl_gene_id":"ENSG00000277342.1","gene_symbol":"AC048344.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32109076,"end":32109602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160886.13","gene_symbol":"LY6K","gene_name":"lymphocyte antigen 6 family member K [Source:HGNC Symbol;Acc:HGNC:24225]","synonyms":"HSJ001348,FLJ35226,CT97","biotype":"protein_coding","ncbi_id":"54742","summary":null,"start":142700111,"end":142705127,"strand":1,"description":"lymphocyte antigen 6 family member K [Source:HGNC Symbol;Acc:HGNC:24225]"}, {"versioned_ensembl_gene_id":"ENSG00000119514.6","gene_symbol":"GALNT12","gene_name":"polypeptide N-acetylgalactosaminyltransferase 12 [Source:HGNC Symbol;Acc:HGNC:19877]","synonyms":"GalNAc-T12","biotype":"protein_coding","ncbi_id":"79695","summary":"This gene encodes a member of a family of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferases, which catalyze the transfer of N-acetylgalactosamine (GalNAc) from UDP-GalNAc to a serine or threonine residue on a polypeptide acceptor in the initial step of O-linked protein glycosylation. Mutations in this gene are associated with an increased susceptibility to colorectal cancer.[provided by RefSeq, Mar 2011]","start":98807699,"end":98850081,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 12 [Source:HGNC Symbol;Acc:HGNC:19877]"}, {"versioned_ensembl_gene_id":"ENSG00000249761.1","gene_symbol":"AC074133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97336858,"end":97337040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244234.1","gene_symbol":"GMCL1P1","gene_name":"germ cell-less, spermatogenesis associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19717]","synonyms":"GMCL1L,GCL,GMCL2","biotype":"processed_pseudogene","ncbi_id":"64396","summary":"This locus shares a high degree of identity with the multi-exon germ cell-less gene on chromosome 2. Despite its single-exon nature, this chromosome 5 locus contains an open reading frame that could putatively encode a full-length germ cell-less related protein. [provided by RefSeq, Jul 2008]","start":178185719,"end":178187299,"strand":-1,"description":"germ cell-less, spermatogenesis associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19717]"}, {"versioned_ensembl_gene_id":"ENSG00000254502.1","gene_symbol":"AP003097.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86195132,"end":86196266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213630.3","gene_symbol":"BOLA3P3","gene_name":"bolA family member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644754","summary":null,"start":126663337,"end":126663568,"strand":-1,"description":"bolA family member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51442]"}, {"versioned_ensembl_gene_id":"ENSG00000172320.3","gene_symbol":"OR5A1","gene_name":"olfactory receptor family 5 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8319]","synonyms":"OST181,OR5A1P","biotype":"protein_coding","ncbi_id":"219982","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59436469,"end":59451380,"strand":1,"description":"olfactory receptor family 5 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8319]"}, {"versioned_ensembl_gene_id":"ENSG00000100036.12","gene_symbol":"SLC35E4","gene_name":"solute carrier family 35 member E4 [Source:HGNC Symbol;Acc:HGNC:17058]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339665","summary":null,"start":30635652,"end":30669016,"strand":1,"description":"solute carrier family 35 member E4 [Source:HGNC Symbol;Acc:HGNC:17058]"}, {"versioned_ensembl_gene_id":"ENSG00000250318.1","gene_symbol":"AC003072.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30653877,"end":30654814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186369.10","gene_symbol":"LINC00643","gene_name":"long intergenic non-protein coding RNA 643 [Source:HGNC Symbol;Acc:HGNC:44296]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"646113","summary":null,"start":62114353,"end":62130962,"strand":1,"description":"long intergenic non-protein coding RNA 643 [Source:HGNC Symbol;Acc:HGNC:44296]"}, {"versioned_ensembl_gene_id":"ENSG00000257431.1","gene_symbol":"AC089998.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82512677,"end":82515817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281982.1","gene_symbol":"AC003070.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45396932,"end":45397477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124610.4","gene_symbol":"HIST1H1A","gene_name":"histone cluster 1 H1 family member a [Source:HGNC Symbol;Acc:HGNC:4715]","synonyms":"H1F1,H1a,H1.1","biotype":"protein_coding","ncbi_id":"3024","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26017085,"end":26017732,"strand":-1,"description":"histone cluster 1 H1 family member a [Source:HGNC Symbol;Acc:HGNC:4715]"}, {"versioned_ensembl_gene_id":"ENSG00000077522.12","gene_symbol":"ACTN2","gene_name":"actinin alpha 2 [Source:HGNC Symbol;Acc:HGNC:164]","synonyms":null,"biotype":"protein_coding","ncbi_id":"88","summary":"Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with multiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. This gene encodes a muscle-specific, alpha actinin isoform that is expressed in both skeletal and cardiac muscles. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]","start":236686454,"end":236764631,"strand":1,"description":"actinin alpha 2 [Source:HGNC Symbol;Acc:HGNC:164]"}, {"versioned_ensembl_gene_id":"ENSG00000165138.17","gene_symbol":"ANKS6","gene_name":"ankyrin repeat and sterile alpha motif domain containing 6 [Source:HGNC Symbol;Acc:HGNC:26724]","synonyms":"SAMD6,NPHP16,FLJ36928,ANKRD14","biotype":"protein_coding","ncbi_id":"203286","summary":"This gene encodes a protein containing multiple ankyrin repeats and a SAM domain. It is thought that this protein may localize to the proximal region of the primary cilium, and may play a role in renal and cardiovascular development. Mutations in this gene have been shown to cause a form of nephronophthisis (NPHP16), a chronic tubulo-interstitial nephritis. [provided by RefSeq, Jul 2015]","start":98731329,"end":98796965,"strand":-1,"description":"ankyrin repeat and sterile alpha motif domain containing 6 [Source:HGNC Symbol;Acc:HGNC:26724]"}, {"versioned_ensembl_gene_id":"ENSG00000279900.1","gene_symbol":"AP001767.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":83083687,"end":83084138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254660.1","gene_symbol":"AP002512.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56509573,"end":56510195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213760.10","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"ATP6G2,NG38,ATP6G,Em:AC004181.3,Vma10","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31544462,"end":31548427,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000234423.1","gene_symbol":"LINC01250","gene_name":"long intergenic non-protein coding RNA 1250 [Source:HGNC Symbol;Acc:HGNC:49844]","synonyms":"FLJ37991","biotype":"lincRNA","ncbi_id":"101927554","summary":null,"start":2895048,"end":3126026,"strand":-1,"description":"long intergenic non-protein coding RNA 1250 [Source:HGNC Symbol;Acc:HGNC:49844]"}, {"versioned_ensembl_gene_id":"ENSG00000267104.2","gene_symbol":"TBC1D3P1-DHX40P1","gene_name":"TBC1D3P1-DHX40P1 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42362]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"653645","summary":"This locus represents naturally-occurring readthrough transcription that extends through two unprocessed pseudogenes, TBC1D3P1 (TBC1 domain family member 3 pseudogene 1) and DHX40P1 (DEAH-box helicase 40 pseudogene 1), to protein-coding RNFT1 (ring finger protein, transmembrane 1). The individual pseudogene loci are not curated as transcribed regions. The readthrough transcript likely does not encode a functional protein, since translation of the long open reading frames would render the transcript a candidate for nonsense-mediated decay (NMD). [provided by RefSeq, Jan 2016]","start":59962363,"end":60018975,"strand":-1,"description":"TBC1D3P1-DHX40P1 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42362]"}, {"versioned_ensembl_gene_id":"ENSG00000266265.2","gene_symbol":"KLF14","gene_name":"Kruppel like factor 14 [Source:HGNC Symbol;Acc:HGNC:23025]","synonyms":"BTEB5","biotype":"protein_coding","ncbi_id":"136259","summary":"This intronless gene encodes a member of the Kruppel-like family of transcription factors. The encoded protein functions as a transcriptional co-repressor, and is induced by transforming growth factor-beta (TGF-beta) to repress TGF-beta receptor II gene expression. This gene exhibits imprinted expression from the maternal allele in embryonic and extra-embryonic tissues. [provided by RefSeq, Jul 2013]","start":130731235,"end":130734061,"strand":-1,"description":"Kruppel like factor 14 [Source:HGNC Symbol;Acc:HGNC:23025]"}, {"versioned_ensembl_gene_id":"ENSG00000265190.6","gene_symbol":"ANXA8","gene_name":"annexin A8 [Source:HGNC Symbol;Acc:HGNC:546]","synonyms":"ANX8","biotype":"protein_coding","ncbi_id":"653145","summary":"This gene encodes a member of the annexin family of evolutionarily conserved Ca2+ and phospholipid binding proteins. The encoded protein may function as an an anticoagulant that indirectly inhibits the thromboplastin-specific complex. Overexpression of this gene has been associated with acute myelocytic leukemia. A highly similar duplicated copy of this gene is found in close proximity on the long arm of chromosome 10. [provided by RefSeq, Jul 2008]","start":47460162,"end":47484158,"strand":-1,"description":"annexin A8 [Source:HGNC Symbol;Acc:HGNC:546]"}, {"versioned_ensembl_gene_id":"ENSG00000172057.9","gene_symbol":"ORMDL3","gene_name":"ORMDL sphingolipid biosynthesis regulator 3 [Source:HGNC Symbol;Acc:HGNC:16038]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94103","summary":null,"start":39921041,"end":39927601,"strand":-1,"description":"ORMDL sphingolipid biosynthesis regulator 3 [Source:HGNC Symbol;Acc:HGNC:16038]"}, {"versioned_ensembl_gene_id":"ENSG00000225087.1","gene_symbol":"AL583808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72748921,"end":72899140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132446.6","gene_symbol":"FTHL17","gene_name":"ferritin heavy chain like 17 [Source:HGNC Symbol;Acc:HGNC:3987]","synonyms":"CT38","biotype":"protein_coding","ncbi_id":"53940","summary":"This gene encodes a ferritin heavy chain-like protein. This gene is primarily expressed in embryonic germ cells. The encoded protein may lack ferroxidase activity. Multiple pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Oct 2016]","start":31071241,"end":31072053,"strand":-1,"description":"ferritin heavy chain like 17 [Source:HGNC Symbol;Acc:HGNC:3987]"}, {"versioned_ensembl_gene_id":"ENSG00000232235.1","gene_symbol":"CDY3P","gene_name":"chromodomain Y-linked 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:23849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286556","summary":null,"start":9166085,"end":9167702,"strand":-1,"description":"chromodomain Y-linked 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:23849]"}, {"versioned_ensembl_gene_id":"ENSG00000271314.1","gene_symbol":"AL161729.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95494924,"end":95495379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227364.1","gene_symbol":"AC018685.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2729908,"end":2730957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231988.1","gene_symbol":"OFD1P3Y","gene_name":"OFD1 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:23875]","synonyms":"OFDYP3,OFD1PY3,OFD1PY19,OFD1P3,OFD1P19Y,OFD1P19","biotype":"unprocessed_pseudogene","ncbi_id":"386687","summary":null,"start":9030594,"end":9039988,"strand":1,"description":"OFD1 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:23875]"}, {"versioned_ensembl_gene_id":"ENSG00000226127.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"HSBLMHC1,BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32460601,"end":32473766,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000276925.1","gene_symbol":"AC099778.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47469777,"end":47469987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166313.18","gene_symbol":"APBB1","gene_name":"amyloid beta precursor protein binding family B member 1 [Source:HGNC Symbol;Acc:HGNC:581]","synonyms":"RIR,Fe65","biotype":"protein_coding","ncbi_id":"322","summary":"The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer's disease amyloid precursor protein (APP), transcription factor CP2/LSF/LBP1 and the low-density lipoprotein receptor-related protein. APP functions as a cytosolic anchoring site that can prevent the gene product's nuclear translocation. This encoded protein could play an important role in the pathogenesis of Alzheimer's disease. It is thought to regulate transcription. Also it is observed to block cell cycle progression by downregulating thymidylate synthase expression. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012]","start":6395124,"end":6419414,"strand":-1,"description":"amyloid beta precursor protein binding family B member 1 [Source:HGNC Symbol;Acc:HGNC:581]"}, {"versioned_ensembl_gene_id":"ENSG00000267028.1","gene_symbol":"TCF4-AS1","gene_name":"TCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51642]","synonyms":"MIR4529HG","biotype":"antisense_RNA","ncbi_id":"105372127","summary":null,"start":55452533,"end":55482940,"strand":1,"description":"TCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51642]"}, {"versioned_ensembl_gene_id":"ENSG00000242320.2","gene_symbol":"RPL21P126","gene_name":"ribosomal protein L21 pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:35959]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271449","summary":null,"start":55635833,"end":55636310,"strand":1,"description":"ribosomal protein L21 pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:35959]"}, {"versioned_ensembl_gene_id":"ENSG00000146433.8","gene_symbol":"TMEM181","gene_name":"transmembrane protein 181 [Source:HGNC Symbol;Acc:HGNC:20958]","synonyms":"KIAA1423,GPR178","biotype":"protein_coding","ncbi_id":"57583","summary":"The TMEM181 gene encodes a putative G protein-coupled receptor expressed on the cell surface (Carette et al., 2009 [PubMed 19965467]; Wollscheid et al., 2009 [PubMed 19349973]).[supplied by OMIM, Jan 2010]","start":158536436,"end":158635428,"strand":1,"description":"transmembrane protein 181 [Source:HGNC Symbol;Acc:HGNC:20958]"}, {"versioned_ensembl_gene_id":"ENSG00000091138.12","gene_symbol":"SLC26A3","gene_name":"solute carrier family 26 member 3 [Source:HGNC Symbol;Acc:HGNC:3018]","synonyms":"DRA,CLD","biotype":"protein_coding","ncbi_id":"1811","summary":"The protein encoded by this gene is a transmembrane glycoprotein that transports chloride ions across the cell membrane in exchange for bicarbonate ions. It is localized to the mucosa of the lower intestinal tract, particularly to the apical membrane of columnar epithelium and some goblet cells. The protein is essential for intestinal chloride absorption, and mutations in this gene have been associated with congenital chloride diarrhea. [provided by RefSeq, Oct 2008]","start":107765467,"end":107803225,"strand":-1,"description":"solute carrier family 26 member 3 [Source:HGNC Symbol;Acc:HGNC:3018]"}, {"versioned_ensembl_gene_id":"ENSG00000179997.8","gene_symbol":"AC010894.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174501952,"end":174502312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164463.12","gene_symbol":"CREBRF","gene_name":"CREB3 regulatory factor [Source:HGNC Symbol;Acc:HGNC:24050]","synonyms":"LRF,C5orf41","biotype":"protein_coding","ncbi_id":"153222","summary":null,"start":173056352,"end":173139284,"strand":1,"description":"CREB3 regulatory factor [Source:HGNC Symbol;Acc:HGNC:24050]"}, {"versioned_ensembl_gene_id":"ENSG00000227078.1","gene_symbol":"LINC02094","gene_name":"long intergenic non-protein coding RNA 2094 [Source:HGNC Symbol;Acc:HGNC:52945]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984995","summary":null,"start":19419035,"end":19424357,"strand":1,"description":"long intergenic non-protein coding RNA 2094 [Source:HGNC Symbol;Acc:HGNC:52945]"}, {"versioned_ensembl_gene_id":"ENSG00000231477.2","gene_symbol":"AC004448.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19457080,"end":19458399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252690.3","gene_symbol":"SCARNA15","gene_name":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]","synonyms":"ACA45,ACA45","biotype":"processed_transcript","ncbi_id":"677778","summary":null,"start":82752884,"end":82757208,"strand":1,"description":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]"}, {"versioned_ensembl_gene_id":"ENSG00000259753.1","gene_symbol":"AC068234.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":47253897,"end":47344292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259442.1","gene_symbol":"AC105339.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82744223,"end":82750289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186081.11","gene_symbol":"KRT5","gene_name":"keratin 5 [Source:HGNC Symbol;Acc:HGNC:6442]","synonyms":"KRT5A,EBS2","biotype":"protein_coding","ncbi_id":"3852","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the basal layer of the epidermis with family member KRT14. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52514575,"end":52520687,"strand":-1,"description":"keratin 5 [Source:HGNC Symbol;Acc:HGNC:6442]"}, {"versioned_ensembl_gene_id":"ENSG00000279758.1","gene_symbol":"AC105339.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82738386,"end":82739122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232380.1","gene_symbol":"ZDHHC20P4","gene_name":"zinc finger DHHC-type containing 20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730239","summary":null,"start":68985058,"end":68986064,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39776]"}, {"versioned_ensembl_gene_id":"ENSG00000230405.1","gene_symbol":"RPS3AP52","gene_name":"ribosomal protein S3a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:42004]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873818","summary":null,"start":68634190,"end":68634486,"strand":1,"description":"ribosomal protein S3a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:42004]"}, {"versioned_ensembl_gene_id":"ENSG00000225055.1","gene_symbol":"AL606490.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48357125,"end":48359495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188368.9","gene_symbol":"PRR19","gene_name":"proline rich 19 [Source:HGNC Symbol;Acc:HGNC:33728]","synonyms":"MGC70924","biotype":"protein_coding","ncbi_id":"284338","summary":null,"start":42302098,"end":42310821,"strand":1,"description":"proline rich 19 [Source:HGNC Symbol;Acc:HGNC:33728]"}, {"versioned_ensembl_gene_id":"ENSG00000280434.1","gene_symbol":"AL031595.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":44139365,"end":44153626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165584.15","gene_symbol":"SSX3","gene_name":"SSX family member 3 [Source:HGNC Symbol;Acc:HGNC:11337]","synonyms":"CT5.3","biotype":"protein_coding","ncbi_id":"10214","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. While some of the related SSX genes are involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas, this gene does not appear to be involved in such translocations. [provided by RefSeq, Jul 2013]","start":48346428,"end":48356707,"strand":-1,"description":"SSX family member 3 [Source:HGNC Symbol;Acc:HGNC:11337]"}, {"versioned_ensembl_gene_id":"ENSG00000242882.1","gene_symbol":"RPL5P11","gene_name":"ribosomal protein L5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35483]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402193","summary":null,"start":173419245,"end":173420137,"strand":-1,"description":"ribosomal protein L5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35483]"}, {"versioned_ensembl_gene_id":"ENSG00000256100.1","gene_symbol":"AP000721.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63974620,"end":63988346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176340.3","gene_symbol":"COX8A","gene_name":"cytochrome c oxidase subunit 8A [Source:HGNC Symbol;Acc:HGNC:2294]","synonyms":"VIII-L,VIII,COX8L,COX8-2,COX8,COX","biotype":"protein_coding","ncbi_id":"1351","summary":"The protein encoded by this gene is the terminal enzyme of the respiratory chain, coupling the transfer of electrons from cytochrome c to molecular oxygen, with the concomitant production of a proton electrochemical gradient across the inner mitochondrial membrane. In addition to 3 mitochondrially encoded subunits, which perform the catalytic function, the eukaryotic enzyme contains nuclear-encoded smaller subunits, ranging in number from 4 in some organisms to 10 in mammals. It has been proposed that nuclear-encoded subunits may be involved in the modulation of the catalytic function. This gene encodes one of the nuclear-encoded subunits. [provided by RefSeq, Jul 2008]","start":63974607,"end":63976543,"strand":1,"description":"cytochrome c oxidase subunit 8A [Source:HGNC Symbol;Acc:HGNC:2294]"}, {"versioned_ensembl_gene_id":"ENSG00000256341.1","gene_symbol":"AP006333.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64118272,"end":64119210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275111.4","gene_symbol":"ZNF2","gene_name":"zinc finger protein 2 [Source:HGNC Symbol;Acc:HGNC:12991]","synonyms":"ZNF661,Zfp661,A1-5","biotype":"protein_coding","ncbi_id":"7549","summary":"The protein encoded by this gene belongs to the C2H2-type zinc-finger protein family. The exact function of this gene is not known, however, zinc-finger proteins are known to interact with DNA and function as transcription regulators. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":95165432,"end":95184317,"strand":1,"description":"zinc finger protein 2 [Source:HGNC Symbol;Acc:HGNC:12991]"}, {"versioned_ensembl_gene_id":"ENSG00000163399.15","gene_symbol":"ATP1A1","gene_name":"ATPase Na+/K+ transporting subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:799]","synonyms":null,"biotype":"protein_coding","ncbi_id":"476","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 1 subunit. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":116372668,"end":116410261,"strand":1,"description":"ATPase Na+/K+ transporting subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:799]"}, {"versioned_ensembl_gene_id":"ENSG00000254267.1","gene_symbol":"AP003438.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98371355,"end":98388247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256249.1","gene_symbol":"AC026333.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122687125,"end":122715979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240520.6","gene_symbol":"UOX","gene_name":"urate oxidase (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12575]","synonyms":"UOXP","biotype":"transcribed_unitary_pseudogene","ncbi_id":"391051","summary":"Urate oxidase is an enzyme that catalyzes the oxidation of uric acid to allantoin. This gene has been inactivated by mutation and is nonfunctional in humans and some other primates. [provided by RefSeq, Jul 2008]","start":84363706,"end":84397831,"strand":-1,"description":"urate oxidase (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12575]"}, {"versioned_ensembl_gene_id":"ENSG00000110713.15","gene_symbol":"NUP98","gene_name":"nucleoporin 98 [Source:HGNC Symbol;Acc:HGNC:8068]","synonyms":"NUP96","biotype":"protein_coding","ncbi_id":"4928","summary":"Nuclear pore complexes (NPCs) regulate the transport of macromolecules between the nucleus and cytoplasm, and are composed of many polypeptide subunits, many of which belong to the nucleoporin family. This gene belongs to the nucleoporin gene family and encodes a 186 kDa precursor protein that undergoes autoproteolytic cleavage to generate a 98 kDa nucleoporin and 96 kDa nucleoporin. The 98 kDa nucleoporin contains a Gly-Leu-Phe-Gly (GLGF) repeat domain and participates in many cellular processes, including nuclear import, nuclear export, mitotic progression, and regulation of gene expression. The 96 kDa nucleoporin is a scaffold component of the NPC. Proteolytic cleavage is important for targeting of the proteins to the NPC. Translocations between this gene and many other partner genes have been observed in different leukemias. Rearrangements typically result in chimeras with the N-terminal GLGF domain of this gene to the C-terminus of the partner gene. Alternative splicing results in multiple transcript variants encoding different isoforms, at least two of which are proteolytically processed. Some variants lack the region that encodes the 96 kDa nucleoporin. [provided by RefSeq, Feb 2016]","start":3671083,"end":3797792,"strand":-1,"description":"nucleoporin 98 [Source:HGNC Symbol;Acc:HGNC:8068]"}, {"versioned_ensembl_gene_id":"ENSG00000136457.9","gene_symbol":"CHAD","gene_name":"chondroadherin [Source:HGNC Symbol;Acc:HGNC:1909]","synonyms":"SLRR4A","biotype":"protein_coding","ncbi_id":"1101","summary":"Chondroadherin is a cartilage matrix protein thought to mediate adhesion of isolated chondrocytes. The protein contains 11 leucine-rich repeats flanked by cysteine-rich regions. The chondroadherin messenger RNA is present in chondrocytes at all ages. [provided by RefSeq, Jul 2008]","start":50464496,"end":50468966,"strand":-1,"description":"chondroadherin [Source:HGNC Symbol;Acc:HGNC:1909]"}, {"versioned_ensembl_gene_id":"ENSG00000176148.15","gene_symbol":"TCP11L1","gene_name":"t-complex 11 like 1 [Source:HGNC Symbol;Acc:HGNC:25655]","synonyms":"FLJ11336","biotype":"protein_coding","ncbi_id":"55346","summary":null,"start":33039417,"end":33105943,"strand":1,"description":"t-complex 11 like 1 [Source:HGNC Symbol;Acc:HGNC:25655]"}, {"versioned_ensembl_gene_id":"ENSG00000204520.12","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31399784,"end":31415315,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000254993.1","gene_symbol":"TRIM77BP","gene_name":"tripartite motif containing 77B, pseudogene [Source:HGNC Symbol;Acc:HGNC:43980]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646770","summary":null,"start":49117019,"end":49124570,"strand":-1,"description":"tripartite motif containing 77B, pseudogene [Source:HGNC Symbol;Acc:HGNC:43980]"}, {"versioned_ensembl_gene_id":"ENSG00000278308.2","gene_symbol":"NPIPA3","gene_name":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642778","summary":null,"start":14708949,"end":14726344,"strand":1,"description":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]"}, {"versioned_ensembl_gene_id":"ENSG00000104205.12","gene_symbol":"SGK3","gene_name":"serum/glucocorticoid regulated kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:10812]","synonyms":"SGKL,SGK2","biotype":"protein_coding","ncbi_id":"23678","summary":"This gene is a member of the Ser/Thr protein kinase family and encodes a phosphoprotein with a PX (phox homology) domain. The protein phosphorylates several target proteins and has a role in neutral amino acid transport and activation of potassium and chloride channels. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":66712418,"end":66862022,"strand":1,"description":"serum/glucocorticoid regulated kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:10812]"}, {"versioned_ensembl_gene_id":"ENSG00000230350.1","gene_symbol":"RPL35AP3","gene_name":"ribosomal protein L35a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21117]","synonyms":"bA55K22.4","biotype":"processed_pseudogene","ncbi_id":"387074","summary":null,"start":136973930,"end":136974217,"strand":-1,"description":"ribosomal protein L35a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21117]"}, {"versioned_ensembl_gene_id":"ENSG00000223702.1","gene_symbol":"ZDHHC20P2","gene_name":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]","synonyms":"OTTHUMG00000133740","biotype":"processed_pseudogene","ncbi_id":"100048908","summary":null,"start":31380411,"end":31380839,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]"}, {"versioned_ensembl_gene_id":"ENSG00000276623.1","gene_symbol":"AC106872.12","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165016887,"end":165017433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250887.1","gene_symbol":"AC106872.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165007086,"end":165007959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236399.7","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30214604,"end":30227224,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000259550.2","gene_symbol":"HNRNPA1P74","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:48804]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421430","summary":null,"start":54320731,"end":54321565,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:48804]"}, {"versioned_ensembl_gene_id":"ENSG00000006016.10","gene_symbol":"CRLF1","gene_name":"cytokine receptor like factor 1 [Source:HGNC Symbol;Acc:HGNC:2364]","synonyms":"CLF-1,CLF,CISS1,CISS","biotype":"protein_coding","ncbi_id":"9244","summary":"This gene encodes a member of the cytokine type I receptor family. The protein forms a secreted complex with cardiotrophin-like cytokine factor 1 and acts on cells expressing ciliary neurotrophic factor receptors. The complex can promote survival of neuronal cells. Mutations in this gene result in Crisponi syndrome and cold-induced sweating syndrome. [provided by RefSeq, Oct 2009]","start":18572220,"end":18607741,"strand":-1,"description":"cytokine receptor like factor 1 [Source:HGNC Symbol;Acc:HGNC:2364]"}, {"versioned_ensembl_gene_id":"ENSG00000274198.1","gene_symbol":"AC025521.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58747055,"end":58747340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276717.1","gene_symbol":"AL136097.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92177235,"end":92188652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121089.4","gene_symbol":"NACA3P","gene_name":"NACA family member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:33442]","synonyms":"NACA3","biotype":"processed_pseudogene","ncbi_id":"389240","summary":null,"start":164943290,"end":164943937,"strand":1,"description":"NACA family member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:33442]"}, {"versioned_ensembl_gene_id":"ENSG00000236164.1","gene_symbol":"AL161618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46758296,"end":46761158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245571.6","gene_symbol":"AP001258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59130133,"end":59143015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236438.7","gene_symbol":"FAM157A","gene_name":"family with sequence similarity 157 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34079]","synonyms":"GTF2IP18","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728262","summary":null,"start":198153287,"end":198222513,"strand":1,"description":"family with sequence similarity 157 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34079]"}, {"versioned_ensembl_gene_id":"ENSG00000225987.7","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"G17,PBX2MHC,HOX12","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32251742,"end":32257192,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000230062.5","gene_symbol":"ANKRD66","gene_name":"ankyrin repeat domain 66 [Source:HGNC Symbol;Acc:HGNC:44669]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287718","summary":null,"start":46746917,"end":46759506,"strand":1,"description":"ankyrin repeat domain 66 [Source:HGNC Symbol;Acc:HGNC:44669]"}, {"versioned_ensembl_gene_id":"ENSG00000256560.1","gene_symbol":"LINC01486","gene_name":"long intergenic non-protein coding RNA 1486 [Source:HGNC Symbol;Acc:HGNC:51137]","synonyms":"TCONS_00021407","biotype":"lincRNA","ncbi_id":"101928138","summary":null,"start":109354083,"end":109359488,"strand":-1,"description":"long intergenic non-protein coding RNA 1486 [Source:HGNC Symbol;Acc:HGNC:51137]"}, {"versioned_ensembl_gene_id":"ENSG00000242386.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"RING7,D6S221E","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32968079,"end":32986577,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000156269.4","gene_symbol":"NAA11","gene_name":"N(alpha)-acetyltransferase 11, NatA catalytic subunit [Source:HGNC Symbol;Acc:HGNC:28125]","synonyms":"hARD2,ARD2,ARD1B","biotype":"protein_coding","ncbi_id":"84779","summary":null,"start":79225694,"end":79326050,"strand":-1,"description":"N(alpha)-acetyltransferase 11, NatA catalytic subunit [Source:HGNC Symbol;Acc:HGNC:28125]"}, {"versioned_ensembl_gene_id":"ENSG00000226987.1","gene_symbol":"AL157938.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131240687,"end":131241724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264150.1","gene_symbol":"AP005136.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2568392,"end":2569122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198055.10","gene_symbol":"GRK6","gene_name":"G protein-coupled receptor kinase 6 [Source:HGNC Symbol;Acc:HGNC:4545]","synonyms":"GPRK6","biotype":"protein_coding","ncbi_id":"2870","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating their deactivation. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":177403204,"end":177442901,"strand":1,"description":"G protein-coupled receptor kinase 6 [Source:HGNC Symbol;Acc:HGNC:4545]"}, {"versioned_ensembl_gene_id":"ENSG00000086061.15","gene_symbol":"DNAJA1","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 [Source:HGNC Symbol;Acc:HGNC:5229]","synonyms":"HSPF4,HSJ2,hdj-2,dj-2,NEDD7","biotype":"protein_coding","ncbi_id":"3301","summary":"This gene encodes a member of the DnaJ family of proteins, which act as heat shock protein 70 cochaperones. Heat shock proteins facilitate protein folding, trafficking, prevention of aggregation, and proteolytic degradation. Members of this family are characterized by a highly conserved N-terminal J domain, a glycine/phenylalanine-rich region, four CxxCxGxG zinc finger repeats, and a C-terminal substrate-binding domain. The J domain mediates the interaction with heat shock protein 70 to recruit substrates and regulate ATP hydrolysis activity. In humans, this gene has been implicated in positive regulation of virus replication through co-option by the influenza A virus. Several pseudogenes of this gene are found on other chromosomes. [provided by RefSeq, Sep 2015]","start":33025211,"end":33039907,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member A1 [Source:HGNC Symbol;Acc:HGNC:5229]"}, {"versioned_ensembl_gene_id":"ENSG00000090054.13","gene_symbol":"SPTLC1","gene_name":"serine palmitoyltransferase long chain base subunit 1 [Source:HGNC Symbol;Acc:HGNC:11277]","synonyms":"SPTI,LCB1,HSN1,HSAN1,hLCB1","biotype":"protein_coding","ncbi_id":"10558","summary":"This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013]","start":92031999,"end":92115384,"strand":-1,"description":"serine palmitoyltransferase long chain base subunit 1 [Source:HGNC Symbol;Acc:HGNC:11277]"}, {"versioned_ensembl_gene_id":"ENSG00000268231.1","gene_symbol":"AC008743.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50555370,"end":50557969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250597.5","gene_symbol":"AC093689.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34657606,"end":34669432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096717.11","gene_symbol":"SIRT1","gene_name":"sirtuin 1 [Source:HGNC Symbol;Acc:HGNC:14929]","synonyms":"SIR2L1","biotype":"protein_coding","ncbi_id":"23411","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the sirtuin family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":67884669,"end":67918390,"strand":1,"description":"sirtuin 1 [Source:HGNC Symbol;Acc:HGNC:14929]"}, {"versioned_ensembl_gene_id":"ENSG00000232258.6","gene_symbol":"TMEM114","gene_name":"transmembrane protein 114 [Source:HGNC Symbol;Acc:HGNC:33227]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283953","summary":"This gene encodes a glycosylated transmembrane protein that plays a role in lens and eye development. Mutations in this gene, including a t(16;22)(p13.3;q11.2) translocation, are associated with congenital and juvenile cataract disorders. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":8537605,"end":8590193,"strand":-1,"description":"transmembrane protein 114 [Source:HGNC Symbol;Acc:HGNC:33227]"}, {"versioned_ensembl_gene_id":"ENSG00000279683.1","gene_symbol":"AC090517.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56795382,"end":56795522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276524.1","gene_symbol":"AC010999.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56887107,"end":56888219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253370.2","gene_symbol":"AC027308.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":156458398,"end":156458507,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271810.5","gene_symbol":"AL603832.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":112702614,"end":112711433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239983.1","gene_symbol":"AC016687.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33968174,"end":33968526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282664.1","gene_symbol":"LINC00552","gene_name":"long intergenic non-protein coding RNA 552 [Source:HGNC Symbol;Acc:HGNC:43692]","synonyms":null,"biotype":"TEC","ncbi_id":"100130386","summary":null,"start":113749533,"end":113752109,"strand":-1,"description":"long intergenic non-protein coding RNA 552 [Source:HGNC Symbol;Acc:HGNC:43692]"}, {"versioned_ensembl_gene_id":"ENSG00000171466.9","gene_symbol":"ZNF562","gene_name":"zinc finger protein 562 [Source:HGNC Symbol;Acc:HGNC:25950]","synonyms":"FLJ20079","biotype":"protein_coding","ncbi_id":"54811","summary":null,"start":9641808,"end":9675086,"strand":-1,"description":"zinc finger protein 562 [Source:HGNC Symbol;Acc:HGNC:25950]"}, {"versioned_ensembl_gene_id":"ENSG00000284739.1","gene_symbol":"BX005132.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4963954,"end":4973298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226211.1","gene_symbol":"AL445466.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221133865,"end":221134221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237022.10","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"PSORS1,HLA-JY3,D6S204","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31312208,"end":31315579,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000275202.1","gene_symbol":"AL161421.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48974967,"end":48976867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198836.8","gene_symbol":"OPA1","gene_name":"OPA1, mitochondrial dynamin like GTPase [Source:HGNC Symbol;Acc:HGNC:8140]","synonyms":"NTG,NPG,MGM1,KIAA0567,FLJ12460","biotype":"protein_coding","ncbi_id":"4976","summary":"The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017]","start":193593144,"end":193697823,"strand":1,"description":"OPA1, mitochondrial dynamin like GTPase [Source:HGNC Symbol;Acc:HGNC:8140]"}, {"versioned_ensembl_gene_id":"ENSG00000143862.7","gene_symbol":"ARL8A","gene_name":"ADP ribosylation factor like GTPase 8A [Source:HGNC Symbol;Acc:HGNC:25192]","synonyms":"Gie2,FLJ45195,ARL10B","biotype":"protein_coding","ncbi_id":"127829","summary":null,"start":202133404,"end":202144743,"strand":-1,"description":"ADP ribosylation factor like GTPase 8A [Source:HGNC Symbol;Acc:HGNC:25192]"}, {"versioned_ensembl_gene_id":"ENSG00000228005.1","gene_symbol":"AC020743.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50141540,"end":50142823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249581.2","gene_symbol":"CLRN2","gene_name":"clarin 2 [Source:HGNC Symbol;Acc:HGNC:33939]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645104","summary":"This gene belongs to the clarin family of genes. The clarins appear to belong to a large superfamily of small integral membrane glycoproteins with four transmembrane domains. The exact function of this gene is unknown. [provided by RefSeq, Oct 2008]","start":17515165,"end":17527104,"strand":1,"description":"clarin 2 [Source:HGNC Symbol;Acc:HGNC:33939]"}, {"versioned_ensembl_gene_id":"ENSG00000253333.1","gene_symbol":"AC146944.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70495100,"end":70500903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250687.6","gene_symbol":"AC146944.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70462244,"end":70479215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134160.13","gene_symbol":"TRPM1","gene_name":"transient receptor potential cation channel subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:7146]","synonyms":"LTRPC1,CSNB1C,MLSN1,LTRPC1,CSNB1C,MLSN1","biotype":"protein_coding","ncbi_id":"4308","summary":"This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":31001061,"end":31161273,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:7146]"}, {"versioned_ensembl_gene_id":"ENSG00000234618.1","gene_symbol":"RPSAP9","gene_name":"ribosomal protein SA pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:31463]","synonyms":"LAMR1P9","biotype":"processed_pseudogene","ncbi_id":"653162","summary":null,"start":76398699,"end":76399586,"strand":1,"description":"ribosomal protein SA pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:31463]"}, {"versioned_ensembl_gene_id":"ENSG00000236389.1","gene_symbol":"AL121970.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134706060,"end":134707349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105722.9","gene_symbol":"ERF","gene_name":"ETS2 repressor factor [Source:HGNC Symbol;Acc:HGNC:3444]","synonyms":"PE2,PE-2","biotype":"protein_coding","ncbi_id":"2077","summary":"ETS2 is a transcription factor and protooncogene involved in development, apoptosis, and the regulation of telomerase. The protein encoded by this gene binds to the ETS2 promoter and is a strong repressor of ETS2 transcription. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":42247572,"end":42255157,"strand":-1,"description":"ETS2 repressor factor [Source:HGNC Symbol;Acc:HGNC:3444]"}, {"versioned_ensembl_gene_id":"ENSG00000248779.1","gene_symbol":"AC093297.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44752949,"end":44765744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176040.13","gene_symbol":"TMPRSS7","gene_name":"transmembrane protease, serine 7 [Source:HGNC Symbol;Acc:HGNC:30846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344805","summary":null,"start":112034843,"end":112081269,"strand":1,"description":"transmembrane protease, serine 7 [Source:HGNC Symbol;Acc:HGNC:30846]"}, {"versioned_ensembl_gene_id":"ENSG00000251629.6","gene_symbol":"LINC02241","gene_name":"long intergenic non-protein coding RNA 2241 [Source:HGNC Symbol;Acc:HGNC:53126]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374676","summary":null,"start":20611840,"end":20937691,"strand":1,"description":"long intergenic non-protein coding RNA 2241 [Source:HGNC Symbol;Acc:HGNC:53126]"}, {"versioned_ensembl_gene_id":"ENSG00000266149.1","gene_symbol":"AP001094.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8360820,"end":8367034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274624.1","gene_symbol":"AC007671.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22104491,"end":22105320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197161.7","gene_symbol":"AC023080.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48345351,"end":48352447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119471.14","gene_symbol":"HSDL2","gene_name":"hydroxysteroid dehydrogenase like 2 [Source:HGNC Symbol;Acc:HGNC:18572]","synonyms":"SDR13C1,C9orf99","biotype":"protein_coding","ncbi_id":"84263","summary":null,"start":112379937,"end":112472410,"strand":1,"description":"hydroxysteroid dehydrogenase like 2 [Source:HGNC Symbol;Acc:HGNC:18572]"}, {"versioned_ensembl_gene_id":"ENSG00000187908.16","gene_symbol":"DMBT1","gene_name":"deleted in malignant brain tumors 1 [Source:HGNC Symbol;Acc:HGNC:2926]","synonyms":"vomeroglandin,SALSA,muclin,hensin,GP340,Gp-340","biotype":"protein_coding","ncbi_id":"1755","summary":"Loss of sequences from human chromosome 10q has been associated with the progression of human cancers. This gene was originally isolated based on its deletion in a medulloblastoma cell line. This gene is expressed with transcripts of 6.0, 7.5, and 8.0 kb in fetal lung and with one transcript of 8.0 kb in adult lung, although the 7.5 kb transcript has not been characterized. The encoded protein precursor is a glycoprotein containing multiple scavenger receptor cysteine-rich (SRCR) domains separated by SRCR-interspersed domains (SID). Transcript variant 2 (8.0 kb) has been shown to bind surfactant protein D independently of carbohydrate recognition. This indicates that DMBT1 may not be a classical tumor suppressor gene, but rather play a role in the interaction of tumor cells and the immune system. [provided by RefSeq, Mar 2016]","start":122560665,"end":122643736,"strand":1,"description":"deleted in malignant brain tumors 1 [Source:HGNC Symbol;Acc:HGNC:2926]"}, {"versioned_ensembl_gene_id":"ENSG00000228638.1","gene_symbol":"FCF1P2","gene_name":"FCF1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060195","summary":null,"start":48290793,"end":48291375,"strand":-1,"description":"FCF1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44614]"}, {"versioned_ensembl_gene_id":"ENSG00000176555.1","gene_symbol":"OR4S1","gene_name":"olfactory receptor family 4 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:14705]","synonyms":null,"biotype":"protein_coding","ncbi_id":"256148","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48306223,"end":48307152,"strand":1,"description":"olfactory receptor family 4 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:14705]"}, {"versioned_ensembl_gene_id":"ENSG00000254926.1","gene_symbol":"AP000445.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58748999,"end":58761053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155966.13","gene_symbol":"AFF2","gene_name":"AF4/FMR2 family member 2 [Source:HGNC Symbol;Acc:HGNC:3776]","synonyms":"FRAXE,FMR2","biotype":"protein_coding","ncbi_id":"2334","summary":"This gene encodes a putative transcriptional activator that is a member of the AF4\\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked cognitive disability. In addition, this gene contains 6-25 GCC repeats that are expanded to >200 repeats in the disease state. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jul 2016]","start":148500619,"end":149000663,"strand":1,"description":"AF4/FMR2 family member 2 [Source:HGNC Symbol;Acc:HGNC:3776]"}, {"versioned_ensembl_gene_id":"ENSG00000165185.14","gene_symbol":"KIAA1958","gene_name":"KIAA1958 [Source:HGNC Symbol;Acc:HGNC:23427]","synonyms":"FLJ39294","biotype":"protein_coding","ncbi_id":"158405","summary":null,"start":112486847,"end":112669397,"strand":1,"description":"KIAA1958 [Source:HGNC Symbol;Acc:HGNC:23427]"}, {"versioned_ensembl_gene_id":"ENSG00000168542.14","gene_symbol":"COL3A1","gene_name":"collagen type III alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2201]","synonyms":"EDS4A","biotype":"protein_coding","ncbi_id":"1281","summary":"This gene encodes the pro-alpha1 chains of type III collagen, a fibrillar collagen that is found in extensible connective tissues such as skin, lung, uterus, intestine and the vascular system, frequently in association with type I collagen. Mutations in this gene are associated with Ehlers-Danlos syndrome types IV, and with aortic and arterial aneurysms. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]","start":188974320,"end":189012746,"strand":1,"description":"collagen type III alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2201]"}, {"versioned_ensembl_gene_id":"ENSG00000250116.2","gene_symbol":"AC018682.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46568256,"end":46580238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251434.1","gene_symbol":"AC104071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31350284,"end":31351725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158747.13","gene_symbol":"NBL1","gene_name":"neuroblastoma 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:7650]","synonyms":"NO3,NB,DAND1,DAN,D1S1733E","biotype":"protein_coding","ncbi_id":"4681","summary":"This gene product is the founding member of the evolutionarily conserved CAN (Cerberus and DAN) family of proteins, which contain a domain resembling the CTCK (C-terminal cystine knot-like) motif found in a number of signaling molecules. These proteins are secreted, and act as BMP (bone morphogenetic protein) antagonists by binding to BMPs and preventing them from interacting with their receptors. They may thus play an important role during growth and development. Alternatively spliced transcript variants have been identified for this gene. Read-through transcripts between this locus and the upstream mitochondrial inner membrane organizing system 1 gene (GeneID 440574) have been observed. [provided by RefSeq, May 2013]","start":19640554,"end":19658456,"strand":1,"description":"neuroblastoma 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:7650]"}, {"versioned_ensembl_gene_id":"ENSG00000239516.1","gene_symbol":"FLYWCH1P1","gene_name":"FLYWCH-type zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38033]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130898","summary":null,"start":180827977,"end":180829850,"strand":-1,"description":"FLYWCH-type zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38033]"}, {"versioned_ensembl_gene_id":"ENSG00000175619.3","gene_symbol":"OR4B1","gene_name":"olfactory receptor family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:8290]","synonyms":"OST208","biotype":"protein_coding","ncbi_id":"119765","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48216810,"end":48217739,"strand":1,"description":"olfactory receptor family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:8290]"}, {"versioned_ensembl_gene_id":"ENSG00000250020.1","gene_symbol":"AC113430.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58198,"end":58915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232310.6","gene_symbol":"AL078590.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134525314,"end":134659836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227723.1","gene_symbol":"AL596188.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134636489,"end":134642495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236986.6","gene_symbol":"AL157938.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131132852,"end":131167505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254867.1","gene_symbol":"AP006287.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65983679,"end":65984331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250197.1","gene_symbol":"HMGN1P15","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39359]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874441","summary":null,"start":115289036,"end":115289330,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39359]"}, {"versioned_ensembl_gene_id":"ENSG00000231995.2","gene_symbol":"AL590399.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62266319,"end":62266919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169605.5","gene_symbol":"GKN1","gene_name":"gastrokine 1 [Source:HGNC Symbol;Acc:HGNC:23217]","synonyms":"CA11,BRICD1,AMP18","biotype":"protein_coding","ncbi_id":"56287","summary":"The protein encoded by this gene is found to be down-regulated in human gastric cancer tissue as compared to normal gastric mucosa. [provided by RefSeq, Jul 2008]","start":68974573,"end":68980974,"strand":1,"description":"gastrokine 1 [Source:HGNC Symbol;Acc:HGNC:23217]"}, {"versioned_ensembl_gene_id":"ENSG00000233456.1","gene_symbol":"LINC01077","gene_name":"long intergenic non-protein coding RNA 1077 [Source:HGNC Symbol;Acc:HGNC:49120]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107080621","summary":null,"start":48570639,"end":48573317,"strand":-1,"description":"long intergenic non-protein coding RNA 1077 [Source:HGNC Symbol;Acc:HGNC:49120]"}, {"versioned_ensembl_gene_id":"ENSG00000118217.5","gene_symbol":"ATF6","gene_name":"activating transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:791]","synonyms":"ATF6A","biotype":"protein_coding","ncbi_id":"22926","summary":"This gene encodes a transcription factor that activates target genes for the unfolded protein response (UPR) during endoplasmic reticulum (ER) stress. Although it is a transcription factor, this protein is unusual in that it is synthesized as a transmembrane protein that is embedded in the ER. It functions as an ER stress sensor/transducer, and following ER stress-induced proteolysis, it functions as a nuclear transcription factor via a cis-acting ER stress response element (ERSE) that is present in the promoters of genes encoding ER chaperones. This protein has been identified as a survival factor for quiescent but not proliferative squamous carcinoma cells. There have been conflicting reports about the association of polymorphisms in this gene with diabetes in different populations, but another polymorphism has been associated with increased plasma cholesterol levels. This gene is also thought to be a potential therapeutic target for cystic fibrosis. [provided by RefSeq, Aug 2011]","start":161766294,"end":161964070,"strand":1,"description":"activating transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:791]"}, {"versioned_ensembl_gene_id":"ENSG00000236266.1","gene_symbol":"Z98884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7810242,"end":7827342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114942.13","gene_symbol":"EEF1B2","gene_name":"eukaryotic translation elongation factor 1 beta 2 [Source:HGNC Symbol;Acc:HGNC:3208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1933","summary":"This gene encodes a translation elongation factor. The protein is a guanine nucleotide exchange factor involved in the transfer of aminoacylated tRNAs to the ribosome. Alternative splicing results in three transcript variants which differ only in the 5' UTR. [provided by RefSeq, Jul 2008]","start":206159585,"end":206162928,"strand":1,"description":"eukaryotic translation elongation factor 1 beta 2 [Source:HGNC Symbol;Acc:HGNC:3208]"}, {"versioned_ensembl_gene_id":"ENSG00000151704.15","gene_symbol":"KCNJ1","gene_name":"potassium voltage-gated channel subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:6255]","synonyms":"ROMK1,Kir1.1","biotype":"protein_coding","ncbi_id":"3758","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":128836315,"end":128867373,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:6255]"}, {"versioned_ensembl_gene_id":"ENSG00000278550.4","gene_symbol":"SLC43A2","gene_name":"solute carrier family 43 member 2 [Source:HGNC Symbol;Acc:HGNC:23087]","synonyms":"MGC34680","biotype":"protein_coding","ncbi_id":"124935","summary":"This gene encodes a member of the L-amino acid transporter-3 or SLC43 family of transporters. The encoded protein mediates sodium-, chloride-, and pH-independent transport of L-isomers of neutral amino acids, including leucine, phenylalanine, valine and methionine. This protein may contribute to the transfer of amino acids across the placental membrane to the fetus. [provided by RefSeq, Mar 2016]","start":1569973,"end":1628886,"strand":-1,"description":"solute carrier family 43 member 2 [Source:HGNC Symbol;Acc:HGNC:23087]"}, {"versioned_ensembl_gene_id":"ENSG00000232783.5","gene_symbol":"FRG2FP","gene_name":"FSHD region gene 2 family member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:51366]","synonyms":"TCONS_l2_00020053","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100128827","summary":null,"start":198110112,"end":198111878,"strand":1,"description":"FSHD region gene 2 family member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:51366]"}, {"versioned_ensembl_gene_id":"ENSG00000262006.1","gene_symbol":"AC005920.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50909637,"end":50910232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273368.1","gene_symbol":"AC006566.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8154558,"end":8155070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229394.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33193611,"end":33194234,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000218305.3","gene_symbol":"CDC14C","gene_name":"cell division cycle 14C, pseudogene [Source:HGNC Symbol;Acc:HGNC:22427]","synonyms":"MGC26484,CDC14CP,CDC14Bretro,CDC14B2","biotype":"processed_pseudogene","ncbi_id":"168448","summary":"This gene represents a retrogene of cell division cycle 14B (CDC14B), which is located on chromosome 9. The introns in the coding sequence have been processed out relative to the CDC14B locus, but there is an intact open reading frame that is missing only some sequence at the N-terminus, including the nuclear localiztion signal, relative to proteins encoded by the CDC14B gene. There is a difference in the subcellular localization of the protein encoded by this gene, relative to its parental gene product. While the parental gene product displays microtubular localization, GFP chimeras of the protein encoded by this gene localize to the endoplasmic reticulum, indicating a possible new functional role for this gene. [provided by RefSeq, Nov 2017]","start":48919765,"end":48926013,"strand":1,"description":"cell division cycle 14C, pseudogene [Source:HGNC Symbol;Acc:HGNC:22427]"}, {"versioned_ensembl_gene_id":"ENSG00000226889.3","gene_symbol":"AL359541.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161765325,"end":161766227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270378.1","gene_symbol":"AC020891.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51351100,"end":51351192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220267.1","gene_symbol":"ACTBP8","gene_name":"actin, beta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:141]","synonyms":"ACTBP2","biotype":"processed_pseudogene","ncbi_id":"68","summary":null,"start":88275882,"end":88276989,"strand":-1,"description":"actin, beta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:141]"}, {"versioned_ensembl_gene_id":"ENSG00000280813.1","gene_symbol":"AC092902.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125800930,"end":125801709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281363.1","gene_symbol":"AF186996.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125756086,"end":125756441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280996.1","gene_symbol":"AF186996.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125747135,"end":125748058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108387.14","gene_symbol":"SEPT4","gene_name":"septin 4 [Source:HGNC Symbol;Acc:HGNC:9165]","synonyms":"ARTS,PNUTL2,MART,hucep-7,hCDCREL-2,H5,CE5B3","biotype":"protein_coding","ncbi_id":"5414","summary":"This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer. [provided by RefSeq, Nov 2010]","start":58520250,"end":58540818,"strand":-1,"description":"septin 4 [Source:HGNC Symbol;Acc:HGNC:9165]"}, {"versioned_ensembl_gene_id":"ENSG00000228173.1","gene_symbol":"AC091770.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48660575,"end":48663305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226324.1","gene_symbol":"AL358453.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71367054,"end":71367303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185662.9","gene_symbol":"SMIM23","gene_name":"small integral membrane protein 23 [Source:HGNC Symbol;Acc:HGNC:34440]","synonyms":"LOC644994,C5orf50","biotype":"protein_coding","ncbi_id":"644994","summary":null,"start":171782432,"end":171796126,"strand":1,"description":"small integral membrane protein 23 [Source:HGNC Symbol;Acc:HGNC:34440]"}, {"versioned_ensembl_gene_id":"ENSG00000236614.1","gene_symbol":"ZNF90P2","gene_name":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]","synonyms":"ZNF463P,dJ111M5.3","biotype":"processed_pseudogene","ncbi_id":"100419606","summary":null,"start":28888823,"end":28889897,"strand":-1,"description":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]"}, {"versioned_ensembl_gene_id":"ENSG00000182107.6","gene_symbol":"TMEM30B","gene_name":"transmembrane protein 30B [Source:HGNC Symbol;Acc:HGNC:27254]","synonyms":"CDC50B","biotype":"protein_coding","ncbi_id":"161291","summary":null,"start":61277370,"end":61281840,"strand":-1,"description":"transmembrane protein 30B [Source:HGNC Symbol;Acc:HGNC:27254]"}, {"versioned_ensembl_gene_id":"ENSG00000087884.14","gene_symbol":"AAMDC","gene_name":"adipogenesis associated Mth938 domain containing [Source:HGNC Symbol;Acc:HGNC:30205]","synonyms":"PTD015,FLJ21035,CK067,C11orf67","biotype":"protein_coding","ncbi_id":"28971","summary":null,"start":77821109,"end":77918432,"strand":1,"description":"adipogenesis associated Mth938 domain containing [Source:HGNC Symbol;Acc:HGNC:30205]"}, {"versioned_ensembl_gene_id":"ENSG00000206072.12","gene_symbol":"SERPINB11","gene_name":"serpin family B member 11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14221]","synonyms":"EPIPIN","biotype":"protein_coding","ncbi_id":"89778","summary":null,"start":63647579,"end":63726432,"strand":1,"description":"serpin family B member 11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14221]"}, {"versioned_ensembl_gene_id":"ENSG00000255115.2","gene_symbol":"AP002812.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77914990,"end":77915275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144827.8","gene_symbol":"ABHD10","gene_name":"abhydrolase domain containing 10 [Source:HGNC Symbol;Acc:HGNC:25656]","synonyms":"FLJ11342","biotype":"protein_coding","ncbi_id":"55347","summary":"This gene encodes a mitochondrially-localized enzyme that acts in liver cells as a hydrolase. The encoded protein removes glucuronide from mycophenolic acid acyl-glucuronide. There is a pseudogene for this gene on chromosome 6. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":111979010,"end":111993363,"strand":1,"description":"abhydrolase domain containing 10 [Source:HGNC Symbol;Acc:HGNC:25656]"}, {"versioned_ensembl_gene_id":"ENSG00000238032.1","gene_symbol":"AC245047.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48177731,"end":48178023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280025.1","gene_symbol":"AL008638.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27102766,"end":27107019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231405.1","gene_symbol":"AL008638.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27143478,"end":27159878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156427.7","gene_symbol":"FGF18","gene_name":"fibroblast growth factor 18 [Source:HGNC Symbol;Acc:HGNC:3674]","synonyms":"FGF-18,ZFGF5","biotype":"protein_coding","ncbi_id":"8817","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. It has been shown in vitro that this protein is able to induce neurite outgrowth in PC12 cells. Studies of the similar proteins in mouse and chick suggested that this protein is a pleiotropic growth factor that stimulates proliferation in a number of tissues, most notably the liver and small intestine. Knockout studies of the similar gene in mice implied the role of this protein in regulating proliferation and differentiation of midline cerebellar structures. [provided by RefSeq, Jul 2008]","start":171419656,"end":171457623,"strand":1,"description":"fibroblast growth factor 18 [Source:HGNC Symbol;Acc:HGNC:3674]"}, {"versioned_ensembl_gene_id":"ENSG00000140262.17","gene_symbol":"TCF12","gene_name":"transcription factor 12 [Source:HGNC Symbol;Acc:HGNC:11623]","synonyms":"HTF4,HsT17266,HEB,bHLHb20","biotype":"protein_coding","ncbi_id":"6938","summary":"The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. This encoded protein is expressed in many tissues, among them skeletal muscle, thymus, B- and T-cells, and may participate in regulating lineage-specific gene expression through the formation of heterodimers with other bHLH E-proteins. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":56918623,"end":57299281,"strand":1,"description":"transcription factor 12 [Source:HGNC Symbol;Acc:HGNC:11623]"}, {"versioned_ensembl_gene_id":"ENSG00000075618.17","gene_symbol":"FSCN1","gene_name":"fascin actin-bundling protein 1 [Source:HGNC Symbol;Acc:HGNC:11148]","synonyms":"SNL,p55,FLJ38511","biotype":"protein_coding","ncbi_id":"6624","summary":"This gene encodes a member of the fascin family of actin-binding proteins. Fascin proteins organize F-actin into parallel bundles, and are required for the formation of actin-based cellular protrusions. The encoded protein plays a critical role in cell migration, motility, adhesion and cellular interactions. Expression of this gene is known to be regulated by several microRNAs, and overexpression of this gene may play a role in the metastasis of multiple types of cancer by increasing cell motility. Expression of this gene is also a marker for Reed-Sternberg cells in Hodgkin's lymphoma. A pseudogene of this gene is located on the long arm of chromosome 15. [provided by RefSeq, Sep 2011]","start":5592823,"end":5606655,"strand":1,"description":"fascin actin-bundling protein 1 [Source:HGNC Symbol;Acc:HGNC:11148]"}, {"versioned_ensembl_gene_id":"ENSG00000227399.1","gene_symbol":"AL391219.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92006062,"end":92006544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233994.2","gene_symbol":"GDI2P2","gene_name":"GDP dissociation inhibitor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420259","summary":null,"start":72274552,"end":72275159,"strand":1,"description":"GDP dissociation inhibitor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37976]"}, {"versioned_ensembl_gene_id":"ENSG00000271123.1","gene_symbol":"ELOCP5","gene_name":"elongin C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38140]","synonyms":"TCEB1P5","biotype":"processed_pseudogene","ncbi_id":"100288493","summary":null,"start":21631683,"end":21632015,"strand":-1,"description":"elongin C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38140]"}, {"versioned_ensembl_gene_id":"ENSG00000281274.1","gene_symbol":"AL139246.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2493437,"end":2494479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269476.1","gene_symbol":"AC010326.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57876765,"end":57916591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172260.14","gene_symbol":"NEGR1","gene_name":"neuronal growth regulator 1 [Source:HGNC Symbol;Acc:HGNC:17302]","synonyms":"Ntra,MGC46680,KILON,IGLON4","biotype":"protein_coding","ncbi_id":"257194","summary":null,"start":71395940,"end":72282734,"strand":-1,"description":"neuronal growth regulator 1 [Source:HGNC Symbol;Acc:HGNC:17302]"}, {"versioned_ensembl_gene_id":"ENSG00000107614.21","gene_symbol":"TRDMT1","gene_name":"tRNA aspartic acid methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2977]","synonyms":"RNMT1,DNMT2","biotype":"protein_coding","ncbi_id":"1787","summary":"This gene encodes a protein responsible for the methylation of aspartic acid transfer RNA, specifically at the cytosine-38 residue in the anticodon loop. This enzyme also possesses residual DNA-(cytosine-C5) methyltransferase activity. While similar in sequence and structure to DNA cytosine methyltransferases, this gene is distinct and highly conserved in its function among taxa. [provided by RefSeq, Jun 2010]","start":17142254,"end":17202054,"strand":-1,"description":"tRNA aspartic acid methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2977]"}, {"versioned_ensembl_gene_id":"ENSG00000260891.1","gene_symbol":"AC020978.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68212401,"end":68221671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261864.1","gene_symbol":"AC130462.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":68077340,"end":68122271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243187.1","gene_symbol":"CCDC39-AS1","gene_name":"CCDC39 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41089]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874112","summary":null,"start":180680084,"end":180700449,"strand":1,"description":"CCDC39 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41089]"}, {"versioned_ensembl_gene_id":"ENSG00000231527.5","gene_symbol":"CR769775.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":61972240,"end":61976380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241473.1","gene_symbol":"AC108734.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180820544,"end":180821612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182810.6","gene_symbol":"DDX28","gene_name":"DEAD-box helicase 28 [Source:HGNC Symbol;Acc:HGNC:17330]","synonyms":"MDDX28,FLJ11282","biotype":"protein_coding","ncbi_id":"55794","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene is intronless. It encodes an RNA-dependent ATPase. The encoded protein is localized in the mitochondria and the nucleus, and can be transported between the mitochondria and the nucleus. [provided by RefSeq, Jul 2008]","start":68021274,"end":68023442,"strand":-1,"description":"DEAD-box helicase 28 [Source:HGNC Symbol;Acc:HGNC:17330]"}, {"versioned_ensembl_gene_id":"ENSG00000282556.1","gene_symbol":"AC068733.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6323554,"end":6324023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231971.5","gene_symbol":"AL078590.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134428240,"end":134520585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204514.9","gene_symbol":"ZNF814","gene_name":"zinc finger protein 814 [Source:HGNC Symbol;Acc:HGNC:33258]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730051","summary":null,"start":57848731,"end":57889074,"strand":-1,"description":"zinc finger protein 814 [Source:HGNC Symbol;Acc:HGNC:33258]"}, {"versioned_ensembl_gene_id":"ENSG00000166415.14","gene_symbol":"WDR72","gene_name":"WD repeat domain 72 [Source:HGNC Symbol;Acc:HGNC:26790]","synonyms":"FLJ38736","biotype":"protein_coding","ncbi_id":"256764","summary":"This gene encodes a protein with eight WD-40 repeats. Mutations in this gene have been associated with amelogenesis imperfecta hypomaturation type 2A3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":53513741,"end":53762878,"strand":-1,"description":"WD repeat domain 72 [Source:HGNC Symbol;Acc:HGNC:26790]"}, {"versioned_ensembl_gene_id":"ENSG00000276845.1","gene_symbol":"CR769775.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61944232,"end":61945136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255522.1","gene_symbol":"SNRPCP5","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49820]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480290","summary":null,"start":3531420,"end":3531608,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49820]"}, {"versioned_ensembl_gene_id":"ENSG00000250067.11","gene_symbol":"YJEFN3","gene_name":"YjeF N-terminal domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24785]","synonyms":"hYjeF_N3-19p13.11,FLJ44968","biotype":"protein_coding","ncbi_id":"374887","summary":null,"start":19528861,"end":19537581,"strand":1,"description":"YjeF N-terminal domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24785]"}, {"versioned_ensembl_gene_id":"ENSG00000136630.12","gene_symbol":"HLX","gene_name":"H2.0 like homeobox [Source:HGNC Symbol;Acc:HGNC:4978]","synonyms":"HLX1,HB24","biotype":"protein_coding","ncbi_id":"3142","summary":null,"start":220879400,"end":220885059,"strand":1,"description":"H2.0 like homeobox [Source:HGNC Symbol;Acc:HGNC:4978]"}, {"versioned_ensembl_gene_id":"ENSG00000279848.1","gene_symbol":"AL008638.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27044001,"end":27045315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236858.1","gene_symbol":"AL008638.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27048144,"end":27060518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238195.1","gene_symbol":"AL021153.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27204211,"end":27205126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151475.5","gene_symbol":"SLC25A31","gene_name":"solute carrier family 25 member 31 [Source:HGNC Symbol;Acc:HGNC:25319]","synonyms":"DKFZP434N1235,ANT4","biotype":"protein_coding","ncbi_id":"83447","summary":"The protein encoded by this gene is a member of the ADP/ATP carrier family of proteins that exchange cytosolic ADP for matrix ATP in the mitochondria. Cells over-expressing this gene have been shown to display an anti-apoptotic phenotype. This protein is also thought to play a role in spermatogenesis, where it is believed to associate with a part of the flagellar cytoskeleton and with glycolytic enzymes. Male mice with mutations in the mouse ortholog of this gene are sterile and spermatocytes display an early meiotic arrest phenotype. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":127730378,"end":127774299,"strand":1,"description":"solute carrier family 25 member 31 [Source:HGNC Symbol;Acc:HGNC:25319]"}, {"versioned_ensembl_gene_id":"ENSG00000284674.1","gene_symbol":"BX005132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4973381,"end":4981568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234754.1","gene_symbol":"C1orf140","gene_name":"uncharacterized LOC400804 [Source:NCBI gene;Acc:400804]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400804","summary":null,"start":221330080,"end":221336296,"strand":-1,"description":"uncharacterized LOC400804 [Source:NCBI gene;Acc:400804]"}, {"versioned_ensembl_gene_id":"ENSG00000267656.1","gene_symbol":"AP001357.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13139780,"end":13140489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198729.4","gene_symbol":"PPP1R14C","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14C [Source:HGNC Symbol;Acc:HGNC:14952]","synonyms":"NY-BR-81,KEPI,CPI17-like","biotype":"protein_coding","ncbi_id":"81706","summary":"The degree of protein phosphorylation is regulated by a balance of protein kinase and phosphatase activities. Protein phosphatase-1 (PP1; see MIM 176875) is a signal-transducing phosphatase that influences neuronal activity, protein synthesis, metabolism, muscle contraction, and cell division. PPP1R14C is an inhibitor of PP1 (Liu et al., 2002 [PubMed 11812771]).[supplied by OMIM, Feb 2010]","start":150143076,"end":150250357,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14C [Source:HGNC Symbol;Acc:HGNC:14952]"}, {"versioned_ensembl_gene_id":"ENSG00000231510.1","gene_symbol":"AL691497.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5086459,"end":5090899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231197.1","gene_symbol":"BX927141.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878153,"end":29879115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111863.12","gene_symbol":"ADTRP","gene_name":"androgen dependent TFPI regulating protein [Source:HGNC Symbol;Acc:HGNC:21214]","synonyms":"dJ413H6.1,C6orf105,AIG1L","biotype":"protein_coding","ncbi_id":"84830","summary":null,"start":11712054,"end":11807046,"strand":-1,"description":"androgen dependent TFPI regulating protein [Source:HGNC Symbol;Acc:HGNC:21214]"}, {"versioned_ensembl_gene_id":"ENSG00000232436.1","gene_symbol":"AL360013.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221508559,"end":221510979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227585.2","gene_symbol":"AL360013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221549786,"end":221550643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267032.1","gene_symbol":"AP001357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13151637,"end":13152689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235498.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29848896,"end":29849024,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000284616.1","gene_symbol":"AL139823.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5301928,"end":5307394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253550.1","gene_symbol":"AC016065.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6473845,"end":6474288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267286.1","gene_symbol":"AP001198.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13183402,"end":13185617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143507.17","gene_symbol":"DUSP10","gene_name":"dual specificity phosphatase 10 [Source:HGNC Symbol;Acc:HGNC:3065]","synonyms":"MKP5,MKP-5","biotype":"protein_coding","ncbi_id":"11221","summary":"Dual specificity protein phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the MAP kinase superfamily, which is associated with cellular proliferation and differentiation. Different members of this family of dual specificity phosphatases show distinct substrate specificities for MAP kinases, different tissue distribution and subcellular localization, and different modes of expression induction by extracellular stimuli. This gene product binds to and inactivates p38 and SAPK/JNK. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":221701424,"end":221742176,"strand":-1,"description":"dual specificity phosphatase 10 [Source:HGNC Symbol;Acc:HGNC:3065]"}, {"versioned_ensembl_gene_id":"ENSG00000271743.1","gene_symbol":"AF287957.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6615604,"end":6617198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224801.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824278,"end":29825257,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000233418.8","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DDX16,PRPF2,DBP2,Prp2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30643349,"end":30663298,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000224375.1","gene_symbol":"AC009276.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134684144,"end":134687990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109956.12","gene_symbol":"B3GAT1","gene_name":"beta-1,3-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:921]","synonyms":"LEU7,HNK-1,GlcAT-P,CD57,NK-1","biotype":"protein_coding","ncbi_id":"27087","summary":"The protein encoded by this gene is a member of the glucuronyltransferase gene family. These enzymes exhibit strict acceptor specificity, recognizing nonreducing terminal sugars and their anomeric linkages. This gene product functions as the key enzyme in a glucuronyl transfer reaction during the biosynthesis of the carbohydrate epitope HNK-1 (human natural killer-1, also known as CD57 and LEU7). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":134378504,"end":134411918,"strand":-1,"description":"beta-1,3-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:921]"}, {"versioned_ensembl_gene_id":"ENSG00000237161.4","gene_symbol":"AC068446.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21293653,"end":21295201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230101.5","gene_symbol":"TUBB3P2","gene_name":"tubulin beta 3 class III pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42181]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130187","summary":null,"start":134734898,"end":134735129,"strand":-1,"description":"tubulin beta 3 class III pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42181]"}, {"versioned_ensembl_gene_id":"ENSG00000108587.15","gene_symbol":"GOSR1","gene_name":"golgi SNAP receptor complex member 1 [Source:HGNC Symbol;Acc:HGNC:4430]","synonyms":"GOLIM2,P28,GS28,GOS28,GOS-28","biotype":"protein_coding","ncbi_id":"9527","summary":"This gene encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi and between Golgi compartments. This protein is considered an essential component of the Golgi SNAP receptor (SNARE) complex. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30477362,"end":30527592,"strand":1,"description":"golgi SNAP receptor complex member 1 [Source:HGNC Symbol;Acc:HGNC:4430]"}, {"versioned_ensembl_gene_id":"ENSG00000233471.2","gene_symbol":"KRT18P62","gene_name":"keratin 18 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287635","summary":null,"start":19257520,"end":19258806,"strand":1,"description":"keratin 18 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48889]"}, {"versioned_ensembl_gene_id":"ENSG00000164048.13","gene_symbol":"ZNF589","gene_name":"zinc finger protein 589 [Source:HGNC Symbol;Acc:HGNC:16747]","synonyms":"SZF1","biotype":"protein_coding","ncbi_id":"51385","summary":null,"start":48241100,"end":48299253,"strand":1,"description":"zinc finger protein 589 [Source:HGNC Symbol;Acc:HGNC:16747]"}, {"versioned_ensembl_gene_id":"ENSG00000235116.1","gene_symbol":"BX649210.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32624375,"end":32624782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196610.13","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32684806,"end":32692245,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000103495.13","gene_symbol":"MAZ","gene_name":"MYC associated zinc finger protein [Source:HGNC Symbol;Acc:HGNC:6914]","synonyms":"ZNF801,Zif87,ZF87,Pur-1","biotype":"protein_coding","ncbi_id":"4150","summary":null,"start":29806106,"end":29811164,"strand":1,"description":"MYC associated zinc finger protein [Source:HGNC Symbol;Acc:HGNC:6914]"}, {"versioned_ensembl_gene_id":"ENSG00000278153.1","gene_symbol":"AL121782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13368291,"end":13368703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267677.1","gene_symbol":"AC016229.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59360700,"end":59386749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236989.5","gene_symbol":"AC130710.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16085222,"end":16105841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229662.2","gene_symbol":"AC245047.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48244894,"end":48245745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168484.12","gene_symbol":"SFTPC","gene_name":"surfactant protein C [Source:HGNC Symbol;Acc:HGNC:10802]","synonyms":"SP-C,SMDP2,SFTP2,PSP-C,BRICD6","biotype":"protein_coding","ncbi_id":"6440","summary":"This gene encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.[provided by RefSeq, Feb 2010]","start":22156913,"end":22164479,"strand":1,"description":"surfactant protein C [Source:HGNC Symbol;Acc:HGNC:10802]"}, {"versioned_ensembl_gene_id":"ENSG00000226764.2","gene_symbol":"AC010145.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15997049,"end":16062885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241207.1","gene_symbol":"AC245047.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48276704,"end":48277578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227105.1","gene_symbol":"PARP1P1","gene_name":"poly(ADP-ribose) polymerase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:275]","synonyms":"PPOLP1,ADPRTP1","biotype":"processed_pseudogene","ncbi_id":"144","summary":null,"start":110936759,"end":110939784,"strand":1,"description":"poly(ADP-ribose) polymerase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:275]"}, {"versioned_ensembl_gene_id":"ENSG00000275582.1","gene_symbol":"AL031670.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3921279,"end":3923400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236289.2","gene_symbol":"GACAT3","gene_name":"gastric cancer associated transcript 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50847]","synonyms":"lncRNA-AC130710,LINC01458","biotype":"lincRNA","ncbi_id":"104797537","summary":null,"start":16050427,"end":16085801,"strand":1,"description":"gastric cancer associated transcript 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50847]"}, {"versioned_ensembl_gene_id":"ENSG00000224087.1","gene_symbol":"AC018865.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130107684,"end":130109741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126752.7","gene_symbol":"SSX1","gene_name":"SSX family member 1 [Source:HGNC Symbol;Acc:HGNC:11335]","synonyms":"CT5.1","biotype":"protein_coding","ncbi_id":"6756","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. This gene, and also the SSX2 and SSX4 family members, have been involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Jul 2013]","start":48255317,"end":48267444,"strand":1,"description":"SSX family member 1 [Source:HGNC Symbol;Acc:HGNC:11335]"}, {"versioned_ensembl_gene_id":"ENSG00000228471.1","gene_symbol":"AC018865.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130082092,"end":130082220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196604.12","gene_symbol":"POTEF","gene_name":"POTE ankyrin domain family member F [Source:HGNC Symbol;Acc:HGNC:33905]","synonyms":"POTEACTIN,POTE2alpha,A26C1B","biotype":"protein_coding","ncbi_id":"728378","summary":null,"start":130074030,"end":130129222,"strand":-1,"description":"POTE ankyrin domain family member F [Source:HGNC Symbol;Acc:HGNC:33905]"}, {"versioned_ensembl_gene_id":"ENSG00000160224.16","gene_symbol":"AIRE","gene_name":"autoimmune regulator [Source:HGNC Symbol;Acc:HGNC:360]","synonyms":"PGA1,APS1,APECED","biotype":"protein_coding","ncbi_id":"326","summary":"This gene encodes a transcriptional regulator that forms nuclear bodies and interacts with the transcriptional coactivator CREB binding protein. The encoded protein plays an important role in immunity by regulating the expression of autoantigens and negative selection of autoreactive T-cells in the thymus. Mutations in this gene cause the rare autosomal-recessive systemic autoimmune disease termed autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (APECED). [provided by RefSeq, Jun 2012]","start":44285838,"end":44298648,"strand":1,"description":"autoimmune regulator [Source:HGNC Symbol;Acc:HGNC:360]"}, {"versioned_ensembl_gene_id":"ENSG00000125779.21","gene_symbol":"PANK2","gene_name":"pantothenate kinase 2 [Source:HGNC Symbol;Acc:HGNC:15894]","synonyms":"PKAN,NBIA1,HSS,HARP,FLJ11729,C20orf48","biotype":"protein_coding","ncbi_id":"80025","summary":"This gene encodes a protein belonging to the pantothenate kinase family and is the only member of that family to be expressed in mitochondria. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by acyl CoA species. Mutations in this gene are associated with HARP syndrome and pantothenate kinase-associated neurodegeneration (PKAN), formerly Hallervorden-Spatz syndrome. Alternative splicing, involving the use of alternate first exons, results in multiple transcripts encoding different isoforms. [provided by RefSeq, Jul 2008]","start":3888839,"end":3929882,"strand":1,"description":"pantothenate kinase 2 [Source:HGNC Symbol;Acc:HGNC:15894]"}, {"versioned_ensembl_gene_id":"ENSG00000264080.1","gene_symbol":"AP005057.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1780329,"end":1782064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266602.1","gene_symbol":"AC008109.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1509183,"end":1647097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258674.5","gene_symbol":"AC011448.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":19516227,"end":19536076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183230.16","gene_symbol":"CTNNA3","gene_name":"catenin alpha 3 [Source:HGNC Symbol;Acc:HGNC:2511]","synonyms":"VR22,MGC26194","biotype":"protein_coding","ncbi_id":"29119","summary":"This gene encodes a protein that belongs to the vinculin/alpha-catenin family. The encoded protein plays a role in cell-cell adhesion in muscle cells. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia, familial 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":65912518,"end":67696169,"strand":-1,"description":"catenin alpha 3 [Source:HGNC Symbol;Acc:HGNC:2511]"}, {"versioned_ensembl_gene_id":"ENSG00000070371.15","gene_symbol":"CLTCL1","gene_name":"clathrin heavy chain like 1 [Source:HGNC Symbol;Acc:HGNC:2093]","synonyms":"CLTD,CLTCL,CLH22,CHC22","biotype":"protein_coding","ncbi_id":"8218","summary":"This gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":19179473,"end":19291716,"strand":-1,"description":"clathrin heavy chain like 1 [Source:HGNC Symbol;Acc:HGNC:2093]"}, {"versioned_ensembl_gene_id":"ENSG00000230370.1","gene_symbol":"RPL23AP52","gene_name":"ribosomal protein L23a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36723]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271465","summary":null,"start":11006399,"end":11006876,"strand":-1,"description":"ribosomal protein L23a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36723]"}, {"versioned_ensembl_gene_id":"ENSG00000106443.15","gene_symbol":"PHF14","gene_name":"PHD finger protein 14 [Source:HGNC Symbol;Acc:HGNC:22203]","synonyms":"KIAA0783","biotype":"protein_coding","ncbi_id":"9678","summary":null,"start":10973872,"end":11169630,"strand":1,"description":"PHD finger protein 14 [Source:HGNC Symbol;Acc:HGNC:22203]"}, {"versioned_ensembl_gene_id":"ENSG00000227925.1","gene_symbol":"LINC01655","gene_name":"long intergenic non-protein coding RNA 1655 [Source:HGNC Symbol;Acc:HGNC:52443]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929771","summary":null,"start":221827666,"end":221840666,"strand":-1,"description":"long intergenic non-protein coding RNA 1655 [Source:HGNC Symbol;Acc:HGNC:52443]"}, {"versioned_ensembl_gene_id":"ENSG00000266450.1","gene_symbol":"AC019183.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1655177,"end":1779955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204648.11","gene_symbol":"SSX9","gene_name":"SSX family member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:19655]","synonyms":"SSX9P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"280660","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene appears not to be involved in this type of chromosome translocation. [provided by RefSeq, Jul 2008]","start":48296816,"end":48306179,"strand":-1,"description":"SSX family member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:19655]"}, {"versioned_ensembl_gene_id":"ENSG00000238042.5","gene_symbol":"LINC02257","gene_name":"long intergenic non-protein coding RNA 2257 [Source:HGNC Symbol;Acc:HGNC:53159]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221880981,"end":221978523,"strand":-1,"description":"long intergenic non-protein coding RNA 2257 [Source:HGNC Symbol;Acc:HGNC:53159]"}, {"versioned_ensembl_gene_id":"ENSG00000204368.6","gene_symbol":"AC245047.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48212791,"end":48218010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228437.5","gene_symbol":"LINC02474","gene_name":"long intergenic non-protein coding RNA 2474 [Source:HGNC Symbol;Acc:HGNC:53417]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221966341,"end":221984964,"strand":1,"description":"long intergenic non-protein coding RNA 2474 [Source:HGNC Symbol;Acc:HGNC:53417]"}, {"versioned_ensembl_gene_id":"ENSG00000197566.9","gene_symbol":"ZNF624","gene_name":"zinc finger protein 624 [Source:HGNC Symbol;Acc:HGNC:29254]","synonyms":"KIAA1349","biotype":"protein_coding","ncbi_id":"57547","summary":null,"start":16620737,"end":16653856,"strand":-1,"description":"zinc finger protein 624 [Source:HGNC Symbol;Acc:HGNC:29254]"}, {"versioned_ensembl_gene_id":"ENSG00000237345.1","gene_symbol":"AC245047.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48279423,"end":48281792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225981.1","gene_symbol":"AC102953.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1459937,"end":1464008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232813.1","gene_symbol":"AC245047.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48274904,"end":48275047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234780.1","gene_symbol":"AC245047.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48197221,"end":48199431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231568.1","gene_symbol":"AC245047.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48228833,"end":48228959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165583.14","gene_symbol":"SSX5","gene_name":"SSX family member 5 [Source:HGNC Symbol;Acc:HGNC:11339]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6758","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. While some of the related SSX genes are involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas, this gene does not appear to be involved in such translocations. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2013]","start":48186220,"end":48196763,"strand":-1,"description":"SSX family member 5 [Source:HGNC Symbol;Acc:HGNC:11339]"}, {"versioned_ensembl_gene_id":"ENSG00000225513.1","gene_symbol":"AL158824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112173522,"end":112173971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144834.13","gene_symbol":"TAGLN3","gene_name":"transgelin 3 [Source:HGNC Symbol;Acc:HGNC:29868]","synonyms":"NP25,NP22","biotype":"protein_coding","ncbi_id":"29114","summary":null,"start":111998664,"end":112013887,"strand":1,"description":"transgelin 3 [Source:HGNC Symbol;Acc:HGNC:29868]"}, {"versioned_ensembl_gene_id":"ENSG00000251132.1","gene_symbol":"AC094104.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115031273,"end":115031894,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250242.1","gene_symbol":"AC094104.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115087892,"end":115088475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114446.4","gene_symbol":"IFT57","gene_name":"intraflagellar transport 57 [Source:HGNC Symbol;Acc:HGNC:17367]","synonyms":"FLJ10147,ESRRBL1,MHS4R2,HIPPI","biotype":"protein_coding","ncbi_id":"55081","summary":null,"start":108160812,"end":108222570,"strand":-1,"description":"intraflagellar transport 57 [Source:HGNC Symbol;Acc:HGNC:17367]"}, {"versioned_ensembl_gene_id":"ENSG00000108641.14","gene_symbol":"B9D1","gene_name":"B9 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24123]","synonyms":"MKS9,EPPB9,B9","biotype":"protein_coding","ncbi_id":"27077","summary":"This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]","start":19337554,"end":19378182,"strand":-1,"description":"B9 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24123]"}, {"versioned_ensembl_gene_id":"ENSG00000198739.10","gene_symbol":"LRRTM3","gene_name":"leucine rich repeat transmembrane neuronal 3 [Source:HGNC Symbol;Acc:HGNC:19410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347731","summary":null,"start":66926006,"end":67099830,"strand":1,"description":"leucine rich repeat transmembrane neuronal 3 [Source:HGNC Symbol;Acc:HGNC:19410]"}, {"versioned_ensembl_gene_id":"ENSG00000108821.13","gene_symbol":"COL1A1","gene_name":"collagen type I alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2197]","synonyms":"OI4","biotype":"protein_coding","ncbi_id":"1277","summary":"This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]","start":50183289,"end":50201632,"strand":-1,"description":"collagen type I alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2197]"}, {"versioned_ensembl_gene_id":"ENSG00000112494.9","gene_symbol":"UNC93A","gene_name":"unc-93 homolog A (C. elegans) [Source:HGNC Symbol;Acc:HGNC:12570]","synonyms":"dJ366N23.2,dJ366N23.1","biotype":"protein_coding","ncbi_id":"54346","summary":null,"start":167271169,"end":167316019,"strand":1,"description":"unc-93 homolog A (C. elegans) [Source:HGNC Symbol;Acc:HGNC:12570]"}, {"versioned_ensembl_gene_id":"ENSG00000248693.1","gene_symbol":"LINC02100","gene_name":"long intergenic non-protein coding RNA 2100 [Source:HGNC Symbol;Acc:HGNC:52955]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986408","summary":null,"start":18704433,"end":18746173,"strand":-1,"description":"long intergenic non-protein coding RNA 2100 [Source:HGNC Symbol;Acc:HGNC:52955]"}, {"versioned_ensembl_gene_id":"ENSG00000249191.1","gene_symbol":"UBE2V1P12","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:44897]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479048","summary":null,"start":18886622,"end":18887095,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:44897]"}, {"versioned_ensembl_gene_id":"ENSG00000249927.1","gene_symbol":"AC025768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18893902,"end":18894168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148516.21","gene_symbol":"ZEB1","gene_name":"zinc finger E-box binding homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11642]","synonyms":"Zfhx1a,Zfhep,ZEB,TCF8,PPCD3,NIL-2-A,FECD6,BZP,AREB6","biotype":"protein_coding","ncbi_id":"6935","summary":"This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010]","start":31318495,"end":31529814,"strand":1,"description":"zinc finger E-box binding homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11642]"}, {"versioned_ensembl_gene_id":"ENSG00000132294.14","gene_symbol":"EFR3A","gene_name":"EFR3 homolog A [Source:HGNC Symbol;Acc:HGNC:28970]","synonyms":"KIAA0143","biotype":"protein_coding","ncbi_id":"23167","summary":"The protein encoded by this gene is part of a complex that plays a role in maintaining an active pool of phosphatidylinositol 4-kinase (PI4K) at the plasma membrane. This protein is thought to be a peripheral membrane protein that associates with the plasma membrane through palmitoylation. Studies indicate that this gene product plays a role in controlling G protein-coupled receptor (GPCR) activity by affecting receptor phosphorylation. Whole exome sequencing studies have implicated mutations in this gene with autism spectrum disorders. [provided by RefSeq, Apr 2016]","start":131904088,"end":132013642,"strand":1,"description":"EFR3 homolog A [Source:HGNC Symbol;Acc:HGNC:28970]"}, {"versioned_ensembl_gene_id":"ENSG00000135334.8","gene_symbol":"AKIRIN2","gene_name":"akirin 2 [Source:HGNC Symbol;Acc:HGNC:21407]","synonyms":"FLJ10342,dJ486L4.2,C6orf166","biotype":"protein_coding","ncbi_id":"55122","summary":null,"start":87675072,"end":87702209,"strand":-1,"description":"akirin 2 [Source:HGNC Symbol;Acc:HGNC:21407]"}, {"versioned_ensembl_gene_id":"ENSG00000172186.7","gene_symbol":"HMGN1P35","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39379]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874448","summary":null,"start":69174124,"end":69174717,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39379]"}, {"versioned_ensembl_gene_id":"ENSG00000236978.1","gene_symbol":"AC073873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70837738,"end":70838013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196235.13","gene_symbol":"SUPT5H","gene_name":"SPT5 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11469]","synonyms":"SPT5H,SPT5,FLJ34157","biotype":"protein_coding","ncbi_id":"6829","summary":null,"start":39436156,"end":39476670,"strand":1,"description":"SPT5 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11469]"}, {"versioned_ensembl_gene_id":"ENSG00000215162.1","gene_symbol":"LINC00269","gene_name":"long intergenic non-protein coding RNA 269 [Source:HGNC Symbol;Acc:HGNC:26586]","synonyms":"NCRNA00269,FLJ33610,CXorf62","biotype":"lincRNA","ncbi_id":"100996279","summary":null,"start":69179557,"end":69209924,"strand":1,"description":"long intergenic non-protein coding RNA 269 [Source:HGNC Symbol;Acc:HGNC:26586]"}, {"versioned_ensembl_gene_id":"ENSG00000160392.13","gene_symbol":"C19orf47","gene_name":"chromosome 19 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:26723]","synonyms":"FLJ36888","biotype":"protein_coding","ncbi_id":"126526","summary":null,"start":40319536,"end":40348527,"strand":-1,"description":"chromosome 19 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:26723]"}, {"versioned_ensembl_gene_id":"ENSG00000072736.18","gene_symbol":"NFATC3","gene_name":"nuclear factor of activated T-cells 3 [Source:HGNC Symbol;Acc:HGNC:7777]","synonyms":"NFATX,NFAT4","biotype":"protein_coding","ncbi_id":"4775","summary":"The product of this gene is a member of the nuclear factors of activated T cells DNA-binding transcription complex. This complex consists of at least two components: a preexisting cytosolic component that translocates to the nucleus upon T cell receptor (TCR) stimulation and an inducible nuclear component. Other members of this family participate to form this complex also. The product of this gene plays a role in the regulation of gene expression in T cells and immature thymocytes. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Nov 2010]","start":68084751,"end":68229259,"strand":1,"description":"nuclear factor of activated T-cells 3 [Source:HGNC Symbol;Acc:HGNC:7777]"}, {"versioned_ensembl_gene_id":"ENSG00000233521.5","gene_symbol":"LINC01638","gene_name":"long intergenic non-protein coding RNA 1638 [Source:HGNC Symbol;Acc:HGNC:52425]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372978","summary":null,"start":27221349,"end":27224727,"strand":-1,"description":"long intergenic non-protein coding RNA 1638 [Source:HGNC Symbol;Acc:HGNC:52425]"}, {"versioned_ensembl_gene_id":"ENSG00000230876.6","gene_symbol":"LINC00486","gene_name":"long intergenic non-protein coding RNA 486 [Source:HGNC Symbol;Acc:HGNC:42946]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285045","summary":null,"start":32825443,"end":32926693,"strand":1,"description":"long intergenic non-protein coding RNA 486 [Source:HGNC Symbol;Acc:HGNC:42946]"}, {"versioned_ensembl_gene_id":"ENSG00000282349.1","gene_symbol":"AC237298.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76515627,"end":76520574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267061.1","gene_symbol":"AC090213.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59563709,"end":59568615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233574.1","gene_symbol":"AL020994.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27276240,"end":27286349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276184.4","gene_symbol":"UPK3B","gene_name":"uroplakin 3B [Source:HGNC Symbol;Acc:HGNC:21444]","synonyms":"UPIIIb,p35,MGC10902,FLJ32198","biotype":"protein_coding","ncbi_id":"105375355","summary":"UPK3B is a minor component of the apical plaques of mammalian urothelium that binds and dimerizes with uroplakin-1b (UPK1B; MIM 602380), one of the major conserved urothelium membrane proteins. The other major conserved integral membrane proteins of urothelial plaques are UPK1A (MIM 611557), UPK2 (MIM 611558), and UPK3A (MIM 611559) (Deng et al., 2002 [PubMed 12446744]).[supplied by OMIM, Mar 2008]","start":76510496,"end":76515744,"strand":1,"description":"uroplakin 3B [Source:HGNC Symbol;Acc:HGNC:21444]"}, {"versioned_ensembl_gene_id":"ENSG00000267000.1","gene_symbol":"AC016229.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59459072,"end":59465682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223726.1","gene_symbol":"AL020994.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27307483,"end":27318538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267774.2","gene_symbol":"AC010776.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59696459,"end":59698111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226741.1","gene_symbol":"LINC02554","gene_name":"long intergenic non-protein coding RNA 2554 [Source:HGNC Symbol;Acc:HGNC:53594]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507657","summary":null,"start":27310651,"end":27317456,"strand":1,"description":"long intergenic non-protein coding RNA 2554 [Source:HGNC Symbol;Acc:HGNC:53594]"}, {"versioned_ensembl_gene_id":"ENSG00000183287.13","gene_symbol":"CCBE1","gene_name":"collagen and calcium binding EGF domains 1 [Source:HGNC Symbol;Acc:HGNC:29426]","synonyms":"KIAA1983,FLJ30681","biotype":"protein_coding","ncbi_id":"147372","summary":"This gene is thought to function in extracellular matrix remodeling and migration. It is predominantly expressed in the ovary, but down regulated in ovarian cancer cell lines and primary carcinomas, suggesting its role as a tumour suppressor. Mutations in this gene have been associated with Hennekam lymphangiectasia-lymphedema syndrome, a generalized lymphatic dysplasia in humans. [provided by RefSeq, Mar 2010]","start":59430940,"end":59697380,"strand":-1,"description":"collagen and calcium binding EGF domains 1 [Source:HGNC Symbol;Acc:HGNC:29426]"}, {"versioned_ensembl_gene_id":"ENSG00000249285.1","gene_symbol":"AC114981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18908866,"end":18909543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236854.1","gene_symbol":"AL121656.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32927127,"end":32928405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257342.1","gene_symbol":"AC025165.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57694132,"end":57721510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213246.6","gene_symbol":"SUPT4H1","gene_name":"SPT4 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11467]","synonyms":"Spt4,SUPT4H,Supt4a,SPT4H","biotype":"protein_coding","ncbi_id":"6827","summary":"This gene encodes the small subunit of DRB (5,6-dichloro-1-beta-d-ribofuranosylbenzimidazole) sensitivity-inducing factor (DSIF) complex, which regulates mRNA processing and transcription elongation by RNA polymerase II. The encoded protein is localized to the nucleus and interacts with the large subunit (SUPT5H) to form the DSIF complex. Related pseudogenes have been identified on chromosomes 2 and 12. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2012]","start":58345175,"end":58353093,"strand":-1,"description":"SPT4 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11467]"}, {"versioned_ensembl_gene_id":"ENSG00000225299.1","gene_symbol":"AL139240.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67052609,"end":67055028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271643.1","gene_symbol":"AC112220.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33795688,"end":33796950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226448.1","gene_symbol":"RPL7AP51","gene_name":"ribosomal protein L7a pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271533","summary":null,"start":67334123,"end":67334882,"strand":1,"description":"ribosomal protein L7a pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36826]"}, {"versioned_ensembl_gene_id":"ENSG00000239327.1","gene_symbol":"AL163195.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20616644,"end":20616991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280364.1","gene_symbol":"AC005858.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126106459,"end":126107047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135506.15","gene_symbol":"OS9","gene_name":"OS9, endoplasmic reticulum lectin [Source:HGNC Symbol;Acc:HGNC:16994]","synonyms":"OS-9,ERLEC2","biotype":"protein_coding","ncbi_id":"10956","summary":"This gene encodes a protein that is highly expressed in osteosarcomas. This protein binds to the hypoxia-inducible factor 1 (HIF-1), a key regulator of the hypoxic response and angiogenesis, and promotes the degradation of one of its subunits. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":57693955,"end":57721557,"strand":1,"description":"OS9, endoplasmic reticulum lectin [Source:HGNC Symbol;Acc:HGNC:16994]"}, {"versioned_ensembl_gene_id":"ENSG00000271020.1","gene_symbol":"AC112220.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33797149,"end":33797681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277056.1","gene_symbol":"AL607023.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66837457,"end":66837704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273360.1","gene_symbol":"AC022017.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66079243,"end":66118326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115944.14","gene_symbol":"COX7A2L","gene_name":"cytochrome c oxidase subunit 7A2 like [Source:HGNC Symbol;Acc:HGNC:2289]","synonyms":"SIG81,EB1,COX7RP,COX7AR","biotype":"protein_coding","ncbi_id":"9167","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein similar to polypeptides 1 and 2 of subunit VIIa in the C-terminal region, and also highly similar to the mouse Sig81 protein sequence. This gene is expressed in all tissues, and upregulated in a breast cancer cell line after estrogen treatment. It is possible that this gene represents a regulatory subunit of COX and mediates the higher level of energy production in target cells by estrogen. Several transcript variants, some protein-coding and others non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016]","start":42333546,"end":42425088,"strand":-1,"description":"cytochrome c oxidase subunit 7A2 like [Source:HGNC Symbol;Acc:HGNC:2289]"}, {"versioned_ensembl_gene_id":"ENSG00000232832.1","gene_symbol":"LMLN-AS1","gene_name":"LMLN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40738]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873947","summary":null,"start":198038321,"end":198039234,"strand":-1,"description":"LMLN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40738]"}, {"versioned_ensembl_gene_id":"ENSG00000223760.4","gene_symbol":"MED15P9","gene_name":"mediator complex subunit 15 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44130]","synonyms":"MED15P2,CCDC74B-AS1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285103","summary":null,"start":130129621,"end":130139417,"strand":1,"description":"mediator complex subunit 15 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44130]"}, {"versioned_ensembl_gene_id":"ENSG00000237012.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30637275,"end":30643339,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000185621.11","gene_symbol":"LMLN","gene_name":"leishmanolysin like peptidase [Source:HGNC Symbol;Acc:HGNC:15991]","synonyms":"Msp,Gp63","biotype":"protein_coding","ncbi_id":"89782","summary":"This gene encodes a zinc-metallopeptidase. The encoded protein may play a role in cell migration and invasion. Studies of a similar protein in Drosophila indicate a potential role in mitotic progression. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":197960200,"end":198043720,"strand":1,"description":"leishmanolysin like peptidase [Source:HGNC Symbol;Acc:HGNC:15991]"}, {"versioned_ensembl_gene_id":"ENSG00000274468.1","gene_symbol":"AL512638.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":115479428,"end":115481572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267269.1","gene_symbol":"AC010776.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59685820,"end":59688400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111907.20","gene_symbol":"TPD52L1","gene_name":"tumor protein D52 like 1 [Source:HGNC Symbol;Acc:HGNC:12006]","synonyms":"hD53,D53","biotype":"protein_coding","ncbi_id":"7164","summary":"This gene encodes a member of a family of proteins that contain coiled-coil domains and may form hetero- or homomers. The encoded protein is involved in cell proliferation and calcium signaling. It also interacts with the mitogen-activated protein kinase kinase kinase 5 (MAP3K5/ASK1) and positively regulates MAP3K5-induced apoptosis. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2016]","start":125119049,"end":125264407,"strand":1,"description":"tumor protein D52 like 1 [Source:HGNC Symbol;Acc:HGNC:12006]"}, {"versioned_ensembl_gene_id":"ENSG00000231706.2","gene_symbol":"CYCSP43","gene_name":"cytochrome c, somatic pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:24417]","synonyms":"HCP43","biotype":"processed_pseudogene","ncbi_id":"360187","summary":null,"start":69485343,"end":69485652,"strand":-1,"description":"cytochrome c, somatic pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:24417]"}, {"versioned_ensembl_gene_id":"ENSG00000152076.18","gene_symbol":"CCDC74B","gene_name":"coiled-coil domain containing 74B [Source:HGNC Symbol;Acc:HGNC:25267]","synonyms":"DKFZp434E2321","biotype":"protein_coding","ncbi_id":"91409","summary":null,"start":130139287,"end":130145134,"strand":-1,"description":"coiled-coil domain containing 74B [Source:HGNC Symbol;Acc:HGNC:25267]"}, {"versioned_ensembl_gene_id":"ENSG00000108375.12","gene_symbol":"RNF43","gene_name":"ring finger protein 43 [Source:HGNC Symbol;Acc:HGNC:18505]","synonyms":"URCC,FLJ20315,DKFZp781H0392","biotype":"protein_coding","ncbi_id":"54894","summary":"The protein encoded by this gene is a RING-type E3 ubiquitin ligase and is predicted to contain a transmembrane domain, a protease-associated domain, an ectodomain, and a cytoplasmic RING domain. This protein is thought to negatively regulate Wnt signaling, and expression of this gene results in an increase in ubiquitination of frizzled receptors, an alteration in their subcellular distribution, resulting in reduced surface levels of these receptors. Mutations in this gene have been reported in multiple tumor cells, including colorectal and endometrial cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]","start":58352500,"end":58417595,"strand":-1,"description":"ring finger protein 43 [Source:HGNC Symbol;Acc:HGNC:18505]"}, {"versioned_ensembl_gene_id":"ENSG00000130054.4","gene_symbol":"FAM155B","gene_name":"family with sequence similarity 155 member B [Source:HGNC Symbol;Acc:HGNC:30701]","synonyms":"TMEM28,TED,CXorf63","biotype":"protein_coding","ncbi_id":"27112","summary":"This gene encodes a product belonging to a family of proteins with unknown function. The presence of two transmembrane domains suggests that this protein is a multi-pass membrane protein. [provided by RefSeq, Sep 2011]","start":69505241,"end":69532508,"strand":1,"description":"family with sequence similarity 155 member B [Source:HGNC Symbol;Acc:HGNC:30701]"}, {"versioned_ensembl_gene_id":"ENSG00000116138.12","gene_symbol":"DNAJC16","gene_name":"DnaJ heat shock protein family (Hsp40) member C16 [Source:HGNC Symbol;Acc:HGNC:29157]","synonyms":"KIAA0962","biotype":"protein_coding","ncbi_id":"23341","summary":null,"start":15526813,"end":15592379,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C16 [Source:HGNC Symbol;Acc:HGNC:29157]"}, {"versioned_ensembl_gene_id":"ENSG00000247765.2","gene_symbol":"AC068446.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21298233,"end":21325241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275839.1","gene_symbol":"AC243654.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37454171,"end":37454931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273965.1","gene_symbol":"AC243654.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37407936,"end":37408594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280703.1","gene_symbol":"AC060814.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21342171,"end":21343958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160396.8","gene_symbol":"HIPK4","gene_name":"homeodomain interacting protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:19007]","synonyms":"FLJ32818","biotype":"protein_coding","ncbi_id":"147746","summary":"This gene encodes a member of the homeodomain interacting protein kinase (HIPK) family of proteins. While other members of this family are found throughout vertebrates, this member is present only in mammals. Compared to other members of this family, the encoded protein lacks a nuclear localization signal and a C-terminal autoinhibitory domain. The encoded protein exhibits kinase activity and may phosphorylate the tumor suppressor protein p53. [provided by RefSeq, Jul 2016]","start":40379271,"end":40390187,"strand":-1,"description":"homeodomain interacting protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:19007]"}, {"versioned_ensembl_gene_id":"ENSG00000280881.1","gene_symbol":"AC060814.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21328380,"end":21343881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236608.1","gene_symbol":"EIF4A1P6","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390407","summary":null,"start":60636888,"end":60638097,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37925]"}, {"versioned_ensembl_gene_id":"ENSG00000276234.4","gene_symbol":"TADA2A","gene_name":"transcriptional adaptor 2A [Source:HGNC Symbol;Acc:HGNC:11531]","synonyms":"hADA2,ADA2A,ADA2,TADA2L","biotype":"protein_coding","ncbi_id":"6871","summary":"Many DNA-binding transcriptional activator proteins enhance the initiation rate of RNA polymerase II-mediated gene transcription by interacting functionally with the general transcription machinery bound at the basal promoter. Adaptor proteins are usually required for this activation, possibly to acetylate and destabilize nucleosomes, thereby relieving chromatin constraints at the promoter. The protein encoded by this gene is a transcriptional activator adaptor and has been found to be part of the PCAF histone acetylase complex. Several alternatively spliced transcript variants encoding different isoforms of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2009]","start":37406874,"end":37479730,"strand":1,"description":"transcriptional adaptor 2A [Source:HGNC Symbol;Acc:HGNC:11531]"}, {"versioned_ensembl_gene_id":"ENSG00000258415.2","gene_symbol":"AC060814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21344548,"end":21345085,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239780.1","gene_symbol":"AC090638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50457887,"end":50458795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235049.1","gene_symbol":"LINC00940","gene_name":"long intergenic non-protein coding RNA 940 [Source:HGNC Symbol;Acc:HGNC:48634]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100271702","summary":null,"start":1929202,"end":1936574,"strand":-1,"description":"long intergenic non-protein coding RNA 940 [Source:HGNC Symbol;Acc:HGNC:48634]"}, {"versioned_ensembl_gene_id":"ENSG00000180113.15","gene_symbol":"TDRD6","gene_name":"tudor domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21339]","synonyms":"SPATA36,NY-CO-45,CT41.2,bA446F17.4","biotype":"protein_coding","ncbi_id":"221400","summary":"This gene encodes a tudor domain-containing protein and component of the chromatoid body, a type of ribonucleoprotein granule present in male germ cells. Studies in rodents have demonstrated a role for the encoded protein in spermiogenesis and the nonsense mediated decay (NMD) pathway. This protein is a major autoantigen in human patients with autoimmune polyendocrine syndrome type 1 (APS1). [provided by RefSeq, Oct 2016]","start":46687875,"end":46704319,"strand":1,"description":"tudor domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21339]"}, {"versioned_ensembl_gene_id":"ENSG00000241832.1","gene_symbol":"CECR3","gene_name":"cat eye syndrome chromosome region, candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1841]","synonyms":null,"biotype":"lincRNA","ncbi_id":"27442","summary":null,"start":17256859,"end":17266733,"strand":-1,"description":"cat eye syndrome chromosome region, candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1841]"}, {"versioned_ensembl_gene_id":"ENSG00000280893.1","gene_symbol":"AC009133.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29812261,"end":29820092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279759.1","gene_symbol":"AC118344.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40355842,"end":40360606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157557.11","gene_symbol":"ETS2","gene_name":"ETS proto-oncogene 2, transcription factor [Source:HGNC Symbol;Acc:HGNC:3489]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2114","summary":"This gene encodes a transcription factor which regulates genes involved in development and apoptosis. The encoded protein is also a protooncogene and shown to be involved in regulation of telomerase. A pseudogene of this gene is located on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":38805307,"end":38824955,"strand":1,"description":"ETS proto-oncogene 2, transcription factor [Source:HGNC Symbol;Acc:HGNC:3489]"}, {"versioned_ensembl_gene_id":"ENSG00000242973.6","gene_symbol":"AL591242.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46670444,"end":46688165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167371.17","gene_symbol":"PRRT2","gene_name":"proline rich transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:30500]","synonyms":"PKC,IFITMD1,ICCA,FLJ25513,FICCA,EKD1,DYT10,DSPB3,DKFZp547J199","biotype":"protein_coding","ncbi_id":"112476","summary":"This gene encodes a transmembrane protein containing a proline-rich domain in its N-terminal half. Studies in mice suggest that it is predominantly expressed in brain and spinal cord in embryonic and postnatal stages. Mutations in this gene are associated with episodic kinesigenic dyskinesia-1. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":29811382,"end":29815892,"strand":1,"description":"proline rich transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:30500]"}, {"versioned_ensembl_gene_id":"ENSG00000232021.6","gene_symbol":"LEF1-AS1","gene_name":"LEF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40339]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"641518","summary":null,"start":108167525,"end":108256836,"strand":1,"description":"LEF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40339]"}, {"versioned_ensembl_gene_id":"ENSG00000262788.3","gene_symbol":"UTP4","gene_name":"UTP4, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:1983]","synonyms":"TEX292,NAIC,KIAA1988,FLJ14728,CIRHIN,CIRH1A","biotype":"protein_coding","ncbi_id":"84916","summary":"This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":69142116,"end":69169025,"strand":1,"description":"UTP4, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:1983]"}, {"versioned_ensembl_gene_id":"ENSG00000227567.7","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"G3a,ApoM,NG20","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31634594,"end":31640388,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000104738.16","gene_symbol":"MCM4","gene_name":"minichromosome maintenance complex component 4 [Source:HGNC Symbol;Acc:HGNC:6947]","synonyms":"P1-Cdc21,MGC33310,hCdc21,CDC54,CDC21","biotype":"protein_coding","ncbi_id":"4173","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 6 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of this protein by CDC2 kinase reduces the DNA helicase activity and chromatin binding of the MCM complex. This gene is mapped to a region on the chromosome 8 head-to-head next to the PRKDC/DNA-PK, a DNA-activated protein kinase involved in the repair of DNA double-strand breaks. Alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":47960185,"end":47978160,"strand":1,"description":"minichromosome maintenance complex component 4 [Source:HGNC Symbol;Acc:HGNC:6947]"}, {"versioned_ensembl_gene_id":"ENSG00000146070.16","gene_symbol":"PLA2G7","gene_name":"phospholipase A2 group VII [Source:HGNC Symbol;Acc:HGNC:9040]","synonyms":"PAFAH,LDL-PLA2","biotype":"protein_coding","ncbi_id":"7941","summary":"The protein encoded by this gene is a secreted enzyme that catalyzes the degradation of platelet-activating factor to biologically inactive products. Defects in this gene are a cause of platelet-activating factor acetylhydrolase deficiency. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2009]","start":46704201,"end":46735693,"strand":-1,"description":"phospholipase A2 group VII [Source:HGNC Symbol;Acc:HGNC:9040]"}, {"versioned_ensembl_gene_id":"ENSG00000148180.19","gene_symbol":"GSN","gene_name":"gelsolin [Source:HGNC Symbol;Acc:HGNC:4620]","synonyms":"DKFZp313L0718","biotype":"protein_coding","ncbi_id":"2934","summary":"The protein encoded by this gene binds to the \"plus\" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":121207794,"end":121332843,"strand":1,"description":"gelsolin [Source:HGNC Symbol;Acc:HGNC:4620]"}, {"versioned_ensembl_gene_id":"ENSG00000099399.5","gene_symbol":"MAGEB2","gene_name":"MAGE family member B2 [Source:HGNC Symbol;Acc:HGNC:6809]","synonyms":"DAM6,CT3.2,MGC26438,MAGE-XP-2","biotype":"protein_coding","ncbi_id":"4113","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is localized in the DSS (dosage-sensitive sex reversal) critical region. It is expressed in testis and placenta, and in a significant fraction of tumors of various histological types. The MAGEB genes are clustered on chromosome Xp22-p21. [provided by RefSeq, Jul 2008]","start":30215560,"end":30220089,"strand":1,"description":"MAGE family member B2 [Source:HGNC Symbol;Acc:HGNC:6809]"}, {"versioned_ensembl_gene_id":"ENSG00000256681.1","gene_symbol":"CCDC58P5","gene_name":"coiled-coil domain containing 58 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420588","summary":null,"start":73850469,"end":73851211,"strand":-1,"description":"coiled-coil domain containing 58 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45028]"}, {"versioned_ensembl_gene_id":"ENSG00000281950.1","gene_symbol":"SPDYE16","gene_name":"speedy/RINGO cell cycle regulator family member E16 [Source:HGNC Symbol;Acc:HGNC:51512]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723555","summary":null,"start":76519194,"end":76529340,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E16 [Source:HGNC Symbol;Acc:HGNC:51512]"}, {"versioned_ensembl_gene_id":"ENSG00000237586.3","gene_symbol":"AC090192.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124301315,"end":124301804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175581.13","gene_symbol":"MRPL48","gene_name":"mitochondrial ribosomal protein L48 [Source:HGNC Symbol;Acc:HGNC:16653]","synonyms":"CGI-118","biotype":"protein_coding","ncbi_id":"51642","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. A pseudogene corresponding to this gene is found on chromosome 6p. Several transcript variants, some protein-coding and some non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016]","start":73787316,"end":73865133,"strand":1,"description":"mitochondrial ribosomal protein L48 [Source:HGNC Symbol;Acc:HGNC:16653]"}, {"versioned_ensembl_gene_id":"ENSG00000034533.11","gene_symbol":"ASTE1","gene_name":"asteroid homolog 1 [Source:HGNC Symbol;Acc:HGNC:25021]","synonyms":"HT001","biotype":"protein_coding","ncbi_id":"28990","summary":null,"start":131013875,"end":131027649,"strand":-1,"description":"asteroid homolog 1 [Source:HGNC Symbol;Acc:HGNC:25021]"}, {"versioned_ensembl_gene_id":"ENSG00000138795.9","gene_symbol":"LEF1","gene_name":"lymphoid enhancer binding factor 1 [Source:HGNC Symbol;Acc:HGNC:6551]","synonyms":"TCF7L3,TCF1ALPHA,TCF10","biotype":"protein_coding","ncbi_id":"51176","summary":"This gene encodes a transcription factor belonging to a family of proteins that share homology with the high mobility group protein-1. The protein encoded by this gene can bind to a functionally important site in the T-cell receptor-alpha enhancer, thereby conferring maximal enhancer activity. This transcription factor is involved in the Wnt signaling pathway, and it may function in hair cell differentiation and follicle morphogenesis. Mutations in this gene have been found in somatic sebaceous tumors. This gene has also been linked to other cancers, including androgen-independent prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":108047545,"end":108168956,"strand":-1,"description":"lymphoid enhancer binding factor 1 [Source:HGNC Symbol;Acc:HGNC:6551]"}, {"versioned_ensembl_gene_id":"ENSG00000145835.6","gene_symbol":"CDKN2AIPNLP2","gene_name":"CDKN2A interacting protein N-terminal like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128579","summary":null,"start":26827169,"end":26827520,"strand":-1,"description":"CDKN2A interacting protein N-terminal like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39855]"}, {"versioned_ensembl_gene_id":"ENSG00000164983.7","gene_symbol":"TMEM65","gene_name":"transmembrane protein 65 [Source:HGNC Symbol;Acc:HGNC:25203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"157378","summary":null,"start":124306189,"end":124372692,"strand":-1,"description":"transmembrane protein 65 [Source:HGNC Symbol;Acc:HGNC:25203]"}, {"versioned_ensembl_gene_id":"ENSG00000198798.5","gene_symbol":"MAGEB3","gene_name":"MAGE family member B3 [Source:HGNC Symbol;Acc:HGNC:6810]","synonyms":"CT3.5","biotype":"protein_coding","ncbi_id":"4114","summary":"This gene is a MAGE-B subfamily member of the MAGE gene family. MAGE family member proteins direct the expression of tumor antigens recognized on a human melanoma by autologous cytolytic T lymphocytes. There are two known clusters of MAGE genes on chromosome X. The members of the MAGE-A subfamily are located in the Xq28 region, while the members of the MAGE-B subfamily are clustered in the Xp21 region. [provided by RefSeq, Jul 2008]","start":30230436,"end":30237492,"strand":1,"description":"MAGE family member B3 [Source:HGNC Symbol;Acc:HGNC:6810]"}, {"versioned_ensembl_gene_id":"ENSG00000120289.11","gene_symbol":"MAGEB4","gene_name":"MAGE family member B4 [Source:HGNC Symbol;Acc:HGNC:6811]","synonyms":"MGC33144,CT3.6","biotype":"protein_coding","ncbi_id":"4115","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEB genes are clustered on chromosome Xp22-p21. This gene sequence ends in the first intron of MAGEB1, another family member. This gene is expressed in testis. [provided by RefSeq, Jul 2008]","start":30242052,"end":30244193,"strand":1,"description":"MAGE family member B4 [Source:HGNC Symbol;Acc:HGNC:6811]"}, {"versioned_ensembl_gene_id":"ENSG00000206422.2","gene_symbol":"LRRC30","gene_name":"leucine rich repeat containing 30 [Source:HGNC Symbol;Acc:HGNC:30219]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339291","summary":null,"start":7231125,"end":7232047,"strand":1,"description":"leucine rich repeat containing 30 [Source:HGNC Symbol;Acc:HGNC:30219]"}, {"versioned_ensembl_gene_id":"ENSG00000214107.7","gene_symbol":"MAGEB1","gene_name":"MAGE family member B1 [Source:HGNC Symbol;Acc:HGNC:6808]","synonyms":"MGC9322,MAGEL1,MAGE-Xp,DAM10,CT3.1","biotype":"protein_coding","ncbi_id":"4112","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is localized in the DSS (dosage-sensitive sex reversal) critical region, and expressed in testis and in a significant fraction of tumors of various histological types. This gene and other MAGEB members are clustered on chromosome Xp22-p21. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene, however, the full length nature of some variants has not been defined. [provided by RefSeq, Jul 2008]","start":30243730,"end":30252038,"strand":1,"description":"MAGE family member B1 [Source:HGNC Symbol;Acc:HGNC:6808]"}, {"versioned_ensembl_gene_id":"ENSG00000229539.1","gene_symbol":"AL353194.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3888239,"end":3888868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234455.1","gene_symbol":"AC067960.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121081437,"end":121088726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226298.1","gene_symbol":"RAD23BP3","gene_name":"RAD23 homolog B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9814]","synonyms":"RAD23BLP","biotype":"processed_pseudogene","ncbi_id":"54034","summary":null,"start":15694300,"end":15696581,"strand":-1,"description":"RAD23 homolog B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9814]"}, {"versioned_ensembl_gene_id":"ENSG00000260392.5","gene_symbol":"AC090518.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":56542952,"end":56629592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250190.1","gene_symbol":"LINC02364","gene_name":"long intergenic non-protein coding RNA 2364 [Source:HGNC Symbol;Acc:HGNC:53288]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723764","summary":null,"start":28996524,"end":29014594,"strand":1,"description":"long intergenic non-protein coding RNA 2364 [Source:HGNC Symbol;Acc:HGNC:53288]"}, {"versioned_ensembl_gene_id":"ENSG00000103126.14","gene_symbol":"AXIN1","gene_name":"axin 1 [Source:HGNC Symbol;Acc:HGNC:903]","synonyms":"PPP1R49","biotype":"protein_coding","ncbi_id":"8312","summary":"This gene encodes a cytoplasmic protein which contains a regulation of G-protein signaling (RGS) domain and a dishevelled and axin (DIX) domain. The encoded protein interacts with adenomatosis polyposis coli, catenin beta-1, glycogen synthase kinase 3 beta, protein phosphate 2, and itself. This protein functions as a negative regulator of the wingless-type MMTV integration site family, member 1 (WNT) signaling pathway and can induce apoptosis. The crystal structure of a portion of this protein, alone and in a complex with other proteins, has been resolved. Mutations in this gene have been associated with hepatocellular carcinoma, hepatoblastomas, ovarian endometriod adenocarcinomas, and medullablastomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":287440,"end":352673,"strand":-1,"description":"axin 1 [Source:HGNC Symbol;Acc:HGNC:903]"}, {"versioned_ensembl_gene_id":"ENSG00000248872.1","gene_symbol":"LINC02431","gene_name":"long intergenic non-protein coding RNA 2431 [Source:HGNC Symbol;Acc:HGNC:53362]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506122","summary":null,"start":171040602,"end":171059163,"strand":1,"description":"long intergenic non-protein coding RNA 2431 [Source:HGNC Symbol;Acc:HGNC:53362]"}, {"versioned_ensembl_gene_id":"ENSG00000276940.1","gene_symbol":"PLCE1P1","gene_name":"phospholipase C epsilon 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51906]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420075","summary":null,"start":30290047,"end":30290351,"strand":-1,"description":"phospholipase C epsilon 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51906]"}, {"versioned_ensembl_gene_id":"ENSG00000169297.7","gene_symbol":"NR0B1","gene_name":"nuclear receptor subfamily 0 group B member 1 [Source:HGNC Symbol;Acc:HGNC:7960]","synonyms":"DSS,DAX1,AHCH,AHC","biotype":"protein_coding","ncbi_id":"190","summary":"This gene encodes a protein that contains a DNA-binding domain. The encoded protein acts as a dominant-negative regulator of transcription which is mediated by the retinoic acid receptor. This protein also functions as an anti-testis gene by acting antagonistically to Sry. Mutations in this gene result in both X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism. [provided by RefSeq, Jul 2008]","start":30304206,"end":30309598,"strand":-1,"description":"nuclear receptor subfamily 0 group B member 1 [Source:HGNC Symbol;Acc:HGNC:7960]"}, {"versioned_ensembl_gene_id":"ENSG00000249525.1","gene_symbol":"AC034159.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171113789,"end":171114581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145246.13","gene_symbol":"ATP10D","gene_name":"ATPase phospholipid transporting 10D (putative) [Source:HGNC Symbol;Acc:HGNC:13549]","synonyms":"KIAA1487,ATPVD","biotype":"protein_coding","ncbi_id":"57205","summary":null,"start":47485288,"end":47593486,"strand":1,"description":"ATPase phospholipid transporting 10D (putative) [Source:HGNC Symbol;Acc:HGNC:13549]"}, {"versioned_ensembl_gene_id":"ENSG00000265206.5","gene_symbol":"AC004687.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58330884,"end":58332508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273230.1","gene_symbol":"AC102953.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1464497,"end":1467522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228257.1","gene_symbol":"AC010141.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21531839,"end":21534011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166482.11","gene_symbol":"MFAP4","gene_name":"microfibril associated protein 4 [Source:HGNC Symbol;Acc:HGNC:7035]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4239","summary":"This gene encodes a protein with similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in cell adhesion or intercellular interactions. The gene is located within the Smith-Magenis syndrome region. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":19383442,"end":19387240,"strand":-1,"description":"microfibril associated protein 4 [Source:HGNC Symbol;Acc:HGNC:7035]"}, {"versioned_ensembl_gene_id":"ENSG00000005379.15","gene_symbol":"TSPOAP1","gene_name":"TSPO associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16831]","synonyms":"PRAX-1,KIAA0612,BZRAP1,RIMBP1,RIM-BP1","biotype":"protein_coding","ncbi_id":"9256","summary":null,"start":58301228,"end":58328760,"strand":-1,"description":"TSPO associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16831]"}, {"versioned_ensembl_gene_id":"ENSG00000234414.7","gene_symbol":"RBMY1A1","gene_name":"RNA binding motif protein, Y-linked, family 1, member A1 [Source:HGNC Symbol;Acc:HGNC:9912]","synonyms":"YRRM2,YRRM1,RBM2,RBM1","biotype":"protein_coding","ncbi_id":"5940","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. This protein is thought to function as a splicing regulator during spermatogenesis. Multiple closely related paralogs of this gene are found in a gene cluster in the AZFb azoospermia factor region of chromosome Y. Most of these related copies are thought to be pseudogenes, though several likely encode functional proteins. [provided by RefSeq, Mar 2016]","start":21511372,"end":21549326,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member A1 [Source:HGNC Symbol;Acc:HGNC:9912]"}, {"versioned_ensembl_gene_id":"ENSG00000251080.1","gene_symbol":"AC024132.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27133996,"end":27140051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075336.11","gene_symbol":"TIMM21","gene_name":"translocase of inner mitochondrial membrane 21 [Source:HGNC Symbol;Acc:HGNC:25010]","synonyms":"TIM21,HSPC154,C18orf55","biotype":"protein_coding","ncbi_id":"29090","summary":null,"start":74148511,"end":74160530,"strand":1,"description":"translocase of inner mitochondrial membrane 21 [Source:HGNC Symbol;Acc:HGNC:25010]"}, {"versioned_ensembl_gene_id":"ENSG00000238045.9","gene_symbol":"AC009133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29808636,"end":29821252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251325.1","gene_symbol":"AC024132.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27262506,"end":27267254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120280.5","gene_symbol":"CXorf21","gene_name":"chromosome X open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:25667]","synonyms":"FLJ11577","biotype":"protein_coding","ncbi_id":"80231","summary":null,"start":30558824,"end":30577844,"strand":-1,"description":"chromosome X open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:25667]"}, {"versioned_ensembl_gene_id":"ENSG00000205830.1","gene_symbol":"AC024132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27207505,"end":27218404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268061.5","gene_symbol":"NAPA-AS1","gene_name":"NAPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44118]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505681","summary":null,"start":47484282,"end":47501597,"strand":1,"description":"NAPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44118]"}, {"versioned_ensembl_gene_id":"ENSG00000235865.2","gene_symbol":"GSN-AS1","gene_name":"GSN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23372]","synonyms":"MOST2,C9orf31","biotype":"antisense_RNA","ncbi_id":"57000","summary":null,"start":121280768,"end":121285530,"strand":-1,"description":"GSN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23372]"}, {"versioned_ensembl_gene_id":"ENSG00000249699.1","gene_symbol":"LINC02261","gene_name":"long intergenic non-protein coding RNA 2261 [Source:HGNC Symbol;Acc:HGNC:53173]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929199","summary":null,"start":27217479,"end":27282225,"strand":1,"description":"long intergenic non-protein coding RNA 2261 [Source:HGNC Symbol;Acc:HGNC:53173]"}, {"versioned_ensembl_gene_id":"ENSG00000214651.4","gene_symbol":"AL513122.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121238117,"end":121240089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277789.4","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160591,"end":54173655,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000174792.10","gene_symbol":"C4orf26","gene_name":"chromosome 4 open reading frame 26 [Source:HGNC Symbol;Acc:HGNC:26300]","synonyms":"FLJ23657,AI2A4","biotype":"protein_coding","ncbi_id":"152816","summary":"Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene is thought to encode an extracellular matrix acidic phosphoprotein that has a function in enamel mineralization during amelogenesis. Mutations in this gene are associated with recessive hypomineralized amelogenesis imperfecta. [provided by RefSeq, Oct 2012]","start":75556048,"end":75565885,"strand":1,"description":"chromosome 4 open reading frame 26 [Source:HGNC Symbol;Acc:HGNC:26300]"}, {"versioned_ensembl_gene_id":"ENSG00000237886.1","gene_symbol":"NALT1","gene_name":"NOTCH1 associated lncRNA in T-cell acute lymphoblastic leukemia 1 [Source:HGNC Symbol;Acc:HGNC:51192]","synonyms":"TCONS_l2_00029132,MIR4674HG,LINC01573","biotype":"antisense_RNA","ncbi_id":"101928483","summary":null,"start":136546212,"end":136549893,"strand":1,"description":"NOTCH1 associated lncRNA in T-cell acute lymphoblastic leukemia 1 [Source:HGNC Symbol;Acc:HGNC:51192]"}, {"versioned_ensembl_gene_id":"ENSG00000279861.1","gene_symbol":"AC073548.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47487638,"end":47489519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250858.1","gene_symbol":"IGBP1P5","gene_name":"immunoglobulin (CD79A) binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391642","summary":null,"start":27585145,"end":27586144,"strand":1,"description":"immunoglobulin (CD79A) binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43614]"}, {"versioned_ensembl_gene_id":"ENSG00000181458.10","gene_symbol":"TMEM45A","gene_name":"transmembrane protein 45A [Source:HGNC Symbol;Acc:HGNC:25480]","synonyms":"FLJ10134,DERP7","biotype":"protein_coding","ncbi_id":"55076","summary":null,"start":100492619,"end":100577444,"strand":1,"description":"transmembrane protein 45A [Source:HGNC Symbol;Acc:HGNC:25480]"}, {"versioned_ensembl_gene_id":"ENSG00000105402.7","gene_symbol":"NAPA","gene_name":"NSF attachment protein alpha [Source:HGNC Symbol;Acc:HGNC:7641]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8775","summary":"This gene encodes a member of the soluble NSF attachment protein (SNAP) family. SNAP proteins play a critical role in the docking and fusion of vesicles to target membranes as part of the 20S NSF-SNAP-SNARE complex. The encoded protein plays a role in the completion of membrane fusion by mediating the interaction of N-ethylmaleimide-sensitive factor (NSF) with the vesicle-associated and membrane-associated SNAP receptor (SNARE) complex, and stimulating the ATPase activity of NSF. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jun 2011]","start":47487637,"end":47515240,"strand":-1,"description":"NSF attachment protein alpha [Source:HGNC Symbol;Acc:HGNC:7641]"}, {"versioned_ensembl_gene_id":"ENSG00000279141.3","gene_symbol":"LINC01451","gene_name":"long intergenic non-protein coding RNA 1451 [Source:NCBI gene;Acc:401561]","synonyms":"HCCAT4","biotype":"lincRNA","ncbi_id":"401561","summary":null,"start":136612024,"end":136617181,"strand":-1,"description":"long intergenic non-protein coding RNA 1451 [Source:NCBI gene;Acc:401561]"}, {"versioned_ensembl_gene_id":"ENSG00000251579.1","gene_symbol":"AC055733.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130927754,"end":130928276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251410.1","gene_symbol":"AC007106.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27967723,"end":27985063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250592.1","gene_symbol":"AC055733.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130899414,"end":130929976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250038.5","gene_symbol":"AC109588.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28362279,"end":28402864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250608.1","gene_symbol":"AC010210.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":131325092,"end":131381475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225249.5","gene_symbol":"LINC00378","gene_name":"long intergenic non-protein coding RNA 378 [Source:HGNC Symbol;Acc:HGNC:42704]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926930","summary":null,"start":60685199,"end":60694528,"strand":1,"description":"long intergenic non-protein coding RNA 378 [Source:HGNC Symbol;Acc:HGNC:42704]"}, {"versioned_ensembl_gene_id":"ENSG00000153291.15","gene_symbol":"SLC25A27","gene_name":"solute carrier family 25 member 27 [Source:HGNC Symbol;Acc:HGNC:21065]","synonyms":"UCP4,FLJ33552","biotype":"protein_coding","ncbi_id":"9481","summary":"Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. Tissue specificity occurs for the different UCPs and the exact methods of how UCPs transfer H+/OH- are not known. UCPs contain the three homologous protein domains of MACPs. Transcripts of this gene are only detected in brain tissue and are specifically modulated by various environmental conditions. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011]","start":46652915,"end":46678193,"strand":1,"description":"solute carrier family 25 member 27 [Source:HGNC Symbol;Acc:HGNC:21065]"}, {"versioned_ensembl_gene_id":"ENSG00000284095.1","gene_symbol":"AC055733.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130868004,"end":130869357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167945.1","gene_symbol":"PRR25","gene_name":"proline rich 25 [Source:HGNC Symbol;Acc:HGNC:37230]","synonyms":"gs64","biotype":"protein_coding","ncbi_id":"388199","summary":null,"start":805443,"end":813861,"strand":1,"description":"proline rich 25 [Source:HGNC Symbol;Acc:HGNC:37230]"}, {"versioned_ensembl_gene_id":"ENSG00000249098.1","gene_symbol":"AC055733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130918226,"end":130919120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275438.1","gene_symbol":"AL031008.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":848525,"end":849065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279657.1","gene_symbol":"AL161901.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":60730176,"end":60733600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158482.10","gene_symbol":"SNX29P1","gene_name":"sorting nexin 29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31913]","synonyms":"RUNDC2B","biotype":"unprocessed_pseudogene","ncbi_id":"100652781","summary":null,"start":21376648,"end":21386064,"strand":1,"description":"sorting nexin 29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31913]"}, {"versioned_ensembl_gene_id":"ENSG00000250064.1","gene_symbol":"AC097480.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28435449,"end":28600275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228401.4","gene_symbol":"HSPC324","gene_name":"uncharacterized LOC101928612 [Source:NCBI gene;Acc:101928612]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928612","summary":null,"start":136648610,"end":136660421,"strand":-1,"description":"uncharacterized LOC101928612 [Source:NCBI gene;Acc:101928612]"}, {"versioned_ensembl_gene_id":"ENSG00000268531.3","gene_symbol":"AC060814.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21368459,"end":21370621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166033.11","gene_symbol":"HTRA1","gene_name":"HtrA serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:9476]","synonyms":"HtrA,ARMD7,PRSS11,IGFBP5-protease","biotype":"protein_coding","ncbi_id":"5654","summary":"This gene encodes a member of the trypsin family of serine proteases. This protein is a secreted enzyme that is proposed to regulate the availability of insulin-like growth factors (IGFs) by cleaving IGF-binding proteins. It has also been suggested to be a regulator of cell growth. Variations in the promoter region of this gene are the cause of susceptibility to age-related macular degeneration type 7. [provided by RefSeq, Jul 2008]","start":122461525,"end":122514908,"strand":1,"description":"HtrA serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:9476]"}, {"versioned_ensembl_gene_id":"ENSG00000227510.3","gene_symbol":"LINC01442","gene_name":"long intergenic non-protein coding RNA 1442 [Source:HGNC Symbol;Acc:HGNC:50764]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103456507","summary":null,"start":60917001,"end":60941768,"strand":1,"description":"long intergenic non-protein coding RNA 1442 [Source:HGNC Symbol;Acc:HGNC:50764]"}, {"versioned_ensembl_gene_id":"ENSG00000262879.5","gene_symbol":"AC068152.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46984045,"end":47100323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228797.2","gene_symbol":"FAM207BP","gene_name":"family with sequence similarity 207 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:39715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729535","summary":null,"start":18697003,"end":18697507,"strand":1,"description":"family with sequence similarity 207 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:39715]"}, {"versioned_ensembl_gene_id":"ENSG00000231004.2","gene_symbol":"CECR9","gene_name":"cat eye syndrome chromosome region, candidate 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1847]","synonyms":null,"biotype":"TEC","ncbi_id":"30847","summary":null,"start":17329034,"end":17329232,"strand":1,"description":"cat eye syndrome chromosome region, candidate 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1847]"}, {"versioned_ensembl_gene_id":"ENSG00000172889.15","gene_symbol":"EGFL7","gene_name":"EGF like domain multiple 7 [Source:HGNC Symbol;Acc:HGNC:20594]","synonyms":"ZNEU1","biotype":"protein_coding","ncbi_id":"51162","summary":"This gene encodes a secreted endothelial cell protein that contains two epidermal growth factor-like domains. The encoded protein may play a role in regulating vasculogenesis. This protein may be involved in the growth and proliferation of tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":136658856,"end":136672678,"strand":1,"description":"EGF like domain multiple 7 [Source:HGNC Symbol;Acc:HGNC:20594]"}, {"versioned_ensembl_gene_id":"ENSG00000230931.2","gene_symbol":"GXYLT1P1","gene_name":"glucoside xylosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101111","summary":null,"start":18724415,"end":18724904,"strand":-1,"description":"glucoside xylosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39676]"}, {"versioned_ensembl_gene_id":"ENSG00000271315.1","gene_symbol":"AC174048.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16149251,"end":16149394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250927.1","gene_symbol":"MESTP3","gene_name":"mesoderm specific transcript pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645641","summary":null,"start":28823244,"end":28824211,"strand":-1,"description":"mesoderm specific transcript pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38553]"}, {"versioned_ensembl_gene_id":"ENSG00000182574.8","gene_symbol":"Z97985.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100956593,"end":100957538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231331.1","gene_symbol":"AC103563.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94953161,"end":94953593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140545.14","gene_symbol":"MFGE8","gene_name":"milk fat globule-EGF factor 8 protein [Source:HGNC Symbol;Acc:HGNC:7036]","synonyms":"OAcGD3S,MFG-E8,HsT19888,hP47,EDIL1,BA46,SPAG10,SED1","biotype":"protein_coding","ncbi_id":"4240","summary":"This gene encodes a preproprotein that is proteolytically processed to form multiple protein products. The major encoded protein product, lactadherin, is a membrane glycoprotein that promotes phagocytosis of apoptotic cells. This protein has also been implicated in wound healing, autoimmune disease, and cancer. Lactadherin can be further processed to form a smaller cleavage product, medin, which comprises the major protein component of aortic medial amyloid (AMA). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":88898683,"end":88913411,"strand":-1,"description":"milk fat globule-EGF factor 8 protein [Source:HGNC Symbol;Acc:HGNC:7036]"}, {"versioned_ensembl_gene_id":"ENSG00000134222.16","gene_symbol":"PSRC1","gene_name":"proline and serine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:24472]","synonyms":"DDA3","biotype":"protein_coding","ncbi_id":"84722","summary":"This gene encodes a proline-rich protein that is a target for regulation by the tumor suppressor protein p53. The encoded protein plays an important role in mitosis by recruiting and regulating microtubule depolymerases that destabalize microtubules. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Apr 2014]","start":109279556,"end":109283186,"strand":-1,"description":"proline and serine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:24472]"}, {"versioned_ensembl_gene_id":"ENSG00000099800.7","gene_symbol":"TIMM13","gene_name":"translocase of inner mitochondrial membrane 13 [Source:HGNC Symbol;Acc:HGNC:11816]","synonyms":"TIMM13B,Tim13","biotype":"protein_coding","ncbi_id":"26517","summary":"This gene encodes a member of the evolutionarily conserved TIMM (translocase of inner mitochondrial membrane) family of proteins that function as chaperones in the import of proteins from the cytoplasm into the mitochondrial inner membrane. Proteins of this family play a role in collecting substrate proteins from the translocase of the outer mitochondrial membrane (TOM) complex and delivering them to either the sorting and assembly machinery in the outer mitochondrial membrane (SAM) complex or the TIMM22 complex in the inner mitochondrial membrane. The encoded protein and the translocase of mitochondrial inner membrane 8a protein form a 70 kDa complex in the intermembrane space. [provided by RefSeq, Jul 2013]","start":2425624,"end":2427894,"strand":-1,"description":"translocase of inner mitochondrial membrane 13 [Source:HGNC Symbol;Acc:HGNC:11816]"}, {"versioned_ensembl_gene_id":"ENSG00000242875.6","gene_symbol":"RBMY1B","gene_name":"RNA binding motif protein, Y-linked, family 1, member B [Source:HGNC Symbol;Acc:HGNC:23914]","synonyms":null,"biotype":"protein_coding","ncbi_id":"378948","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. This protein likely functions as a splicing factor during spermatogenesis. Multiple closely related paralogs of this gene are found in a gene cluster in the AZFb azoospermia factor region of chromosome Y. Most of these related copies are thought to be pseudogenes, though several likely encode functional proteins. [provided by RefSeq, Mar 2016]","start":21511338,"end":21549094,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member B [Source:HGNC Symbol;Acc:HGNC:23914]"}, {"versioned_ensembl_gene_id":"ENSG00000084764.10","gene_symbol":"MAPRE3","gene_name":"microtubule associated protein RP/EB family member 3 [Source:HGNC Symbol;Acc:HGNC:6892]","synonyms":"RP3,EB3","biotype":"protein_coding","ncbi_id":"22924","summary":" The protein encoded by this gene is a member of the RP/EB family of genes. The protein localizes to the cytoplasmic microtubule network and binds APCL, a homolog of the adenomatous polyposis coli tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":26970612,"end":27027196,"strand":1,"description":"microtubule associated protein RP/EB family member 3 [Source:HGNC Symbol;Acc:HGNC:6892]"}, {"versioned_ensembl_gene_id":"ENSG00000244155.1","gene_symbol":"CYP4F34P","gene_name":"cytochrome P450 family 4 subfamily F member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:39953]","synonyms":"CYP4F-se7[6:7:8]","biotype":"unprocessed_pseudogene","ncbi_id":"100422247","summary":null,"start":18741730,"end":18742718,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:39953]"}, {"versioned_ensembl_gene_id":"ENSG00000179673.4","gene_symbol":"RPRML","gene_name":"reprimo like [Source:HGNC Symbol;Acc:HGNC:32422]","synonyms":"MGC43894","biotype":"protein_coding","ncbi_id":"388394","summary":null,"start":46978156,"end":46979248,"strand":-1,"description":"reprimo like [Source:HGNC Symbol;Acc:HGNC:32422]"}, {"versioned_ensembl_gene_id":"ENSG00000164932.12","gene_symbol":"CTHRC1","gene_name":"collagen triple helix repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:18831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115908","summary":"This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":103371515,"end":103382997,"strand":1,"description":"collagen triple helix repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:18831]"}, {"versioned_ensembl_gene_id":"ENSG00000263142.5","gene_symbol":"LRRC37A17P","gene_name":"leucine rich repeat containing 37 member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48365]","synonyms":"LRRC37A5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644397","summary":null,"start":46978481,"end":47054569,"strand":1,"description":"leucine rich repeat containing 37 member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48365]"}, {"versioned_ensembl_gene_id":"ENSG00000277377.4","gene_symbol":"SERPINA1","gene_name":"serpin family A member 1 [Source:HGNC Symbol;Acc:HGNC:8941]","synonyms":"alpha-1-antitrypsin,AAT,A1AT,A1A,PI1,PI,alpha1AT","biotype":"protein_coding","ncbi_id":"5265","summary":"The protein encoded by this gene is a serine protease inhibitor belonging to the serpin superfamily whose targets include elastase, plasmin, thrombin, trypsin, chymotrypsin, and plasminogen activator. This protein is produced in the liver, the bone marrow, by lymphocytic and monocytic cells in lymphoid tissue, and by the Paneth cells of the gut. Defects in this gene are associated with chronic obstructive pulmonary disease, emphysema, and chronic liver disease. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2020]","start":94378757,"end":94392703,"strand":-1,"description":"serpin family A member 1 [Source:HGNC Symbol;Acc:HGNC:8941]"}, {"versioned_ensembl_gene_id":"ENSG00000256232.1","gene_symbol":"LINC02387","gene_name":"long intergenic non-protein coding RNA 2387 [Source:HGNC Symbol;Acc:HGNC:53313]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929027","summary":null,"start":31363481,"end":31369301,"strand":-1,"description":"long intergenic non-protein coding RNA 2387 [Source:HGNC Symbol;Acc:HGNC:53313]"}, {"versioned_ensembl_gene_id":"ENSG00000227568.1","gene_symbol":"SNX18P26","gene_name":"sorting nexin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39634]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419038","summary":null,"start":18807279,"end":18808018,"strand":-1,"description":"sorting nexin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39634]"}, {"versioned_ensembl_gene_id":"ENSG00000020181.17","gene_symbol":"ADGRA2","gene_name":"adhesion G protein-coupled receptor A2 [Source:HGNC Symbol;Acc:HGNC:17849]","synonyms":"TEM5,KIAA1531,GPR124,FLJ14390,DKFZp434J0911,DKFZp434C211","biotype":"protein_coding","ncbi_id":"25960","summary":null,"start":37784191,"end":37844896,"strand":1,"description":"adhesion G protein-coupled receptor A2 [Source:HGNC Symbol;Acc:HGNC:17849]"}, {"versioned_ensembl_gene_id":"ENSG00000230194.1","gene_symbol":"AC000081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19238443,"end":19238739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178297.12","gene_symbol":"TMPRSS9","gene_name":"transmembrane protease, serine 9 [Source:HGNC Symbol;Acc:HGNC:30079]","synonyms":null,"biotype":"protein_coding","ncbi_id":"360200","summary":"The protein encoded by this gene is a membrane-bound type II serine polyprotease that is cleaved to release three different proteases. Two of the proteases are active and can be inhibited by serine protease inhibitors, and one is thought to be catalytically inactive. This gene enhances the invasive capability of pancreatic cancer cells and may be involved in cancer progression. [provided by RefSeq, Jul 2016]","start":2389771,"end":2426239,"strand":1,"description":"transmembrane protease, serine 9 [Source:HGNC Symbol;Acc:HGNC:30079]"}, {"versioned_ensembl_gene_id":"ENSG00000262633.2","gene_symbol":"AC005670.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46923133,"end":47049932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186732.13","gene_symbol":"MPPED1","gene_name":"metallophosphoesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1306]","synonyms":"C22orf1,239AB,FAM1A","biotype":"protein_coding","ncbi_id":"758","summary":null,"start":43411196,"end":43507848,"strand":1,"description":"metallophosphoesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1306]"}, {"versioned_ensembl_gene_id":"ENSG00000284666.1","gene_symbol":"Z98259.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5480787,"end":5482028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260972.1","gene_symbol":"Z98259.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5492978,"end":5494674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284692.1","gene_symbol":"Z98259.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5478736,"end":5493057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236145.1","gene_symbol":"AC079988.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121178327,"end":121182580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108433.16","gene_symbol":"GOSR2","gene_name":"golgi SNAP receptor complex member 2 [Source:HGNC Symbol;Acc:HGNC:4431]","synonyms":"GS27,Bos1","biotype":"protein_coding","ncbi_id":"9570","summary":"This gene encodes a trafficking membrane protein which transports proteins among the medial- and trans-Golgi compartments. Due to its chromosomal location and trafficking function, this gene may be involved in familial essential hypertension. [provided by RefSeq, Mar 2016]","start":46923075,"end":46975524,"strand":1,"description":"golgi SNAP receptor complex member 2 [Source:HGNC Symbol;Acc:HGNC:4431]"}, {"versioned_ensembl_gene_id":"ENSG00000267239.1","gene_symbol":"AP001198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13203774,"end":13216367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169764.15","gene_symbol":"UGP2","gene_name":"UDP-glucose pyrophosphorylase 2 [Source:HGNC Symbol;Acc:HGNC:12527]","synonyms":"UGPP1,UGP1","biotype":"protein_coding","ncbi_id":"7360","summary":"The enzyme encoded by this gene is an important intermediary in mammalian carbohydrate interconversions. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP-glucose and MgPPi. In liver and muscle tissue, UDP-glucose is a direct precursor of glycogen; in lactating mammary gland it is converted to UDP-galactose which is then converted to lactose. The eukaryotic enzyme has no significant sequence similarity to the prokaryotic enzyme. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63840940,"end":63891562,"strand":1,"description":"UDP-glucose pyrophosphorylase 2 [Source:HGNC Symbol;Acc:HGNC:12527]"}, {"versioned_ensembl_gene_id":"ENSG00000283356.1","gene_symbol":"Z97988.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5554747,"end":5554881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248254.1","gene_symbol":"AC107398.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47556731,"end":47560259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242431.2","gene_symbol":"AC107398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47490967,"end":47491471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225016.1","gene_symbol":"LINC00328-2P","gene_name":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]","synonyms":"NCRNA00328B,NCRNA00328-2P","biotype":"processed_pseudogene","ncbi_id":"100874404","summary":null,"start":18809830,"end":18810048,"strand":1,"description":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]"}, {"versioned_ensembl_gene_id":"ENSG00000236948.2","gene_symbol":"AL365255.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5561709,"end":5668295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232594.1","gene_symbol":"AC103563.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94961047,"end":94961503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183665.5","gene_symbol":"TRMT12","gene_name":"tRNA methyltransferase 12 homolog [Source:HGNC Symbol;Acc:HGNC:26091]","synonyms":"TYW2,Trm12,FLJ20772","biotype":"protein_coding","ncbi_id":"55039","summary":"Wybutosine (yW) is a hypermodified guanosine at the 3-prime position adjacent to the anticodon of phenylalanine tRNA that stabilizes codon-anticodon interactions during decoding on the ribosome. TRMT12 is the human homolog of a yeast gene essential for yW synthesis (Noma and Suzuki, 2006).[supplied by OMIM, Mar 2008]","start":124450820,"end":124462150,"strand":1,"description":"tRNA methyltransferase 12 homolog [Source:HGNC Symbol;Acc:HGNC:26091]"}, {"versioned_ensembl_gene_id":"ENSG00000115112.7","gene_symbol":"TFCP2L1","gene_name":"transcription factor CP2 like 1 [Source:HGNC Symbol;Acc:HGNC:17925]","synonyms":"LBP-9,CRTR1","biotype":"protein_coding","ncbi_id":"29842","summary":null,"start":121216587,"end":121285207,"strand":-1,"description":"transcription factor CP2 like 1 [Source:HGNC Symbol;Acc:HGNC:17925]"}, {"versioned_ensembl_gene_id":"ENSG00000206192.7","gene_symbol":"ANKRD20A9P","gene_name":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"284232","summary":null,"start":18816718,"end":18871967,"strand":-1,"description":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]"}, {"versioned_ensembl_gene_id":"ENSG00000248989.1","gene_symbol":"STK19B","gene_name":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]","synonyms":"bPG116M5.10,STK19P,RP2","biotype":"unprocessed_pseudogene","ncbi_id":"373159","summary":null,"start":32005925,"end":32006441,"strand":1,"description":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]"}, {"versioned_ensembl_gene_id":"ENSG00000182162.10","gene_symbol":"P2RY8","gene_name":"purinergic receptor P2Y8 [Source:HGNC Symbol;Acc:HGNC:15524]","synonyms":"P2Y8","biotype":"protein_coding","ncbi_id":"286530","summary":"The protein encoded by this gene belongs to the family of G-protein coupled receptors, that are preferentially activated by adenosine and uridine nucleotides. This gene is moderately expressed in undifferentiated HL60 cells, and is located on both chromosomes X and Y. [provided by RefSeq, Jul 2008]","start":1462572,"end":1537107,"strand":-1,"description":"purinergic receptor P2Y8 [Source:HGNC Symbol;Acc:HGNC:15524]"}, {"versioned_ensembl_gene_id":"ENSG00000245149.3","gene_symbol":"RNF139-AS1","gene_name":"RNF139 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48940]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927612","summary":null,"start":124462485,"end":124474576,"strand":-1,"description":"RNF139 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48940]"}, {"versioned_ensembl_gene_id":"ENSG00000280165.1","gene_symbol":"PCDH20","gene_name":"protocadherin 20 [Source:HGNC Symbol;Acc:HGNC:14257]","synonyms":"PCDH13,FLJ22218","biotype":"protein_coding","ncbi_id":"64881","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. This gene encodes a protein which contains 6 extracellular cadherin domains, a transmembrane domain and a cytoplasmic tail differing from those of the classical cadherins. Although its specific function is undetermined, the cadherin-related neuronal receptor is thought to play a role in the establishment and function of specific cell-cell connections in the brain. [provided by RefSeq, Jul 2008]","start":61409685,"end":61415522,"strand":-1,"description":"protocadherin 20 [Source:HGNC Symbol;Acc:HGNC:14257]"}, {"versioned_ensembl_gene_id":"ENSG00000237301.1","gene_symbol":"AL121992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15586136,"end":15603626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279797.1","gene_symbol":"LINC02339","gene_name":"long intergenic non-protein coding RNA 2339 [Source:HGNC Symbol;Acc:HGNC:53259]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926951","summary":null,"start":61424689,"end":61427946,"strand":-1,"description":"long intergenic non-protein coding RNA 2339 [Source:HGNC Symbol;Acc:HGNC:53259]"}, {"versioned_ensembl_gene_id":"ENSG00000116771.5","gene_symbol":"AGMAT","gene_name":"agmatinase [Source:HGNC Symbol;Acc:HGNC:18407]","synonyms":"FLJ23384","biotype":"protein_coding","ncbi_id":"79814","summary":null,"start":15572353,"end":15585110,"strand":-1,"description":"agmatinase [Source:HGNC Symbol;Acc:HGNC:18407]"}, {"versioned_ensembl_gene_id":"ENSG00000176619.12","gene_symbol":"LMNB2","gene_name":"lamin B2 [Source:HGNC Symbol;Acc:HGNC:6638]","synonyms":"LMN2","biotype":"protein_coding","ncbi_id":"84823","summary":"This gene encodes a B type nuclear lamin. The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Mutations in this gene are associated with acquired partial lipodystrophy. [provided by RefSeq, May 2012]","start":2427638,"end":2456996,"strand":-1,"description":"lamin B2 [Source:HGNC Symbol;Acc:HGNC:6638]"}, {"versioned_ensembl_gene_id":"ENSG00000197991.11","gene_symbol":"AL592490.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61409858,"end":61427849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172113.8","gene_symbol":"NME6","gene_name":"NME/NM23 nucleoside diphosphate kinase 6 [Source:HGNC Symbol;Acc:HGNC:20567]","synonyms":"NM23-H6,IPIA-ALPHA","biotype":"protein_coding","ncbi_id":"10201","summary":"Nucleoside diphosphate (NDP) kinases (EC 2.7.4.6), such as NME6, are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates (Mehus et al., 1999 [PubMed 10453732]).[supplied by OMIM, Jul 2010]","start":48293264,"end":48301685,"strand":-1,"description":"NME/NM23 nucleoside diphosphate kinase 6 [Source:HGNC Symbol;Acc:HGNC:20567]"}, {"versioned_ensembl_gene_id":"ENSG00000256263.1","gene_symbol":"DDX11L8","gene_name":"DEAD/H-box helicase 11 like 8 [Source:HGNC Symbol;Acc:HGNC:37101]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100302090","summary":null,"start":12310,"end":13501,"strand":1,"description":"DEAD/H-box helicase 11 like 8 [Source:HGNC Symbol;Acc:HGNC:37101]"}, {"versioned_ensembl_gene_id":"ENSG00000228520.3","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33186401,"end":33190628,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000223923.1","gene_symbol":"AC010136.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":217978707,"end":217992615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233105.1","gene_symbol":"AC103563.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94964473,"end":94964836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262411.1","gene_symbol":"LINC02066","gene_name":"long intergenic non-protein coding RNA 2066 [Source:HGNC Symbol;Acc:HGNC:52911]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374158","summary":null,"start":151637174,"end":151657956,"strand":1,"description":"long intergenic non-protein coding RNA 2066 [Source:HGNC Symbol;Acc:HGNC:52911]"}, {"versioned_ensembl_gene_id":"ENSG00000136936.10","gene_symbol":"XPA","gene_name":"XPA, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12814]","synonyms":"XPAC,XP1","biotype":"protein_coding","ncbi_id":"7507","summary":"This gene encodes a zinc finger protein plays a central role in nucleotide excision repair (NER), a specialized type of DNA repair. NER is responsible for repair of UV radiation-induced photoproducts and DNA adducts induced by chemical carcinogens and chemotherapeutic drugs. The encoded protein interacts with DNA and several NER proteins, acting as a scaffold to assemble the NER incision complex at sites of DNA damage. Mutations in this gene cause Xeroderma pigmentosum complementation group A (XP-A), an autosomal recessive skin disorder featuring hypersensitivity to sunlight and increased risk for skin cancer. [provided by RefSeq, Aug 2017]","start":97674909,"end":97697357,"strand":-1,"description":"XPA, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12814]"}, {"versioned_ensembl_gene_id":"ENSG00000249228.1","gene_symbol":"AC068944.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29046591,"end":29048765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181803.3","gene_symbol":"OR6S1","gene_name":"olfactory receptor family 6 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15363]","synonyms":"OR6S1Q","biotype":"protein_coding","ncbi_id":"341799","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20640696,"end":20641691,"strand":-1,"description":"olfactory receptor family 6 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15363]"}, {"versioned_ensembl_gene_id":"ENSG00000248176.1","gene_symbol":"AC109349.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29118308,"end":29202770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168874.12","gene_symbol":"ATOH8","gene_name":"atonal bHLH transcription factor 8 [Source:HGNC Symbol;Acc:HGNC:24126]","synonyms":"bHLHa21,FLJ14708,HATH6","biotype":"protein_coding","ncbi_id":"84913","summary":null,"start":85751344,"end":85788066,"strand":1,"description":"atonal bHLH transcription factor 8 [Source:HGNC Symbol;Acc:HGNC:24126]"}, {"versioned_ensembl_gene_id":"ENSG00000224585.1","gene_symbol":"AC103563.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94971954,"end":94972167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248338.1","gene_symbol":"LINC02472","gene_name":"long intergenic non-protein coding RNA 2472 [Source:HGNC Symbol;Acc:HGNC:53411]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374561","summary":null,"start":29214398,"end":29221162,"strand":1,"description":"long intergenic non-protein coding RNA 2472 [Source:HGNC Symbol;Acc:HGNC:53411]"}, {"versioned_ensembl_gene_id":"ENSG00000251373.1","gene_symbol":"AC092593.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29407100,"end":29408012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276548.1","gene_symbol":"AC008740.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21401089,"end":21401198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186714.12","gene_symbol":"CCDC73","gene_name":"coiled-coil domain containing 73 [Source:HGNC Symbol;Acc:HGNC:23261]","synonyms":"NY-SAR-79","biotype":"protein_coding","ncbi_id":"493860","summary":null,"start":32602246,"end":32794658,"strand":-1,"description":"coiled-coil domain containing 73 [Source:HGNC Symbol;Acc:HGNC:23261]"}, {"versioned_ensembl_gene_id":"ENSG00000233447.1","gene_symbol":"AC103563.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94974544,"end":94974838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160072.19","gene_symbol":"ATAD3B","gene_name":"ATPase family, AAA domain containing 3B [Source:HGNC Symbol;Acc:HGNC:24007]","synonyms":"TOB3,KIAA1273","biotype":"protein_coding","ncbi_id":"83858","summary":"The protein encoded by this gene is localized to the mitochondrial inner membrane, where it can bind to a highly-related protein, ATAD3A. ATAD3A appears to interact with matrix nucleoid complexes, and the encoded protein negatively regulates that interaction. This gene is expressed almost exclusively in pluripotent embryonic stem cells and some cancer cells. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":1471769,"end":1497848,"strand":1,"description":"ATPase family, AAA domain containing 3B [Source:HGNC Symbol;Acc:HGNC:24007]"}, {"versioned_ensembl_gene_id":"ENSG00000235186.1","gene_symbol":"AC103563.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94991880,"end":94994362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259171.1","gene_symbol":"AL163636.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":20684587,"end":20700576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272501.1","gene_symbol":"AL662844.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31195200,"end":31198037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251113.2","gene_symbol":"AC092593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29465701,"end":29467850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206344.7","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"lincRNA","ncbi_id":"253018","summary":null,"start":31197760,"end":31203968,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000105711.11","gene_symbol":"SCN1B","gene_name":"sodium voltage-gated channel beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:10586]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6324","summary":"Voltage-gated sodium channels are heteromeric proteins that function in the generation and propagation of action potentials in muscle and neuronal cells. They are composed of one alpha and two beta subunits, where the alpha subunit provides channel activity and the beta-1 subunit modulates the kinetics of channel inactivation. This gene encodes a sodium channel beta-1 subunit. Mutations in this gene result in generalized epilepsy with febrile seizures plus, Brugada syndrome 5, and defects in cardiac conduction. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":35030466,"end":35040449,"strand":1,"description":"sodium voltage-gated channel beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:10586]"}, {"versioned_ensembl_gene_id":"ENSG00000214274.9","gene_symbol":"ANG","gene_name":"angiogenin [Source:HGNC Symbol;Acc:HGNC:483]","synonyms":"RNASE5,RAA1","biotype":"protein_coding","ncbi_id":"283","summary":"The protein encoded by this gene is a member of the RNase A superfamily though it has relatively weak ribonucleolytic activity. This protein is a potent mediator of new blood vessel formation and thus, in addition to the name RNase5, is commonly called angiogenin. This protein induces angiogenesis after binding to actin on the surface of endothelial cells. This protein also accumulates at the nucleolus where it stimulates ribosomal transcription. Under stress conditions this protein translocates to the cytosol where it hydrolyzes cellular tRNAs and influences protein synthesis. A signal peptide is cleaved from the precursor protein to produce a mature protein which contains a nuclear localization signal, a cell binding motif, and a catalytic domain. This protein has been shown to be both neurotrophic and neuroprotective and the mature protein has antimicrobial activity against some bacteria and fungi, including S. pneumoniae and C. albicans. Due to its effect on rRNA production and angiogenesis this gene plays important roles in cell growth and tumor progression. Mutations in this gene are associated with progression of amyotrophic lateral sclerosis (ALS). This gene and the neighboring RNase4 gene share promoters and 5' exons though each gene then splices to a distinct 3' exon containing the complete coding region of each gene. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2020]","start":20684177,"end":20698971,"strand":1,"description":"angiogenin [Source:HGNC Symbol;Acc:HGNC:483]"}, {"versioned_ensembl_gene_id":"ENSG00000242756.2","gene_symbol":"RHOT1P3","gene_name":"ras homolog family member T1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37839]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462810","summary":null,"start":18837768,"end":18838098,"strand":-1,"description":"ras homolog family member T1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37839]"}, {"versioned_ensembl_gene_id":"ENSG00000248755.1","gene_symbol":"AC092639.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171169209,"end":171169942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248339.1","gene_symbol":"LINC02504","gene_name":"long intergenic non-protein coding RNA 2504 [Source:HGNC Symbol;Acc:HGNC:53493]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928288","summary":null,"start":171289475,"end":171298267,"strand":-1,"description":"long intergenic non-protein coding RNA 2504 [Source:HGNC Symbol;Acc:HGNC:53493]"}, {"versioned_ensembl_gene_id":"ENSG00000272510.1","gene_symbol":"AL121992.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15565611,"end":15565956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251176.1","gene_symbol":"AC074254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":171553000,"end":171564267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228216.1","gene_symbol":"AL355607.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90957260,"end":90965393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260965.1","gene_symbol":"RPL23AP91","gene_name":"ribosomal protein L23a pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:51625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480337","summary":null,"start":57321352,"end":57322117,"strand":1,"description":"ribosomal protein L23a pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:51625]"}, {"versioned_ensembl_gene_id":"ENSG00000134588.12","gene_symbol":"USP26","gene_name":"ubiquitin specific peptidase 26 [Source:HGNC Symbol;Acc:HGNC:13485]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83844","summary":"This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases and is a deubiquitinating enzyme (DUB) with His and Cys domains. It is specifically expressed in testis tissue. Mutations in this gene have been associated with Sertoli cell-only syndrome and male infertility. [provided by RefSeq, Jul 2008]","start":133024631,"end":133097109,"strand":-1,"description":"ubiquitin specific peptidase 26 [Source:HGNC Symbol;Acc:HGNC:13485]"}, {"versioned_ensembl_gene_id":"ENSG00000082516.8","gene_symbol":"GEMIN5","gene_name":"gem nuclear organelle associated protein 5 [Source:HGNC Symbol;Acc:HGNC:20043]","synonyms":null,"biotype":"protein_coding","ncbi_id":"25929","summary":"This gene encodes a WD repeat protein that is a component of the survival of motor neurons (SMN) complex. The SMN complex plays a critical role in mRNA splicing through the assembly of spliceosomal small nuclear ribonucleoproteins (snRNPs), and may also mediate the assembly and transport of other classes of ribonucleoproteins. The encoded protein is the snRNA-binding component of the SMN complex. Dysregulation of this gene may play a role in alternative mRNA splicing and tumor cell motility. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":154887416,"end":154938209,"strand":-1,"description":"gem nuclear organelle associated protein 5 [Source:HGNC Symbol;Acc:HGNC:20043]"}, {"versioned_ensembl_gene_id":"ENSG00000271821.1","gene_symbol":"AL662844.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31200165,"end":31201918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249297.1","gene_symbol":"LINC02174","gene_name":"long intergenic non-protein coding RNA 2174 [Source:HGNC Symbol;Acc:HGNC:53037]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377536","summary":null,"start":171602683,"end":171638763,"strand":-1,"description":"long intergenic non-protein coding RNA 2174 [Source:HGNC Symbol;Acc:HGNC:53037]"}, {"versioned_ensembl_gene_id":"ENSG00000230537.1","gene_symbol":"AL158071.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91104957,"end":91107304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237036.4","gene_symbol":"ZEB1-AS1","gene_name":"ZEB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42354]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"220930","summary":"This locus produces long non-coding RNA that is transcribed from a shared bi-directional promoter with zinc finger E-box binding homeobox 1 (ZEB1). This transcript binds lysine methyltransferase 2A and promotes histone modifications that are thought to promote expression of ZEB1. Expression of this gene is correlated with tumor progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]","start":31206278,"end":31320447,"strand":-1,"description":"ZEB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42354]"}, {"versioned_ensembl_gene_id":"ENSG00000104221.12","gene_symbol":"BRF2","gene_name":"BRF2, RNA polymerase III transcription initiation factor subunit [Source:HGNC Symbol;Acc:HGNC:17298]","synonyms":"TFIIIB50,FLJ11052,BRFU","biotype":"protein_coding","ncbi_id":"55290","summary":"This gene encodes one of the multiple subunits of the RNA polymerase III transcription factor complex required for transcription of genes with promoter elements upstream of the initiation site. The product of this gene, a TFIIB-like factor, is directly recruited to the TATA-box of polymerase III small nuclear RNA gene promoters through its interaction with the TATA-binding protein. [provided by RefSeq, Jul 2008]","start":37843268,"end":37849904,"strand":-1,"description":"BRF2, RNA polymerase III transcription initiation factor subunit [Source:HGNC Symbol;Acc:HGNC:17298]"}, {"versioned_ensembl_gene_id":"ENSG00000271456.1","gene_symbol":"AC108081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57332379,"end":57332599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233850.1","gene_symbol":"AC103563.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95025193,"end":95026709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258451.1","gene_symbol":"AL163636.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20693480,"end":20707120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231062.1","gene_symbol":"AC103563.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95051395,"end":95053176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223622.2","gene_symbol":"GSTA6P","gene_name":"glutathione S-transferase alpha 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:4630]","synonyms":"GSTAP1","biotype":"unprocessed_pseudogene","ncbi_id":"2942","summary":null,"start":52805613,"end":52813460,"strand":-1,"description":"glutathione S-transferase alpha 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:4630]"}, {"versioned_ensembl_gene_id":"ENSG00000237422.1","gene_symbol":"AL158071.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91119138,"end":91163087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274474.3","gene_symbol":"YWHAE","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Source:HGNC Symbol;Acc:HGNC:12851]","synonyms":"FLJ45465","biotype":"protein_coding","ncbi_id":"7531","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 100% identical to the mouse ortholog. It interacts with CDC25 phosphatases, RAF1 and IRS1 proteins, suggesting its role in diverse biochemical activities related to signal transduction, such as cell division and regulation of insulin sensitivity. It has also been implicated in the pathogenesis of small cell lung cancer. Two transcript variants, one protein-coding and the other non-protein-coding, have been found for this gene. [provided by RefSeq, Aug 2008]","start":1247054,"end":1303157,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Source:HGNC Symbol;Acc:HGNC:12851]"}, {"versioned_ensembl_gene_id":"ENSG00000258818.3","gene_symbol":"RNASE4","gene_name":"ribonuclease A family member 4 [Source:HGNC Symbol;Acc:HGNC:10047]","synonyms":"RAB1","biotype":"protein_coding","ncbi_id":"6038","summary":"The protein encoded by this gene belongs to the pancreatic ribonuclease family. It plays an important role in mRNA cleavage and has marked specificity towards the 3' side of uridine nucleotides. Alternative splicing results in four transcript variants encoding the same protein. This gene and the gene that encodes angiogenin share promoters and 5' exons. Each gene splices to a unique downstream exon that contains its complete coding region. [provided by RefSeq, Aug 2013]","start":20684100,"end":20701215,"strand":1,"description":"ribonuclease A family member 4 [Source:HGNC Symbol;Acc:HGNC:10047]"}, {"versioned_ensembl_gene_id":"ENSG00000172005.10","gene_symbol":"MAL","gene_name":"mal, T-cell differentiation protein [Source:HGNC Symbol;Acc:HGNC:6817]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4118","summary":"The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]","start":95025677,"end":95053996,"strand":1,"description":"mal, T-cell differentiation protein [Source:HGNC Symbol;Acc:HGNC:6817]"}, {"versioned_ensembl_gene_id":"ENSG00000229694.6","gene_symbol":"LINC00484","gene_name":"long intergenic non-protein coding RNA 484 [Source:NCBI gene;Acc:100129347]","synonyms":"C9orf73,C9orf73","biotype":"lincRNA","ncbi_id":"100129347","summary":null,"start":91119062,"end":91182762,"strand":1,"description":"long intergenic non-protein coding RNA 484 [Source:NCBI gene;Acc:100129347]"}, {"versioned_ensembl_gene_id":"ENSG00000249998.1","gene_symbol":"AC106894.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16973275,"end":17073903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251212.1","gene_symbol":"MTND5P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42306]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873200","summary":null,"start":17061878,"end":17062165,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42306]"}, {"versioned_ensembl_gene_id":"ENSG00000272381.1","gene_symbol":"AL356258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31187883,"end":31261910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244203.2","gene_symbol":"FOXP1-AS1","gene_name":"FOXP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41942]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104502416","summary":null,"start":71289769,"end":71305853,"strand":1,"description":"FOXP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41942]"}, {"versioned_ensembl_gene_id":"ENSG00000230397.1","gene_symbol":"SPTLC1P1","gene_name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39668]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100874511","summary":null,"start":31360955,"end":31361215,"strand":1,"description":"serine palmitoyltransferase long chain base subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39668]"}, {"versioned_ensembl_gene_id":"ENSG00000230147.2","gene_symbol":"AL158071.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91169585,"end":91170045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225949.1","gene_symbol":"Z77249.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133141300,"end":133143940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110031.12","gene_symbol":"LPXN","gene_name":"leupaxin [Source:HGNC Symbol;Acc:HGNC:14061]","synonyms":"LDPL","biotype":"protein_coding","ncbi_id":"9404","summary":"The product encoded by this gene is preferentially expressed in hematopoietic cells and belongs to the paxillin protein family. Similar to other members of this focal-adhesion-associated adaptor-protein family, it has four leucine-rich LD-motifs in the N-terminus and four LIM domains in the C-terminus. It may function in cell type-specific signaling by associating with PYK2, a member of focal adhesion kinase family. As a substrate for a tyrosine kinase in lymphoid cells, this protein may also function in, and be regulated by, tyrosine kinase activity. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Jan 2009]","start":58526871,"end":58578220,"strand":-1,"description":"leupaxin [Source:HGNC Symbol;Acc:HGNC:14061]"}, {"versioned_ensembl_gene_id":"ENSG00000102962.4","gene_symbol":"CCL22","gene_name":"C-C motif chemokine ligand 22 [Source:HGNC Symbol;Acc:HGNC:10621]","synonyms":"SCYA22,MGC34554,MDC,DC/B-CK,ABCD-1,A-152E5.1,STCP-1","biotype":"protein_coding","ncbi_id":"6367","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 16. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for monocytes, dendritic cells, natural killer cells and for chronically activated T lymphocytes. It also displays a mild activity for primary activated T lymphocytes and has no chemoattractant activity for neutrophils, eosinophils and resting T lymphocytes. The product of this gene binds to chemokine receptor CCR4. This chemokine may play a role in the trafficking of activated T lymphocytes to inflammatory sites and other aspects of activated T lymphocyte physiology. [provided by RefSeq, Sep 2014]","start":57358772,"end":57366190,"strand":1,"description":"C-C motif chemokine ligand 22 [Source:HGNC Symbol;Acc:HGNC:10621]"}, {"versioned_ensembl_gene_id":"ENSG00000205500.8","gene_symbol":"AC013472.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":26984776,"end":27014612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235641.4","gene_symbol":"LINC00484","gene_name":"long intergenic non-protein coding RNA 484 [Source:HGNC Symbol;Acc:HGNC:27862]","synonyms":"C9orf73,C9orf73","biotype":"lincRNA","ncbi_id":"100129347","summary":null,"start":91159573,"end":91165658,"strand":1,"description":"long intergenic non-protein coding RNA 484 [Source:HGNC Symbol;Acc:HGNC:27862]"}, {"versioned_ensembl_gene_id":"ENSG00000250819.1","gene_symbol":"LINC02493","gene_name":"long intergenic non-protein coding RNA 2493 [Source:HGNC Symbol;Acc:HGNC:53477]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929123","summary":null,"start":17171757,"end":17186059,"strand":-1,"description":"long intergenic non-protein coding RNA 2493 [Source:HGNC Symbol;Acc:HGNC:53477]"}, {"versioned_ensembl_gene_id":"ENSG00000261211.1","gene_symbol":"AL031123.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6680309,"end":6683633,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152503.9","gene_symbol":"TRIM36","gene_name":"tripartite motif containing 36 [Source:HGNC Symbol;Acc:HGNC:16280]","synonyms":"RBCC728,HAPRIN,RNF98","biotype":"protein_coding","ncbi_id":"55521","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":115124762,"end":115180546,"strand":-1,"description":"tripartite motif containing 36 [Source:HGNC Symbol;Acc:HGNC:16280]"}, {"versioned_ensembl_gene_id":"ENSG00000223523.1","gene_symbol":"AC092598.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":188598791,"end":188839445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270903.1","gene_symbol":"HNRNPA3P9","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48755]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421415","summary":null,"start":32591793,"end":32592771,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48755]"}, {"versioned_ensembl_gene_id":"ENSG00000229498.1","gene_symbol":"AC105053.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85815130,"end":85825391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174325.4","gene_symbol":"DIRC1","gene_name":"disrupted in renal carcinoma 1 [Source:HGNC Symbol;Acc:HGNC:15760]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116093","summary":"Disruption of DIRC1 by translocation is associated with familial clear cell renal cancer. Overexpression of DIRC1 is associated with tumor progression and poor prognosis in gastric cancer. [provided by RefSeq, Mar 2019]","start":188734155,"end":188790104,"strand":-1,"description":"disrupted in renal carcinoma 1 [Source:HGNC Symbol;Acc:HGNC:15760]"}, {"versioned_ensembl_gene_id":"ENSG00000151651.15","gene_symbol":"ADAM8","gene_name":"ADAM metallopeptidase domain 8 [Source:HGNC Symbol;Acc:HGNC:215]","synonyms":"MS2,CD156a,CD156","biotype":"protein_coding","ncbi_id":"101","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene may be involved in cell adhesion during neurodegeneration, and it is thought to be a target for allergic respiratory diseases, including asthma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2009]","start":133262403,"end":133276868,"strand":-1,"description":"ADAM metallopeptidase domain 8 [Source:HGNC Symbol;Acc:HGNC:215]"}, {"versioned_ensembl_gene_id":"ENSG00000244535.1","gene_symbol":"AL049714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32758268,"end":32758614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267393.1","gene_symbol":"AP002439.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13362203,"end":13366243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254780.1","gene_symbol":"AC023232.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47905323,"end":47905607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233157.1","gene_symbol":"Z97055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43759199,"end":43759910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272746.1","gene_symbol":"AP005131.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":13526078,"end":13526688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230286.1","gene_symbol":"AC013472.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26950308,"end":27009807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279020.1","gene_symbol":"C18orf15","gene_name":"chromosome 18 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:26447]","synonyms":"HsT3231,FLJ31338","biotype":"TEC","ncbi_id":"147276","summary":null,"start":13239543,"end":13242076,"strand":1,"description":"chromosome 18 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:26447]"}, {"versioned_ensembl_gene_id":"ENSG00000169246.16","gene_symbol":"NPIPB3","gene_name":"nuclear pore complex interacting protein family member B3 [Source:HGNC Symbol;Acc:HGNC:28989]","synonyms":"KIAA0220,NPIPL3","biotype":"protein_coding","ncbi_id":"23117","summary":null,"start":21402237,"end":21448567,"strand":-1,"description":"nuclear pore complex interacting protein family member B3 [Source:HGNC Symbol;Acc:HGNC:28989]"}, {"versioned_ensembl_gene_id":"ENSG00000149100.12","gene_symbol":"EIF3M","gene_name":"eukaryotic translation initiation factor 3 subunit M [Source:HGNC Symbol;Acc:HGNC:24460]","synonyms":"TANGO7,PCID1,hfl-B5,GA17,FLJ29030,eIF3m","biotype":"protein_coding","ncbi_id":"10480","summary":"This gene encodes a protein that is part of the eurkaryotic translation initiation factor 3 complete (eIF-3) required for protein synthesis. Elevated levels of the encoded protein are present in cancer cell lines. Inactivation of the encoded protein has been shown to interfere with translation of herpes virus mRNAs by preventing the association of mRNAs with the ribosomes. A pseudogene of this gene is located on the X chromosome. [provided by RefSeq, Dec 2011]","start":32583798,"end":32606262,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit M [Source:HGNC Symbol;Acc:HGNC:24460]"}, {"versioned_ensembl_gene_id":"ENSG00000249542.2","gene_symbol":"EEF1A1P21","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421807","summary":null,"start":29748757,"end":29750100,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37894]"}, {"versioned_ensembl_gene_id":"ENSG00000260566.2","gene_symbol":"AC127459.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":23061406,"end":23064173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234730.1","gene_symbol":"AP001117.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21566763,"end":21615437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183434.9","gene_symbol":"TFDP3","gene_name":"transcription factor Dp family member 3 [Source:HGNC Symbol;Acc:HGNC:24603]","synonyms":"HCA661,E2F-like,CT30","biotype":"protein_coding","ncbi_id":"51270","summary":"This gene encodes a member of the DP family of transcription factors. These factors heterodimerize with E2F proteins to enhance their DNA-binding activity and promote transcription from E2F target genes. This protein functions as a negative regulator and inhibits the DNA binding and transcriptional activities of E2F factors.[provided by RefSeq, May 2010]","start":133216669,"end":133218348,"strand":-1,"description":"transcription factor Dp family member 3 [Source:HGNC Symbol;Acc:HGNC:24603]"}, {"versioned_ensembl_gene_id":"ENSG00000186976.14","gene_symbol":"EFCAB6","gene_name":"EF-hand calcium binding domain 6 [Source:HGNC Symbol;Acc:HGNC:24204]","synonyms":"dJ185D5.1,KIAA1672,HSCBCIP1,FLJ23588,DJBP","biotype":"protein_coding","ncbi_id":"64800","summary":"This gene encodes a protein which directly binds the oncogene DJ-1 and androgen receptor to form a ternary complex in cells. This binding protein recruits histone-deacetylase complexes in order to repress transcription activity of androgen receptor. This protein may also play a role in spermatogenesis and fertilization. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":43528744,"end":43812337,"strand":-1,"description":"EF-hand calcium binding domain 6 [Source:HGNC Symbol;Acc:HGNC:24204]"}, {"versioned_ensembl_gene_id":"ENSG00000157851.16","gene_symbol":"DPYSL5","gene_name":"dihydropyrimidinase like 5 [Source:HGNC Symbol;Acc:HGNC:20637]","synonyms":"Ulip6,CRMP5,CRMP-5,CRAM","biotype":"protein_coding","ncbi_id":"56896","summary":"This gene encodes a member of the CRMP (collapsing response mediator protein) family thought to be involved in neural development. Antibodies to the encoded protein were found in some patients with neurologic symptoms who had paraneoplastic syndrome. A pseudogene of this gene is found on chromosome 11. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Dec 2011]","start":26847747,"end":26950351,"strand":1,"description":"dihydropyrimidinase like 5 [Source:HGNC Symbol;Acc:HGNC:20637]"}, {"versioned_ensembl_gene_id":"ENSG00000168675.18","gene_symbol":"LDLRAD4","gene_name":"low density lipoprotein receptor class A domain containing 4 [Source:HGNC Symbol;Acc:HGNC:1224]","synonyms":"C18orf1","biotype":"protein_coding","ncbi_id":"753","summary":null,"start":13217498,"end":13652755,"strand":1,"description":"low density lipoprotein receptor class A domain containing 4 [Source:HGNC Symbol;Acc:HGNC:1224]"}, {"versioned_ensembl_gene_id":"ENSG00000215278.4","gene_symbol":"RPS7P6","gene_name":"ribosomal protein S7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270869","summary":null,"start":17427696,"end":17428274,"strand":-1,"description":"ribosomal protein S7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36334]"}, {"versioned_ensembl_gene_id":"ENSG00000254951.7","gene_symbol":"AC044810.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":7754393,"end":7905955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220598.1","gene_symbol":"SSR1P1","gene_name":"signal sequence receptor subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39273]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420476","summary":null,"start":150384307,"end":150385120,"strand":-1,"description":"signal sequence receptor subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39273]"}, {"versioned_ensembl_gene_id":"ENSG00000183303.2","gene_symbol":"OR5P2","gene_name":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]","synonyms":"JCG3","biotype":"protein_coding","ncbi_id":"120065","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7795905,"end":7796973,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]"}, {"versioned_ensembl_gene_id":"ENSG00000161921.14","gene_symbol":"CXCL16","gene_name":"C-X-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:16642]","synonyms":"SRPSOX,SR-PSOX,CXCLG16","biotype":"protein_coding","ncbi_id":"58191","summary":null,"start":4733526,"end":4739922,"strand":-1,"description":"C-X-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:16642]"}, {"versioned_ensembl_gene_id":"ENSG00000009765.14","gene_symbol":"IYD","gene_name":"iodotyrosine deiodinase [Source:HGNC Symbol;Acc:HGNC:21071]","synonyms":"dJ422F24.1,DEHAL1,C6orf71","biotype":"protein_coding","ncbi_id":"389434","summary":"This gene encodes an enzyme that catalyzes the oxidative NADPH-dependent deiodination of mono- and diiodotyrosine, which are the halogenated byproducts of thyroid hormone production. The N-terminus of the protein functions as a membrane anchor. Mutations in this gene cause congenital hypothyroidism due to dyshormonogenesis type 4, which is also referred to as deiodinase deficiency, or iodotyrosine dehalogenase deficiency, or thyroid hormonogenesis type 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":150368892,"end":150405969,"strand":1,"description":"iodotyrosine deiodinase [Source:HGNC Symbol;Acc:HGNC:21071]"}, {"versioned_ensembl_gene_id":"ENSG00000174473.15","gene_symbol":"GALNTL6","gene_name":"polypeptide N-acetylgalactosaminyltransferase like 6 [Source:HGNC Symbol;Acc:HGNC:33844]","synonyms":"GALNT17,GalNAc-T6L","biotype":"protein_coding","ncbi_id":"442117","summary":null,"start":171812254,"end":173041559,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase like 6 [Source:HGNC Symbol;Acc:HGNC:33844]"}, {"versioned_ensembl_gene_id":"ENSG00000261846.2","gene_symbol":"AADACL2","gene_name":"arylacetamide deacetylase like 2 [Source:HGNC Symbol;Acc:HGNC:24427]","synonyms":"MGC72001","biotype":"protein_coding","ncbi_id":"344752","summary":null,"start":151744454,"end":151770036,"strand":1,"description":"arylacetamide deacetylase like 2 [Source:HGNC Symbol;Acc:HGNC:24427]"}, {"versioned_ensembl_gene_id":"ENSG00000170688.4","gene_symbol":"OR5E1P","gene_name":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]","synonyms":"TPCR24,OR5E1,HSTPCR24","biotype":"unprocessed_pseudogene","ncbi_id":"26343","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7848700,"end":7849626,"strand":1,"description":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]"}, {"versioned_ensembl_gene_id":"ENSG00000241008.1","gene_symbol":"AC044810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7783697,"end":7784407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076716.8","gene_symbol":"GPC4","gene_name":"glypican 4 [Source:HGNC Symbol;Acc:HGNC:4452]","synonyms":"K-glypican","biotype":"protein_coding","ncbi_id":"2239","summary":"Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The GPC4 gene is adjacent to the 3' end of GPC3 and may also play a role in Simpson-Golabi-Behmel syndrome. [provided by RefSeq, Jul 2008]","start":133300103,"end":133415490,"strand":-1,"description":"glypican 4 [Source:HGNC Symbol;Acc:HGNC:4452]"}, {"versioned_ensembl_gene_id":"ENSG00000231453.1","gene_symbol":"LINC01305","gene_name":"long intergenic non-protein coding RNA 1305 [Source:HGNC Symbol;Acc:HGNC:27690]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285084","summary":null,"start":174326027,"end":174330643,"strand":1,"description":"long intergenic non-protein coding RNA 1305 [Source:HGNC Symbol;Acc:HGNC:27690]"}, {"versioned_ensembl_gene_id":"ENSG00000272486.1","gene_symbol":"AC090922.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124579631,"end":124580648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226422.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31218662,"end":31222831,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000258853.1","gene_symbol":"AC021979.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27684498,"end":27685768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227892.1","gene_symbol":"OR5P4P","gene_name":"olfactory receptor family 5 subfamily P member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15295]","synonyms":"OST730","biotype":"unprocessed_pseudogene","ncbi_id":"81185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7745990,"end":7746906,"strand":1,"description":"olfactory receptor family 5 subfamily P member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15295]"}, {"versioned_ensembl_gene_id":"ENSG00000227180.1","gene_symbol":"AC013467.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174299324,"end":174300956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137673.8","gene_symbol":"MMP7","gene_name":"matrix metallopeptidase 7 [Source:HGNC Symbol;Acc:HGNC:7174]","synonyms":"PUMP-1,MPSL1","biotype":"protein_coding","ncbi_id":"4316","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down proteoglycans, fibronectin, elastin and casein and differs from most MMP family members in that it lacks a conserved C-terminal hemopexin domain. The enzyme is involved in wound healing, and studies in mice suggest that it regulates the activity of defensins in intestinal mucosa. The gene is part of a cluster of MMP genes on chromosome 11. This gene exhibits elevated expression levels in multiple human cancers. [provided by RefSeq, Jan 2016]","start":102520508,"end":102530753,"strand":-1,"description":"matrix metallopeptidase 7 [Source:HGNC Symbol;Acc:HGNC:7174]"}, {"versioned_ensembl_gene_id":"ENSG00000275612.1","gene_symbol":"AC104237.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7698951,"end":7699393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229101.1","gene_symbol":"ELOCP20","gene_name":"elongin C pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38156]","synonyms":"TCEB1P20","biotype":"unprocessed_pseudogene","ncbi_id":"100287778","summary":null,"start":115556826,"end":115557475,"strand":1,"description":"elongin C pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38156]"}, {"versioned_ensembl_gene_id":"ENSG00000166408.4","gene_symbol":"OR5P1P","gene_name":"olfactory receptor family 5 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14779]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79283","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7772890,"end":7773814,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14779]"}, {"versioned_ensembl_gene_id":"ENSG00000275989.1","gene_symbol":"AL442128.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110952722,"end":110952811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176716.5","gene_symbol":"OR10AB1P","gene_name":"olfactory receptor family 10 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14804]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390091","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7726436,"end":7729684,"strand":1,"description":"olfactory receptor family 10 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14804]"}, {"versioned_ensembl_gene_id":"ENSG00000237804.1","gene_symbol":"HNRNPA1P39","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:48768]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402112","summary":null,"start":174310015,"end":174310974,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:48768]"}, {"versioned_ensembl_gene_id":"ENSG00000182334.2","gene_symbol":"OR5P3","gene_name":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]","synonyms":"JCG1","biotype":"protein_coding","ncbi_id":"120066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7824818,"end":7830840,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]"}, {"versioned_ensembl_gene_id":"ENSG00000262466.5","gene_symbol":"AADACL2-AS1","gene_name":"AADACL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50301]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928142","summary":null,"start":151761981,"end":151765669,"strand":-1,"description":"AADACL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50301]"}, {"versioned_ensembl_gene_id":"ENSG00000271758.2","gene_symbol":"AC044810.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7704628,"end":7882947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235180.1","gene_symbol":"LINC00601","gene_name":"long intergenic non-protein coding RNA 601 [Source:HGNC Symbol;Acc:HGNC:43916]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101101772","summary":null,"start":126413869,"end":126421879,"strand":-1,"description":"long intergenic non-protein coding RNA 601 [Source:HGNC Symbol;Acc:HGNC:43916]"}, {"versioned_ensembl_gene_id":"ENSG00000226141.1","gene_symbol":"AC244107.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":154654546,"end":154655325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255492.1","gene_symbol":"AC104383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11856490,"end":11856859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254707.1","gene_symbol":"AC104237.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7705288,"end":7709517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232679.1","gene_symbol":"LINC01705","gene_name":"long intergenic non-protein coding RNA 1705 [Source:HGNC Symbol;Acc:HGNC:52493]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985307","summary":null,"start":222041705,"end":222064763,"strand":-1,"description":"long intergenic non-protein coding RNA 1705 [Source:HGNC Symbol;Acc:HGNC:52493]"}, {"versioned_ensembl_gene_id":"ENSG00000234033.1","gene_symbol":"RAC1P8","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42005]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874398","summary":null,"start":61805150,"end":61805676,"strand":1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42005]"}, {"versioned_ensembl_gene_id":"ENSG00000261898.2","gene_symbol":"AC091153.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4731756,"end":4732371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170242.17","gene_symbol":"USP47","gene_name":"ubiquitin specific peptidase 47 [Source:HGNC Symbol;Acc:HGNC:20076]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55031","summary":null,"start":11841423,"end":11959323,"strand":1,"description":"ubiquitin specific peptidase 47 [Source:HGNC Symbol;Acc:HGNC:20076]"}, {"versioned_ensembl_gene_id":"ENSG00000183378.11","gene_symbol":"OVCH2","gene_name":"ovochymase 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:29970]","synonyms":"OVTN","biotype":"protein_coding","ncbi_id":"341277","summary":null,"start":7689438,"end":7706421,"strand":-1,"description":"ovochymase 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:29970]"}, {"versioned_ensembl_gene_id":"ENSG00000226210.3","gene_symbol":"AC215219.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14522,"end":32015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213252.3","gene_symbol":"AP001282.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106826392,"end":106827890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183214.12","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31389818,"end":31406373,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000161920.9","gene_symbol":"MED11","gene_name":"mediator complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:32687]","synonyms":"MGC88387,HSPC296","biotype":"protein_coding","ncbi_id":"400569","summary":"MED11 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008]","start":4731428,"end":4733610,"strand":1,"description":"mediator complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:32687]"}, {"versioned_ensembl_gene_id":"ENSG00000111906.17","gene_symbol":"HDDC2","gene_name":"HD domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21078]","synonyms":"dJ167O5.2,CGI-130,C6orf74","biotype":"protein_coding","ncbi_id":"51020","summary":null,"start":125219962,"end":125302078,"strand":-1,"description":"HD domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21078]"}, {"versioned_ensembl_gene_id":"ENSG00000236230.1","gene_symbol":"AL356108.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222089169,"end":222387434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265148.5","gene_symbol":"TSPOAP1-AS1","gene_name":"TSPOAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44148]","synonyms":"BZRAP1-AS1","biotype":"antisense_RNA","ncbi_id":"100506779","summary":null,"start":58325450,"end":58415766,"strand":1,"description":"TSPOAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44148]"}, {"versioned_ensembl_gene_id":"ENSG00000227613.1","gene_symbol":"QRSL1P2","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43668]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422330","summary":null,"start":222261833,"end":222262796,"strand":-1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43668]"}, {"versioned_ensembl_gene_id":"ENSG00000270856.1","gene_symbol":"AL353765.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61927090,"end":61927272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225760.2","gene_symbol":"LINC00431","gene_name":"long intergenic non-protein coding RNA 431 [Source:HGNC Symbol;Acc:HGNC:42766]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"104355135","summary":null,"start":110965704,"end":110990579,"strand":1,"description":"long intergenic non-protein coding RNA 431 [Source:HGNC Symbol;Acc:HGNC:42766]"}, {"versioned_ensembl_gene_id":"ENSG00000242654.1","gene_symbol":"RPL32P14","gene_name":"ribosomal protein L32 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:37038]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270994","summary":null,"start":19041009,"end":19041386,"strand":1,"description":"ribosomal protein L32 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:37038]"}, {"versioned_ensembl_gene_id":"ENSG00000251487.1","gene_symbol":"AC106744.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19035197,"end":19038799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226643.2","gene_symbol":"AL513314.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222452738,"end":222454705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266289.1","gene_symbol":"AC012213.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103383078,"end":103383854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228160.1","gene_symbol":"AL158069.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69569669,"end":69570357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229578.2","gene_symbol":"LINC00358","gene_name":"long intergenic non-protein coding RNA 358 [Source:HGNC Symbol;Acc:HGNC:42678]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874143","summary":null,"start":62003525,"end":62029548,"strand":-1,"description":"long intergenic non-protein coding RNA 358 [Source:HGNC Symbol;Acc:HGNC:42678]"}, {"versioned_ensembl_gene_id":"ENSG00000251000.1","gene_symbol":"AC008592.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95834424,"end":95835046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249174.1","gene_symbol":"AC106744.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18965861,"end":19142346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258186.2","gene_symbol":"SLC7A5P2","gene_name":"solute carrier family 7 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24951]","synonyms":"IMAA,hLAT1-3TM","biotype":"transcribed_processed_pseudogene","ncbi_id":"387254","summary":null,"start":21519830,"end":21520365,"strand":-1,"description":"solute carrier family 7 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24951]"}, {"versioned_ensembl_gene_id":"ENSG00000249557.2","gene_symbol":"HSPD1P15","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35130]","synonyms":"HSPD1-15P","biotype":"processed_pseudogene","ncbi_id":"646273","summary":null,"start":19233366,"end":19234487,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35130]"}, {"versioned_ensembl_gene_id":"ENSG00000234419.1","gene_symbol":"CICP13","gene_name":"capicua transcriptional repressor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37907]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728615","summary":null,"start":222468094,"end":222470882,"strand":1,"description":"capicua transcriptional repressor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37907]"}, {"versioned_ensembl_gene_id":"ENSG00000249564.1","gene_symbol":"AC097510.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29907659,"end":29907791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180747.15","gene_symbol":"SMG1P3","gene_name":"SMG1P3, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49860]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100271836","summary":null,"start":21446683,"end":21520444,"strand":-1,"description":"SMG1P3, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49860]"}, {"versioned_ensembl_gene_id":"ENSG00000230142.2","gene_symbol":"LINC01075","gene_name":"long intergenic non-protein coding RNA 1075 [Source:HGNC Symbol;Acc:HGNC:49118]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103752583","summary":null,"start":62212577,"end":62249947,"strand":1,"description":"long intergenic non-protein coding RNA 1075 [Source:HGNC Symbol;Acc:HGNC:49118]"}, {"versioned_ensembl_gene_id":"ENSG00000271114.1","gene_symbol":"AL590392.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87891424,"end":87891869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219722.1","gene_symbol":"AL356057.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75499705,"end":75500136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244031.3","gene_symbol":"RPS3AP17","gene_name":"ribosomal protein S3a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36083]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271130","summary":null,"start":29962644,"end":29963758,"strand":-1,"description":"ribosomal protein S3a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36083]"}, {"versioned_ensembl_gene_id":"ENSG00000248637.1","gene_symbol":"AC108064.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172380028,"end":172380487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237619.1","gene_symbol":"OR3B1P","gene_name":"olfactory receptor family 3 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14839]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392561","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":154658790,"end":154659682,"strand":-1,"description":"olfactory receptor family 3 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14839]"}, {"versioned_ensembl_gene_id":"ENSG00000220730.2","gene_symbol":"AL356057.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75586122,"end":75586461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251409.1","gene_symbol":"AC008592.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95835943,"end":95852721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227611.1","gene_symbol":"LINC01074","gene_name":"long intergenic non-protein coding RNA 1074 [Source:HGNC Symbol;Acc:HGNC:49117]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144607","summary":null,"start":62321305,"end":62322398,"strand":1,"description":"long intergenic non-protein coding RNA 1074 [Source:HGNC Symbol;Acc:HGNC:49117]"}, {"versioned_ensembl_gene_id":"ENSG00000256480.1","gene_symbol":"AC018653.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7237432,"end":7240986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236882.7","gene_symbol":"LINC01554","gene_name":"long intergenic non-protein coding RNA 1554 [Source:HGNC Symbol;Acc:HGNC:24687]","synonyms":"FLJ38821,FIS,C5orf27","biotype":"lincRNA","ncbi_id":"202299","summary":null,"start":95852232,"end":95860133,"strand":1,"description":"long intergenic non-protein coding RNA 1554 [Source:HGNC Symbol;Acc:HGNC:24687]"}, {"versioned_ensembl_gene_id":"ENSG00000248281.1","gene_symbol":"AC106868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30006951,"end":30008316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276668.1","gene_symbol":"AC104237.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7699562,"end":7699988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006210.6","gene_symbol":"CX3CL1","gene_name":"C-X3-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10647]","synonyms":"SCYD1,NTN,neurotactin,fractalkine,CXC3C,CXC3,C3Xkine,ABCD-3","biotype":"protein_coding","ncbi_id":"6376","summary":"This gene belongs to the CX3C subgroup of chemokines, characterized by the number of amino acids located between the conserved cysteine residues. This is the only member of the CX3C subgroup, which contains three amino acids between cysteine residues, resulting in a Cys-X-X-X-Cys configuration. The encoded protein contains an extended mucin-like stalk with a chemokine domain on top, and exists in both a membrane-anchored form where it acts as a binding molecule, or, in soluble form, as a chemotactic cytokine. The mature form of this protein can be cleaved at the cell surface, yielding different soluble forms that can interact with the G-protein coupled receptor, C-X3-C motif chemokine receptor 1 gene product. This gene plays a role in a wide range of diseases, including cancer, vasculitis, neuropathies, atherosclerosis, inflammatory diseases, and in human immunodeficiency virus infections. [provided by RefSeq, Sep 2017]","start":57372458,"end":57385048,"strand":1,"description":"C-X3-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10647]"}, {"versioned_ensembl_gene_id":"ENSG00000229307.1","gene_symbol":"LINC00459","gene_name":"long intergenic non-protein coding RNA 459 [Source:HGNC Symbol;Acc:HGNC:42808]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874180","summary":null,"start":62323657,"end":62328833,"strand":1,"description":"long intergenic non-protein coding RNA 459 [Source:HGNC Symbol;Acc:HGNC:42808]"}, {"versioned_ensembl_gene_id":"ENSG00000215009.5","gene_symbol":"ACSM4","gene_name":"acyl-CoA synthetase medium chain family member 4 [Source:HGNC Symbol;Acc:HGNC:32016]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341392","summary":null,"start":7304284,"end":7328724,"strand":1,"description":"acyl-CoA synthetase medium chain family member 4 [Source:HGNC Symbol;Acc:HGNC:32016]"}, {"versioned_ensembl_gene_id":"ENSG00000128596.16","gene_symbol":"CCDC136","gene_name":"coiled-coil domain containing 136 [Source:HGNC Symbol;Acc:HGNC:22225]","synonyms":"NAG6,KIAA1793,DKFZP434G156","biotype":"protein_coding","ncbi_id":"64753","summary":null,"start":128790757,"end":128822132,"strand":1,"description":"coiled-coil domain containing 136 [Source:HGNC Symbol;Acc:HGNC:22225]"}, {"versioned_ensembl_gene_id":"ENSG00000185274.11","gene_symbol":"GALNT17","gene_name":"polypeptide N-acetylgalactosaminyltransferase 17 [Source:HGNC Symbol;Acc:HGNC:16347]","synonyms":"GalNAc-T5L,GalNAc-T19,GalNAc-T17,WBSCR17,ppGalNAc-T17,GALNTL3","biotype":"protein_coding","ncbi_id":"64409","summary":"This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]","start":71132169,"end":71713600,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 17 [Source:HGNC Symbol;Acc:HGNC:16347]"}, {"versioned_ensembl_gene_id":"ENSG00000225870.1","gene_symbol":"LINC00368","gene_name":"long intergenic non-protein coding RNA 368 [Source:HGNC Symbol;Acc:HGNC:42690]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927802","summary":null,"start":111095838,"end":111103097,"strand":1,"description":"long intergenic non-protein coding RNA 368 [Source:HGNC Symbol;Acc:HGNC:42690]"}, {"versioned_ensembl_gene_id":"ENSG00000232105.1","gene_symbol":"RPL32P28","gene_name":"ribosomal protein L32 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36328]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133193","summary":null,"start":62327988,"end":62328384,"strand":1,"description":"ribosomal protein L32 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36328]"}, {"versioned_ensembl_gene_id":"ENSG00000263513.5","gene_symbol":"FAM72C","gene_name":"family with sequence similarity 72 member C [Source:HGNC Symbol;Acc:HGNC:30602]","synonyms":"RP5-998N21.9","biotype":"protein_coding","ncbi_id":"554282","summary":null,"start":143955364,"end":143971965,"strand":-1,"description":"family with sequence similarity 72 member C [Source:HGNC Symbol;Acc:HGNC:30602]"}, {"versioned_ensembl_gene_id":"ENSG00000078053.16","gene_symbol":"AMPH","gene_name":"amphiphysin [Source:HGNC Symbol;Acc:HGNC:471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"273","summary":"This gene encodes a protein associated with the cytoplasmic surface of synaptic vesicles. A subset of patients with stiff-man syndrome who were also affected by breast cancer are positive for autoantibodies against this protein. Alternate splicing of this gene results in two transcript variants encoding different isoforms. Additional splice variants have been described, but their full length sequences have not been determined. A pseudogene of this gene is found on chromosome 11.[provided by RefSeq, Nov 2010]","start":38383704,"end":38631567,"strand":-1,"description":"amphiphysin [Source:HGNC Symbol;Acc:HGNC:471]"}, {"versioned_ensembl_gene_id":"ENSG00000272021.1","gene_symbol":"AC008592.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95849309,"end":95849855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242689.2","gene_symbol":"CNTF","gene_name":"ciliary neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:2169]","synonyms":"HCNTF","biotype":"protein_coding","ncbi_id":"1270","summary":"The protein encoded by this gene is a polypeptide hormone whose actions appear to be restricted to the nervous system where it promotes neurotransmitter synthesis and neurite outgrowth in certain neuronal populations. The protein is a potent survival factor for neurons and oligodendrocytes and may be relevant in reducing tissue destruction during inflammatory attacks. A mutation in this gene, which results in aberrant splicing, leads to ciliary neurotrophic factor deficiency, but this phenotype is not causally related to neurologic disease. A read-through transcript variant composed of the upstream ZFP91 gene and CNTF sequence has been identified, but it is thought to be non-coding. Read-through transcription of ZFP91 and CNTF has also been observed in mouse. [provided by RefSeq, Oct 2010]","start":58622673,"end":58625733,"strand":1,"description":"ciliary neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:2169]"}, {"versioned_ensembl_gene_id":"ENSG00000276149.1","gene_symbol":"BX005040.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":61202718,"end":61203087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176988.8","gene_symbol":"FMR1NB","gene_name":"FMR1 neighbor [Source:HGNC Symbol;Acc:HGNC:26372]","synonyms":"NY-SAR-35,FLJ25736,CT37","biotype":"protein_coding","ncbi_id":"158521","summary":null,"start":147981329,"end":148026667,"strand":1,"description":"FMR1 neighbor [Source:HGNC Symbol;Acc:HGNC:26372]"}, {"versioned_ensembl_gene_id":"ENSG00000276040.4","gene_symbol":"SPATA31A7","gene_name":"SPATA31 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:32007]","synonyms":"SPATA31A4,FAM75A7,FAM75A4","biotype":"protein_coding","ncbi_id":"26165","summary":null,"start":61190003,"end":61196280,"strand":1,"description":"SPATA31 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:32007]"}, {"versioned_ensembl_gene_id":"ENSG00000255545.7","gene_symbol":"AP004608.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":134436473,"end":134505661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269570.2","gene_symbol":"AP001350.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58611119,"end":58612642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255073.8","gene_symbol":"ZFP91-CNTF","gene_name":"ZFP91-CNTF readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:33441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"386607","summary":"This gene represents a read-through transcript composed of ZFP91 and CNTF sequence. This transcript is thought to be non-coding because it would be subject to nonsense-mediated mRNA decay (NMD). Read-through transcription of ZFP91 and CNTF has also been observed in mouse. [provided by RefSeq, Aug 2008]","start":58579172,"end":58624639,"strand":1,"description":"ZFP91-CNTF readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:33441]"}, {"versioned_ensembl_gene_id":"ENSG00000154493.17","gene_symbol":"C10orf90","gene_name":"chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:HGNC:26563]","synonyms":"FLJ32938,FATS,bA422P15.2","biotype":"protein_coding","ncbi_id":"118611","summary":null,"start":126424997,"end":126670446,"strand":-1,"description":"chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:HGNC:26563]"}, {"versioned_ensembl_gene_id":"ENSG00000249406.1","gene_symbol":"AC015909.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50208972,"end":50214459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182793.11","gene_symbol":"GSTA5","gene_name":"glutathione S-transferase alpha 5 [Source:HGNC Symbol;Acc:HGNC:19662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"221357","summary":"The glutathione S-transferases (GST; EC 2.5.1.18) catalyze the conjugation of reduced glutathiones and a variety of electrophiles, including many known carcinogens and mutagens. The cytosolic GSTs belong to a large superfamily, with members located on different chromosomes. For additional information on GSTs, see GSTA1 (MIM 138359).[supplied by OMIM, Sep 2008]","start":52831655,"end":52846095,"strand":-1,"description":"glutathione S-transferase alpha 5 [Source:HGNC Symbol;Acc:HGNC:19662]"}, {"versioned_ensembl_gene_id":"ENSG00000263176.1","gene_symbol":"AC015909.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50212933,"end":50215357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236913.1","gene_symbol":"AC025750.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42469817,"end":42470266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223843.4","gene_symbol":"EFCAB6-AS1","gene_name":"EFCAB6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39999]","synonyms":"CITF22-123F2.1","biotype":"antisense_RNA","ncbi_id":"100874197","summary":null,"start":43516107,"end":43537117,"strand":1,"description":"EFCAB6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39999]"}, {"versioned_ensembl_gene_id":"ENSG00000256496.1","gene_symbol":"AC073913.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127317709,"end":127319986,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158488.15","gene_symbol":"CD1E","gene_name":"CD1e molecule [Source:HGNC Symbol;Acc:HGNC:1638]","synonyms":null,"biotype":"protein_coding","ncbi_id":"913","summary":"This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes within Golgi compartments, endosomes, and lysosomes, and is cleaved into a stable soluble form. The soluble form is required for the intracellular processing of some glycolipids into a form that can be presented by other CD1 family members. Many alternatively spliced transcript variants encoding different isoforms have been described. Additional transcript variants have been found; however, their biological validity has not been determined. [provided by RefSeq, Jun 2010]","start":158353696,"end":158357553,"strand":1,"description":"CD1e molecule [Source:HGNC Symbol;Acc:HGNC:1638]"}, {"versioned_ensembl_gene_id":"ENSG00000232526.1","gene_symbol":"VDAC1P13","gene_name":"voltage dependent anion channel 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50515]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420568","summary":null,"start":42463139,"end":42463997,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50515]"}, {"versioned_ensembl_gene_id":"ENSG00000251085.1","gene_symbol":"LINC01969","gene_name":"long intergenic non-protein coding RNA 1969 [Source:HGNC Symbol;Acc:HGNC:52795]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927230","summary":null,"start":50214694,"end":50215420,"strand":1,"description":"long intergenic non-protein coding RNA 1969 [Source:HGNC Symbol;Acc:HGNC:52795]"}, {"versioned_ensembl_gene_id":"ENSG00000254573.1","gene_symbol":"AP004550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134563396,"end":134573056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171126.7","gene_symbol":"KCNG3","gene_name":"potassium voltage-gated channel modifier subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:18306]","synonyms":"Kv6.3","biotype":"protein_coding","ncbi_id":"170850","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This member is a gamma subunit functioning as a modulatory molecule. Alternative splicing results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":42442017,"end":42494097,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:18306]"}, {"versioned_ensembl_gene_id":"ENSG00000274929.1","gene_symbol":"AL157813.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48532013,"end":48532599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249838.1","gene_symbol":"SUMO2P7","gene_name":"SUMO2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131823","summary":null,"start":50235845,"end":50236129,"strand":1,"description":"SUMO2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39017]"}, {"versioned_ensembl_gene_id":"ENSG00000254989.1","gene_symbol":"AP001999.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134671426,"end":134672024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239300.5","gene_symbol":"AC080162.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9505445,"end":9512412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136161.12","gene_symbol":"RCBTB2","gene_name":"RCC1 and BTB domain containing protein 2 [Source:HGNC Symbol;Acc:HGNC:1914]","synonyms":"CHC1L","biotype":"protein_coding","ncbi_id":"1102","summary":"This gene encodes a protein containing two C-terminal BTB/POZ domains that is related to regulator of chromosome condensation (RCC). The encoded protein may act as a guanine nucleotide exchange factor. This gene is observed to be lost or underexpressed in prostate cancers. There is a pseudogene of this gene on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":48488959,"end":48533256,"strand":-1,"description":"RCC1 and BTB domain containing protein 2 [Source:HGNC Symbol;Acc:HGNC:1914]"}, {"versioned_ensembl_gene_id":"ENSG00000186660.14","gene_symbol":"ZFP91","gene_name":"ZFP91 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:14983]","synonyms":"ZNF757,PZF","biotype":"protein_coding","ncbi_id":"80829","summary":"The protein encoded by this gene is a member of the zinc finger family of proteins. The gene product contains C2H2-type domains, which are the classical zinc finger domains found in numerous nucleic acid-binding proteins. This protein functions as a regulator of the non-canonical NF-kappaB pathway in lymphotoxin-beta receptor signaling. Alternative splicing results in multiple transcript variants. A read-through transcript variant composed of ZFP91 and the downstream CNTF gene sequence has been identified, but it is thought to be non-coding. Read-through transcription of ZFP91 and CNTF has also been observed in mouse. A ZFP91-related pseudogene has also been identified on chromosome 2. [provided by RefSeq, Oct 2010]","start":58579111,"end":58621042,"strand":1,"description":"ZFP91 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:14983]"}, {"versioned_ensembl_gene_id":"ENSG00000255344.1","gene_symbol":"AP001999.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134714542,"end":134715922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251226.1","gene_symbol":"AP001999.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134735596,"end":134763810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185988.12","gene_symbol":"PLK5","gene_name":"polo like kinase 5 [Source:HGNC Symbol;Acc:HGNC:27001]","synonyms":"SgK384ps,PLK5P","biotype":"protein_coding","ncbi_id":"126520","summary":null,"start":1524074,"end":1535456,"strand":1,"description":"polo like kinase 5 [Source:HGNC Symbol;Acc:HGNC:27001]"}, {"versioned_ensembl_gene_id":"ENSG00000151694.12","gene_symbol":"ADAM17","gene_name":"ADAM metallopeptidase domain 17 [Source:HGNC Symbol;Acc:HGNC:195]","synonyms":"CD156B,TACE,cSVP","biotype":"protein_coding","ncbi_id":"6868","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature protease. The encoded protease functions in the ectodomain shedding of tumor necrosis factor-alpha, in which soluble tumor necrosis factor-alpha is released from the membrane-bound precursor. This protease also functions in the processing of numerous other substrates, including cell adhesion proteins, cytokine and growth factor receptors and epidermal growth factor (EGF) receptor ligands, and plays a prominent role in the activation of the Notch signaling pathway. Elevated expression of this gene has been observed in specific cell types derived from psoriasis, rheumatoid arthritis, multiple sclerosis and Crohn's disease patients, suggesting that the encoded protein may play a role in autoimmune disease. Additionally, this protease may play a role in viral infection through its cleavage of ACE2, the cellular receptor for SARS-CoV and SARS-CoV-2. [provided by RefSeq, Aug 2020]","start":9488486,"end":9555792,"strand":-1,"description":"ADAM metallopeptidase domain 17 [Source:HGNC Symbol;Acc:HGNC:195]"}, {"versioned_ensembl_gene_id":"ENSG00000248546.3","gene_symbol":"ANP32C","gene_name":"acidic nuclear phosphoprotein 32 family member C [Source:HGNC Symbol;Acc:HGNC:16675]","synonyms":"PP32R1","biotype":"processed_pseudogene","ncbi_id":"23520","summary":null,"start":164197007,"end":164197711,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member C [Source:HGNC Symbol;Acc:HGNC:16675]"}, {"versioned_ensembl_gene_id":"ENSG00000250746.1","gene_symbol":"AC105250.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164188311,"end":164190367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164934.13","gene_symbol":"DCAF13","gene_name":"DDB1 and CUL4 associated factor 13 [Source:HGNC Symbol;Acc:HGNC:24535]","synonyms":"Sof1,HSPC064,Gm83,DKFZP564O0463,WDSOF1","biotype":"protein_coding","ncbi_id":"25879","summary":null,"start":103414714,"end":103443453,"strand":1,"description":"DDB1 and CUL4 associated factor 13 [Source:HGNC Symbol;Acc:HGNC:24535]"}, {"versioned_ensembl_gene_id":"ENSG00000259078.2","gene_symbol":"PTBP1P","gene_name":"polypyrimidine tract binding protein 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:20030]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122888","summary":null,"start":65279267,"end":65281166,"strand":1,"description":"polypyrimidine tract binding protein 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:20030]"}, {"versioned_ensembl_gene_id":"ENSG00000203688.4","gene_symbol":"LINC02487","gene_name":"long intergenic non-protein coding RNA 2487 [Source:HGNC Symbol;Acc:HGNC:53466]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441178","summary":null,"start":167679626,"end":167683787,"strand":-1,"description":"long intergenic non-protein coding RNA 2487 [Source:HGNC Symbol;Acc:HGNC:53466]"}, {"versioned_ensembl_gene_id":"ENSG00000169692.12","gene_symbol":"AGPAT2","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:325]","synonyms":"LPAAT-beta,BSCL","biotype":"protein_coding","ncbi_id":"10555","summary":"This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. The protein is located within the endoplasmic reticulum membrane and converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. Mutations in this gene have been associated with congenital generalized lipodystrophy (CGL), or Berardinelli-Seip syndrome, a disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":136673143,"end":136687423,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:325]"}, {"versioned_ensembl_gene_id":"ENSG00000255726.1","gene_symbol":"AL662844.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31222913,"end":31223093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145416.13","gene_symbol":"MARCH1","gene_name":"membrane associated ring-CH-type finger 1 [Source:HGNC Symbol;Acc:HGNC:26077]","synonyms":"RNF171,MARCH-I,FLJ20668","biotype":"protein_coding","ncbi_id":"55016","summary":"MARCH1 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH1 downregulates the surface expression of major histocompatibility complex (MHC) class II molecules (see MIM 142880) and other glycoproteins by directing them to the late endosomal/lysosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Thibodeau et al., 2008 [PubMed 18389477]; De Gassart et al., 2008 [PubMed 18305173]).[supplied by OMIM, Mar 2010]","start":163524298,"end":164384050,"strand":-1,"description":"membrane associated ring-CH-type finger 1 [Source:HGNC Symbol;Acc:HGNC:26077]"}, {"versioned_ensembl_gene_id":"ENSG00000147684.7","gene_symbol":"NDUFB9","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 [Source:HGNC Symbol;Acc:HGNC:7704]","synonyms":"UQOR22,LYRM3,B22","biotype":"protein_coding","ncbi_id":"4715","summary":"The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":124539103,"end":124568510,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B9 [Source:HGNC Symbol;Acc:HGNC:7704]"}, {"versioned_ensembl_gene_id":"ENSG00000165879.8","gene_symbol":"FRAT1","gene_name":"FRAT1, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:3944]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10023","summary":"The protein encoded by this gene belongs to the GSK-3-binding protein family. The protein inhibits GSK-3-mediated phosphorylation of beta-catenin and positively regulates the Wnt signaling pathway. It may function in tumor progression and in lymphomagenesis. [provided by RefSeq, Oct 2008]","start":97319267,"end":97321915,"strand":1,"description":"FRAT1, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:3944]"}, {"versioned_ensembl_gene_id":"ENSG00000255899.1","gene_symbol":"AL662844.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31224342,"end":31225058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178372.7","gene_symbol":"CALML5","gene_name":"calmodulin like 5 [Source:HGNC Symbol;Acc:HGNC:18180]","synonyms":"CLSP","biotype":"protein_coding","ncbi_id":"51806","summary":"This gene encodes a novel calcium binding protein expressed in the epidermis and related to the calmodulin family of calcium binding proteins. Functional studies with recombinant protein demonstrate it does bind calcium and undergoes a conformational change when it does so. Abundant expression is detected only in reconstructed epidermis and is restricted to differentiating keratinocytes. In addition, it can associate with transglutaminase 3, shown to be a key enzyme in the terminal differentiation of keratinocytes. [provided by RefSeq, Jul 2008]","start":5498697,"end":5499555,"strand":-1,"description":"calmodulin like 5 [Source:HGNC Symbol;Acc:HGNC:18180]"}, {"versioned_ensembl_gene_id":"ENSG00000164508.4","gene_symbol":"HIST1H2AA","gene_name":"histone cluster 1 H2A family member a [Source:HGNC Symbol;Acc:HGNC:18729]","synonyms":"bA317E16.2,H2AFR","biotype":"protein_coding","ncbi_id":"221613","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":25726132,"end":25726527,"strand":-1,"description":"histone cluster 1 H2A family member a [Source:HGNC Symbol;Acc:HGNC:18729]"}, {"versioned_ensembl_gene_id":"ENSG00000206403.11","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"BAT5,NG26,D6S82E","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31677180,"end":31693655,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000250472.1","gene_symbol":"TRIM36-IT1","gene_name":"TRIM36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41422]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874338","summary":null,"start":115148764,"end":115149644,"strand":-1,"description":"TRIM36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41422]"}, {"versioned_ensembl_gene_id":"ENSG00000075073.14","gene_symbol":"TACR2","gene_name":"tachykinin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11527]","synonyms":"TAC2R,SKR,NKNAR,NK2R","biotype":"protein_coding","ncbi_id":"6865","summary":"This gene belongs to a family of genes that function as receptors for tachykinins. Receptor affinities are specified by variations in the 5'-end of the sequence. The receptors belonging to this family are characterized by interactions with G proteins and 7 hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin neuropeptide substance K, also referred to as neurokinin A. [provided by RefSeq, Jul 2008]","start":69403903,"end":69416867,"strand":-1,"description":"tachykinin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11527]"}, {"versioned_ensembl_gene_id":"ENSG00000164933.11","gene_symbol":"SLC25A32","gene_name":"solute carrier family 25 member 32 [Source:HGNC Symbol;Acc:HGNC:29683]","synonyms":"MFTC","biotype":"protein_coding","ncbi_id":"81034","summary":"This gene encodes a member of the P(I/L)W subfamily of mitochondrial carrier family transport proteins. The encoded protein transports folate across the inner mitochondrial membrane. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2013]","start":103398635,"end":103415189,"strand":-1,"description":"solute carrier family 25 member 32 [Source:HGNC Symbol;Acc:HGNC:29683]"}, {"versioned_ensembl_gene_id":"ENSG00000267702.1","gene_symbol":"AP005131.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":13486462,"end":13490676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178363.4","gene_symbol":"CALML3","gene_name":"calmodulin like 3 [Source:HGNC Symbol;Acc:HGNC:1452]","synonyms":"CLP","biotype":"protein_coding","ncbi_id":"810","summary":null,"start":5524009,"end":5526771,"strand":1,"description":"calmodulin like 3 [Source:HGNC Symbol;Acc:HGNC:1452]"}, {"versioned_ensembl_gene_id":"ENSG00000179832.17","gene_symbol":"MROH1","gene_name":"maestro heat like repeat family member 1 [Source:HGNC Symbol;Acc:HGNC:26958]","synonyms":"KIAA1833,HEATR7A","biotype":"protein_coding","ncbi_id":"727957","summary":null,"start":144148016,"end":144261940,"strand":1,"description":"maestro heat like repeat family member 1 [Source:HGNC Symbol;Acc:HGNC:26958]"}, {"versioned_ensembl_gene_id":"ENSG00000267529.3","gene_symbol":"AP005131.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":13471012,"end":13472709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267503.1","gene_symbol":"AP005131.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13561399,"end":13565035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170248.13","gene_symbol":"PDCD6IP","gene_name":"programmed cell death 6 interacting protein [Source:HGNC Symbol;Acc:HGNC:8766]","synonyms":"Hp95,Alix,AIP1","biotype":"protein_coding","ncbi_id":"10015","summary":"This gene encodes a protein that functions within the ESCRT pathway in the abscission stage of cytokinesis, in intralumenal endosomal vesicle formation, and in enveloped virus budding. Studies using mouse cells have shown that overexpression of this protein can block apoptosis. In addition, the product of this gene binds to the product of the PDCD6 gene, a protein required for apoptosis, in a calcium-dependent manner. This gene product also binds to endophilins, proteins that regulate membrane shape during endocytosis. Overexpression of this gene product and endophilins results in cytoplasmic vacuolization, which may be partly responsible for the protection against cell death. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. Related pseudogenes have been identified on chromosome 15. [provided by RefSeq, Jan 2012]","start":33798352,"end":33869707,"strand":1,"description":"programmed cell death 6 interacting protein [Source:HGNC Symbol;Acc:HGNC:8766]"}, {"versioned_ensembl_gene_id":"ENSG00000121481.10","gene_symbol":"RNF2","gene_name":"ring finger protein 2 [Source:HGNC Symbol;Acc:HGNC:10061]","synonyms":"DING,BAP1,BAP-1,RING2,RING1B,HIPI3","biotype":"protein_coding","ncbi_id":"6045","summary":"Polycomb group (PcG) of proteins form the multiprotein complexes that are important for the transcription repression of various genes involved in development and cell proliferation. The protein encoded by this gene is one of the PcG proteins. It has been shown to interact with, and suppress the activity of, transcription factor CP2 (TFCP2/CP2). Studies of the mouse counterpart suggested the involvement of this gene in the specification of anterior-posterior axis, as well as in cell proliferation in early development. This protein was also found to interact with huntingtin interacting protein 2 (HIP2), an ubiquitin-conjugating enzyme, and possess ubiquitin ligase activity. [provided by RefSeq, Jul 2008]","start":185045364,"end":185102608,"strand":1,"description":"ring finger protein 2 [Source:HGNC Symbol;Acc:HGNC:10061]"}, {"versioned_ensembl_gene_id":"ENSG00000132669.12","gene_symbol":"RIN2","gene_name":"Ras and Rab interactor 2 [Source:HGNC Symbol;Acc:HGNC:18750]","synonyms":"RASSF4","biotype":"protein_coding","ncbi_id":"54453","summary":"The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011]","start":19886521,"end":20002457,"strand":1,"description":"Ras and Rab interactor 2 [Source:HGNC Symbol;Acc:HGNC:18750]"}, {"versioned_ensembl_gene_id":"ENSG00000267694.1","gene_symbol":"AP005131.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13461020,"end":13470823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256462.1","gene_symbol":"AL732437.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5524976,"end":5525742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255002.1","gene_symbol":"LINC02324","gene_name":"long intergenic non-protein coding RNA 2324 [Source:HGNC Symbol;Acc:HGNC:53244]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128233","summary":null,"start":65212893,"end":65222347,"strand":-1,"description":"long intergenic non-protein coding RNA 2324 [Source:HGNC Symbol;Acc:HGNC:53244]"}, {"versioned_ensembl_gene_id":"ENSG00000205488.8","gene_symbol":"CALML3-AS1","gene_name":"CALML3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44682]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132159","summary":null,"start":5514244,"end":5526246,"strand":-1,"description":"CALML3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44682]"}, {"versioned_ensembl_gene_id":"ENSG00000118434.8","gene_symbol":"SPACA1","gene_name":"sperm acrosome associated 1 [Source:HGNC Symbol;Acc:HGNC:14967]","synonyms":"SAMP32","biotype":"protein_coding","ncbi_id":"81833","summary":"The correlation of anti-sperm antibodies with cases of unexplained infertility implicates a role for these antibodies in blocking fertilization. Improved diagnosis and treatment of immunologic infertility, as well as identification of proteins for targeted contraception, are dependent on the identification and characterization of relevant sperm antigens. The protein expressed by this gene is recognized by anti-sperm antibodies from infertile males. Furthermore, antibodies generated against the recombinant protein block in vitro fertilization. This protein localizes to the acrosomal membrane of spermatids and mature spermatozoa where it is thought to play a role in acrosomal morphogenesis and in sperm-egg binding and fusion, respectively. [provided by RefSeq, Jul 2008]","start":88047789,"end":88066832,"strand":1,"description":"sperm acrosome associated 1 [Source:HGNC Symbol;Acc:HGNC:14967]"}, {"versioned_ensembl_gene_id":"ENSG00000226217.1","gene_symbol":"RPL19P1","gene_name":"ribosomal protein L19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16595]","synonyms":"dJ860F19.2","biotype":"processed_pseudogene","ncbi_id":"140759","summary":null,"start":2780614,"end":2781041,"strand":1,"description":"ribosomal protein L19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16595]"}, {"versioned_ensembl_gene_id":"ENSG00000267690.1","gene_symbol":"LDLRAD4-AS1","gene_name":"LDLRAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48592]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288122","summary":null,"start":13419421,"end":13427480,"strand":-1,"description":"LDLRAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48592]"}, {"versioned_ensembl_gene_id":"ENSG00000277412.1","gene_symbol":"BX005040.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61194211,"end":61203446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229759.1","gene_symbol":"MRPS18AP1","gene_name":"mitochondrial ribosomal protein S18A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359761","summary":null,"start":48256350,"end":48256938,"strand":-1,"description":"mitochondrial ribosomal protein S18A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29740]"}, {"versioned_ensembl_gene_id":"ENSG00000203690.11","gene_symbol":"TCP10","gene_name":"t-complex 10 [Source:HGNC Symbol;Acc:HGNC:11656]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6953","summary":null,"start":167357031,"end":167384510,"strand":-1,"description":"t-complex 10 [Source:HGNC Symbol;Acc:HGNC:11656]"}, {"versioned_ensembl_gene_id":"ENSG00000267177.1","gene_symbol":"AP002505.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13234945,"end":13236470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276997.4","gene_symbol":"AL513314.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222477252,"end":222504622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170807.11","gene_symbol":"LMOD2","gene_name":"leiomodin 2 [Source:HGNC Symbol;Acc:HGNC:6648]","synonyms":null,"biotype":"protein_coding","ncbi_id":"442721","summary":null,"start":123655807,"end":123664290,"strand":1,"description":"leiomodin 2 [Source:HGNC Symbol;Acc:HGNC:6648]"}, {"versioned_ensembl_gene_id":"ENSG00000204718.3","gene_symbol":"CNN2P12","gene_name":"calponin 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39834]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131550","summary":null,"start":18726706,"end":18727414,"strand":1,"description":"calponin 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39834]"}, {"versioned_ensembl_gene_id":"ENSG00000279275.1","gene_symbol":"AP002505.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":13279415,"end":13280110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266954.1","gene_symbol":"AP001010.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13644815,"end":13645685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267366.1","gene_symbol":"AP005131.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13500641,"end":13501289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267136.1","gene_symbol":"AP005131.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13514520,"end":13522888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232185.1","gene_symbol":"CNOT7P2","gene_name":"CCR4-NOT transcription complex subunit 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44249]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132332","summary":null,"start":115564601,"end":115565432,"strand":1,"description":"CCR4-NOT transcription complex subunit 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44249]"}, {"versioned_ensembl_gene_id":"ENSG00000258878.1","gene_symbol":"AL355076.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65234515,"end":65235101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175513.9","gene_symbol":"TSGA10IP","gene_name":"testis specific 10 interacting protein [Source:HGNC Symbol;Acc:HGNC:26555]","synonyms":"FLJ32880,FAM161C","biotype":"protein_coding","ncbi_id":"254187","summary":null,"start":65945445,"end":65959963,"strand":1,"description":"testis specific 10 interacting protein [Source:HGNC Symbol;Acc:HGNC:26555]"}, {"versioned_ensembl_gene_id":"ENSG00000213347.10","gene_symbol":"MXD3","gene_name":"MAX dimerization protein 3 [Source:HGNC Symbol;Acc:HGNC:14008]","synonyms":"MAD3,bHLHc13","biotype":"protein_coding","ncbi_id":"83463","summary":"This gene encodes a member of the Myc superfamily of basic helix-loop-helix leucine zipper transcriptional regulators. The encoded protein forms a heterodimer with the cofactor MAX which binds specific E-box DNA motifs in the promoters of target genes and regulates their transcription. Disruption of the MAX-MXD3 complex is associated with uncontrolled cell proliferation and tumorigenesis. Transcript variants of this gene encoding different isoforms have been described.[provided by RefSeq, Dec 2008]","start":177301461,"end":177312757,"strand":-1,"description":"MAX dimerization protein 3 [Source:HGNC Symbol;Acc:HGNC:14008]"}, {"versioned_ensembl_gene_id":"ENSG00000236898.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33232201,"end":33237743,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000180150.5","gene_symbol":"HMGN2P9","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:4987]","synonyms":"HMGN2L9,HMG17L1,dJ388M5.2","biotype":"processed_pseudogene","ncbi_id":"23605","summary":null,"start":43802544,"end":43802772,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:4987]"}, {"versioned_ensembl_gene_id":"ENSG00000273153.1","gene_symbol":"AC067747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17137336,"end":17137585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258760.1","gene_symbol":"AL355076.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65236480,"end":65318790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170873.18","gene_symbol":"MTSS1","gene_name":"MTSS1, I-BAR domain containing [Source:HGNC Symbol;Acc:HGNC:20443]","synonyms":"MIM,KIAA0429,MIMB,MIMA","biotype":"protein_coding","ncbi_id":"9788","summary":null,"start":124550790,"end":124728429,"strand":-1,"description":"MTSS1, I-BAR domain containing [Source:HGNC Symbol;Acc:HGNC:20443]"}, {"versioned_ensembl_gene_id":"ENSG00000270631.1","gene_symbol":"AL592436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115577229,"end":115577786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235500.2","gene_symbol":"SNX19P2","gene_name":"sorting nexin 19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38115]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400094","summary":null,"start":18892260,"end":18895230,"strand":-1,"description":"sorting nexin 19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38115]"}, {"versioned_ensembl_gene_id":"ENSG00000102970.10","gene_symbol":"CCL17","gene_name":"C-C motif chemokine ligand 17 [Source:HGNC Symbol;Acc:HGNC:10615]","synonyms":"TARC,SCYA17,ABCD-2","biotype":"protein_coding","ncbi_id":"6361","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 16. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for T lymphocytes, but not monocytes or granulocytes. The product of this gene binds to chemokine receptors CCR4 and CCR8. This chemokine plays important roles in T cell development in thymus as well as in trafficking and activation of mature T cells. [provided by RefSeq, Sep 2014]","start":57404767,"end":57416062,"strand":1,"description":"C-C motif chemokine ligand 17 [Source:HGNC Symbol;Acc:HGNC:10615]"}, {"versioned_ensembl_gene_id":"ENSG00000214759.3","gene_symbol":"AL355076.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65268829,"end":65269098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258613.1","gene_symbol":"RPL21P7","gene_name":"ribosomal protein L21 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"145370","summary":null,"start":65266638,"end":65267690,"strand":-1,"description":"ribosomal protein L21 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19772]"}, {"versioned_ensembl_gene_id":"ENSG00000280414.1","gene_symbol":"AC018470.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":174334438,"end":174337566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217236.1","gene_symbol":"SP9","gene_name":"Sp9 transcription factor [Source:HGNC Symbol;Acc:HGNC:30690]","synonyms":"ZNF990","biotype":"protein_coding","ncbi_id":"100131390","summary":null,"start":174334946,"end":174338492,"strand":1,"description":"Sp9 transcription factor [Source:HGNC Symbol;Acc:HGNC:30690]"}, {"versioned_ensembl_gene_id":"ENSG00000178556.8","gene_symbol":"CKS1BP6","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24608]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652904","summary":null,"start":30617454,"end":30617693,"strand":1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24608]"}, {"versioned_ensembl_gene_id":"ENSG00000106299.7","gene_symbol":"WASL","gene_name":"Wiskott-Aldrich syndrome like [Source:HGNC Symbol;Acc:HGNC:12735]","synonyms":"WASPB,NWASP,N-WASP","biotype":"protein_coding","ncbi_id":"8976","summary":"This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family. Wiskott-Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin-related protein-2/3 (ARP2/3) complex. The encoded protein may be involved in the formation of long actin microspikes, and in neurite extension. [provided by RefSeq, Jul 2013]","start":123681935,"end":123749067,"strand":-1,"description":"Wiskott-Aldrich syndrome like [Source:HGNC Symbol;Acc:HGNC:12735]"}, {"versioned_ensembl_gene_id":"ENSG00000267305.2","gene_symbol":"AL592148.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":222510169,"end":222519732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280629.1","gene_symbol":"AC233280.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232368.1","gene_symbol":"FTLP2","gene_name":"ferritin light chain pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4001]","synonyms":"FTLL2","biotype":"processed_pseudogene","ncbi_id":"392437","summary":null,"start":30630298,"end":30630825,"strand":1,"description":"ferritin light chain pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4001]"}, {"versioned_ensembl_gene_id":"ENSG00000225809.1","gene_symbol":"RBMY2KP","gene_name":"RNA binding motif protein, Y-linked, family 2, member K pseudogene [Source:HGNC Symbol;Acc:HGNC:23888]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"140100","summary":null,"start":8264449,"end":8277188,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member K pseudogene [Source:HGNC Symbol;Acc:HGNC:23888]"}, {"versioned_ensembl_gene_id":"ENSG00000281798.1","gene_symbol":"AC233280.16","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226513.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33244216,"end":33247752,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000250362.1","gene_symbol":"AC008592.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":95861786,"end":95874519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197635.9","gene_symbol":"DPP4","gene_name":"dipeptidyl peptidase 4 [Source:HGNC Symbol;Acc:HGNC:3009]","synonyms":"DPPIV,CD26,ADCP2","biotype":"protein_coding","ncbi_id":"1803","summary":"The DPP4 gene encodes dipeptidyl peptidase 4, which is identical to adenosine deaminase complexing protein-2, and to the T-cell activation antigen CD26. It is an intrinsic type II transmembrane glycoprotein and a serine exopeptidase that cleaves X-proline dipeptides from the N-terminus of polypeptides. Dipeptidyl peptidase 4 is highly involved in glucose and insulin metabolism, as well as in immune regulation. This protein was shown to be a functional receptor for Middle East respiratory syndrome coronavirus (MERS-CoV), and protein modeling suggests that it may play a similar role with SARS-CoV-2, the virus responsible for COVID-19. [provided by RefSeq, Apr 2020]","start":161992241,"end":162074542,"strand":-1,"description":"dipeptidyl peptidase 4 [Source:HGNC Symbol;Acc:HGNC:3009]"}, {"versioned_ensembl_gene_id":"ENSG00000236195.1","gene_symbol":"RNMTL1P2","gene_name":"RNA methyltransferase like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44906]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420223","summary":null,"start":17962079,"end":17963029,"strand":1,"description":"RNA methyltransferase like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44906]"}, {"versioned_ensembl_gene_id":"ENSG00000272927.1","gene_symbol":"AC107464.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":661209,"end":661945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162746.14","gene_symbol":"FCRLB","gene_name":"Fc receptor like B [Source:HGNC Symbol;Acc:HGNC:26431]","synonyms":"FREB-2,FLJ31052,FCRLY,FCRLM2,FCRL2","biotype":"protein_coding","ncbi_id":"127943","summary":"FCRL2 belongs to the Fc receptor family. Fc receptors are involved in phagocytosis, antibody-dependent cell cytotoxicity, immediate hypersensitivity, and transcytosis of immunoglobulins via their ability to bind immunoglobulin (Ig) constant regions (Chikaev et al., 2005 [PubMed 15676285]).[supplied by OMIM, Mar 2008]","start":161721563,"end":161728143,"strand":1,"description":"Fc receptor like B [Source:HGNC Symbol;Acc:HGNC:26431]"}, {"versioned_ensembl_gene_id":"ENSG00000280340.1","gene_symbol":"AC080080.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18000290,"end":18000879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100142.14","gene_symbol":"POLR2F","gene_name":"RNA polymerase II subunit F [Source:HGNC Symbol;Acc:HGNC:9193]","synonyms":"RPB6,HRBP14.4","biotype":"protein_coding","ncbi_id":"5435","summary":"This gene encodes the sixth largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. In yeast, this polymerase subunit, in combination with at least two other subunits, forms a structure that stabilizes the transcribing polymerase on the DNA template. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":37952607,"end":38041915,"strand":1,"description":"RNA polymerase II subunit F [Source:HGNC Symbol;Acc:HGNC:9193]"}, {"versioned_ensembl_gene_id":"ENSG00000236905.2","gene_symbol":"AC104333.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212824027,"end":212824505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281160.1","gene_symbol":"AC018358.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42264989,"end":42266390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168379.8","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33252873,"end":33269193,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000281246.1","gene_symbol":"AF186996.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125703375,"end":125704277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229716.2","gene_symbol":"RPL23AP19","gene_name":"ribosomal protein L23a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36708]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131143","summary":null,"start":8831007,"end":8831375,"strand":1,"description":"ribosomal protein L23a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36708]"}, {"versioned_ensembl_gene_id":"ENSG00000133256.12","gene_symbol":"PDE6B","gene_name":"phosphodiesterase 6B [Source:HGNC Symbol;Acc:HGNC:8786]","synonyms":"rd1,PDEB,CSNBAD2,CSNB3,RP40","biotype":"protein_coding","ncbi_id":"5158","summary":"Photon absorption triggers a signaling cascade in rod photoreceptors that activates cGMP phosphodiesterase (PDE), resulting in the rapid hydrolysis of cGMP, closure of cGMP-gated cation channels, and hyperpolarization of the cell. PDE is a peripheral membrane heterotrimeric enzyme made up of alpha, beta, and gamma subunits. This gene encodes the beta subunit. Mutations in this gene result in retinitis pigmentosa and autosomal dominant congenital stationary night blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":625584,"end":670782,"strand":1,"description":"phosphodiesterase 6B [Source:HGNC Symbol;Acc:HGNC:8786]"}, {"versioned_ensembl_gene_id":"ENSG00000139874.5","gene_symbol":"SSTR1","gene_name":"somatostatin receptor 1 [Source:HGNC Symbol;Acc:HGNC:11330]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6751","summary":"Somatostatins are peptide hormones that regulate diverse cellular functions such as neurotransmission, cell proliferation, and endocrine signaling as well as inhibiting the release of many hormones and other secretory proteins. Somatostatin has two active forms of 14 and 28 amino acids. The biological effects of somatostatins are mediated by a family of G-protein coupled somatostatin receptors that are expressed in a tissue-specific manner. The protein encoded by this gene is a member of the superfamily of somatostatin receptors having seven transmembrane segments. Somatostatin receptors form homodimers and heterodimers with other members of the superfamily as well as with other G-protein coupled receptors and receptor tyrosine kinases. This somatostatin receptor has greater affinity for somatostatin-14 than -28. [provided by RefSeq, Jul 2012]","start":38207999,"end":38213067,"strand":1,"description":"somatostatin receptor 1 [Source:HGNC Symbol;Acc:HGNC:11330]"}, {"versioned_ensembl_gene_id":"ENSG00000273381.1","gene_symbol":"AL158071.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91206175,"end":91210299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173218.14","gene_symbol":"VANGL1","gene_name":"VANGL planar cell polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:15512]","synonyms":"STB2","biotype":"protein_coding","ncbi_id":"81839","summary":"This gene encodes a member of the tretraspanin family. The encoded protein may be involved in mediating intestinal trefoil factor induced wound healing in the intestinal mucosa. Mutations in this gene are associated with neural tube defects. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":115641953,"end":115698224,"strand":1,"description":"VANGL planar cell polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:15512]"}, {"versioned_ensembl_gene_id":"ENSG00000273449.1","gene_symbol":"AC093788.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163529771,"end":163530697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229937.6","gene_symbol":"PRPS1L1","gene_name":"phosphoribosyl pyrophosphate synthetase 1-like 1 [Source:HGNC Symbol;Acc:HGNC:9463]","synonyms":"PRPSL,PRPS3","biotype":"protein_coding","ncbi_id":"221823","summary":"This intronless gene is specifically expressed in the testis, and encodes a protein that is highly homologous to the two subunits of phosphoribosylpyrophosphate synthetase encoded by human X-linked genes, PRPS1 and PRPS2. These enzymes convert pyrimidine, purine or pyridine bases to the corresponding ribonucleoside monophosphates. In vitro transcription/translation and site-directed mutagenesis studies indicate that translation of this mRNA initiates exclusively at a non-AUG (ACG) codon. [provided by RefSeq, Jul 2008]","start":18026774,"end":18027863,"strand":-1,"description":"phosphoribosyl pyrophosphate synthetase 1-like 1 [Source:HGNC Symbol;Acc:HGNC:9463]"}, {"versioned_ensembl_gene_id":"ENSG00000177803.7","gene_symbol":"AC112247.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163932526,"end":163933182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185523.6","gene_symbol":"SPATA45","gene_name":"spermatogenesis associated 45 [Source:HGNC Symbol;Acc:HGNC:33709]","synonyms":"LOC149643,C1orf227","biotype":"protein_coding","ncbi_id":"149643","summary":null,"start":212830141,"end":212847649,"strand":-1,"description":"spermatogenesis associated 45 [Source:HGNC Symbol;Acc:HGNC:33709]"}, {"versioned_ensembl_gene_id":"ENSG00000232734.1","gene_symbol":"ATP5G1P7","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39510]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130962","summary":null,"start":69432972,"end":69433371,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39510]"}, {"versioned_ensembl_gene_id":"ENSG00000282327.1","gene_symbol":"AC134503.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180201159,"end":180201212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280982.1","gene_symbol":"AF186996.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125712140,"end":125713051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213158.6","gene_symbol":"GAPDHP36","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37790]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647249","summary":null,"start":180212191,"end":180213108,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37790]"}, {"versioned_ensembl_gene_id":"ENSG00000281785.1","gene_symbol":"AF186996.14","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125724567,"end":125725463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272686.1","gene_symbol":"AC006333.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123749068,"end":123751166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134330.18","gene_symbol":"IAH1","gene_name":"isoamyl acetate-hydrolyzing esterase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285148","summary":null,"start":9473658,"end":9496543,"strand":1,"description":"isoamyl acetate-hydrolyzing esterase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27696]"}, {"versioned_ensembl_gene_id":"ENSG00000232792.2","gene_symbol":"FTH1P25","gene_name":"ferritin heavy chain 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37643]","synonyms":"FTHL25","biotype":"processed_pseudogene","ncbi_id":"100462799","summary":null,"start":185071567,"end":185072035,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37643]"}, {"versioned_ensembl_gene_id":"ENSG00000230375.1","gene_symbol":"GSTA11P","gene_name":"glutathione S-transferase alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:49905]","synonyms":"GSTAP3","biotype":"unprocessed_pseudogene","ncbi_id":"647175","summary":null,"start":52847910,"end":52870329,"strand":-1,"description":"glutathione S-transferase alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:49905]"}, {"versioned_ensembl_gene_id":"ENSG00000236317.1","gene_symbol":"AC104333.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212855175,"end":212855366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239880.1","gene_symbol":"AC068760.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180323107,"end":180325059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227107.1","gene_symbol":"AC104667.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":237612977,"end":237626525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198468.7","gene_symbol":"FLVCR1-AS1","gene_name":"FLVCR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39077]","synonyms":"NCRNA00292,LQK1","biotype":"lincRNA","ncbi_id":"642946","summary":null,"start":212852108,"end":212858088,"strand":-1,"description":"FLVCR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39077]"}, {"versioned_ensembl_gene_id":"ENSG00000255867.1","gene_symbol":"DENND5B-AS1","gene_name":"DENND5B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42517]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874249","summary":null,"start":31589923,"end":31615666,"strand":1,"description":"DENND5B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42517]"}, {"versioned_ensembl_gene_id":"ENSG00000241696.1","gene_symbol":"LINC02053","gene_name":"long intergenic non-protein coding RNA 2053 [Source:HGNC Symbol;Acc:HGNC:52893]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505609","summary":null,"start":180414174,"end":180422506,"strand":1,"description":"long intergenic non-protein coding RNA 2053 [Source:HGNC Symbol;Acc:HGNC:52893]"}, {"versioned_ensembl_gene_id":"ENSG00000275769.1","gene_symbol":"AC068792.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31443792,"end":31444208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120440.13","gene_symbol":"TTLL2","gene_name":"tubulin tyrosine ligase like 2 [Source:HGNC Symbol;Acc:HGNC:21211]","synonyms":"NYD-TSPG,dJ366N23.3,C6orf104","biotype":"protein_coding","ncbi_id":"83887","summary":null,"start":167325086,"end":167359503,"strand":1,"description":"tubulin tyrosine ligase like 2 [Source:HGNC Symbol;Acc:HGNC:21211]"}, {"versioned_ensembl_gene_id":"ENSG00000235182.1","gene_symbol":"AC104333.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212853280,"end":212853426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263749.1","gene_symbol":"OOSP1P2","gene_name":"oocyte secreted protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49241]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480252","summary":null,"start":32343774,"end":32344124,"strand":-1,"description":"oocyte secreted protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49241]"}, {"versioned_ensembl_gene_id":"ENSG00000105609.16","gene_symbol":"LILRB5","gene_name":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]","synonyms":"LIR8,LIR-8,CD85c","biotype":"protein_coding","ncbi_id":"10990","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54249431,"end":54257301,"strand":-1,"description":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]"}, {"versioned_ensembl_gene_id":"ENSG00000225349.2","gene_symbol":"AC022080.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31534715,"end":31535247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225850.3","gene_symbol":"AL355490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97334564,"end":97343203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088882.7","gene_symbol":"CPXM1","gene_name":"carboxypeptidase X, M14 family member 1 [Source:HGNC Symbol;Acc:HGNC:15771]","synonyms":"CPXM,CPX1,CPX-1","biotype":"protein_coding","ncbi_id":"56265","summary":"This gene likely encodes a member of the carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a carboxypeptidase domain, but the protein appears to lack residues necessary for carboxypeptidase activity.[provided by RefSeq, May 2010]","start":2794069,"end":2800637,"strand":-1,"description":"carboxypeptidase X, M14 family member 1 [Source:HGNC Symbol;Acc:HGNC:15771]"}, {"versioned_ensembl_gene_id":"ENSG00000152128.13","gene_symbol":"TMEM163","gene_name":"transmembrane protein 163 [Source:HGNC Symbol;Acc:HGNC:25380]","synonyms":"SV31,DKFZP566N034","biotype":"protein_coding","ncbi_id":"81615","summary":null,"start":134455759,"end":134719000,"strand":-1,"description":"transmembrane protein 163 [Source:HGNC Symbol;Acc:HGNC:25380]"}, {"versioned_ensembl_gene_id":"ENSG00000241946.1","gene_symbol":"AC068298.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180589887,"end":180590047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181274.6","gene_symbol":"FRAT2","gene_name":"FRAT2, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:16048]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23401","summary":"The protein encoded by this intronless gene belongs to the GSK-3-binding protein family. Studies show that this protein plays a role as a positive regulator of the WNT signaling pathway. It may be upregulated in tumor progression. [provided by RefSeq, Jul 2008]","start":97332497,"end":97334709,"strand":-1,"description":"FRAT2, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:16048]"}, {"versioned_ensembl_gene_id":"ENSG00000170456.15","gene_symbol":"DENND5B","gene_name":"DENN domain containing 5B [Source:HGNC Symbol;Acc:HGNC:28338]","synonyms":"MGC24039","biotype":"protein_coding","ncbi_id":"160518","summary":null,"start":31382223,"end":31591097,"strand":-1,"description":"DENN domain containing 5B [Source:HGNC Symbol;Acc:HGNC:28338]"}, {"versioned_ensembl_gene_id":"ENSG00000239774.1","gene_symbol":"AC125618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180566718,"end":180601935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213606.3","gene_symbol":"AKR1B10P1","gene_name":"aldo-keto reductase family 1 member B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340888","summary":null,"start":67750284,"end":67751225,"strand":1,"description":"aldo-keto reductase family 1 member B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45062]"}, {"versioned_ensembl_gene_id":"ENSG00000148090.11","gene_symbol":"AUH","gene_name":"AU RNA binding methylglutaconyl-CoA hydratase [Source:HGNC Symbol;Acc:HGNC:890]","synonyms":null,"biotype":"protein_coding","ncbi_id":"549","summary":"This gene encodes bifunctional mitochondrial protein that has both RNA-binding and hydratase activities. The encoded protein is a methylglutaconyl-CoA hydratase that catalyzes the hydration of 3-methylglutaconyl-CoA to 3-hydroxy-3-methyl-glutaryl-CoA, a critical step in the leucine degradation pathway. This protein also binds AU-rich elements (AREs) found in the 3' UTRs of rapidly decaying mRNAs including c-fos, c-myc and granulocyte/ macrophage colony stimulating factor. ARE elements are involved in directing RNA to rapid degradation and deadenylation. This protein is localizes to the mitochondrial matrix and the inner mitochondrial membrane and may be involved in mitochondrial protein synthesis. Mutations in this gene are the cause of 3-methylglutaconic aciduria, type I. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":91213815,"end":91361913,"strand":-1,"description":"AU RNA binding methylglutaconyl-CoA hydratase [Source:HGNC Symbol;Acc:HGNC:890]"}, {"versioned_ensembl_gene_id":"ENSG00000263745.6","gene_symbol":"AP005230.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1883524,"end":2489426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217447.1","gene_symbol":"AL021331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167347472,"end":167348053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223635.1","gene_symbol":"AL121990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":229508501,"end":229514272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248774.1","gene_symbol":"AC097534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173322206,"end":173329694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109586.11","gene_symbol":"GALNT7","gene_name":"polypeptide N-acetylgalactosaminyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4129]","synonyms":"GALNAC-T7","biotype":"protein_coding","ncbi_id":"51809","summary":"This gene encodes GalNAc transferase 7, a member of the GalNAc-transferase family. The enzyme encoded by this gene controls the initiation step of mucin-type O-linked protein glycosylation and transfer of N-acetylgalactosamine to serine and threonine amino acid residues. This enzyme is a type II transmembrane protein and shares common sequence motifs with other family members. Unlike other family members, this enzyme shows exclusive specificity for partially GalNAc-glycosylated acceptor substrates and shows no activity with non-glycosylated peptides. This protein may function as a follow-up enzyme in the initiation step of O-glycosylation. [provided by RefSeq, Jul 2008]","start":173168753,"end":173323967,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4129]"}, {"versioned_ensembl_gene_id":"ENSG00000077150.18","gene_symbol":"NFKB2","gene_name":"nuclear factor kappa B subunit 2 [Source:HGNC Symbol;Acc:HGNC:7795]","synonyms":"p52,p49/p100,p105,NF-kB2,LYT-10","biotype":"protein_coding","ncbi_id":"4791","summary":"This gene encodes a subunit of the transcription factor complex nuclear factor-kappa-B (NFkB). The NFkB complex is expressed in numerous cell types and functions as a central activator of genes involved in inflammation and immune function. The protein encoded by this gene can function as both a transcriptional activator or repressor depending on its dimerization partner. The p100 full-length protein is co-translationally processed into a p52 active form. Chromosomal rearrangements and translocations of this locus have been observed in B cell lymphomas, some of which may result in the formation of fusion proteins. There is a pseudogene for this gene on chromosome 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":102394110,"end":102402529,"strand":1,"description":"nuclear factor kappa B subunit 2 [Source:HGNC Symbol;Acc:HGNC:7795]"}, {"versioned_ensembl_gene_id":"ENSG00000260161.1","gene_symbol":"MTCYBP28","gene_name":"mitochondrially encoded cytochrome b pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:51994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075134","summary":null,"start":82120638,"end":82121769,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:51994]"}, {"versioned_ensembl_gene_id":"ENSG00000261235.1","gene_symbol":"AC092142.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82044336,"end":82139631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146047.6","gene_symbol":"HIST1H2BA","gene_name":"histone cluster 1 H2B family member a [Source:HGNC Symbol;Acc:HGNC:18730]","synonyms":"TSH2B,STBP,H2BFU,bA317E16.3","biotype":"protein_coding","ncbi_id":"255626","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a testis/sperm-specific member of the histone H2B family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":25726777,"end":25727292,"strand":1,"description":"histone cluster 1 H2B family member a [Source:HGNC Symbol;Acc:HGNC:18730]"}, {"versioned_ensembl_gene_id":"ENSG00000269038.1","gene_symbol":"AP001462.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64778954,"end":64779405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169230.9","gene_symbol":"PRELID1","gene_name":"PRELI domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30255]","synonyms":"PRELI,CGI-106,PX19","biotype":"protein_coding","ncbi_id":"27166","summary":"This gene encodes a member of the late embryogenesis abundant motif-containing protein family. The encoded protein is localized to mitochondria and may function as a cytoprotectant by regulating cell death and differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. Several related pseudogenes have been identified. [provided by RefSeq, Nov 2012]","start":177303774,"end":177306959,"strand":1,"description":"PRELI domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30255]"}, {"versioned_ensembl_gene_id":"ENSG00000086696.10","gene_symbol":"HSD17B2","gene_name":"hydroxysteroid 17-beta dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:5211]","synonyms":"SDR9C2,HSD17","biotype":"protein_coding","ncbi_id":"3294","summary":null,"start":82035004,"end":82098534,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:5211]"}, {"versioned_ensembl_gene_id":"ENSG00000170876.7","gene_symbol":"TMEM43","gene_name":"transmembrane protein 43 [Source:HGNC Symbol;Acc:HGNC:28472]","synonyms":"LUMA,DKFZp586G1919,ARVD5,MGC3222","biotype":"protein_coding","ncbi_id":"79188","summary":"This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element for PPAR gamma (an adipogenic transcription factor), which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC. [provided by RefSeq, Oct 2008]","start":14124940,"end":14143679,"strand":1,"description":"transmembrane protein 43 [Source:HGNC Symbol;Acc:HGNC:28472]"}, {"versioned_ensembl_gene_id":"ENSG00000143771.11","gene_symbol":"CNIH4","gene_name":"cornichon family AMPA receptor auxiliary protein 4 [Source:HGNC Symbol;Acc:HGNC:25013]","synonyms":"HSPC163","biotype":"protein_coding","ncbi_id":"29097","summary":null,"start":224356850,"end":224379459,"strand":1,"description":"cornichon family AMPA receptor auxiliary protein 4 [Source:HGNC Symbol;Acc:HGNC:25013]"}, {"versioned_ensembl_gene_id":"ENSG00000238148.2","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31242712,"end":31243133,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000048649.13","gene_symbol":"RSF1","gene_name":"remodeling and spacing factor 1 [Source:HGNC Symbol;Acc:HGNC:18118]","synonyms":"XAP8,RSF-1,p325,HBXAP","biotype":"protein_coding","ncbi_id":"51773","summary":"This gene encodes a nuclear protein that interacts with hepatitis B virus X protein (HBX) and facilitates transcription of hepatitis B virus genes by the HBX transcription activator, suggesting a role for this interaction in the virus life cycle. This protein also interacts with SNF2H protein to form the RSF chromatin-remodeling complex, where the SNF2H subunit functions as the nucleosome-dependent ATPase, and this protein as the histone chaperone. [provided by RefSeq, Sep 2011]","start":77659996,"end":77821017,"strand":-1,"description":"remodeling and spacing factor 1 [Source:HGNC Symbol;Acc:HGNC:18118]"}, {"versioned_ensembl_gene_id":"ENSG00000264189.1","gene_symbol":"AP005262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1927727,"end":1929094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264958.2","gene_symbol":"ALOX12P1","gene_name":"arachidonate 12-lipoxygenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:431]","synonyms":"ALOX12P","biotype":"unprocessed_pseudogene","ncbi_id":"243","summary":null,"start":30529688,"end":30542416,"strand":1,"description":"arachidonate 12-lipoxygenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:431]"}, {"versioned_ensembl_gene_id":"ENSG00000059378.12","gene_symbol":"PARP12","gene_name":"poly(ADP-ribose) polymerase family member 12 [Source:HGNC Symbol;Acc:HGNC:21919]","synonyms":"PARP-12,FLJ22693,ZC3HDC1,ZC3H1","biotype":"protein_coding","ncbi_id":"64761","summary":null,"start":140023744,"end":140063721,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 12 [Source:HGNC Symbol;Acc:HGNC:21919]"}, {"versioned_ensembl_gene_id":"ENSG00000228454.7","gene_symbol":"C4B","gene_name":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]","synonyms":"CO4,C4B3,CH,C4B1,CPAMD3,C4F","biotype":"protein_coding","ncbi_id":"721","summary":"This gene encodes the basic form of complement factor 4, and together with the C4A gene, is part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, May 2020]","start":32007416,"end":32028073,"strand":1,"description":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]"}, {"versioned_ensembl_gene_id":"ENSG00000215601.3","gene_symbol":"TSPY24P","gene_name":"testis specific protein, Y-linked 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:38725]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874287","summary":null,"start":8280198,"end":8282209,"strand":1,"description":"testis specific protein, Y-linked 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:38725]"}, {"versioned_ensembl_gene_id":"ENSG00000267713.1","gene_symbol":"AC012433.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":50669510,"end":50670215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100146.16","gene_symbol":"SOX10","gene_name":"SRY-box 10 [Source:HGNC Symbol;Acc:HGNC:11190]","synonyms":"WS4,WS2E,DOM","biotype":"protein_coding","ncbi_id":"6663","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008]","start":37970686,"end":37987422,"strand":-1,"description":"SRY-box 10 [Source:HGNC Symbol;Acc:HGNC:11190]"}, {"versioned_ensembl_gene_id":"ENSG00000151552.11","gene_symbol":"QDPR","gene_name":"quinoid dihydropteridine reductase [Source:HGNC Symbol;Acc:HGNC:9752]","synonyms":"PKU2,DHPR,SDR33C1","biotype":"protein_coding","ncbi_id":"5860","summary":"This gene encodes the enzyme dihydropteridine reductase, which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin. This enzyme is an essential component of the pterin-dependent aromatic amino acid hydroxylating systems. Mutations in this gene resulting in QDPR deficiency include aberrant splicing, amino acid substitutions, insertions, or premature terminations. Dihydropteridine reductase deficiency presents as atypical phenylketonuria due to insufficient production of biopterin, a cofactor for phenylalanine hydroxylase. [provided by RefSeq, Jul 2008]","start":17460261,"end":17512234,"strand":-1,"description":"quinoid dihydropteridine reductase [Source:HGNC Symbol;Acc:HGNC:9752]"}, {"versioned_ensembl_gene_id":"ENSG00000141639.11","gene_symbol":"MAPK4","gene_name":"mitogen-activated protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:6878]","synonyms":"Erk4,Erk3-related,PRKM4","biotype":"protein_coding","ncbi_id":"5596","summary":"Mitogen-activated protein kinase 4 is a member of the mitogen-activated protein kinase family. Tyrosine kinase growth factor receptors activate mitogen-activated protein kinases which then translocate into the nucleus and phosphorylate nuclear targets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":50560078,"end":50731824,"strand":1,"description":"mitogen-activated protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:6878]"}, {"versioned_ensembl_gene_id":"ENSG00000263674.1","gene_symbol":"AC026620.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32280387,"end":32280953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224634.1","gene_symbol":"ZNF736P6Y","gene_name":"zinc finger protein 736 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:38440]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419732","summary":null,"start":8350931,"end":8352143,"strand":1,"description":"zinc finger protein 736 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:38440]"}, {"versioned_ensembl_gene_id":"ENSG00000251162.1","gene_symbol":"AC074198.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164597719,"end":164597976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162769.12","gene_symbol":"FLVCR1","gene_name":"feline leukemia virus subgroup C cellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:24682]","synonyms":"PCA,MFSD7B,FLVCR,AXPC1","biotype":"protein_coding","ncbi_id":"28982","summary":"This gene encodes a member of the major facilitator superfamily of transporter proteins. The encoded protein is a heme transporter that may play a critical role in erythropoiesis by protecting developing erythroid cells from heme toxicity. This gene may play a role in posterior column ataxia with retinitis pigmentosa and the hematological disorder Diamond-Blackfan syndrome. [provided by RefSeq, Jan 2011]","start":212858255,"end":212899363,"strand":1,"description":"feline leukemia virus subgroup C cellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:24682]"}, {"versioned_ensembl_gene_id":"ENSG00000248766.2","gene_symbol":"AC093303.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20158662,"end":20158956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141314.12","gene_symbol":"RHBDL3","gene_name":"rhomboid like 3 [Source:HGNC Symbol;Acc:HGNC:16502]","synonyms":"VRHO,RHBDL4","biotype":"protein_coding","ncbi_id":"162494","summary":null,"start":32266176,"end":32324661,"strand":1,"description":"rhomboid like 3 [Source:HGNC Symbol;Acc:HGNC:16502]"}, {"versioned_ensembl_gene_id":"ENSG00000261668.1","gene_symbol":"AC093591.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127840198,"end":127844040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214132.4","gene_symbol":"AC094103.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20304045,"end":20305448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137094.14","gene_symbol":"DNAJB5","gene_name":"DnaJ heat shock protein family (Hsp40) member B5 [Source:HGNC Symbol;Acc:HGNC:14887]","synonyms":"Hsc40","biotype":"protein_coding","ncbi_id":"25822","summary":"This gene encodes a member of the DNAJ heat shock protein 40 family of co-chaperone proteins. The encoded protein contains an N-terminal DNAJ domain and a C-terminal substrate binding domain but lacks the cysteine-rich domain found in other DNAJ family members. In mice, a multi-protein complex containing this protein, thioredoxin 1, and histone deacetylase 4, serves as a master negative regulator of cardiac hypertrophy. [provided by RefSeq, Mar 2017]","start":34989641,"end":34998900,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B5 [Source:HGNC Symbol;Acc:HGNC:14887]"}, {"versioned_ensembl_gene_id":"ENSG00000244021.4","gene_symbol":"AC093591.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127812720,"end":127813200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124570.17","gene_symbol":"SERPINB6","gene_name":"serpin family B member 6 [Source:HGNC Symbol;Acc:HGNC:8950]","synonyms":"PTI,PI6,DFNB91,CAP","biotype":"protein_coding","ncbi_id":"5269","summary":"The protein encoded by this gene is a member of the serpin (serine proteinase inhibitor) superfamily, and ovalbumin(ov)-serpin subfamily. It was originally discovered as a placental thrombin inhibitor. The mouse homolog was found to be expressed in the hair cells of the inner ear. Mutations in this gene are associated with nonsyndromic progressive hearing loss, suggesting that this serpin plays an important role in the inner ear in the protection against leakage of lysosomal content during stress, and that loss of this protection results in cell death and sensorineural hearing loss. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]","start":2948159,"end":2972165,"strand":-1,"description":"serpin family B member 6 [Source:HGNC Symbol;Acc:HGNC:8950]"}, {"versioned_ensembl_gene_id":"ENSG00000249854.1","gene_symbol":"CDH18-AS1","gene_name":"CDH18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53088]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102725105","summary":null,"start":20305565,"end":20331456,"strand":1,"description":"CDH18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53088]"}, {"versioned_ensembl_gene_id":"ENSG00000282855.1","gene_symbol":"AC093591.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127809170,"end":127809477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145526.11","gene_symbol":"CDH18","gene_name":"cadherin 18 [Source:HGNC Symbol;Acc:HGNC:1757]","synonyms":"EY-CADHERIN,CDH14","biotype":"protein_coding","ncbi_id":"1016","summary":"This gene encodes a type II classical cadherin from the cadherin superfamily of integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. This particular cadherin is expressed specifically in the central nervous system and is putatively involved in synaptic adhesion, axon outgrowth and guidance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":19472951,"end":20575873,"strand":-1,"description":"cadherin 18 [Source:HGNC Symbol;Acc:HGNC:1757]"}, {"versioned_ensembl_gene_id":"ENSG00000164070.11","gene_symbol":"HSPA4L","gene_name":"heat shock protein family A (Hsp70) member 4 like [Source:HGNC Symbol;Acc:HGNC:17041]","synonyms":"Osp94,HSPH3,APG-1","biotype":"protein_coding","ncbi_id":"22824","summary":"The protein encoded by this gene is heat shock inducible and may act as a chaperone. The encoded protein can protect the heat-shocked cell against the harmful effects of aggregated proteins. This gene is highly expressed in leukemia cells and may be a good target for therapeutic intervention. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":127781821,"end":127840733,"strand":1,"description":"heat shock protein family A (Hsp70) member 4 like [Source:HGNC Symbol;Acc:HGNC:17041]"}, {"versioned_ensembl_gene_id":"ENSG00000245213.6","gene_symbol":"AC105285.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173131928,"end":173169652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260022.1","gene_symbol":"AL031716.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":883780,"end":885090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276931.1","gene_symbol":"AC009041.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":968375,"end":969012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230051.1","gene_symbol":"AL020994.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27331787,"end":27379265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103227.18","gene_symbol":"LMF1","gene_name":"lipase maturation factor 1 [Source:HGNC Symbol;Acc:HGNC:14154]","synonyms":"TMEM112A,TMEM112,JFP11,FLJ22302,FLJ12681,C16orf26","biotype":"protein_coding","ncbi_id":"64788","summary":null,"start":853634,"end":981318,"strand":-1,"description":"lipase maturation factor 1 [Source:HGNC Symbol;Acc:HGNC:14154]"}, {"versioned_ensembl_gene_id":"ENSG00000233597.3","gene_symbol":"AC133435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142043623,"end":142044198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280445.1","gene_symbol":"AL049536.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27414462,"end":27419713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167105.7","gene_symbol":"TMEM92","gene_name":"transmembrane protein 92 [Source:HGNC Symbol;Acc:HGNC:26579]","synonyms":"FLJ33318","biotype":"protein_coding","ncbi_id":"162461","summary":null,"start":50271406,"end":50281485,"strand":1,"description":"transmembrane protein 92 [Source:HGNC Symbol;Acc:HGNC:26579]"}, {"versioned_ensembl_gene_id":"ENSG00000227880.1","gene_symbol":"AL050402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27457247,"end":27460060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114126.17","gene_symbol":"TFDP2","gene_name":"transcription factor Dp-2 [Source:HGNC Symbol;Acc:HGNC:11751]","synonyms":"Dp-2","biotype":"protein_coding","ncbi_id":"7029","summary":"The gene is a member of the transcription factor DP family. The encoded protein forms heterodimers with the E2F transcription factors resulting in transcriptional activation of cell cycle regulated genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":141944428,"end":142149544,"strand":-1,"description":"transcription factor Dp-2 [Source:HGNC Symbol;Acc:HGNC:11751]"}, {"versioned_ensembl_gene_id":"ENSG00000231788.4","gene_symbol":"RPL31P50","gene_name":"ribosomal protein L31 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341356","summary":null,"start":31597114,"end":31597409,"strand":-1,"description":"ribosomal protein L31 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36799]"}, {"versioned_ensembl_gene_id":"ENSG00000203437.3","gene_symbol":"AC022080.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31465062,"end":31465842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256159.1","gene_symbol":"AC022080.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31477506,"end":31477987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226250.1","gene_symbol":"LINC00408","gene_name":"long intergenic non-protein coding RNA 408 [Source:HGNC Symbol;Acc:HGNC:42740]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652856","summary":null,"start":18905439,"end":18907810,"strand":1,"description":"long intergenic non-protein coding RNA 408 [Source:HGNC Symbol;Acc:HGNC:42740]"}, {"versioned_ensembl_gene_id":"ENSG00000279010.3","gene_symbol":"AL031587.6","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":37948352,"end":38002889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231358.2","gene_symbol":"AL355516.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18921889,"end":18923765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272582.1","gene_symbol":"AL031587.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37950965,"end":37951778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270975.1","gene_symbol":"MAGOH3P","gene_name":"mago homolog 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:20020]","synonyms":"MAGOHP1,MAGOHP","biotype":"unprocessed_pseudogene","ncbi_id":"90352","summary":null,"start":68861762,"end":68862525,"strand":1,"description":"mago homolog 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:20020]"}, {"versioned_ensembl_gene_id":"ENSG00000226599.1","gene_symbol":"AL450344.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150650772,"end":150652025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227139.1","gene_symbol":"AC241644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147697794,"end":147699335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069424.14","gene_symbol":"KCNAB2","gene_name":"potassium voltage-gated channel subfamily A regulatory beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:6229]","synonyms":"KCNA2B,HKvbeta2.2,HKvbeta2.1,AKR6A5","biotype":"protein_coding","ncbi_id":"8514","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member is one of the beta subunits, which are auxiliary proteins associating with functional Kv-alpha subunits. This member alters functional properties of the KCNA4 gene product. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2010]","start":5991466,"end":6101193,"strand":1,"description":"potassium voltage-gated channel subfamily A regulatory beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:6229]"}, {"versioned_ensembl_gene_id":"ENSG00000278948.1","gene_symbol":"AL031587.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37943050,"end":37944898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169228.13","gene_symbol":"RAB24","gene_name":"RAB24, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53917","summary":"RAB24 is a small GTPase of the Rab subfamily of Ras-related proteins that regulate intracellular protein trafficking (Olkkonen et al., 1993 [PubMed 8126105]).[supplied by OMIM, Aug 2009]","start":177301198,"end":177303744,"strand":-1,"description":"RAB24, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9765]"}, {"versioned_ensembl_gene_id":"ENSG00000128346.10","gene_symbol":"C22orf23","gene_name":"chromosome 22 open reading frame 23 [Source:HGNC Symbol;Acc:HGNC:18589]","synonyms":"FLJ32787,EVG1,LOC84645","biotype":"protein_coding","ncbi_id":"84645","summary":null,"start":37943050,"end":37953669,"strand":-1,"description":"chromosome 22 open reading frame 23 [Source:HGNC Symbol;Acc:HGNC:18589]"}, {"versioned_ensembl_gene_id":"ENSG00000230918.1","gene_symbol":"AC008063.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162073256,"end":162075169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268649.5","gene_symbol":"AL132655.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58817132,"end":58817725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263201.1","gene_symbol":"AC040162.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":68013436,"end":68015911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270872.2","gene_symbol":"SRGAP2D","gene_name":"SLIT-ROBO Rho GTPase activating protein 2D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43932]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996712","summary":"This locus encodes a member of the SLIT-ROBO Rho GTPase activating protein family. This human-specific locus resulted from segmental duplication of the SLIT-ROBO Rho GTPase activating protein 2B locus. This duplicated locus lacks an internal exon, and thus this gene copy may not be functional. Expression of this locus appears to be much lower than the similar SLIT-ROBO Rho GTPase activating protein 2C (SRGAP2C) locus. The SRGAP2C locus has been shown to encode a protein that functions antagonistically to SLIT-ROBO Rho GTPase activating protein 2 in cortical neuron development. [provided by RefSeq, May 2014]","start":143975087,"end":144068350,"strand":1,"description":"SLIT-ROBO Rho GTPase activating protein 2D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43932]"}, {"versioned_ensembl_gene_id":"ENSG00000257043.1","gene_symbol":"AP006296.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18665050,"end":18665548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262514.1","gene_symbol":"AC020978.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68199795,"end":68200981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128944.13","gene_symbol":"KNSTRN","gene_name":"kinetochore localized astrin/SPAG5 binding protein [Source:HGNC Symbol;Acc:HGNC:30767]","synonyms":"TRAF4AF1,SKAP,kinastrin,FLJ14502,C15orf23","biotype":"protein_coding","ncbi_id":"90417","summary":null,"start":40382721,"end":40394246,"strand":1,"description":"kinetochore localized astrin/SPAG5 binding protein [Source:HGNC Symbol;Acc:HGNC:30767]"}, {"versioned_ensembl_gene_id":"ENSG00000262160.1","gene_symbol":"AC020978.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68225969,"end":68229145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110436.11","gene_symbol":"SLC1A2","gene_name":"solute carrier family 1 member 2 [Source:HGNC Symbol;Acc:HGNC:10940]","synonyms":"EAAT2,GLT-1","biotype":"protein_coding","ncbi_id":"6506","summary":"This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Improper regulation of this gene is thought to be associated with several neurological disorders. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Jun 2017]","start":35251206,"end":35420063,"strand":-1,"description":"solute carrier family 1 member 2 [Source:HGNC Symbol;Acc:HGNC:10940]"}, {"versioned_ensembl_gene_id":"ENSG00000103067.13","gene_symbol":"ESRP2","gene_name":"epithelial splicing regulatory protein 2 [Source:HGNC Symbol;Acc:HGNC:26152]","synonyms":"RBM35B,FLJ21918","biotype":"protein_coding","ncbi_id":"80004","summary":"ESPR2 is an epithelial cell-type-specific splicing regulator (Warzecha et al., 2009 [PubMed 19285943]).[supplied by OMIM, Aug 2009]","start":68229111,"end":68238102,"strand":-1,"description":"epithelial splicing regulatory protein 2 [Source:HGNC Symbol;Acc:HGNC:26152]"}, {"versioned_ensembl_gene_id":"ENSG00000214417.4","gene_symbol":"KRT18P13","gene_name":"keratin 18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:6432]","synonyms":"KRT18L3","biotype":"processed_pseudogene","ncbi_id":"392371","summary":null,"start":97698922,"end":97700734,"strand":1,"description":"keratin 18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:6432]"}, {"versioned_ensembl_gene_id":"ENSG00000260677.1","gene_symbol":"AL445531.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97743208,"end":97744935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236130.1","gene_symbol":"PTCSC2","gene_name":"papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44086]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928337","summary":null,"start":97805935,"end":97810008,"strand":-1,"description":"papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44086]"}, {"versioned_ensembl_gene_id":"ENSG00000165030.3","gene_symbol":"NFIL3","gene_name":"nuclear factor, interleukin 3 regulated [Source:HGNC Symbol;Acc:HGNC:7787]","synonyms":"NFIL3A,NF-IL3A,IL3BP1,E4BP4","biotype":"protein_coding","ncbi_id":"4783","summary":"The protein encoded by this gene is a transcriptional regulator that binds as a homodimer to activating transcription factor (ATF) sites in many cellular and viral promoters. The encoded protein represses PER1 and PER2 expression and therefore plays a role in the regulation of circadian rhythm. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2014]","start":91409045,"end":91423862,"strand":-1,"description":"nuclear factor, interleukin 3 regulated [Source:HGNC Symbol;Acc:HGNC:7787]"}, {"versioned_ensembl_gene_id":"ENSG00000082515.17","gene_symbol":"MRPL22","gene_name":"mitochondrial ribosomal protein L22 [Source:HGNC Symbol;Acc:HGNC:14480]","synonyms":"RPML25,MRP-L25,HSPC158","biotype":"protein_coding","ncbi_id":"29093","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L22 ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 4q. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":154941070,"end":154969411,"strand":1,"description":"mitochondrial ribosomal protein L22 [Source:HGNC Symbol;Acc:HGNC:14480]"}, {"versioned_ensembl_gene_id":"ENSG00000232685.4","gene_symbol":"LINC00442","gene_name":"long intergenic non-protein coding RNA 442 [Source:HGNC Symbol;Acc:HGNC:42779]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"348021","summary":null,"start":19008259,"end":19012559,"strand":1,"description":"long intergenic non-protein coding RNA 442 [Source:HGNC Symbol;Acc:HGNC:42779]"}, {"versioned_ensembl_gene_id":"ENSG00000120645.11","gene_symbol":"IQSEC3","gene_name":"IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:HGNC:29193]","synonyms":"KIAA1110,MGC30156","biotype":"protein_coding","ncbi_id":"440073","summary":null,"start":66765,"end":178460,"strand":1,"description":"IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:HGNC:29193]"}, {"versioned_ensembl_gene_id":"ENSG00000178919.8","gene_symbol":"FOXE1","gene_name":"forkhead box E1 [Source:HGNC Symbol;Acc:HGNC:3806]","synonyms":"FOXE2,FKHL15,TTF-2,TITF2,HFKH4","biotype":"protein_coding","ncbi_id":"2304","summary":"This intronless gene encodes a protein that belongs to the forkhead family of transcription factors. Members of this family contain a conserved 100-amino acid DNA-binding 'forkhead' domain. The encoded protein functions as a thyroid transcription factor that plays a role in thyroid morphogenesis. Mutations in this gene are associated with the Bamforth-Lazarus syndrome, and with susceptibility to nonmedullary thyroid cancer-4. [provided by RefSeq, Nov 2016]","start":97853254,"end":97856715,"strand":1,"description":"forkhead box E1 [Source:HGNC Symbol;Acc:HGNC:3806]"}, {"versioned_ensembl_gene_id":"ENSG00000188917.14","gene_symbol":"TRMT2B","gene_name":"tRNA methyltransferase 2 homolog B [Source:HGNC Symbol;Acc:HGNC:25748]","synonyms":"FLJ12687,CXorf34","biotype":"protein_coding","ncbi_id":"79979","summary":"This gene encodes a homolog of the TRM2 gene in S. cerevisiae. The yeast gene encodes a tRNA methyltransferase that plays a role in tRNA maturation. The yeast protein also has endo-exonuclease activity and may be involved in DNA double strand break repair. Alternative splicing results in multiple transcripts encoding different isoforms. [provided by RefSeq, Nov 2009]","start":101009346,"end":101052116,"strand":-1,"description":"tRNA methyltransferase 2 homolog B [Source:HGNC Symbol;Acc:HGNC:25748]"}, {"versioned_ensembl_gene_id":"ENSG00000179088.14","gene_symbol":"C12orf42","gene_name":"chromosome 12 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:24729]","synonyms":"FLJ25323","biotype":"protein_coding","ncbi_id":"374470","summary":null,"start":103237591,"end":103496010,"strand":-1,"description":"chromosome 12 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:24729]"}, {"versioned_ensembl_gene_id":"ENSG00000227376.1","gene_symbol":"FTH1P16","gene_name":"ferritin heavy chain 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:3986]","synonyms":"FTHL16,FTH2","biotype":"processed_pseudogene","ncbi_id":"2508","summary":null,"start":77734475,"end":77735026,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:3986]"}, {"versioned_ensembl_gene_id":"ENSG00000263860.1","gene_symbol":"AC011840.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30550493,"end":30551189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255409.1","gene_symbol":"RSF1-IT1","gene_name":"RSF1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41439]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874308","summary":null,"start":77738680,"end":77739568,"strand":-1,"description":"RSF1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41439]"}, {"versioned_ensembl_gene_id":"ENSG00000219622.1","gene_symbol":"AL451061.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150504811,"end":150510300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219529.2","gene_symbol":"AP000580.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77813319,"end":77813676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254985.1","gene_symbol":"RSF1-IT2","gene_name":"RSF1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41438]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874307","summary":null,"start":77717712,"end":77718411,"strand":-1,"description":"RSF1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41438]"}, {"versioned_ensembl_gene_id":"ENSG00000170860.3","gene_symbol":"LSM3","gene_name":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17874]","synonyms":"YLR438C,USS2,SMX4","biotype":"protein_coding","ncbi_id":"27258","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]","start":14178358,"end":14201119,"strand":1,"description":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17874]"}, {"versioned_ensembl_gene_id":"ENSG00000136932.13","gene_symbol":"TRMO","gene_name":"tRNA methyltransferase O [Source:HGNC Symbol;Acc:HGNC:30967]","synonyms":"HSPC219,C9orf156","biotype":"protein_coding","ncbi_id":"51531","summary":null,"start":97904489,"end":97922570,"strand":-1,"description":"tRNA methyltransferase O [Source:HGNC Symbol;Acc:HGNC:30967]"}, {"versioned_ensembl_gene_id":"ENSG00000279431.1","gene_symbol":"AC011840.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30551193,"end":30551802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164880.15","gene_symbol":"INTS1","gene_name":"integrator complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24555]","synonyms":"NET28,KIAA1440,INT1,DKFZp586J0619","biotype":"protein_coding","ncbi_id":"26173","summary":"INTS1 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":1470277,"end":1504367,"strand":-1,"description":"integrator complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24555]"}, {"versioned_ensembl_gene_id":"ENSG00000233081.1","gene_symbol":"AL353764.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91426238,"end":91427144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086504.15","gene_symbol":"MRPL28","gene_name":"mitochondrial ribosomal protein L28 [Source:HGNC Symbol;Acc:HGNC:14484]","synonyms":"p15,MAAT1","biotype":"protein_coding","ncbi_id":"10573","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein, a part of which was originally isolated by its ability to recognize tyrosinase in an HLA-A24-restricted fashion. [provided by RefSeq, Jul 2008]","start":367384,"end":370527,"strand":-1,"description":"mitochondrial ribosomal protein L28 [Source:HGNC Symbol;Acc:HGNC:14484]"}, {"versioned_ensembl_gene_id":"ENSG00000108666.9","gene_symbol":"C17orf75","gene_name":"chromosome 17 open reading frame 75 [Source:HGNC Symbol;Acc:HGNC:30173]","synonyms":"SRI2,NJMU-R1","biotype":"protein_coding","ncbi_id":"64149","summary":null,"start":32324565,"end":32350023,"strand":-1,"description":"chromosome 17 open reading frame 75 [Source:HGNC Symbol;Acc:HGNC:30173]"}, {"versioned_ensembl_gene_id":"ENSG00000266733.5","gene_symbol":"TBC1D29","gene_name":"TBC1 domain family member 29 [Source:HGNC Symbol;Acc:HGNC:24509]","synonyms":"DKFZP434O047","biotype":"protein_coding","ncbi_id":"26083","summary":null,"start":30557112,"end":30563493,"strand":1,"description":"TBC1 domain family member 29 [Source:HGNC Symbol;Acc:HGNC:24509]"}, {"versioned_ensembl_gene_id":"ENSG00000222044.1","gene_symbol":"AL031587.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38032165,"end":38034228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135776.4","gene_symbol":"ABCB10","gene_name":"ATP binding cassette subfamily B member 10 [Source:HGNC Symbol;Acc:HGNC:41]","synonyms":"MTABC2,M-ABC2,EST20237","biotype":"protein_coding","ncbi_id":"23456","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The function of this mitochondrial protein is unknown. [provided by RefSeq, Jul 2008]","start":229516582,"end":229558695,"strand":-1,"description":"ATP binding cassette subfamily B member 10 [Source:HGNC Symbol;Acc:HGNC:41]"}, {"versioned_ensembl_gene_id":"ENSG00000264765.1","gene_symbol":"AC098850.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16653904,"end":16654787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264359.1","gene_symbol":"NEK4P2","gene_name":"NIMA-related kinase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39650]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421734","summary":null,"start":16666107,"end":16667118,"strand":-1,"description":"NIMA-related kinase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39650]"}, {"versioned_ensembl_gene_id":"ENSG00000260569.2","gene_symbol":"AC090398.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74211391,"end":74240555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231458.2","gene_symbol":"AC098850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16683438,"end":16684227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178762.4","gene_symbol":"HIST1H2BPS1","gene_name":"histone cluster 1 H2B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18719]","synonyms":"H2BFVP,bA317E16.4","biotype":"unprocessed_pseudogene","ncbi_id":"100288742","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 6. [provided by RefSeq, Oct 2015]","start":25731782,"end":25732091,"strand":-1,"description":"histone cluster 1 H2B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18719]"}, {"versioned_ensembl_gene_id":"ENSG00000075624.13","gene_symbol":"ACTB","gene_name":"actin beta [Source:HGNC Symbol;Acc:HGNC:132]","synonyms":null,"biotype":"protein_coding","ncbi_id":"60","summary":"This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome. [provided by RefSeq, Aug 2017]","start":5527151,"end":5563784,"strand":-1,"description":"actin beta [Source:HGNC Symbol;Acc:HGNC:132]"}, {"versioned_ensembl_gene_id":"ENSG00000216436.2","gene_symbol":"AL512384.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25732497,"end":25732827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185339.8","gene_symbol":"TCN2","gene_name":"transcobalamin 2 [Source:HGNC Symbol;Acc:HGNC:11653]","synonyms":"TC2,D22S750,D22S676","biotype":"protein_coding","ncbi_id":"6948","summary":"This gene encodes a member of the vitamin B12-binding protein family. This family of proteins, alternatively referred to as R binders, is expressed in various tissues and secretions. This plasma protein binds cobalamin and mediates the transport of cobalamin into cells. This protein and other mammalian cobalamin-binding proteins, such as transcobalamin I and gastric intrisic factor, may have evolved by duplication of a common ancestral gene. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":30606838,"end":30627278,"strand":1,"description":"transcobalamin 2 [Source:HGNC Symbol;Acc:HGNC:11653]"}, {"versioned_ensembl_gene_id":"ENSG00000223767.5","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"G16,RING5,RMA1,NG2","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32245363,"end":32247802,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000118432.12","gene_symbol":"CNR1","gene_name":"cannabinoid receptor 1 [Source:HGNC Symbol;Acc:HGNC:2159]","synonyms":"CNR,CB1K5,CB1A,CB1,CB-R,CANN6","biotype":"protein_coding","ncbi_id":"1268","summary":"This gene encodes one of two cannabinoid receptors. The cannabinoids, principally delta-9-tetrahydrocannabinol and synthetic analogs, are psychoactive ingredients of marijuana. The cannabinoid receptors are members of the guanine-nucleotide-binding protein (G-protein) coupled receptor family, which inhibit adenylate cyclase activity in a dose-dependent, stereoselective and pertussis toxin-sensitive manner. The two receptors have been found to be involved in the cannabinoid-induced CNS effects (including alterations in mood and cognition) experienced by users of marijuana. Multiple transcript variants encoding two different protein isoforms have been described for this gene. [provided by RefSeq, May 2009]","start":88139864,"end":88166359,"strand":-1,"description":"cannabinoid receptor 1 [Source:HGNC Symbol;Acc:HGNC:2159]"}, {"versioned_ensembl_gene_id":"ENSG00000154767.14","gene_symbol":"XPC","gene_name":"XPC complex subunit, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12816]","synonyms":"XPCC,RAD4","biotype":"protein_coding","ncbi_id":"7508","summary":"The protein encoded by this gene is a key component of the XPC complex, which plays an important role in the early steps of global genome nucleotide excision repair (NER). The encoded protein is important for damage sensing and DNA binding, and shows a preference for single-stranded DNA. Mutations in this gene or some other NER components can result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]","start":14145147,"end":14178783,"strand":-1,"description":"XPC complex subunit, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12816]"}, {"versioned_ensembl_gene_id":"ENSG00000185650.9","gene_symbol":"ZFP36L1","gene_name":"ZFP36 ring finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:1107]","synonyms":"TIS11B,RNF162B,ERF1,cMG1,BRF1,Berg36","biotype":"protein_coding","ncbi_id":"677","summary":"This gene is a member of the TIS11 family of early response genes, which are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. This gene is well conserved across species and has a promoter that contains motifs seen in other early-response genes. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":68787660,"end":68796253,"strand":-1,"description":"ZFP36 ring finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:1107]"}, {"versioned_ensembl_gene_id":"ENSG00000089123.15","gene_symbol":"TASP1","gene_name":"taspase 1 [Source:HGNC Symbol;Acc:HGNC:15859]","synonyms":"dJ585I14.2,C20orf13,FLJ20212","biotype":"protein_coding","ncbi_id":"55617","summary":"This gene encodes an endopeptidase that cleaves specific substrates following aspartate residues. The encoded protein undergoes posttranslational autoproteolytic processing to generate alpha and beta subunits, which reassemble into the active alpha2-beta2 heterotetramer. It is required to cleave MLL, a protein required for the maintenance of HOX gene expression, and TFIIA, a basal transcription factor. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":13389392,"end":13638940,"strand":-1,"description":"taspase 1 [Source:HGNC Symbol;Acc:HGNC:15859]"}, {"versioned_ensembl_gene_id":"ENSG00000266775.1","gene_symbol":"AC011840.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30557732,"end":30558502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264242.2","gene_symbol":"AC011840.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30553697,"end":30558962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280010.1","gene_symbol":"AP001350.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58627435,"end":58628528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242686.4","gene_symbol":"AC107464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":652850,"end":656213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251012.1","gene_symbol":"AC083800.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":119147375,"end":119187807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254588.1","gene_symbol":"AP003397.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128526142,"end":128530389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163424.8","gene_symbol":"C3orf30","gene_name":"chromosome 3 open reading frame 30 [Source:HGNC Symbol;Acc:HGNC:26553]","synonyms":"TSCPA,FLJ32859","biotype":"protein_coding","ncbi_id":"152405","summary":null,"start":119146150,"end":119160042,"strand":1,"description":"chromosome 3 open reading frame 30 [Source:HGNC Symbol;Acc:HGNC:26553]"}, {"versioned_ensembl_gene_id":"ENSG00000134954.14","gene_symbol":"ETS1","gene_name":"ETS proto-oncogene 1, transcription factor [Source:HGNC Symbol;Acc:HGNC:3488]","synonyms":"FLJ10768,EWSR2,ETS-1","biotype":"protein_coding","ncbi_id":"2113","summary":"This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transcriptional activators or repressors of numerous genes, and are involved in stem cell development, cell senescence and death, and tumorigenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]","start":128458761,"end":128587558,"strand":-1,"description":"ETS proto-oncogene 1, transcription factor [Source:HGNC Symbol;Acc:HGNC:3488]"}, {"versioned_ensembl_gene_id":"ENSG00000100395.14","gene_symbol":"L3MBTL2","gene_name":"L3MBTL2, polycomb repressive complex 1 subunit [Source:HGNC Symbol;Acc:HGNC:18594]","synonyms":"dJ756G23.3,H-l(3)mbt-l,DKFZP761I141","biotype":"protein_coding","ncbi_id":"83746","summary":null,"start":41205205,"end":41231271,"strand":1,"description":"L3MBTL2, polycomb repressive complex 1 subunit [Source:HGNC Symbol;Acc:HGNC:18594]"}, {"versioned_ensembl_gene_id":"ENSG00000227784.1","gene_symbol":"ZNF965P","gene_name":"zinc finger protein 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:42025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132598","summary":null,"start":18734080,"end":18734896,"strand":1,"description":"zinc finger protein 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:42025]"}, {"versioned_ensembl_gene_id":"ENSG00000279445.2","gene_symbol":"AC135068.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21683038,"end":21683962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249084.1","gene_symbol":"AC027627.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177343004,"end":177357032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176435.6","gene_symbol":"CLEC14A","gene_name":"C-type lectin domain containing 14A [Source:HGNC Symbol;Acc:HGNC:19832]","synonyms":"C14orf27","biotype":"protein_coding","ncbi_id":"161198","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This family member plays a role in cell-cell adhesion and angiogenesis. It functions in filopodia formation, cell migration and tube formation. Due to its presence at higher levels in tumor endothelium than in normal tissue endothelium, it is considered to be a candidate for tumor vascular targeting. [provided by RefSeq, Jan 2012]","start":38254103,"end":38256369,"strand":-1,"description":"C-type lectin domain containing 14A [Source:HGNC Symbol;Acc:HGNC:19832]"}, {"versioned_ensembl_gene_id":"ENSG00000120278.15","gene_symbol":"PLEKHG1","gene_name":"pleckstrin homology and RhoGEF domain containing G1 [Source:HGNC Symbol;Acc:HGNC:20884]","synonyms":"KIAA1209,ARHGEF41","biotype":"protein_coding","ncbi_id":"57480","summary":null,"start":150599883,"end":150843665,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G1 [Source:HGNC Symbol;Acc:HGNC:20884]"}, {"versioned_ensembl_gene_id":"ENSG00000259072.1","gene_symbol":"AL161751.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38290953,"end":38311930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174225.14","gene_symbol":"ARL13A","gene_name":"ADP ribosylation factor like GTPase 13A [Source:HGNC Symbol;Acc:HGNC:31709]","synonyms":"ARL13","biotype":"protein_coding","ncbi_id":"392509","summary":null,"start":100969708,"end":100990829,"strand":1,"description":"ADP ribosylation factor like GTPase 13A [Source:HGNC Symbol;Acc:HGNC:31709]"}, {"versioned_ensembl_gene_id":"ENSG00000271468.1","gene_symbol":"AL357094.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38605255,"end":38606098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240435.2","gene_symbol":"AC020978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68209442,"end":68209778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273664.1","gene_symbol":"AC010776.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59700523,"end":59700946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224161.3","gene_symbol":"AC098847.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59761558,"end":59761905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274583.1","gene_symbol":"FAM74A4","gene_name":"family with sequence similarity 74 member A4 [Source:HGNC Symbol;Acc:HGNC:32032]","synonyms":"FLJ45202,FAM74A2","biotype":"transcribed_processed_pseudogene","ncbi_id":"401508","summary":null,"start":61205258,"end":61212373,"strand":1,"description":"family with sequence similarity 74 member A4 [Source:HGNC Symbol;Acc:HGNC:32032]"}, {"versioned_ensembl_gene_id":"ENSG00000279368.1","gene_symbol":"AL031123.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6685148,"end":6686984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114638.7","gene_symbol":"UPK1B","gene_name":"uroplakin 1B [Source:HGNC Symbol;Acc:HGNC:12578]","synonyms":"UPK1,TSPAN20","biotype":"protein_coding","ncbi_id":"7348","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is found in the asymmetrical unit membrane (AUM) where it can form a complex with other transmembrane 4 superfamily proteins. It may play a role in normal bladder epithelial physiology, possibly in regulating membrane permeability of superficial umbrella cells or in stabilizing the apical membrane through AUM/cytoskeletal interactions. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]","start":119173517,"end":119205153,"strand":1,"description":"uroplakin 1B [Source:HGNC Symbol;Acc:HGNC:12578]"}, {"versioned_ensembl_gene_id":"ENSG00000255327.1","gene_symbol":"AP003062.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134950708,"end":134951568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249791.1","gene_symbol":"AC008494.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115188563,"end":115188932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267486.1","gene_symbol":"GLUD1P4","gene_name":"glutamate dehydrogenase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4339]","synonyms":"GLUDP4","biotype":"processed_pseudogene","ncbi_id":"2750","summary":null,"start":59778572,"end":59778989,"strand":1,"description":"glutamate dehydrogenase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4339]"}, {"versioned_ensembl_gene_id":"ENSG00000167264.17","gene_symbol":"DUS2","gene_name":"dihydrouridine synthase 2 [Source:HGNC Symbol;Acc:HGNC:26014]","synonyms":"FLJ20399,DUS2L,SMM1","biotype":"protein_coding","ncbi_id":"54920","summary":"This gene encodes a cytoplasmic protein that catalyzes the conversion of uridine residues to dihydrouridine in the D-loop of tRNA. The resulting modified bases confer enhanced regional flexibility to tRNA. The encoded protein may increase the rate of translation by inhibiting an interferon-induced protein kinase. This gene has been implicated in pulmonary carcinogenesis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]","start":67987746,"end":68079320,"strand":1,"description":"dihydrouridine synthase 2 [Source:HGNC Symbol;Acc:HGNC:26014]"}, {"versioned_ensembl_gene_id":"ENSG00000279046.1","gene_symbol":"AP003062.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134985683,"end":134986799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258948.2","gene_symbol":"KRT8P1","gene_name":"keratin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20281]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338017","summary":null,"start":38727275,"end":38728481,"strand":1,"description":"keratin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20281]"}, {"versioned_ensembl_gene_id":"ENSG00000255512.1","gene_symbol":"AP005135.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135061781,"end":135075899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271581.1","gene_symbol":"AL671883.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31356647,"end":31357637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251179.1","gene_symbol":"TMEM92-AS1","gene_name":"TMEM92 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50442]","synonyms":"TCONS_00025237,RP11-893F2.9,lncRNA-508851","biotype":"antisense_RNA","ncbi_id":"103752589","summary":null,"start":50281577,"end":50287855,"strand":-1,"description":"TMEM92 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50442]"}, {"versioned_ensembl_gene_id":"ENSG00000226281.2","gene_symbol":"AL031123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6692744,"end":6711002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227939.1","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31280317,"end":31281519,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000275676.1","gene_symbol":"BX005040.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61229913,"end":61231863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233644.1","gene_symbol":"ARHGEF7-IT1","gene_name":"ARHGEF7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41408]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874371","summary":null,"start":111122652,"end":111144264,"strand":1,"description":"ARHGEF7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41408]"}, {"versioned_ensembl_gene_id":"ENSG00000204525.16","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31268749,"end":31272130,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000176160.10","gene_symbol":"HSF5","gene_name":"heat shock transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:26862]","synonyms":"FLJ40311","biotype":"protein_coding","ncbi_id":"124535","summary":null,"start":58420167,"end":58488384,"strand":-1,"description":"heat shock transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:26862]"}, {"versioned_ensembl_gene_id":"ENSG00000282156.1","gene_symbol":"AL512324.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45187292,"end":45198323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206299.8","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"ABCB3,PSF2,D6S217E,RING11","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32750528,"end":32767476,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000283378.1","gene_symbol":"BX088645.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61330717,"end":61453030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260439.1","gene_symbol":"LMF1-AS1","gene_name":"LMF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50469]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929387","summary":null,"start":921033,"end":934495,"strand":1,"description":"LMF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50469]"}, {"versioned_ensembl_gene_id":"ENSG00000276674.1","gene_symbol":"IGKV1OR1-1","gene_name":"immunoglobulin kappa variable 1/OR1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5764]","synonyms":"IGKVP1,IGKV1/OR1-1","biotype":"IG_V_pseudogene","ncbi_id":"3525","summary":null,"start":144085628,"end":144086098,"strand":1,"description":"immunoglobulin kappa variable 1/OR1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5764]"}, {"versioned_ensembl_gene_id":"ENSG00000224029.1","gene_symbol":"AL450344.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":150624677,"end":150626086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227352.1","gene_symbol":"ARHGEF7-AS1","gene_name":"ARHGEF7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39816]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874226","summary":null,"start":111144305,"end":111144733,"strand":-1,"description":"ARHGEF7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39816]"}, {"versioned_ensembl_gene_id":"ENSG00000224532.2","gene_symbol":"AL136361.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6758276,"end":6759291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126950.7","gene_symbol":"TMEM35A","gene_name":"transmembrane protein 35A [Source:HGNC Symbol;Acc:HGNC:25864]","synonyms":"TMEM35,FLJ14084","biotype":"protein_coding","ncbi_id":"59353","summary":null,"start":101078720,"end":101096364,"strand":1,"description":"transmembrane protein 35A [Source:HGNC Symbol;Acc:HGNC:25864]"}, {"versioned_ensembl_gene_id":"ENSG00000232891.1","gene_symbol":"AL450344.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":150600834,"end":150605850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275075.1","gene_symbol":"AC244015.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144168752,"end":144168850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213089.4","gene_symbol":"PDCL3P5","gene_name":"phosducin-like 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44506]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644850","summary":null,"start":150827663,"end":150828384,"strand":1,"description":"phosducin-like 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44506]"}, {"versioned_ensembl_gene_id":"ENSG00000260316.2","gene_symbol":"AL008727.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":898967,"end":905224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230432.1","gene_symbol":"AC114803.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219299002,"end":219304130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266648.1","gene_symbol":"SETP3","gene_name":"SET pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31115]","synonyms":"SETP13","biotype":"processed_pseudogene","ncbi_id":"619349","summary":null,"start":58476138,"end":58476950,"strand":-1,"description":"SET pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31115]"}, {"versioned_ensembl_gene_id":"ENSG00000275767.1","gene_symbol":"AC244015.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144179777,"end":144211729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259070.5","gene_symbol":"LINC00639","gene_name":"long intergenic non-protein coding RNA 639 [Source:HGNC Symbol;Acc:HGNC:27502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283547","summary":null,"start":38749339,"end":38948273,"strand":-1,"description":"long intergenic non-protein coding RNA 639 [Source:HGNC Symbol;Acc:HGNC:27502]"}, {"versioned_ensembl_gene_id":"ENSG00000260807.6","gene_symbol":"AC009041.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":975761,"end":981596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158813.17","gene_symbol":"EDA","gene_name":"ectodysplasin A [Source:HGNC Symbol;Acc:HGNC:3157]","synonyms":"EDA-A1,ED1-A2,ED1-A1,ED1,XLHED,XHED,ODT1,HED,EDA2,EDA1,EDA-A2","biotype":"protein_coding","ncbi_id":"1896","summary":"The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":69616067,"end":70039469,"strand":1,"description":"ectodysplasin A [Source:HGNC Symbol;Acc:HGNC:3157]"}, {"versioned_ensembl_gene_id":"ENSG00000165716.10","gene_symbol":"FAM69B","gene_name":"family with sequence similarity 69 member B [Source:HGNC Symbol;Acc:HGNC:28290]","synonyms":"MGC20262,C9orf136","biotype":"protein_coding","ncbi_id":"138311","summary":"This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011]","start":136712570,"end":136724050,"strand":1,"description":"family with sequence similarity 69 member B [Source:HGNC Symbol;Acc:HGNC:28290]"}, {"versioned_ensembl_gene_id":"ENSG00000054356.13","gene_symbol":"PTPRN","gene_name":"protein tyrosine phosphatase, receptor type N [Source:HGNC Symbol;Acc:HGNC:9676]","synonyms":"IA-2","biotype":"protein_coding","ncbi_id":"5798","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single catalytic domain, and thus represents a receptor-type PTP. This PTP was found to be an autoantigen that is reactive with insulin-dependent diabetes mellitus (IDDM) patient sera, and thus may be a potential target of autoimmunity in diabetes mellitus. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010]","start":219289623,"end":219309648,"strand":-1,"description":"protein tyrosine phosphatase, receptor type N [Source:HGNC Symbol;Acc:HGNC:9676]"}, {"versioned_ensembl_gene_id":"ENSG00000225839.2","gene_symbol":"TRMT2B-AS1","gene_name":"TRMT2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41116]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"106481789","summary":null,"start":101043564,"end":101094476,"strand":-1,"description":"TRMT2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41116]"}, {"versioned_ensembl_gene_id":"ENSG00000177459.10","gene_symbol":"ERICH5","gene_name":"glutamate rich 5 [Source:HGNC Symbol;Acc:HGNC:26823]","synonyms":"FLJ39553,C8orf47","biotype":"protein_coding","ncbi_id":"203111","summary":null,"start":98064311,"end":98093610,"strand":1,"description":"glutamate rich 5 [Source:HGNC Symbol;Acc:HGNC:26823]"}, {"versioned_ensembl_gene_id":"ENSG00000232527.7","gene_symbol":"AC245595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144227030,"end":144250288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078269.14","gene_symbol":"SYNJ2","gene_name":"synaptojanin 2 [Source:HGNC Symbol;Acc:HGNC:11504]","synonyms":"INPP5H","biotype":"protein_coding","ncbi_id":"8871","summary":"The gene is a member of the inositol-polyphosphate 5-phosphatase family. The encoded protein interacts with the ras-related C3 botulinum toxin substrate 1, which causes translocation of the encoded protein to the plasma membrane where it inhibits clathrin-mediated endocytosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":157981887,"end":158099176,"strand":1,"description":"synaptojanin 2 [Source:HGNC Symbol;Acc:HGNC:11504]"}, {"versioned_ensembl_gene_id":"ENSG00000232723.1","gene_symbol":"AC013399.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121309995,"end":121310412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236117.1","gene_symbol":"LINC01639","gene_name":"long intergenic non-protein coding RNA 1639 [Source:HGNC Symbol;Acc:HGNC:52426]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373054","summary":null,"start":43400331,"end":43409681,"strand":1,"description":"long intergenic non-protein coding RNA 1639 [Source:HGNC Symbol;Acc:HGNC:52426]"}, {"versioned_ensembl_gene_id":"ENSG00000230081.2","gene_symbol":"HSPE1P28","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49347]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"171420","summary":null,"start":112280978,"end":112281335,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49347]"}, {"versioned_ensembl_gene_id":"ENSG00000272815.1","gene_symbol":"AC098850.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":16788057,"end":16816540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251147.1","gene_symbol":"AC084871.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184910889,"end":184911352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119314.15","gene_symbol":"PTBP3","gene_name":"polypyrimidine tract binding protein 3 [Source:HGNC Symbol;Acc:HGNC:10253]","synonyms":"ROD1,DKFZp781I1117","biotype":"protein_coding","ncbi_id":"9991","summary":"The protein encoded by this gene binds RNA and is a regulator of cell differentiation. The encoded protein preferentially binds to poly(G) and poly(U) sequences in vitro. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":112217716,"end":112333667,"strand":-1,"description":"polypyrimidine tract binding protein 3 [Source:HGNC Symbol;Acc:HGNC:10253]"}, {"versioned_ensembl_gene_id":"ENSG00000188933.14","gene_symbol":"USP32P1","gene_name":"ubiquitin specific peptidase 32 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43570]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"162632","summary":null,"start":16786489,"end":16804455,"strand":1,"description":"ubiquitin specific peptidase 32 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43570]"}, {"versioned_ensembl_gene_id":"ENSG00000102606.17","gene_symbol":"ARHGEF7","gene_name":"Rho guanine nucleotide exchange factor 7 [Source:HGNC Symbol;Acc:HGNC:15607]","synonyms":"P85,P50BP,P50,Nbla10314,KIAA0142,DKFZp761K1021,DKFZp686C12170,COOL1,BETA-PIX,PIXB,PAK3,P85SPR,P85COOL1","biotype":"protein_coding","ncbi_id":"8874","summary":"This gene encodes a protein that belongs to a family of cytoplasmic proteins that activate the Ras-like family of Rho proteins by exchanging bound GDP for GTP. It forms a complex with the small GTP binding protein Rac1 and recruits Rac1 to membrane ruffles and to focal adhesions. Multiple alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Mar 2016]","start":111114559,"end":111305737,"strand":1,"description":"Rho guanine nucleotide exchange factor 7 [Source:HGNC Symbol;Acc:HGNC:15607]"}, {"versioned_ensembl_gene_id":"ENSG00000108389.9","gene_symbol":"MTMR4","gene_name":"myotubularin related protein 4 [Source:HGNC Symbol;Acc:HGNC:7452]","synonyms":"ZFYVE11,KIAA0647","biotype":"protein_coding","ncbi_id":"9110","summary":null,"start":58489529,"end":58517905,"strand":-1,"description":"myotubularin related protein 4 [Source:HGNC Symbol;Acc:HGNC:7452]"}, {"versioned_ensembl_gene_id":"ENSG00000228595.1","gene_symbol":"PAICSP2","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8589]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780815","summary":null,"start":91611343,"end":91612492,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8589]"}, {"versioned_ensembl_gene_id":"ENSG00000228974.5","gene_symbol":"AC006483.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5560743,"end":5561055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258680.2","gene_symbol":"AL132994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38835389,"end":38835788,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169071.14","gene_symbol":"ROR2","gene_name":"receptor tyrosine kinase like orphan receptor 2 [Source:HGNC Symbol;Acc:HGNC:10257]","synonyms":"NTRKR2,BDB1,BDB","biotype":"protein_coding","ncbi_id":"4920","summary":"The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]","start":91563091,"end":91950162,"strand":-1,"description":"receptor tyrosine kinase like orphan receptor 2 [Source:HGNC Symbol;Acc:HGNC:10257]"}, {"versioned_ensembl_gene_id":"ENSG00000226619.1","gene_symbol":"AL137001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19027837,"end":19028701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277109.1","gene_symbol":"AL935212.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61581813,"end":61582675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272719.1","gene_symbol":"AC006483.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5556731,"end":5557245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187721.8","gene_symbol":"GTF2IP3","gene_name":"general transcription factor IIi pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42640]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"645686","summary":null,"start":19026001,"end":19032626,"strand":-1,"description":"general transcription factor IIi pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42640]"}, {"versioned_ensembl_gene_id":"ENSG00000268030.1","gene_symbol":"AC005253.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18557775,"end":18561560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233016.6","gene_symbol":"SNHG7","gene_name":"small nucleolar RNA host gene 7 [Source:HGNC Symbol;Acc:HGNC:28254]","synonyms":"MGC16037,NCRNA00061","biotype":"antisense_RNA","ncbi_id":"84973","summary":null,"start":136721366,"end":136728184,"strand":-1,"description":"small nucleolar RNA host gene 7 [Source:HGNC Symbol;Acc:HGNC:28254]"}, {"versioned_ensembl_gene_id":"ENSG00000281870.1","gene_symbol":"AC208814.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30406695,"end":30413531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231248.2","gene_symbol":"AL935212.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61615876,"end":61627683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105700.10","gene_symbol":"KXD1","gene_name":"KxDL motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28420]","synonyms":"MGC2749,KXDL,FLJ25480,C19orf50,BORCS4","biotype":"protein_coding","ncbi_id":"79036","summary":null,"start":18557762,"end":18569387,"strand":1,"description":"KxDL motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28420]"}, {"versioned_ensembl_gene_id":"ENSG00000236811.1","gene_symbol":"GAPDHP2","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16577]","synonyms":"dJ585I14.1,GAPDP2","biotype":"processed_pseudogene","ncbi_id":"170516","summary":null,"start":13392677,"end":13393674,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16577]"}, {"versioned_ensembl_gene_id":"ENSG00000118017.3","gene_symbol":"A4GNT","gene_name":"alpha-1,4-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:17968]","synonyms":"alpha4GnT","biotype":"protein_coding","ncbi_id":"51146","summary":"This gene encodes a protein from the glycosyltransferase 32 family. The enzyme catalyzes the transfer of N-acetylglucosamine (GlcNAc) to core 2 branched O-glycans. It forms a unique glycan, GlcNAcalpha1-->4Galbeta-->R and is largely associated with the Golgi apparatus membrane. [provided by RefSeq, Jul 2008]","start":138123718,"end":138132387,"strand":-1,"description":"alpha-1,4-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:17968]"}, {"versioned_ensembl_gene_id":"ENSG00000276586.1","gene_symbol":"AL356102.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62397645,"end":62397916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219986.2","gene_symbol":"BTF3P7","gene_name":"basic transcription factor 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38569]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652960","summary":null,"start":6794915,"end":6795402,"strand":-1,"description":"basic transcription factor 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38569]"}, {"versioned_ensembl_gene_id":"ENSG00000253106.1","gene_symbol":"AC090198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124488510,"end":124491643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219507.4","gene_symbol":"FTH1P8","gene_name":"ferritin heavy chain 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:3995]","synonyms":"FTHL8","biotype":"processed_pseudogene","ncbi_id":"2501","summary":null,"start":148052233,"end":148052746,"strand":1,"description":"ferritin heavy chain 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:3995]"}, {"versioned_ensembl_gene_id":"ENSG00000197976.11","gene_symbol":"AKAP17A","gene_name":"A-kinase anchoring protein 17A [Source:HGNC Symbol;Acc:HGNC:18783]","synonyms":"XE7Y,XE7,SFRS17A,MGC39904,DXYS155E,CXYorf3,CCDC133,721P","biotype":"protein_coding","ncbi_id":"8227","summary":"This locus encodes a protein kinase A anchoring protein. The encoded protein is part of the spliceosome complex and is involved in the regulation of alternate splicing in some mRNA precursors. Alternatively spliced transcript variants have been identified for this gene.[provided by RefSeq, Sep 2010]","start":1591593,"end":1602514,"strand":1,"description":"A-kinase anchoring protein 17A [Source:HGNC Symbol;Acc:HGNC:18783]"}, {"versioned_ensembl_gene_id":"ENSG00000271465.1","gene_symbol":"SQSTM1P1","gene_name":"sequestosome 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480677","summary":null,"start":62406058,"end":62406916,"strand":-1,"description":"sequestosome 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49099]"}, {"versioned_ensembl_gene_id":"ENSG00000147687.18","gene_symbol":"TATDN1","gene_name":"TatD DNase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24220]","synonyms":"CDA11","biotype":"protein_coding","ncbi_id":"83940","summary":null,"start":124488485,"end":124539458,"strand":-1,"description":"TatD DNase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24220]"}, {"versioned_ensembl_gene_id":"ENSG00000231061.1","gene_symbol":"LINC00395","gene_name":"long intergenic non-protein coding RNA 395 [Source:HGNC Symbol;Acc:HGNC:42723]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874157","summary":null,"start":63667681,"end":63738018,"strand":-1,"description":"long intergenic non-protein coding RNA 395 [Source:HGNC Symbol;Acc:HGNC:42723]"}, {"versioned_ensembl_gene_id":"ENSG00000281562.1","gene_symbol":"AC233280.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284740.1","gene_symbol":"AL645728.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1503250,"end":1509452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100399.15","gene_symbol":"CHADL","gene_name":"chondroadherin like [Source:HGNC Symbol;Acc:HGNC:25165]","synonyms":"SLRR4B","biotype":"protein_coding","ncbi_id":"150356","summary":null,"start":41229510,"end":41240934,"strand":-1,"description":"chondroadherin like [Source:HGNC Symbol;Acc:HGNC:25165]"}, {"versioned_ensembl_gene_id":"ENSG00000100029.17","gene_symbol":"PES1","gene_name":"pescadillo ribosomal biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:8848]","synonyms":"PES,NOP7","biotype":"protein_coding","ncbi_id":"23481","summary":"This gene encodes a nuclear protein that contains a breast cancer associated gene 1 (BRCA1) C-terminal interaction domain. The encoded protein interacts with BOP1 and WDR12 to form the PeBoW complex, which plays a critical role in cell proliferation via pre-rRNA processing and 60S ribosomal subunit maturation. Expression of this gene may play an important role in breast cancer proliferation and tumorigenicity. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Pseudogenes of this gene are located on the long arm of chromosome 4 and the short arm of chromosome 9. [provided by RefSeq, Aug 2011]","start":30576625,"end":30607083,"strand":-1,"description":"pescadillo ribosomal biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:8848]"}, {"versioned_ensembl_gene_id":"ENSG00000226057.6","gene_symbol":"PHF2P2","gene_name":"PHD finger protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38808]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100873793","summary":null,"start":18946755,"end":19062718,"strand":-1,"description":"PHD finger protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38808]"}, {"versioned_ensembl_gene_id":"ENSG00000255004.1","gene_symbol":"AL133330.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35281813,"end":35286009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255542.1","gene_symbol":"AC090625.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35419057,"end":35421002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169851.15","gene_symbol":"PCDH7","gene_name":"protocadherin 7 [Source:HGNC Symbol;Acc:HGNC:8659]","synonyms":"PPP1R120,BH-Pcdh","biotype":"protein_coding","ncbi_id":"5099","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The gene encodes a protein with an extracellular domain containing 7 cadherin repeats. The gene product is an integral membrane protein that is thought to function in cell-cell recognition and adhesion. Alternative splicing yields isoforms with unique cytoplasmic tails. [provided by RefSeq, Jul 2008]","start":30720415,"end":31146805,"strand":1,"description":"protocadherin 7 [Source:HGNC Symbol;Acc:HGNC:8659]"}, {"versioned_ensembl_gene_id":"ENSG00000215380.2","gene_symbol":"AC090625.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35374265,"end":35374474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268279.4","gene_symbol":"AC090004.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14135217,"end":14148252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229375.1","gene_symbol":"USP24P1","gene_name":"ubiquitin specific peptidase 24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42014]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874248","summary":null,"start":19015487,"end":19019336,"strand":-1,"description":"ubiquitin specific peptidase 24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42014]"}, {"versioned_ensembl_gene_id":"ENSG00000174963.17","gene_symbol":"ZIC4","gene_name":"Zic family member 4 [Source:HGNC Symbol;Acc:HGNC:20393]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84107","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. Members of this family are important during development, and have been associated with X-linked visceral heterotaxy and holoprosencephaly type 5. This gene is closely linked to the gene encoding zinc finger protein of the cerebellum 1, a related family member on chromosome 3. Heterozygous deletion of these linked genes is involved in Dandy-Walker malformation, which is a congenital cerebellar malformation. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Dec 2009]","start":147386046,"end":147406860,"strand":-1,"description":"Zic family member 4 [Source:HGNC Symbol;Acc:HGNC:20393]"}, {"versioned_ensembl_gene_id":"ENSG00000223447.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33271325,"end":33271451,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000228242.6","gene_symbol":"AC093495.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14144637,"end":14165978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233229.1","gene_symbol":"CNOT7P1","gene_name":"CCR4-NOT transcription complex subunit 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44248]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421338","summary":null,"start":69937166,"end":69938017,"strand":-1,"description":"CCR4-NOT transcription complex subunit 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44248]"}, {"versioned_ensembl_gene_id":"ENSG00000175467.14","gene_symbol":"SART1","gene_name":"SART1, U4/U6.U5 tri-snRNP-associated protein 1 [Source:HGNC Symbol;Acc:HGNC:10538]","synonyms":"Snu66,SNRNP110,HAF,Ara1","biotype":"protein_coding","ncbi_id":"9092","summary":"This gene encodes two proteins, the SART1(800) protein expressed in the nucleus of the majority of proliferating cells, and the SART1(259) protein expressed in the cytosol of epithelial cancers. The SART1(259) protein is translated by the mechanism of -1 frameshifting during posttranscriptional regulation; its full-length sequence is not published yet. The two encoded proteins are thought to be involved in the regulation of proliferation. Both proteins have tumor-rejection antigens. The SART1(259) protein possesses tumor epitopes capable of inducing HLA-A2402-restricted cytotoxic T lymphocytes in cancer patients. This SART1(259) antigen may be useful in specific immunotherapy for cancer patients and may serve as a paradigmatic tool for the diagnosis and treatment of patients with atopy. The SART1(259) protein is found to be essential for the recruitment of the tri-snRNP to the pre-spliceosome in the spliceosome assembly pathway. [provided by RefSeq, Jul 2008]","start":65961689,"end":65979828,"strand":1,"description":"SART1, U4/U6.U5 tri-snRNP-associated protein 1 [Source:HGNC Symbol;Acc:HGNC:10538]"}, {"versioned_ensembl_gene_id":"ENSG00000254337.1","gene_symbol":"AC083967.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68848742,"end":68852763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267669.1","gene_symbol":"AC098847.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":59821040,"end":59825261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154114.12","gene_symbol":"TBCEL","gene_name":"tubulin folding cofactor E like [Source:HGNC Symbol;Acc:HGNC:28115]","synonyms":"MGC10233,LRRC35","biotype":"protein_coding","ncbi_id":"219899","summary":null,"start":121024072,"end":121090775,"strand":1,"description":"tubulin folding cofactor E like [Source:HGNC Symbol;Acc:HGNC:28115]"}, {"versioned_ensembl_gene_id":"ENSG00000126550.8","gene_symbol":"HTN1","gene_name":"histatin 1 [Source:HGNC Symbol;Acc:HGNC:5283]","synonyms":"HIS1","biotype":"protein_coding","ncbi_id":"3346","summary":"This gene encodes a member of the histatin family of small, histidine-rich, cationic proteins. They function as antimicrobial peptides and are important components of the innate immune system. Histatins are found in saliva and exhibit antibacterial, antifungal activities and function in wound healing. [provided by RefSeq, Aug 2014]","start":70050402,"end":70058845,"strand":1,"description":"histatin 1 [Source:HGNC Symbol;Acc:HGNC:5283]"}, {"versioned_ensembl_gene_id":"ENSG00000198586.13","gene_symbol":"TLK1","gene_name":"tousled like kinase 1 [Source:HGNC Symbol;Acc:HGNC:11841]","synonyms":"PKU-BETA,KIAA0137","biotype":"protein_coding","ncbi_id":"9874","summary":"The protein encoded by this gene is a serine/threonine kinase that may be involved in the regulation of chromatin assembly. The encoded protein is only active when it is phosphorylated, and this phosphorylation is cell cycle-dependent, with the maximal activity of this protein coming during S phase. The catalytic activity of this protein is diminished by DNA damage and by blockage of DNA replication. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":170990823,"end":171231314,"strand":-1,"description":"tousled like kinase 1 [Source:HGNC Symbol;Acc:HGNC:11841]"}, {"versioned_ensembl_gene_id":"ENSG00000274052.1","gene_symbol":"OR7E156P","gene_name":"olfactory receptor family 7 subfamily E member 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:31311]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"283491","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":63742341,"end":63742804,"strand":1,"description":"olfactory receptor family 7 subfamily E member 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:31311]"}, {"versioned_ensembl_gene_id":"ENSG00000281564.1","gene_symbol":"AC233280.12","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237378.2","gene_symbol":"AL445989.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63746741,"end":63751080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142949.16","gene_symbol":"PTPRF","gene_name":"protein tyrosine phosphatase, receptor type F [Source:HGNC Symbol;Acc:HGNC:9670]","synonyms":"LAR","biotype":"protein_coding","ncbi_id":"5792","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains three Ig-like domains, and nine non-Ig like domains similar to that of neural-cell adhesion molecule. This PTP was shown to function in the regulation of epithelial cell-cell contacts at adherents junctions, as well as in the control of beta-catenin signaling. An increased expression level of this protein was found in the insulin-responsive tissue of obese, insulin-resistant individuals, and may contribute to the pathogenesis of insulin resistance. Two alternatively spliced transcript variants of this gene, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008]","start":43525187,"end":43623666,"strand":1,"description":"protein tyrosine phosphatase, receptor type F [Source:HGNC Symbol;Acc:HGNC:9670]"}, {"versioned_ensembl_gene_id":"ENSG00000141682.11","gene_symbol":"PMAIP1","gene_name":"phorbol-12-myristate-13-acetate-induced protein 1 [Source:HGNC Symbol;Acc:HGNC:9108]","synonyms":"APR,NOXA","biotype":"protein_coding","ncbi_id":"5366","summary":"This gene belongs to a pro-apoptotic subfamily within the BCL-2 protein family, referred to as the BCL-2 homology domain 3 (BH3)-only subfamily, which determine whether a cell commits to apoptosis. In response to death-inducing stimuli, BH3-only members inhibit the anti-apoptotic BCL-2 family members, which under steady-state conditions keep the multi-BH domain proteins BAX and BAK, in an inactive state. [provided by RefSeq, Aug 2020]","start":59899948,"end":59904306,"strand":1,"description":"phorbol-12-myristate-13-acetate-induced protein 1 [Source:HGNC Symbol;Acc:HGNC:9108]"}, {"versioned_ensembl_gene_id":"ENSG00000250624.1","gene_symbol":"MTCYBP43","gene_name":"mitochondrially encoded cytochrome b pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52311]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729119","summary":null,"start":30884443,"end":30885182,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52311]"}, {"versioned_ensembl_gene_id":"ENSG00000249678.1","gene_symbol":"AC097716.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30776257,"end":30793970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261442.1","gene_symbol":"AC023830.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4634329,"end":4640623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264892.1","gene_symbol":"NOS2P4","gene_name":"nitric oxide synthase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266619","summary":null,"start":16812447,"end":16812651,"strand":1,"description":"nitric oxide synthase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50720]"}, {"versioned_ensembl_gene_id":"ENSG00000228669.1","gene_symbol":"LINC00448","gene_name":"long intergenic non-protein coding RNA 448 [Source:HGNC Symbol;Acc:HGNC:42785]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874176","summary":null,"start":62672285,"end":62732359,"strand":-1,"description":"long intergenic non-protein coding RNA 448 [Source:HGNC Symbol;Acc:HGNC:42785]"}, {"versioned_ensembl_gene_id":"ENSG00000010244.18","gene_symbol":"ZNF207","gene_name":"zinc finger protein 207 [Source:HGNC Symbol;Acc:HGNC:12998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7756","summary":null,"start":32350117,"end":32381886,"strand":1,"description":"zinc finger protein 207 [Source:HGNC Symbol;Acc:HGNC:12998]"}, {"versioned_ensembl_gene_id":"ENSG00000146039.10","gene_symbol":"SLC17A4","gene_name":"solute carrier family 17 member 4 [Source:HGNC Symbol;Acc:HGNC:10932]","synonyms":"KIAA2138","biotype":"protein_coding","ncbi_id":"10050","summary":"Phosphate homeostasis is maintained by regulating intake, intestinal absorption, bone deposition and resorption, and renal excretion of phosphate. The central molecule in the control of phosphate excretion from the kidney is the sodium/phosphate cotransporter NPT1 (SLC17A1; MIM 182308), which is located in the renal proximal tubule. NPT1 uses the transmembrane electrochemical potential gradient of sodium to transport phosphate across the cell membrane. SLC17A4 is a similar sodium/phosphate cotransporter in the intestinal mucosa that plays an important role in the absorption of phosphate from the intestine (summary by Shibui et al., 1999 [PubMed 10319585]).[supplied by OMIM, Feb 2011]","start":25754699,"end":25781191,"strand":1,"description":"solute carrier family 17 member 4 [Source:HGNC Symbol;Acc:HGNC:10932]"}, {"versioned_ensembl_gene_id":"ENSG00000266302.6","gene_symbol":"AC098850.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16690261,"end":16804453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102858.12","gene_symbol":"MGRN1","gene_name":"mahogunin ring finger 1 [Source:HGNC Symbol;Acc:HGNC:20254]","synonyms":"RNF156,KIAA0544","biotype":"protein_coding","ncbi_id":"23295","summary":"Mahogunin (MGRN1) is a C3HC4 RING-containing protein with E3 ubiquitin ligase activity in vitro.[supplied by OMIM, Apr 2004]","start":4616493,"end":4690974,"strand":1,"description":"mahogunin ring finger 1 [Source:HGNC Symbol;Acc:HGNC:20254]"}, {"versioned_ensembl_gene_id":"ENSG00000239593.1","gene_symbol":"AL513122.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121279863,"end":121282730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233467.2","gene_symbol":"U40455.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148198014,"end":148198878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119396.10","gene_symbol":"RAB14","gene_name":"RAB14, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16524]","synonyms":"RAB-14,FBP","biotype":"protein_coding","ncbi_id":"51552","summary":"RAB14 belongs to the large RAB family of low molecular mass GTPases that are involved in intracellular membrane trafficking. These proteins act as molecular switches that flip between an inactive GDP-bound state and an active GTP-bound state in which they recruit downstream effector proteins onto membranes (Junutula et al., 2004 [PubMed 15004230]).[supplied by OMIM, Mar 2009]","start":121178137,"end":121223014,"strand":-1,"description":"RAB14, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16524]"}, {"versioned_ensembl_gene_id":"ENSG00000280892.1","gene_symbol":"AL161638.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30414392,"end":30416755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259928.1","gene_symbol":"AC011840.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30564057,"end":30565576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176970.8","gene_symbol":"RPL7L1P11","gene_name":"ribosomal protein L7 like 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347509","summary":null,"start":148464708,"end":148465428,"strand":1,"description":"ribosomal protein L7 like 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39493]"}, {"versioned_ensembl_gene_id":"ENSG00000249054.2","gene_symbol":"FAM138D","gene_name":"family with sequence similarity 138 member D [Source:HGNC Symbol;Acc:HGNC:33583]","synonyms":"F379,F379","biotype":"lincRNA","ncbi_id":"677784","summary":null,"start":36602,"end":38133,"strand":-1,"description":"family with sequence similarity 138 member D [Source:HGNC Symbol;Acc:HGNC:33583]"}, {"versioned_ensembl_gene_id":"ENSG00000264673.1","gene_symbol":"AC098850.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16788248,"end":16789234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273550.1","gene_symbol":"AL354810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63034992,"end":63097797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282718.1","gene_symbol":"AC104333.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212916787,"end":212917577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198830.10","gene_symbol":"HMGN2","gene_name":"high mobility group nucleosomal binding domain 2 [Source:HGNC Symbol;Acc:HGNC:4986]","synonyms":"HMG17","biotype":"protein_coding","ncbi_id":"3151","summary":"The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMGN1, the encoded protein may help maintain an open chromatin configuration around transcribable genes. The protein has also been found to have antimicrobial activity against bacteria, viruses and fungi. [provided by RefSeq, Oct 2014]","start":26472450,"end":26475972,"strand":1,"description":"high mobility group nucleosomal binding domain 2 [Source:HGNC Symbol;Acc:HGNC:4986]"}, {"versioned_ensembl_gene_id":"ENSG00000237741.1","gene_symbol":"AC002368.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148498113,"end":148500615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170160.17","gene_symbol":"CCDC144A","gene_name":"coiled-coil domain containing 144A [Source:HGNC Symbol;Acc:HGNC:29072]","synonyms":"KIAA0565,FLJ43983","biotype":"protein_coding","ncbi_id":"9720","summary":null,"start":16689537,"end":16777881,"strand":1,"description":"coiled-coil domain containing 144A [Source:HGNC Symbol;Acc:HGNC:29072]"}, {"versioned_ensembl_gene_id":"ENSG00000231870.4","gene_symbol":"KRT17P3","gene_name":"keratin 17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33697]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729682","summary":null,"start":30567700,"end":30571748,"strand":-1,"description":"keratin 17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33697]"}, {"versioned_ensembl_gene_id":"ENSG00000227564.2","gene_symbol":"LINC00376","gene_name":"long intergenic non-protein coding RNA 376 [Source:HGNC Symbol;Acc:HGNC:42701]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355293","summary":null,"start":63183101,"end":63328094,"strand":-1,"description":"long intergenic non-protein coding RNA 376 [Source:HGNC Symbol;Acc:HGNC:42701]"}, {"versioned_ensembl_gene_id":"ENSG00000281104.1","gene_symbol":"AL161638.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30420942,"end":30426225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281188.1","gene_symbol":"AC233280.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195639990,"end":195640460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235590.7","gene_symbol":"GNAS-AS1","gene_name":"GNAS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24872]","synonyms":"GNASAS,GNAS1AS,GNAS-AS,SANG,NESPAS,NESP-AS,NCRNA00075","biotype":"antisense_RNA","ncbi_id":"149775","summary":"This gene produces a paternally-imprinted antisense RNA transcript that helps regulate the GNAS complex locus, which encodes the alpha subunit of the stimulatory G protein. Defects in this gene are a cause of pseudohypoparathyroidism type Ib.[provided by RefSeq, Jun 2010]","start":58818919,"end":58850903,"strand":-1,"description":"GNAS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24872]"}, {"versioned_ensembl_gene_id":"ENSG00000282536.1","gene_symbol":"LINC00328-2P","gene_name":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]","synonyms":"NCRNA00328B,NCRNA00328-2P","biotype":"processed_pseudogene","ncbi_id":"100874404","summary":null,"start":18809830,"end":18810048,"strand":1,"description":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]"}, {"versioned_ensembl_gene_id":"ENSG00000225806.7","gene_symbol":"AL121917.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58863528,"end":58888809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224027.1","gene_symbol":"AL133456.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27563839,"end":27573573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235513.1","gene_symbol":"AL035681.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41209122,"end":41217627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227838.1","gene_symbol":"AL121885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27676559,"end":27714970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231495.1","gene_symbol":"AL121885.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27707580,"end":27709931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099937.10","gene_symbol":"SERPIND1","gene_name":"serpin family D member 1 [Source:HGNC Symbol;Acc:HGNC:4838]","synonyms":"HLS2,HCF2,HC2,HC-II,D22S673","biotype":"protein_coding","ncbi_id":"3053","summary":"This gene belongs to the serpin gene superfamily. Serpins play roles in many processes including inflammation, blood clotting, and cancer metastasis. Members of this family have highly conserved secondary structures with a reactive center loop that interacts with the protease active site to inhibit protease activity. This gene encodes a plasma serine protease that functions as a thrombin and chymotrypsin inhibitor. The protein is activated by heparin, dermatan sulfate, and glycosaminoglycans. Allelic variations in this gene are associated with heparin cofactor II deficiency. [provided by RefSeq, Jul 2015]","start":20773879,"end":20787720,"strand":1,"description":"serpin family D member 1 [Source:HGNC Symbol;Acc:HGNC:4838]"}, {"versioned_ensembl_gene_id":"ENSG00000274829.4","gene_symbol":"PARN","gene_name":"poly(A)-specific ribonuclease [Source:HGNC Symbol;Acc:HGNC:8609]","synonyms":"DAN","biotype":"protein_coding","ncbi_id":"5073","summary":"The protein encoded by this gene is a 3'-exoribonuclease, with similarity to the RNase D family of 3'-exonucleases. It prefers poly(A) as the substrate, hence, efficiently degrades poly(A) tails of mRNAs. Exonucleolytic degradation of the poly(A) tail is often the first step in the decay of eukaryotic mRNAs. This protein is also involved in silencing of certain maternal mRNAs during oocyte maturation and early embryonic development, as well as in nonsense-mediated decay (NMD) of mRNAs that contain premature stop codons. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":14435701,"end":14632727,"strand":-1,"description":"poly(A)-specific ribonuclease [Source:HGNC Symbol;Acc:HGNC:8609]"}, {"versioned_ensembl_gene_id":"ENSG00000226169.1","gene_symbol":"AL121885.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27716480,"end":27721677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238170.1","gene_symbol":"C4A-AS1","gene_name":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478955","summary":null,"start":32025384,"end":32028913,"strand":-1,"description":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]"}, {"versioned_ensembl_gene_id":"ENSG00000254479.1","gene_symbol":"SLC25A1P1","gene_name":"solute carrier family 25 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43845]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131457","summary":null,"start":85934737,"end":85935663,"strand":1,"description":"solute carrier family 25 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43845]"}, {"versioned_ensembl_gene_id":"ENSG00000267291.1","gene_symbol":"AC008649.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38596346,"end":38601694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087460.24","gene_symbol":"GNAS","gene_name":"GNAS complex locus [Source:HGNC Symbol;Acc:HGNC:4392]","synonyms":"NESP55,NESP,GPSA,GNASXL,GNAS1,SgVI,SCG6","biotype":"protein_coding","ncbi_id":"2778","summary":"This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]","start":58839718,"end":58911192,"strand":1,"description":"GNAS complex locus [Source:HGNC Symbol;Acc:HGNC:4392]"}, {"versioned_ensembl_gene_id":"ENSG00000166347.18","gene_symbol":"CYB5A","gene_name":"cytochrome b5 type A [Source:HGNC Symbol;Acc:HGNC:2570]","synonyms":"CYB5","biotype":"protein_coding","ncbi_id":"1528","summary":"The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":74250847,"end":74292016,"strand":-1,"description":"cytochrome b5 type A [Source:HGNC Symbol;Acc:HGNC:2570]"}, {"versioned_ensembl_gene_id":"ENSG00000239393.1","gene_symbol":"AC146507.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177346073,"end":177346426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169223.14","gene_symbol":"LMAN2","gene_name":"lectin, mannose binding 2 [Source:HGNC Symbol;Acc:HGNC:16986]","synonyms":"VIP36,GP36B,C5orf8","biotype":"protein_coding","ncbi_id":"10960","summary":"This gene encodes a type I transmembrane lectin that shuttles between the endoplasmic reticulum, the Golgi apparatus and the plasma membrane. The encoded protein binds high mannose type glycoproteins and may facilitate their sorting, trafficking and quality control. [provided by RefSeq, Oct 2008]","start":177331562,"end":177351852,"strand":-1,"description":"lectin, mannose binding 2 [Source:HGNC Symbol;Acc:HGNC:16986]"}, {"versioned_ensembl_gene_id":"ENSG00000125531.6","gene_symbol":"FNDC11","gene_name":"fibronectin type III domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28764]","synonyms":"MGC5356,C20orf195","biotype":"protein_coding","ncbi_id":"79025","summary":null,"start":63547891,"end":63556708,"strand":1,"description":"fibronectin type III domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28764]"}, {"versioned_ensembl_gene_id":"ENSG00000104814.12","gene_symbol":"MAP4K1","gene_name":"mitogen-activated protein kinase kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6863]","synonyms":"HPK1","biotype":"protein_coding","ncbi_id":"11184","summary":null,"start":38587641,"end":38618882,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6863]"}, {"versioned_ensembl_gene_id":"ENSG00000250220.1","gene_symbol":"AC053527.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73259209,"end":73317953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231955.1","gene_symbol":"AC007383.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206115547,"end":206122323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249976.2","gene_symbol":"AC108157.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73337233,"end":73337771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237580.1","gene_symbol":"GCSHP3","gene_name":"glycine cleavage system protein H pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100329109","summary":null,"start":206116110,"end":206116500,"strand":-1,"description":"glycine cleavage system protein H pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43929]"}, {"versioned_ensembl_gene_id":"ENSG00000223342.2","gene_symbol":"AL158817.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6901022,"end":6918715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271797.1","gene_symbol":"AC008494.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115262505,"end":115263448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250650.1","gene_symbol":"AC093534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117019548,"end":117019679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099940.11","gene_symbol":"SNAP29","gene_name":"synaptosome associated protein 29 [Source:HGNC Symbol;Acc:HGNC:11133]","synonyms":"SNAP-29,CEDNIK","biotype":"protein_coding","ncbi_id":"9342","summary":"This gene, a member of the SNAP25 gene family, encodes a protein involved in multiple membrane trafficking steps. Two other members of this gene family, SNAP23 and SNAP25, encode proteins that bind a syntaxin protein and mediate synaptic vesicle membrane docking and fusion to the plasma membrane. The protein encoded by this gene binds tightly to multiple syntaxins and is localized to intracellular membrane structures rather than to the plasma membrane. While the protein is mostly membrane-bound, a significant fraction of it is found free in the cytoplasm. Use of multiple polyadenylation sites has been noted for this gene. [provided by RefSeq, Jul 2008]","start":20858983,"end":20891218,"strand":1,"description":"synaptosome associated protein 29 [Source:HGNC Symbol;Acc:HGNC:11133]"}, {"versioned_ensembl_gene_id":"ENSG00000023228.13","gene_symbol":"NDUFS1","gene_name":"NADH:ubiquinone oxidoreductase core subunit S1 [Source:HGNC Symbol;Acc:HGNC:7707]","synonyms":"CI-75k","biotype":"protein_coding","ncbi_id":"4719","summary":"The protein encoded by this gene belongs to the complex I 75 kDa subunit family. Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. This protein is the largest subunit of complex I and it is a component of the iron-sulfur (IP) fragment of the enzyme. It may form part of the active site crevice where NADH is oxidized. Mutations in this gene are associated with complex I deficiency. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":206114817,"end":206159603,"strand":-1,"description":"NADH:ubiquinone oxidoreductase core subunit S1 [Source:HGNC Symbol;Acc:HGNC:7707]"}, {"versioned_ensembl_gene_id":"ENSG00000225922.1","gene_symbol":"RPL21P92","gene_name":"ribosomal protein L21 pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:35606]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130400","summary":null,"start":67793770,"end":67794245,"strand":1,"description":"ribosomal protein L21 pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:35606]"}, {"versioned_ensembl_gene_id":"ENSG00000164219.9","gene_symbol":"PGGT1B","gene_name":"protein geranylgeranyltransferase type I subunit beta [Source:HGNC Symbol;Acc:HGNC:8895]","synonyms":"BGGI,GGTI","biotype":"protein_coding","ncbi_id":"5229","summary":"Protein geranylgeranyltransferase type I (GGTase-I) transfers a geranylgeranyl group to the cysteine residue of candidate proteins containing a C-terminal CAAX motif in which 'A' is an aliphatic amino acid and 'X' is leucine (summarized by Zhang et al., 1994 [PubMed 8106351]). The enzyme is composed of a 48-kD alpha subunit (FNTA; MIM 134635) and a 43-kD beta subunit, encoded by the PGGT1B gene. The FNTA gene encodes the alpha subunit for both GGTase-I and the related enzyme farnesyltransferase.[supplied by OMIM, Mar 2010]","start":115204012,"end":115262872,"strand":-1,"description":"protein geranylgeranyltransferase type I subunit beta [Source:HGNC Symbol;Acc:HGNC:8895]"}, {"versioned_ensembl_gene_id":"ENSG00000067225.17","gene_symbol":"PKM","gene_name":"pyruvate kinase, muscle [Source:HGNC Symbol;Acc:HGNC:9021]","synonyms":"THBP1,PKM2,PK3,OIP3","biotype":"protein_coding","ncbi_id":"5315","summary":"This gene encodes a protein involved in glycolysis. The encoded protein is a pyruvate kinase that catalyzes the transfer of a phosphoryl group from phosphoenolpyruvate to ADP, generating ATP and pyruvate. This protein has been shown to interact with thyroid hormone and may mediate cellular metabolic effects induced by thyroid hormones. This protein has been found to bind Opa protein, a bacterial outer membrane protein involved in gonococcal adherence to and invasion of human cells, suggesting a role of this protein in bacterial pathogenesis. Several alternatively spliced transcript variants encoding a few distinct isoforms have been reported. [provided by RefSeq, May 2011]","start":72199029,"end":72231822,"strand":-1,"description":"pyruvate kinase, muscle [Source:HGNC Symbol;Acc:HGNC:9021]"}, {"versioned_ensembl_gene_id":"ENSG00000267066.1","gene_symbol":"AC107990.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59929226,"end":59930330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152223.12","gene_symbol":"EPG5","gene_name":"ectopic P-granules autophagy protein 5 homolog [Source:HGNC Symbol;Acc:HGNC:29331]","synonyms":"KIAA1632,hEPG5","biotype":"protein_coding","ncbi_id":"57724","summary":"This gene encodes a large coiled coil domain-containing protein that functions in autophagy during starvation conditions. Mutations in this gene cause Vici syndrome. [provided by RefSeq, Aug 2015]","start":45847609,"end":45967274,"strand":-1,"description":"ectopic P-granules autophagy protein 5 homolog [Source:HGNC Symbol;Acc:HGNC:29331]"}, {"versioned_ensembl_gene_id":"ENSG00000267497.1","gene_symbol":"NFE2L3P1","gene_name":"nuclear factor, erythroid 2 like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22278]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642996","summary":null,"start":59969438,"end":59971396,"strand":1,"description":"nuclear factor, erythroid 2 like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22278]"}, {"versioned_ensembl_gene_id":"ENSG00000224043.7","gene_symbol":"CCNT2-AS1","gene_name":"CCNT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40130]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129961","summary":null,"start":134735464,"end":134918710,"strand":-1,"description":"CCNT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40130]"}, {"versioned_ensembl_gene_id":"ENSG00000237141.1","gene_symbol":"DNAJC19P1","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45064]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129853","summary":null,"start":67833763,"end":67834081,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45064]"}, {"versioned_ensembl_gene_id":"ENSG00000108176.14","gene_symbol":"DNAJC12","gene_name":"DnaJ heat shock protein family (Hsp40) member C12 [Source:HGNC Symbol;Acc:HGNC:28908]","synonyms":"JDP1","biotype":"protein_coding","ncbi_id":"56521","summary":"This gene encodes a member of a subclass of the HSP40/DnaJ protein family. Members of this family of proteins are associated with complex assembly, protein folding, and export. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":67796665,"end":67838166,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C12 [Source:HGNC Symbol;Acc:HGNC:28908]"}, {"versioned_ensembl_gene_id":"ENSG00000234682.1","gene_symbol":"VDAC2P4","gene_name":"voltage dependent anion channel 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420574","summary":null,"start":134797169,"end":134797879,"strand":1,"description":"voltage dependent anion channel 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51932]"}, {"versioned_ensembl_gene_id":"ENSG00000223955.1","gene_symbol":"MTND6P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38730]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499469","summary":null,"start":8363536,"end":8363959,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38730]"}, {"versioned_ensembl_gene_id":"ENSG00000268983.1","gene_symbol":"AC005253.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18568506,"end":18569375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187094.11","gene_symbol":"CCK","gene_name":"cholecystokinin [Source:HGNC Symbol;Acc:HGNC:1569]","synonyms":null,"biotype":"protein_coding","ncbi_id":"885","summary":"This gene encodes a member of the gastrin/cholecystokinin family of proteins. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the peptide hormones cholecystokinin-8, -12, -33, and others. The encoded peptides have been shown to regulate gastric acid secretion and food intake. A sulfated form of cholecystokinin-8 may modulate neuronal activity in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":42257825,"end":42266207,"strand":-1,"description":"cholecystokinin [Source:HGNC Symbol;Acc:HGNC:1569]"}, {"versioned_ensembl_gene_id":"ENSG00000228098.1","gene_symbol":"AC110620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134816362,"end":134816589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235079.1","gene_symbol":"ZRANB2-AS1","gene_name":"ZRANB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43594]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132618","summary":null,"start":71048855,"end":71067184,"strand":1,"description":"ZRANB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43594]"}, {"versioned_ensembl_gene_id":"ENSG00000231966.1","gene_symbol":"AL359853.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179829609,"end":179836124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204814.5","gene_symbol":"AL935212.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61659733,"end":61662690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254879.1","gene_symbol":"PTPRJ-AS1","gene_name":"PTPRJ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50634]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104326192","summary":null,"start":48014406,"end":48015855,"strand":-1,"description":"PTPRJ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50634]"}, {"versioned_ensembl_gene_id":"ENSG00000279792.1","gene_symbol":"AC015909.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50362967,"end":50365232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241973.10","gene_symbol":"PI4KA","gene_name":"phosphatidylinositol 4-kinase alpha [Source:HGNC Symbol;Acc:HGNC:8983]","synonyms":"PIK4CA,pi4K230,PI4K-ALPHA","biotype":"protein_coding","ncbi_id":"5297","summary":"This gene encodes a phosphatidylinositol (PI) 4-kinase which catalyzes the first committed step in the biosynthesis of phosphatidylinositol 4,5-bisphosphate. The mammalian PI 4-kinases have been classified into two types, II and III, based on their molecular mass, and modulation by detergent and adenosine. The protein encoded by this gene is a type III enzyme that is not inhibited by adenosine. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2018]","start":20707691,"end":20859417,"strand":-1,"description":"phosphatidylinositol 4-kinase alpha [Source:HGNC Symbol;Acc:HGNC:8983]"}, {"versioned_ensembl_gene_id":"ENSG00000082258.12","gene_symbol":"CCNT2","gene_name":"cyclin T2 [Source:HGNC Symbol;Acc:HGNC:1600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"905","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin and its kinase partner CDK9 were found to be subunits of the transcription elongation factor p-TEFb. The p-TEFb complex containing this cyclin was reported to interact with, and act as a negative regulator of human immunodeficiency virus type 1 (HIV-1) Tat protein. A pseudogene of this gene is found on chromosome 1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010]","start":134918235,"end":134959342,"strand":1,"description":"cyclin T2 [Source:HGNC Symbol;Acc:HGNC:1600]"}, {"versioned_ensembl_gene_id":"ENSG00000249203.1","gene_symbol":"LINC02224","gene_name":"long intergenic non-protein coding RNA 2224 [Source:HGNC Symbol;Acc:HGNC:53093]","synonyms":"ENST00000505706,BRCAT107","biotype":"lincRNA","ncbi_id":"102723839","summary":null,"start":44495618,"end":44510282,"strand":-1,"description":"long intergenic non-protein coding RNA 2224 [Source:HGNC Symbol;Acc:HGNC:53093]"}, {"versioned_ensembl_gene_id":"ENSG00000132485.13","gene_symbol":"ZRANB2","gene_name":"zinc finger RANBP2-type containing 2 [Source:HGNC Symbol;Acc:HGNC:13058]","synonyms":"ZNF265,ZIS2,ZIS1,ZIS","biotype":"protein_coding","ncbi_id":"9406","summary":null,"start":71063291,"end":71081297,"strand":-1,"description":"zinc finger RANBP2-type containing 2 [Source:HGNC Symbol;Acc:HGNC:13058]"}, {"versioned_ensembl_gene_id":"ENSG00000250418.1","gene_symbol":"AC093292.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44698431,"end":44700808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161405.16","gene_symbol":"IKZF3","gene_name":"IKAROS family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:13178]","synonyms":"ZNFN1A3,Aiolos","biotype":"protein_coding","ncbi_id":"22806","summary":"This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This gene product is a transcription factor that is important in the regulation of B lymphocyte proliferation and differentiation. Both Ikaros and Aiolos can participate in chromatin remodeling. Regulation of gene expression in B lymphocytes by Aiolos is complex as it appears to require the sequential formation of Ikaros homodimers, Ikaros/Aiolos heterodimers, and Aiolos homodimers. Several alternative transcripts encoding different isoforms have been described, as well as some non-protein coding variants. [provided by RefSeq, Apr 2012]","start":39757715,"end":39864188,"strand":-1,"description":"IKAROS family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:13178]"}, {"versioned_ensembl_gene_id":"ENSG00000234179.1","gene_symbol":"MTCYBP1","gene_name":"mitochondrially encoded cytochrome b pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38729]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499418","summary":null,"start":8364032,"end":8365150,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38729]"}, {"versioned_ensembl_gene_id":"ENSG00000257176.2","gene_symbol":"AC009318.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29280418,"end":29317848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270160.1","gene_symbol":"AP001995.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128614340,"end":128615236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064763.10","gene_symbol":"FAR2","gene_name":"fatty acyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:25531]","synonyms":"SDR10E2,MLSTD1,FLJ10462","biotype":"protein_coding","ncbi_id":"55711","summary":"This gene belongs to the short chain dehydrogenase/reductase superfamily. It encodes a reductase enzyme involved in the first step of wax biosynthesis wherein fatty acids are converted to fatty alcohols. The encoded peroxisomal protein utilizes saturated fatty acids of 16 or 18 carbons as preferred substrates. Alternatively spliced transcript variants have been observed for this gene. Related pseudogenes have been identified on chromosomes 2, 14 and 22. [provided by RefSeq, Nov 2012]","start":29149103,"end":29340980,"strand":1,"description":"fatty acyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:25531]"}, {"versioned_ensembl_gene_id":"ENSG00000240296.1","gene_symbol":"AC245052.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54268005,"end":54269045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255465.3","gene_symbol":"AP001995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128615867,"end":128621806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139445.17","gene_symbol":"FOXN4","gene_name":"forkhead box N4 [Source:HGNC Symbol;Acc:HGNC:21399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"121643","summary":"Members of the winged-helix/forkhead family of transcription factors, such as FOXN4, are characterized by a 110-amino acid DNA-binding domain that can fold into a variant of the helix-turn-helix motif consisting of 3 alpha helices flanked by 2 large loops or wings. These transcription factors are involved in a variety of biologic processes as key regulators in development and metabolism (Li et al., 2004 [PubMed 15363391]).[supplied by OMIM, Mar 2008]","start":109277979,"end":109309220,"strand":-1,"description":"forkhead box N4 [Source:HGNC Symbol;Acc:HGNC:21399]"}, {"versioned_ensembl_gene_id":"ENSG00000243495.1","gene_symbol":"GMFBP1","gene_name":"glia maturation factor beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38654]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499251","summary":null,"start":100665050,"end":100665476,"strand":-1,"description":"glia maturation factor beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38654]"}, {"versioned_ensembl_gene_id":"ENSG00000241202.1","gene_symbol":"ZIC4-AS1","gene_name":"ZIC4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40920]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873950","summary":null,"start":147386967,"end":147387453,"strand":1,"description":"ZIC4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40920]"}, {"versioned_ensembl_gene_id":"ENSG00000152977.9","gene_symbol":"ZIC1","gene_name":"Zic family member 1 [Source:HGNC Symbol;Acc:HGNC:12872]","synonyms":"ZIC,ZNF201","biotype":"protein_coding","ncbi_id":"7545","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. Members of this family are important during development. Aberrant expression of this gene is seen in medulloblastoma, a childhood brain tumor. This gene is closely linked to the gene encoding zinc finger protein of the cerebellum 4, a related family member on chromosome 3. This gene encodes a transcription factor that can bind and transactivate the apolipoprotein E gene. [provided by RefSeq, Jul 2008]","start":147393422,"end":147510293,"strand":1,"description":"Zic family member 1 [Source:HGNC Symbol;Acc:HGNC:12872]"}, {"versioned_ensembl_gene_id":"ENSG00000102891.3","gene_symbol":"MT4","gene_name":"metallothionein 4 [Source:HGNC Symbol;Acc:HGNC:18705]","synonyms":"MTIV","biotype":"protein_coding","ncbi_id":"84560","summary":null,"start":56565049,"end":56568957,"strand":1,"description":"metallothionein 4 [Source:HGNC Symbol;Acc:HGNC:18705]"}, {"versioned_ensembl_gene_id":"ENSG00000144820.7","gene_symbol":"ADGRG7","gene_name":"adhesion G protein-coupled receptor G7 [Source:HGNC Symbol;Acc:HGNC:19241]","synonyms":"GPR128,FLJ14454","biotype":"protein_coding","ncbi_id":"84873","summary":null,"start":100609589,"end":100695479,"strand":1,"description":"adhesion G protein-coupled receptor G7 [Source:HGNC Symbol;Acc:HGNC:19241]"}, {"versioned_ensembl_gene_id":"ENSG00000272549.1","gene_symbol":"LINC02538","gene_name":"long intergenic non-protein coding RNA 2538 [Source:HGNC Symbol;Acc:HGNC:53571]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401286","summary":null,"start":167666840,"end":167679270,"strand":-1,"description":"long intergenic non-protein coding RNA 2538 [Source:HGNC Symbol;Acc:HGNC:53571]"}, {"versioned_ensembl_gene_id":"ENSG00000105707.13","gene_symbol":"HPN","gene_name":"hepsin [Source:HGNC Symbol;Acc:HGNC:5155]","synonyms":"TMPRSS1","biotype":"protein_coding","ncbi_id":"3249","summary":"This gene encodes a type II transmembrane serine protease that may be involved in diverse cellular functions, including blood coagulation and the maintenance of cell morphology. Expression of the encoded protein is associated with the growth and progression of cancers, particularly prostate cancer. The protein is cleaved into a catalytic serine protease chain and a non-catalytic scavenger receptor cysteine-rich chain, which associate via a single disulfide bond. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":35040506,"end":35066571,"strand":1,"description":"hepsin [Source:HGNC Symbol;Acc:HGNC:5155]"}, {"versioned_ensembl_gene_id":"ENSG00000149177.12","gene_symbol":"PTPRJ","gene_name":"protein tyrosine phosphatase, receptor type J [Source:HGNC Symbol;Acc:HGNC:9673]","synonyms":"HPTPeta,DEP1,CD148","biotype":"protein_coding","ncbi_id":"5795","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes, including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region containing five fibronectin type III repeats, a single transmembrane region, and a single intracytoplasmic catalytic domain, and thus represents a receptor-type PTP. This protein is present in all hematopoietic lineages, and was shown to negatively regulate T cell receptor signaling possibly through interfering with the phosphorylation of Phospholipase C Gamma 1 and Linker for Activation of T Cells. This protein can also dephosphorylate the PDGF beta receptor, and may be involved in UV-induced signal transduction. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":47980558,"end":48170841,"strand":1,"description":"protein tyrosine phosphatase, receptor type J [Source:HGNC Symbol;Acc:HGNC:9673]"}, {"versioned_ensembl_gene_id":"ENSG00000015532.9","gene_symbol":"XYLT2","gene_name":"xylosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15517]","synonyms":"XT-II,PXYLT2","biotype":"protein_coding","ncbi_id":"64132","summary":"The protein encoded by this gene is an isoform of xylosyltransferase, which belongs to a family of glycosyltransferases. This enzyme transfers xylose from UDP-xylose to specific serine residues of the core protein and initiates the biosynthesis of glycosaminoglycan chains in proteoglycans including chondroitin sulfate, heparan sulfate, heparin and dermatan sulfate. The enzyme activity, which is increased in scleroderma patients, is a diagnostic marker for the determination of sclerotic activity in systemic sclerosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]","start":50346092,"end":50363138,"strand":1,"description":"xylosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15517]"}, {"versioned_ensembl_gene_id":"ENSG00000272892.1","gene_symbol":"AL133551.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67849525,"end":67850746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229367.1","gene_symbol":"HMGN2P19","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39383]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874466","summary":null,"start":229570532,"end":229570796,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39383]"}, {"versioned_ensembl_gene_id":"ENSG00000267462.1","gene_symbol":"AC090377.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60010281,"end":60014258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260689.2","gene_symbol":"HNRNPA3P11","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48757]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421431","summary":null,"start":57246960,"end":57247893,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48757]"}, {"versioned_ensembl_gene_id":"ENSG00000256704.3","gene_symbol":"SDCCAG3P1","gene_name":"serologically defined colon cancer antigen 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29375]","synonyms":"SDCCAG3L","biotype":"processed_pseudogene","ncbi_id":"388478","summary":null,"start":60009994,"end":60011143,"strand":-1,"description":"serologically defined colon cancer antigen 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29375]"}, {"versioned_ensembl_gene_id":"ENSG00000248162.1","gene_symbol":"AC074198.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164725310,"end":164726706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213065.2","gene_symbol":"AL009178.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167767083,"end":167768568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275343.1","gene_symbol":"AC010999.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56908312,"end":56908635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225625.4","gene_symbol":"AC090517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56846340,"end":56846605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219932.6","gene_symbol":"RPL12P8","gene_name":"ribosomal protein L12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23735]","synonyms":"bA57G10.3","biotype":"processed_pseudogene","ncbi_id":"645161","summary":null,"start":67874332,"end":67874911,"strand":1,"description":"ribosomal protein L12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23735]"}, {"versioned_ensembl_gene_id":"ENSG00000256686.1","gene_symbol":"AC019209.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25782706,"end":25814171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245008.3","gene_symbol":"AP001122.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128629653,"end":128686922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255725.2","gene_symbol":"TDGP1","gene_name":"thymine-DNA glycosylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49891]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645233","summary":null,"start":25803298,"end":25804526,"strand":1,"description":"thymine-DNA glycosylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49891]"}, {"versioned_ensembl_gene_id":"ENSG00000269155.2","gene_symbol":"AL009178.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167795530,"end":167798248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137871.19","gene_symbol":"ZNF280D","gene_name":"zinc finger protein 280D [Source:HGNC Symbol;Acc:HGNC:25953]","synonyms":"ZNF634,SUHW4,FLJ20086","biotype":"protein_coding","ncbi_id":"54816","summary":null,"start":56630181,"end":56918571,"strand":-1,"description":"zinc finger protein 280D [Source:HGNC Symbol;Acc:HGNC:25953]"}, {"versioned_ensembl_gene_id":"ENSG00000146521.9","gene_symbol":"LINC01558","gene_name":"long intergenic non-protein coding RNA 1558 [Source:HGNC Symbol;Acc:HGNC:21235]","synonyms":"LINC01557,HGC6.2,dJ431P23.4,C6orf123","biotype":"lincRNA","ncbi_id":"26238","summary":null,"start":167784537,"end":167796859,"strand":-1,"description":"long intergenic non-protein coding RNA 1558 [Source:HGNC Symbol;Acc:HGNC:21235]"}, {"versioned_ensembl_gene_id":"ENSG00000256440.1","gene_symbol":"AC019209.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25831416,"end":25834182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151702.16","gene_symbol":"FLI1","gene_name":"Fli-1 proto-oncogene, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3749]","synonyms":"SIC-1,EWSR2","biotype":"protein_coding","ncbi_id":"2313","summary":"This gene encodes a transcription factor containing an ETS DNA-binding domain. The gene can undergo a t(11;22)(q24;q12) translocation with the Ewing sarcoma gene on chromosome 22, which results in a fusion gene that is present in the majority of Ewing sarcoma cases. An acute lymphoblastic leukemia-associated t(4;11)(q21;q23) translocation involving this gene has also been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":128686535,"end":128813267,"strand":1,"description":"Fli-1 proto-oncogene, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3749]"}, {"versioned_ensembl_gene_id":"ENSG00000256256.1","gene_symbol":"AC019209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25882955,"end":25885855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235581.1","gene_symbol":"AC005011.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71942259,"end":71942468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087250.8","gene_symbol":"MT3","gene_name":"metallothionein 3 [Source:HGNC Symbol;Acc:HGNC:7408]","synonyms":"GIF","biotype":"protein_coding","ncbi_id":"4504","summary":"This gene is a member of the metallothionein family of genes. Proteins encoded by this gene family are low in molecular weight, are cysteine-rich, lack aromatic residues, and bind divalent heavy metal ions. This gene family member displays tissue-specific expression, and contains a threonine insert near its N-terminus and a glutamate-rich hexapeptide insert near its C-terminus relative to the proteins encoded by other gene family members. It plays an important role in zinc and copper homeostasis, and is induced under hypoxic conditions. The encoded protein is a growth inhibitory factor, and reduced levels of the protein are observed in the brains of individuals with some metal-linked neurodegenerative disorders such as Alzheimer's disease. [provided by RefSeq, Sep 2017]","start":56589074,"end":56591088,"strand":1,"description":"metallothionein 3 [Source:HGNC Symbol;Acc:HGNC:7408]"}, {"versioned_ensembl_gene_id":"ENSG00000276756.4","gene_symbol":"AC245595.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144276484,"end":144305180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264729.1","gene_symbol":"AC022596.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16804627,"end":16805707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228769.1","gene_symbol":"ABCF2P2","gene_name":"ATP binding cassette subfamily F member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48842]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422059","summary":null,"start":72103181,"end":72104209,"strand":1,"description":"ATP binding cassette subfamily F member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48842]"}, {"versioned_ensembl_gene_id":"ENSG00000266129.1","gene_symbol":"SRP68P1","gene_name":"signal recognition particle 68 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30427]","synonyms":"SRPSMCR","biotype":"processed_pseudogene","ncbi_id":"252841","summary":null,"start":16787235,"end":16788141,"strand":-1,"description":"signal recognition particle 68 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30427]"}, {"versioned_ensembl_gene_id":"ENSG00000183166.10","gene_symbol":"CALN1","gene_name":"calneuron 1 [Source:HGNC Symbol;Acc:HGNC:13248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83698","summary":"This gene encodes a protein with high similarity to the calcium-binding proteins of the calmodulin family. The encoded protein contains two EF-hand domains and potential calcium-binding sites. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":71779491,"end":72447151,"strand":-1,"description":"calneuron 1 [Source:HGNC Symbol;Acc:HGNC:13248]"}, {"versioned_ensembl_gene_id":"ENSG00000266486.1","gene_symbol":"FAM106CP","gene_name":"family with sequence similarity 106 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:38396]","synonyms":"FAM106C","biotype":"processed_pseudogene","ncbi_id":"100129396","summary":null,"start":16788901,"end":16789407,"strand":1,"description":"family with sequence similarity 106 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:38396]"}, {"versioned_ensembl_gene_id":"ENSG00000226478.3","gene_symbol":"UPF3AP1","gene_name":"UPF3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30568]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"147226","summary":null,"start":16745636,"end":16746761,"strand":-1,"description":"UPF3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30568]"}, {"versioned_ensembl_gene_id":"ENSG00000175658.4","gene_symbol":"DRD5P2","gene_name":"dopamine receptor D5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1818","summary":null,"start":144274892,"end":144277993,"strand":-1,"description":"dopamine receptor D5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3028]"}, {"versioned_ensembl_gene_id":"ENSG00000135801.9","gene_symbol":"TAF5L","gene_name":"TATA-box binding protein associated factor 5 like [Source:HGNC Symbol;Acc:HGNC:17304]","synonyms":"PAF65B","biotype":"protein_coding","ncbi_id":"27097","summary":"The product of this gene belongs to the WD-repeat TAF5 family of proteins. This gene encodes a protein that is a component of the PCAF histone acetylase complex. The PCAF histone acetylase complex, which is composed of more than 20 polypeptides some of which are TAFs, is required for myogenic transcription and differentiation. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors to facilitate complex assembly and transcription initiation. The encoded protein is structurally similar to one of the histone-like TAFs, TAF5. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":229593111,"end":229626047,"strand":-1,"description":"TATA-box binding protein associated factor 5 like [Source:HGNC Symbol;Acc:HGNC:17304]"}, {"versioned_ensembl_gene_id":"ENSG00000274671.4","gene_symbol":"MARVELD2","gene_name":"MARVEL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26401]","synonyms":"TRIC,MRVLDC2,FLJ30532,DFNB49","biotype":"protein_coding","ncbi_id":"153562","summary":"The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":69415353,"end":69444141,"strand":1,"description":"MARVEL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26401]"}, {"versioned_ensembl_gene_id":"ENSG00000271567.1","gene_symbol":"PPIAL4E","gene_name":"peptidylprolyl isomerase A like 4E [Source:HGNC Symbol;Acc:HGNC:33997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730262","summary":null,"start":144372875,"end":144373659,"strand":-1,"description":"peptidylprolyl isomerase A like 4E [Source:HGNC Symbol;Acc:HGNC:33997]"}, {"versioned_ensembl_gene_id":"ENSG00000121486.11","gene_symbol":"TRMT1L","gene_name":"tRNA methyltransferase 1 like [Source:HGNC Symbol;Acc:HGNC:16782]","synonyms":"C1orf25","biotype":"protein_coding","ncbi_id":"81627","summary":"This gene encodes a protein that has some similarity to N2,N2-dimethylguanosine tRNA methyltransferase from other organisms. Studies of the mouse ortholog have shown that this protein plays a role in motor coordination and exploratory behavior, and it may also be involved in modulating postnatal neuronal functions. Alternatively spliced transcripts have been identified for this gene. [provided by RefSeq, Jan 2011]","start":185118098,"end":185157072,"strand":-1,"description":"tRNA methyltransferase 1 like [Source:HGNC Symbol;Acc:HGNC:16782]"}, {"versioned_ensembl_gene_id":"ENSG00000271439.1","gene_symbol":"AC246785.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144401069,"end":144401355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233586.1","gene_symbol":"AC246785.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144418678,"end":144419190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269425.1","gene_symbol":"AC104521.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4339577,"end":4343491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237343.1","gene_symbol":"AC246785.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144418113,"end":144419192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231402.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31287510,"end":31288964,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000248771.5","gene_symbol":"SMIM31","gene_name":"small integral membrane protein 31 [Source:HGNC Symbol;Acc:HGNC:49638]","synonyms":"LINC01207","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":164754064,"end":164803795,"strand":1,"description":"small integral membrane protein 31 [Source:HGNC Symbol;Acc:HGNC:49638]"}, {"versioned_ensembl_gene_id":"ENSG00000178078.11","gene_symbol":"STAP2","gene_name":"signal transducing adaptor family member 2 [Source:HGNC Symbol;Acc:HGNC:30430]","synonyms":"STAP-2,BKS","biotype":"protein_coding","ncbi_id":"55620","summary":"This gene encodes the substrate of breast tumor kinase, an Src-type non-receptor tyrosine kinase. The encoded protein possesses domains and several tyrosine phosphorylation sites characteristic of adaptor proteins that mediate the interactions linking proteins involved in signal transduction pathways. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":4324043,"end":4342786,"strand":-1,"description":"signal transducing adaptor family member 2 [Source:HGNC Symbol;Acc:HGNC:30430]"}, {"versioned_ensembl_gene_id":"ENSG00000256166.1","gene_symbol":"AL671883.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31293908,"end":31301642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279000.3","gene_symbol":"OR10A6","gene_name":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"390093","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":7924592,"end":7931268,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]"}, {"versioned_ensembl_gene_id":"ENSG00000163818.16","gene_symbol":"LZTFL1","gene_name":"leucine zipper transcription factor like 1 [Source:HGNC Symbol;Acc:HGNC:6741]","synonyms":"BBS17","biotype":"protein_coding","ncbi_id":"54585","summary":"This gene encodes a ubiquitously expressed protein that localizes to the cytoplasm. This protein interacts with Bardet-Biedl Syndrome (BBS) proteins and, through its interaction with BBS protein complexes, regulates protein trafficking to the ciliary membrane. Nonsense mutations in this gene cause a form of Bardet-Biedl Syndrome; a ciliopathy characterized in part by polydactyly, obesity, cognitive impairment, hypogonadism, and kidney failure. This gene may also function as a tumor suppressor; possibly by interacting with E-cadherin and the actin cytoskeleton and thereby regulating the transition of epithelial cells to mesenchymal cells. [provided by RefSeq, Aug 2020]","start":45823316,"end":45916042,"strand":-1,"description":"leucine zipper transcription factor like 1 [Source:HGNC Symbol;Acc:HGNC:6741]"}, {"versioned_ensembl_gene_id":"ENSG00000177483.11","gene_symbol":"RBM44","gene_name":"RNA binding motif protein 44 [Source:HGNC Symbol;Acc:HGNC:24756]","synonyms":"FLJ40411","biotype":"protein_coding","ncbi_id":"375316","summary":null,"start":237798389,"end":237842808,"strand":1,"description":"RNA binding motif protein 44 [Source:HGNC Symbol;Acc:HGNC:24756]"}, {"versioned_ensembl_gene_id":"ENSG00000234175.1","gene_symbol":"AL355355.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13139196,"end":13139533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256540.1","gene_symbol":"AC007406.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166856,"end":182399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234745.10","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31269491,"end":31357188,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000257415.1","gene_symbol":"AC084364.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103503381,"end":103504936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234427.1","gene_symbol":"AL022724.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11810602,"end":11811248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215124.2","gene_symbol":"AMD1P4","gene_name":"adenosylmethionine decarboxylase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51609]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129761","summary":null,"start":11861626,"end":11862970,"strand":-1,"description":"adenosylmethionine decarboxylase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51609]"}, {"versioned_ensembl_gene_id":"ENSG00000170683.6","gene_symbol":"OR10A3","gene_name":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]","synonyms":"HTPCRX12,HSHTPCRX12","biotype":"protein_coding","ncbi_id":"26496","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7937171,"end":7941708,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]"}, {"versioned_ensembl_gene_id":"ENSG00000198221.8","gene_symbol":"AFDN-AS1","gene_name":"AFDN antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:21236]","synonyms":"MLLT4-AS1,HGC6.4,dJ431P23.3,C6orf124","biotype":"lincRNA","ncbi_id":"653483","summary":null,"start":167823876,"end":167826709,"strand":-1,"description":"AFDN antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:21236]"}, {"versioned_ensembl_gene_id":"ENSG00000225102.1","gene_symbol":"AL157373.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11990343,"end":11992012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257994.1","gene_symbol":"AC084364.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":103505411,"end":103506174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257762.5","gene_symbol":"LINC02401","gene_name":"long intergenic non-protein coding RNA 2401 [Source:HGNC Symbol;Acc:HGNC:53328]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929084","summary":null,"start":103547794,"end":103559815,"strand":1,"description":"long intergenic non-protein coding RNA 2401 [Source:HGNC Symbol;Acc:HGNC:53328]"}, {"versioned_ensembl_gene_id":"ENSG00000108239.8","gene_symbol":"TBC1D12","gene_name":"TBC1 domain family member 12 [Source:HGNC Symbol;Acc:HGNC:29082]","synonyms":"KIAA0608","biotype":"protein_coding","ncbi_id":"23232","summary":null,"start":94402504,"end":94535930,"strand":1,"description":"TBC1 domain family member 12 [Source:HGNC Symbol;Acc:HGNC:29082]"}, {"versioned_ensembl_gene_id":"ENSG00000130589.16","gene_symbol":"HELZ2","gene_name":"helicase with zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:30021]","synonyms":"PRIC285,PDIP1,KIAA1769","biotype":"protein_coding","ncbi_id":"85441","summary":"The protein encoded by this gene is a nuclear transcriptional co-activator for peroxisome proliferator activated receptor alpha. The encoded protein contains a zinc finger and is a helicase that appears to be part of the peroxisome proliferator activated receptor alpha interacting complex. This gene is a member of the DNA2/NAM7 helicase gene family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63558086,"end":63574239,"strand":-1,"description":"helicase with zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:30021]"}, {"versioned_ensembl_gene_id":"ENSG00000274315.1","gene_symbol":"AC009318.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29331434,"end":29331936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275476.1","gene_symbol":"AC009318.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29277397,"end":29277882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275278.1","gene_symbol":"AC012150.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29156448,"end":29156991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182261.3","gene_symbol":"NLRP10","gene_name":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]","synonyms":"Pynod,PAN5,NOD8,NALP10,CLR11.1","biotype":"protein_coding","ncbi_id":"338322","summary":"Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). The protein encoded by this gene belongs to the NALP protein family despite lacking the LRR region. This protein likely plays a regulatory role in the innate immune system. The protein belongs to the signal-induced multiprotein complex, the inflammasome, that activates the pro-inflammatory caspases, caspase-1 and caspase-5. Other experiments indicate that this gene acts as a multifunctional negative regulator of inflammation and apoptosis. [provided by RefSeq, Jul 2008]","start":7959424,"end":7965426,"strand":-1,"description":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]"}, {"versioned_ensembl_gene_id":"ENSG00000253261.1","gene_symbol":"AC008410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154993598,"end":154994445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087502.17","gene_symbol":"ERGIC2","gene_name":"ERGIC and golgi 2 [Source:HGNC Symbol;Acc:HGNC:30208]","synonyms":"PTX1,Erv41","biotype":"protein_coding","ncbi_id":"51290","summary":"ERGIC2, or PTX1, is a ubiquitously expressed nuclear protein that is downregulated in prostate carcinoma (Kwok et al., 2001 [PubMed 11445006]).[supplied by OMIM, Aug 2008]","start":29337352,"end":29381189,"strand":-1,"description":"ERGIC and golgi 2 [Source:HGNC Symbol;Acc:HGNC:30208]"}, {"versioned_ensembl_gene_id":"ENSG00000160570.13","gene_symbol":"DEDD2","gene_name":"death effector domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24450]","synonyms":"FLAME-3","biotype":"protein_coding","ncbi_id":"162989","summary":"This gene encodes a nuclear-localized protein containing a death effector domain (DED). The encoded protein may regulate the trafficking of caspases and other proteins into the nucleus during death receptor-induced apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":42198598,"end":42220140,"strand":-1,"description":"death effector domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24450]"}, {"versioned_ensembl_gene_id":"ENSG00000274356.1","gene_symbol":"AL355987.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":136728953,"end":136729855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114455.13","gene_symbol":"HHLA2","gene_name":"HERV-H LTR-associating 2 [Source:HGNC Symbol;Acc:HGNC:4905]","synonyms":"B7y,B7H7,B7-H5","biotype":"protein_coding","ncbi_id":"11148","summary":"This gene encodes a protein ligand found on the surface of monocytes. The encoded protein is thought to regulate cell-mediated immunity by binding to a receptor on T lymphocytes and inhibiting the proliferation of these cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":108296490,"end":108378285,"strand":1,"description":"HERV-H LTR-associating 2 [Source:HGNC Symbol;Acc:HGNC:4905]"}, {"versioned_ensembl_gene_id":"ENSG00000267742.1","gene_symbol":"FAM60CP","gene_name":"family with sequence similarity 60 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728115","summary":null,"start":60016778,"end":60017441,"strand":-1,"description":"family with sequence similarity 60 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31737]"}, {"versioned_ensembl_gene_id":"ENSG00000228330.1","gene_symbol":"AL355355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13142185,"end":13142977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267686.1","gene_symbol":"AC090771.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60125033,"end":60161195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144158.4","gene_symbol":"AL078621.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113657908,"end":113658675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227989.1","gene_symbol":"AC010141.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21555852,"end":21558070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239622.1","gene_symbol":"AC005165.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25689580,"end":25689959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153086.13","gene_symbol":"ACMSD","gene_name":"aminocarboxymuconate semialdehyde decarboxylase [Source:HGNC Symbol;Acc:HGNC:19288]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130013","summary":"The neuronal excitotoxin quinolinate is an intermediate in the de novo synthesis pathway of NAD from tryptophan, and has been implicated in the pathogenesis of several neurodegenerative disorders. Quinolinate is derived from alpha-amino-beta-carboxy-muconate-epsilon-semialdehyde (ACMS). ACMSD (ACMS decarboxylase; EC 4.1.1.45) can divert ACMS to a benign catabolite and thus prevent the accumulation of quinolinate from ACMS.[supplied by OMIM, Oct 2004]","start":134838547,"end":134902034,"strand":1,"description":"aminocarboxymuconate semialdehyde decarboxylase [Source:HGNC Symbol;Acc:HGNC:19288]"}, {"versioned_ensembl_gene_id":"ENSG00000226650.5","gene_symbol":"KIF4B","gene_name":"kinesin family member 4B [Source:HGNC Symbol;Acc:HGNC:6322]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285643","summary":"This gene is an intronless retrocopy of kinesin family member 4A. The protein encoded by this gene is a microtubule-based motor protein that plays vital roles in anaphase spindle dynamics and cytokinesis. [provided by RefSeq, Jul 2016]","start":155013755,"end":155018132,"strand":1,"description":"kinesin family member 4B [Source:HGNC Symbol;Acc:HGNC:6322]"}, {"versioned_ensembl_gene_id":"ENSG00000253646.1","gene_symbol":"AC010476.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155111184,"end":155112324,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023734.10","gene_symbol":"STRAP","gene_name":"serine/threonine kinase receptor associated protein [Source:HGNC Symbol;Acc:HGNC:30796]","synonyms":"UNRIP,pt-wd,MAWD","biotype":"protein_coding","ncbi_id":"11171","summary":null,"start":15882391,"end":15903478,"strand":1,"description":"serine/threonine kinase receptor associated protein [Source:HGNC Symbol;Acc:HGNC:30796]"}, {"versioned_ensembl_gene_id":"ENSG00000101443.17","gene_symbol":"WFDC2","gene_name":"WAP four-disulfide core domain 2 [Source:HGNC Symbol;Acc:HGNC:15939]","synonyms":"WAP5,HE4,EDDM4,dJ461P17.6","biotype":"protein_coding","ncbi_id":"10406","summary":"This gene encodes a protein that is a member of the WFDC domain family. The WFDC domain, or WAP Signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many family members. This gene is expressed in pulmonary epithelial cells, and was also found to be expressed in some ovarian cancers. The encoded protein is a small secretory protein, which may be involved in sperm maturation. [provided by RefSeq, Jul 2008]","start":45469706,"end":45481532,"strand":1,"description":"WAP four-disulfide core domain 2 [Source:HGNC Symbol;Acc:HGNC:15939]"}, {"versioned_ensembl_gene_id":"ENSG00000169184.5","gene_symbol":"MN1","gene_name":"MN1 proto-oncogene, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:7180]","synonyms":"MGCR1-PEN,MGCR1,MGCR","biotype":"protein_coding","ncbi_id":"4330","summary":"Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by RefSeq, Jul 2008]","start":27748277,"end":27801498,"strand":-1,"description":"MN1 proto-oncogene, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:7180]"}, {"versioned_ensembl_gene_id":"ENSG00000282128.1","gene_symbol":"AC207965.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70312831,"end":70374969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234391.1","gene_symbol":"AL606490.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48306769,"end":48309055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244332.1","gene_symbol":"AL138759.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":94577439,"end":94611238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279489.1","gene_symbol":"AL355377.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35001913,"end":35003663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282637.1","gene_symbol":"MAP3K14","gene_name":"mitogen-activated protein kinase kinase kinase 14 [Source:HGNC Symbol;Acc:HGNC:6853]","synonyms":"FTDCR1B,NIK,HSNIK,HS","biotype":"processed_transcript","ncbi_id":"9020","summary":"This gene encodes mitogen-activated protein kinase kinase kinase 14, which is a serine/threonine protein-kinase. This kinase binds to TRAF2 and stimulates NF-kappaB activity. It shares sequence similarity with several other MAPKK kinases. It participates in an NF-kappaB-inducing signalling cascade common to receptors of the tumour-necrosis/nerve-growth factor (TNF/NGF) family and to the interleukin-1 type-I receptor. [provided by RefSeq, Jul 2008]","start":45316960,"end":45317040,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 14 [Source:HGNC Symbol;Acc:HGNC:6853]"}, {"versioned_ensembl_gene_id":"ENSG00000273597.1","gene_symbol":"AL355377.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35001342,"end":35002994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227302.1","gene_symbol":"SSXP9","gene_name":"SSX family pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30645]","synonyms":"psiSSX9","biotype":"unprocessed_pseudogene","ncbi_id":"326586","summary":null,"start":48322349,"end":48326683,"strand":1,"description":"SSX family pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30645]"}, {"versioned_ensembl_gene_id":"ENSG00000119969.14","gene_symbol":"HELLS","gene_name":"helicase, lymphoid specific [Source:HGNC Symbol;Acc:HGNC:4861]","synonyms":"SMARCA6,PASG,Nbla10143,LSH","biotype":"protein_coding","ncbi_id":"3070","summary":"This gene encodes a lymphoid-specific helicase. Other helicases function in processes involving DNA strand separation, including replication, repair, recombination, and transcription. This protein is thought to be involved with cellular proliferation and may play a role in leukemogenesis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2014]","start":94501434,"end":94613905,"strand":1,"description":"helicase, lymphoid specific [Source:HGNC Symbol;Acc:HGNC:4861]"}, {"versioned_ensembl_gene_id":"ENSG00000282563.1","gene_symbol":"AC003070.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45371402,"end":45372057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223831.1","gene_symbol":"AC005006.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30598309,"end":30606687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230100.1","gene_symbol":"AL606490.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48333675,"end":48334439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229986.1","gene_symbol":"AP001042.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38846247,"end":38848644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203498.2","gene_symbol":"AL139390.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6993191,"end":6995554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233496.1","gene_symbol":"SYNJ2-IT1","gene_name":"SYNJ2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41387]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874300","summary":null,"start":158001107,"end":158002383,"strand":1,"description":"SYNJ2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41387]"}, {"versioned_ensembl_gene_id":"ENSG00000235185.1","gene_symbol":"AL031727.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19591802,"end":19596832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179066.7","gene_symbol":"AC020907.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35105969,"end":35107318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227392.1","gene_symbol":"HPN-AS1","gene_name":"HPN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:47041]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128675","summary":null,"start":35059059,"end":35106304,"strand":-1,"description":"HPN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:47041]"}, {"versioned_ensembl_gene_id":"ENSG00000249695.6","gene_symbol":"AC026369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137411,"end":149169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136929.12","gene_symbol":"HEMGN","gene_name":"hemogen [Source:HGNC Symbol;Acc:HGNC:17509]","synonyms":"NDR,EDAG,CT155","biotype":"protein_coding","ncbi_id":"55363","summary":null,"start":97926791,"end":97944856,"strand":-1,"description":"hemogen [Source:HGNC Symbol;Acc:HGNC:17509]"}, {"versioned_ensembl_gene_id":"ENSG00000187922.13","gene_symbol":"LCN10","gene_name":"lipocalin 10 [Source:HGNC Symbol;Acc:HGNC:20892]","synonyms":null,"biotype":"protein_coding","ncbi_id":"414332","summary":"Members of the lipocalin family, such as LCN10, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al., 2004 [PubMed 15363845]).[supplied by OMIM, Aug 2009]","start":136738167,"end":136743356,"strand":-1,"description":"lipocalin 10 [Source:HGNC Symbol;Acc:HGNC:20892]"}, {"versioned_ensembl_gene_id":"ENSG00000229925.1","gene_symbol":"AP001043.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38888772,"end":38903905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270713.1","gene_symbol":"AL132994.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38973399,"end":38974085,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227721.1","gene_symbol":"RPSAP64","gene_name":"ribosomal protein SA pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:39642]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873797","summary":null,"start":38894917,"end":38895252,"strand":1,"description":"ribosomal protein SA pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:39642]"}, {"versioned_ensembl_gene_id":"ENSG00000231454.2","gene_symbol":"AL935212.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61665579,"end":61666386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256694.1","gene_symbol":"AC026369.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":164664,"end":166321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205622.9","gene_symbol":"AP001043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38863676,"end":38956467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256948.1","gene_symbol":"AC026369.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106524,"end":111850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154537.4","gene_symbol":"FAM27C","gene_name":"family with sequence similarity 27 member C [Source:HGNC Symbol;Acc:HGNC:23668]","synonyms":"FAM27A,bA7G23.5,bA374M1.5,FAM27A3,FAM27A1","biotype":"lincRNA","ncbi_id":"100132948","summary":null,"start":61854162,"end":61855331,"strand":1,"description":"family with sequence similarity 27 member C [Source:HGNC Symbol;Acc:HGNC:23668]"}, {"versioned_ensembl_gene_id":"ENSG00000261172.1","gene_symbol":"AC133919.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90110574,"end":90168225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161677.11","gene_symbol":"JOSD2","gene_name":"Josephin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28853]","synonyms":"SBBI54","biotype":"protein_coding","ncbi_id":"126119","summary":"This gene encodes a protein containing a Josephin domain. Josephin domain-containing proteins are deubiquitinating enzymes which catalyze the hydrolysis of the bond between the C-terminal glycine of the ubiquitin peptide and protein substrates. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":50505998,"end":50511353,"strand":-1,"description":"Josephin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28853]"}, {"versioned_ensembl_gene_id":"ENSG00000277624.1","gene_symbol":"AL391987.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61858710,"end":61858908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229823.1","gene_symbol":"CR847794.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31245121,"end":31245594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243304.3","gene_symbol":"AC008494.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115264669,"end":115265464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179978.11","gene_symbol":"AC140134.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70094659,"end":70128434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166589.12","gene_symbol":"CDH16","gene_name":"cadherin 16 [Source:HGNC Symbol;Acc:HGNC:1755]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1014","summary":"This gene is a member of the cadherin superfamily, genes encoding calcium-dependent, membrane-associated glycoproteins. Mapped to a previously identified cluster of cadherin genes on chromosome 16q22.1, the gene localizes with superfamily members CDH1, CDH3, CDH5, CDH8 and CDH11. The protein consists of an extracellular domain containing 6 cadherin domains, a transmembrane region and a truncated cytoplasmic domain but lacks the prosequence and tripeptide HAV adhesion recognition sequence typical of most classical cadherins. Expression is exclusively in kidney, where the protein functions as the principal mediator of homotypic cellular recognition, playing a role in the morphogenic direction of tissue development. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2011]","start":66908122,"end":66918984,"strand":-1,"description":"cadherin 16 [Source:HGNC Symbol;Acc:HGNC:1755]"}, {"versioned_ensembl_gene_id":"ENSG00000213529.3","gene_symbol":"AL359073.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112362714,"end":112363116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254703.2","gene_symbol":"SENCR","gene_name":"smooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:44177]","synonyms":"FLI1-AS1","biotype":"antisense_RNA","ncbi_id":"100507392","summary":null,"start":128691672,"end":128696023,"strand":-1,"description":"smooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:44177]"}, {"versioned_ensembl_gene_id":"ENSG00000204805.8","gene_symbol":"FAM27E4","gene_name":"family with sequence similarity 27 member E4 [Source:HGNC Symbol;Acc:HGNC:44415]","synonyms":"FAM27E4P","biotype":"processed_pseudogene","ncbi_id":"107987001","summary":null,"start":61861995,"end":61862336,"strand":1,"description":"family with sequence similarity 27 member E4 [Source:HGNC Symbol;Acc:HGNC:44415]"}, {"versioned_ensembl_gene_id":"ENSG00000170152.4","gene_symbol":"AL391987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61861853,"end":61862567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276023.4","gene_symbol":"DUSP14","gene_name":"dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:HGNC:17007]","synonyms":"MKP6,MKP-L","biotype":"protein_coding","ncbi_id":"11072","summary":"Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP14 contains the consensus DUSP C-terminal catalytic domain but lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]","start":37489831,"end":37513501,"strand":1,"description":"dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:HGNC:17007]"}, {"versioned_ensembl_gene_id":"ENSG00000258565.1","gene_symbol":"BLZF2P","gene_name":"basic leucine zipper nuclear factor 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:20049]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"317729","summary":null,"start":68867857,"end":68869951,"strand":-1,"description":"basic leucine zipper nuclear factor 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:20049]"}, {"versioned_ensembl_gene_id":"ENSG00000253492.1","gene_symbol":"CDH12P3","gene_name":"cadherin 12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37699]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100093624","summary":null,"start":70132679,"end":70132973,"strand":1,"description":"cadherin 12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37699]"}, {"versioned_ensembl_gene_id":"ENSG00000106302.9","gene_symbol":"HYAL4","gene_name":"hyaluronoglucosaminidase 4 [Source:HGNC Symbol;Acc:HGNC:5323]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23553","summary":"This gene encodes a protein which is similar in structure to hyaluronidases but lacks hyaluronidase activity. The encoded protein acts as a chondroitin-sulfate-specific endo-beta-N-acetylgalactosaminidase; that is, it exhibits hydrolytic activity toward chondroitin sulfate chains and degrades them into oligosaccharides. Proteoglycans are formed by the covalent linkage of chondroitin sulfate chains to protein. Proteoglycans are ubiquitous components of the extracellular matrix of connective tissues and are also found at the surface of many cell types where they participate in a variety of cellular processes such as cell proliferation, differentiation, migration, cell-cell recognition, extracellular matrix deposition, and tissue morphogenesis. The expression of this gene is highest in testes and placenta. [provided by RefSeq, Apr 2019]","start":123828983,"end":123877478,"strand":1,"description":"hyaluronoglucosaminidase 4 [Source:HGNC Symbol;Acc:HGNC:5323]"}, {"versioned_ensembl_gene_id":"ENSG00000235659.1","gene_symbol":"AL391987.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61865755,"end":61866965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272600.1","gene_symbol":"AC007308.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20889206,"end":20891214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230332.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"HZFw1,LIRF","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30148763,"end":30154384,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000236896.1","gene_symbol":"AL354726.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97986551,"end":97987656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254701.3","gene_symbol":"AC138866.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70197255,"end":70207745,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136938.8","gene_symbol":"ANP32B","gene_name":"acidic nuclear phosphoprotein 32 family member B [Source:HGNC Symbol;Acc:HGNC:16677]","synonyms":"SSP29,PHAPI2,APRIL","biotype":"protein_coding","ncbi_id":"10541","summary":null,"start":97983361,"end":98015943,"strand":1,"description":"acidic nuclear phosphoprotein 32 family member B [Source:HGNC Symbol;Acc:HGNC:16677]"}, {"versioned_ensembl_gene_id":"ENSG00000223379.1","gene_symbol":"AL391987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61868727,"end":61887084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253816.3","gene_symbol":"AC138866.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70219918,"end":70258930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135763.9","gene_symbol":"URB2","gene_name":"URB2 ribosome biogenesis 2 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:28967]","synonyms":"KIAA0133,NPA2,NET10","biotype":"protein_coding","ncbi_id":"9816","summary":null,"start":229626234,"end":229660199,"strand":1,"description":"URB2 ribosome biogenesis 2 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:28967]"}, {"versioned_ensembl_gene_id":"ENSG00000228211.2","gene_symbol":"HYALP1","gene_name":"hyaluronoglucosaminidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5324]","synonyms":"HYAL6","biotype":"unitary_pseudogene","ncbi_id":"26062","summary":null,"start":123814139,"end":123829252,"strand":1,"description":"hyaluronoglucosaminidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5324]"}, {"versioned_ensembl_gene_id":"ENSG00000237403.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30145206,"end":30148830,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000224057.1","gene_symbol":"EGFR-AS1","gene_name":"EGFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40207]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507500","summary":null,"start":55179750,"end":55188934,"strand":-1,"description":"EGFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40207]"}, {"versioned_ensembl_gene_id":"ENSG00000242060.1","gene_symbol":"RPS3AP49","gene_name":"ribosomal protein S3a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:36810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400652","summary":null,"start":60149576,"end":60150365,"strand":1,"description":"ribosomal protein S3a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:36810]"}, {"versioned_ensembl_gene_id":"ENSG00000204003.8","gene_symbol":"AL355987.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":136738167,"end":136748453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175509.8","gene_symbol":"AL078621.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113667478,"end":113668621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233479.1","gene_symbol":"AC017074.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113669166,"end":113673191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138231.12","gene_symbol":"DBR1","gene_name":"debranching RNA lariats 1 [Source:HGNC Symbol;Acc:HGNC:15594]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51163","summary":"The protein encoded by this gene is an RNA lariat debranching enzyme that hydrolyzes 2'-5' prime branched phosphodiester bonds. The encoded protein specifically targets the bonds at the branch point of excised lariat intron RNA, converting them to linear molecules that are then degraded. This protein may also be involved in retroviral replication. [provided by RefSeq, Nov 2011]","start":138161012,"end":138174949,"strand":-1,"description":"debranching RNA lariats 1 [Source:HGNC Symbol;Acc:HGNC:15594]"}, {"versioned_ensembl_gene_id":"ENSG00000173250.2","gene_symbol":"GPR151","gene_name":"G protein-coupled receptor 151 [Source:HGNC Symbol;Acc:HGNC:23624]","synonyms":"PGR7,GALR4","biotype":"protein_coding","ncbi_id":"134391","summary":"This gene encodes an orphan member of the class A rhodopsin-like family of G-protein-coupled receptors (GPCRs). Within the rhodopsin-like family, this gene is a member of the SOG subfamily that includes somatostatin, opioid, galanin, and kisspeptin receptors. The orthologous mouse gene has a restricted pattern of neuronal expression which is induced following nerve injury. All GPCRs have a transmembrane domain that includes seven transmembrane alpha-helices. A general feature of GPCR signaling is the agonist-induced conformational change in the receptor, leading to activation of the heterotrimeric G protein. The activated G protein then binds to and activates numerous downstream effector proteins, which generate second messengers that mediate a broad range of cellular and physiological processes. [provided by RefSeq, Jul 2017]","start":146513103,"end":146516190,"strand":-1,"description":"G protein-coupled receptor 151 [Source:HGNC Symbol;Acc:HGNC:23624]"}, {"versioned_ensembl_gene_id":"ENSG00000236930.1","gene_symbol":"AC099782.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45883640,"end":45884113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173585.15","gene_symbol":"CCR9","gene_name":"C-C motif chemokine receptor 9 [Source:HGNC Symbol;Acc:HGNC:1610]","synonyms":"GPR28,GPR-9-6,CDw199","biotype":"protein_coding","ncbi_id":"10803","summary":"The protein encoded by this gene is a G protein-coupled receptor with seven transmembrane domains that belongs to the beta chemokine receptor family. Chemokines and their receptors are key regulators of thymocyte migration and maturation in normal and inflammation conditions. This gene is differentially expressed in T lymphocytes of the small intestine and colon, and its interaction with chemokine 25 contributes to intestinal intra-epithelial lymphocyte homing to the small intestine. This suggests a role for this gene in directing immune responses to different segments of the gastrointestinal tract. This gene and its exclusive ligand, chemokine 25, are overexpressed in a variety of malignant tumors and are closely associated with tumor proliferation, apoptosis, invasion, migration and drug resistance. This gene maps to the chemokine receptor gene cluster. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2020]","start":45886504,"end":45903177,"strand":1,"description":"C-C motif chemokine receptor 9 [Source:HGNC Symbol;Acc:HGNC:1610]"}, {"versioned_ensembl_gene_id":"ENSG00000232722.3","gene_symbol":"MROH4P","gene_name":"maestro heat like repeat family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:44902]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"101154686","summary":null,"start":142567260,"end":142577881,"strand":-1,"description":"maestro heat like repeat family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:44902]"}, {"versioned_ensembl_gene_id":"ENSG00000267206.5","gene_symbol":"LCN6","gene_name":"lipocalin 6 [Source:HGNC Symbol;Acc:HGNC:17337]","synonyms":null,"biotype":"protein_coding","ncbi_id":"158062","summary":null,"start":136744011,"end":136748528,"strand":-1,"description":"lipocalin 6 [Source:HGNC Symbol;Acc:HGNC:17337]"}, {"versioned_ensembl_gene_id":"ENSG00000228100.1","gene_symbol":"LINC01820","gene_name":"long intergenic non-protein coding RNA 1820 [Source:HGNC Symbol;Acc:HGNC:52625]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374582","summary":null,"start":46392297,"end":46394167,"strand":-1,"description":"long intergenic non-protein coding RNA 1820 [Source:HGNC Symbol;Acc:HGNC:52625]"}, {"versioned_ensembl_gene_id":"ENSG00000197785.13","gene_symbol":"ATAD3A","gene_name":"ATPase family, AAA domain containing 3A [Source:HGNC Symbol;Acc:HGNC:25567]","synonyms":"FLJ10709","biotype":"protein_coding","ncbi_id":"55210","summary":"This gene encodes a ubiquitously expressed mitochondrial membrane protein that contributes to mitochondrial dynamics, nucleoid organization, protein translation, cell growth, and cholesterol metabolism. This gene is a member of the ATPase family AAA-domain containing 3 gene family which, in humans, includes two other paralogs. Naturally occurring mutations in this gene are associated with distinct neurological syndromes including Harel-Yoon syndrome. High-level expression of this gene is associated with poor survival in breast cancer patients. A homozygous knockout of the orthologous gene in mice results in embryonic lethality at day 7.5 due to growth retardation and defective development of the trophoblast lineage. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":1512151,"end":1534687,"strand":1,"description":"ATPase family, AAA domain containing 3A [Source:HGNC Symbol;Acc:HGNC:25567]"}, {"versioned_ensembl_gene_id":"ENSG00000107872.12","gene_symbol":"FBXL15","gene_name":"F-box and leucine rich repeat protein 15 [Source:HGNC Symbol;Acc:HGNC:28155]","synonyms":"MGC11279,FBXO37,Fbl15","biotype":"protein_coding","ncbi_id":"79176","summary":null,"start":102419189,"end":102423136,"strand":1,"description":"F-box and leucine rich repeat protein 15 [Source:HGNC Symbol;Acc:HGNC:28155]"}, {"versioned_ensembl_gene_id":"ENSG00000177575.12","gene_symbol":"CD163","gene_name":"CD163 molecule [Source:HGNC Symbol;Acc:HGNC:1631]","synonyms":"SCARI1,MM130,M130","biotype":"protein_coding","ncbi_id":"9332","summary":"The protein encoded by this gene is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, and is exclusively expressed in monocytes and macrophages. It functions as an acute phase-regulated receptor involved in the clearance and endocytosis of hemoglobin/haptoglobin complexes by macrophages, and may thereby protect tissues from free hemoglobin-mediated oxidative damage. This protein may also function as an innate immune sensor for bacteria and inducer of local inflammation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":7470813,"end":7503893,"strand":-1,"description":"CD163 molecule [Source:HGNC Symbol;Acc:HGNC:1631]"}, {"versioned_ensembl_gene_id":"ENSG00000266826.2","gene_symbol":"AC011195.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":58660424,"end":58692018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243188.1","gene_symbol":"HNRNPA1P17","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39135]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421376","summary":null,"start":108325520,"end":108326814,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39135]"}, {"versioned_ensembl_gene_id":"ENSG00000227523.1","gene_symbol":"RPS20P15","gene_name":"ribosomal protein S20 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271085","summary":null,"start":27462506,"end":27462816,"strand":1,"description":"ribosomal protein S20 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36340]"}, {"versioned_ensembl_gene_id":"ENSG00000198326.9","gene_symbol":"TMEM239","gene_name":"transmembrane protein 239 [Source:HGNC Symbol;Acc:HGNC:40044]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288797","summary":null,"start":2816302,"end":2820284,"strand":1,"description":"transmembrane protein 239 [Source:HGNC Symbol;Acc:HGNC:40044]"}, {"versioned_ensembl_gene_id":"ENSG00000203414.2","gene_symbol":"BTBD7P1","gene_name":"BTB domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44875]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441548","summary":null,"start":13156684,"end":13158136,"strand":-1,"description":"BTB domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44875]"}, {"versioned_ensembl_gene_id":"ENSG00000181924.6","gene_symbol":"COA4","gene_name":"cytochrome c oxidase assembly factor 4 homolog [Source:HGNC Symbol;Acc:HGNC:24604]","synonyms":"E2IG2,CMC3,CHCHD8","biotype":"protein_coding","ncbi_id":"51287","summary":null,"start":73872667,"end":73876988,"strand":-1,"description":"cytochrome c oxidase assembly factor 4 homolog [Source:HGNC Symbol;Acc:HGNC:24604]"}, {"versioned_ensembl_gene_id":"ENSG00000263517.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30211301,"end":30211463,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000170881.4","gene_symbol":"RNF139","gene_name":"ring finger protein 139 [Source:HGNC Symbol;Acc:HGNC:17023]","synonyms":"TRC8,RCA1,HRCA1","biotype":"protein_coding","ncbi_id":"11236","summary":"The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP. [provided by RefSeq, Jul 2008]","start":124474738,"end":124487914,"strand":1,"description":"ring finger protein 139 [Source:HGNC Symbol;Acc:HGNC:17023]"}, {"versioned_ensembl_gene_id":"ENSG00000237540.1","gene_symbol":"RPL36AP36","gene_name":"ribosomal protein L36a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644834","summary":null,"start":13159477,"end":13159777,"strand":-1,"description":"ribosomal protein L36a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36326]"}, {"versioned_ensembl_gene_id":"ENSG00000155313.15","gene_symbol":"USP25","gene_name":"ubiquitin specific peptidase 25 [Source:HGNC Symbol;Acc:HGNC:12624]","synonyms":"USP21","biotype":"protein_coding","ncbi_id":"29761","summary":"Ubiquitin (MIM 191339) is a highly conserved 76-amino acid protein involved in regulation of intracellular protein breakdown, cell cycle regulation, and stress response. Ubiquitin is released from degraded proteins by disassembly of the polyubiquitin chains, which is mediated by ubiquitin-specific proteases (USPs), such as USP25 (Valero et al., 1999 [PubMed 10644437]).[supplied by OMIM, Mar 2008]","start":15730025,"end":15880069,"strand":1,"description":"ubiquitin specific peptidase 25 [Source:HGNC Symbol;Acc:HGNC:12624]"}, {"versioned_ensembl_gene_id":"ENSG00000121101.15","gene_symbol":"TEX14","gene_name":"testis expressed 14, intercellular bridge forming factor [Source:HGNC Symbol;Acc:HGNC:11737]","synonyms":"CT113","biotype":"protein_coding","ncbi_id":"56155","summary":"The protein encoded by this gene is necessary for intercellular bridges in germ cells, which are required for spermatogenesis. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2011]","start":58556678,"end":58692055,"strand":-1,"description":"testis expressed 14, intercellular bridge forming factor [Source:HGNC Symbol;Acc:HGNC:11737]"}, {"versioned_ensembl_gene_id":"ENSG00000173480.10","gene_symbol":"ZNF417","gene_name":"zinc finger protein 417 [Source:HGNC Symbol;Acc:HGNC:20646]","synonyms":"MGC34079","biotype":"protein_coding","ncbi_id":"147687","summary":null,"start":57900296,"end":57916610,"strand":-1,"description":"zinc finger protein 417 [Source:HGNC Symbol;Acc:HGNC:20646]"}, {"versioned_ensembl_gene_id":"ENSG00000258713.2","gene_symbol":"C20orf141","gene_name":"chromosome 20 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:16134]","synonyms":"dJ860F19.4","biotype":"protein_coding","ncbi_id":"128653","summary":null,"start":2814987,"end":2815833,"strand":1,"description":"chromosome 20 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:16134]"}, {"versioned_ensembl_gene_id":"ENSG00000273609.1","gene_symbol":"AC005562.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30617680,"end":30617790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223756.6","gene_symbol":"TSSC2","gene_name":"tumor suppressing subtransferable candidate 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:12384]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"650368","summary":null,"start":3380961,"end":3408978,"strand":1,"description":"tumor suppressing subtransferable candidate 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:12384]"}, {"versioned_ensembl_gene_id":"ENSG00000154545.16","gene_symbol":"MAGED4","gene_name":"MAGE family member D4 [Source:HGNC Symbol;Acc:HGNC:23793]","synonyms":"MGC3210,MAGE1,MAGE-E1,KIAA1859","biotype":"protein_coding","ncbi_id":"728239","summary":null,"start":52184823,"end":52192268,"strand":1,"description":"MAGE family member D4 [Source:HGNC Symbol;Acc:HGNC:23793]"}, {"versioned_ensembl_gene_id":"ENSG00000214719.11","gene_symbol":"AC005562.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30576464,"end":30672789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059915.16","gene_symbol":"PSD","gene_name":"pleckstrin and Sec7 domain containing [Source:HGNC Symbol;Acc:HGNC:9507]","synonyms":"EFA6A,EFA6,TYL,PSD1,KIAA2011","biotype":"protein_coding","ncbi_id":"5662","summary":"This gene encodes a Plekstrin homology and SEC7 domains-containing protein that functions as a guanine nucleotide exchange factor. The encoded protein regulates signal transduction by activating ADP-ribosylation factor 6. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":102402617,"end":102421539,"strand":-1,"description":"pleckstrin and Sec7 domain containing [Source:HGNC Symbol;Acc:HGNC:9507]"}, {"versioned_ensembl_gene_id":"ENSG00000273680.1","gene_symbol":"AC009318.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29332733,"end":29333383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000033867.16","gene_symbol":"SLC4A7","gene_name":"solute carrier family 4 member 7 [Source:HGNC Symbol;Acc:HGNC:11033]","synonyms":"SLC4A6,SBC2,NBC3","biotype":"protein_coding","ncbi_id":"9497","summary":"This locus encodes a sodium bicarbonate cotransporter. The encoded transmembrane protein appears to transport sodium and bicarbonate ions in a 1:1 ratio, and is thus considered an electroneutral cotransporter. The encoded protein likely plays a critical role in regulation of intracellular pH involved in visual and auditory sensory transmission. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Apr 2012]","start":27372721,"end":27484420,"strand":-1,"description":"solute carrier family 4 member 7 [Source:HGNC Symbol;Acc:HGNC:11033]"}, {"versioned_ensembl_gene_id":"ENSG00000237211.2","gene_symbol":"SETP4","gene_name":"SET pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642869","summary":null,"start":84755136,"end":84756003,"strand":1,"description":"SET pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42923]"}, {"versioned_ensembl_gene_id":"ENSG00000131697.17","gene_symbol":"NPHP4","gene_name":"nephrocystin 4 [Source:HGNC Symbol;Acc:HGNC:19104]","synonyms":"SLSN4,POC10,KIAA0673","biotype":"protein_coding","ncbi_id":"261734","summary":"This gene encodes a protein involved in renal tubular development and function. This protein interacts with nephrocystin, and belongs to a multifunctional complex that is localized to actin- and microtubule-based structures. Mutations in this gene are associated with nephronophthisis type 4, a renal disease, and with Senior-Loken syndrome type 4, a combination of nephronophthisis and retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":5862811,"end":5992473,"strand":-1,"description":"nephrocystin 4 [Source:HGNC Symbol;Acc:HGNC:19104]"}, {"versioned_ensembl_gene_id":"ENSG00000229896.2","gene_symbol":"AL157373.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12007670,"end":12008856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124831.18","gene_symbol":"LRRFIP1","gene_name":"LRR binding FLII interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:6702]","synonyms":"TRIP,HUFI-1,GCF-2,FLIIAP1,FLAP-1","biotype":"protein_coding","ncbi_id":"9208","summary":null,"start":237627576,"end":237813682,"strand":1,"description":"LRR binding FLII interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:6702]"}, {"versioned_ensembl_gene_id":"ENSG00000241690.3","gene_symbol":"AL035460.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2814968,"end":2818066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270435.1","gene_symbol":"AC068733.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6297189,"end":6298606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198466.11","gene_symbol":"ZNF587","gene_name":"zinc finger protein 587 [Source:HGNC Symbol;Acc:HGNC:30955]","synonyms":"FLJ14710,ZF6,UBF-fl,FLJ20813","biotype":"protein_coding","ncbi_id":"84914","summary":null,"start":57849857,"end":57865112,"strand":1,"description":"zinc finger protein 587 [Source:HGNC Symbol;Acc:HGNC:30955]"}, {"versioned_ensembl_gene_id":"ENSG00000095951.16","gene_symbol":"HIVEP1","gene_name":"human immunodeficiency virus type I enhancer binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4920]","synonyms":"CIRIP,ZNF40A,ZNF40,ZAS1,Schnurri-1,PRDII-BF1,MBP-1,CRYBP1","biotype":"protein_coding","ncbi_id":"3096","summary":"This gene encodes a transcription factor belonging to the ZAS family, members of which are large proteins that contain a ZAS domain - a modular protein structure consisting of a pair of C2H2 zinc fingers with an acidic-rich region and a serine/threonine-rich sequence. These proteins bind specifically to the DNA sequence motif, GGGACTTTCC, found in the enhancer elements of several viral promoters, including human immunodeficiency virus (HIV), and to related sequences found in the enhancer elements of a number of cellular promoters. This protein binds to this sequence motif, suggesting a role in the transcriptional regulation of both viral and cellular genes. [provided by RefSeq, Oct 2011]","start":12008762,"end":12164999,"strand":1,"description":"human immunodeficiency virus type I enhancer binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4920]"}, {"versioned_ensembl_gene_id":"ENSG00000198576.3","gene_symbol":"ARC","gene_name":"activity regulated cytoskeleton associated protein [Source:HGNC Symbol;Acc:HGNC:648]","synonyms":"KIAA0278,Arg3.1","biotype":"protein_coding","ncbi_id":"23237","summary":null,"start":142611044,"end":142614472,"strand":-1,"description":"activity regulated cytoskeleton associated protein [Source:HGNC Symbol;Acc:HGNC:648]"}, {"versioned_ensembl_gene_id":"ENSG00000167470.12","gene_symbol":"MIDN","gene_name":"midnolin [Source:HGNC Symbol;Acc:HGNC:16298]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90007","summary":null,"start":1248553,"end":1259140,"strand":1,"description":"midnolin [Source:HGNC Symbol;Acc:HGNC:16298]"}, {"versioned_ensembl_gene_id":"ENSG00000183607.9","gene_symbol":"GKN2","gene_name":"gastrokine 2 [Source:HGNC Symbol;Acc:HGNC:24588]","synonyms":"GDDR,BRICD1B,blottin,VLTI465,TFIZ1,PRO813","biotype":"protein_coding","ncbi_id":"200504","summary":"The secretory protein encoded by this gene is produced in gastric surface mucous cells, where it can bind trefoil factor family peptide 1 or gastrokine-1. This gene may be a tumor suppressor gene, as its expression is markedly decreased in gastric cancer tissues. The encoded protein interacts with gastrokine-1 and regulates homeostasis of the gastric mucosa. [provided by RefSeq, Dec 2015]","start":68945232,"end":68952970,"strand":-1,"description":"gastrokine 2 [Source:HGNC Symbol;Acc:HGNC:24588]"}, {"versioned_ensembl_gene_id":"ENSG00000227709.4","gene_symbol":"AC091607.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156175852,"end":156176911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227359.1","gene_symbol":"AC017074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113677702,"end":113704078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248568.1","gene_symbol":"KRT8P48","gene_name":"keratin 8 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:48344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100887067","summary":null,"start":146706381,"end":146707600,"strand":-1,"description":"keratin 8 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:48344]"}, {"versioned_ensembl_gene_id":"ENSG00000181588.16","gene_symbol":"MEX3D","gene_name":"mex-3 RNA binding family member D [Source:HGNC Symbol;Acc:HGNC:16734]","synonyms":"OK/SW-cl.4,KIAA2031,Tino,RNF193,RKHD1","biotype":"protein_coding","ncbi_id":"399664","summary":null,"start":1554669,"end":1568058,"strand":-1,"description":"mex-3 RNA binding family member D [Source:HGNC Symbol;Acc:HGNC:16734]"}, {"versioned_ensembl_gene_id":"ENSG00000242370.1","gene_symbol":"KCNAB1-AS1","gene_name":"KCNAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40316]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874084","summary":null,"start":156441157,"end":156446905,"strand":-1,"description":"KCNAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40316]"}, {"versioned_ensembl_gene_id":"ENSG00000264943.1","gene_symbol":"SH3GL1P2","gene_name":"SH3 domain containing GRB2 like 1, endophilin A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10836]","synonyms":"SH3GLP2,CNSA-P2","biotype":"processed_pseudogene","ncbi_id":"6459","summary":null,"start":30624413,"end":30625494,"strand":1,"description":"SH3 domain containing GRB2 like 1, endophilin A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10836]"}, {"versioned_ensembl_gene_id":"ENSG00000250407.1","gene_symbol":"AC008728.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146563226,"end":146617004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178660.6","gene_symbol":"ARMC10P1","gene_name":"armadillo repeat containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389137","summary":null,"start":94506766,"end":94507620,"strand":-1,"description":"armadillo repeat containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43646]"}, {"versioned_ensembl_gene_id":"ENSG00000189398.5","gene_symbol":"OR7E12P","gene_name":"olfactory receptor family 7 subfamily E member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:8383]","synonyms":"OR7E79P,OR7E58P,OR11-3","biotype":"unprocessed_pseudogene","ncbi_id":"10821","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3390780,"end":3391752,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:8383]"}, {"versioned_ensembl_gene_id":"ENSG00000248121.8","gene_symbol":"SMURF2P1","gene_name":"SMAD specific E3 ubiquitin protein ligase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44402]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107133516","summary":null,"start":30600796,"end":30615980,"strand":1,"description":"SMAD specific E3 ubiquitin protein ligase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44402]"}, {"versioned_ensembl_gene_id":"ENSG00000271477.1","gene_symbol":"AC010591.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155397291,"end":155398353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242911.1","gene_symbol":"AC140059.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94935760,"end":94936120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169282.17","gene_symbol":"KCNAB1","gene_name":"potassium voltage-gated channel subfamily A member regulatory beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:6228]","synonyms":"KCNA1B,hKvBeta3,hKvb3,AKR6A3,Kvb1.3","biotype":"protein_coding","ncbi_id":"7881","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member includes distinct isoforms which are encoded by alternatively spliced transcript variants of this gene. Some of these isoforms are beta subunits, which form heteromultimeric complexes with alpha subunits and modulate the activity of the pore-forming alpha subunits. [provided by RefSeq, Apr 2015]","start":156037701,"end":156539138,"strand":1,"description":"potassium voltage-gated channel subfamily A member regulatory beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:6228]"}, {"versioned_ensembl_gene_id":"ENSG00000270442.1","gene_symbol":"AC008725.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155491336,"end":155493598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234629.1","gene_symbol":"WDR82P1","gene_name":"WD repeat domain 82 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32447]","synonyms":"WDR82B,WDR82,SW2,hCG26824","biotype":"processed_pseudogene","ncbi_id":"728505","summary":null,"start":94937086,"end":94938024,"strand":-1,"description":"WD repeat domain 82 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32447]"}, {"versioned_ensembl_gene_id":"ENSG00000156475.18","gene_symbol":"PPP2R2B","gene_name":"protein phosphatase 2 regulatory subunit Bbeta [Source:HGNC Symbol;Acc:HGNC:9305]","synonyms":"SCA12,PR55-BETA,PR52B,B55beta","biotype":"protein_coding","ncbi_id":"5521","summary":"The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a beta isoform of the regulatory subunit B55 subfamily. Defects in this gene cause autosomal dominant spinocerebellar ataxia 12 (SCA12), a disease caused by degeneration of the cerebellum, sometimes involving the brainstem and spinal cord, and in resulting in poor coordination of speech and body movements. Multiple alternatively spliced variants, which encode different isoforms, have been identified for this gene. The 5' UTR of some of these variants includes a CAG trinucleotide repeat sequence (7-28 copies) that can be expanded to 55-78 copies in cases of SCA12. [provided by RefSeq, Jul 2016]","start":146581146,"end":147084784,"strand":-1,"description":"protein phosphatase 2 regulatory subunit Bbeta [Source:HGNC Symbol;Acc:HGNC:9305]"}, {"versioned_ensembl_gene_id":"ENSG00000231268.9","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32247977,"end":32251333,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000231421.7","gene_symbol":"AC011840.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30573471,"end":30577000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246695.7","gene_symbol":"RASSF8-AS1","gene_name":"RASSF8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48637]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506451","summary":null,"start":25939329,"end":25959765,"strand":-1,"description":"RASSF8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48637]"}, {"versioned_ensembl_gene_id":"ENSG00000199282.1","gene_symbol":"SNORA9","gene_name":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]","synonyms":"ACA9,SNORA9A","biotype":"snoRNA","ncbi_id":"677798","summary":null,"start":72586680,"end":72586810,"strand":1,"description":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]"}, {"versioned_ensembl_gene_id":"ENSG00000269304.1","gene_symbol":"FKBP1AP1","gene_name":"FK506 binding protein 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3714]","synonyms":"FKBP1P1","biotype":"processed_pseudogene","ncbi_id":"2282","summary":null,"start":57826461,"end":57826778,"strand":-1,"description":"FK506 binding protein 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3714]"}, {"versioned_ensembl_gene_id":"ENSG00000138433.15","gene_symbol":"CIR1","gene_name":"corepressor interacting with RBPJ, 1 [Source:HGNC Symbol;Acc:HGNC:24217]","synonyms":"CIR","biotype":"protein_coding","ncbi_id":"9541","summary":null,"start":174348022,"end":174395715,"strand":-1,"description":"corepressor interacting with RBPJ, 1 [Source:HGNC Symbol;Acc:HGNC:24217]"}, {"versioned_ensembl_gene_id":"ENSG00000268750.6","gene_symbol":"AC010522.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57819719,"end":57858941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250462.8","gene_symbol":"LRRC37BP1","gene_name":"leucine rich repeat containing 37B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25390]","synonyms":"LRRC37B2,DKFZp667M2411","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"147172","summary":null,"start":30629680,"end":30637466,"strand":1,"description":"leucine rich repeat containing 37B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25390]"}, {"versioned_ensembl_gene_id":"ENSG00000255449.1","gene_symbol":"AP002812.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77866412,"end":77870091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265794.5","gene_symbol":"AC005899.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32324431,"end":32360700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149262.16","gene_symbol":"INTS4","gene_name":"integrator complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:25048]","synonyms":"MST093,MGC16733,INT4","biotype":"protein_coding","ncbi_id":"92105","summary":"INTS4 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":77878720,"end":77994678,"strand":-1,"description":"integrator complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:25048]"}, {"versioned_ensembl_gene_id":"ENSG00000226529.1","gene_symbol":"MTND1P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38728]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499468","summary":null,"start":8371663,"end":8372030,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38728]"}, {"versioned_ensembl_gene_id":"ENSG00000083828.15","gene_symbol":"ZNF586","gene_name":"zinc finger protein 586 [Source:HGNC Symbol;Acc:HGNC:25949]","synonyms":"FLJ20070","biotype":"protein_coding","ncbi_id":"54807","summary":null,"start":57769655,"end":57819939,"strand":1,"description":"zinc finger protein 586 [Source:HGNC Symbol;Acc:HGNC:25949]"}, {"versioned_ensembl_gene_id":"ENSG00000161016.17","gene_symbol":"RPL8","gene_name":"ribosomal protein L8 [Source:HGNC Symbol;Acc:HGNC:10368]","synonyms":"L8","biotype":"protein_coding","ncbi_id":"6132","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L2P family of ribosomal proteins. It is located in the cytoplasm. In rat, the protein associates with the 5.8S rRNA, very likely participates in the binding of aminoacyl-tRNA, and is a constituent of the elongation factor 2-binding site at the ribosomal subunit interface. Alternatively spliced transcript variants encoding the same protein exist. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":144789765,"end":144792587,"strand":-1,"description":"ribosomal protein L8 [Source:HGNC Symbol;Acc:HGNC:10368]"}, {"versioned_ensembl_gene_id":"ENSG00000175575.12","gene_symbol":"PAAF1","gene_name":"proteasomal ATPase associated factor 1 [Source:HGNC Symbol;Acc:HGNC:25687]","synonyms":"WDR71,Rpn14,FLJ11848","biotype":"protein_coding","ncbi_id":"80227","summary":"This gene encodes a WD repeat-containing protein involved in regulation of association of proteasome components. During HIV infection, the encoded protein is thought to promote provirus transcription through recruitment of the 19S regulatory complex. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2012]","start":73876699,"end":73931124,"strand":1,"description":"proteasomal ATPase associated factor 1 [Source:HGNC Symbol;Acc:HGNC:25687]"}, {"versioned_ensembl_gene_id":"ENSG00000282715.1","gene_symbol":"ANKRD20A9P","gene_name":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"284232","summary":null,"start":18816718,"end":18880683,"strand":-1,"description":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]"}, {"versioned_ensembl_gene_id":"ENSG00000265139.1","gene_symbol":"AC005899.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32328441,"end":32329395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125247.15","gene_symbol":"TMTC4","gene_name":"transmembrane and tetratricopeptide repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:25904]","synonyms":"FLJ22153,FLJ14624","biotype":"protein_coding","ncbi_id":"84899","summary":"This gene encodes a transmembrane protein that belongs to family of proteins containing an N-terminal transmembrane domain and a C-terminal tetratricopeptide repeat (TPR) domain. TPR domains mediate protein-protein interactions in various cellular processes, such as synaptic vesicle fusion, protein folding, and protein translocation. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, Apr 2017]","start":100603927,"end":100675093,"strand":-1,"description":"transmembrane and tetratricopeptide repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:25904]"}, {"versioned_ensembl_gene_id":"ENSG00000281804.1","gene_symbol":"AC068446.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21250180,"end":21260147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166492.9","gene_symbol":"FAM86GP","gene_name":"family with sequence similarity 86 member G, pseudogene [Source:HGNC Symbol;Acc:HGNC:42358]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387745","summary":null,"start":3410352,"end":3422496,"strand":-1,"description":"family with sequence similarity 86 member G, pseudogene [Source:HGNC Symbol;Acc:HGNC:42358]"}, {"versioned_ensembl_gene_id":"ENSG00000229547.4","gene_symbol":"UBE2DNL","gene_name":"ubiquitin conjugating enzyme E2 D N-terminal like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:28656]","synonyms":"MGC42638","biotype":"transcribed_processed_pseudogene","ncbi_id":"100131816","summary":null,"start":84934151,"end":84934890,"strand":1,"description":"ubiquitin conjugating enzyme E2 D N-terminal like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:28656]"}, {"versioned_ensembl_gene_id":"ENSG00000143494.15","gene_symbol":"VASH2","gene_name":"vasohibin 2 [Source:HGNC Symbol;Acc:HGNC:25723]","synonyms":"FLJ12505","biotype":"protein_coding","ncbi_id":"79805","summary":null,"start":212950520,"end":212992037,"strand":1,"description":"vasohibin 2 [Source:HGNC Symbol;Acc:HGNC:25723]"}, {"versioned_ensembl_gene_id":"ENSG00000131042.14","gene_symbol":"LILRB2","gene_name":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]","synonyms":"LIR-2,MIR10,ILT4,MIR-10,CD85d,LIR2","biotype":"protein_coding","ncbi_id":"10288","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54273821,"end":54281184,"strand":-1,"description":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]"}, {"versioned_ensembl_gene_id":"ENSG00000143512.12","gene_symbol":"HHIPL2","gene_name":"HHIP like 2 [Source:HGNC Symbol;Acc:HGNC:25842]","synonyms":"KIAA1822L,FLJ13840","biotype":"protein_coding","ncbi_id":"79802","summary":null,"start":222522258,"end":222548103,"strand":-1,"description":"HHIP like 2 [Source:HGNC Symbol;Acc:HGNC:25842]"}, {"versioned_ensembl_gene_id":"ENSG00000229697.2","gene_symbol":"AL391987.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61898805,"end":61911022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237852.1","gene_symbol":"AC119800.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65486406,"end":65494188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269867.1","gene_symbol":"AC010326.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":57867038,"end":57868172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237226.1","gene_symbol":"AC127526.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3549745,"end":3550519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270804.1","gene_symbol":"AC010326.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":57867885,"end":57868834,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234743.1","gene_symbol":"EIF5AP4","gene_name":"eukaryotic translation initiation factor 5A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31442]","synonyms":"EIF5AL3","biotype":"processed_pseudogene","ncbi_id":"642592","summary":null,"start":80247219,"end":80247683,"strand":-1,"description":"eukaryotic translation initiation factor 5A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31442]"}, {"versioned_ensembl_gene_id":"ENSG00000123094.15","gene_symbol":"RASSF8","gene_name":"Ras association domain family member 8 [Source:HGNC Symbol;Acc:HGNC:13232]","synonyms":"HoJ-1,C12orf2","biotype":"protein_coding","ncbi_id":"11228","summary":"This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":25959029,"end":26079892,"strand":1,"description":"Ras association domain family member 8 [Source:HGNC Symbol;Acc:HGNC:13232]"}, {"versioned_ensembl_gene_id":"ENSG00000284639.1","gene_symbol":"AP006294.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3580927,"end":3581135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234850.1","gene_symbol":"MTND2P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38727]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499457","summary":null,"start":8372241,"end":8372710,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38727]"}, {"versioned_ensembl_gene_id":"ENSG00000284605.1","gene_symbol":"AC127526.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3429758,"end":3500621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078401.6","gene_symbol":"EDN1","gene_name":"endothelin 1 [Source:HGNC Symbol;Acc:HGNC:3176]","synonyms":"ET1","biotype":"protein_coding","ncbi_id":"1906","summary":"This gene encodes a preproprotein that is proteolytically processed to generate a secreted peptide that belongs to the endothelin/sarafotoxin family. This peptide is a potent vasoconstrictor and its cognate receptors are therapeutic targets in the treatment of pulmonary arterial hypertension. Aberrant expression of this gene may promote tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":12290363,"end":12297194,"strand":1,"description":"endothelin 1 [Source:HGNC Symbol;Acc:HGNC:3176]"}, {"versioned_ensembl_gene_id":"ENSG00000178935.5","gene_symbol":"ZNF552","gene_name":"zinc finger protein 552 [Source:HGNC Symbol;Acc:HGNC:26135]","synonyms":"FLJ21603","biotype":"protein_coding","ncbi_id":"79818","summary":null,"start":57803841,"end":57814913,"strand":-1,"description":"zinc finger protein 552 [Source:HGNC Symbol;Acc:HGNC:26135]"}, {"versioned_ensembl_gene_id":"ENSG00000223688.2","gene_symbol":"AC127526.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3559657,"end":3560022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255367.3","gene_symbol":"AC127526.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":3481520,"end":3581211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224570.1","gene_symbol":"AC097063.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65576129,"end":65578380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213118.4","gene_symbol":"CHCHD2P4","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874507","summary":null,"start":134393142,"end":134393900,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39588]"}, {"versioned_ensembl_gene_id":"ENSG00000222300.1","gene_symbol":"RNU2-21P","gene_name":"RNA, U2 small nuclear 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:48514]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480206","summary":null,"start":158935798,"end":158935985,"strand":-1,"description":"RNA, U2 small nuclear 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:48514]"}, {"versioned_ensembl_gene_id":"ENSG00000207569.2","gene_symbol":"MIR433","gene_name":"microRNA 433 [Source:HGNC Symbol;Acc:HGNC:32026]","synonyms":"MIRN433,hsa-mir-433","biotype":"miRNA","ncbi_id":"574034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100881886,"end":100881978,"strand":1,"description":"microRNA 433 [Source:HGNC Symbol;Acc:HGNC:32026]"}, {"versioned_ensembl_gene_id":"ENSG00000264966.1","gene_symbol":"MIR5094","gene_name":"microRNA 5094 [Source:HGNC Symbol;Acc:HGNC:43519]","synonyms":"hsa-mir-5094","biotype":"miRNA","ncbi_id":"100847059","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89850637,"end":89850721,"strand":-1,"description":"microRNA 5094 [Source:HGNC Symbol;Acc:HGNC:43519]"}, {"versioned_ensembl_gene_id":"ENSG00000274941.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000224614.1","gene_symbol":"TNK2-AS1","gene_name":"TNK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49093]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128262","summary":null,"start":195908076,"end":195911257,"strand":1,"description":"TNK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49093]"}, {"versioned_ensembl_gene_id":"ENSG00000206150.3","gene_symbol":"RNASE13","gene_name":"ribonuclease A family member 13 (inactive) [Source:HGNC Symbol;Acc:HGNC:25285]","synonyms":"RAL1","biotype":"protein_coding","ncbi_id":"440163","summary":null,"start":21032820,"end":21034785,"strand":-1,"description":"ribonuclease A family member 13 (inactive) [Source:HGNC Symbol;Acc:HGNC:25285]"}, {"versioned_ensembl_gene_id":"ENSG00000173621.8","gene_symbol":"LRFN4","gene_name":"leucine rich repeat and fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28456]","synonyms":"SALM3.,MGC3103,FIGLER6","biotype":"protein_coding","ncbi_id":"78999","summary":null,"start":66856647,"end":66860475,"strand":1,"description":"leucine rich repeat and fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28456]"}, {"versioned_ensembl_gene_id":"ENSG00000266736.1","gene_symbol":"GTF2IP6","gene_name":"general transcription factor IIi pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51718]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927390","summary":null,"start":27019527,"end":27047934,"strand":-1,"description":"general transcription factor IIi pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51718]"}, {"versioned_ensembl_gene_id":"ENSG00000141854.9","gene_symbol":"MISP3","gene_name":"MISP family member 3 [Source:HGNC Symbol;Acc:HGNC:26963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113230","summary":null,"start":14072536,"end":14075062,"strand":1,"description":"MISP family member 3 [Source:HGNC Symbol;Acc:HGNC:26963]"}, {"versioned_ensembl_gene_id":"ENSG00000169683.7","gene_symbol":"LRRC45","gene_name":"leucine rich repeat containing 45 [Source:HGNC Symbol;Acc:HGNC:28302]","synonyms":"MGC20806","biotype":"protein_coding","ncbi_id":"201255","summary":null,"start":82023302,"end":82031151,"strand":1,"description":"leucine rich repeat containing 45 [Source:HGNC Symbol;Acc:HGNC:28302]"}, {"versioned_ensembl_gene_id":"ENSG00000235296.1","gene_symbol":"AC145207.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81941869,"end":81947601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263585.1","gene_symbol":"AC145207.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81932398,"end":81933058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267670.1","gene_symbol":"AC022098.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14030855,"end":14031557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274226.5","gene_symbol":"TBC1D3H","gene_name":"TBC1 domain family member 3H [Source:HGNC Symbol;Acc:HGNC:30708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729877","summary":null,"start":36377531,"end":36388423,"strand":-1,"description":"TBC1 domain family member 3H [Source:HGNC Symbol;Acc:HGNC:30708]"}, {"versioned_ensembl_gene_id":"ENSG00000234384.1","gene_symbol":"LINC01049","gene_name":"long intergenic non-protein coding RNA 1049 [Source:HGNC Symbol;Acc:HGNC:49043]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927224","summary":null,"start":90493287,"end":90535080,"strand":1,"description":"long intergenic non-protein coding RNA 1049 [Source:HGNC Symbol;Acc:HGNC:49043]"}, {"versioned_ensembl_gene_id":"ENSG00000133706.17","gene_symbol":"LARS","gene_name":"leucyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6512]","synonyms":"RNTLS,LEUS,LARS1,HSPC192,FLJ21788,FLJ10595","biotype":"protein_coding","ncbi_id":"51520","summary":"This gene encodes a cytosolic leucine-tRNA synthetase, a member of the class I aminoacyl-tRNA synthetase family. The encoded enzyme catalyzes the ATP-dependent ligation of L-leucine to tRNA(Leu). It is found in the cytoplasm as part of a multisynthetase complex and interacts with the arginine tRNA synthetase through its C-terminal domain. A mutation in this gene was found in affected individuals with infantile liver failure syndrome 1. Alternatively spliced transcript variants of this gene have been observed. [provided by RefSeq, Dec 2015]","start":146113038,"end":146182660,"strand":-1,"description":"leucyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6512]"}, {"versioned_ensembl_gene_id":"ENSG00000258672.1","gene_symbol":"AL160313.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99691445,"end":99693648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270294.1","gene_symbol":"XIAPP1","gene_name":"X-linked inhibitor of apoptosis pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996851","summary":null,"start":109680442,"end":109681041,"strand":1,"description":"X-linked inhibitor of apoptosis pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52375]"}, {"versioned_ensembl_gene_id":"ENSG00000268681.1","gene_symbol":"COX6CP7","gene_name":"cytochrome c oxidase subunit 6C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49359]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480265","summary":null,"start":49502432,"end":49502639,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49359]"}, {"versioned_ensembl_gene_id":"ENSG00000229775.6","gene_symbol":"AL353148.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106140264,"end":106188722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198561.13","gene_symbol":"CTNND1","gene_name":"catenin delta 1 [Source:HGNC Symbol;Acc:HGNC:2515]","synonyms":"p120ctn,p120cas,p120,KIAA0384,CTNND","biotype":"protein_coding","ncbi_id":"1500","summary":"This gene encodes a member of the Armadillo protein family, which function in adhesion between cells and signal transduction. Multiple translation initiation codons and alternative splicing result in many different isoforms being translated. Not all of the full-length natures of the described transcript variants have been determined. Read-through transcription also exists between this gene and the neighboring upstream thioredoxin-related transmembrane protein 2 (TMX2) gene. [provided by RefSeq, Dec 2010]","start":57753243,"end":57819546,"strand":1,"description":"catenin delta 1 [Source:HGNC Symbol;Acc:HGNC:2515]"}, {"versioned_ensembl_gene_id":"ENSG00000250747.1","gene_symbol":"AC116345.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73152416,"end":73152938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226387.2","gene_symbol":"SORCS3-AS1","gene_name":"SORCS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45244]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505890","summary":null,"start":104664608,"end":104666200,"strand":-1,"description":"SORCS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45244]"}, {"versioned_ensembl_gene_id":"ENSG00000280070.1","gene_symbol":"AL049833.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96992864,"end":96996601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213128.3","gene_symbol":"AC109327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80542203,"end":80542605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262979.1","gene_symbol":"AC124319.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":80315651,"end":80316633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225748.9","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"BAT2,G2,D6S51E","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31697009,"end":31714058,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000181045.14","gene_symbol":"SLC26A11","gene_name":"solute carrier family 26 member 11 [Source:HGNC Symbol;Acc:HGNC:14471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284129","summary":"This gene encodes a member of the solute linked carrier 26 family of anion exchangers. Members of this family of proteins are essential for numerous cellular functions including homeostasis and intracellular electrolyte balance. The encoded protein is a sodium independent sulfate transporter that is sensitive to the anion exchanger inhibitor 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":80219699,"end":80253500,"strand":1,"description":"solute carrier family 26 member 11 [Source:HGNC Symbol;Acc:HGNC:14471]"}, {"versioned_ensembl_gene_id":"ENSG00000168676.10","gene_symbol":"KCTD19","gene_name":"potassium channel tetramerization domain containing 19 [Source:HGNC Symbol;Acc:HGNC:24753]","synonyms":"FLJ40162","biotype":"protein_coding","ncbi_id":"146212","summary":null,"start":67289428,"end":67326763,"strand":-1,"description":"potassium channel tetramerization domain containing 19 [Source:HGNC Symbol;Acc:HGNC:24753]"}, {"versioned_ensembl_gene_id":"ENSG00000141519.14","gene_symbol":"CCDC40","gene_name":"coiled-coil domain containing 40 [Source:HGNC Symbol;Acc:HGNC:26090]","synonyms":"CILD15,KIAA1640,FLJ32021,FLJ20753,FAP172","biotype":"protein_coding","ncbi_id":"55036","summary":"This gene encodes a protein that is necessary for motile cilia function. It functions in correct left-right axis formation by regulating the assembly of the inner dynein arm and the dynein regulatory complexes, which control ciliary beat. Mutations in this gene cause ciliary dyskinesia type 15, a disorder due to defects in cilia motility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":80036632,"end":80100613,"strand":1,"description":"coiled-coil domain containing 40 [Source:HGNC Symbol;Acc:HGNC:26090]"}, {"versioned_ensembl_gene_id":"ENSG00000163485.16","gene_symbol":"ADORA1","gene_name":"adenosine A1 receptor [Source:HGNC Symbol;Acc:HGNC:262]","synonyms":"RDC7","biotype":"protein_coding","ncbi_id":"134","summary":"The protein encoded by this gene is an adenosine receptor that belongs to the G-protein coupled receptor 1 family. There are 3 types of adenosine receptors, each with a specific pattern of ligand binding and tissue distribution, and together they regulate a diverse set of physiologic functions. The type A1 receptors inhibit adenylyl cyclase, and play a role in the fertilization process. Animal studies also suggest a role for A1 receptors in kidney function and ethanol intoxication. Transcript variants with alternative splicing in the 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]","start":203090654,"end":203167405,"strand":1,"description":"adenosine A1 receptor [Source:HGNC Symbol;Acc:HGNC:262]"}, {"versioned_ensembl_gene_id":"ENSG00000224671.2","gene_symbol":"AC105940.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203144694,"end":203152579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234775.1","gene_symbol":"AC105940.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203127259,"end":203127954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262172.1","gene_symbol":"AC116025.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79991944,"end":79992841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088038.17","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54137728,"end":54155681,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000223745.7","gene_symbol":"CCDC18-AS1","gene_name":"CCDC18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52262]","synonyms":"ENST00000440778.1","biotype":"processed_transcript","ncbi_id":"100131564","summary":null,"start":93262186,"end":93346025,"strand":-1,"description":"CCDC18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52262]"}, {"versioned_ensembl_gene_id":"ENSG00000206513.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555518,"end":29559832,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000278822.1","gene_symbol":"WT1-AS_1","gene_name":"WT1 antisense RNA conserved region 1 [Source:RFAM;Acc:RF02203]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32435738,"end":32435846,"strand":1,"description":"WT1 antisense RNA conserved region 1 [Source:RFAM;Acc:RF02203]"}, {"versioned_ensembl_gene_id":"ENSG00000136811.16","gene_symbol":"ODF2","gene_name":"outer dense fiber of sperm tails 2 [Source:HGNC Symbol;Acc:HGNC:8114]","synonyms":"ODF84,CT134","biotype":"protein_coding","ncbi_id":"4957","summary":"The outer dense fibers are cytoskeletal structures that surround the axoneme in the middle piece and principal piece of the sperm tail. The fibers function in maintaining the elastic structure and recoil of the sperm tail as well as in protecting the tail from shear forces during epididymal transport and ejaculation. Defects in the outer dense fibers lead to abnormal sperm morphology and infertility. This gene encodes one of the major outer dense fiber proteins. Alternative splicing results in multiple transcript variants. The longer transcripts, also known as 'Cenexins', encode proteins with a C-terminal extension that are differentially targeted to somatic centrioles and thought to be crucial for the formation of microtubule organizing centers. [provided by RefSeq, Oct 2010]","start":128455186,"end":128501292,"strand":1,"description":"outer dense fiber of sperm tails 2 [Source:HGNC Symbol;Acc:HGNC:8114]"}, {"versioned_ensembl_gene_id":"ENSG00000113578.17","gene_symbol":"FGF1","gene_name":"fibroblast growth factor 1 [Source:HGNC Symbol;Acc:HGNC:3665]","synonyms":"FGF-alpha,ECGFB,ECGFA,ECGF-beta,ECGF,AFGF,HBGF1,GLIO703,FGFA","biotype":"protein_coding","ncbi_id":"2246","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein functions as a modifier of endothelial cell migration and proliferation, as well as an angiogenic factor. It acts as a mitogen for a variety of mesoderm- and neuroectoderm-derived cells in vitro, thus is thought to be involved in organogenesis. Multiple alternatively spliced variants encoding different isoforms have been described. [provided by RefSeq, Jan 2009]","start":142592178,"end":142698070,"strand":-1,"description":"fibroblast growth factor 1 [Source:HGNC Symbol;Acc:HGNC:3665]"}, {"versioned_ensembl_gene_id":"ENSG00000233330.1","gene_symbol":"AL078581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149591755,"end":149592663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231804.1","gene_symbol":"AL353748.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88484852,"end":88485325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232170.5","gene_symbol":"LINC00708","gene_name":"long intergenic non-protein coding RNA 708 [Source:HGNC Symbol;Acc:HGNC:44694]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507143","summary":null,"start":8259331,"end":8268305,"strand":-1,"description":"long intergenic non-protein coding RNA 708 [Source:HGNC Symbol;Acc:HGNC:44694]"}, {"versioned_ensembl_gene_id":"ENSG00000131013.3","gene_symbol":"PPIL4","gene_name":"peptidylprolyl isomerase like 4 [Source:HGNC Symbol;Acc:HGNC:15702]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85313","summary":"This gene is a member of the cyclophilin family of peptidylprolyl isomerases. The cyclophilins are a highly conserved family, members of which play an important role in protein folding, immunosuppression by cyclosporin A, and infection of HIV-1 virions. [provided by RefSeq, Jul 2008]","start":149504733,"end":149546038,"strand":-1,"description":"peptidylprolyl isomerase like 4 [Source:HGNC Symbol;Acc:HGNC:15702]"}, {"versioned_ensembl_gene_id":"ENSG00000255292.7","gene_symbol":"SDHD","gene_name":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]","synonyms":"PGL,cybS,PGL1","biotype":"protein_coding","ncbi_id":"6392","summary":"This gene encodes a member of complex II of the respiratory chain, which is responsible for the oxidation of succinate. The encoded protein is one of two integral membrane proteins anchoring the complex to the matrix side of the mitochondrial inner membrane. Mutations in this gene are associated with the formation of tumors, including hereditary paraganglioma. Transmission of disease occurs almost exclusively through the paternal allele, suggesting that this locus may be maternally imprinted. There are pseudogenes for this gene on chromosomes 1, 2, 3, 7, and 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]","start":112086824,"end":112193805,"strand":1,"description":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]"}, {"versioned_ensembl_gene_id":"ENSG00000220749.4","gene_symbol":"RPL21P28","gene_name":"ribosomal protein L21 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36258]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131205","summary":null,"start":212051524,"end":212052006,"strand":-1,"description":"ribosomal protein L21 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36258]"}, {"versioned_ensembl_gene_id":"ENSG00000267601.1","gene_symbol":"AC022966.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78855478,"end":78855844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267491.1","gene_symbol":"AC100788.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78903263,"end":78905024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108561.8","gene_symbol":"C1QBP","gene_name":"complement C1q binding protein [Source:HGNC Symbol;Acc:HGNC:1243]","synonyms":"SF2p32,p32,HABP1,gC1qR,gC1Q-R","biotype":"protein_coding","ncbi_id":"708","summary":"The human complement subcomponent C1q associates with C1r and C1s in order to yield the first component of the serum complement system. The protein encoded by this gene is known to bind to the globular heads of C1q molecules and inhibit C1 activation. This protein has also been identified as the p32 subunit of pre-mRNA splicing factor SF2, as well as a hyaluronic acid-binding protein. [provided by RefSeq, Jul 2008]","start":5432777,"end":5448830,"strand":-1,"description":"complement C1q binding protein [Source:HGNC Symbol;Acc:HGNC:1243]"}, {"versioned_ensembl_gene_id":"ENSG00000150768.15","gene_symbol":"DLAT","gene_name":"dihydrolipoamide S-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2896]","synonyms":"PDC-E2,DLTA","biotype":"protein_coding","ncbi_id":"1737","summary":"This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvate and transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and early childhood.[provided by RefSeq, Oct 2009]","start":112024814,"end":112064390,"strand":1,"description":"dihydrolipoamide S-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2896]"}, {"versioned_ensembl_gene_id":"ENSG00000253146.1","gene_symbol":"CIR1P1","gene_name":"corepressor interacting with RBPJ, 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131740","summary":null,"start":154559308,"end":154560440,"strand":-1,"description":"corepressor interacting with RBPJ, 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44011]"}, {"versioned_ensembl_gene_id":"ENSG00000113555.5","gene_symbol":"PCDH12","gene_name":"protocadherin 12 [Source:HGNC Symbol;Acc:HGNC:8657]","synonyms":"VE-cadherin-2","biotype":"protein_coding","ncbi_id":"51294","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 6 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene localizes to the region on chromosome 5 where the protocadherin gene clusters reside. The exon organization of this transcript is similar to that of the gene cluster transcripts, notably the first large exon, but no significant sequence homology exists. The function of this cellular adhesion protein is undetermined but mouse protocadherin 12 does not bind catenins and appears to have no affect on cell migration or growth. [provided by RefSeq, Jul 2008]","start":141943585,"end":141969741,"strand":-1,"description":"protocadherin 12 [Source:HGNC Symbol;Acc:HGNC:8657]"}, {"versioned_ensembl_gene_id":"ENSG00000270547.5","gene_symbol":"LINC01235","gene_name":"long intergenic non-protein coding RNA 1235 [Source:HGNC Symbol;Acc:HGNC:49769]","synonyms":"FLJ41200","biotype":"lincRNA","ncbi_id":"401492","summary":null,"start":13406380,"end":13433053,"strand":-1,"description":"long intergenic non-protein coding RNA 1235 [Source:HGNC Symbol;Acc:HGNC:49769]"}, {"versioned_ensembl_gene_id":"ENSG00000206519.3","gene_symbol":"BX000688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582427,"end":29582944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182704.7","gene_symbol":"TSKU","gene_name":"tsukushi, small leucine rich proteoglycan [Source:HGNC Symbol;Acc:HGNC:28850]","synonyms":"TSK,LRRC54,E2IG4","biotype":"protein_coding","ncbi_id":"25987","summary":null,"start":76782251,"end":76798154,"strand":1,"description":"tsukushi, small leucine rich proteoglycan [Source:HGNC Symbol;Acc:HGNC:28850]"}, {"versioned_ensembl_gene_id":"ENSG00000108669.16","gene_symbol":"CYTH1","gene_name":"cytohesin 1 [Source:HGNC Symbol;Acc:HGNC:9501]","synonyms":"PSCD1,D17S811E,cytohesin-1,B2-1","biotype":"protein_coding","ncbi_id":"9267","summary":"The protein encoded by this gene is a member of the PSCD family. Members of this family have identical structural organization that consists of an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein activity, and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes. Members of this family appear to mediate the regulation of protein sorting and membrane trafficking. This gene is highly expressed in natural killer and peripheral T cells, and regulates the adhesiveness of integrins at the plasma membrane of lymphocytes. A pseudogene of this gene has been defined on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":78674048,"end":78782297,"strand":-1,"description":"cytohesin 1 [Source:HGNC Symbol;Acc:HGNC:9501]"}, {"versioned_ensembl_gene_id":"ENSG00000279154.1","gene_symbol":"AL353726.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88177695,"end":88178578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101353.14","gene_symbol":"MROH8","gene_name":"maestro heat like repeat family member 8 [Source:HGNC Symbol;Acc:HGNC:16125]","synonyms":"dJ621N11.3,C20orf132,C20orf131,dJ621N11.4","biotype":"protein_coding","ncbi_id":"140699","summary":"The protein encoded by this gene belongs to the maestro heat-like repeat family. The exact function of this gene is not known, however, in a genome-wide association study using hippocampal atrophy as a quantitative trait, this gene has been associated with Alzheimer's disease (PMID:19668339). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":37101226,"end":37179588,"strand":-1,"description":"maestro heat like repeat family member 8 [Source:HGNC Symbol;Acc:HGNC:16125]"}, {"versioned_ensembl_gene_id":"ENSG00000230716.3","gene_symbol":"KRT8P7","gene_name":"keratin 8 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729131","summary":null,"start":119602875,"end":119604306,"strand":-1,"description":"keratin 8 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33361]"}, {"versioned_ensembl_gene_id":"ENSG00000099338.22","gene_symbol":"CATSPERG","gene_name":"cation channel sperm associated auxiliary subunit gamma [Source:HGNC Symbol;Acc:HGNC:25243]","synonyms":"FLJ46353,DKFZp434A1022,C19orf15","biotype":"protein_coding","ncbi_id":"57828","summary":"CATSPERG is a subunit of the CATSPER (see CATSPER1; MIM 606389) sperm calcium channel, which is required for sperm hyperactivated motility and male fertility (Wang et al., 2009 [PubMed 19516020]).[supplied by OMIM, Jul 2010]","start":38335775,"end":38370943,"strand":1,"description":"cation channel sperm associated auxiliary subunit gamma [Source:HGNC Symbol;Acc:HGNC:25243]"}, {"versioned_ensembl_gene_id":"ENSG00000187775.16","gene_symbol":"DNAH17","gene_name":"dynein axonemal heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]","synonyms":"FLJ40457,DNEL2,DNAHL1","biotype":"protein_coding","ncbi_id":"8632","summary":"Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. DNAH17 is a heavy chain associated with axonemal dynein (Milisav and Affara, 1998 [PubMed 9545504]).[supplied by OMIM, Mar 2008]","start":78423697,"end":78577394,"strand":-1,"description":"dynein axonemal heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]"}, {"versioned_ensembl_gene_id":"ENSG00000267166.5","gene_symbol":"AC007993.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43922775,"end":43927388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236146.2","gene_symbol":"AL353803.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129380136,"end":129380470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224307.1","gene_symbol":"AL161785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129282458,"end":129285728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204529.4","gene_symbol":"GUCY2EP","gene_name":"guanylate cyclase 2E, pseudogene [Source:HGNC Symbol;Acc:HGNC:4690]","synonyms":"GUCY2E,GC-E","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390226","summary":"This olfactory specific guanylyl cyclase is part of the mammalian olfactory system and and encodes a protein involved in chemosensation in rodents. The gene has become inactivated to become a pseudogene is humans and most primates. [provided by RefSeq, Oct 2008]","start":76694041,"end":76719801,"strand":-1,"description":"guanylate cyclase 2E, pseudogene [Source:HGNC Symbol;Acc:HGNC:4690]"}, {"versioned_ensembl_gene_id":"ENSG00000075388.3","gene_symbol":"FGF4","gene_name":"fibroblast growth factor 4 [Source:HGNC Symbol;Acc:HGNC:3682]","synonyms":"KFGF,K-FGF,HSTF1,HST-1,HST,HBGF-4","biotype":"protein_coding","ncbi_id":"2249","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its oncogenic transforming activity. This gene and FGF3, another oncogenic growth factor, are located closely on chromosome 11. Co-amplification of both genes was found in various kinds of human tumors. Studies on the mouse homolog suggested a function in bone morphogenesis and limb development through the sonic hedgehog (SHH) signaling pathway. [provided by RefSeq, Jul 2008]","start":69771016,"end":69775403,"strand":-1,"description":"fibroblast growth factor 4 [Source:HGNC Symbol;Acc:HGNC:3682]"}, {"versioned_ensembl_gene_id":"ENSG00000217824.1","gene_symbol":"SNRPEP6","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43571]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874414","summary":null,"start":148567378,"end":148567654,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43571]"}, {"versioned_ensembl_gene_id":"ENSG00000268707.1","gene_symbol":"AL158151.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129170434,"end":129170940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188483.7","gene_symbol":"IER5L","gene_name":"immediate early response 5 like [Source:HGNC Symbol;Acc:HGNC:23679]","synonyms":"bA247A12.2","biotype":"protein_coding","ncbi_id":"389792","summary":null,"start":129175552,"end":129178262,"strand":-1,"description":"immediate early response 5 like [Source:HGNC Symbol;Acc:HGNC:23679]"}, {"versioned_ensembl_gene_id":"ENSG00000277797.1","gene_symbol":"AL359693.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81551686,"end":81554092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258703.1","gene_symbol":"AL161757.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56759379,"end":56765757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143774.16","gene_symbol":"GUK1","gene_name":"guanylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:4693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2987","summary":"The protein encoded by this gene is an enzyme that catalyzes the transfer of a phosphate group from ATP to guanosine monophosphate (GMP) to form guanosine diphosphate (GDP). The encoded protein is thought to be a good target for cancer chemotherapy. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":228139962,"end":228148984,"strand":1,"description":"guanylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:4693]"}, {"versioned_ensembl_gene_id":"ENSG00000250194.1","gene_symbol":"AC109458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125074665,"end":125074980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249365.1","gene_symbol":"AC110009.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125108204,"end":125149929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253310.1","gene_symbol":"IGHVIII-76-1","gene_name":"immunoglobulin heavy variable (III)-76-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5708]","synonyms":"IGHV(III)-76-1","biotype":"IG_V_pseudogene","ncbi_id":"28339","summary":null,"start":106831767,"end":106832052,"strand":-1,"description":"immunoglobulin heavy variable (III)-76-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5708]"}, {"versioned_ensembl_gene_id":"ENSG00000260066.1","gene_symbol":"AC112176.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1725149,"end":1728172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167874.6","gene_symbol":"TMEM88","gene_name":"transmembrane protein 88 [Source:HGNC Symbol;Acc:HGNC:32371]","synonyms":"MGC71744,FLJ20025","biotype":"protein_coding","ncbi_id":"92162","summary":null,"start":7855065,"end":7856099,"strand":1,"description":"transmembrane protein 88 [Source:HGNC Symbol;Acc:HGNC:32371]"}, {"versioned_ensembl_gene_id":"ENSG00000118495.18","gene_symbol":"PLAGL1","gene_name":"PLAG1 like zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:9046]","synonyms":"ZAC,LOT1","biotype":"protein_coding","ncbi_id":"5325","summary":"This gene encodes a C2H2 zinc finger protein that functions as a suppressor of cell growth. This gene is often deleted or methylated and silenced in cancer cells. In addition, overexpression of this gene during fetal development is thought to be the causal factor for transient neonatal diabetes mellitus (TNDM). Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding two different protein isoforms. The P1 downstream promoter of this gene is imprinted, with preferential expression from the paternal allele in many tissues. [provided by RefSeq, Nov 2015]","start":143940300,"end":144064599,"strand":-1,"description":"PLAG1 like zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:9046]"}, {"versioned_ensembl_gene_id":"ENSG00000265168.1","gene_symbol":"AC005726.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28573117,"end":28574243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211456.10","gene_symbol":"SACM1L","gene_name":"SAC1 like phosphatidylinositide phosphatase [Source:HGNC Symbol;Acc:HGNC:17059]","synonyms":"SAC1,KIAA0851","biotype":"protein_coding","ncbi_id":"22908","summary":"This gene encodes an integral membrane protein, which is localized to the endoplasmic reticulum, and functions as a phosphoinositide phosphatase that hydrolyzes phosphatidylinositol 3-phosphate, phosphatidylinositol 4-phosphate, and phosphatidylinositol 3,5-bisphosphate. Deletion of this gene in mouse results in preimplantation lethality. Other studies suggest that this gene is also involved in the organization of golgi membranes and mitotic spindles. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame, downstream translation termination codon via a stop codon readthrough mechanism.[provided by RefSeq, Dec 2017]","start":45689056,"end":45745424,"strand":1,"description":"SAC1 like phosphatidylinositide phosphatase [Source:HGNC Symbol;Acc:HGNC:17059]"}, {"versioned_ensembl_gene_id":"ENSG00000167941.2","gene_symbol":"SOST","gene_name":"sclerostin [Source:HGNC Symbol;Acc:HGNC:13771]","synonyms":"VBCH,DAND6","biotype":"protein_coding","ncbi_id":"50964","summary":"Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease. [provided by RefSeq, Jul 2008]","start":43753731,"end":43758788,"strand":-1,"description":"sclerostin [Source:HGNC Symbol;Acc:HGNC:13771]"}, {"versioned_ensembl_gene_id":"ENSG00000258784.1","gene_symbol":"AL355773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55748208,"end":55773203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104901.6","gene_symbol":"DKKL1","gene_name":"dickkopf like acrosomal protein 1 [Source:HGNC Symbol;Acc:HGNC:16528]","synonyms":"SGY-1,CT34","biotype":"protein_coding","ncbi_id":"27120","summary":"The dickkopf protein family interacts with the Wnt signaling pathway and its members are characterized by two conserved cysteine-rich domains. This gene encodes a secreted protein that has low sequence similarity to the dickkopf-3 protein. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":49361783,"end":49375116,"strand":1,"description":"dickkopf like acrosomal protein 1 [Source:HGNC Symbol;Acc:HGNC:16528]"}, {"versioned_ensembl_gene_id":"ENSG00000134940.13","gene_symbol":"ACRV1","gene_name":"acrosomal vesicle protein 1 [Source:HGNC Symbol;Acc:HGNC:127]","synonyms":"SP-10,D11S4365,SPACA2","biotype":"protein_coding","ncbi_id":"56","summary":"This gene encodes a testis-specific, differentiation antigen, acrosomal vesicle protein 1, that arises within the acrosomal vesicle during spermatogenesis, and is associated with the acrosomal membranes and matrix of mature sperm. The acrosomal vesicle protein 1 may be involved in sperm-zona binding or penetration. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2010]","start":125671522,"end":125681123,"strand":-1,"description":"acrosomal vesicle protein 1 [Source:HGNC Symbol;Acc:HGNC:127]"}, {"versioned_ensembl_gene_id":"ENSG00000109814.11","gene_symbol":"UGDH","gene_name":"UDP-glucose 6-dehydrogenase [Source:HGNC Symbol;Acc:HGNC:12525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7358","summary":"The protein encoded by this gene converts UDP-glucose to UDP-glucuronate and thereby participates in the biosynthesis of glycosaminoglycans such as hyaluronan, chondroitin sulfate, and heparan sulfate. These glycosylated compounds are common components of the extracellular matrix and likely play roles in signal transduction, cell migration, and cancer growth and metastasis. The expression of this gene is up-regulated by transforming growth factor beta and down-regulated by hypoxia. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":39498755,"end":39528311,"strand":-1,"description":"UDP-glucose 6-dehydrogenase [Source:HGNC Symbol;Acc:HGNC:12525]"}, {"versioned_ensembl_gene_id":"ENSG00000196344.11","gene_symbol":"ADH7","gene_name":"alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [Source:HGNC Symbol;Acc:HGNC:256]","synonyms":"ADH-4","biotype":"protein_coding","ncbi_id":"131","summary":"This gene encodes class IV alcohol dehydrogenase 7 mu or sigma subunit, which is a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. The enzyme encoded by this gene is inefficient in ethanol oxidation, but is the most active as a retinol dehydrogenase; thus it may participate in the synthesis of retinoic acid, a hormone important for cellular differentiation. The expression of this gene is much more abundant in stomach than liver, thus differing from the other known gene family members. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":99412261,"end":99435737,"strand":-1,"description":"alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [Source:HGNC Symbol;Acc:HGNC:256]"}, {"versioned_ensembl_gene_id":"ENSG00000186652.9","gene_symbol":"PRG2","gene_name":"proteoglycan 2, pro eosinophil major basic protein [Source:HGNC Symbol;Acc:HGNC:9362]","synonyms":"proMBP,MBP,BMPG","biotype":"protein_coding","ncbi_id":"5553","summary":"The protein encoded by this gene is the predominant constituent of the crystalline core of the eosinophil granule. High levels of the proform of this protein are also present in placenta and pregnancy serum, where it exists as a complex with several other proteins including pregnancy-associated plasma protein A (PAPPA), angiotensinogen (AGT), and C3dg. This protein may be involved in antiparasitic defense mechanisms as a cytotoxin and helminthotoxin, and in immune hypersensitivity reactions. The encoded protein contains a peptide that displays potent antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, and fungi. It is directly implicated in epithelial cell damage, exfoliation, and bronchospasm in allergic diseases. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":57386794,"end":57390657,"strand":-1,"description":"proteoglycan 2, pro eosinophil major basic protein [Source:HGNC Symbol;Acc:HGNC:9362]"}, {"versioned_ensembl_gene_id":"ENSG00000267508.5","gene_symbol":"ZNF285","gene_name":"zinc finger protein 285 [Source:HGNC Symbol;Acc:HGNC:13079]","synonyms":"ZNF285A","biotype":"protein_coding","ncbi_id":"26974","summary":null,"start":44382298,"end":44401608,"strand":-1,"description":"zinc finger protein 285 [Source:HGNC Symbol;Acc:HGNC:13079]"}, {"versioned_ensembl_gene_id":"ENSG00000198453.12","gene_symbol":"ZNF568","gene_name":"zinc finger protein 568 [Source:HGNC Symbol;Acc:HGNC:25392]","synonyms":"DKFZp686B0797","biotype":"protein_coding","ncbi_id":"374900","summary":null,"start":36916329,"end":36998700,"strand":1,"description":"zinc finger protein 568 [Source:HGNC Symbol;Acc:HGNC:25392]"}, {"versioned_ensembl_gene_id":"ENSG00000162851.7","gene_symbol":"TFB2M","gene_name":"transcription factor B2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:18559]","synonyms":"Hkp1,FLJ23182,FLJ22661","biotype":"protein_coding","ncbi_id":"64216","summary":null,"start":246540560,"end":246566324,"strand":-1,"description":"transcription factor B2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:18559]"}, {"versioned_ensembl_gene_id":"ENSG00000278077.1","gene_symbol":"AL591926.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41644771,"end":41644981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254851.1","gene_symbol":"AP005018.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":117135528,"end":117138582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153395.9","gene_symbol":"LPCAT1","gene_name":"lysophosphatidylcholine acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25718]","synonyms":"FLJ12443,AYTL2,AGPAT9,AGPAT10","biotype":"protein_coding","ncbi_id":"79888","summary":"This gene encodes a member of the 1-acyl-sn-glycerol-3-phosphate acyltransferase family of proteins. The encoded enzyme plays a role in phospholipid metabolism, specifically in the conversion of lysophosphatidylcholine to phosphatidylcholine in the presence of acyl-CoA. This process is important in the synthesis of lung surfactant and platelet-activating factor (PAF). Elevated expression of this gene may contribute to the progression of oral squamous cell, prostate, breast, and other human cancers. [provided by RefSeq, Sep 2016]","start":1456480,"end":1523977,"strand":-1,"description":"lysophosphatidylcholine acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25718]"}, {"versioned_ensembl_gene_id":"ENSG00000222206.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27223319,"end":27223427,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280735.1","gene_symbol":"AC217779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46062345,"end":46062802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226257.9","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31953357,"end":31965001,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000131504.15","gene_symbol":"DIAPH1","gene_name":"diaphanous related formin 1 [Source:HGNC Symbol;Acc:HGNC:2876]","synonyms":"LFHL1,hDIA1,DFNA1","biotype":"protein_coding","ncbi_id":"1729","summary":"This gene is a homolog of the Drosophila diaphanous gene, and has been linked to autosomal dominant, fully penetrant, nonsyndromic sensorineural progressive low-frequency hearing loss. Actin polymerization involves proteins known to interact with diaphanous protein in Drosophila and mouse. It has therefore been speculated that this gene may have a role in the regulation of actin polymerization in hair cells of the inner ear. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":141515016,"end":141619055,"strand":-1,"description":"diaphanous related formin 1 [Source:HGNC Symbol;Acc:HGNC:2876]"}, {"versioned_ensembl_gene_id":"ENSG00000211962.2","gene_symbol":"IGHV1-46","gene_name":"immunoglobulin heavy variable 1-46 [Source:HGNC Symbol;Acc:HGNC:5554]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28465","summary":null,"start":106511117,"end":106511856,"strand":-1,"description":"immunoglobulin heavy variable 1-46 [Source:HGNC Symbol;Acc:HGNC:5554]"}, {"versioned_ensembl_gene_id":"ENSG00000253465.1","gene_symbol":"IGHVIV-44-1","gene_name":"immunoglobulin heavy variable (IV)-44-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5710]","synonyms":"IGHV(IV)-44-1","biotype":"IG_V_pseudogene","ncbi_id":"28337","summary":null,"start":106489345,"end":106489756,"strand":-1,"description":"immunoglobulin heavy variable (IV)-44-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5710]"}, {"versioned_ensembl_gene_id":"ENSG00000268818.2","gene_symbol":"AL049747.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35626988,"end":35635134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269994.1","gene_symbol":"AL513318.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87008455,"end":87042126,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268582.1","gene_symbol":"AC243960.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41652676,"end":41652963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235722.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30104215,"end":30107221,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000268997.1","gene_symbol":"DNAJC19P3","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861443","summary":null,"start":41638569,"end":41638899,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45066]"}, {"versioned_ensembl_gene_id":"ENSG00000253622.1","gene_symbol":"AC027419.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":117128455,"end":117130299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172900.12","gene_symbol":"FLJ42102","gene_name":"uncharacterized LOC399923 [Source:NCBI gene;Acc:399923]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"399923","summary":null,"start":71382601,"end":71423423,"strand":-1,"description":"uncharacterized LOC399923 [Source:NCBI gene;Acc:399923]"}, {"versioned_ensembl_gene_id":"ENSG00000213433.5","gene_symbol":"AC091982.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":151765859,"end":151766378,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125898.12","gene_symbol":"FAM110A","gene_name":"family with sequence similarity 110 member A [Source:HGNC Symbol;Acc:HGNC:16188]","synonyms":"C20orf55,bA371L19.3","biotype":"protein_coding","ncbi_id":"83541","summary":null,"start":833715,"end":857463,"strand":1,"description":"family with sequence similarity 110 member A [Source:HGNC Symbol;Acc:HGNC:16188]"}, {"versioned_ensembl_gene_id":"ENSG00000167881.14","gene_symbol":"SRP68","gene_name":"signal recognition particle 68 [Source:HGNC Symbol;Acc:HGNC:11302]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6730","summary":"This gene encodes a subunit of the signal recognition particle (SRP). The SRP is a ribonucleoprotein complex that transports secreted and membrane proteins to the endoplasmic reticulum for processing. The complex includes a 7S RNA and six protein subunits. The encoded protein is the 68kDa component of the SRP, and forms a heterodimer with the 72kDa subunit that is required for SRP function. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and three pseudogenes of this gene are located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, May 2012]","start":76038775,"end":76072653,"strand":-1,"description":"signal recognition particle 68 [Source:HGNC Symbol;Acc:HGNC:11302]"}, {"versioned_ensembl_gene_id":"ENSG00000278259.4","gene_symbol":"MYO19","gene_name":"myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]","synonyms":"MYOHD1,FLJ22865","biotype":"protein_coding","ncbi_id":"80179","summary":null,"start":36495633,"end":36543435,"strand":-1,"description":"myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]"}, {"versioned_ensembl_gene_id":"ENSG00000226812.2","gene_symbol":"AL117382.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44347552,"end":44355185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269292.1","gene_symbol":"AC093503.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46609277,"end":46610779,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101074.3","gene_symbol":"R3HDML","gene_name":"R3H domain containing like [Source:HGNC Symbol;Acc:HGNC:16249]","synonyms":"dJ881L22.3","biotype":"protein_coding","ncbi_id":"140902","summary":null,"start":44336986,"end":44351235,"strand":1,"description":"R3H domain containing like [Source:HGNC Symbol;Acc:HGNC:16249]"}, {"versioned_ensembl_gene_id":"ENSG00000272479.1","gene_symbol":"AC010857.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40519565,"end":40520158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255321.1","gene_symbol":"AC068389.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60551957,"end":60553036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118492.16","gene_symbol":"ADGB","gene_name":"androglobin [Source:HGNC Symbol;Acc:HGNC:21212]","synonyms":"FLJ23121,dJ408K24.1,CAPN16,C6orf103","biotype":"protein_coding","ncbi_id":"79747","summary":null,"start":146598965,"end":146815462,"strand":1,"description":"androglobin [Source:HGNC Symbol;Acc:HGNC:21212]"}, {"versioned_ensembl_gene_id":"ENSG00000280014.1","gene_symbol":"AC243960.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41551568,"end":41552274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160294.10","gene_symbol":"MCM3AP","gene_name":"minichromosome maintenance complex component 3 associated protein [Source:HGNC Symbol;Acc:HGNC:6946]","synonyms":"SAC3,Map80,KIAA0572,GANP","biotype":"protein_coding","ncbi_id":"8888","summary":"The minichromosome maintenance protein 3 (MCM3) is one of the MCM proteins essential for the initiation of DNA replication. The protein encoded by this gene is a MCM3 binding protein. It was reported to have phosphorylation-dependent DNA-primase activity, which was up-regulated in antigen immunization induced germinal center. This protein was demonstrated to be an acetyltransferase that acetylates MCM3 and plays a role in DNA replication. The mutagenesis of a nuclear localization signal of MCM3 affects the binding of this protein with MCM3, suggesting that this protein may also facilitate MCM3 nuclear localization. This gene is expressed in the brain or in neuronal tissue. An allelic variant encoding amino acid Lys at 915, instead of conserved Glu, has been identified in patients with mild intellectual disability. [provided by RefSeq, Jan 2014]","start":46235126,"end":46286297,"strand":-1,"description":"minichromosome maintenance complex component 3 associated protein [Source:HGNC Symbol;Acc:HGNC:6946]"}, {"versioned_ensembl_gene_id":"ENSG00000174788.9","gene_symbol":"PCP2","gene_name":"Purkinje cell protein 2 [Source:HGNC Symbol;Acc:HGNC:30209]","synonyms":"MGC41903,GPSM4","biotype":"protein_coding","ncbi_id":"126006","summary":null,"start":7631611,"end":7633748,"strand":-1,"description":"Purkinje cell protein 2 [Source:HGNC Symbol;Acc:HGNC:30209]"}, {"versioned_ensembl_gene_id":"ENSG00000226009.1","gene_symbol":"KCNIP2-AS1","gene_name":"KCNIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48680]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289509","summary":null,"start":101819078,"end":101828779,"strand":1,"description":"KCNIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48680]"}, {"versioned_ensembl_gene_id":"ENSG00000185420.18","gene_symbol":"SMYD3","gene_name":"SET and MYND domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15513]","synonyms":"ZNFN3A1,ZMYND1,KMT3E","biotype":"protein_coding","ncbi_id":"64754","summary":"This gene encodes a histone methyltransferase which functions in RNA polymerase II complexes by an interaction with a specific RNA helicase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":245749342,"end":246507312,"strand":-1,"description":"SET and MYND domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15513]"}, {"versioned_ensembl_gene_id":"ENSG00000103353.15","gene_symbol":"UBFD1","gene_name":"ubiquitin family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30565]","synonyms":"UBPH,FLJ42145,FLJ38870","biotype":"protein_coding","ncbi_id":"56061","summary":null,"start":23557362,"end":23574389,"strand":1,"description":"ubiquitin family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30565]"}, {"versioned_ensembl_gene_id":"ENSG00000212240.1","gene_symbol":"RNU6-930P","gene_name":"RNA, U6 small nuclear 930, pseudogene [Source:HGNC Symbol;Acc:HGNC:47893]","synonyms":"RNU6-1173P","biotype":"snRNA","ncbi_id":"106480622","summary":null,"start":28915645,"end":28915744,"strand":1,"description":"RNA, U6 small nuclear 930, pseudogene [Source:HGNC Symbol;Acc:HGNC:47893]"}, {"versioned_ensembl_gene_id":"ENSG00000130528.11","gene_symbol":"HRC","gene_name":"histidine rich calcium binding protein [Source:HGNC Symbol;Acc:HGNC:5178]","synonyms":"MGC133236","biotype":"protein_coding","ncbi_id":"3270","summary":"This gene encodes a luminal sarcoplasmic reticulum protein identified by its ability to bind low-density lipoprotein with high affinity. The protein interacts with the cytoplasmic domain of triadin, the main transmembrane protein of the junctional sarcoplasmic reticulum (SR) of skeletal muscle. The protein functions in the regulation of releasable calcium into the SR. [provided by RefSeq, Sep 2008]","start":49151198,"end":49155424,"strand":-1,"description":"histidine rich calcium binding protein [Source:HGNC Symbol;Acc:HGNC:5178]"}, {"versioned_ensembl_gene_id":"ENSG00000233712.1","gene_symbol":"AL135929.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157636300,"end":157640301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279348.1","gene_symbol":"AC012513.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":216211404,"end":216213519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257272.1","gene_symbol":"AL162311.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35873857,"end":35875303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254954.1","gene_symbol":"SLC2A13P1","gene_name":"SLC2A13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480239","summary":null,"start":60141821,"end":60142142,"strand":1,"description":"SLC2A13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48929]"}, {"versioned_ensembl_gene_id":"ENSG00000282887.2","gene_symbol":"AL358215.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110472543,"end":110474980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283999.1","gene_symbol":"AL358215.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":110473756,"end":110488663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250161.1","gene_symbol":"TRMT112P5","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44024]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480784","summary":null,"start":139845078,"end":139845411,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44024]"}, {"versioned_ensembl_gene_id":"ENSG00000240194.7","gene_symbol":"CYMP","gene_name":"chymosin pseudogene [Source:HGNC Symbol;Acc:HGNC:2588]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"643160","summary":null,"start":110480752,"end":110491277,"strand":1,"description":"chymosin pseudogene [Source:HGNC Symbol;Acc:HGNC:2588]"}, {"versioned_ensembl_gene_id":"ENSG00000260581.1","gene_symbol":"AC011374.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151652275,"end":151655449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270380.1","gene_symbol":"AL358215.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110456505,"end":110457354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254045.1","gene_symbol":"IGHVIII-22-2","gene_name":"immunoglobulin heavy variable (III)-22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5696]","synonyms":"IGHV(III)-22-2","biotype":"IG_V_pseudogene","ncbi_id":"28349","summary":null,"start":106264688,"end":106264715,"strand":-1,"description":"immunoglobulin heavy variable (III)-22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5696]"}, {"versioned_ensembl_gene_id":"ENSG00000103855.17","gene_symbol":"CD276","gene_name":"CD276 molecule [Source:HGNC Symbol;Acc:HGNC:19137]","synonyms":"B7-H3,B7RP-2,B7H3","biotype":"protein_coding","ncbi_id":"80381","summary":"The protein encoded by this gene belongs to the immunoglobulin superfamily, and thought to participate in the regulation of T-cell-mediated immune response. Studies show that while the transcript of this gene is ubiquitously expressed in normal tissues and solid tumors, the protein is preferentially expressed only in tumor tissues. Additionally, it was observed that the 3' UTR of this transcript contains a target site for miR29 microRNA, and there is an inverse correlation between the expression of this protein and miR29 levels, suggesting regulation of expression of this gene product by miR29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":73683966,"end":73714518,"strand":1,"description":"CD276 molecule [Source:HGNC Symbol;Acc:HGNC:19137]"}, {"versioned_ensembl_gene_id":"ENSG00000258224.1","gene_symbol":"AC090049.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91871122,"end":91871230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235910.1","gene_symbol":"APOA1-AS","gene_name":"APOA1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40079]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104326055","summary":null,"start":116836117,"end":116855729,"strand":1,"description":"APOA1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40079]"}, {"versioned_ensembl_gene_id":"ENSG00000261268.1","gene_symbol":"AC112236.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139618136,"end":139623232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251455.1","gene_symbol":"AC092611.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151674483,"end":151677893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006071.12","gene_symbol":"ABCC8","gene_name":"ATP binding cassette subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:59]","synonyms":"TNDM2,SUR1,SUR,PHHI,MRP8,HRINS,HI,HHF1,ABC36","biotype":"protein_coding","ncbi_id":"6833","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations in the ABCC8 gene and deficiencies in the encoded protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II, an autosomal dominant disease of defective insulin secretion. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2020]","start":17392885,"end":17476845,"strand":-1,"description":"ATP binding cassette subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:59]"}, {"versioned_ensembl_gene_id":"ENSG00000235687.9","gene_symbol":"LINC00993","gene_name":"long intergenic non-protein coding RNA 993 [Source:HGNC Symbol;Acc:HGNC:48948]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101929520","summary":null,"start":37248118,"end":37347031,"strand":1,"description":"long intergenic non-protein coding RNA 993 [Source:HGNC Symbol;Acc:HGNC:48948]"}, {"versioned_ensembl_gene_id":"ENSG00000197324.8","gene_symbol":"LRP10","gene_name":"LDL receptor related protein 10 [Source:HGNC Symbol;Acc:HGNC:14553]","synonyms":"MSTP087,MST087,MGC8675,LRP9,DKFZP564C1940","biotype":"protein_coding","ncbi_id":"26020","summary":"This gene encodes a low density lipoprotein receptor family protein. A similar protein in mouse is thought to play a role in the uptake of apolipoprotein E-containing lipoproteins. [provided by RefSeq, Jul 2016]","start":22871613,"end":22881580,"strand":1,"description":"LDL receptor related protein 10 [Source:HGNC Symbol;Acc:HGNC:14553]"}, {"versioned_ensembl_gene_id":"ENSG00000237970.1","gene_symbol":"TMEM161BP1","gene_name":"transmembrane protein 161B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646360","summary":null,"start":37337415,"end":37338871,"strand":1,"description":"transmembrane protein 161B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44973]"}, {"versioned_ensembl_gene_id":"ENSG00000101166.15","gene_symbol":"PRELID3B","gene_name":"PRELI domain containing 3B [Source:HGNC Symbol;Acc:HGNC:15892]","synonyms":"SLMO2,dJ543J19.5,C20orf45","biotype":"protein_coding","ncbi_id":"51012","summary":null,"start":59033145,"end":59042909,"strand":-1,"description":"PRELI domain containing 3B [Source:HGNC Symbol;Acc:HGNC:15892]"}, {"versioned_ensembl_gene_id":"ENSG00000122133.16","gene_symbol":"PAEP","gene_name":"progestagen associated endometrial protein [Source:HGNC Symbol;Acc:HGNC:8573]","synonyms":"PAEG,MGC142288,MGC138509,GdS,GdF,GdA,GD,PP14,PEP","biotype":"protein_coding","ncbi_id":"5047","summary":"This gene is a member of the kernel lipocalin superfamily whose members share relatively low sequence similarity but have highly conserved exon/intron structure and three-dimensional protein folding. Most lipocalins are clustered on the long arm of chromosome 9. The encoded glycoprotein has been previously referred to as pregnancy-associated endometrial alpha-2-globulin, placental protein 14, and glycodelin, but has been officially named progestagen-associated endometrial protein. Three distinct forms, with identical protein backbones but different glycosylation profiles, are found in amniotic fluid, follicular fluid and seminal plasma of the reproductive system. These glycoproteins have distinct and essential roles in regulating a uterine environment suitable for pregnancy and in the timing and occurrence of the appropriate sequence of events in the fertilization process. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":135561756,"end":135566955,"strand":1,"description":"progestagen associated endometrial protein [Source:HGNC Symbol;Acc:HGNC:8573]"}, {"versioned_ensembl_gene_id":"ENSG00000240303.7","gene_symbol":"ACAD11","gene_name":"acyl-CoA dehydrogenase family member 11 [Source:HGNC Symbol;Acc:HGNC:30211]","synonyms":"FLJ12592","biotype":"protein_coding","ncbi_id":"84129","summary":"This gene encodes an acyl-CoA dehydrogenase enzyme with a preference for carbon chain lengths between 20 and 26. Naturally occurring read-through transcription occurs between the upstream gene NPHP3 (nephronophthisis 3 (adolescent)) and this gene. [provided by RefSeq, Aug 2015]","start":132558138,"end":132660723,"strand":-1,"description":"acyl-CoA dehydrogenase family member 11 [Source:HGNC Symbol;Acc:HGNC:30211]"}, {"versioned_ensembl_gene_id":"ENSG00000101134.11","gene_symbol":"DOK5","gene_name":"docking protein 5 [Source:HGNC Symbol;Acc:HGNC:16173]","synonyms":"dJ805C22.1,C20orf180","biotype":"protein_coding","ncbi_id":"55816","summary":"The protein encoded by this gene is a member of the DOK family of membrane proteins, which are adapter proteins involved in signal transduction. The encoded protein interacts with phosphorylated receptor tyrosine kinases to mediate neurite outgrowth and activation of the MAP kinase pathway. Unlike other DOK family proteins, this protein does not interact with RASGAP. This protein is up-regulated in patients with systemic sclerosis and is associated with fibrosis induced by insulin-like growth factor binding protein 5. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":54475597,"end":54651171,"strand":1,"description":"docking protein 5 [Source:HGNC Symbol;Acc:HGNC:16173]"}, {"versioned_ensembl_gene_id":"ENSG00000238276.5","gene_symbol":"AL354863.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":118241564,"end":118267710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250948.1","gene_symbol":"AC091180.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49375380,"end":49380094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234715.1","gene_symbol":"AC005064.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103445207,"end":103514007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278861.1","gene_symbol":"AC117503.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123655528,"end":123656128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267022.1","gene_symbol":"AC067968.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":44025354,"end":44087318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222009.8","gene_symbol":"BTBD19","gene_name":"BTB domain containing 19 [Source:HGNC Symbol;Acc:HGNC:27145]","synonyms":null,"biotype":"protein_coding","ncbi_id":"149478","summary":null,"start":44808482,"end":44815585,"strand":1,"description":"BTB domain containing 19 [Source:HGNC Symbol;Acc:HGNC:27145]"}, {"versioned_ensembl_gene_id":"ENSG00000262154.1","gene_symbol":"EIF1P4","gene_name":"eukaryotic translation initiation factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130566","summary":null,"start":2822659,"end":2822993,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49617]"}, {"versioned_ensembl_gene_id":"ENSG00000275423.1","gene_symbol":"AC092650.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47989625,"end":47990526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204438.10","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31661229,"end":31666283,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000204956.5","gene_symbol":"PCDHGA1","gene_name":"protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:HGNC:8696]","synonyms":"PCDH-GAMMA-A1","biotype":"protein_coding","ncbi_id":"56114","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141330571,"end":141512981,"strand":1,"description":"protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:HGNC:8696]"}, {"versioned_ensembl_gene_id":"ENSG00000213140.3","gene_symbol":"ELK2AP","gene_name":"ELK2A, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3323]","synonyms":"ELK2P1,ELK2.1,ELK2","biotype":"processed_pseudogene","ncbi_id":"2003","summary":null,"start":105672308,"end":105673314,"strand":-1,"description":"ELK2A, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3323]"}, {"versioned_ensembl_gene_id":"ENSG00000107560.10","gene_symbol":"RAB11FIP2","gene_name":"RAB11 family interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29152]","synonyms":"Rab11-FIP2,nRip11,KIAA0941","biotype":"protein_coding","ncbi_id":"22841","summary":null,"start":118004916,"end":118046603,"strand":-1,"description":"RAB11 family interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29152]"}, {"versioned_ensembl_gene_id":"ENSG00000119686.9","gene_symbol":"FLVCR2","gene_name":"feline leukemia virus subgroup C cellular receptor family member 2 [Source:HGNC Symbol;Acc:HGNC:20105]","synonyms":"MFSD7C,FLJ20371,C14orf58","biotype":"protein_coding","ncbi_id":"55640","summary":"This gene encodes a member of the major facilitator superfamily. The encoded transmembrane protein is a calcium transporter. Unlike the related protein feline leukemia virus subgroup C receptor 1, the protein encoded by this locus does not bind to feline leukemia virus subgroup C envelope protein. The encoded protein may play a role in development of brain vascular endothelial cells, as mutations at this locus have been associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome. Alternatively spliced transcript variants have been described.[provided by RefSeq, Aug 2010]","start":75578617,"end":75663214,"strand":1,"description":"feline leukemia virus subgroup C cellular receptor family member 2 [Source:HGNC Symbol;Acc:HGNC:20105]"}, {"versioned_ensembl_gene_id":"ENSG00000279191.1","gene_symbol":"AC068491.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":111321433,"end":111324812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242180.3","gene_symbol":"OR51B5","gene_name":"olfactory receptor family 51 subfamily B member 5 [Source:HGNC Symbol;Acc:HGNC:19599]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282763","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5342586,"end":5343524,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 5 [Source:HGNC Symbol;Acc:HGNC:19599]"}, {"versioned_ensembl_gene_id":"ENSG00000131437.15","gene_symbol":"KIF3A","gene_name":"kinesin family member 3A [Source:HGNC Symbol;Acc:HGNC:6319]","synonyms":"KLP-20,FLA10","biotype":"protein_coding","ncbi_id":"11127","summary":null,"start":132692628,"end":132737638,"strand":-1,"description":"kinesin family member 3A [Source:HGNC Symbol;Acc:HGNC:6319]"}, {"versioned_ensembl_gene_id":"ENSG00000236881.1","gene_symbol":"BX005428.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720705,"end":29721695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261308.2","gene_symbol":"FIGNL2","gene_name":"fidgetin like 2 [Source:HGNC Symbol;Acc:HGNC:13287]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401720","summary":null,"start":51817840,"end":51848766,"strand":-1,"description":"fidgetin like 2 [Source:HGNC Symbol;Acc:HGNC:13287]"}, {"versioned_ensembl_gene_id":"ENSG00000165802.22","gene_symbol":"NSMF","gene_name":"NMDA receptor synaptonuclear signaling and neuronal migration factor [Source:HGNC Symbol;Acc:HGNC:29843]","synonyms":"NELF","biotype":"protein_coding","ncbi_id":"26012","summary":"The protein encoded by this gene is involved in guidance of olfactory axon projections and migration of luteinizing hormone-releasing hormone neurons. Defects in this gene are a cause of idiopathic hypogonadotropic hypogonadism (IHH). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":137447573,"end":137459334,"strand":-1,"description":"NMDA receptor synaptonuclear signaling and neuronal migration factor [Source:HGNC Symbol;Acc:HGNC:29843]"}, {"versioned_ensembl_gene_id":"ENSG00000213619.9","gene_symbol":"NDUFS3","gene_name":"NADH:ubiquinone oxidoreductase core subunit S3 [Source:HGNC Symbol;Acc:HGNC:7710]","synonyms":"CI-30","biotype":"protein_coding","ncbi_id":"4722","summary":"This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.[provided by RefSeq, Apr 2009]","start":47565336,"end":47584562,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit S3 [Source:HGNC Symbol;Acc:HGNC:7710]"}, {"versioned_ensembl_gene_id":"ENSG00000275416.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,cl-5,nkat4b,nkat4,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850500,"end":54867258,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000278206.1","gene_symbol":"AL031320.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":143484979,"end":143507327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104863.11","gene_symbol":"LIN7B","gene_name":"lin-7 homolog B, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17788]","synonyms":"VELI2,MALS-2,LIN-7B","biotype":"protein_coding","ncbi_id":"64130","summary":null,"start":49114324,"end":49118460,"strand":1,"description":"lin-7 homolog B, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17788]"}, {"versioned_ensembl_gene_id":"ENSG00000110848.8","gene_symbol":"CD69","gene_name":"CD69 molecule [Source:HGNC Symbol;Acc:HGNC:1694]","synonyms":"CLEC2C","biotype":"protein_coding","ncbi_id":"969","summary":"This gene encodes a member of the calcium dependent lectin superfamily of type II transmembrane receptors. Expression of the encoded protein is induced upon activation of T lymphocytes, and may play a role in proliferation. Furthermore, the protein may act to transmit signals in natural killer cells and platelets. [provided by RefSeq, Aug 2011]","start":9752486,"end":9760901,"strand":-1,"description":"CD69 molecule [Source:HGNC Symbol;Acc:HGNC:1694]"}, {"versioned_ensembl_gene_id":"ENSG00000239544.1","gene_symbol":"AL442663.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72963645,"end":72964008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196843.15","gene_symbol":"ARID5A","gene_name":"AT-rich interaction domain 5A [Source:HGNC Symbol;Acc:HGNC:17361]","synonyms":"RP11-363D14,MRF-1","biotype":"protein_coding","ncbi_id":"10865","summary":"Members of the ARID protein family, including ARID5A, have diverse functions but all appear to play important roles in development, tissue-specific gene expression, and regulation of cell growth (Patsialou et al., 2005 [PubMed 15640446]).[supplied by OMIM, Mar 2008]","start":96536743,"end":96552638,"strand":1,"description":"AT-rich interaction domain 5A [Source:HGNC Symbol;Acc:HGNC:17361]"}, {"versioned_ensembl_gene_id":"ENSG00000104848.1","gene_symbol":"KCNA7","gene_name":"potassium voltage-gated channel subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:6226]","synonyms":"Kv1.7,HAK6","biotype":"protein_coding","ncbi_id":"3743","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. The gene is expressed preferentially in skeletal muscle, heart and kidney. It is a candidate gene for inherited cardiac disorders. [provided by RefSeq, Jul 2008]","start":49067418,"end":49072941,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:6226]"}, {"versioned_ensembl_gene_id":"ENSG00000225361.3","gene_symbol":"PPP1R26-AS1","gene_name":"PPP1R26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48717]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506599","summary":null,"start":135462727,"end":135480777,"strand":-1,"description":"PPP1R26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48717]"}, {"versioned_ensembl_gene_id":"ENSG00000120329.6","gene_symbol":"SLC25A2","gene_name":"solute carrier family 25 member 2 [Source:HGNC Symbol;Acc:HGNC:22921]","synonyms":"ORNT2","biotype":"protein_coding","ncbi_id":"83884","summary":"This intronless gene encodes a protein that localizes to the mitochondrial inner membrane and likely functions as a transporter of small molecules such as ornithine. This gene is located between the protocadherin beta and gamma gene clusters on chromosome 5. [provided by RefSeq, Dec 2014]","start":141302629,"end":141304045,"strand":-1,"description":"solute carrier family 25 member 2 [Source:HGNC Symbol;Acc:HGNC:22921]"}, {"versioned_ensembl_gene_id":"ENSG00000253923.2","gene_symbol":"AP002981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102417979,"end":102418953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273723.1","gene_symbol":"AL139089.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52651305,"end":52652279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239920.1","gene_symbol":"AC015691.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5572322,"end":5624896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196422.10","gene_symbol":"PPP1R26","gene_name":"protein phosphatase 1 regulatory subunit 26 [Source:HGNC Symbol;Acc:HGNC:29089]","synonyms":"KIAA0649","biotype":"protein_coding","ncbi_id":"9858","summary":null,"start":135479079,"end":135488893,"strand":1,"description":"protein phosphatase 1 regulatory subunit 26 [Source:HGNC Symbol;Acc:HGNC:29089]"}, {"versioned_ensembl_gene_id":"ENSG00000240040.6","gene_symbol":"AC244205.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":88811186,"end":88861563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267334.1","gene_symbol":"AC015936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44947912,"end":44948939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259023.2","gene_symbol":"LINC00524","gene_name":"long intergenic non-protein coding RNA 524 [Source:HGNC Symbol;Acc:HGNC:20118]","synonyms":"C14orf71","biotype":"lincRNA","ncbi_id":"338002","summary":null,"start":101405987,"end":101407922,"strand":-1,"description":"long intergenic non-protein coding RNA 524 [Source:HGNC Symbol;Acc:HGNC:20118]"}, {"versioned_ensembl_gene_id":"ENSG00000142959.4","gene_symbol":"BEST4","gene_name":"bestrophin 4 [Source:HGNC Symbol;Acc:HGNC:17106]","synonyms":"VMD2L2","biotype":"protein_coding","ncbi_id":"266675","summary":"This gene is a member of the bestrophin gene family of anion channels. Bestrophin genes share a similar gene structure with highly conserved exon-intron boundaries, but with distinct 3' ends. Bestrophins are transmembrane proteins that contain a homologous region rich in aromatic residues, including an invariant arg-phe-pro motif. Mutation in one of the family members (bestrophin 1) is associated with vitelliform macular dystrophy. The bestrophin 4 gene is predominantly expressed in the colon. [provided by RefSeq, Jul 2008]","start":44783585,"end":44787705,"strand":-1,"description":"bestrophin 4 [Source:HGNC Symbol;Acc:HGNC:17106]"}, {"versioned_ensembl_gene_id":"ENSG00000223851.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30678268,"end":30678534,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000163812.13","gene_symbol":"ZDHHC3","gene_name":"zinc finger DHHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18470]","synonyms":"ZNF373,GODZ,DHHC3","biotype":"protein_coding","ncbi_id":"51304","summary":null,"start":44915257,"end":44976185,"strand":-1,"description":"zinc finger DHHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18470]"}, {"versioned_ensembl_gene_id":"ENSG00000170949.17","gene_symbol":"ZNF160","gene_name":"zinc finger protein 160 [Source:HGNC Symbol;Acc:HGNC:12948]","synonyms":"HKr18,FLJ00032,F11,KR18,KIAA1611,HZF5","biotype":"protein_coding","ncbi_id":"90338","summary":"The protein encoded by this gene is a Kruppel-related zinc finger protein which is characterized by the presence of an N-terminal repressor domain, the Kruppel-associated box (KRAB). The KRAB domain is a potent repressor of transcription; thus this protein may function in transcription regulation. Multiple transcript variants have been found for this gene. [provided by RefSeq, Apr 2016]","start":53066606,"end":53103436,"strand":-1,"description":"zinc finger protein 160 [Source:HGNC Symbol;Acc:HGNC:12948]"}, {"versioned_ensembl_gene_id":"ENSG00000229109.1","gene_symbol":"AL137847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83219331,"end":83234242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275718.1","gene_symbol":"CCL15","gene_name":"C-C motif chemokine ligand 15 [Source:HGNC Symbol;Acc:HGNC:10613]","synonyms":"NCC-3,MIP-5,MIP-1d,Lkn-1,HMRP-2B,HCC-2,SCYL3,SCYA15","biotype":"protein_coding","ncbi_id":"6359","summary":"This gene is located in a cluster of similar genes in the same region of chromosome 17. These genes encode CC cytokines, which are secreted proteins characterized by two adjacent cysteines. The product of this gene is chemotactic for T cells and monocytes, and acts through C-C chemokine receptor type 1 (CCR1). The proprotein is further processed into numerous smaller functional peptides. Naturally-occurring readthrough transcripts occur from this gene into the downstream gene, CCL14 (chemokine (C-C motif) ligand 14). [provided by RefSeq, Jan 2013]","start":35996440,"end":36002038,"strand":-1,"description":"C-C motif chemokine ligand 15 [Source:HGNC Symbol;Acc:HGNC:10613]"}, {"versioned_ensembl_gene_id":"ENSG00000273784.4","gene_symbol":"AL137058.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":52600042,"end":52642542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120328.6","gene_symbol":"PCDHB12","gene_name":"protocadherin beta 12 [Source:HGNC Symbol;Acc:HGNC:8683]","synonyms":"PCDH-BETA12","biotype":"protein_coding","ncbi_id":"56124","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141208697,"end":141212571,"strand":1,"description":"protocadherin beta 12 [Source:HGNC Symbol;Acc:HGNC:8683]"}, {"versioned_ensembl_gene_id":"ENSG00000281708.1","gene_symbol":"ERC2-IT1","gene_name":"ERC2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1229]","synonyms":"C3orf51,C1orf1,Po42","biotype":"sense_intronic","ncbi_id":"711","summary":"This gene is a putative tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":55657206,"end":55659382,"strand":-1,"description":"ERC2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1229]"}, {"versioned_ensembl_gene_id":"ENSG00000113248.5","gene_symbol":"PCDHB15","gene_name":"protocadherin beta 15 [Source:HGNC Symbol;Acc:HGNC:8686]","synonyms":"PCDH-BETA15","biotype":"protein_coding","ncbi_id":"56121","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141245349,"end":141249365,"strand":1,"description":"protocadherin beta 15 [Source:HGNC Symbol;Acc:HGNC:8686]"}, {"versioned_ensembl_gene_id":"ENSG00000188488.13","gene_symbol":"SERPINA5","gene_name":"serpin family A member 5 [Source:HGNC Symbol;Acc:HGNC:8723]","synonyms":"PROCI,PLANH3,PCI,PAI3","biotype":"protein_coding","ncbi_id":"5104","summary":"The protein encoded by this gene is a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. This gene is one in a cluster of serpin genes located on the q arm of chromosome 14. This family member is a glycoprotein that can inhibit several serine proteases, including protein C and various plasminogen activators and kallikreins, and it thus plays diverse roles in hemostasis and thrombosis in multiple organs. [provided by RefSeq, Aug 2012]","start":94561442,"end":94593120,"strand":1,"description":"serpin family A member 5 [Source:HGNC Symbol;Acc:HGNC:8723]"}, {"versioned_ensembl_gene_id":"ENSG00000236911.6","gene_symbol":"AL137789.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":207551925,"end":207606555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233342.1","gene_symbol":"AL391361.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160926369,"end":160927162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235984.5","gene_symbol":"GPC5-AS1","gene_name":"GPC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39886]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873969","summary":null,"start":92701389,"end":92721614,"strand":-1,"description":"GPC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39886]"}, {"versioned_ensembl_gene_id":"ENSG00000282865.1","gene_symbol":"AL157815.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":92239835,"end":92241951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282993.1","gene_symbol":"AL356737.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":92658994,"end":92659227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273259.3","gene_symbol":"AL049839.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":94592058,"end":94624646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229287.1","gene_symbol":"FABP5P4","gene_name":"fatty acid binding protein 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31061]","synonyms":"FABP5L4","biotype":"processed_pseudogene","ncbi_id":"404766","summary":null,"start":92180715,"end":92180885,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31061]"}, {"versioned_ensembl_gene_id":"ENSG00000231880.2","gene_symbol":"KF459542.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47577725,"end":47578277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008438.4","gene_symbol":"PGLYRP1","gene_name":"peptidoglycan recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:8904]","synonyms":"TNFSF3L,TAG7,PGRPS,PGRP-S,PGRP,PGLYRP","biotype":"protein_coding","ncbi_id":"8993","summary":null,"start":46019153,"end":46023065,"strand":-1,"description":"peptidoglycan recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:8904]"}, {"versioned_ensembl_gene_id":"ENSG00000113971.19","gene_symbol":"NPHP3","gene_name":"nephrocystin 3 [Source:HGNC Symbol;Acc:HGNC:7907]","synonyms":"CFAP31,SLSN3,NPH3,MKS7,KIAA2000,FLJ36696,FLJ30691","biotype":"protein_coding","ncbi_id":"27031","summary":"This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011]","start":132680609,"end":132722442,"strand":-1,"description":"nephrocystin 3 [Source:HGNC Symbol;Acc:HGNC:7907]"}, {"versioned_ensembl_gene_id":"ENSG00000275722.4","gene_symbol":"LYZL6","gene_name":"lysozyme like 6 [Source:HGNC Symbol;Acc:HGNC:29614]","synonyms":"TKAL754,PRO1485,LYC1","biotype":"protein_coding","ncbi_id":"57151","summary":"This gene encodes a member of the C-type lysozyme/alpha-lactalbumin family. C-type lysozymes are bacteriolytic factors that play a role in host defense, whereas alpha-lactalbumins mediate lactose biosynthesis. The encoded protein contains catalytic residues characteristic of C-type lysozymes and may play a role in male reproduction. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jan 2011]","start":35934518,"end":35943699,"strand":-1,"description":"lysozyme like 6 [Source:HGNC Symbol;Acc:HGNC:29614]"}, {"versioned_ensembl_gene_id":"ENSG00000174373.16","gene_symbol":"RALGAPA1","gene_name":"Ral GTPase activating protein catalytic alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:17770]","synonyms":"Tulip1,RalGAPalpha1,KIAA0884,GRIPE,GARNL1,DKFZp667F074","biotype":"protein_coding","ncbi_id":"253959","summary":"This gene encodes a major subunit of the RAL-GTPase activating protein. A similar protein in mouse binds E12, a transcriptional regulator of immunoglobulin genes. The mouse protein also functions in skeletal muscle by binding to the regulatory 14-3-3 proteins upon stimulation with insulin or muscle contraction. A pseudogene of this gene has been identified on chromosome 9. [provided by RefSeq, Oct 2016]","start":35538352,"end":35809304,"strand":-1,"description":"Ral GTPase activating protein catalytic alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:17770]"}, {"versioned_ensembl_gene_id":"ENSG00000231562.1","gene_symbol":"AL512593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106978776,"end":106979554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260879.1","gene_symbol":"AL359258.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108199926,"end":108201491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000044115.20","gene_symbol":"CTNNA1","gene_name":"catenin alpha 1 [Source:HGNC Symbol;Acc:HGNC:2509]","synonyms":"CAP102","biotype":"protein_coding","ncbi_id":"1495","summary":"This gene encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell. The encoded mechanosensing protein contains three vinculin homology domains and undergoes conformational changes in response to cytoskeletal tension, resulting in the reconfiguration of cadherin-actin filament connections. Certain mutations in this gene cause butterfly-shaped pigment dystrophy. [provided by RefSeq, May 2016]","start":138610967,"end":138935034,"strand":1,"description":"catenin alpha 1 [Source:HGNC Symbol;Acc:HGNC:2509]"}, {"versioned_ensembl_gene_id":"ENSG00000236051.7","gene_symbol":"MYCBP2-AS1","gene_name":"MYCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41023]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874212","summary":null,"start":77026767,"end":77129717,"strand":1,"description":"MYCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41023]"}, {"versioned_ensembl_gene_id":"ENSG00000234474.2","gene_symbol":"MIR3663HG","gene_name":"MIR3663 host gene [Source:HGNC Symbol;Acc:HGNC:50676]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927704","summary":null,"start":117158656,"end":117169059,"strand":-1,"description":"MIR3663 host gene [Source:HGNC Symbol;Acc:HGNC:50676]"}, {"versioned_ensembl_gene_id":"ENSG00000225475.1","gene_symbol":"AC099789.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56619409,"end":56619549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271484.1","gene_symbol":"ABI1P1","gene_name":"abl interactor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20035]","synonyms":"SSH3BP1P,ABI1P","biotype":"unprocessed_pseudogene","ncbi_id":"326268","summary":null,"start":55546674,"end":55548123,"strand":1,"description":"abl interactor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20035]"}, {"versioned_ensembl_gene_id":"ENSG00000122194.18","gene_symbol":"PLG","gene_name":"plasminogen [Source:HGNC Symbol;Acc:HGNC:9071]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5340","summary":"The plasminogen protein encoded by this gene is a serine protease that circulates in blood plasma as an inactive zymogen and is converted to the active protease, plasmin, by several plasminogen activators such as tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, and factor XII (Hageman factor). The conversion of plasminogen to plasmin involves the cleavage of the peptide bond between Arg-561 and Val-562. Plasmin cleavage also releases the angiostatin protein which inhibits angiogenesis. Plasmin degrades many blood plasma proteins, including fibrin-containing blood clots. As a serine protease, plasmin cleaves many products in addition to fibrin such as fibronectin, thrombospondin, laminin, and von Willebrand factor. Plasmin is inactivated by proteins such as alpha-2-macroglobulin and alpha-2-antiplasmin in addition to inhibitors of the various plasminogen activators. Plasminogen also interacts with plasminogen receptors which results in the retention of plasmin on cell surfaces and in plasmin-induced cell signaling. The localization of plasminogen on cell surfaces plays a role in the degradation of extracellular matrices, cell migration, inflamation, wound healing, oncogenesis, metastasis, myogenesis, muscle regeneration, neurite outgrowth, and fibrinolysis. This protein may also play a role in acute respiratory distress syndrome (ARDS) which, in part, is caused by enhanced clot formation and the suppression of fibrinolysis. Compared to other mammals, the cluster of plasminogen-like genes to which this gene belongs has been rearranged in catarrhine primates. [provided by RefSeq, May 2020]","start":160702238,"end":160753315,"strand":1,"description":"plasminogen [Source:HGNC Symbol;Acc:HGNC:9071]"}, {"versioned_ensembl_gene_id":"ENSG00000233259.4","gene_symbol":"FABP3P2","gene_name":"fatty acid binding protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3558]","synonyms":"FABP3P,FABP3-ps","biotype":"processed_pseudogene","ncbi_id":"56677","summary":null,"start":42369259,"end":42369657,"strand":-1,"description":"fatty acid binding protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3558]"}, {"versioned_ensembl_gene_id":"ENSG00000112319.17","gene_symbol":"EYA4","gene_name":"EYA transcriptional coactivator and phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:3522]","synonyms":"DFNA10,CMD1J","biotype":"protein_coding","ncbi_id":"2070","summary":"This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":133240598,"end":133532120,"strand":1,"description":"EYA transcriptional coactivator and phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:3522]"}, {"versioned_ensembl_gene_id":"ENSG00000163864.15","gene_symbol":"NMNAT3","gene_name":"nicotinamide nucleotide adenylyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:20989]","synonyms":"PNAT3","biotype":"protein_coding","ncbi_id":"349565","summary":"This gene encodes a member of the nicotinamide/nicotinic acid mononucleotide adenylyltransferase family. These enzymes use ATP to catalyze the synthesis of nicotinamide adenine dinucleotide or nicotinic acid adenine dinucleotide from nicotinamide mononucleotide or nicotinic acid mononucleotide, respectively. The encoded protein is localized to mitochondria and may also play a neuroprotective role as a molecular chaperone. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":139560180,"end":139678017,"strand":-1,"description":"nicotinamide nucleotide adenylyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:20989]"}, {"versioned_ensembl_gene_id":"ENSG00000224477.5","gene_symbol":"AL109933.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160698288,"end":160700632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090861.15","gene_symbol":"AARS","gene_name":"alanyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:20]","synonyms":"CMT2N,AlaRS","biotype":"protein_coding","ncbi_id":"16","summary":"The human alanyl-tRNA synthetase (AARS) belongs to a family of tRNA synthases, of the class II enzymes. Class II tRNA synthases evolved early in evolution and are highly conserved. This is reflected by the fact that 498 of the 968-residue polypeptide human AARS shares 41% identity witht the E.coli protein. tRNA synthases are the enzymes that interpret the RNA code and attach specific aminoacids to the tRNAs that contain the cognate trinucleotide anticodons. They consist of a catalytic domain which interacts with the amino acid acceptor-T psi C helix of the tRNA, and a second domain which interacts with the rest of the tRNA structure. [provided by RefSeq, Jul 2008]","start":70252295,"end":70289543,"strand":-1,"description":"alanyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:20]"}, {"versioned_ensembl_gene_id":"ENSG00000227954.6","gene_symbol":"TARID","gene_name":"TCF21 antisense RNA inducing promoter demethylation [Source:HGNC Symbol;Acc:HGNC:50506]","synonyms":"EYA4-AS1","biotype":"antisense_RNA","ncbi_id":"100507308","summary":null,"start":133502252,"end":133892802,"strand":-1,"description":"TCF21 antisense RNA inducing promoter demethylation [Source:HGNC Symbol;Acc:HGNC:50506]"}, {"versioned_ensembl_gene_id":"ENSG00000272428.1","gene_symbol":"AL450270.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133540784,"end":133541174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223586.5","gene_symbol":"LINC01312","gene_name":"long intergenic non-protein coding RNA 1312 [Source:HGNC Symbol;Acc:HGNC:28525]","synonyms":"MGC34034","biotype":"lincRNA","ncbi_id":"154089","summary":null,"start":133821147,"end":133851800,"strand":1,"description":"long intergenic non-protein coding RNA 1312 [Source:HGNC Symbol;Acc:HGNC:28525]"}, {"versioned_ensembl_gene_id":"ENSG00000226397.8","gene_symbol":"C12orf77","gene_name":"chromosome 12 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:27282]","synonyms":null,"biotype":"lincRNA","ncbi_id":"196415","summary":null,"start":24993424,"end":25006403,"strand":-1,"description":"chromosome 12 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:27282]"}, {"versioned_ensembl_gene_id":"ENSG00000263219.1","gene_symbol":"AC087742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4222091,"end":4223828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263165.1","gene_symbol":"AC087292.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4163910,"end":4164713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225205.5","gene_symbol":"AC078883.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172480840,"end":172556596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279632.1","gene_symbol":"AP003108.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61426448,"end":61427325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256591.5","gene_symbol":"AP003108.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61429220,"end":61485822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189159.15","gene_symbol":"JPT1","gene_name":"Jupiter microtubule associated homolog 1 [Source:HGNC Symbol;Acc:HGNC:14569]","synonyms":"HN1A,HN1,ARM2","biotype":"protein_coding","ncbi_id":"51155","summary":null,"start":75135248,"end":75168281,"strand":-1,"description":"Jupiter microtubule associated homolog 1 [Source:HGNC Symbol;Acc:HGNC:14569]"}, {"versioned_ensembl_gene_id":"ENSG00000148660.20","gene_symbol":"CAMK2G","gene_name":"calcium/calmodulin dependent protein kinase II gamma [Source:HGNC Symbol;Acc:HGNC:1463]","synonyms":"CAMKG","biotype":"protein_coding","ncbi_id":"818","summary":"The product of this gene is one of the four subunits of an enzyme which belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells the enzyme is composed of four different chains: alpha, beta, gamma, and delta. The product of this gene is a gamma chain. Many alternatively spliced transcripts encoding different isoforms have been described but the full-length nature of all the variants has not been determined.[provided by RefSeq, Mar 2011]","start":73812501,"end":73874591,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II gamma [Source:HGNC Symbol;Acc:HGNC:1463]"}, {"versioned_ensembl_gene_id":"ENSG00000261446.2","gene_symbol":"LINC00559","gene_name":"long intergenic non-protein coding RNA 559 [Source:HGNC Symbol;Acc:HGNC:43703]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874187","summary":null,"start":90060247,"end":90119719,"strand":-1,"description":"long intergenic non-protein coding RNA 559 [Source:HGNC Symbol;Acc:HGNC:43703]"}, {"versioned_ensembl_gene_id":"ENSG00000237566.1","gene_symbol":"AC090955.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5099627,"end":5099861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279456.1","gene_symbol":"AL353763.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41061290,"end":41062917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156508.17","gene_symbol":"EEF1A1","gene_name":"eukaryotic translation elongation factor 1 alpha 1 [Source:HGNC Symbol;Acc:HGNC:3189]","synonyms":"EEF1A,EE1A1,LENG7,EF1A","biotype":"protein_coding","ncbi_id":"1915","summary":"This gene encodes an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas, and the other isoform (alpha 2) is expressed in brain, heart and skeletal muscle. This isoform is identified as an autoantigen in 66% of patients with Felty syndrome. This gene has been found to have multiple copies on many chromosomes, some of which, if not all, represent different pseudogenes. [provided by RefSeq, Jul 2008]","start":73515750,"end":73523797,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 [Source:HGNC Symbol;Acc:HGNC:3189]"}, {"versioned_ensembl_gene_id":"ENSG00000228970.6","gene_symbol":"UBTFL6","gene_name":"upstream binding transcription factor, RNA polymerase I-like 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35406]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643615","summary":null,"start":97636780,"end":97637803,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35406]"}, {"versioned_ensembl_gene_id":"ENSG00000186051.6","gene_symbol":"TAL2","gene_name":"TAL bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11557]","synonyms":"bHLHa19","biotype":"protein_coding","ncbi_id":"6887","summary":"This intronless gene encodes a helix-loop-helix protein. Translocations between this gene on chromosome 9 and the T-cell receptor beta-chain locus on chromosome 7 have been associated with activation of the T-cell acute lymphocytic leukemia 2 gene and T-cell acute lymphoblastic leukemia. [provided by RefSeq, Mar 2009]","start":105662457,"end":105663112,"strand":1,"description":"TAL bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11557]"}, {"versioned_ensembl_gene_id":"ENSG00000272629.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859613,"end":28863339,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000273122.1","gene_symbol":"AL844539.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861404,"end":28862035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272473.1","gene_symbol":"AC006273.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":781002,"end":781862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227147.9","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"ZNF178,RNF93,ZNFB7","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30153123,"end":30162613,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000120526.10","gene_symbol":"NUDCD1","gene_name":"NudC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24306]","synonyms":"FLJ14991,CML66","biotype":"protein_coding","ncbi_id":"84955","summary":null,"start":109240919,"end":109334385,"strand":-1,"description":"NudC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24306]"}, {"versioned_ensembl_gene_id":"ENSG00000066827.15","gene_symbol":"ZFAT","gene_name":"zinc finger and AT-hook domain containing [Source:HGNC Symbol;Acc:HGNC:19899]","synonyms":"ZNF406,ZFAT1,KIAA1485","biotype":"protein_coding","ncbi_id":"57623","summary":"This gene encodes a protein that likely binds DNA and functions as a transcriptional regulator involved in apoptosis and cell survival. This gene resides in a susceptibility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009]","start":134477788,"end":134713049,"strand":-1,"description":"zinc finger and AT-hook domain containing [Source:HGNC Symbol;Acc:HGNC:19899]"}, {"versioned_ensembl_gene_id":"ENSG00000248230.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29739210,"end":29746446,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000205940.8","gene_symbol":"HSP90AB2P","gene_name":"heat shock protein 90 alpha family class B member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32537]","synonyms":"HSP90BB","biotype":"transcribed_processed_pseudogene","ncbi_id":"391634","summary":null,"start":13333414,"end":13338657,"strand":1,"description":"heat shock protein 90 alpha family class B member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32537]"}, {"versioned_ensembl_gene_id":"ENSG00000111432.4","gene_symbol":"FZD10","gene_name":"frizzled class receptor 10 [Source:HGNC Symbol;Acc:HGNC:4039]","synonyms":"CD350","biotype":"protein_coding","ncbi_id":"11211","summary":"This gene is a member of the frizzled gene family. Members of this family encode 7-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. Using array analysis, expression of this intronless gene is significantly up-regulated in two cases of primary colon cancer. [provided by RefSeq, Jul 2008]","start":130162459,"end":130165740,"strand":1,"description":"frizzled class receptor 10 [Source:HGNC Symbol;Acc:HGNC:4039]"}, {"versioned_ensembl_gene_id":"ENSG00000139625.12","gene_symbol":"MAP3K12","gene_name":"mitogen-activated protein kinase kinase kinase 12 [Source:HGNC Symbol;Acc:HGNC:6851]","synonyms":"ZPKP1,ZPK,MUK,MEKK12,DLK","biotype":"protein_coding","ncbi_id":"7786","summary":"This gene encodes a member of the serine/threonine protein kinase family. This kinase contains a leucine-zipper domain and is predominately expressed in neuronal cells. The phosphorylation state of this kinase in synaptic terminals was shown to be regulated by membrane depolarization via calcineurin. This kinase forms heterodimers with leucine zipper containing transcription factors, such as cAMP responsive element binding protein (CREB) and MYC, and thus may play a regulatory role in PKA or retinoic acid induced neuronal differentiation. Alternatively spliced transcript variants encoding different proteins have been described.[provided by RefSeq, Jul 2010]","start":53479669,"end":53500063,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 12 [Source:HGNC Symbol;Acc:HGNC:6851]"}, {"versioned_ensembl_gene_id":"ENSG00000271180.1","gene_symbol":"AL158801.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55240622,"end":55241080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231937.1","gene_symbol":"AC116666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152138883,"end":152186857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258991.1","gene_symbol":"DUX4L19","gene_name":"double homeobox 4 like 19 [Source:HGNC Symbol;Acc:HGNC:37718]","synonyms":"DUXY4","biotype":"unprocessed_pseudogene","ncbi_id":"643034","summary":null,"start":11332329,"end":11333595,"strand":1,"description":"double homeobox 4 like 19 [Source:HGNC Symbol;Acc:HGNC:37718]"}, {"versioned_ensembl_gene_id":"ENSG00000248867.1","gene_symbol":"AC010625.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109448349,"end":109449063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168679.17","gene_symbol":"SLC16A4","gene_name":"solute carrier family 16 member 4 [Source:HGNC Symbol;Acc:HGNC:10925]","synonyms":"MCT5,MCT4","biotype":"protein_coding","ncbi_id":"9122","summary":null,"start":110362848,"end":110391082,"strand":-1,"description":"solute carrier family 16 member 4 [Source:HGNC Symbol;Acc:HGNC:10925]"}, {"versioned_ensembl_gene_id":"ENSG00000231649.3","gene_symbol":"SPATA31B1P","gene_name":"SPATA31 subfamily B member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:31411]","synonyms":"SPATA31B1,FAM75B,C9orf36B,bA388B24.2","biotype":"unprocessed_pseudogene","ncbi_id":"404770","summary":null,"start":82057647,"end":82063682,"strand":-1,"description":"SPATA31 subfamily B member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:31411]"}, {"versioned_ensembl_gene_id":"ENSG00000256906.1","gene_symbol":"LINC02419","gene_name":"long intergenic non-protein coding RNA 2419 [Source:HGNC Symbol;Acc:HGNC:53349]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370078","summary":null,"start":130070325,"end":130072685,"strand":1,"description":"long intergenic non-protein coding RNA 2419 [Source:HGNC Symbol;Acc:HGNC:53349]"}, {"versioned_ensembl_gene_id":"ENSG00000187164.19","gene_symbol":"SHTN1","gene_name":"shootin 1 [Source:HGNC Symbol;Acc:HGNC:29319]","synonyms":"shootin1,shootin-1,KIAA1598","biotype":"protein_coding","ncbi_id":"57698","summary":null,"start":116881482,"end":117126586,"strand":-1,"description":"shootin 1 [Source:HGNC Symbol;Acc:HGNC:29319]"}, {"versioned_ensembl_gene_id":"ENSG00000169641.13","gene_symbol":"LUZP1","gene_name":"leucine zipper protein 1 [Source:HGNC Symbol;Acc:HGNC:14985]","synonyms":"LUZP","biotype":"protein_coding","ncbi_id":"7798","summary":"This gene encodes a protein that contains a leucine zipper motif. The exact function of the encoded protein is not known. In mice this gene affects neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":23084023,"end":23177808,"strand":-1,"description":"leucine zipper protein 1 [Source:HGNC Symbol;Acc:HGNC:14985]"}, {"versioned_ensembl_gene_id":"ENSG00000276042.4","gene_symbol":"LILRB4","gene_name":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]","synonyms":"CD85k,LIR-5,ILT3,HM18,LIR5","biotype":"protein_coding","ncbi_id":"11006","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54592642,"end":54600251,"strand":1,"description":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]"}, {"versioned_ensembl_gene_id":"ENSG00000266200.6","gene_symbol":"PNLIPRP2","gene_name":"pancreatic lipase related protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:9157]","synonyms":"PLRP2","biotype":"polymorphic_pseudogene","ncbi_id":"5408","summary":"This gene encodes a lipase that hydrolyzes galactolipids, the main components of plant membrane lipids. An allelic polymorphism in this gene results in both coding and non-coding variants; the reference genome represents the non-coding allele. [provided by RefSeq, Aug 2015]","start":116620953,"end":116645143,"strand":1,"description":"pancreatic lipase related protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:9157]"}, {"versioned_ensembl_gene_id":"ENSG00000168792.4","gene_symbol":"ABHD15","gene_name":"abhydrolase domain containing 15 [Source:HGNC Symbol;Acc:HGNC:26971]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116236","summary":null,"start":29560547,"end":29567137,"strand":-1,"description":"abhydrolase domain containing 15 [Source:HGNC Symbol;Acc:HGNC:26971]"}, {"versioned_ensembl_gene_id":"ENSG00000184564.8","gene_symbol":"SLITRK6","gene_name":"SLIT and NTRK like family member 6 [Source:HGNC Symbol;Acc:HGNC:23503]","synonyms":"FLJ22774","biotype":"protein_coding","ncbi_id":"84189","summary":"This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014]","start":85792790,"end":85799488,"strand":-1,"description":"SLIT and NTRK like family member 6 [Source:HGNC Symbol;Acc:HGNC:23503]"}, {"versioned_ensembl_gene_id":"ENSG00000259017.1","gene_symbol":"AL133163.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35447003,"end":35447625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266919.3","gene_symbol":"AC104984.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30117079,"end":30117172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154342.5","gene_symbol":"WNT3A","gene_name":"Wnt family member 3A [Source:HGNC Symbol;Acc:HGNC:15983]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89780","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 96% amino acid identity to mouse Wnt3A protein, and 84% to human WNT3 protein, another WNT gene product. This gene is clustered with WNT14 gene, another family member, in chromosome 1q42 region. [provided by RefSeq, Jul 2008]","start":228007051,"end":228061260,"strand":1,"description":"Wnt family member 3A [Source:HGNC Symbol;Acc:HGNC:15983]"}, {"versioned_ensembl_gene_id":"ENSG00000226317.2","gene_symbol":"LINC00351","gene_name":"long intergenic non-protein coding RNA 351 [Source:HGNC Symbol;Acc:HGNC:42669]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874137","summary":null,"start":85363601,"end":85544570,"strand":1,"description":"long intergenic non-protein coding RNA 351 [Source:HGNC Symbol;Acc:HGNC:42669]"}, {"versioned_ensembl_gene_id":"ENSG00000271490.1","gene_symbol":"AC013244.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50806335,"end":50806437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167720.12","gene_symbol":"SRR","gene_name":"serine racemase [Source:HGNC Symbol;Acc:HGNC:14398]","synonyms":"ISO1,ILV1","biotype":"protein_coding","ncbi_id":"63826","summary":null,"start":2303383,"end":2325260,"strand":1,"description":"serine racemase [Source:HGNC Symbol;Acc:HGNC:14398]"}, {"versioned_ensembl_gene_id":"ENSG00000232907.7","gene_symbol":"DLGAP4-AS1","gene_name":"DLGAP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51223]","synonyms":"CCAT7","biotype":"antisense_RNA","ncbi_id":"101926987","summary":null,"start":36507702,"end":36573391,"strand":-1,"description":"DLGAP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51223]"}, {"versioned_ensembl_gene_id":"ENSG00000244245.1","gene_symbol":"AC133134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108593609,"end":108593967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186268.3","gene_symbol":"OR10D4P","gene_name":"olfactory receptor family 10 subfamily D member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14770]","synonyms":"OR10D6P,OR10D4","biotype":"unprocessed_pseudogene","ncbi_id":"390266","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124093582,"end":124094532,"strand":-1,"description":"olfactory receptor family 10 subfamily D member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14770]"}, {"versioned_ensembl_gene_id":"ENSG00000182634.8","gene_symbol":"OR10G7","gene_name":"olfactory receptor family 10 subfamily G member 7 [Source:HGNC Symbol;Acc:HGNC:14842]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390265","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124036013,"end":124041325,"strand":-1,"description":"olfactory receptor family 10 subfamily G member 7 [Source:HGNC Symbol;Acc:HGNC:14842]"}, {"versioned_ensembl_gene_id":"ENSG00000103404.14","gene_symbol":"USP31","gene_name":"ubiquitin specific peptidase 31 [Source:HGNC Symbol;Acc:HGNC:20060]","synonyms":"KIAA1203","biotype":"protein_coding","ncbi_id":"57478","summary":null,"start":23061406,"end":23149270,"strand":-1,"description":"ubiquitin specific peptidase 31 [Source:HGNC Symbol;Acc:HGNC:20060]"}, {"versioned_ensembl_gene_id":"ENSG00000280400.1","gene_symbol":"AC127459.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23061767,"end":23062232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182979.17","gene_symbol":"MTA1","gene_name":"metastasis associated 1 [Source:HGNC Symbol;Acc:HGNC:7410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9112","summary":"This gene encodes a protein that was identified in a screen for genes expressed in metastatic cells, specifically, mammary adenocarcinoma cell lines. Expression of this gene has been correlated with the metastatic potential of at least two types of carcinomas although it is also expressed in many normal tissues. The role it plays in metastasis is unclear. It was initially thought to be the 70kD component of a nucleosome remodeling deacetylase complex, NuRD, but it is more likely that this component is a different but very similar protein. These two proteins are so closely related, though, that they share the same types of domains. These domains include two DNA binding domains, a dimerization domain, and a domain commonly found in proteins that methylate DNA. The profile and activity of this gene product suggest that it is involved in regulating transcription and that this may be accomplished by chromatin remodeling. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":105419820,"end":105470729,"strand":1,"description":"metastasis associated 1 [Source:HGNC Symbol;Acc:HGNC:7410]"}, {"versioned_ensembl_gene_id":"ENSG00000185198.11","gene_symbol":"PRSS57","gene_name":"protease, serine 57 [Source:HGNC Symbol;Acc:HGNC:31397]","synonyms":"PRSSL1,UNQ782","biotype":"protein_coding","ncbi_id":"400668","summary":"This gene encodes an arginine-specific serine protease and member of the peptidase S1 family of proteins. The encoded protein may undergo proteolytic activation before storage in azurophil granules, in neutrophil cells of the immune system. Following neutrophil activation, the protease is released into the pericellular environment, where it may play a role in defense against microbial pathogens. [provided by RefSeq, Jul 2016]","start":685546,"end":695498,"strand":-1,"description":"protease, serine 57 [Source:HGNC Symbol;Acc:HGNC:31397]"}, {"versioned_ensembl_gene_id":"ENSG00000122254.6","gene_symbol":"HS3ST2","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:5195]","synonyms":"3OST2","biotype":"protein_coding","ncbi_id":"9956","summary":"Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. The enzyme encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. It is a type II integral membrane protein and possesses heparan sulfate glucosaminyl 3-O-sulfotransferase activity. This gene is expressed predominantly in brain and may play a role in the nervous system. [provided by RefSeq, Jul 2008]","start":22814177,"end":22916338,"strand":1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:5195]"}, {"versioned_ensembl_gene_id":"ENSG00000103769.9","gene_symbol":"RAB11A","gene_name":"RAB11A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9760]","synonyms":"YL8","biotype":"protein_coding","ncbi_id":"8766","summary":"The protein encoded by this gene belongs to the Rab family of the small GTPase superfamily. It is associated with both constitutive and regulated secretory pathways, and may be involved in protein transport. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":65726054,"end":65891991,"strand":1,"description":"RAB11A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9760]"}, {"versioned_ensembl_gene_id":"ENSG00000184349.12","gene_symbol":"EFNA5","gene_name":"ephrin A5 [Source:HGNC Symbol;Acc:HGNC:3225]","synonyms":"LERK7,EPLG7,AF1","biotype":"protein_coding","ncbi_id":"1946","summary":"Ephrin-A5, a member of the ephrin gene family, prevents axon bundling in cocultures of cortical neurons with astrocytes, a model of late stage nervous system development and differentiation. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. EPH receptors typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin ligands and receptors have been named by the Eph Nomenclature Committee (1997). Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are similarly divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. [provided by RefSeq, Jul 2008]","start":107376889,"end":107670895,"strand":-1,"description":"ephrin A5 [Source:HGNC Symbol;Acc:HGNC:3225]"}, {"versioned_ensembl_gene_id":"ENSG00000096696.13","gene_symbol":"DSP","gene_name":"desmoplakin [Source:HGNC Symbol;Acc:HGNC:3052]","synonyms":"PPKS2,KPPS2,DPII,DPI","biotype":"protein_coding","ncbi_id":"1832","summary":"This gene encodes a protein that anchors intermediate filaments to desmosomal plaques and forms an obligate component of functional desmosomes. Mutations in this gene are the cause of several cardiomyopathies and keratodermas, including skin fragility-woolly hair syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":7541575,"end":7586717,"strand":1,"description":"desmoplakin [Source:HGNC Symbol;Acc:HGNC:3052]"}, {"versioned_ensembl_gene_id":"ENSG00000120705.12","gene_symbol":"ETF1","gene_name":"eukaryotic translation termination factor 1 [Source:HGNC Symbol;Acc:HGNC:3477]","synonyms":"SUP45L1,RF1,ERF1,ERF,TB3-1","biotype":"protein_coding","ncbi_id":"2107","summary":"This gene encodes a class-1 polypeptide chain release factor. The encoded protein plays an essential role in directing termination of mRNA translation from the termination codons UAA, UAG and UGA. This protein is a component of the SURF complex which promotes degradation of prematurely terminated mRNAs via the mechanism of nonsense-mediated mRNA decay (NMD). Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 6, 7, and X. [provided by RefSeq, Aug 2013]","start":138506095,"end":138543300,"strand":-1,"description":"eukaryotic translation termination factor 1 [Source:HGNC Symbol;Acc:HGNC:3477]"}, {"versioned_ensembl_gene_id":"ENSG00000250364.6","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29374013,"end":29450575,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000102287.18","gene_symbol":"GABRE","gene_name":"gamma-aminobutyric acid type A receptor epsilon subunit [Source:HGNC Symbol;Acc:HGNC:4085]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2564","summary":"The product of this gene belongs to the ligand-gated ionic channel (TC 1.A.9) family. It encodes the gamma-aminobutyric acid (GABA) A receptor which is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. This gene encodes an epsilon subunit. It is mapped to chromosome Xq28 in a cluster comprised of genes encoding alpha 3, beta 4 and theta subunits of the same receptor. Alternatively spliced transcript variants have been identified, but only one is thought to encode a protein. [provided by RefSeq, Oct 2008]","start":151953124,"end":151974680,"strand":-1,"description":"gamma-aminobutyric acid type A receptor epsilon subunit [Source:HGNC Symbol;Acc:HGNC:4085]"}, {"versioned_ensembl_gene_id":"ENSG00000103024.7","gene_symbol":"NME3","gene_name":"NME/NM23 nucleoside diphosphate kinase 3 [Source:HGNC Symbol;Acc:HGNC:7851]","synonyms":"NM23-H3,NDPKC,DR-nm23","biotype":"protein_coding","ncbi_id":"4832","summary":null,"start":1770286,"end":1771730,"strand":-1,"description":"NME/NM23 nucleoside diphosphate kinase 3 [Source:HGNC Symbol;Acc:HGNC:7851]"}, {"versioned_ensembl_gene_id":"ENSG00000258417.3","gene_symbol":"AC100868.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":132024238,"end":132085655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116039.11","gene_symbol":"ATP6V1B1","gene_name":"ATPase H+ transporting V1 subunit B1 [Source:HGNC Symbol;Acc:HGNC:853]","synonyms":"ATP6B1,VPP3,Vma2,VATB,RTA1B","biotype":"protein_coding","ncbi_id":"525","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain B subunit isoforms and is found in the kidney. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. [provided by RefSeq, Jul 2008]","start":70935882,"end":70965406,"strand":1,"description":"ATPase H+ transporting V1 subunit B1 [Source:HGNC Symbol;Acc:HGNC:853]"}, {"versioned_ensembl_gene_id":"ENSG00000224538.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29901898,"end":29902760,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000237072.1","gene_symbol":"AL161727.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81488308,"end":81488837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272735.1","gene_symbol":"AC007881.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71067519,"end":71068125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180616.8","gene_symbol":"SSTR2","gene_name":"somatostatin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11331]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6752","summary":"Somatostatin acts at many sites to inhibit the release of many hormones and other secretory proteins. The biologic effects of somatostatin are probably mediated by a family of G protein-coupled receptors that are expressed in a tissue-specific manner. SSTR2 is a member of the superfamily of receptors having seven transmembrane segments and is expressed in highest levels in cerebrum and kidney. [provided by RefSeq, Jul 2008]","start":73165012,"end":73176633,"strand":1,"description":"somatostatin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11331]"}, {"versioned_ensembl_gene_id":"ENSG00000282407.1","gene_symbol":"AC229888.6","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142577660,"end":142578143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125503.12","gene_symbol":"PPP1R12C","gene_name":"protein phosphatase 1 regulatory subunit 12C [Source:HGNC Symbol;Acc:HGNC:14947]","synonyms":"p85,p84,MBS85,LENG3,DKFZP434D0412","biotype":"protein_coding","ncbi_id":"54776","summary":"The gene encodes a subunit of myosin phosphatase. The encoded protein regulates the catalytic activity of protein phosphatase 1 delta and assembly of the actin cytoskeleton. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]","start":55090913,"end":55117559,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 12C [Source:HGNC Symbol;Acc:HGNC:14947]"}, {"versioned_ensembl_gene_id":"ENSG00000266501.1","gene_symbol":"AC025198.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73067870,"end":73068288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230359.5","gene_symbol":"TPI1P2","gene_name":"triosephosphate isomerase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38069]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"286016","summary":null,"start":129055223,"end":129057239,"strand":1,"description":"triosephosphate isomerase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38069]"}, {"versioned_ensembl_gene_id":"ENSG00000154265.15","gene_symbol":"ABCA5","gene_name":"ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]","synonyms":"EST90625","biotype":"protein_coding","ncbi_id":"23461","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":69244311,"end":69327244,"strand":-1,"description":"ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]"}, {"versioned_ensembl_gene_id":"ENSG00000248853.1","gene_symbol":"AC113352.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121059244,"end":121060953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239552.2","gene_symbol":"HOXB-AS2","gene_name":"HOXB cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40284]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874350","summary":null,"start":48557262,"end":48560333,"strand":1,"description":"HOXB cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40284]"}, {"versioned_ensembl_gene_id":"ENSG00000248394.1","gene_symbol":"FOSL1P1","gene_name":"FOS like 1, AP-1 transcription factor subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419062","summary":null,"start":128155389,"end":128156204,"strand":1,"description":"FOS like 1, AP-1 transcription factor subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44055]"}, {"versioned_ensembl_gene_id":"ENSG00000103429.10","gene_symbol":"BFAR","gene_name":"bifunctional apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:17613]","synonyms":"RNF47,BAR","biotype":"protein_coding","ncbi_id":"51283","summary":null,"start":14632815,"end":14669236,"strand":1,"description":"bifunctional apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:17613]"}, {"versioned_ensembl_gene_id":"ENSG00000240934.2","gene_symbol":"AC066616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58200606,"end":58201018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259293.1","gene_symbol":"LIPC-AS1","gene_name":"LIPC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52294]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928694","summary":null,"start":58434890,"end":58498735,"strand":-1,"description":"LIPC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52294]"}, {"versioned_ensembl_gene_id":"ENSG00000280461.1","gene_symbol":"ABCB10P1","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]","synonyms":"ABCB10P2,ABCB10P,MABC2,M-ABC2","biotype":"processed_pseudogene","ncbi_id":"56476","summary":null,"start":23183337,"end":23185517,"strand":1,"description":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]"}, {"versioned_ensembl_gene_id":"ENSG00000259626.2","gene_symbol":"MTND3P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52072]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075160","summary":null,"start":58150635,"end":58150962,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52072]"}, {"versioned_ensembl_gene_id":"ENSG00000132305.20","gene_symbol":"IMMT","gene_name":"inner membrane mitochondrial protein [Source:HGNC Symbol;Acc:HGNC:6047]","synonyms":"P89,P87,MINOS2,Mic60,HMP","biotype":"protein_coding","ncbi_id":"10989","summary":null,"start":86143932,"end":86195770,"strand":-1,"description":"inner membrane mitochondrial protein [Source:HGNC Symbol;Acc:HGNC:6047]"}, {"versioned_ensembl_gene_id":"ENSG00000278616.1","gene_symbol":"BEND3P3","gene_name":"BEN domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"650623","summary":null,"start":79682997,"end":79685436,"strand":1,"description":"BEN domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45016]"}, {"versioned_ensembl_gene_id":"ENSG00000272489.1","gene_symbol":"AL132656.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79663192,"end":79664786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282704.1","gene_symbol":"TRBV7-6","gene_name":"T-cell receptor beta variable 7-6 [Source:HGNC Symbol;Acc:HGNC:12240]","synonyms":"TRBV76,TCRBV7S6,TCRBV6S3A1N1T","biotype":"TR_V_gene","ncbi_id":"28592","summary":null,"start":142513848,"end":142514385,"strand":1,"description":"T-cell receptor beta variable 7-6 [Source:HGNC Symbol;Acc:HGNC:12240]"}, {"versioned_ensembl_gene_id":"ENSG00000213863.2","gene_symbol":"AL731661.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170725197,"end":170728488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232548.1","gene_symbol":"LINC01809","gene_name":"long intergenic non-protein coding RNA 1809 [Source:HGNC Symbol;Acc:HGNC:52612]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928031","summary":null,"start":83522814,"end":83523502,"strand":1,"description":"long intergenic non-protein coding RNA 1809 [Source:HGNC Symbol;Acc:HGNC:52612]"}, {"versioned_ensembl_gene_id":"ENSG00000236762.1","gene_symbol":"RPL19P16","gene_name":"ribosomal protein L19 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36596]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646255","summary":null,"start":121133090,"end":121133723,"strand":-1,"description":"ribosomal protein L19 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36596]"}, {"versioned_ensembl_gene_id":"ENSG00000259600.2","gene_symbol":"AC066616.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58151033,"end":58152513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207101.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41803349,"end":41803450,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000099250.17","gene_symbol":"NRP1","gene_name":"neuropilin 1 [Source:HGNC Symbol;Acc:HGNC:8004]","synonyms":"VEGF165R,NRP,CD304","biotype":"protein_coding","ncbi_id":"8829","summary":"This gene encodes one of two neuropilins, which contain specific protein domains which allow them to participate in several different types of signaling pathways that control cell migration. Neuropilins contain a large N-terminal extracellular domain, made up of complement-binding, coagulation factor V/VIII, and meprin domains. These proteins also contains a short membrane-spanning domain and a small cytoplasmic domain. Neuropilins bind many ligands and various types of co-receptors; they affect cell survival, migration, and attraction. Some of the ligands and co-receptors bound by neuropilins are vascular endothelial growth factor (VEGF) and semaphorin family members. This protein has also been determined to act as a co-receptor for SARS-CoV-2 (which causes COVID-19) to infect host cells. [provided by RefSeq, Nov 2020]","start":33177492,"end":33336262,"strand":-1,"description":"neuropilin 1 [Source:HGNC Symbol;Acc:HGNC:8004]"}, {"versioned_ensembl_gene_id":"ENSG00000117407.16","gene_symbol":"ARTN","gene_name":"artemin [Source:HGNC Symbol;Acc:HGNC:727]","synonyms":"NBN,EVN,ENOVIN","biotype":"protein_coding","ncbi_id":"9048","summary":"This gene encodes a secreted ligand of the glial cell line-derived neurotrophic factor (GDNF) subfamily and TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein signals through the RET receptor and GFR alpha 3 coreceptor, and supports the survival of a number of peripheral neuron populations and at least one population of dopaminergic CNS neurons. This protein has also been shown to promote tumor growth, metastasis, and drug resistance in mammary carcinoma. [provided by RefSeq, Aug 2016]","start":43933320,"end":43937241,"strand":1,"description":"artemin [Source:HGNC Symbol;Acc:HGNC:727]"}, {"versioned_ensembl_gene_id":"ENSG00000238002.2","gene_symbol":"NPAP1P6","gene_name":"nuclear pore associated protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533675","summary":null,"start":79863019,"end":79866875,"strand":1,"description":"nuclear pore associated protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45023]"}, {"versioned_ensembl_gene_id":"ENSG00000061337.15","gene_symbol":"LZTS1","gene_name":"leucine zipper tumor suppressor 1 [Source:HGNC Symbol;Acc:HGNC:13861]","synonyms":"FEZ1","biotype":"protein_coding","ncbi_id":"11178","summary":"This gene encodes a tumor suppressor protein that is ubiquitously expressed in normal tissues. In uveal melanomas, expression of this protein is silenced in rapidly metastasizing and metastatic tumor cells but has normal expression in slowly metastasizing or nonmetastasizing tumor cells. This protein may have a role in cell-cycle control by interacting with the Cdk1/cyclinB1 complex. This gene is located on chromosomal region 8p22. Loss of heterozygosity (LOH) in the 8p arm is a common characteristic of many types of cancer. [provided by RefSeq, Nov 2009]","start":20246165,"end":20303963,"strand":-1,"description":"leucine zipper tumor suppressor 1 [Source:HGNC Symbol;Acc:HGNC:13861]"}, {"versioned_ensembl_gene_id":"ENSG00000185982.6","gene_symbol":"DEFB128","gene_name":"defensin beta 128 [Source:HGNC Symbol;Acc:HGNC:18106]","synonyms":"DEFB-28","biotype":"protein_coding","ncbi_id":"245939","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":187853,"end":189681,"strand":-1,"description":"defensin beta 128 [Source:HGNC Symbol;Acc:HGNC:18106]"}, {"versioned_ensembl_gene_id":"ENSG00000260163.1","gene_symbol":"AC012508.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127025211,"end":127029686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173369.15","gene_symbol":"C1QB","gene_name":"complement C1q B chain [Source:HGNC Symbol;Acc:HGNC:1242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"713","summary":"This gene encodes the B-chain polypeptide of serum complement subcomponent C1q, which associates with C1r and C1s to yield the first component of the serum complement system. C1q is composed of 18 polypeptide chains which include 6 A-chains, 6 B-chains, and 6 C-chains. Each chain contains an N-terminal collagen-like region and a C-terminal C1q globular domain. C1q deficiency is associated with lupus erythematosus and glomerulonephritis. [provided by RefSeq, Dec 2016]","start":22652762,"end":22661538,"strand":1,"description":"complement C1q B chain [Source:HGNC Symbol;Acc:HGNC:1242]"}, {"versioned_ensembl_gene_id":"ENSG00000229011.1","gene_symbol":"LINC01038","gene_name":"long intergenic non-protein coding RNA 1038 [Source:HGNC Symbol;Acc:HGNC:49026]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724076","summary":null,"start":79804418,"end":79805685,"strand":1,"description":"long intergenic non-protein coding RNA 1038 [Source:HGNC Symbol;Acc:HGNC:49026]"}, {"versioned_ensembl_gene_id":"ENSG00000076053.10","gene_symbol":"RBM7","gene_name":"RNA binding motif protein 7 [Source:HGNC Symbol;Acc:HGNC:9904]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10179","summary":null,"start":114400030,"end":114414203,"strand":1,"description":"RNA binding motif protein 7 [Source:HGNC Symbol;Acc:HGNC:9904]"}, {"versioned_ensembl_gene_id":"ENSG00000159322.17","gene_symbol":"ADPGK","gene_name":"ADP dependent glucokinase [Source:HGNC Symbol;Acc:HGNC:25250]","synonyms":"DKFZp434B195,ADP-GK","biotype":"protein_coding","ncbi_id":"83440","summary":"ADPGK (EC 2.7.1.147) catalyzes the ADP-dependent phosphorylation of glucose to glucose-6-phosphate and may play a role in glycolysis, possibly during ischemic conditions (Ronimus and Morgan, 2004 [PubMed 14975750]).[supplied by OMIM, Mar 2008]","start":72751369,"end":72785846,"strand":-1,"description":"ADP dependent glucokinase [Source:HGNC Symbol;Acc:HGNC:25250]"}, {"versioned_ensembl_gene_id":"ENSG00000129991.12","gene_symbol":"TNNI3","gene_name":"troponin I3, cardiac type [Source:HGNC Symbol;Acc:HGNC:11947]","synonyms":"TNNC1,CMH7,CMD2A","biotype":"protein_coding","ncbi_id":"7137","summary":"Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. This gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM). Troponin I is useful in making a diagnosis of heart failure, and of ischemic heart disease. An elevated level of troponin is also now used as indicator of acute myocardial injury in patients hospitalized with moderate/severe Coronavirus Disease 2019 (COVID-19). Such elevation has also been associated with higher risk of mortality in cardiovascular disease patients hospitalized due to COVID-19. [provided by RefSeq, Aug 2020]","start":55151767,"end":55157773,"strand":-1,"description":"troponin I3, cardiac type [Source:HGNC Symbol;Acc:HGNC:11947]"}, {"versioned_ensembl_gene_id":"ENSG00000171446.6","gene_symbol":"KRT27","gene_name":"keratin 27 [Source:HGNC Symbol;Acc:HGNC:30841]","synonyms":"KRT25C","biotype":"protein_coding","ncbi_id":"342574","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40776808,"end":40782534,"strand":-1,"description":"keratin 27 [Source:HGNC Symbol;Acc:HGNC:30841]"}, {"versioned_ensembl_gene_id":"ENSG00000214857.4","gene_symbol":"SEM1P1","gene_name":"SEM1, 26S proteasome complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24454]","synonyms":"SHFM1P1,SHFM1P,DSS1P1","biotype":"processed_pseudogene","ncbi_id":"153842","summary":null,"start":81892490,"end":81892721,"strand":1,"description":"SEM1, 26S proteasome complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24454]"}, {"versioned_ensembl_gene_id":"ENSG00000274695.1","gene_symbol":"AC108704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128826836,"end":128827579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201420.1","gene_symbol":"RNA5SP512","gene_name":"RNA, 5S ribosomal pseudogene 512 [Source:HGNC Symbol;Acc:HGNC:43412]","synonyms":"RN5S512","biotype":"rRNA","ncbi_id":"100873563","summary":null,"start":111669829,"end":111669948,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 512 [Source:HGNC Symbol;Acc:HGNC:43412]"}, {"versioned_ensembl_gene_id":"ENSG00000249743.5","gene_symbol":"AC116345.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73213947,"end":73294934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136942.14","gene_symbol":"RPL35","gene_name":"ribosomal protein L35 [Source:HGNC Symbol;Acc:HGNC:10344]","synonyms":"L35","biotype":"protein_coding","ncbi_id":"11224","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L29P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":124857880,"end":124861981,"strand":-1,"description":"ribosomal protein L35 [Source:HGNC Symbol;Acc:HGNC:10344]"}, {"versioned_ensembl_gene_id":"ENSG00000109906.13","gene_symbol":"ZBTB16","gene_name":"zinc finger and BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:12930]","synonyms":"ZNF145,PLZF","biotype":"protein_coding","ncbi_id":"7704","summary":"This gene is a member of the Krueppel C2H2-type zinc-finger protein family and encodes a zinc finger transcription factor that contains nine Kruppel-type zinc finger domains at the carboxyl terminus. This protein is located in the nucleus, is involved in cell cycle progression, and interacts with a histone deacetylase. Specific instances of aberrant gene rearrangement at this locus have been associated with acute promyelocytic leukemia (APL). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":114059593,"end":114250676,"strand":1,"description":"zinc finger and BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:12930]"}, {"versioned_ensembl_gene_id":"ENSG00000070808.15","gene_symbol":"CAMK2A","gene_name":"calcium/calmodulin dependent protein kinase II alpha [Source:HGNC Symbol;Acc:HGNC:1460]","synonyms":"KIAA0968,CaMKIINalpha,CAMKA","biotype":"protein_coding","ncbi_id":"815","summary":"The product of this gene belongs to the serine/threonine protein kinases family, and to the Ca(2+)/calmodulin-dependent protein kinases subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. This calcium calmodulin-dependent protein kinase is composed of four different chains: alpha, beta, gamma, and delta. The alpha chain encoded by this gene is required for hippocampal long-term potentiation (LTP) and spatial learning. In addition to its calcium-calmodulin (CaM)-dependent activity, this protein can undergo autophosphorylation, resulting in CaM-independent activity. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2018]","start":150219491,"end":150290291,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II alpha [Source:HGNC Symbol;Acc:HGNC:1460]"}, {"versioned_ensembl_gene_id":"ENSG00000237300.2","gene_symbol":"MTCO1P19","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075144","summary":null,"start":102796251,"end":102797093,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52021]"}, {"versioned_ensembl_gene_id":"ENSG00000030419.16","gene_symbol":"IKZF2","gene_name":"IKAROS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13177]","synonyms":"ZNFN1A2,Helios","biotype":"protein_coding","ncbi_id":"22807","summary":"This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This protein forms homo- or hetero-dimers with other Ikaros family members, and is thought to function predominantly in early hematopoietic development. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":212999691,"end":213152427,"strand":-1,"description":"IKAROS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13177]"}, {"versioned_ensembl_gene_id":"ENSG00000234429.1","gene_symbol":"AC105342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81194337,"end":81201184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234424.2","gene_symbol":"AL353743.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85753306,"end":85786575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261751.1","gene_symbol":"AC007603.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49920730,"end":49924154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148200.16","gene_symbol":"NR6A1","gene_name":"nuclear receptor subfamily 6 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7985]","synonyms":"CT150,RTR,GCNF1,GCNF","biotype":"protein_coding","ncbi_id":"2649","summary":"This gene encodes an orphan nuclear receptor which is a member of the nuclear hormone receptor family. Its expression pattern suggests that it may be involved in neurogenesis and germ cell development. The protein can homodimerize and bind DNA, but in vivo targets have not been identified. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jun 2013]","start":124517275,"end":124771310,"strand":-1,"description":"nuclear receptor subfamily 6 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7985]"}, {"versioned_ensembl_gene_id":"ENSG00000117360.12","gene_symbol":"PRPF3","gene_name":"pre-mRNA processing factor 3 [Source:HGNC Symbol;Acc:HGNC:17348]","synonyms":"SNRNP90,RP18,Prp3,hPrp3","biotype":"protein_coding","ncbi_id":"9129","summary":"The removal of introns from nuclear pre-mRNAs occurs on complexes called spliceosomes, which are made up of 4 small nuclear ribonucleoprotein (snRNP) particles and an undefined number of transiently associated splicing factors. This gene product is one of several proteins that associate with U4 and U6 snRNPs. Mutations in this gene are associated with retinitis pigmentosa-18. [provided by RefSeq, Jul 2008]","start":150321476,"end":150353195,"strand":1,"description":"pre-mRNA processing factor 3 [Source:HGNC Symbol;Acc:HGNC:17348]"}, {"versioned_ensembl_gene_id":"ENSG00000147655.10","gene_symbol":"RSPO2","gene_name":"R-spondin 2 [Source:HGNC Symbol;Acc:HGNC:28583]","synonyms":"MGC35555","biotype":"protein_coding","ncbi_id":"340419","summary":"This gene encodes a member of the R-spondin family of proteins. These proteins are secreted ligands of leucine-rich repeat containing G protein-coupled receptors that enhance Wnt signaling through the inhibition of ubiquitin E3 ligases. A chromosomal translocation including this locus that results in the formation of a gene fusion has been identified in multiple human cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":107899316,"end":108083648,"strand":-1,"description":"R-spondin 2 [Source:HGNC Symbol;Acc:HGNC:28583]"}, {"versioned_ensembl_gene_id":"ENSG00000165494.11","gene_symbol":"PCF11","gene_name":"PCF11 cleavage and polyadenylation factor subunit [Source:HGNC Symbol;Acc:HGNC:30097]","synonyms":"KIAA0824","biotype":"protein_coding","ncbi_id":"51585","summary":"The protein encoded by this gene binds to CLP1 to form pre-mRNA cleavage factor IIm. The encoded protein is necessary for efficient Pol II transcription termination and may be involved in degradation of the 3' product of polyA site cleavage. [provided by RefSeq, Oct 2016]","start":83156988,"end":83187451,"strand":1,"description":"PCF11 cleavage and polyadenylation factor subunit [Source:HGNC Symbol;Acc:HGNC:30097]"}, {"versioned_ensembl_gene_id":"ENSG00000251639.2","gene_symbol":"AC092535.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1100016,"end":1101558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274780.2","gene_symbol":"PHRF1","gene_name":"PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:24351]","synonyms":"PPP1R125,KIAA1542,RNF221","biotype":"protein_coding","ncbi_id":"57661","summary":null,"start":576501,"end":612474,"strand":1,"description":"PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:24351]"}, {"versioned_ensembl_gene_id":"ENSG00000273243.1","gene_symbol":"Z82243.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45155539,"end":45156011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177045.7","gene_symbol":"SIX5","gene_name":"SIX homeobox 5 [Source:HGNC Symbol;Acc:HGNC:10891]","synonyms":"DMAHP","biotype":"protein_coding","ncbi_id":"147912","summary":"The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2. [provided by RefSeq, Jul 2009]","start":45764785,"end":45769226,"strand":-1,"description":"SIX homeobox 5 [Source:HGNC Symbol;Acc:HGNC:10891]"}, {"versioned_ensembl_gene_id":"ENSG00000201161.1","gene_symbol":"RN7SKP10","gene_name":"RNA, 7SK small nuclear pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42628]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873873","summary":null,"start":109915096,"end":109915420,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42628]"}, {"versioned_ensembl_gene_id":"ENSG00000263468.1","gene_symbol":"hsa-mir-3130-1","gene_name":"hsa-mir-3130-1 [Source:miRBase;Acc:MI0014147]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":206783234,"end":206783308,"strand":1,"description":"hsa-mir-3130-1 [Source:miRBase;Acc:MI0014147]"}, {"versioned_ensembl_gene_id":"ENSG00000261879.5","gene_symbol":"AC087500.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5192084,"end":5248069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263164.1","gene_symbol":"AC087500.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5240508,"end":5241543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089737.16","gene_symbol":"DDX24","gene_name":"DEAD-box helicase 24 [Source:HGNC Symbol;Acc:HGNC:13266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57062","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which shows little similarity to any of the other known human DEAD box proteins, but shows a high similarity to mouse Ddx24 at the amino acid level. [provided by RefSeq, Jul 2008]","start":94048291,"end":94081245,"strand":-1,"description":"DEAD-box helicase 24 [Source:HGNC Symbol;Acc:HGNC:13266]"}, {"versioned_ensembl_gene_id":"ENSG00000226328.6","gene_symbol":"NUP50-AS1","gene_name":"NUP50 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506714","summary":null,"start":45133020,"end":45163781,"strand":-1,"description":"NUP50 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50502]"}, {"versioned_ensembl_gene_id":"ENSG00000130822.15","gene_symbol":"PNCK","gene_name":"pregnancy up-regulated nonubiquitous CaM kinase [Source:HGNC Symbol;Acc:HGNC:13415]","synonyms":"MGC45419,CaMK1b","biotype":"protein_coding","ncbi_id":"139728","summary":"PNCK is a member of the calcium/calmodulin-dependent protein kinase family of protein serine/threonine kinases (see CAMK1; MIM 604998) (Gardner et al., 2000 [PubMed 10673339]).[supplied by OMIM, Mar 2008]","start":153669730,"end":153689010,"strand":-1,"description":"pregnancy up-regulated nonubiquitous CaM kinase [Source:HGNC Symbol;Acc:HGNC:13415]"}, {"versioned_ensembl_gene_id":"ENSG00000270807.1","gene_symbol":"AC024153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33717853,"end":33718217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113460.12","gene_symbol":"BRIX1","gene_name":"BRX1, biogenesis of ribosomes [Source:HGNC Symbol;Acc:HGNC:24170]","synonyms":"FLJ11100,BXDC2,BRIX","biotype":"protein_coding","ncbi_id":"55299","summary":null,"start":34915376,"end":34925996,"strand":1,"description":"BRX1, biogenesis of ribosomes [Source:HGNC Symbol;Acc:HGNC:24170]"}, {"versioned_ensembl_gene_id":"ENSG00000227542.1","gene_symbol":"AC092614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191229165,"end":191246172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118194.18","gene_symbol":"TNNT2","gene_name":"troponin T2, cardiac type [Source:HGNC Symbol;Acc:HGNC:11949]","synonyms":"CMPD2,CMH2,CMD1D","biotype":"protein_coding","ncbi_id":"7139","summary":"The protein encoded by this gene is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. Transcripts for this gene undergo alternative splicing that results in many tissue-specific isoforms, however, the full-length nature of some of these variants has not yet been determined. [provided by RefSeq, Jul 2008]","start":201359008,"end":201377762,"strand":-1,"description":"troponin T2, cardiac type [Source:HGNC Symbol;Acc:HGNC:11949]"}, {"versioned_ensembl_gene_id":"ENSG00000108963.17","gene_symbol":"DPH1","gene_name":"diphthamide biosynthesis 1 [Source:HGNC Symbol;Acc:HGNC:3003]","synonyms":"OVCA1,DPH2L1,DPH2L","biotype":"protein_coding","ncbi_id":"1801","summary":"The protein encoded by this gene is an enzyme involved in the biosynthesis of diphthamide, a modified histidine found only in elongation factor-2 (EEF2). Diphthamide residues in EEF2 are targeted for ADP-ribosylation by diphtheria toxin and Pseudomonas exotoxin A. Defects in this gene have been associated with both ovarian cancer and autosomal recessive intellectual disability with short stature, craniofacial, and ectodermal anomalies. [provided by RefSeq, Oct 2016]","start":2030110,"end":2043430,"strand":1,"description":"diphthamide biosynthesis 1 [Source:HGNC Symbol;Acc:HGNC:3003]"}, {"versioned_ensembl_gene_id":"ENSG00000237010.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"processed_transcript","ncbi_id":"414760","summary":null,"start":28897398,"end":28898188,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000268434.5","gene_symbol":"AC011530.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":45779437,"end":45785973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256538.1","gene_symbol":"AC046130.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34037438,"end":34056740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233387.1","gene_symbol":"AL121748.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33096257,"end":33116672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197355.10","gene_symbol":"UAP1L1","gene_name":"UDP-N-acetylglucosamine pyrophosphorylase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28082]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91373","summary":null,"start":137077501,"end":137084539,"strand":1,"description":"UDP-N-acetylglucosamine pyrophosphorylase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28082]"}, {"versioned_ensembl_gene_id":"ENSG00000251802.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":34892417,"end":34892549,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000252920.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":153012482,"end":153012614,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000199088.5","gene_symbol":"MIR379","gene_name":"microRNA 379 [Source:HGNC Symbol;Acc:HGNC:31872]","synonyms":"MIRN379,hsa-mir-379","biotype":"miRNA","ncbi_id":"494328","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101022066,"end":101022132,"strand":1,"description":"microRNA 379 [Source:HGNC Symbol;Acc:HGNC:31872]"}, {"versioned_ensembl_gene_id":"ENSG00000278063.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868122,"end":54868228,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000275254.1","gene_symbol":"FTX_3","gene_name":"FTX transcript, XIST regulator conserved region 3 [Source:RFAM;Acc:RF02121]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74280936,"end":74281082,"strand":1,"description":"FTX transcript, XIST regulator conserved region 3 [Source:RFAM;Acc:RF02121]"}, {"versioned_ensembl_gene_id":"ENSG00000252213.1","gene_symbol":"SNORA74D","gene_name":"small nucleolar RNA, H/ACA box 74D [Source:HGNC Symbol;Acc:HGNC:52219]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616975","summary":null,"start":139276180,"end":139276320,"strand":1,"description":"small nucleolar RNA, H/ACA box 74D [Source:HGNC Symbol;Acc:HGNC:52219]"}, {"versioned_ensembl_gene_id":"ENSG00000265848.1","gene_symbol":"MIR3689D1","gene_name":"microRNA 3689d-1 [Source:HGNC Symbol;Acc:HGNC:41621]","synonyms":"hsa-mir-3689d-1","biotype":"miRNA","ncbi_id":"100616131","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134849609,"end":134849682,"strand":-1,"description":"microRNA 3689d-1 [Source:HGNC Symbol;Acc:HGNC:41621]"}, {"versioned_ensembl_gene_id":"ENSG00000278002.1","gene_symbol":"AL627171.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49863072,"end":49864379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274748.1","gene_symbol":"AC233702.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21678086,"end":21678418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284447.1","gene_symbol":"MIR9-2","gene_name":"microRNA 9-2 [Source:HGNC Symbol;Acc:HGNC:31642]","synonyms":"MIRN9-2,hsa-mir-9-2","biotype":"miRNA","ncbi_id":"407047","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88666853,"end":88666939,"strand":-1,"description":"microRNA 9-2 [Source:HGNC Symbol;Acc:HGNC:31642]"}, {"versioned_ensembl_gene_id":"ENSG00000275935.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000278617.1","gene_symbol":"MIR8074","gene_name":"microRNA 8074 [Source:HGNC Symbol;Acc:HGNC:50105]","synonyms":"hsa-mir-8074","biotype":"miRNA","ncbi_id":"102465873","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51206929,"end":51207009,"strand":-1,"description":"microRNA 8074 [Source:HGNC Symbol;Acc:HGNC:50105]"}, {"versioned_ensembl_gene_id":"ENSG00000222418.1","gene_symbol":"RNA5SP113","gene_name":"RNA, 5S ribosomal pseudogene 113 [Source:HGNC Symbol;Acc:HGNC:42911]","synonyms":"RN5S113","biotype":"rRNA","ncbi_id":"100873383","summary":null,"start":182048822,"end":182048905,"strand":1,"description":"RNA, 5S ribosomal pseudogene 113 [Source:HGNC Symbol;Acc:HGNC:42911]"}, {"versioned_ensembl_gene_id":"ENSG00000277153.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54868939,"end":54869045,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000238540.1","gene_symbol":"RNU7-93P","gene_name":"RNA, U7 small nuclear 93 pseudogene [Source:HGNC Symbol;Acc:HGNC:45627]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480813","summary":null,"start":36405214,"end":36405274,"strand":1,"description":"RNA, U7 small nuclear 93 pseudogene [Source:HGNC Symbol;Acc:HGNC:45627]"}, {"versioned_ensembl_gene_id":"ENSG00000283824.1","gene_symbol":"MIR22","gene_name":"microRNA 22 [Source:HGNC Symbol;Acc:HGNC:31599]","synonyms":"MIRN22,hsa-mir-22","biotype":"miRNA","ncbi_id":"407004","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1713903,"end":1713987,"strand":-1,"description":"microRNA 22 [Source:HGNC Symbol;Acc:HGNC:31599]"}, {"versioned_ensembl_gene_id":"ENSG00000199005.4","gene_symbol":"MIR370","gene_name":"microRNA 370 [Source:HGNC Symbol;Acc:HGNC:31784]","synonyms":"MIRN370,hsa-mir-370","biotype":"miRNA","ncbi_id":"442915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100911139,"end":100911213,"strand":1,"description":"microRNA 370 [Source:HGNC Symbol;Acc:HGNC:31784]"}, {"versioned_ensembl_gene_id":"ENSG00000275869.1","gene_symbol":"AC136612.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":933862,"end":936467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276094.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":41573512,"end":41573606,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000202514.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":42949388,"end":42949495,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000282878.1","gene_symbol":"AC093151.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41242373,"end":41284861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275574.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46833127,"end":46833407,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201510.1","gene_symbol":"RN7SKP217","gene_name":"RNA, 7SK small nuclear pseudogene 217 [Source:HGNC Symbol;Acc:HGNC:45941]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479191","summary":null,"start":76736641,"end":76736980,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 217 [Source:HGNC Symbol;Acc:HGNC:45941]"}, {"versioned_ensembl_gene_id":"ENSG00000281067.1","gene_symbol":"ST13P19","gene_name":"ST13, Hsp70 interacting protein pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131961","summary":null,"start":210265636,"end":210267241,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38862]"}, {"versioned_ensembl_gene_id":"ENSG00000260157.3","gene_symbol":"AC233702.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21614487,"end":21641536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263375.1","gene_symbol":"AC233702.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21592794,"end":21594180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198780.11","gene_symbol":"FAM169A","gene_name":"family with sequence similarity 169 member A [Source:HGNC Symbol;Acc:HGNC:29138]","synonyms":"KIAA0888,SLAP75","biotype":"protein_coding","ncbi_id":"26049","summary":null,"start":74777574,"end":74866951,"strand":-1,"description":"family with sequence similarity 169 member A [Source:HGNC Symbol;Acc:HGNC:29138]"}, {"versioned_ensembl_gene_id":"ENSG00000271714.1","gene_symbol":"AC010501.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74865893,"end":74867854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150764.13","gene_symbol":"DIXDC1","gene_name":"DIX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23695]","synonyms":"KIAA1735,Dixin","biotype":"protein_coding","ncbi_id":"85458","summary":"The protein encoded by this gene is a positive regulator of the Wnt signaling pathway. The encoded protein is found associated with gamma tubulin at the centrosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]","start":111927144,"end":112022584,"strand":1,"description":"DIX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23695]"}, {"versioned_ensembl_gene_id":"ENSG00000265370.1","gene_symbol":"MIR4682","gene_name":"microRNA 4682 [Source:HGNC Symbol;Acc:HGNC:41788]","synonyms":"hsa-mir-4682","biotype":"miRNA","ncbi_id":"100616322","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119958513,"end":119958592,"strand":1,"description":"microRNA 4682 [Source:HGNC Symbol;Acc:HGNC:41788]"}, {"versioned_ensembl_gene_id":"ENSG00000207805.3","gene_symbol":"MIR483","gene_name":"microRNA 483 [Source:HGNC Symbol;Acc:HGNC:32340]","synonyms":"MIRN483,hsa-mir-483","biotype":"miRNA","ncbi_id":"619552","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2134134,"end":2134209,"strand":-1,"description":"microRNA 483 [Source:HGNC Symbol;Acc:HGNC:32340]"}, {"versioned_ensembl_gene_id":"ENSG00000207862.1","gene_symbol":"MIR518B","gene_name":"microRNA 518b [Source:HGNC Symbol;Acc:HGNC:32106]","synonyms":"MIRN518B,hsa-mir-518b","biotype":"miRNA","ncbi_id":"574474","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53702737,"end":53702819,"strand":1,"description":"microRNA 518b [Source:HGNC Symbol;Acc:HGNC:32106]"}, {"versioned_ensembl_gene_id":"ENSG00000221792.1","gene_symbol":"MIR1282","gene_name":"microRNA 1282 [Source:HGNC Symbol;Acc:HGNC:35360]","synonyms":"MIRN1282,hsa-mir-1282","biotype":"miRNA","ncbi_id":"100302254","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43793659,"end":43793759,"strand":-1,"description":"microRNA 1282 [Source:HGNC Symbol;Acc:HGNC:35360]"}, {"versioned_ensembl_gene_id":"ENSG00000266593.1","gene_symbol":"MIR4713","gene_name":"microRNA 4713 [Source:HGNC Symbol;Acc:HGNC:41899]","synonyms":"hsa-mir-4713","biotype":"miRNA","ncbi_id":"100616369","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51242190,"end":51242264,"strand":1,"description":"microRNA 4713 [Source:HGNC Symbol;Acc:HGNC:41899]"}, {"versioned_ensembl_gene_id":"ENSG00000207128.1","gene_symbol":"RNU6-729P","gene_name":"RNA, U6 small nuclear 729, pseudogene [Source:HGNC Symbol;Acc:HGNC:47692]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481410","summary":null,"start":10476223,"end":10476329,"strand":1,"description":"RNA, U6 small nuclear 729, pseudogene [Source:HGNC Symbol;Acc:HGNC:47692]"}, {"versioned_ensembl_gene_id":"ENSG00000199730.1","gene_symbol":"RN7SKP95","gene_name":"RNA, 7SK small nuclear pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:45819]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480862","summary":null,"start":58703852,"end":58704154,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:45819]"}, {"versioned_ensembl_gene_id":"ENSG00000212145.2","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":41899111,"end":41899253,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000207308.1","gene_symbol":"RNU6-878P","gene_name":"RNA, U6 small nuclear 878, pseudogene [Source:HGNC Symbol;Acc:HGNC:47841]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479954","summary":null,"start":2321718,"end":2321827,"strand":1,"description":"RNA, U6 small nuclear 878, pseudogene [Source:HGNC Symbol;Acc:HGNC:47841]"}, {"versioned_ensembl_gene_id":"ENSG00000221697.1","gene_symbol":"MIR1275","gene_name":"microRNA 1275 [Source:HGNC Symbol;Acc:HGNC:35346]","synonyms":"MIRN1275,hsa-mir-1275","biotype":"miRNA","ncbi_id":"100302123","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33999972,"end":34000051,"strand":-1,"description":"microRNA 1275 [Source:HGNC Symbol;Acc:HGNC:35346]"}, {"versioned_ensembl_gene_id":"ENSG00000211520.2","gene_symbol":"MIR216B","gene_name":"microRNA 216b [Source:HGNC Symbol;Acc:HGNC:33668]","synonyms":"MIRN216B,hsa-mir-216b","biotype":"miRNA","ncbi_id":"100126319","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56000714,"end":56000795,"strand":-1,"description":"microRNA 216b [Source:HGNC Symbol;Acc:HGNC:33668]"}, {"versioned_ensembl_gene_id":"ENSG00000278422.1","gene_symbol":"RN7SL331P","gene_name":"RNA, 7SL, cytoplasmic 331, pseudogene [Source:HGNC Symbol;Acc:HGNC:46347]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479344","summary":null,"start":84205454,"end":84205700,"strand":-1,"description":"RNA, 7SL, cytoplasmic 331, pseudogene [Source:HGNC Symbol;Acc:HGNC:46347]"}, {"versioned_ensembl_gene_id":"ENSG00000208009.1","gene_symbol":"MIR130A","gene_name":"microRNA 130a [Source:HGNC Symbol;Acc:HGNC:31514]","synonyms":"MIRN130A,hsa-mir-130a","biotype":"miRNA","ncbi_id":"406919","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57641198,"end":57641286,"strand":1,"description":"microRNA 130a [Source:HGNC Symbol;Acc:HGNC:31514]"}, {"versioned_ensembl_gene_id":"ENSG00000281420.1","gene_symbol":"AP001052.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":43748365,"end":43748468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277856.1","gene_symbol":"AC233755.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":26241,"end":26534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199311.1","gene_symbol":"SNORD115-34","gene_name":"small nucleolar RNA, C/D box 115-34 [Source:HGNC Symbol;Acc:HGNC:33053]","synonyms":"HBII-52-34","biotype":"snoRNA","ncbi_id":"100033808","summary":null,"start":25232387,"end":25232468,"strand":1,"description":"small nucleolar RNA, C/D box 115-34 [Source:HGNC Symbol;Acc:HGNC:33053]"}, {"versioned_ensembl_gene_id":"ENSG00000200638.1","gene_symbol":"SNORD115-37","gene_name":"small nucleolar RNA, C/D box 115-37 [Source:HGNC Symbol;Acc:HGNC:33056]","synonyms":"HBII-52-37","biotype":"snoRNA","ncbi_id":"100033811","summary":null,"start":25237986,"end":25238067,"strand":1,"description":"small nucleolar RNA, C/D box 115-37 [Source:HGNC Symbol;Acc:HGNC:33056]"}, {"versioned_ensembl_gene_id":"ENSG00000283592.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29575060,"end":29575171,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242673.3","gene_symbol":"RN7SL167P","gene_name":"RNA, 7SL, cytoplasmic 167, pseudogene [Source:HGNC Symbol;Acc:HGNC:46183]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480966","summary":null,"start":131004128,"end":131004429,"strand":-1,"description":"RNA, 7SL, cytoplasmic 167, pseudogene [Source:HGNC Symbol;Acc:HGNC:46183]"}, {"versioned_ensembl_gene_id":"ENSG00000265223.1","gene_symbol":"RNU1-79P","gene_name":"RNA, U1 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:48421]","synonyms":null,"biotype":"snRNA","ncbi_id":"107521942","summary":null,"start":32441551,"end":32441699,"strand":-1,"description":"RNA, U1 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:48421]"}, {"versioned_ensembl_gene_id":"ENSG00000243124.3","gene_symbol":"RN7SL643P","gene_name":"RNA, 7SL, cytoplasmic 643, pseudogene [Source:HGNC Symbol;Acc:HGNC:46659]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481098","summary":null,"start":86435848,"end":86436138,"strand":1,"description":"RNA, 7SL, cytoplasmic 643, pseudogene [Source:HGNC Symbol;Acc:HGNC:46659]"}, {"versioned_ensembl_gene_id":"ENSG00000274574.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":144560668,"end":144560831,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000283372.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":98026042,"end":98026139,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207389.1","gene_symbol":"RNU1-4","gene_name":"RNA, U1 small nuclear 4 [Source:HGNC Symbol;Acc:HGNC:10128]","synonyms":"U1F,U1E2,U1D2,U1B2,RNU1G2,RNU1G1,RNU1F1,RNU1E2,RNU1D2,HSD7,HSD6,HSD5,HSD2","biotype":"snRNA","ncbi_id":"6060","summary":null,"start":16740516,"end":16740679,"strand":1,"description":"RNA, U1 small nuclear 4 [Source:HGNC Symbol;Acc:HGNC:10128]"}, {"versioned_ensembl_gene_id":"ENSG00000277818.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":79562745,"end":79562846,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252686.1","gene_symbol":"RNU6-1234P","gene_name":"RNA, U6 small nuclear 1234, pseudogene [Source:HGNC Symbol;Acc:HGNC:48197]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480106","summary":null,"start":29811916,"end":29812018,"strand":1,"description":"RNA, U6 small nuclear 1234, pseudogene [Source:HGNC Symbol;Acc:HGNC:48197]"}, {"versioned_ensembl_gene_id":"ENSG00000221475.1","gene_symbol":"SNORA11D","gene_name":"small nucleolar RNA, H/ACA box 11D [Source:HGNC Symbol;Acc:HGNC:33622]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124541","summary":null,"start":52190621,"end":52190748,"strand":1,"description":"small nucleolar RNA, H/ACA box 11D [Source:HGNC Symbol;Acc:HGNC:33622]"}, {"versioned_ensembl_gene_id":"ENSG00000207330.1","gene_symbol":"RNU6-73P","gene_name":"RNA, U6 small nuclear 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:42563]","synonyms":"RNU6-73","biotype":"snRNA","ncbi_id":"106478989","summary":null,"start":27828763,"end":27828869,"strand":1,"description":"RNA, U6 small nuclear 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:42563]"}, {"versioned_ensembl_gene_id":"ENSG00000206679.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":95125511,"end":95125609,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265237.1","gene_symbol":"MIR3142","gene_name":"microRNA 3142 [Source:HGNC Symbol;Acc:HGNC:38297]","synonyms":"hsa-mir-3142","biotype":"miRNA","ncbi_id":"100422938","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160474402,"end":160474483,"strand":1,"description":"microRNA 3142 [Source:HGNC Symbol;Acc:HGNC:38297]"}, {"versioned_ensembl_gene_id":"ENSG00000171617.13","gene_symbol":"ENC1","gene_name":"ectodermal-neural cortex 1 [Source:HGNC Symbol;Acc:HGNC:3345]","synonyms":"TP53I10,PIG10,NRPB,KLHL37,ENC-1","biotype":"protein_coding","ncbi_id":"8507","summary":"This gene encodes a member of the kelch-related family of actin-binding proteins. The encoded protein plays a role in the oxidative stress response as a regulator of the transcription factor Nrf2, and expression of this gene may play a role in malignant transformation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":74627406,"end":74641424,"strand":-1,"description":"ectodermal-neural cortex 1 [Source:HGNC Symbol;Acc:HGNC:3345]"}, {"versioned_ensembl_gene_id":"ENSG00000231057.3","gene_symbol":"AC096637.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":211675762,"end":211690103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251076.1","gene_symbol":"AC104126.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112228283,"end":112257309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238901.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":122671291,"end":122671394,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000275843.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"NALP2,PYPAF2,NBS1,CLR19.9,FLJ20510,NBS1,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54998440,"end":55034296,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000277666.1","gene_symbol":"AC136352.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":100123,"end":101141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199731.1","gene_symbol":"RNU6-1079P","gene_name":"RNA, U6 small nuclear 1079, pseudogene [Source:HGNC Symbol;Acc:HGNC:48042]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480040","summary":null,"start":32234766,"end":32234875,"strand":-1,"description":"RNA, U6 small nuclear 1079, pseudogene [Source:HGNC Symbol;Acc:HGNC:48042]"}, {"versioned_ensembl_gene_id":"ENSG00000241406.3","gene_symbol":"RN7SL515P","gene_name":"RNA, 7SL, cytoplasmic 515, pseudogene [Source:HGNC Symbol;Acc:HGNC:46531]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481063","summary":null,"start":41807677,"end":41807973,"strand":1,"description":"RNA, 7SL, cytoplasmic 515, pseudogene [Source:HGNC Symbol;Acc:HGNC:46531]"}, {"versioned_ensembl_gene_id":"ENSG00000202189.1","gene_symbol":"SNORA30B","gene_name":"small nucleolar RNA, H/ACA box 30B [Source:HGNC Symbol;Acc:HGNC:52200]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616992","summary":null,"start":20786927,"end":20787055,"strand":1,"description":"small nucleolar RNA, H/ACA box 30B [Source:HGNC Symbol;Acc:HGNC:52200]"}, {"versioned_ensembl_gene_id":"ENSG00000200367.1","gene_symbol":"SNORD113-8","gene_name":"small nucleolar RNA, C/D box 113-8 [Source:HGNC Symbol;Acc:HGNC:32987]","synonyms":"14q(I-8)","biotype":"snoRNA","ncbi_id":"767568","summary":null,"start":100943451,"end":100943524,"strand":1,"description":"small nucleolar RNA, C/D box 113-8 [Source:HGNC Symbol;Acc:HGNC:32987]"}, {"versioned_ensembl_gene_id":"ENSG00000278328.1","gene_symbol":"MIR6802","gene_name":"microRNA 6802 [Source:HGNC Symbol;Acc:HGNC:50154]","synonyms":"hsa-mir-6802","biotype":"miRNA","ncbi_id":"102465481","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55239912,"end":55239976,"strand":-1,"description":"microRNA 6802 [Source:HGNC Symbol;Acc:HGNC:50154]"}, {"versioned_ensembl_gene_id":"ENSG00000274841.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":137638128,"end":137638408,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275696.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":186629936,"end":186630211,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212495.1","gene_symbol":"RNU6-332P","gene_name":"RNA, U6 small nuclear 332, pseudogene [Source:HGNC Symbol;Acc:HGNC:47295]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481284","summary":null,"start":94003815,"end":94003922,"strand":-1,"description":"RNA, U6 small nuclear 332, pseudogene [Source:HGNC Symbol;Acc:HGNC:47295]"}, {"versioned_ensembl_gene_id":"ENSG00000200872.1","gene_symbol":"RNA5SP456","gene_name":"RNA, 5S ribosomal pseudogene 456 [Source:HGNC Symbol;Acc:HGNC:43356]","synonyms":"RN5S456","biotype":"rRNA","ncbi_id":"100873701","summary":null,"start":48475487,"end":48475600,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 456 [Source:HGNC Symbol;Acc:HGNC:43356]"}, {"versioned_ensembl_gene_id":"ENSG00000274597.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54940339,"end":54940445,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000263419.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28974068,"end":28974366,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207634.1","gene_symbol":"MIR521-1","gene_name":"microRNA 521-1 [Source:HGNC Symbol;Acc:HGNC:32126]","synonyms":"MIRN521-1,hsa-mir-521-1","biotype":"miRNA","ncbi_id":"574494","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53748636,"end":53748722,"strand":1,"description":"microRNA 521-1 [Source:HGNC Symbol;Acc:HGNC:32126]"}, {"versioned_ensembl_gene_id":"ENSG00000221545.1","gene_symbol":"MIR1255B2","gene_name":"microRNA 1255b-2 [Source:HGNC Symbol;Acc:HGNC:35367]","synonyms":"MIRN1255B2,hsa-mir-1255b-2","biotype":"miRNA","ncbi_id":"100313835","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":167998660,"end":167998726,"strand":1,"description":"microRNA 1255b-2 [Source:HGNC Symbol;Acc:HGNC:35367]"}, {"versioned_ensembl_gene_id":"ENSG00000206723.1","gene_symbol":"RNU6-1056P","gene_name":"RNA, U6 small nuclear 1056, pseudogene [Source:HGNC Symbol;Acc:HGNC:48019]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481514","summary":null,"start":48724455,"end":48724561,"strand":-1,"description":"RNA, U6 small nuclear 1056, pseudogene [Source:HGNC Symbol;Acc:HGNC:48019]"}, {"versioned_ensembl_gene_id":"ENSG00000252067.1","gene_symbol":"RNU4-71P","gene_name":"RNA, U4 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:47007]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481194","summary":null,"start":23600026,"end":23600138,"strand":-1,"description":"RNA, U4 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:47007]"}, {"versioned_ensembl_gene_id":"ENSG00000229654.1","gene_symbol":"LINC02526","gene_name":"long intergenic non-protein coding RNA 2526 [Source:HGNC Symbol;Acc:HGNC:53550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377926","summary":null,"start":106695535,"end":106699994,"strand":1,"description":"long intergenic non-protein coding RNA 2526 [Source:HGNC Symbol;Acc:HGNC:53550]"}, {"versioned_ensembl_gene_id":"ENSG00000267614.1","gene_symbol":"AC245748.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44536263,"end":44536613,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275527.1","gene_symbol":"AC100835.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74598919,"end":74599397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221649.1","gene_symbol":"MIR1233-1","gene_name":"microRNA 1233-1 [Source:HGNC Symbol;Acc:HGNC:33929]","synonyms":"MIRN1233,MIR1233,hsa-mir-1233","biotype":"miRNA","ncbi_id":"100302160","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34382069,"end":34382150,"strand":-1,"description":"microRNA 1233-1 [Source:HGNC Symbol;Acc:HGNC:33929]"}, {"versioned_ensembl_gene_id":"ENSG00000207500.1","gene_symbol":"SNORD102","gene_name":"small nucleolar RNA, C/D box 102 [Source:HGNC Symbol;Acc:HGNC:10099]","synonyms":"U102,RNU102","biotype":"snoRNA","ncbi_id":"26771","summary":null,"start":27255064,"end":27255135,"strand":1,"description":"small nucleolar RNA, C/D box 102 [Source:HGNC Symbol;Acc:HGNC:10099]"}, {"versioned_ensembl_gene_id":"ENSG00000274822.1","gene_symbol":"MIR6762","gene_name":"microRNA 6762 [Source:HGNC Symbol;Acc:HGNC:50168]","synonyms":"hsa-mir-6762","biotype":"miRNA","ncbi_id":"102465457","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113291523,"end":113291608,"strand":1,"description":"microRNA 6762 [Source:HGNC Symbol;Acc:HGNC:50168]"}, {"versioned_ensembl_gene_id":"ENSG00000276150.1","gene_symbol":"TTC28-AS1_2","gene_name":"TTC28 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02199]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27922022,"end":27922178,"strand":1,"description":"TTC28 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02199]"}, {"versioned_ensembl_gene_id":"ENSG00000200597.1","gene_symbol":"RNU1-87P","gene_name":"RNA, U1 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:48429]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480178","summary":null,"start":37915573,"end":37915742,"strand":1,"description":"RNA, U1 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:48429]"}, {"versioned_ensembl_gene_id":"ENSG00000207062.1","gene_symbol":"SNORA15B-1","gene_name":"small nucleolar RNA, H/ACA box 15B-1 [Source:HGNC Symbol;Acc:HGNC:52191]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616962","summary":null,"start":65070538,"end":65070672,"strand":1,"description":"small nucleolar RNA, H/ACA box 15B-1 [Source:HGNC Symbol;Acc:HGNC:52191]"}, {"versioned_ensembl_gene_id":"ENSG00000274884.1","gene_symbol":"AL117190.3","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100826284,"end":100826370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243991.3","gene_symbol":"RN7SL447P","gene_name":"RNA, 7SL, cytoplasmic 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:46463]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479386","summary":null,"start":193740471,"end":193740715,"strand":-1,"description":"RNA, 7SL, cytoplasmic 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:46463]"}, {"versioned_ensembl_gene_id":"ENSG00000206675.1","gene_symbol":"RNU6-32P","gene_name":"RNA, U6 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:34276]","synonyms":"RNU6-32","biotype":"snRNA","ncbi_id":"106480708","summary":null,"start":39297605,"end":39297711,"strand":-1,"description":"RNA, U6 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:34276]"}, {"versioned_ensembl_gene_id":"ENSG00000206692.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":171253906,"end":171254022,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264073.1","gene_symbol":"MIR3199-1","gene_name":"microRNA 3199-1 [Source:HGNC Symbol;Acc:HGNC:38294]","synonyms":"hsa-mir-3199-1","biotype":"miRNA","ncbi_id":"100423034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27920525,"end":27920612,"strand":-1,"description":"microRNA 3199-1 [Source:HGNC Symbol;Acc:HGNC:38294]"}, {"versioned_ensembl_gene_id":"ENSG00000252279.1","gene_symbol":"RNU6-406P","gene_name":"RNA, U6 small nuclear 406, pseudogene [Source:HGNC Symbol;Acc:HGNC:47369]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481306","summary":null,"start":43445507,"end":43445613,"strand":1,"description":"RNA, U6 small nuclear 406, pseudogene [Source:HGNC Symbol;Acc:HGNC:47369]"}, {"versioned_ensembl_gene_id":"ENSG00000202058.1","gene_symbol":"RN7SKP80","gene_name":"RNA, 7SK small nuclear pseudogene 80 [Source:HGNC Symbol;Acc:HGNC:45804]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479130","summary":null,"start":42565048,"end":42565330,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 80 [Source:HGNC Symbol;Acc:HGNC:45804]"}, {"versioned_ensembl_gene_id":"ENSG00000221365.1","gene_symbol":"MIR1228","gene_name":"microRNA 1228 [Source:HGNC Symbol;Acc:HGNC:33928]","synonyms":"MIRN1228,hsa-mir-1228","biotype":"miRNA","ncbi_id":"100302201","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57194504,"end":57194576,"strand":1,"description":"microRNA 1228 [Source:HGNC Symbol;Acc:HGNC:33928]"}, {"versioned_ensembl_gene_id":"ENSG00000266308.2","gene_symbol":"RN7SL510P","gene_name":"RNA, 7SL, cytoplasmic 510, pseudogene [Source:HGNC Symbol;Acc:HGNC:46526]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479410","summary":null,"start":75895040,"end":75895302,"strand":1,"description":"RNA, 7SL, cytoplasmic 510, pseudogene [Source:HGNC Symbol;Acc:HGNC:46526]"}, {"versioned_ensembl_gene_id":"ENSG00000201547.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67408774,"end":67408881,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240151.3","gene_symbol":"RN7SL826P","gene_name":"RNA, 7SL, cytoplasmic 826, pseudogene [Source:HGNC Symbol;Acc:HGNC:46842]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479523","summary":null,"start":117163968,"end":117164255,"strand":1,"description":"RNA, 7SL, cytoplasmic 826, pseudogene [Source:HGNC Symbol;Acc:HGNC:46842]"}, {"versioned_ensembl_gene_id":"ENSG00000200555.1","gene_symbol":"RNU6-525P","gene_name":"RNA, U6 small nuclear 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:47488]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479799","summary":null,"start":180444509,"end":180444612,"strand":1,"description":"RNA, U6 small nuclear 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:47488]"}, {"versioned_ensembl_gene_id":"ENSG00000260679.1","gene_symbol":"AP007216.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69921638,"end":69926813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269236.1","gene_symbol":"AC008751.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58166166,"end":58167145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276584.1","gene_symbol":"MIR6737","gene_name":"microRNA 6737 [Source:HGNC Symbol;Acc:HGNC:50273]","synonyms":"hsa-mir-6737","biotype":"miRNA","ncbi_id":"102465441","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153962351,"end":153962420,"strand":-1,"description":"microRNA 6737 [Source:HGNC Symbol;Acc:HGNC:50273]"}, {"versioned_ensembl_gene_id":"ENSG00000212497.1","gene_symbol":"RNA5SP465","gene_name":"RNA, 5S ribosomal pseudogene 465 [Source:HGNC Symbol;Acc:HGNC:43365]","synonyms":"RN5S465","biotype":"rRNA","ncbi_id":"100873709","summary":null,"start":12027913,"end":12028021,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 465 [Source:HGNC Symbol;Acc:HGNC:43365]"}, {"versioned_ensembl_gene_id":"ENSG00000277359.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000251861.1","gene_symbol":"SCARNA20","gene_name":"Small Cajal body specific RNA 20 [Source:RFAM;Acc:RF00601]","synonyms":"ACA66","biotype":"scaRNA","ncbi_id":"677681","summary":null,"start":204727991,"end":204728106,"strand":1,"description":"Small Cajal body specific RNA 20 [Source:RFAM;Acc:RF00601]"}, {"versioned_ensembl_gene_id":"ENSG00000278050.1","gene_symbol":"NEAT1_2","gene_name":"Nuclear enriched abundant transcript 1 conserved region 2 [Source:RFAM;Acc:RF01956]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65423638,"end":65423742,"strand":1,"description":"Nuclear enriched abundant transcript 1 conserved region 2 [Source:RFAM;Acc:RF01956]"}, {"versioned_ensembl_gene_id":"ENSG00000264163.1","gene_symbol":"MIR3689B","gene_name":"microRNA 3689b [Source:HGNC Symbol;Acc:HGNC:38924]","synonyms":"hsa-mir-3689b","biotype":"miRNA","ncbi_id":"100500906","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134850125,"end":134850272,"strand":-1,"description":"microRNA 3689b [Source:HGNC Symbol;Acc:HGNC:38924]"}, {"versioned_ensembl_gene_id":"ENSG00000265247.1","gene_symbol":"MIR4472-1","gene_name":"microRNA 4472-1 [Source:HGNC Symbol;Acc:HGNC:41644]","synonyms":"hsa-mir-4472-1","biotype":"miRNA","ncbi_id":"100616268","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":142176339,"end":142176418,"strand":1,"description":"microRNA 4472-1 [Source:HGNC Symbol;Acc:HGNC:41644]"}, {"versioned_ensembl_gene_id":"ENSG00000283298.1","gene_symbol":"MIR4272","gene_name":"microRNA 4272 [Source:HGNC Symbol;Acc:HGNC:38303]","synonyms":"hsa-mir-4272","biotype":"miRNA","ncbi_id":"100422941","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67225464,"end":67225527,"strand":1,"description":"microRNA 4272 [Source:HGNC Symbol;Acc:HGNC:38303]"}, {"versioned_ensembl_gene_id":"ENSG00000283764.1","gene_symbol":"MIR6850","gene_name":"microRNA 6850 [Source:HGNC Symbol;Acc:HGNC:50093]","synonyms":"hsa-mir-6850","biotype":"miRNA","ncbi_id":"102465978","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144791931,"end":144791991,"strand":-1,"description":"microRNA 6850 [Source:HGNC Symbol;Acc:HGNC:50093]"}, {"versioned_ensembl_gene_id":"ENSG00000284328.1","gene_symbol":"AC132825.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22531876,"end":22532172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284263.1","gene_symbol":"AC132825.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22532166,"end":22532522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266691.1","gene_symbol":"AC138761.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22277867,"end":22279289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282885.1","gene_symbol":"AL627171.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49861176,"end":49864326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164347.17","gene_symbol":"GFM2","gene_name":"G elongation factor mitochondrial 2 [Source:HGNC Symbol;Acc:HGNC:29682]","synonyms":"FLJ21661,EFG2","biotype":"protein_coding","ncbi_id":"84340","summary":"Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors, which is a GTPase that plays a role at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA . Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013]","start":74721204,"end":74767371,"strand":-1,"description":"G elongation factor mitochondrial 2 [Source:HGNC Symbol;Acc:HGNC:29682]"}, {"versioned_ensembl_gene_id":"ENSG00000264245.1","gene_symbol":"AC233702.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21573770,"end":21574073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266673.1","gene_symbol":"AC233702.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21552509,"end":21552711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266466.1","gene_symbol":"AC233702.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21532974,"end":21542786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173653.7","gene_symbol":"RCE1","gene_name":"Ras converting CAAX endopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:13721]","synonyms":"RCE1B,RCE1A,hRCE1,FACE2,FACE-2","biotype":"protein_coding","ncbi_id":"9986","summary":"This gene encodes an integral membrane protein which is classified as a member of the metalloproteinase family. This enzyme is thought to function in the maintenance and processing of CAAX-type prenylated proteins. [provided by RefSeq, Jul 2008]","start":66842835,"end":66846546,"strand":1,"description":"Ras converting CAAX endopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:13721]"}, {"versioned_ensembl_gene_id":"ENSG00000278910.3","gene_symbol":"BANCR","gene_name":"BRAF-activated non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:43877]","synonyms":"LINC00586","biotype":"lincRNA","ncbi_id":"100885775","summary":"This gene produces a long non-coding RNA that plays a role in tumor progression and epithelial to mesenchymal transition. This transcript acts through the MAP kinase signaling pathway. [provided by RefSeq, Dec 2017]","start":69296682,"end":69306977,"strand":-1,"description":"BRAF-activated non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:43877]"}, {"versioned_ensembl_gene_id":"ENSG00000135063.17","gene_symbol":"FAM189A2","gene_name":"family with sequence similarity 189 member A2 [Source:HGNC Symbol;Acc:HGNC:24820]","synonyms":"X123,C9orf61","biotype":"protein_coding","ncbi_id":"9413","summary":null,"start":69324572,"end":69392455,"strand":1,"description":"family with sequence similarity 189 member A2 [Source:HGNC Symbol;Acc:HGNC:24820]"}, {"versioned_ensembl_gene_id":"ENSG00000196405.12","gene_symbol":"EVL","gene_name":"Enah/Vasp-like [Source:HGNC Symbol;Acc:HGNC:20234]","synonyms":"RNB6","biotype":"protein_coding","ncbi_id":"51466","summary":null,"start":99971449,"end":100144236,"strand":1,"description":"Enah/Vasp-like [Source:HGNC Symbol;Acc:HGNC:20234]"}, {"versioned_ensembl_gene_id":"ENSG00000258693.1","gene_symbol":"AL133368.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99977115,"end":99978098,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196387.9","gene_symbol":"ZNF140","gene_name":"zinc finger protein 140 [Source:HGNC Symbol;Acc:HGNC:12925]","synonyms":"pHZ-39","biotype":"protein_coding","ncbi_id":"7699","summary":null,"start":133079838,"end":133107544,"strand":1,"description":"zinc finger protein 140 [Source:HGNC Symbol;Acc:HGNC:12925]"}, {"versioned_ensembl_gene_id":"ENSG00000279466.1","gene_symbol":"AC073911.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133073516,"end":133073983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232728.1","gene_symbol":"PHB2P1","gene_name":"prohibitin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45249]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645318","summary":null,"start":109528119,"end":109529008,"strand":1,"description":"prohibitin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45249]"}, {"versioned_ensembl_gene_id":"ENSG00000224498.1","gene_symbol":"MAPKAPK5P1","gene_name":"mitogen-activated protein kinase-activated protein kinase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45246]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533849","summary":null,"start":108848186,"end":108849561,"strand":1,"description":"mitogen-activated protein kinase-activated protein kinase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45246]"}, {"versioned_ensembl_gene_id":"ENSG00000234544.2","gene_symbol":"PTGES3P5","gene_name":"prostaglandin E synthase 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480359","summary":null,"start":108296099,"end":108296532,"strand":1,"description":"prostaglandin E synthase 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43826]"}, {"versioned_ensembl_gene_id":"ENSG00000136878.12","gene_symbol":"USP20","gene_name":"ubiquitin specific peptidase 20 [Source:HGNC Symbol;Acc:HGNC:12619]","synonyms":"KIAA1003","biotype":"protein_coding","ncbi_id":"10868","summary":"This gene encodes a ubiquitin specific processing protease that was first identified as a substrate of the VHL (von Hippel-Lindau disease) protein E3 ubiquitin ligase complex. In addition to being ubiquitinated by the VHL-E3 ligase complex, this enzyme deubiquitinates hypoxia-inducible factor (HIF)-1 alpha and thereby causes increased expression of HIF-1alpha targeted genes which play a role in angiogenesis, glucose metabolism, cell proliferation and metastasis. The enzyme encoded by this gene also regulates G-protein coupled receptor signaling by mediating the deubiquitination of beta-2 adrenergic receptor (ADRB2). This enzyme is a ubiquitously expressed thiolester hydrolase. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jan 2013]","start":129834698,"end":129881838,"strand":1,"description":"ubiquitin specific peptidase 20 [Source:HGNC Symbol;Acc:HGNC:12619]"}, {"versioned_ensembl_gene_id":"ENSG00000136819.15","gene_symbol":"C9orf78","gene_name":"chromosome 9 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:24932]","synonyms":"HSPC220,HCA59","biotype":"protein_coding","ncbi_id":"51759","summary":null,"start":129827290,"end":129835863,"strand":-1,"description":"chromosome 9 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:24932]"}, {"versioned_ensembl_gene_id":"ENSG00000234528.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SUMO2P,SMT3Bp,dJ271M21,SMT3H2P","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29635969,"end":29636252,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000259058.1","gene_symbol":"AF111169.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76921840,"end":76924649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213201.3","gene_symbol":"FABP5P10","gene_name":"fatty acid binding protein 5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:31066]","synonyms":"FABP5L10","biotype":"processed_pseudogene","ncbi_id":"344332","summary":null,"start":151186188,"end":151186595,"strand":1,"description":"fatty acid binding protein 5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:31066]"}, {"versioned_ensembl_gene_id":"ENSG00000234789.1","gene_symbol":"AL590369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129640476,"end":129641282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228510.2","gene_symbol":"AL359091.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128444587,"end":128446628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233626.2","gene_symbol":"AC092814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211936249,"end":211936634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225385.3","gene_symbol":"AL353572.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88066915,"end":88068037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204277.1","gene_symbol":"LINC01993","gene_name":"long intergenic non-protein coding RNA 1993 [Source:HGNC Symbol;Acc:HGNC:52826]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996291","summary":null,"start":78261349,"end":78278492,"strand":-1,"description":"long intergenic non-protein coding RNA 1993 [Source:HGNC Symbol;Acc:HGNC:52826]"}, {"versioned_ensembl_gene_id":"ENSG00000267737.1","gene_symbol":"AC087645.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78315729,"end":78347798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267676.1","gene_symbol":"THA1P","gene_name":"threonine aldolase 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18004]","synonyms":"GLY1","biotype":"unitary_pseudogene","ncbi_id":"390816","summary":null,"start":78248493,"end":78254416,"strand":-1,"description":"threonine aldolase 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18004]"}, {"versioned_ensembl_gene_id":"ENSG00000283914.1","gene_symbol":"AC087645.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78248193,"end":78251440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178217.13","gene_symbol":"SH2D4B","gene_name":"SH2 domain containing 4B [Source:HGNC Symbol;Acc:HGNC:31440]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387694","summary":null,"start":80537902,"end":80646560,"strand":1,"description":"SH2 domain containing 4B [Source:HGNC Symbol;Acc:HGNC:31440]"}, {"versioned_ensembl_gene_id":"ENSG00000204054.13","gene_symbol":"LINC00963","gene_name":"long intergenic non-protein coding RNA 963 [Source:HGNC Symbol;Acc:HGNC:48716]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506190","summary":null,"start":129483451,"end":129513686,"strand":1,"description":"long intergenic non-protein coding RNA 963 [Source:HGNC Symbol;Acc:HGNC:48716]"}, {"versioned_ensembl_gene_id":"ENSG00000254978.2","gene_symbol":"ALG1L9P","gene_name":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:44378]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285407","summary":null,"start":71800541,"end":71804640,"strand":-1,"description":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:44378]"}, {"versioned_ensembl_gene_id":"ENSG00000260422.1","gene_symbol":"Z97205.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164084023,"end":164085661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272774.1","gene_symbol":"AC112219.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72178279,"end":72178810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254186.1","gene_symbol":"AC091901.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162558685,"end":162623461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255319.5","gene_symbol":"ENPP7P8","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48691]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421860","summary":null,"start":71711740,"end":71781183,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48691]"}, {"versioned_ensembl_gene_id":"ENSG00000214144.3","gene_symbol":"AL390728.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247229940,"end":247231880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251187.5","gene_symbol":"AC010261.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112192020,"end":112210139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261334.1","gene_symbol":"AL353803.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129480605,"end":129482538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108639.7","gene_symbol":"SYNGR2","gene_name":"synaptogyrin 2 [Source:HGNC Symbol;Acc:HGNC:11499]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9144","summary":"This gene encodes an integral membrane protein containing four transmembrane regions and a C-terminal cytoplasmic tail that is tyrosine phosphorylated. The exact function of this protein is unclear, but studies of a similar rat protein suggest that it may play a role in regulating membrane traffic in non-neuronal cells. The gene belongs to the synaptogyrin gene family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":78168558,"end":78173527,"strand":1,"description":"synaptogyrin 2 [Source:HGNC Symbol;Acc:HGNC:11499]"}, {"versioned_ensembl_gene_id":"ENSG00000166851.14","gene_symbol":"PLK1","gene_name":"polo like kinase 1 [Source:HGNC Symbol;Acc:HGNC:9077]","synonyms":"PLK","biotype":"protein_coding","ncbi_id":"5347","summary":"The Ser/Thr protein kinase encoded by this gene belongs to the CDC5/Polo subfamily. It is highly expressed during mitosis and elevated levels are found in many different types of cancer. Depletion of this protein in cancer cells dramatically inhibited cell proliferation and induced apoptosis; hence, it is a target for cancer therapy. [provided by RefSeq, Sep 2015]","start":23677656,"end":23690367,"strand":1,"description":"polo like kinase 1 [Source:HGNC Symbol;Acc:HGNC:9077]"}, {"versioned_ensembl_gene_id":"ENSG00000170909.13","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094668,"end":54102692,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000255261.1","gene_symbol":"OR7E4P","gene_name":"olfactory receptor family 7 subfamily E member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:8424]","synonyms":"OR7F4P,OR11-11a","biotype":"unprocessed_pseudogene","ncbi_id":"8585","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71620020,"end":71621032,"strand":1,"description":"olfactory receptor family 7 subfamily E member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:8424]"}, {"versioned_ensembl_gene_id":"ENSG00000117650.12","gene_symbol":"NEK2","gene_name":"NIMA related kinase 2 [Source:HGNC Symbol;Acc:HGNC:7745]","synonyms":"RP67,PPP1R111,NLK1,NEK2A","biotype":"protein_coding","ncbi_id":"4751","summary":"This gene encodes a serine/threonine-protein kinase that is involved in mitotic regulation. This protein is localized to the centrosome, and undetectable during G1 phase, but accumulates progressively throughout the S phase, reaching maximal levels in late G2 phase. Alternatively spliced transcript variants encoding different isoforms with distinct C-termini have been noted for this gene. [provided by RefSeq, Feb 2011]","start":211658657,"end":211675630,"strand":-1,"description":"NIMA related kinase 2 [Source:HGNC Symbol;Acc:HGNC:7745]"}, {"versioned_ensembl_gene_id":"ENSG00000134398.14","gene_symbol":"ERN2","gene_name":"endoplasmic reticulum to nucleus signaling 2 [Source:HGNC Symbol;Acc:HGNC:16942]","synonyms":"IRE1b","biotype":"protein_coding","ncbi_id":"10595","summary":null,"start":23690326,"end":23713500,"strand":-1,"description":"endoplasmic reticulum to nucleus signaling 2 [Source:HGNC Symbol;Acc:HGNC:16942]"}, {"versioned_ensembl_gene_id":"ENSG00000147676.13","gene_symbol":"MAL2","gene_name":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114569","summary":"This gene encodes a multispan transmembrane protein belonging to the MAL proteolipid family. The protein is a component of lipid rafts and, in polarized cells, it primarily localizes to endosomal structures beneath the apical membrane. It is required for transcytosis, an intracellular transport pathway used to deliver membrane-bound proteins and exogenous cargos from the basolateral to the apical surface. [provided by RefSeq, Jul 2008]","start":119165034,"end":119245673,"strand":1,"description":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]"}, {"versioned_ensembl_gene_id":"ENSG00000105281.12","gene_symbol":"SLC1A5","gene_name":"solute carrier family 1 member 5 [Source:HGNC Symbol;Acc:HGNC:10943]","synonyms":"RDRC,M7V1,ASCT2,AAAT","biotype":"protein_coding","ncbi_id":"6510","summary":"The SLC1A5 gene encodes a sodium-dependent neutral amino acid transporter that can act as a receptor for RD114/type D retrovirus (Larriba et al., 2001 [PubMed 11781704]).[supplied by OMIM, Jan 2011]","start":46774883,"end":46788594,"strand":-1,"description":"solute carrier family 1 member 5 [Source:HGNC Symbol;Acc:HGNC:10943]"}, {"versioned_ensembl_gene_id":"ENSG00000250699.1","gene_symbol":"AP000892.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117316362,"end":117328038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271412.1","gene_symbol":"PRR13P3","gene_name":"proline rich 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129201","summary":null,"start":117336256,"end":117336631,"strand":-1,"description":"proline rich 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50616]"}, {"versioned_ensembl_gene_id":"ENSG00000254278.1","gene_symbol":"AC107953.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119062942,"end":119068782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184374.2","gene_symbol":"COLEC10","gene_name":"collectin subfamily member 10 [Source:HGNC Symbol;Acc:HGNC:2220]","synonyms":"CL-L1","biotype":"protein_coding","ncbi_id":"10584","summary":"This gene encodes a member of the C-lectin family, proteins that possess collagen-like sequences and carbohydrate recognition domains. The other members of this family are secreted proteins and bind to carbohydrate antigens on microorganisms facilitating their recognition and removal. This gene product is a cytosolic protein, a characteristic that suggests that it may have different biological functions than other C-lectins. [provided by RefSeq, Jul 2008]","start":118995452,"end":119106582,"strand":1,"description":"collectin subfamily member 10 [Source:HGNC Symbol;Acc:HGNC:2220]"}, {"versioned_ensembl_gene_id":"ENSG00000053770.11","gene_symbol":"AP5M1","gene_name":"adaptor related protein complex 5 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:20192]","synonyms":"MUDENG,MuD,mu5,FLJ10813,C14orf108","biotype":"protein_coding","ncbi_id":"55745","summary":null,"start":57268909,"end":57298742,"strand":1,"description":"adaptor related protein complex 5 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:20192]"}, {"versioned_ensembl_gene_id":"ENSG00000267790.1","gene_symbol":"LINC01987","gene_name":"long intergenic non-protein coding RNA 1987 [Source:HGNC Symbol;Acc:HGNC:52819]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132174","summary":null,"start":77722872,"end":77728559,"strand":-1,"description":"long intergenic non-protein coding RNA 1987 [Source:HGNC Symbol;Acc:HGNC:52819]"}, {"versioned_ensembl_gene_id":"ENSG00000183514.4","gene_symbol":"TDGF1P2","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:11702]","synonyms":"TDGF2,CRIPTO-2,CR-2","biotype":"processed_pseudogene","ncbi_id":"22816","summary":null,"start":227870083,"end":227870644,"strand":-1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:11702]"}, {"versioned_ensembl_gene_id":"ENSG00000167414.4","gene_symbol":"GNG8","gene_name":"G protein subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:19664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94235","summary":null,"start":46634076,"end":46634685,"strand":-1,"description":"G protein subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:19664]"}, {"versioned_ensembl_gene_id":"ENSG00000213087.3","gene_symbol":"AL356535.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151225550,"end":151225947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181027.10","gene_symbol":"FKRP","gene_name":"fukutin related protein [Source:HGNC Symbol;Acc:HGNC:17997]","synonyms":"MDC1C,LGMD2I","biotype":"protein_coding","ncbi_id":"79147","summary":"This gene encodes a protein which is targeted to the medial Golgi apparatus and is necessary for posttranslational modification of dystroglycan. Mutations in this gene have been associated with congenital muscular dystrophy, cognitive disability, and cerebellar cysts. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2008]","start":46746046,"end":46776988,"strand":1,"description":"fukutin related protein [Source:HGNC Symbol;Acc:HGNC:17997]"}, {"versioned_ensembl_gene_id":"ENSG00000265121.1","gene_symbol":"AC068594.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77264180,"end":77264776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263718.2","gene_symbol":"AC068594.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77257737,"end":77281897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231291.3","gene_symbol":"AC106799.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4512262,"end":4516776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162344.3","gene_symbol":"FGF19","gene_name":"fibroblast growth factor 19 [Source:HGNC Symbol;Acc:HGNC:3675]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9965","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This growth factor is a high affinity, heparin dependent ligand for FGFR4. Expression of this gene was detected only in fetal but not adult brain tissue. Synergistic interaction of the chick homolog and Wnt-8c has been shown to be required for initiation of inner ear development. [provided by RefSeq, Jul 2008]","start":69698232,"end":69704642,"strand":-1,"description":"fibroblast growth factor 19 [Source:HGNC Symbol;Acc:HGNC:3675]"}, {"versioned_ensembl_gene_id":"ENSG00000234460.1","gene_symbol":"AL772337.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87864166,"end":87866290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227924.2","gene_symbol":"RBPJP6","gene_name":"RBPJ pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643198","summary":null,"start":42497704,"end":42499134,"strand":-1,"description":"RBPJ pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37486]"}, {"versioned_ensembl_gene_id":"ENSG00000248118.1","gene_symbol":"LINC01019","gene_name":"long intergenic non-protein coding RNA 1019 [Source:HGNC Symbol;Acc:HGNC:27742]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285577","summary":null,"start":3417152,"end":3536094,"strand":-1,"description":"long intergenic non-protein coding RNA 1019 [Source:HGNC Symbol;Acc:HGNC:27742]"}, {"versioned_ensembl_gene_id":"ENSG00000249830.1","gene_symbol":"LINC02162","gene_name":"long intergenic non-protein coding RNA 2162 [Source:HGNC Symbol;Acc:HGNC:53023]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374624","summary":null,"start":3452816,"end":3461660,"strand":1,"description":"long intergenic non-protein coding RNA 2162 [Source:HGNC Symbol;Acc:HGNC:53023]"}, {"versioned_ensembl_gene_id":"ENSG00000064201.15","gene_symbol":"TSPAN32","gene_name":"tetraspanin 32 [Source:HGNC Symbol;Acc:HGNC:13410]","synonyms":"TSSC6,PHEMX","biotype":"protein_coding","ncbi_id":"10077","summary":"This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes imprinting. This gene may play a role in malignancies and diseases that involve this region, and it is also involved in hematopoietic cell function. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":2301997,"end":2318200,"strand":1,"description":"tetraspanin 32 [Source:HGNC Symbol;Acc:HGNC:13410]"}, {"versioned_ensembl_gene_id":"ENSG00000258758.1","gene_symbol":"AL137100.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57040885,"end":57042504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198892.6","gene_symbol":"SHISA4","gene_name":"shisa family member 4 [Source:HGNC Symbol;Acc:HGNC:27139]","synonyms":"TMEM58,hShisa4,C1orf40","biotype":"protein_coding","ncbi_id":"149345","summary":null,"start":201888680,"end":201892306,"strand":1,"description":"shisa family member 4 [Source:HGNC Symbol;Acc:HGNC:27139]"}, {"versioned_ensembl_gene_id":"ENSG00000131473.16","gene_symbol":"ACLY","gene_name":"ATP citrate lyase [Source:HGNC Symbol;Acc:HGNC:115]","synonyms":"CLATP,ATPCL,ACL","biotype":"protein_coding","ncbi_id":"47","summary":"ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Dec 2014]","start":41866908,"end":41930542,"strand":-1,"description":"ATP citrate lyase [Source:HGNC Symbol;Acc:HGNC:115]"}, {"versioned_ensembl_gene_id":"ENSG00000203709.11","gene_symbol":"C1orf132","gene_name":"chromosome 1 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:32018]","synonyms":"FLJ35650","biotype":"lincRNA","ncbi_id":"100128537","summary":null,"start":207801518,"end":207879096,"strand":-1,"description":"chromosome 1 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:32018]"}, {"versioned_ensembl_gene_id":"ENSG00000227463.2","gene_symbol":"AL390838.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84063443,"end":84094577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240611.1","gene_symbol":"AC010307.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133172218,"end":133173053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280104.1","gene_symbol":"AC010608.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133457805,"end":133458331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275649.1","gene_symbol":"AL445584.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42231811,"end":42354454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258996.2","gene_symbol":"AL359219.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59181593,"end":59181940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281560.1","gene_symbol":"LSINCT5","gene_name":"long stress-induced non-coding transcript 5 [Source:NCBI gene;Acc:101234261]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101234261","summary":null,"start":2712591,"end":2715237,"strand":1,"description":"long stress-induced non-coding transcript 5 [Source:NCBI gene;Acc:101234261]"}, {"versioned_ensembl_gene_id":"ENSG00000149716.12","gene_symbol":"ORAOV1","gene_name":"oral cancer overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:17589]","synonyms":"TAOS1","biotype":"protein_coding","ncbi_id":"220064","summary":null,"start":69653076,"end":69675416,"strand":-1,"description":"oral cancer overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:17589]"}, {"versioned_ensembl_gene_id":"ENSG00000275733.1","gene_symbol":"AC092266.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2261859,"end":2262023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155329.11","gene_symbol":"ZCCHC10","gene_name":"zinc finger CCHC-type containing 10 [Source:HGNC Symbol;Acc:HGNC:25954]","synonyms":"FLJ20094","biotype":"protein_coding","ncbi_id":"54819","summary":null,"start":132996985,"end":133026604,"strand":-1,"description":"zinc finger CCHC-type containing 10 [Source:HGNC Symbol;Acc:HGNC:25954]"}, {"versioned_ensembl_gene_id":"ENSG00000235183.3","gene_symbol":"AC015795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49795343,"end":49795669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236709.1","gene_symbol":"DAPK1-IT1","gene_name":"DAPK1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43591]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100506897","summary":null,"start":87553454,"end":87554459,"strand":1,"description":"DAPK1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43591]"}, {"versioned_ensembl_gene_id":"ENSG00000250402.2","gene_symbol":"AC109471.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125376828,"end":125377439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258529.5","gene_symbol":"AP001781.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":111786286,"end":111879425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137720.7","gene_symbol":"C11orf1","gene_name":"chromosome 11 open reading frame 1 [Source:HGNC Symbol;Acc:HGNC:1163]","synonyms":"FLJ23499","biotype":"protein_coding","ncbi_id":"64776","summary":null,"start":111878935,"end":111885975,"strand":1,"description":"chromosome 11 open reading frame 1 [Source:HGNC Symbol;Acc:HGNC:1163]"}, {"versioned_ensembl_gene_id":"ENSG00000267344.1","gene_symbol":"AC003070.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45396932,"end":45397477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167840.13","gene_symbol":"ZNF232","gene_name":"zinc finger protein 232 [Source:HGNC Symbol;Acc:HGNC:13026]","synonyms":"ZSCAN11","biotype":"protein_coding","ncbi_id":"7775","summary":null,"start":5105541,"end":5123116,"strand":-1,"description":"zinc finger protein 232 [Source:HGNC Symbol;Acc:HGNC:13026]"}, {"versioned_ensembl_gene_id":"ENSG00000254552.1","gene_symbol":"XIRP2-AS1","gene_name":"XIRP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40679]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874011","summary":null,"start":167123904,"end":167140955,"strand":-1,"description":"XIRP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40679]"}, {"versioned_ensembl_gene_id":"ENSG00000259109.1","gene_symbol":"AC004858.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73189763,"end":73190004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249112.1","gene_symbol":"AC112196.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124707827,"end":124710737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240355.1","gene_symbol":"AC004869.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46476457,"end":46477940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159593.14","gene_symbol":"NAE1","gene_name":"NEDD8 activating enzyme E1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:621]","synonyms":"APPBP1,APP-BP1,ula-1","biotype":"protein_coding","ncbi_id":"8883","summary":"The protein encoded by this gene binds to the beta-amyloid precursor protein. Beta-amyloid precursor protein is a cell surface protein with signal-transducing properties, and it is thought to play a role in the pathogenesis of Alzheimer's disease. In addition, the encoded protein can form a heterodimer with UBE1C and bind and activate NEDD8, a ubiquitin-like protein. This protein is required for cell cycle progression through the S/M checkpoint. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":66802875,"end":66873256,"strand":-1,"description":"NEDD8 activating enzyme E1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:621]"}, {"versioned_ensembl_gene_id":"ENSG00000250411.1","gene_symbol":"AC109458.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125036831,"end":125042239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145494.11","gene_symbol":"NDUFS6","gene_name":"NADH:ubiquinone oxidoreductase subunit S6 [Source:HGNC Symbol;Acc:HGNC:7713]","synonyms":"CI-13kA","biotype":"protein_coding","ncbi_id":"4726","summary":"This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.[provided by RefSeq, Oct 2009]","start":1801400,"end":1816605,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit S6 [Source:HGNC Symbol;Acc:HGNC:7713]"}, {"versioned_ensembl_gene_id":"ENSG00000139946.9","gene_symbol":"PELI2","gene_name":"pellino E3 ubiquitin protein ligase family member 2 [Source:HGNC Symbol;Acc:HGNC:8828]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57161","summary":null,"start":56117814,"end":56301526,"strand":1,"description":"pellino E3 ubiquitin protein ligase family member 2 [Source:HGNC Symbol;Acc:HGNC:8828]"}, {"versioned_ensembl_gene_id":"ENSG00000134627.11","gene_symbol":"PIWIL4","gene_name":"piwi like RNA-mediated gene silencing 4 [Source:HGNC Symbol;Acc:HGNC:18444]","synonyms":"Miwi2,HIWI2,FLJ36156","biotype":"protein_coding","ncbi_id":"143689","summary":"PIWIL4 belongs to the Argonaute family of proteins, which function in development and maintenance of germline stem cells (Sasaki et al., 2003 [PubMed 12906857]).[supplied by OMIM, Mar 2008]","start":94543840,"end":94621421,"strand":1,"description":"piwi like RNA-mediated gene silencing 4 [Source:HGNC Symbol;Acc:HGNC:18444]"}, {"versioned_ensembl_gene_id":"ENSG00000277763.1","gene_symbol":"AL138995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56117316,"end":56117990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262456.1","gene_symbol":"AC006435.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2384847,"end":2386664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159314.11","gene_symbol":"ARHGAP27","gene_name":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]","synonyms":"SH3P20,SH3D20,FLJ43547,CAMGAP1","biotype":"protein_coding","ncbi_id":"201176","summary":"This gene encodes a member of a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein may pay a role in clathrin-mediated endocytosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2013]","start":45393902,"end":45434421,"strand":-1,"description":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]"}, {"versioned_ensembl_gene_id":"ENSG00000255929.5","gene_symbol":"AP000943.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94545330,"end":94740355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254226.5","gene_symbol":"LINC01933","gene_name":"long intergenic non-protein coding RNA 1933 [Source:HGNC Symbol;Acc:HGNC:52756]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927115","summary":null,"start":151949571,"end":152270448,"strand":1,"description":"long intergenic non-protein coding RNA 1933 [Source:HGNC Symbol;Acc:HGNC:52756]"}, {"versioned_ensembl_gene_id":"ENSG00000089916.17","gene_symbol":"GPATCH2L","gene_name":"G-patch domain containing 2 like [Source:HGNC Symbol;Acc:HGNC:20210]","synonyms":"FLJ20689,FLJ10033,C14orf118","biotype":"protein_coding","ncbi_id":"55668","summary":null,"start":76151916,"end":76254342,"strand":1,"description":"G-patch domain containing 2 like [Source:HGNC Symbol;Acc:HGNC:20210]"}, {"versioned_ensembl_gene_id":"ENSG00000261987.2","gene_symbol":"KYNUP1","gene_name":"kynureninase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39199]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729321","summary":null,"start":19166896,"end":19169668,"strand":-1,"description":"kynureninase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39199]"}, {"versioned_ensembl_gene_id":"ENSG00000224650.2","gene_symbol":"IGHV3-74","gene_name":"immunoglobulin heavy variable 3-74 [Source:HGNC Symbol;Acc:HGNC:5624]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28408","summary":null,"start":106810442,"end":106811131,"strand":-1,"description":"immunoglobulin heavy variable 3-74 [Source:HGNC Symbol;Acc:HGNC:5624]"}, {"versioned_ensembl_gene_id":"ENSG00000249295.1","gene_symbol":"AC145146.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69477472,"end":69502466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223392.1","gene_symbol":"CLDN10-AS1","gene_name":"CLDN10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39907]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874194","summary":null,"start":95479444,"end":95533910,"strand":-1,"description":"CLDN10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39907]"}, {"versioned_ensembl_gene_id":"ENSG00000270978.1","gene_symbol":"AC091982.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151848886,"end":151850791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108861.8","gene_symbol":"DUSP3","gene_name":"dual specificity phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:3069]","synonyms":"VHR","biotype":"protein_coding","ncbi_id":"1845","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene maps in a region that contains the BRCA1 locus which confers susceptibility to breast and ovarian cancer. Although DUSP3 is expressed in both breast and ovarian tissues, mutation screening in breast cancer pedigrees and in sporadic tumors was negative, leading to the conclusion that this gene is not BRCA1. [provided by RefSeq, Jul 2008]","start":43766121,"end":43778988,"strand":-1,"description":"dual specificity phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:3069]"}, {"versioned_ensembl_gene_id":"ENSG00000282600.2","gene_symbol":"AC245369.7","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106728163,"end":106728615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275946.5","gene_symbol":"GU182345.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771241,"end":54780725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130005.12","gene_symbol":"GAMT","gene_name":"guanidinoacetate N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:4136]","synonyms":"TP53I2,PIG2","biotype":"protein_coding","ncbi_id":"2593","summary":"The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals. Two transcript variants encoding different isoforms have been described for this gene. Pseudogenes of this gene are found on chromosomes 2 and 13. [provided by RefSeq, Feb 2012]","start":1397026,"end":1401570,"strand":-1,"description":"guanidinoacetate N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:4136]"}, {"versioned_ensembl_gene_id":"ENSG00000149591.16","gene_symbol":"TAGLN","gene_name":"transgelin [Source:HGNC Symbol;Acc:HGNC:11553]","synonyms":"WS3-10,TAGLN1,SMCC,SM22,DKFZp686P11128","biotype":"protein_coding","ncbi_id":"6876","summary":"This gene encodes a shape change and transformation sensitive actin-binding protein which belongs to the calponin family. It is ubiquitously expressed in vascular and visceral smooth muscle, and is an early marker of smooth muscle differentiation. The encoded protein is thought to be involved in calcium-independent smooth muscle contraction. It acts as a tumor suppressor, and the loss of its expression is an early event in cell transformation and the development of some tumors, coinciding with cellular plasticity. The encoded protein has a domain architecture consisting of an N-terminal calponin homology (CH) domain and a C-terminal calponin-like (CLIK) domain. Mice with a knockout of the orthologous gene are viable and fertile but their vascular smooth muscle cells exhibit alterations in the distribution of the actin filament and changes in cytoskeletal organization. [provided by RefSeq, Aug 2017]","start":117199321,"end":117204782,"strand":1,"description":"transgelin [Source:HGNC Symbol;Acc:HGNC:11553]"}, {"versioned_ensembl_gene_id":"ENSG00000172543.7","gene_symbol":"CTSW","gene_name":"cathepsin W [Source:HGNC Symbol;Acc:HGNC:2546]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1521","summary":"The protein encoded by this gene, a member of the peptidase C1 family, is a cysteine proteinase that may have a specific function in the mechanism or regulation of T-cell cytolytic activity. The encoded protein is found associated with the membrane inside the endoplasmic reticulum of natural killer and cytotoxic T-cells. Expression of this gene is up-regulated by interleukin-2. [provided by RefSeq, Jul 2008]","start":65879809,"end":65883741,"strand":1,"description":"cathepsin W [Source:HGNC Symbol;Acc:HGNC:2546]"}, {"versioned_ensembl_gene_id":"ENSG00000273535.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54836140,"end":54846123,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000145681.10","gene_symbol":"HAPLN1","gene_name":"hyaluronan and proteoglycan link protein 1 [Source:HGNC Symbol;Acc:HGNC:2380]","synonyms":"CRTL1","biotype":"protein_coding","ncbi_id":"1404","summary":null,"start":83637805,"end":83721613,"strand":-1,"description":"hyaluronan and proteoglycan link protein 1 [Source:HGNC Symbol;Acc:HGNC:2380]"}, {"versioned_ensembl_gene_id":"ENSG00000232579.1","gene_symbol":"MTCO1P27","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52092]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075168","summary":null,"start":12504665,"end":12504890,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52092]"}, {"versioned_ensembl_gene_id":"ENSG00000233603.1","gene_symbol":"JTBP1","gene_name":"jumping translocation breakpoint pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39180]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874254","summary":null,"start":40798039,"end":40798285,"strand":1,"description":"jumping translocation breakpoint pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39180]"}, {"versioned_ensembl_gene_id":"ENSG00000270038.1","gene_symbol":"AL133467.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95644508,"end":95645232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141576.14","gene_symbol":"RNF157","gene_name":"ring finger protein 157 [Source:HGNC Symbol;Acc:HGNC:29402]","synonyms":"KIAA1917","biotype":"protein_coding","ncbi_id":"114804","summary":null,"start":76142453,"end":76240373,"strand":-1,"description":"ring finger protein 157 [Source:HGNC Symbol;Acc:HGNC:29402]"}, {"versioned_ensembl_gene_id":"ENSG00000279485.1","gene_symbol":"AC016734.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":63517892,"end":63519268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275239.4","gene_symbol":"AL591926.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41657708,"end":41699072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137504.13","gene_symbol":"CREBZF","gene_name":"CREB/ATF bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:24905]","synonyms":"ZF","biotype":"protein_coding","ncbi_id":"58487","summary":null,"start":85659708,"end":85682908,"strand":-1,"description":"CREB/ATF bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:24905]"}, {"versioned_ensembl_gene_id":"ENSG00000269266.1","gene_symbol":"DNAJC19P2","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45065]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861445","summary":null,"start":41605341,"end":41605671,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45065]"}, {"versioned_ensembl_gene_id":"ENSG00000235121.1","gene_symbol":"AL645504.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201723294,"end":201737506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125257.13","gene_symbol":"ABCC4","gene_name":"ATP binding cassette subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:55]","synonyms":"EST170205,MRP4,MOATB,MOAT-B","biotype":"protein_coding","ncbi_id":"10257","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This family member plays a role in cellular detoxification as a pump for its substrate, organic anions. It may also function in prostaglandin-mediated cAMP signaling in ciliogenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":95019829,"end":95301446,"strand":-1,"description":"ATP binding cassette subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:55]"}, {"versioned_ensembl_gene_id":"ENSG00000250584.2","gene_symbol":"LINC01511","gene_name":"long intergenic non-protein coding RNA 1511 [Source:HGNC Symbol;Acc:HGNC:51200]","synonyms":"RP11-325I22.2","biotype":"lincRNA","ncbi_id":"100506791","summary":null,"start":1363582,"end":1380067,"strand":-1,"description":"long intergenic non-protein coding RNA 1511 [Source:HGNC Symbol;Acc:HGNC:51200]"}, {"versioned_ensembl_gene_id":"ENSG00000270147.1","gene_symbol":"AC068620.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56396312,"end":56396871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236390.1","gene_symbol":"AC092800.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201673105,"end":201674144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112742.9","gene_symbol":"TTK","gene_name":"TTK protein kinase [Source:HGNC Symbol;Acc:HGNC:12401]","synonyms":"MPS1L1,MPS1,MPH1,CT96","biotype":"protein_coding","ncbi_id":"7272","summary":"This gene encodes a dual specificity protein kinase with the ability to phosphorylate tyrosine, serine and threonine. Associated with cell proliferation, this protein is essential for chromosome alignment at the centromere during mitosis and is required for centrosome duplication. It has been found to be a critical mitotic checkpoint protein for accurate segregation of chromosomes during mitosis. Tumorigenesis may occur when this protein fails to degrade and produces excess centrosomes resulting in aberrant mitotic spindles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]","start":80003887,"end":80042527,"strand":1,"description":"TTK protein kinase [Source:HGNC Symbol;Acc:HGNC:12401]"}, {"versioned_ensembl_gene_id":"ENSG00000186564.5","gene_symbol":"FOXD2","gene_name":"forkhead box D2 [Source:HGNC Symbol;Acc:HGNC:3803]","synonyms":"FREAC9,FKHL17","biotype":"protein_coding","ncbi_id":"2306","summary":"This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined. [provided by RefSeq, Jul 2008]","start":47436017,"end":47440691,"strand":1,"description":"forkhead box D2 [Source:HGNC Symbol;Acc:HGNC:3803]"}, {"versioned_ensembl_gene_id":"ENSG00000277718.1","gene_symbol":"LINC02255","gene_name":"long intergenic non-protein coding RNA 2255 [Source:HGNC Symbol;Acc:HGNC:53153]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370894","summary":null,"start":74379083,"end":74390535,"strand":1,"description":"long intergenic non-protein coding RNA 2255 [Source:HGNC Symbol;Acc:HGNC:53153]"}, {"versioned_ensembl_gene_id":"ENSG00000238230.1","gene_symbol":"LINC00391","gene_name":"long intergenic non-protein coding RNA 391 [Source:HGNC Symbol;Acc:HGNC:42719]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874154","summary":null,"start":94699694,"end":94702862,"strand":-1,"description":"long intergenic non-protein coding RNA 391 [Source:HGNC Symbol;Acc:HGNC:42719]"}, {"versioned_ensembl_gene_id":"ENSG00000248268.1","gene_symbol":"AC010275.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111277517,"end":111302567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225762.1","gene_symbol":"LINC01389","gene_name":"long intergenic non-protein coding RNA 1389 [Source:HGNC Symbol;Acc:HGNC:50661]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724077","summary":null,"start":47380928,"end":47408477,"strand":-1,"description":"long intergenic non-protein coding RNA 1389 [Source:HGNC Symbol;Acc:HGNC:50661]"}, {"versioned_ensembl_gene_id":"ENSG00000113140.10","gene_symbol":"SPARC","gene_name":"secreted protein acidic and cysteine rich [Source:HGNC Symbol;Acc:HGNC:11219]","synonyms":"ON","biotype":"protein_coding","ncbi_id":"6678","summary":"This gene encodes a cysteine-rich acidic matrix-associated protein. The encoded protein is required for the collagen in bone to become calcified but is also involved in extracellular matrix synthesis and promotion of changes to cell shape. The gene product has been associated with tumor suppression but has also been correlated with metastasis based on changes to cell shape which can promote tumor cell invasion. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2015]","start":151661096,"end":151687165,"strand":-1,"description":"secreted protein acidic and cysteine rich [Source:HGNC Symbol;Acc:HGNC:11219]"}, {"versioned_ensembl_gene_id":"ENSG00000176907.4","gene_symbol":"C8orf4","gene_name":"chromosome 8 open reading frame 4 [Source:HGNC Symbol;Acc:HGNC:1357]","synonyms":"TC1,TC-1,hTC-1","biotype":"protein_coding","ncbi_id":"56892","summary":"This gene encodes a small, monomeric, predominantly unstructured protein that functions as a positive regulator of the Wnt/beta-catenin signaling pathway. This protein interacts with a repressor of beta-catenin mediated transcription at nuclear speckles. It is thought to competitively block interactions of the repressor with beta-catenin, resulting in up-regulation of beta-catenin target genes. The encoded protein may also play a role in the NF-kappaB and ERK1/2 signaling pathways. Expression of this gene may play a role in the proliferation of several types of cancer including thyroid cancer, breast cancer and hematological malignancies. [provided by RefSeq, Nov 2011]","start":40153455,"end":40155308,"strand":1,"description":"chromosome 8 open reading frame 4 [Source:HGNC Symbol;Acc:HGNC:1357]"}, {"versioned_ensembl_gene_id":"ENSG00000255485.1","gene_symbol":"OR5G4P","gene_name":"olfactory receptor family 5 subfamily G member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15288]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81192","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56790206,"end":56790965,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15288]"}, {"versioned_ensembl_gene_id":"ENSG00000160014.16","gene_symbol":"CALM3","gene_name":"calmodulin 3 [Source:HGNC Symbol;Acc:HGNC:1449]","synonyms":"PHKD","biotype":"protein_coding","ncbi_id":"808","summary":"This gene encodes a member of a family of proteins that binds calcium and functions as a enzymatic co-factor. Activity of this protein is important in the regulation of the cell cycle and cytokinesis. Multiple alternatively spliced transcript variants have been observed at this gene. [provided by RefSeq, Aug 2016]","start":46601074,"end":46610793,"strand":1,"description":"calmodulin 3 [Source:HGNC Symbol;Acc:HGNC:1449]"}, {"versioned_ensembl_gene_id":"ENSG00000161533.11","gene_symbol":"ACOX1","gene_name":"acyl-CoA oxidase 1 [Source:HGNC Symbol;Acc:HGNC:119]","synonyms":"PALMCOX","biotype":"protein_coding","ncbi_id":"51","summary":"The protein encoded by this gene is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":75941507,"end":75979363,"strand":-1,"description":"acyl-CoA oxidase 1 [Source:HGNC Symbol;Acc:HGNC:119]"}, {"versioned_ensembl_gene_id":"ENSG00000147394.18","gene_symbol":"ZNF185","gene_name":"zinc finger protein 185 with LIM domain [Source:HGNC Symbol;Acc:HGNC:12976]","synonyms":"SCELL","biotype":"protein_coding","ncbi_id":"7739","summary":"Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a LIM-domain zinc finger protein. The LIM domain is composed of two contiguous zinc finger domains, separated by a two-amino acid residue hydrophobic linker. The LIM domain mediates protein:protein interactions. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, May 2010]","start":152914442,"end":152973480,"strand":1,"description":"zinc finger protein 185 with LIM domain [Source:HGNC Symbol;Acc:HGNC:12976]"}, {"versioned_ensembl_gene_id":"ENSG00000163898.9","gene_symbol":"LIPH","gene_name":"lipase H [Source:HGNC Symbol;Acc:HGNC:18483]","synonyms":"PLA1B,mPA-PLA1alpha,mPA-PLA1,LPDLR","biotype":"protein_coding","ncbi_id":"200879","summary":"This gene encodes a membrane-bound member of the mammalian triglyceride lipase family. It catalyzes the production of 2-acyl lysophosphatidic acid (LPA), which is a lipid mediator with diverse biological properties that include platelet aggregation, smooth muscle contraction, and stimulation of cell proliferation and motility. [provided by RefSeq, Jul 2008]","start":185506262,"end":185552613,"strand":-1,"description":"lipase H [Source:HGNC Symbol;Acc:HGNC:18483]"}, {"versioned_ensembl_gene_id":"ENSG00000257195.1","gene_symbol":"HNRNPA1P50","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728170","summary":null,"start":92883773,"end":92884700,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48780]"}, {"versioned_ensembl_gene_id":"ENSG00000183560.9","gene_symbol":"IZUMO1R","gene_name":"IZUMO1 receptor, JUNO [Source:HGNC Symbol;Acc:HGNC:32565]","synonyms":"JUNO,FOLR4,Folbp3","biotype":"protein_coding","ncbi_id":"390243","summary":null,"start":94305592,"end":94307721,"strand":1,"description":"IZUMO1 receptor, JUNO [Source:HGNC Symbol;Acc:HGNC:32565]"}, {"versioned_ensembl_gene_id":"ENSG00000239210.2","gene_symbol":"RPS26P55","gene_name":"ribosomal protein S26 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129650","summary":null,"start":34533427,"end":34534084,"strand":-1,"description":"ribosomal protein S26 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36500]"}, {"versioned_ensembl_gene_id":"ENSG00000253802.1","gene_symbol":"AC105999.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40298741,"end":40343402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169515.5","gene_symbol":"CCDC8","gene_name":"coiled-coil domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25367]","synonyms":"PPP1R20,DKFZp564K0322,3M3","biotype":"protein_coding","ncbi_id":"83987","summary":"This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a cofactor required for p53-mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin-like 1. Mutations in this gene are a cause of 3M syndrome-3 (3M3). [provided by RefSeq, Dec 2011]","start":46410372,"end":46413584,"strand":-1,"description":"coiled-coil domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25367]"}, {"versioned_ensembl_gene_id":"ENSG00000233164.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30691675,"end":30697740,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000213574.2","gene_symbol":"LDHAP5","gene_name":"lactate dehydrogenase A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:6540]","synonyms":"LDHAL5","biotype":"processed_pseudogene","ncbi_id":"729666","summary":null,"start":118932674,"end":118933295,"strand":-1,"description":"lactate dehydrogenase A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:6540]"}, {"versioned_ensembl_gene_id":"ENSG00000254326.1","gene_symbol":"IGHV7-27","gene_name":"immunoglobulin heavy variable 7-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5663]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28383","summary":null,"start":106317823,"end":106318236,"strand":-1,"description":"immunoglobulin heavy variable 7-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5663]"}, {"versioned_ensembl_gene_id":"ENSG00000238275.2","gene_symbol":"HOMER2P2","gene_name":"homer scaffolding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317769","summary":null,"start":106286811,"end":106287657,"strand":-1,"description":"homer scaffolding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20334]"}, {"versioned_ensembl_gene_id":"ENSG00000259143.1","gene_symbol":"AL356017.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":95185117,"end":95185854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240480.1","gene_symbol":"RPL29P2","gene_name":"ribosomal protein L29 pseudogene 2 [Source:NCBI gene;Acc:118432]","synonyms":"RPL29_10_1510","biotype":"transcribed_processed_pseudogene","ncbi_id":"118432","summary":null,"start":7754320,"end":7754976,"strand":1,"description":"ribosomal protein L29 pseudogene 2 [Source:NCBI gene;Acc:118432]"}, {"versioned_ensembl_gene_id":"ENSG00000280486.1","gene_symbol":"AC005329.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1386804,"end":1389651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172938.3","gene_symbol":"MRGPRD","gene_name":"MAS related GPR family member D [Source:HGNC Symbol;Acc:HGNC:29626]","synonyms":"mrgD","biotype":"protein_coding","ncbi_id":"116512","summary":null,"start":68980021,"end":68980986,"strand":-1,"description":"MAS related GPR family member D [Source:HGNC Symbol;Acc:HGNC:29626]"}, {"versioned_ensembl_gene_id":"ENSG00000136944.17","gene_symbol":"LMX1B","gene_name":"LIM homeobox transcription factor 1 beta [Source:HGNC Symbol;Acc:HGNC:6654]","synonyms":"NPS1","biotype":"protein_coding","ncbi_id":"4010","summary":"This gene encodes a member of LIM-homeodomain family of proteins containing two N-terminal zinc-binding LIM domains, 1 homeodomain, and a C-terminal glutamine-rich domain. It functions as a transcription factor, and is essential for the normal development of dorsal limb structures, the glomerular basement membrane, the anterior segment of the eye, and dopaminergic and serotonergic neurons. Mutations in this gene are associated with nail-patella syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":126614443,"end":126701032,"strand":1,"description":"LIM homeobox transcription factor 1 beta [Source:HGNC Symbol;Acc:HGNC:6654]"}, {"versioned_ensembl_gene_id":"ENSG00000238010.1","gene_symbol":"AL161908.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":126640756,"end":126641293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267801.1","gene_symbol":"AC087289.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75876372,"end":75879546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152760.9","gene_symbol":"TCTEX1D1","gene_name":"Tctex1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26882]","synonyms":"FLJ40873","biotype":"protein_coding","ncbi_id":"200132","summary":null,"start":66752459,"end":66778787,"strand":1,"description":"Tctex1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26882]"}, {"versioned_ensembl_gene_id":"ENSG00000143105.7","gene_symbol":"KCNA10","gene_name":"potassium voltage-gated channel subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:6219]","synonyms":"Kv1.8","biotype":"protein_coding","ncbi_id":"3744","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It is specifically regulated by cGMP and postulated to mediate the effects of substances that increase intracellular cGMP. This gene is intronless, and the gene is clustered with genes KCNA2 and KCNA3 on chromosome 1. [provided by RefSeq, Jul 2008]","start":110517217,"end":110519175,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:6219]"}, {"versioned_ensembl_gene_id":"ENSG00000232725.1","gene_symbol":"U52111.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153735626,"end":153766478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110777.11","gene_symbol":"POU2AF1","gene_name":"POU class 2 associating factor 1 [Source:HGNC Symbol;Acc:HGNC:9211]","synonyms":"OBF1,BOB1","biotype":"protein_coding","ncbi_id":"5450","summary":null,"start":111352252,"end":111455630,"strand":-1,"description":"POU class 2 associating factor 1 [Source:HGNC Symbol;Acc:HGNC:9211]"}, {"versioned_ensembl_gene_id":"ENSG00000197863.8","gene_symbol":"ZNF790","gene_name":"zinc finger protein 790 [Source:HGNC Symbol;Acc:HGNC:33114]","synonyms":"MGC62100,FLJ20350","biotype":"protein_coding","ncbi_id":"388536","summary":null,"start":36817428,"end":36850787,"strand":-1,"description":"zinc finger protein 790 [Source:HGNC Symbol;Acc:HGNC:33114]"}, {"versioned_ensembl_gene_id":"ENSG00000275080.5","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54798381,"end":54812886,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000235407.1","gene_symbol":"CYMP-AS1","gene_name":"CYMP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52509]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440602","summary":null,"start":110487680,"end":110490258,"strand":-1,"description":"CYMP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52509]"}, {"versioned_ensembl_gene_id":"ENSG00000251247.10","gene_symbol":"ZNF345","gene_name":"zinc finger protein 345 [Source:HGNC Symbol;Acc:HGNC:16367]","synonyms":"HZF10","biotype":"protein_coding","ncbi_id":"25850","summary":null,"start":36850361,"end":36913029,"strand":1,"description":"zinc finger protein 345 [Source:HGNC Symbol;Acc:HGNC:16367]"}, {"versioned_ensembl_gene_id":"ENSG00000271419.1","gene_symbol":"AL035410.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114353986,"end":114355178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273698.1","gene_symbol":"MRPL57P1","gene_name":"mitochondrial ribosomal protein L57 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29686]","synonyms":"MRP63P1","biotype":"processed_pseudogene","ncbi_id":"126581","summary":null,"start":114279011,"end":114279275,"strand":-1,"description":"mitochondrial ribosomal protein L57 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29686]"}, {"versioned_ensembl_gene_id":"ENSG00000226687.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529298,"end":29533446,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000234268.1","gene_symbol":"AP000936.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117035797,"end":117036051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254046.1","gene_symbol":"IGHV1-17","gene_name":"immunoglobulin heavy variable 1-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5548]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28469","summary":null,"start":106174342,"end":106174760,"strand":-1,"description":"immunoglobulin heavy variable 1-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5548]"}, {"versioned_ensembl_gene_id":"ENSG00000211944.2","gene_symbol":"IGHV3-16","gene_name":"immunoglobulin heavy variable 3-16 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5583]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28447","summary":null,"start":106165205,"end":106165730,"strand":-1,"description":"immunoglobulin heavy variable 3-16 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5583]"}, {"versioned_ensembl_gene_id":"ENSG00000266980.1","gene_symbol":"AC087289.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75818815,"end":75820055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132382.14","gene_symbol":"MYBBP1A","gene_name":"MYB binding protein 1a [Source:HGNC Symbol;Acc:HGNC:7546]","synonyms":"Pol5,PAP2,P160,FLJ37886","biotype":"protein_coding","ncbi_id":"10514","summary":"This gene encodes a nucleolar transcriptional regulator that was first identified by its ability to bind specifically to the Myb proto-oncogene protein. The encoded protein is thought to play a role in many cellular processes including response to nucleolar stress, tumor suppression and synthesis of ribosomal DNA. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":4538897,"end":4555631,"strand":-1,"description":"MYB binding protein 1a [Source:HGNC Symbol;Acc:HGNC:7546]"}, {"versioned_ensembl_gene_id":"ENSG00000229320.3","gene_symbol":"KRT8P12","gene_name":"keratin 8 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:28057]","synonyms":"KRT8L2","biotype":"transcribed_processed_pseudogene","ncbi_id":"90133","summary":null,"start":160565447,"end":160569248,"strand":1,"description":"keratin 8 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:28057]"}, {"versioned_ensembl_gene_id":"ENSG00000276085.1","gene_symbol":"CCL3L3","gene_name":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]","synonyms":"MGC12815","biotype":"protein_coding","ncbi_id":"414062","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this gene binds to several chemokine receptors, including chemokine binding protein 2 and chemokine (C-C motif) receptor 5 (CCR5). CCR5 is a co-receptor for HIV, and binding of this protein to CCR5 inhibits HIV entry. The copy number of this gene varies among individuals, where most individuals have one to six copies, and a minority of individuals have zero or more than six copies. There are conflicting reports about copy number variation of this gene and its correlation to disease susceptibility.[provided by RefSeq, Apr 2014]","start":36194869,"end":36196758,"strand":-1,"description":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]"}, {"versioned_ensembl_gene_id":"ENSG00000274767.1","gene_symbol":"AC243829.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36183235,"end":36196471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255520.1","gene_symbol":"AC090589.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47123104,"end":47130801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270190.1","gene_symbol":"AC068491.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111266868,"end":111267473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263020.6","gene_symbol":"AL662899.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31666102,"end":31673546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237043.1","gene_symbol":"AL929561.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026665,"end":29027592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226706.1","gene_symbol":"AL161452.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135503273,"end":135506447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125945.14","gene_symbol":"ZNF436","gene_name":"zinc finger protein 436 [Source:HGNC Symbol;Acc:HGNC:20814]","synonyms":"Zfp46,KIAA1710","biotype":"protein_coding","ncbi_id":"80818","summary":null,"start":23359448,"end":23369442,"strand":-1,"description":"zinc finger protein 436 [Source:HGNC Symbol;Acc:HGNC:20814]"}, {"versioned_ensembl_gene_id":"ENSG00000245750.7","gene_symbol":"DRAIC","gene_name":"downregulated RNA in cancer, inhibitor of cell invasion and migration [Source:HGNC Symbol;Acc:HGNC:27082]","synonyms":null,"biotype":"lincRNA","ncbi_id":"145837","summary":null,"start":69463026,"end":69571440,"strand":1,"description":"downregulated RNA in cancer, inhibitor of cell invasion and migration [Source:HGNC Symbol;Acc:HGNC:27082]"}, {"versioned_ensembl_gene_id":"ENSG00000275659.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,CD158e1/2,nkat3,NKB1,CD158e2,NKB1B,cl-11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54814901,"end":54878560,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000241680.1","gene_symbol":"AC002350.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110460988,"end":110461362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279650.1","gene_symbol":"AC073912.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130775694,"end":130776546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270580.5","gene_symbol":"PKD1P6-NPIPP1","gene_name":"PKD1P6-NPIPP1 readthrough [Source:NCBI gene;Acc:105369154]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"105369154","summary":"This locus represents naturally-occurring readthrough transcription between two unprocessed pseudogenes, PKD1P6 (polycystic kidney disease 1 (autosomal dominant) pseudogene 6) and NPIPP1 (nuclear pore complex interacting protein pseudogene 1). The individual pseudogene loci are not curated as transcribed regions. Readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Jan 2016]","start":15104723,"end":15131601,"strand":-1,"description":"PKD1P6-NPIPP1 readthrough [Source:NCBI gene;Acc:105369154]"}, {"versioned_ensembl_gene_id":"ENSG00000221932.6","gene_symbol":"HEPN1","gene_name":"hepatocellular carcinoma, down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:34400]","synonyms":null,"biotype":"protein_coding","ncbi_id":"641654","summary":"This gene is expressed predominantly in the liver. Transient transfection studies show the expression of this gene significantly inhibits cell growth, suggesting a role for this gene in apoptosis. Expression of this gene is down-regulated or lost in hepatocellular carcinomas (HCC), suggesting that loss of this gene is involved in carcinogenesis of hepatocytes (PMID:12971969). This gene maps to the 3'-noncoding region of the HEPACAM gene (GeneID:220296) on the antisense strand. [provided by RefSeq, Aug 2020]","start":124919244,"end":124920677,"strand":1,"description":"hepatocellular carcinoma, down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:34400]"}, {"versioned_ensembl_gene_id":"ENSG00000240801.1","gene_symbol":"AC132217.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":2129121,"end":2129964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280890.1","gene_symbol":"AC073324.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55235965,"end":55255635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167244.18","gene_symbol":"IGF2","gene_name":"insulin like growth factor 2 [Source:HGNC Symbol;Acc:HGNC:5466]","synonyms":"IGF-II,FLJ44734,C11orf43","biotype":"protein_coding","ncbi_id":"3481","summary":"This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":2129112,"end":2141238,"strand":-1,"description":"insulin like growth factor 2 [Source:HGNC Symbol;Acc:HGNC:5466]"}, {"versioned_ensembl_gene_id":"ENSG00000237781.3","gene_symbol":"AL356356.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150548562,"end":150557724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168872.16","gene_symbol":"DDX19A","gene_name":"DEAD-box helicase 19A [Source:HGNC Symbol;Acc:HGNC:25628]","synonyms":"FLJ11126,DDX19L","biotype":"protein_coding","ncbi_id":"55308","summary":null,"start":70346829,"end":70373383,"strand":1,"description":"DEAD-box helicase 19A [Source:HGNC Symbol;Acc:HGNC:25628]"}, {"versioned_ensembl_gene_id":"ENSG00000105821.14","gene_symbol":"DNAJC2","gene_name":"DnaJ heat shock protein family (Hsp40) member C2 [Source:HGNC Symbol;Acc:HGNC:13192]","synonyms":"zuotin,ZUO1,ZRF1,MPP11,MPHOSPH11","biotype":"protein_coding","ncbi_id":"27000","summary":"This gene is a member of the M-phase phosphoprotein (MPP) family. The gene encodes a phosphoprotein with a J domain and a Myb DNA-binding domain which localizes to both the nucleus and the cytosol. The protein is capable of forming a heterodimeric complex that associates with ribosomes, acting as a molecular chaperone for nascent polypeptide chains as they exit the ribosome. This protein was identified as a leukemia-associated antigen and expression of the gene is upregulated in leukemic blasts. Also, chromosomal aberrations involving this gene are associated with primary head and neck squamous cell tumors. This gene has a pseudogene on chromosome 6. Alternatively spliced variants which encode different protein isoforms have been described. [provided by RefSeq, Jul 2008]","start":103312474,"end":103344873,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C2 [Source:HGNC Symbol;Acc:HGNC:13192]"}, {"versioned_ensembl_gene_id":"ENSG00000186026.6","gene_symbol":"ZNF284","gene_name":"zinc finger protein 284 [Source:HGNC Symbol;Acc:HGNC:13078]","synonyms":"DKFZp781F1775","biotype":"protein_coding","ncbi_id":"342909","summary":null,"start":44072144,"end":44089613,"strand":1,"description":"zinc finger protein 284 [Source:HGNC Symbol;Acc:HGNC:13078]"}, {"versioned_ensembl_gene_id":"ENSG00000241069.1","gene_symbol":"AC125388.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53386233,"end":53386388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159885.13","gene_symbol":"ZNF222","gene_name":"zinc finger protein 222 [Source:HGNC Symbol;Acc:HGNC:13015]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7673","summary":null,"start":44025342,"end":44033112,"strand":1,"description":"zinc finger protein 222 [Source:HGNC Symbol;Acc:HGNC:13015]"}, {"versioned_ensembl_gene_id":"ENSG00000160183.13","gene_symbol":"TMPRSS3","gene_name":"transmembrane protease, serine 3 [Source:HGNC Symbol;Acc:HGNC:11877]","synonyms":"DFNB8,DFNB10","biotype":"protein_coding","ncbi_id":"64699","summary":"This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, an LDL receptor-like domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor-associated gene that is overexpressed in ovarian tumors. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":42371890,"end":42396846,"strand":-1,"description":"transmembrane protease, serine 3 [Source:HGNC Symbol;Acc:HGNC:11877]"}, {"versioned_ensembl_gene_id":"ENSG00000269758.1","gene_symbol":"AC092070.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53267870,"end":53270932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255372.1","gene_symbol":"AC107886.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22261209,"end":22262256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253332.1","gene_symbol":"AP005902.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39860219,"end":39860525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253755.1","gene_symbol":"IGHGP","gene_name":"immunoglobulin heavy constant gamma P (non-functional) [Source:HGNC Symbol;Acc:HGNC:5529]","synonyms":"IGHGP1","biotype":"IG_C_pseudogene","ncbi_id":"3505","summary":null,"start":105664633,"end":105669843,"strand":-1,"description":"immunoglobulin heavy constant gamma P (non-functional) [Source:HGNC Symbol;Acc:HGNC:5529]"}, {"versioned_ensembl_gene_id":"ENSG00000197928.10","gene_symbol":"ZNF677","gene_name":"zinc finger protein 677 [Source:HGNC Symbol;Acc:HGNC:28730]","synonyms":"MGC48625","biotype":"protein_coding","ncbi_id":"342926","summary":null,"start":53235381,"end":53254898,"strand":-1,"description":"zinc finger protein 677 [Source:HGNC Symbol;Acc:HGNC:28730]"}, {"versioned_ensembl_gene_id":"ENSG00000231049.2","gene_symbol":"OR52B5P","gene_name":"olfactory receptor family 52 subfamily B member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15210]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81270","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5557096,"end":5564327,"strand":1,"description":"olfactory receptor family 52 subfamily B member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15210]"}, {"versioned_ensembl_gene_id":"ENSG00000197728.9","gene_symbol":"RPS26","gene_name":"ribosomal protein S26 [Source:HGNC Symbol;Acc:HGNC:10414]","synonyms":"S26","biotype":"protein_coding","ncbi_id":"6231","summary":"This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S26E family of ribosomal proteins. Mutations in this gene are found in Diamond-Blackfan anemia 10. There are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Aug 2017]","start":56041853,"end":56044675,"strand":1,"description":"ribosomal protein S26 [Source:HGNC Symbol;Acc:HGNC:10414]"}, {"versioned_ensembl_gene_id":"ENSG00000234952.1","gene_symbol":"AL139121.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117735313,"end":117736407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165416.14","gene_symbol":"SUGT1","gene_name":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone [Source:HGNC Symbol;Acc:HGNC:16987]","synonyms":"SGT1","biotype":"protein_coding","ncbi_id":"10910","summary":"This gene encodes a highly conserved nuclear protein involved in kinetochore function and required for the G1/S and G2/M transitions. This protein interacts with heat shock protein 90. Alternative splicing results in multiple transcript variants. Pseudogenes for this gene have been defined on several different chromosomes. [provided by RefSeq, Mar 2016]","start":52652709,"end":52700909,"strand":1,"description":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone [Source:HGNC Symbol;Acc:HGNC:16987]"}, {"versioned_ensembl_gene_id":"ENSG00000163815.5","gene_symbol":"CLEC3B","gene_name":"C-type lectin domain family 3 member B [Source:HGNC Symbol;Acc:HGNC:11891]","synonyms":"TNA,TN","biotype":"protein_coding","ncbi_id":"7123","summary":null,"start":45001548,"end":45036071,"strand":1,"description":"C-type lectin domain family 3 member B [Source:HGNC Symbol;Acc:HGNC:11891]"}, {"versioned_ensembl_gene_id":"ENSG00000213401.9","gene_symbol":"MAGEA12","gene_name":"MAGE family member A12 [Source:HGNC Symbol;Acc:HGNC:6799]","synonyms":"MAGE12,CT1.12","biotype":"protein_coding","ncbi_id":"4111","summary":"This gene is closely related to several other genes clustered on chromosome X. These genes may be overexpressed in tumors. Multiple alternatively spliced variants encoding the same protein have been identified. [provided by RefSeq, Jun 2014]","start":152733779,"end":152737669,"strand":1,"description":"MAGE family member A12 [Source:HGNC Symbol;Acc:HGNC:6799]"}, {"versioned_ensembl_gene_id":"ENSG00000242599.7","gene_symbol":"CSAG4","gene_name":"CSAG family member 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20923]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100130935","summary":null,"start":152733827,"end":152740985,"strand":1,"description":"CSAG family member 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20923]"}, {"versioned_ensembl_gene_id":"ENSG00000226535.1","gene_symbol":"AL445487.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107169569,"end":107171148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230087.1","gene_symbol":"AC104389.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5354692,"end":5355578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225616.2","gene_symbol":"AL138785.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28982278,"end":28982608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272841.1","gene_symbol":"AL139393.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160990318,"end":160992342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259708.1","gene_symbol":"AC090607.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78250502,"end":78264156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160113.5","gene_symbol":"NR2F6","gene_name":"nuclear receptor subfamily 2 group F member 6 [Source:HGNC Symbol;Acc:HGNC:7977]","synonyms":"ERBAL2,EAR-2","biotype":"protein_coding","ncbi_id":"2063","summary":null,"start":17231883,"end":17245940,"strand":-1,"description":"nuclear receptor subfamily 2 group F member 6 [Source:HGNC Symbol;Acc:HGNC:7977]"}, {"versioned_ensembl_gene_id":"ENSG00000177885.13","gene_symbol":"GRB2","gene_name":"growth factor receptor bound protein 2 [Source:HGNC Symbol;Acc:HGNC:4566]","synonyms":"NCKAP2","biotype":"protein_coding","ncbi_id":"2885","summary":"The protein encoded by this gene binds the epidermal growth factor receptor and contains one SH2 domain and two SH3 domains. Its two SH3 domains direct complex formation with proline-rich regions of other proteins, and its SH2 domain binds tyrosine phosphorylated sequences. This gene is similar to the Sem5 gene of C.elegans, which is involved in the signal transduction pathway. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75318076,"end":75405709,"strand":-1,"description":"growth factor receptor bound protein 2 [Source:HGNC Symbol;Acc:HGNC:4566]"}, {"versioned_ensembl_gene_id":"ENSG00000267372.2","gene_symbol":"AC005330.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1321225,"end":1322846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229521.2","gene_symbol":"MYCBP2-AS2","gene_name":"MYCBP2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41024]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874213","summary":null,"start":77080511,"end":77081190,"strand":-1,"description":"MYCBP2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41024]"}, {"versioned_ensembl_gene_id":"ENSG00000280223.1","gene_symbol":"AL645820.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126004446,"end":126006118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176407.17","gene_symbol":"KCMF1","gene_name":"potassium channel modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:20589]","synonyms":"ZZZ1,PCMF,DKFZP434L1021,DEBT91","biotype":"protein_coding","ncbi_id":"56888","summary":null,"start":84971093,"end":85059472,"strand":1,"description":"potassium channel modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:20589]"}, {"versioned_ensembl_gene_id":"ENSG00000282815.1","gene_symbol":"TEX13C","gene_name":"TEX13 family member C [Source:HGNC Symbol;Acc:HGNC:52277]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129520","summary":null,"start":125320120,"end":125325214,"strand":1,"description":"TEX13 family member C [Source:HGNC Symbol;Acc:HGNC:52277]"}, {"versioned_ensembl_gene_id":"ENSG00000237062.1","gene_symbol":"AL512649.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106615078,"end":106615806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234323.6","gene_symbol":"LINC01505","gene_name":"long intergenic non-protein coding RNA 1505 [Source:HGNC Symbol;Acc:HGNC:51186]","synonyms":"RP11-308N19.1,RP11-308N19.1","biotype":"lincRNA","ncbi_id":"100996590","summary":null,"start":105993310,"end":106740875,"strand":1,"description":"long intergenic non-protein coding RNA 1505 [Source:HGNC Symbol;Acc:HGNC:51186]"}, {"versioned_ensembl_gene_id":"ENSG00000196876.15","gene_symbol":"SCN8A","gene_name":"sodium voltage-gated channel alpha subunit 8 [Source:HGNC Symbol;Acc:HGNC:10596]","synonyms":"PN4,Nav1.6,NaCh6,MED,CIAT,CerIII","biotype":"protein_coding","ncbi_id":"6334","summary":"This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with cognitive disability, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":51590266,"end":51812864,"strand":1,"description":"sodium voltage-gated channel alpha subunit 8 [Source:HGNC Symbol;Acc:HGNC:10596]"}, {"versioned_ensembl_gene_id":"ENSG00000165219.21","gene_symbol":"GAPVD1","gene_name":"GTPase activating protein and VPS9 domains 1 [Source:HGNC Symbol;Acc:HGNC:23375]","synonyms":"KIAA1521,DKFZP434C212","biotype":"protein_coding","ncbi_id":"26130","summary":null,"start":125261794,"end":125367207,"strand":1,"description":"GTPase activating protein and VPS9 domains 1 [Source:HGNC Symbol;Acc:HGNC:23375]"}, {"versioned_ensembl_gene_id":"ENSG00000146648.17","gene_symbol":"EGFR","gene_name":"epidermal growth factor receptor [Source:HGNC Symbol;Acc:HGNC:3236]","synonyms":"ERBB,ERBB1","biotype":"protein_coding","ncbi_id":"1956","summary":"The protein encoded by this gene is a transmembrane glycoprotein that is a member of the protein kinase superfamily. This protein is a receptor for members of the epidermal growth factor family. EGFR is a cell surface protein that binds to epidermal growth factor, thus inducing receptor dimerization and tyrosine autophosphorylation leading to cell proliferation. Mutations in this gene are associated with lung cancer. EGFR is a component of the cytokine storm which contributes to a severe form of Coronavirus Disease 2019 (COVID-19) resulting from infection with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). [provided by RefSeq, Jul 2020]","start":55019021,"end":55211628,"strand":1,"description":"epidermal growth factor receptor [Source:HGNC Symbol;Acc:HGNC:3236]"}, {"versioned_ensembl_gene_id":"ENSG00000265399.1","gene_symbol":"AP005329.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3190397,"end":3247277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126337.13","gene_symbol":"KRT36","gene_name":"keratin 36 [Source:HGNC Symbol;Acc:HGNC:6454]","synonyms":"KRTHA6","biotype":"protein_coding","ncbi_id":"8689","summary":"The protein encoded by this gene is a member of the keratin gene family. This type I hair keratin is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41486136,"end":41492546,"strand":-1,"description":"keratin 36 [Source:HGNC Symbol;Acc:HGNC:6454]"}, {"versioned_ensembl_gene_id":"ENSG00000235416.1","gene_symbol":"AC233728.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53456273,"end":53457029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233211.2","gene_symbol":"GRPEL2P1","gene_name":"GrpE like 2, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874360","summary":null,"start":88978447,"end":88978785,"strand":-1,"description":"GrpE like 2, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41969]"}, {"versioned_ensembl_gene_id":"ENSG00000216721.3","gene_symbol":"AC093850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":215804731,"end":215804981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280123.1","gene_symbol":"AC023632.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":94427712,"end":94429888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228618.1","gene_symbol":"AC012462.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215476667,"end":215480248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230695.1","gene_symbol":"AC012462.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":215436253,"end":215436992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244734.3","gene_symbol":"HBB","gene_name":"hemoglobin subunit beta [Source:HGNC Symbol;Acc:HGNC:4827]","synonyms":"HBD,CD113t-C,beta-globin","biotype":"protein_coding","ncbi_id":"3043","summary":"The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. The normal adult hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta-zero-thalassemia. Reduced amounts of detectable beta globin causes beta-plus-thalassemia. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008]","start":5225464,"end":5229395,"strand":-1,"description":"hemoglobin subunit beta [Source:HGNC Symbol;Acc:HGNC:4827]"}, {"versioned_ensembl_gene_id":"ENSG00000126777.17","gene_symbol":"KTN1","gene_name":"kinectin 1 [Source:HGNC Symbol;Acc:HGNC:6467]","synonyms":"KNT,KIAA0004,CG1","biotype":"protein_coding","ncbi_id":"3895","summary":"This gene encodes an integral membrane protein that is a member of the kinectin protein family. The encoded protein is primarily localized to the endoplasmic reticulum membrane. This protein binds kinesin and may be involved in intracellular organelle motility. This protein also binds translation elongation factor-delta and may be involved in the assembly of the elongation factor-1 complex. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Aug 2012]","start":55559072,"end":55701526,"strand":1,"description":"kinectin 1 [Source:HGNC Symbol;Acc:HGNC:6467]"}, {"versioned_ensembl_gene_id":"ENSG00000034510.5","gene_symbol":"TMSB10","gene_name":"thymosin beta 10 [Source:HGNC Symbol;Acc:HGNC:11879]","synonyms":"TB10","biotype":"protein_coding","ncbi_id":"9168","summary":null,"start":84905625,"end":84906675,"strand":1,"description":"thymosin beta 10 [Source:HGNC Symbol;Acc:HGNC:11879]"}, {"versioned_ensembl_gene_id":"ENSG00000104783.11","gene_symbol":"KCNN4","gene_name":"potassium calcium-activated channel subfamily N member 4 [Source:HGNC Symbol;Acc:HGNC:6293]","synonyms":"KCa3.1,IK,hSK4,hKCa4,hIKCa1","biotype":"protein_coding","ncbi_id":"3783","summary":"The protein encoded by this gene is part of a potentially heterotetrameric voltage-independent potassium channel that is activated by intracellular calcium. Activation is followed by membrane hyperpolarization, which promotes calcium influx. The encoded protein may be part of the predominant calcium-activated potassium channel in T-lymphocytes. This gene is similar to other KCNN family potassium channel genes, but it differs enough to possibly be considered as part of a new subfamily. [provided by RefSeq, Jul 2008]","start":43766533,"end":43781257,"strand":-1,"description":"potassium calcium-activated channel subfamily N member 4 [Source:HGNC Symbol;Acc:HGNC:6293]"}, {"versioned_ensembl_gene_id":"ENSG00000226592.1","gene_symbol":"AC004911.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145269514,"end":145270384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254911.3","gene_symbol":"SCARNA9","gene_name":"small Cajal body-specific RNA 9 [Source:HGNC Symbol;Acc:HGNC:32566]","synonyms":"Z32,mgU2-19/30","biotype":"antisense_RNA","ncbi_id":"619383","summary":null,"start":93721513,"end":93721865,"strand":1,"description":"small Cajal body-specific RNA 9 [Source:HGNC Symbol;Acc:HGNC:32566]"}, {"versioned_ensembl_gene_id":"ENSG00000280405.1","gene_symbol":"AC026336.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130144954,"end":130145691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230595.1","gene_symbol":"RSL24D1P2","gene_name":"ribosomal L24 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129162","summary":null,"start":62561058,"end":62561423,"strand":-1,"description":"ribosomal L24 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37867]"}, {"versioned_ensembl_gene_id":"ENSG00000276825.2","gene_symbol":"DRD4","gene_name":"dopamine receptor D4 [Source:HGNC Symbol;Acc:HGNC:3025]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1815","summary":"This gene encodes the D4 subtype of the dopamine receptor. The D4 subtype is a G-protein coupled receptor which inhibits adenylyl cyclase. It is a target for drugs which treat schizophrenia and Parkinson disease. Mutations in this gene have been associated with various behavioral phenotypes, including autonomic nervous system dysfunction, attention deficit/hyperactivity disorder, and the personality trait of novelty seeking. This gene contains a polymorphic number (2-10 copies) of tandem 48 nt repeats; the sequence shown contains four repeats. [provided by RefSeq, Jul 2008]","start":637525,"end":640936,"strand":1,"description":"dopamine receptor D4 [Source:HGNC Symbol;Acc:HGNC:3025]"}, {"versioned_ensembl_gene_id":"ENSG00000259029.1","gene_symbol":"DUX4L18","gene_name":"double homeobox 4 like 18 [Source:HGNC Symbol;Acc:HGNC:37716]","synonyms":"DUXY2","biotype":"unprocessed_pseudogene","ncbi_id":"100132421","summary":null,"start":11321557,"end":11322823,"strand":1,"description":"double homeobox 4 like 18 [Source:HGNC Symbol;Acc:HGNC:37716]"}, {"versioned_ensembl_gene_id":"ENSG00000213779.4","gene_symbol":"AC107956.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17193489,"end":17194308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228473.1","gene_symbol":"LIN28AP2","gene_name":"LIN28A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38056]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287388","summary":null,"start":87379472,"end":87380258,"strand":-1,"description":"LIN28A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38056]"}, {"versioned_ensembl_gene_id":"ENSG00000184906.10","gene_symbol":"AMYH02020865.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40497850,"end":40566779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124449.6","gene_symbol":"IRGC","gene_name":"immunity related GTPase cinema [Source:HGNC Symbol;Acc:HGNC:28835]","synonyms":"IRGC1,Iigp5,CINEMA","biotype":"protein_coding","ncbi_id":"56269","summary":null,"start":43716010,"end":43720021,"strand":1,"description":"immunity related GTPase cinema [Source:HGNC Symbol;Acc:HGNC:28835]"}, {"versioned_ensembl_gene_id":"ENSG00000161996.18","gene_symbol":"WDR90","gene_name":"WD repeat domain 90 [Source:HGNC Symbol;Acc:HGNC:26960]","synonyms":"C16orf15,KIAA1924,FLJ36483,C16orf19,C16orf18,C16orf17,C16orf16","biotype":"protein_coding","ncbi_id":"197335","summary":null,"start":649311,"end":667833,"strand":1,"description":"WD repeat domain 90 [Source:HGNC Symbol;Acc:HGNC:26960]"}, {"versioned_ensembl_gene_id":"ENSG00000168619.15","gene_symbol":"ADAM18","gene_name":"ADAM metallopeptidase domain 18 [Source:HGNC Symbol;Acc:HGNC:196]","synonyms":"tMDCIII,ADAM27","biotype":"protein_coding","ncbi_id":"8749","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature sperm surface protein. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":39584489,"end":39730064,"strand":1,"description":"ADAM metallopeptidase domain 18 [Source:HGNC Symbol;Acc:HGNC:196]"}, {"versioned_ensembl_gene_id":"ENSG00000139842.14","gene_symbol":"CUL4A","gene_name":"cullin 4A [Source:HGNC Symbol;Acc:HGNC:2554]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8451","summary":"CUL4A is the ubiquitin ligase component of a multimeric complex involved in the degradation of DNA damage-response proteins (Liu et al., 2009 [PubMed 19481525]).[supplied by OMIM, Oct 2009]","start":113208193,"end":113267108,"strand":1,"description":"cullin 4A [Source:HGNC Symbol;Acc:HGNC:2554]"}, {"versioned_ensembl_gene_id":"ENSG00000274502.1","gene_symbol":"ANKRD20A6P","gene_name":"ankyrin repeat domain 20 family member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:37714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728157","summary":null,"start":11173618,"end":11173821,"strand":1,"description":"ankyrin repeat domain 20 family member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:37714]"}, {"versioned_ensembl_gene_id":"ENSG00000253784.1","gene_symbol":"AC090735.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72874859,"end":72881740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230293.11","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31722164,"end":31744857,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000105323.16","gene_symbol":"HNRNPUL1","gene_name":"heterogeneous nuclear ribonucleoprotein U like 1 [Source:HGNC Symbol;Acc:HGNC:17011]","synonyms":"HNRPUL1,FLJ12944,E1BAP5,E1B-AP5","biotype":"protein_coding","ncbi_id":"11100","summary":"This gene encodes a nuclear RNA-binding protein of the heterogeneous nuclear ribonucleoprotein (hnRNP) family. This protein binds specifically to adenovirus early-1B-55kDa oncoprotein. It may play an important role in nucleocytoplasmic RNA transport, and its function is modulated by early-1B-55kDa in adenovirus-infected cells. [provided by RefSeq, Mar 2016]","start":41262496,"end":41307598,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein U like 1 [Source:HGNC Symbol;Acc:HGNC:17011]"}, {"versioned_ensembl_gene_id":"ENSG00000262898.1","gene_symbol":"AC139099.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83144131,"end":83177607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172912.4","gene_symbol":"COX6B1P3","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2283]","synonyms":"COX6BP3","biotype":"processed_pseudogene","ncbi_id":"1343","summary":null,"start":40569286,"end":40569895,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2283]"}, {"versioned_ensembl_gene_id":"ENSG00000004487.15","gene_symbol":"KDM1A","gene_name":"lysine demethylase 1A [Source:HGNC Symbol;Acc:HGNC:29079]","synonyms":"LSD1,KIAA0601,KDM1,BHC110,AOF2","biotype":"protein_coding","ncbi_id":"23028","summary":"This gene encodes a nuclear protein containing a SWIRM domain, a FAD-binding motif, and an amine oxidase domain. This protein is a component of several histone deacetylase complexes, though it silences genes by functioning as a histone demethylase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":23019448,"end":23083689,"strand":1,"description":"lysine demethylase 1A [Source:HGNC Symbol;Acc:HGNC:29079]"}, {"versioned_ensembl_gene_id":"ENSG00000164142.15","gene_symbol":"FAM160A1","gene_name":"family with sequence similarity 160 member A1 [Source:HGNC Symbol;Acc:HGNC:34237]","synonyms":"FLJ43373","biotype":"protein_coding","ncbi_id":"729830","summary":null,"start":151409216,"end":151663632,"strand":1,"description":"family with sequence similarity 160 member A1 [Source:HGNC Symbol;Acc:HGNC:34237]"}, {"versioned_ensembl_gene_id":"ENSG00000240553.1","gene_symbol":"AL031428.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23020147,"end":23088058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243385.2","gene_symbol":"AC094085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83201229,"end":83202141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228236.2","gene_symbol":"TXNP5","gene_name":"thioredoxin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49485]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"151276","summary":null,"start":149068596,"end":149068910,"strand":-1,"description":"thioredoxin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49485]"}, {"versioned_ensembl_gene_id":"ENSG00000019582.14","gene_symbol":"CD74","gene_name":"CD74 molecule [Source:HGNC Symbol;Acc:HGNC:1697]","synonyms":"DHLAG","biotype":"protein_coding","ncbi_id":"972","summary":"The protein encoded by this gene associates with class II major histocompatibility complex (MHC) and is an important chaperone that regulates antigen presentation for immune response. It also serves as cell surface receptor for the cytokine macrophage migration inhibitory factor (MIF) which, when bound to the encoded protein, initiates survival pathways and cell proliferation. This protein also interacts with amyloid precursor protein (APP) and suppresses the production of amyloid beta (Abeta). Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":150401637,"end":150412929,"strand":-1,"description":"CD74 molecule [Source:HGNC Symbol;Acc:HGNC:1697]"}, {"versioned_ensembl_gene_id":"ENSG00000254816.1","gene_symbol":"AC090857.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21169748,"end":21170137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270570.1","gene_symbol":"AC140113.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11107719,"end":11107887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283044.1","gene_symbol":"AL391597.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207401691,"end":207416236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243160.1","gene_symbol":"AC093270.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79529302,"end":79530093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275855.1","gene_symbol":"AC138747.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28361822,"end":28365684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225993.9","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"Ly6-D,NG25,G6D,MEGT1,C6orf23","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31754813,"end":31757257,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000217576.7","gene_symbol":"AL158066.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":52167709,"end":52291557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117013.14","gene_symbol":"KCNQ4","gene_name":"potassium voltage-gated channel subfamily Q member 4 [Source:HGNC Symbol;Acc:HGNC:6298]","synonyms":"Kv7.4,DFNA2","biotype":"protein_coding","ncbi_id":"9132","summary":"The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":40784012,"end":40840452,"strand":1,"description":"potassium voltage-gated channel subfamily Q member 4 [Source:HGNC Symbol;Acc:HGNC:6298]"}, {"versioned_ensembl_gene_id":"ENSG00000226870.2","gene_symbol":"BX276092.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71719142,"end":71721278,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228490.1","gene_symbol":"CT009496.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29881442,"end":29882408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179604.9","gene_symbol":"CDC42EP4","gene_name":"CDC42 effector protein 4 [Source:HGNC Symbol;Acc:HGNC:17147]","synonyms":"BORG4,MGC3740,MGC17125,KAIA1777,CEP4","biotype":"protein_coding","ncbi_id":"23580","summary":"The product of this gene is a member of the CDC42-binding protein family. Members of this family interact with Rho family GTPases and regulate the organization of the actin cytoskeleton. This protein has been shown to bind both CDC42 and TC10 GTPases in a GTP-dependent manner. When overexpressed in fibroblasts, this protein was able to induce pseudopodia formation, which suggested a role in inducing actin filament assembly and cell shape control. [provided by RefSeq, Jul 2008]","start":73283624,"end":73312175,"strand":-1,"description":"CDC42 effector protein 4 [Source:HGNC Symbol;Acc:HGNC:17147]"}, {"versioned_ensembl_gene_id":"ENSG00000253499.2","gene_symbol":"AC025881.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114318400,"end":114318911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144468.16","gene_symbol":"RHBDD1","gene_name":"rhomboid domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23081]","synonyms":"DKFZp547E052","biotype":"protein_coding","ncbi_id":"84236","summary":null,"start":226835581,"end":226999215,"strand":1,"description":"rhomboid domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23081]"}, {"versioned_ensembl_gene_id":"ENSG00000253226.1","gene_symbol":"HAUS1P3","gene_name":"HAUS augmin like complex subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43762]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271703","summary":null,"start":72618722,"end":72619383,"strand":-1,"description":"HAUS augmin like complex subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43762]"}, {"versioned_ensembl_gene_id":"ENSG00000153187.18","gene_symbol":"HNRNPU","gene_name":"heterogeneous nuclear ribonucleoprotein U [Source:HGNC Symbol;Acc:HGNC:5048]","synonyms":"HNRNPU-AS1,hnRNPU,FLJ37978,FLJ30202,C1orf199,SAF-A,NCRNA00201,HNRPU","biotype":"protein_coding","ncbi_id":"3192","summary":"This gene encodes a member of a family of proteins that bind nucleic acids and function in the formation of ribonucleoprotein complexes in the nucleus with heterogeneous nuclear RNA (hnRNA). The encoded protein has affinity for both RNA and DNA, and binds scaffold-attached region (SAR) DNA. Mutations in this gene have been associated with epileptic encephalopathy, early infantile, 54. A pseudogene of this gene has been identified on chromosome 14. [provided by RefSeq, Jun 2017]","start":244840638,"end":244864560,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein U [Source:HGNC Symbol;Acc:HGNC:5048]"}, {"versioned_ensembl_gene_id":"ENSG00000198520.10","gene_symbol":"C1orf228","gene_name":"chromosome 1 open reading frame 228 [Source:HGNC Symbol;Acc:HGNC:34345]","synonyms":"p40,NCRNA00082,MGC33556","biotype":"protein_coding","ncbi_id":"339541","summary":null,"start":44674692,"end":44725591,"strand":1,"description":"chromosome 1 open reading frame 228 [Source:HGNC Symbol;Acc:HGNC:34345]"}, {"versioned_ensembl_gene_id":"ENSG00000176893.5","gene_symbol":"OR51G2","gene_name":"olfactory receptor family 51 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15198]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81282","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4912588,"end":4919350,"strand":-1,"description":"olfactory receptor family 51 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15198]"}, {"versioned_ensembl_gene_id":"ENSG00000235441.5","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"OR10C1P,hs6M1-17,OR10C2","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439782,"end":29441453,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000279261.2","gene_symbol":"AL360294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234757619,"end":234760056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149970.14","gene_symbol":"CNKSR2","gene_name":"connector enhancer of kinase suppressor of Ras 2 [Source:HGNC Symbol;Acc:HGNC:19701]","synonyms":"KSR2,KIAA0902,CNK2","biotype":"protein_coding","ncbi_id":"22866","summary":"This gene encodes a multidomain protein that functions as a scaffold protein to mediate the mitogen-activated protein kinase pathways downstream from Ras. This gene product is induced by vitamin D and inhibits apoptosis in certain cancer cells. It may also play a role in ternary complex assembly of synaptic proteins at the postsynaptic membrane and coupling of signal transduction to membrane/cytoskeletal remodeling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":21374418,"end":21654695,"strand":1,"description":"connector enhancer of kinase suppressor of Ras 2 [Source:HGNC Symbol;Acc:HGNC:19701]"}, {"versioned_ensembl_gene_id":"ENSG00000229309.2","gene_symbol":"AL353633.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81250438,"end":81302407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248778.1","gene_symbol":"AC105391.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105679050,"end":105680094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144031.11","gene_symbol":"ANKRD53","gene_name":"ankyrin repeat domain 53 [Source:HGNC Symbol;Acc:HGNC:25691]","synonyms":"FLJ12056,FLJ36160","biotype":"protein_coding","ncbi_id":"79998","summary":null,"start":70978380,"end":70985499,"strand":1,"description":"ankyrin repeat domain 53 [Source:HGNC Symbol;Acc:HGNC:25691]"}, {"versioned_ensembl_gene_id":"ENSG00000239322.1","gene_symbol":"ATP6V1B1-AS1","gene_name":"ATP6V1B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51118]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927750","summary":null,"start":70941817,"end":70948610,"strand":-1,"description":"ATP6V1B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51118]"}, {"versioned_ensembl_gene_id":"ENSG00000236699.8","gene_symbol":"ARHGEF38","gene_name":"Rho guanine nucleotide exchange factor 38 [Source:HGNC Symbol;Acc:HGNC:25968]","synonyms":"FLJ20184","biotype":"protein_coding","ncbi_id":"54848","summary":null,"start":105552620,"end":105708093,"strand":1,"description":"Rho guanine nucleotide exchange factor 38 [Source:HGNC Symbol;Acc:HGNC:25968]"}, {"versioned_ensembl_gene_id":"ENSG00000226061.1","gene_symbol":"PCMTD1P1","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38804]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874520","summary":null,"start":10173853,"end":10174207,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38804]"}, {"versioned_ensembl_gene_id":"ENSG00000250120.6","gene_symbol":"PCDHA10","gene_name":"protocadherin alpha 10 [Source:HGNC Symbol;Acc:HGNC:8664]","synonyms":"PCDH-ALPHA10,CRNR8,CNRS8,CNRN8,CNR8","biotype":"protein_coding","ncbi_id":"56139","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140855883,"end":141012344,"strand":1,"description":"protocadherin alpha 10 [Source:HGNC Symbol;Acc:HGNC:8664]"}, {"versioned_ensembl_gene_id":"ENSG00000224058.2","gene_symbol":"AC006509.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47731402,"end":47732035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235369.1","gene_symbol":"RPL36AP15","gene_name":"ribosomal protein L36a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271325","summary":null,"start":47797826,"end":47798091,"strand":-1,"description":"ribosomal protein L36a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36648]"}, {"versioned_ensembl_gene_id":"ENSG00000254961.1","gene_symbol":"TUBB4BP4","gene_name":"tubulin beta 4B class IVb pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42333]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480434","summary":null,"start":91949731,"end":91950034,"strand":-1,"description":"tubulin beta 4B class IVb pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42333]"}, {"versioned_ensembl_gene_id":"ENSG00000169047.5","gene_symbol":"IRS1","gene_name":"insulin receptor substrate 1 [Source:HGNC Symbol;Acc:HGNC:6125]","synonyms":"HIRS-1","biotype":"protein_coding","ncbi_id":"3667","summary":"This gene encodes a protein which is phosphorylated by insulin receptor tyrosine kinase. Mutations in this gene are associated with type II diabetes and susceptibility to insulin resistance. [provided by RefSeq, Nov 2009]","start":226731317,"end":226799759,"strand":-1,"description":"insulin receptor substrate 1 [Source:HGNC Symbol;Acc:HGNC:6125]"}, {"versioned_ensembl_gene_id":"ENSG00000235070.3","gene_symbol":"AC062015.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":226180044,"end":226185371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279417.1","gene_symbol":"AC019322.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30344307,"end":30348236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251664.3","gene_symbol":"PCDHA12","gene_name":"protocadherin alpha 12 [Source:HGNC Symbol;Acc:HGNC:8666]","synonyms":"PCDH-ALPHA12","biotype":"protein_coding","ncbi_id":"56137","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140875302,"end":141012344,"strand":1,"description":"protocadherin alpha 12 [Source:HGNC Symbol;Acc:HGNC:8666]"}, {"versioned_ensembl_gene_id":"ENSG00000254026.1","gene_symbol":"AC015468.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20954012,"end":20968904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253199.1","gene_symbol":"LINC02153","gene_name":"long intergenic non-protein coding RNA 2153 [Source:HGNC Symbol;Acc:HGNC:27823]","synonyms":"ENST00000517573","biotype":"lincRNA","ncbi_id":"286114","summary":null,"start":20973797,"end":20995119,"strand":1,"description":"long intergenic non-protein coding RNA 2153 [Source:HGNC Symbol;Acc:HGNC:27823]"}, {"versioned_ensembl_gene_id":"ENSG00000086015.20","gene_symbol":"MAST2","gene_name":"microtubule associated serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:19035]","synonyms":"MAST205,KIAA0807","biotype":"protein_coding","ncbi_id":"23139","summary":null,"start":45786987,"end":46036124,"strand":1,"description":"microtubule associated serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:19035]"}, {"versioned_ensembl_gene_id":"ENSG00000116062.14","gene_symbol":"MSH6","gene_name":"mutS homolog 6 [Source:HGNC Symbol;Acc:HGNC:7329]","synonyms":"GTBP","biotype":"protein_coding","ncbi_id":"2956","summary":"This gene encodes a member of the DNA mismatch repair MutS family. In E. coli, the MutS protein helps in the recognition of mismatched nucleotides prior to their repair. A highly conserved region of approximately 150 aa, called the Walker-A adenine nucleotide binding motif, exists in MutS homologs. The encoded protein heterodimerizes with MSH2 to form a mismatch recognition complex that functions as a bidirectional molecular switch that exchanges ADP and ATP as DNA mismatches are bound and dissociated. Mutations in this gene may be associated with hereditary nonpolyposis colon cancer, colorectal cancer, and endometrial cancer. Transcripts variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013]","start":47695530,"end":47810101,"strand":1,"description":"mutS homolog 6 [Source:HGNC Symbol;Acc:HGNC:7329]"}, {"versioned_ensembl_gene_id":"ENSG00000279744.1","gene_symbol":"AC132938.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82462601,"end":82464255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248468.1","gene_symbol":"AC107027.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131517831,"end":131520880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172410.4","gene_symbol":"INSL5","gene_name":"insulin like 5 [Source:HGNC Symbol;Acc:HGNC:6088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10022","summary":"The protein encoded by this gene contains a classical signature of the insulin superfamily and is highly similar to relaxin 3 (RLN3/INSL7). [provided by RefSeq, Jul 2008]","start":66797741,"end":66801256,"strand":-1,"description":"insulin like 5 [Source:HGNC Symbol;Acc:HGNC:6088]"}, {"versioned_ensembl_gene_id":"ENSG00000167910.3","gene_symbol":"CYP7A1","gene_name":"cytochrome P450 family 7 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2651]","synonyms":"CYP7","biotype":"protein_coding","ncbi_id":"1581","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway in the liver, which converts cholesterol to bile acids. This reaction is the rate limiting step and the major site of regulation of bile acid synthesis, which is the primary mechanism for the removal of cholesterol from the body. Polymorphisms in the promoter of this gene are associated with defects in bile acid synthesis. [provided by RefSeq, Feb 2010]","start":58490178,"end":58500236,"strand":-1,"description":"cytochrome P450 family 7 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2651]"}, {"versioned_ensembl_gene_id":"ENSG00000250195.1","gene_symbol":"AC109927.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138819954,"end":139012646,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070214.15","gene_symbol":"SLC44A1","gene_name":"solute carrier family 44 member 1 [Source:HGNC Symbol;Acc:HGNC:18798]","synonyms":"CTL1,CHTL1,CDW92,CD92","biotype":"protein_coding","ncbi_id":"23446","summary":null,"start":105244622,"end":105439171,"strand":1,"description":"solute carrier family 44 member 1 [Source:HGNC Symbol;Acc:HGNC:18798]"}, {"versioned_ensembl_gene_id":"ENSG00000224712.12","gene_symbol":"NPIPA3","gene_name":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642778","summary":null,"start":14708944,"end":14726338,"strand":1,"description":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]"}, {"versioned_ensembl_gene_id":"ENSG00000185238.12","gene_symbol":"PRMT3","gene_name":"protein arginine methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:30163]","synonyms":"HRMT1L3","biotype":"protein_coding","ncbi_id":"10196","summary":"This gene belongs to the protein arginine methyltransferase (PRMT) family. The encoded enzyme catalyzes the methylation of guanidino nitrogens of arginyl residues of proteins. The enzyme acts on 40S ribosomal protein S2 (rpS2), which is its major in-vivo substrate, and is involved in the proper maturation of the 80S ribosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":20387530,"end":20509294,"strand":1,"description":"protein arginine methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:30163]"}, {"versioned_ensembl_gene_id":"ENSG00000213673.3","gene_symbol":"SLC25A5P3","gene_name":"solute carrier family 25 member 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:507]","synonyms":"ANTP1","biotype":"processed_pseudogene","ncbi_id":"222005","summary":null,"start":54419444,"end":54420328,"strand":1,"description":"solute carrier family 25 member 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:507]"}, {"versioned_ensembl_gene_id":"ENSG00000124767.6","gene_symbol":"GLO1","gene_name":"glyoxalase I [Source:HGNC Symbol;Acc:HGNC:4323]","synonyms":"GLOD1","biotype":"protein_coding","ncbi_id":"2739","summary":"The enzyme encoded by this gene is responsible for the catalysis and formation of S-lactoyl-glutathione from methylglyoxal condensation and reduced glutatione. Glyoxalase I is linked to HLA and is localized to 6p21.3-p21.1, between HLA and the centromere. [provided by RefSeq, Jul 2008]","start":38675925,"end":38703141,"strand":-1,"description":"glyoxalase I [Source:HGNC Symbol;Acc:HGNC:4323]"}, {"versioned_ensembl_gene_id":"ENSG00000171431.3","gene_symbol":"KRT20","gene_name":"keratin 20 [Source:HGNC Symbol;Acc:HGNC:20412]","synonyms":"K20,CK20,MGC35423","biotype":"protein_coding","ncbi_id":"54474","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This cytokeratin is a major cellular protein of mature enterocytes and goblet cells and is specifically expressed in the gastric and intestinal mucosa. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2008]","start":40875941,"end":40885227,"strand":-1,"description":"keratin 20 [Source:HGNC Symbol;Acc:HGNC:20412]"}, {"versioned_ensembl_gene_id":"ENSG00000261399.1","gene_symbol":"AL031710.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1713527,"end":1714208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230054.2","gene_symbol":"AL160275.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":114656304,"end":114662374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254888.2","gene_symbol":"AP000827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90074839,"end":90075096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231874.3","gene_symbol":"TSPY18P","gene_name":"testis specific protein, Y-linked 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:37725]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642796","summary":null,"start":9869664,"end":9870781,"strand":1,"description":"testis specific protein, Y-linked 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:37725]"}, {"versioned_ensembl_gene_id":"ENSG00000182459.4","gene_symbol":"TEX19","gene_name":"testis expressed 19 [Source:HGNC Symbol;Acc:HGNC:33802]","synonyms":"FLJ35767","biotype":"protein_coding","ncbi_id":"400629","summary":null,"start":82359247,"end":82363776,"strand":1,"description":"testis expressed 19 [Source:HGNC Symbol;Acc:HGNC:33802]"}, {"versioned_ensembl_gene_id":"ENSG00000109113.19","gene_symbol":"RAB34","gene_name":"RAB34, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16519]","synonyms":"RAH,RAB39,NARR","biotype":"protein_coding","ncbi_id":"83871","summary":"This gene encodes a protein belonging to the RAB family of proteins, which are small GTPases involved in protein transport. This family member is a Golgi-bound member of the secretory pathway that is involved in the repositioning of lysosomes and the activation of macropinocytosis. Alternative splicing of this gene results in multiple transcript variants. An alternatively spliced transcript variant produces the nine-amino acid residue-repeats (NARR) protein, which is a functionally distinct nucleolar protein resulting from a different reading frame. [provided by RefSeq, Dec 2016]","start":28714281,"end":28718429,"strand":-1,"description":"RAB34, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16519]"}, {"versioned_ensembl_gene_id":"ENSG00000230896.1","gene_symbol":"AL604028.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45694684,"end":45697075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255187.1","gene_symbol":"AP003386.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91158083,"end":91167294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127328.21","gene_symbol":"RAB3IP","gene_name":"RAB3A interacting protein [Source:HGNC Symbol;Acc:HGNC:16508]","synonyms":"RABIN8,RABIN3,FLJ22548","biotype":"protein_coding","ncbi_id":"117177","summary":null,"start":69738681,"end":69823204,"strand":1,"description":"RAB3A interacting protein [Source:HGNC Symbol;Acc:HGNC:16508]"}, {"versioned_ensembl_gene_id":"ENSG00000174165.7","gene_symbol":"ZDHHC24","gene_name":"zinc finger DHHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:27387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"254359","summary":null,"start":66520637,"end":66546238,"strand":-1,"description":"zinc finger DHHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:27387]"}, {"versioned_ensembl_gene_id":"ENSG00000089723.9","gene_symbol":"OTUB2","gene_name":"OTU deubiquitinase, ubiquitin aldehyde binding 2 [Source:HGNC Symbol;Acc:HGNC:20351]","synonyms":"MGC3102,FLJ21916,C14orf137","biotype":"protein_coding","ncbi_id":"78990","summary":"This gene encodes one of several deubiquitylating enzymes. Ubiquitin modification of proteins is needed for their stability and function; to reverse the process, deubiquityling enzymes remove ubiquitin. This protein contains an OTU domain and binds Ubal (ubiquitin aldehyde); an active cysteine protease site is present in the OTU domain. [provided by RefSeq, Aug 2011]","start":94026329,"end":94048930,"strand":1,"description":"OTU deubiquitinase, ubiquitin aldehyde binding 2 [Source:HGNC Symbol;Acc:HGNC:20351]"}, {"versioned_ensembl_gene_id":"ENSG00000093000.18","gene_symbol":"NUP50","gene_name":"nucleoporin 50 [Source:HGNC Symbol;Acc:HGNC:8065]","synonyms":"NPAP60L","biotype":"protein_coding","ncbi_id":"10762","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a member of the FG-repeat containing nucleoporins that functions as a soluble cofactor in importin-alpha:beta-mediated nuclear protein import. Pseudogenes of this gene are found on chromosomes 5, 6, and 14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":45163841,"end":45188015,"strand":1,"description":"nucleoporin 50 [Source:HGNC Symbol;Acc:HGNC:8065]"}, {"versioned_ensembl_gene_id":"ENSG00000139133.6","gene_symbol":"ALG10","gene_name":"ALG10, alpha-1,2-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23162]","synonyms":"FLJ14751,DIE2,ALG10A","biotype":"protein_coding","ncbi_id":"84920","summary":"This gene encodes a membrane-associated protein that adds the third glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation. That is, it transfers the terminal glucose from dolichyl phosphate glucose (Dol-P-Glc) onto the lipid-linked oligosaccharide Glc2Man9GlcNAc(2)-PP-Dol. The rat protein homolog was shown to specifically modulate the gating function of the rat neuronal ether-a-go-go (EAG) potassium ion channel. [provided by RefSeq, Jan 2010]","start":34022281,"end":34029694,"strand":1,"description":"ALG10, alpha-1,2-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23162]"}, {"versioned_ensembl_gene_id":"ENSG00000269235.1","gene_symbol":"ZNF350-AS1","gene_name":"ZNF350 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48598]","synonyms":"uc002pyc,HCCAT3","biotype":"antisense_RNA","ncbi_id":"101669766","summary":null,"start":51949134,"end":51981367,"strand":1,"description":"ZNF350 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48598]"}, {"versioned_ensembl_gene_id":"ENSG00000270987.1","gene_symbol":"AL133338.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100889603,"end":100890338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282221.1","gene_symbol":"AC119427.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201399633,"end":201401190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266654.1","gene_symbol":"AC129510.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82160056,"end":82160452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258458.5","gene_symbol":"AL160314.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":22702611,"end":22766562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213050.5","gene_symbol":"TPM3P1","gene_name":"tropomyosin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16350]","synonyms":"TPM3L2","biotype":"processed_pseudogene","ncbi_id":"252956","summary":null,"start":116972165,"end":116972911,"strand":-1,"description":"tropomyosin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16350]"}, {"versioned_ensembl_gene_id":"ENSG00000277024.1","gene_symbol":"BX005214.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":39359890,"end":39369105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259706.1","gene_symbol":"HSP90B2P","gene_name":"heat shock protein 90 beta family member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12099]","synonyms":"TRAP1,TRA1P1,HSPCP2,GRP94P1,GRP94b","biotype":"processed_pseudogene","ncbi_id":"7190","summary":null,"start":99257632,"end":99260015,"strand":1,"description":"heat shock protein 90 beta family member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12099]"}, {"versioned_ensembl_gene_id":"ENSG00000259257.1","gene_symbol":"AC037479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99337857,"end":99338481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215112.6","gene_symbol":"FAM74A1","gene_name":"family with sequence similarity 74 member A1 [Source:HGNC Symbol;Acc:HGNC:32029]","synonyms":"FAM74A5","biotype":"lincRNA","ncbi_id":"401507","summary":null,"start":39371065,"end":39376916,"strand":1,"description":"family with sequence similarity 74 member A1 [Source:HGNC Symbol;Acc:HGNC:32029]"}, {"versioned_ensembl_gene_id":"ENSG00000155463.12","gene_symbol":"OXA1L","gene_name":"OXA1L, mitochondrial inner membrane protein [Source:HGNC Symbol;Acc:HGNC:8526]","synonyms":"OXA1,MGC133129","biotype":"protein_coding","ncbi_id":"5018","summary":"This gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N-terminal tail of subunit 2 of cytochrome c oxidase, and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain. [provided by RefSeq, Jul 2016]","start":22766522,"end":22773041,"strand":1,"description":"OXA1L, mitochondrial inner membrane protein [Source:HGNC Symbol;Acc:HGNC:8526]"}, {"versioned_ensembl_gene_id":"ENSG00000259392.2","gene_symbol":"AC090877.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32836983,"end":32837326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259228.1","gene_symbol":"HNRNPA1P62","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48792]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480235","summary":null,"start":99284625,"end":99285576,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48792]"}, {"versioned_ensembl_gene_id":"ENSG00000279958.1","gene_symbol":"AC019278.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33105758,"end":33106236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146414.15","gene_symbol":"SHPRH","gene_name":"SNF2 histone linker PHD RING helicase [Source:HGNC Symbol;Acc:HGNC:19336]","synonyms":"KIAA2023,FLJ90837,bA545I5.2","biotype":"protein_coding","ncbi_id":"257218","summary":"SHPRH is a ubiquitously expressed protein that contains motifs characteristics of several DNA repair proteins, transcription factors, and helicases. SHPRH is a functional homolog of S. cerevisiae RAD5 (Unk et al., 2006 [PubMed 17108083]).[supplied by OMIM, Mar 2008]","start":145864245,"end":145964423,"strand":-1,"description":"SNF2 histone linker PHD RING helicase [Source:HGNC Symbol;Acc:HGNC:19336]"}, {"versioned_ensembl_gene_id":"ENSG00000004866.20","gene_symbol":"ST7","gene_name":"suppression of tumorigenicity 7 [Source:HGNC Symbol;Acc:HGNC:11351]","synonyms":"TSG7,SEN4,RAY1,HELG,FAM4A1,FAM4A,ETS7q","biotype":"protein_coding","ncbi_id":"7982","summary":"The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]","start":116953238,"end":117230103,"strand":1,"description":"suppression of tumorigenicity 7 [Source:HGNC Symbol;Acc:HGNC:11351]"}, {"versioned_ensembl_gene_id":"ENSG00000252336.1","gene_symbol":"RNA5SP148","gene_name":"RNA, 5S ribosomal pseudogene 148 [Source:HGNC Symbol;Acc:HGNC:43048]","synonyms":"RN5S148","biotype":"rRNA","ncbi_id":"100873415","summary":null,"start":178429197,"end":178429290,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 148 [Source:HGNC Symbol;Acc:HGNC:43048]"}, {"versioned_ensembl_gene_id":"ENSG00000259686.1","gene_symbol":"HNRNPA1P71","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:48801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421433","summary":null,"start":33012119,"end":33013068,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:48801]"}, {"versioned_ensembl_gene_id":"ENSG00000168904.14","gene_symbol":"LRRC28","gene_name":"leucine rich repeat containing 28 [Source:HGNC Symbol;Acc:HGNC:28355]","synonyms":"MGC24976,FLJ45242,FLJ34269","biotype":"protein_coding","ncbi_id":"123355","summary":null,"start":99251362,"end":99390729,"strand":1,"description":"leucine rich repeat containing 28 [Source:HGNC Symbol;Acc:HGNC:28355]"}, {"versioned_ensembl_gene_id":"ENSG00000250330.1","gene_symbol":"AC016559.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79229904,"end":79230588,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229208.1","gene_symbol":"RBMY2NP","gene_name":"RNA binding motif protein, Y-linked, family 2, member N pseudogene [Source:HGNC Symbol;Acc:HGNC:23919]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378956","summary":null,"start":9831418,"end":9846696,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member N pseudogene [Source:HGNC Symbol;Acc:HGNC:23919]"}, {"versioned_ensembl_gene_id":"ENSG00000233123.1","gene_symbol":"LINC01007","gene_name":"long intergenic non-protein coding RNA 1007 [Source:HGNC Symbol;Acc:HGNC:48973]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506527","summary":null,"start":101562779,"end":101569006,"strand":-1,"description":"long intergenic non-protein coding RNA 1007 [Source:HGNC Symbol;Acc:HGNC:48973]"}, {"versioned_ensembl_gene_id":"ENSG00000273853.1","gene_symbol":"AC023158.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33432311,"end":33432853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259937.2","gene_symbol":"AC023158.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33404872,"end":33405896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123843.12","gene_symbol":"C4BPB","gene_name":"complement component 4 binding protein beta [Source:HGNC Symbol;Acc:HGNC:1328]","synonyms":"C4BP","biotype":"protein_coding","ncbi_id":"725","summary":"This gene encodes a member of a superfamily of proteins composed predominantly of tandemly arrayed short consensus repeats of approximately 60 amino acids. A single, unique beta-chain encoded by this gene assembles with seven identical alpha-chains into the predominant isoform of C4b-binding protein, a multimeric protein that controls activation of the complement cascade through the classical pathway. C4b-binding protein has a regulatory role in the coagulation system also, mediated through the beta-chain binding of protein S, a vitamin K-dependent protein that serves as a cofactor of activated protein C. The genes encoding both alpha and beta chains are located adjacent to each other on human chromosome 1 in the regulator of complement activation gene cluster. Alternative splicing gives rise to multiple transcript variants. [provided by RefSeq, Jul 2008]","start":207088842,"end":207099993,"strand":1,"description":"complement component 4 binding protein beta [Source:HGNC Symbol;Acc:HGNC:1328]"}, {"versioned_ensembl_gene_id":"ENSG00000282459.1","gene_symbol":"TRBV6-6","gene_name":"T-cell receptor beta variable 6-6 [Source:HGNC Symbol;Acc:HGNC:12231]","synonyms":"TRBV66,TCRBV6S6,TCRBV13S6A2T","biotype":"TR_V_gene","ncbi_id":"28601","summary":null,"start":142491254,"end":142491732,"strand":1,"description":"T-cell receptor beta variable 6-6 [Source:HGNC Symbol;Acc:HGNC:12231]"}, {"versioned_ensembl_gene_id":"ENSG00000216098.1","gene_symbol":"MIR892B","gene_name":"microRNA 892b [Source:HGNC Symbol;Acc:HGNC:33649]","synonyms":"MIRN892B,hsa-mir-892b","biotype":"miRNA","ncbi_id":"100126307","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145997198,"end":145997274,"strand":-1,"description":"microRNA 892b [Source:HGNC Symbol;Acc:HGNC:33649]"}, {"versioned_ensembl_gene_id":"ENSG00000212601.1","gene_symbol":"RNA5SP53","gene_name":"RNA, 5S ribosomal pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:42830]","synonyms":"RN5S53","biotype":"rRNA","ncbi_id":"100873291","summary":null,"start":93488333,"end":93488452,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:42830]"}, {"versioned_ensembl_gene_id":"ENSG00000199857.1","gene_symbol":"SNORD50","gene_name":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":76402076,"end":76402146,"strand":1,"description":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]"}, {"versioned_ensembl_gene_id":"ENSG00000201638.2","gene_symbol":"RNY4P16","gene_name":"RNA, Ro-associated Y4 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:34066]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100431173","summary":null,"start":234837976,"end":234838069,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:34066]"}, {"versioned_ensembl_gene_id":"ENSG00000276746.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33562880,"end":33563130,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284142.1","gene_symbol":"MIR6845","gene_name":"microRNA 6845 [Source:HGNC Symbol;Acc:HGNC:49956]","synonyms":"hsa-mir-6845","biotype":"miRNA","ncbi_id":"102466748","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143837756,"end":143837816,"strand":-1,"description":"microRNA 6845 [Source:HGNC Symbol;Acc:HGNC:49956]"}, {"versioned_ensembl_gene_id":"ENSG00000243359.3","gene_symbol":"RN7SL815P","gene_name":"RNA, 7SL, cytoplasmic 815, pseudogene [Source:HGNC Symbol;Acc:HGNC:46831]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479519","summary":null,"start":115837870,"end":115838159,"strand":1,"description":"RNA, 7SL, cytoplasmic 815, pseudogene [Source:HGNC Symbol;Acc:HGNC:46831]"}, {"versioned_ensembl_gene_id":"ENSG00000207746.1","gene_symbol":"MIR575","gene_name":"microRNA 575 [Source:HGNC Symbol;Acc:HGNC:32831]","synonyms":"MIRN575,hsa-mir-575","biotype":"miRNA","ncbi_id":"693160","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82753337,"end":82753430,"strand":-1,"description":"microRNA 575 [Source:HGNC Symbol;Acc:HGNC:32831]"}, {"versioned_ensembl_gene_id":"ENSG00000280263.1","gene_symbol":"ACTR3BP2","gene_name":"ACTR3B pseudogene 2 [Source:NCBI gene;Acc:440888]","synonyms":"FKSG73,FKSG73","biotype":"processed_pseudogene","ncbi_id":"440888","summary":null,"start":16486985,"end":16488322,"strand":1,"description":"ACTR3B pseudogene 2 [Source:NCBI gene;Acc:440888]"}, {"versioned_ensembl_gene_id":"ENSG00000207267.1","gene_symbol":"RNU6-1081P","gene_name":"RNA, U6 small nuclear 1081, pseudogene [Source:HGNC Symbol;Acc:HGNC:48044]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480636","summary":null,"start":11233988,"end":11234094,"strand":1,"description":"RNA, U6 small nuclear 1081, pseudogene [Source:HGNC Symbol;Acc:HGNC:48044]"}, {"versioned_ensembl_gene_id":"ENSG00000267583.5","gene_symbol":"AC007998.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35443869,"end":35467088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266383.1","gene_symbol":"MIR5002","gene_name":"microRNA 5002 [Source:HGNC Symbol;Acc:HGNC:43470]","synonyms":"hsa-mir-5002","biotype":"miRNA","ncbi_id":"100847021","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124132929,"end":124133025,"strand":1,"description":"microRNA 5002 [Source:HGNC Symbol;Acc:HGNC:43470]"}, {"versioned_ensembl_gene_id":"ENSG00000266015.1","gene_symbol":"MIR4309","gene_name":"microRNA 4309 [Source:HGNC Symbol;Acc:HGNC:38336]","synonyms":"hsa-mir-4309","biotype":"miRNA","ncbi_id":"100422954","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102539644,"end":102539726,"strand":1,"description":"microRNA 4309 [Source:HGNC Symbol;Acc:HGNC:38336]"}, {"versioned_ensembl_gene_id":"ENSG00000264902.1","gene_symbol":"MIR5701-3","gene_name":"microRNA 5701-3 [Source:HGNC Symbol;Acc:HGNC:50844]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504741","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21951242,"end":21951323,"strand":1,"description":"microRNA 5701-3 [Source:HGNC Symbol;Acc:HGNC:50844]"}, {"versioned_ensembl_gene_id":"ENSG00000243005.3","gene_symbol":"RN7SL16P","gene_name":"RNA, 7SL, cytoplasmic 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:46032]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479231","summary":null,"start":24563193,"end":24563461,"strand":-1,"description":"RNA, 7SL, cytoplasmic 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:46032]"}, {"versioned_ensembl_gene_id":"ENSG00000273658.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53464720,"end":53464901,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000264881.1","gene_symbol":"MIR1273D","gene_name":"microRNA 1273d [Source:HGNC Symbol;Acc:HGNC:38375]","synonyms":"hsa-mir-1273d","biotype":"miRNA","ncbi_id":"100422970","summary":"This record was withdrawn by miRBase.","start":10227718,"end":10227803,"strand":1,"description":"microRNA 1273d [Source:HGNC Symbol;Acc:HGNC:38375]"}, {"versioned_ensembl_gene_id":"ENSG00000275054.1","gene_symbol":"ST7-OT3_1","gene_name":"ST7 overlapping transcript 3 conserved region 1 [Source:RFAM;Acc:RF02183]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117184126,"end":117184199,"strand":1,"description":"ST7 overlapping transcript 3 conserved region 1 [Source:RFAM;Acc:RF02183]"}, {"versioned_ensembl_gene_id":"ENSG00000252720.1","gene_symbol":"RNU6-1258P","gene_name":"RNA, U6 small nuclear 1258, pseudogene [Source:HGNC Symbol;Acc:HGNC:48221]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480115","summary":null,"start":93437400,"end":93437510,"strand":-1,"description":"RNA, U6 small nuclear 1258, pseudogene [Source:HGNC Symbol;Acc:HGNC:48221]"}, {"versioned_ensembl_gene_id":"ENSG00000278454.1","gene_symbol":"ZFAT-AS1_3","gene_name":"ZFAT antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02213]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":134600257,"end":134600336,"strand":1,"description":"ZFAT antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02213]"}, {"versioned_ensembl_gene_id":"ENSG00000274520.1","gene_symbol":"Six3os1_1","gene_name":"Six3os1 conserved region 1 [Source:RFAM;Acc:RF02246]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44932320,"end":44932406,"strand":1,"description":"Six3os1 conserved region 1 [Source:RFAM;Acc:RF02246]"}, {"versioned_ensembl_gene_id":"ENSG00000222743.1","gene_symbol":"RNU6-1190P","gene_name":"RNA, U6 small nuclear 1190, pseudogene [Source:HGNC Symbol;Acc:HGNC:48153]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480087","summary":null,"start":37619985,"end":37620088,"strand":-1,"description":"RNA, U6 small nuclear 1190, pseudogene [Source:HGNC Symbol;Acc:HGNC:48153]"}, {"versioned_ensembl_gene_id":"ENSG00000222574.1","gene_symbol":"RN7SKP61","gene_name":"RNA, 7SK small nuclear pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:45785]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479122","summary":null,"start":78161698,"end":78161992,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:45785]"}, {"versioned_ensembl_gene_id":"ENSG00000200351.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":98936638,"end":98936747,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251779.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76319376,"end":76319473,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252358.1","gene_symbol":"RN7SKP135","gene_name":"RNA, 7SK small nuclear pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:45859]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480875","summary":null,"start":63609354,"end":63609600,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:45859]"}, {"versioned_ensembl_gene_id":"ENSG00000252098.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27255464,"end":27255567,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000243642.3","gene_symbol":"RN7SL526P","gene_name":"RNA, 7SL, cytoplasmic 526, pseudogene [Source:HGNC Symbol;Acc:HGNC:46542]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479415","summary":null,"start":58069970,"end":58070288,"strand":1,"description":"RNA, 7SL, cytoplasmic 526, pseudogene [Source:HGNC Symbol;Acc:HGNC:46542]"}, {"versioned_ensembl_gene_id":"ENSG00000222667.1","gene_symbol":"RNU6-394P","gene_name":"RNA, U6 small nuclear 394, pseudogene [Source:HGNC Symbol;Acc:HGNC:47357]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480698","summary":null,"start":66676258,"end":66676364,"strand":-1,"description":"RNA, U6 small nuclear 394, pseudogene [Source:HGNC Symbol;Acc:HGNC:47357]"}, {"versioned_ensembl_gene_id":"ENSG00000238783.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30355436,"end":30355540,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241866.3","gene_symbol":"RN7SL401P","gene_name":"RNA, 7SL, cytoplasmic 401, pseudogene [Source:HGNC Symbol;Acc:HGNC:46417]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480507","summary":null,"start":73744935,"end":73745232,"strand":1,"description":"RNA, 7SL, cytoplasmic 401, pseudogene [Source:HGNC Symbol;Acc:HGNC:46417]"}, {"versioned_ensembl_gene_id":"ENSG00000199477.1","gene_symbol":"SNORA31","gene_name":"small nucleolar RNA, H/ACA box 31 [Source:HGNC Symbol;Acc:HGNC:32621]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":45337480,"end":45337609,"strand":-1,"description":"small nucleolar RNA, H/ACA box 31 [Source:HGNC Symbol;Acc:HGNC:32621]"}, {"versioned_ensembl_gene_id":"ENSG00000200231.1","gene_symbol":"RNU1-23P","gene_name":"RNA, U1 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:41964]","synonyms":null,"biotype":"snRNA","ncbi_id":"106478980","summary":null,"start":24237255,"end":24237398,"strand":1,"description":"RNA, U1 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:41964]"}, {"versioned_ensembl_gene_id":"ENSG00000278732.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31975167,"end":31975448,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000198551.9","gene_symbol":"ZNF627","gene_name":"zinc finger protein 627 [Source:HGNC Symbol;Acc:HGNC:30570]","synonyms":"FLJ90365","biotype":"protein_coding","ncbi_id":"199692","summary":null,"start":11559374,"end":11619135,"strand":1,"description":"zinc finger protein 627 [Source:HGNC Symbol;Acc:HGNC:30570]"}, {"versioned_ensembl_gene_id":"ENSG00000238517.1","gene_symbol":"MIR1270","gene_name":"microRNA 1270 [Source:HGNC Symbol;Acc:HGNC:35338]","synonyms":"MIRN1270,MIR1270-2,MIR1270-1,hsa-mir-1270-2,hsa-mir-1270","biotype":"miRNA","ncbi_id":"100302179","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20399272,"end":20399354,"strand":-1,"description":"microRNA 1270 [Source:HGNC Symbol;Acc:HGNC:35338]"}, {"versioned_ensembl_gene_id":"ENSG00000207559.1","gene_symbol":"MIR578","gene_name":"microRNA 578 [Source:HGNC Symbol;Acc:HGNC:32834]","synonyms":"MIRN578,hsa-mir-578","biotype":"miRNA","ncbi_id":"693163","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":165386242,"end":165386337,"strand":1,"description":"microRNA 578 [Source:HGNC Symbol;Acc:HGNC:32834]"}, {"versioned_ensembl_gene_id":"ENSG00000201529.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67617302,"end":67617415,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284158.1","gene_symbol":"MIR6822","gene_name":"microRNA 6822 [Source:HGNC Symbol;Acc:HGNC:49999]","synonyms":"hsa-mir-6822","biotype":"miRNA","ncbi_id":"102466743","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39138206,"end":39138266,"strand":1,"description":"microRNA 6822 [Source:HGNC Symbol;Acc:HGNC:49999]"}, {"versioned_ensembl_gene_id":"ENSG00000278418.1","gene_symbol":"MIR6512","gene_name":"microRNA 6512 [Source:HGNC Symbol;Acc:HGNC:50259]","synonyms":"hsa-mir-6512","biotype":"miRNA","ncbi_id":"102465255","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":177313806,"end":177313882,"strand":-1,"description":"microRNA 6512 [Source:HGNC Symbol;Acc:HGNC:50259]"}, {"versioned_ensembl_gene_id":"ENSG00000201452.1","gene_symbol":"RNU6-1317P","gene_name":"RNA, U6 small nuclear 1317, pseudogene [Source:HGNC Symbol;Acc:HGNC:48280]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481596","summary":null,"start":175767558,"end":175767661,"strand":1,"description":"RNA, U6 small nuclear 1317, pseudogene [Source:HGNC Symbol;Acc:HGNC:48280]"}, {"versioned_ensembl_gene_id":"ENSG00000276656.1","gene_symbol":"MIR6083","gene_name":"microRNA 6083 [Source:HGNC Symbol;Acc:HGNC:50076]","synonyms":"hsa-mir-6083","biotype":"miRNA","ncbi_id":"102464832","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124374332,"end":124374437,"strand":1,"description":"microRNA 6083 [Source:HGNC Symbol;Acc:HGNC:50076]"}, {"versioned_ensembl_gene_id":"ENSG00000199145.1","gene_symbol":"MIR302D","gene_name":"microRNA 302d [Source:HGNC Symbol;Acc:HGNC:31765]","synonyms":"MIRN302D,hsa-mir-302d","biotype":"miRNA","ncbi_id":"442896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112648004,"end":112648071,"strand":-1,"description":"microRNA 302d [Source:HGNC Symbol;Acc:HGNC:31765]"}, {"versioned_ensembl_gene_id":"ENSG00000243591.3","gene_symbol":"RN7SL282P","gene_name":"RNA, 7SL, cytoplasmic 282, pseudogene [Source:HGNC Symbol;Acc:HGNC:46298]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480374","summary":null,"start":6601540,"end":6601836,"strand":1,"description":"RNA, 7SL, cytoplasmic 282, pseudogene [Source:HGNC Symbol;Acc:HGNC:46298]"}, {"versioned_ensembl_gene_id":"ENSG00000202186.1","gene_symbol":"RNU6-497P","gene_name":"RNA, U6 small nuclear 497, pseudogene [Source:HGNC Symbol;Acc:HGNC:47460]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479786","summary":null,"start":47484278,"end":47484381,"strand":-1,"description":"RNA, U6 small nuclear 497, pseudogene [Source:HGNC Symbol;Acc:HGNC:47460]"}, {"versioned_ensembl_gene_id":"ENSG00000265432.1","gene_symbol":"MIR4308","gene_name":"microRNA 4308 [Source:HGNC Symbol;Acc:HGNC:38206]","synonyms":"hsa-mir-4308","biotype":"miRNA","ncbi_id":"100422984","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54878113,"end":54878193,"strand":-1,"description":"microRNA 4308 [Source:HGNC Symbol;Acc:HGNC:38206]"}, {"versioned_ensembl_gene_id":"ENSG00000265462.1","gene_symbol":"MIR3680-1","gene_name":"microRNA 3680-1 [Source:HGNC Symbol;Acc:HGNC:38989]","synonyms":"MIR3680,hsa-mir-3680","biotype":"miRNA","ncbi_id":"100500917","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21506049,"end":21506135,"strand":-1,"description":"microRNA 3680-1 [Source:HGNC Symbol;Acc:HGNC:38989]"}, {"versioned_ensembl_gene_id":"ENSG00000280404.1","gene_symbol":"AC005086.4","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":102161120,"end":102161337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252581.1","gene_symbol":"RNU6-1098P","gene_name":"RNA, U6 small nuclear 1098, pseudogene [Source:HGNC Symbol;Acc:HGNC:48061]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481935","summary":null,"start":149525631,"end":149525726,"strand":1,"description":"RNA, U6 small nuclear 1098, pseudogene [Source:HGNC Symbol;Acc:HGNC:48061]"}, {"versioned_ensembl_gene_id":"ENSG00000252671.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10337277,"end":10337386,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278673.1","gene_symbol":"AC136352.5","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":20741,"end":22392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199626.1","gene_symbol":"RNU6-989P","gene_name":"RNA, U6 small nuclear 989, pseudogene [Source:HGNC Symbol;Acc:HGNC:47952]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481492","summary":null,"start":187270698,"end":187270804,"strand":-1,"description":"RNA, U6 small nuclear 989, pseudogene [Source:HGNC Symbol;Acc:HGNC:47952]"}, {"versioned_ensembl_gene_id":"ENSG00000265388.2","gene_symbol":"RN7SL391P","gene_name":"RNA, 7SL, cytoplasmic 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:46407]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481030","summary":null,"start":6344554,"end":6344837,"strand":1,"description":"RNA, 7SL, cytoplasmic 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:46407]"}, {"versioned_ensembl_gene_id":"ENSG00000252141.1","gene_symbol":"RNU6-65P","gene_name":"RNA, U6 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:42555]","synonyms":"RNU6-65","biotype":"snRNA","ncbi_id":"106480751","summary":null,"start":51565412,"end":51565509,"strand":1,"description":"RNA, U6 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:42555]"}, {"versioned_ensembl_gene_id":"ENSG00000276690.1","gene_symbol":"SOX2OT_exon3","gene_name":"SOX2 overlapping transcript exon 3 [Source:RFAM;Acc:RF01953]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":181699608,"end":181699883,"strand":1,"description":"SOX2 overlapping transcript exon 3 [Source:RFAM;Acc:RF01953]"}, {"versioned_ensembl_gene_id":"ENSG00000240306.2","gene_symbol":"RN7SL100P","gene_name":"RNA, 7SL, cytoplasmic 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:46116]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480948","summary":null,"start":26895678,"end":26895970,"strand":1,"description":"RNA, 7SL, cytoplasmic 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:46116]"}, {"versioned_ensembl_gene_id":"ENSG00000238610.1","gene_symbol":"RNU7-26P","gene_name":"RNA, U7 small nuclear 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:34122]","synonyms":"U7.26","biotype":"snRNA","ncbi_id":"100147813","summary":null,"start":27897504,"end":27897566,"strand":-1,"description":"RNA, U7 small nuclear 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:34122]"}, {"versioned_ensembl_gene_id":"ENSG00000223262.1","gene_symbol":"RNA5SP492","gene_name":"RNA, 5S ribosomal pseudogene 492 [Source:HGNC Symbol;Acc:HGNC:43392]","synonyms":"RN5S492","biotype":"rRNA","ncbi_id":"100873734","summary":null,"start":42221173,"end":42221286,"strand":1,"description":"RNA, 5S ribosomal pseudogene 492 [Source:HGNC Symbol;Acc:HGNC:43392]"}, {"versioned_ensembl_gene_id":"ENSG00000274701.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":94655911,"end":94656208,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253079.1","gene_symbol":"NRON","gene_name":"non-protein coding RNA, repressor of NFAT [Source:HGNC Symbol;Acc:HGNC:37079]","synonyms":"NCRNA00194","biotype":"misc_RNA","ncbi_id":"641373","summary":null,"start":126408041,"end":126408410,"strand":-1,"description":"non-protein coding RNA, repressor of NFAT [Source:HGNC Symbol;Acc:HGNC:37079]"}, {"versioned_ensembl_gene_id":"ENSG00000252461.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":28881480,"end":28881607,"strand":-1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000276159.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000252821.1","gene_symbol":"RNU6-388P","gene_name":"RNA, U6 small nuclear 388, pseudogene [Source:HGNC Symbol;Acc:HGNC:47351]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479737","summary":null,"start":33001950,"end":33002054,"strand":-1,"description":"RNA, U6 small nuclear 388, pseudogene [Source:HGNC Symbol;Acc:HGNC:47351]"}, {"versioned_ensembl_gene_id":"ENSG00000206633.1","gene_symbol":"SNORA80B","gene_name":"small nucleolar RNA, H/ACA box 80B [Source:HGNC Symbol;Acc:HGNC:34355]","synonyms":"ACA67B","biotype":"snoRNA","ncbi_id":"100302743","summary":null,"start":10446714,"end":10446849,"strand":-1,"description":"small nucleolar RNA, H/ACA box 80B [Source:HGNC Symbol;Acc:HGNC:34355]"}, {"versioned_ensembl_gene_id":"ENSG00000199910.1","gene_symbol":"RNA5S10","gene_name":"RNA, 5S ribosomal 10 [Source:HGNC Symbol;Acc:HGNC:34371]","synonyms":"RN5S10","biotype":"rRNA","ncbi_id":"100169761","summary":null,"start":228630390,"end":228630508,"strand":-1,"description":"RNA, 5S ribosomal 10 [Source:HGNC Symbol;Acc:HGNC:34371]"}, {"versioned_ensembl_gene_id":"ENSG00000206845.1","gene_symbol":"RNU6-209P","gene_name":"RNA, U6 small nuclear 209, pseudogene [Source:HGNC 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[Source:HGNC Symbol;Acc:HGNC:46919]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480541","summary":null,"start":22130603,"end":22130729,"strand":-1,"description":"RNA, U6atac small nuclear 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46919]"}, {"versioned_ensembl_gene_id":"ENSG00000202476.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30453997,"end":30454097,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201483.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7187582,"end":7187686,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239333.3","gene_symbol":"RN7SL658P","gene_name":"RNA, 7SL, cytoplasmic 658, pseudogene [Source:HGNC 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Symbol;Acc:HGNC:50065]","synonyms":"hsa-mir-6887","biotype":"miRNA","ncbi_id":"102466205","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35122700,"end":35122764,"strand":1,"description":"microRNA 6887 [Source:HGNC Symbol;Acc:HGNC:50065]"}, {"versioned_ensembl_gene_id":"ENSG00000265178.1","gene_symbol":"MIR4728","gene_name":"microRNA 4728 [Source:HGNC Symbol;Acc:HGNC:41632]","synonyms":"hsa-mir-4728","biotype":"miRNA","ncbi_id":"100616132","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39726495,"end":39726561,"strand":1,"description":"microRNA 4728 [Source:HGNC Symbol;Acc:HGNC:41632]"}, {"versioned_ensembl_gene_id":"ENSG00000274796.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34L,SEN34L,LENG5,LENG5,SEN34,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000278190.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868050,"end":54868156,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000283454.1","gene_symbol":"RNA5SP443","gene_name":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]","synonyms":"RN5S443","biotype":"rRNA","ncbi_id":"106481745","summary":null,"start":45327366,"end":45327497,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]"}, {"versioned_ensembl_gene_id":"ENSG00000221255.1","gene_symbol":"RNU6ATAC37P","gene_name":"RNA, U6atac small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46936]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479558","summary":null,"start":7576841,"end":7576971,"strand":1,"description":"RNA, U6atac small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46936]"}, {"versioned_ensembl_gene_id":"ENSG00000200785.1","gene_symbol":"SNORD8","gene_name":"small nucleolar RNA, C/D box 8 [Source:HGNC Symbol;Acc:HGNC:20159]","synonyms":"RNU6C,mgU6-53","biotype":"snoRNA","ncbi_id":"319103","summary":null,"start":21397292,"end":21397401,"strand":-1,"description":"small nucleolar RNA, C/D box 8 [Source:HGNC Symbol;Acc:HGNC:20159]"}, {"versioned_ensembl_gene_id":"ENSG00000280466.1","gene_symbol":"SCARNA4","gene_name":"small Cajal body-specific RNA 4 [Source:HGNC Symbol;Acc:HGNC:32560]","synonyms":"ACA26,ACA26","biotype":"scaRNA","ncbi_id":"677771","summary":null,"start":155925958,"end":155926085,"strand":-1,"description":"small Cajal body-specific RNA 4 [Source:HGNC Symbol;Acc:HGNC:32560]"}, {"versioned_ensembl_gene_id":"ENSG00000201499.1","gene_symbol":"RNU6-312P","gene_name":"RNA, U6 small nuclear 312, pseudogene [Source:HGNC Symbol;Acc:HGNC:47275]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479706","summary":null,"start":200881715,"end":200881821,"strand":-1,"description":"RNA, U6 small nuclear 312, pseudogene [Source:HGNC Symbol;Acc:HGNC:47275]"}, {"versioned_ensembl_gene_id":"ENSG00000272296.1","gene_symbol":"SNORD96A","gene_name":"small nucleolar RNA, C/D box 96A [Source:HGNC Symbol;Acc:HGNC:32758]","synonyms":"U96a","biotype":"snoRNA","ncbi_id":"619571","summary":null,"start":181241814,"end":181241892,"strand":-1,"description":"small nucleolar RNA, C/D box 96A [Source:HGNC Symbol;Acc:HGNC:32758]"}, {"versioned_ensembl_gene_id":"ENSG00000275796.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"PYPAF2,NBS1,CLR19.9,FLJ20510,NBS1,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54636119,"end":54671975,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000266875.2","gene_symbol":"RN7SL408P","gene_name":"RNA, 7SL, cytoplasmic 408, pseudogene [Source:HGNC Symbol;Acc:HGNC:46424]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481841","summary":null,"start":134133573,"end":134133868,"strand":1,"description":"RNA, 7SL, cytoplasmic 408, pseudogene [Source:HGNC Symbol;Acc:HGNC:46424]"}, {"versioned_ensembl_gene_id":"ENSG00000266059.2","gene_symbol":"RN7SL140P","gene_name":"RNA, 7SL, cytoplasmic 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:46156]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479272","summary":null,"start":20175346,"end":20175639,"strand":1,"description":"RNA, 7SL, cytoplasmic 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:46156]"}, {"versioned_ensembl_gene_id":"ENSG00000222650.1","gene_symbol":"RNU2-70P","gene_name":"RNA, U2 small nuclear 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:48563]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480227","summary":null,"start":236267780,"end":236267958,"strand":1,"description":"RNA, U2 small nuclear 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:48563]"}, {"versioned_ensembl_gene_id":"ENSG00000206963.1","gene_symbol":"RNU6-675P","gene_name":"RNA, U6 small nuclear 675, pseudogene [Source:HGNC Symbol;Acc:HGNC:47638]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479864","summary":null,"start":126702839,"end":126702942,"strand":-1,"description":"RNA, U6 small nuclear 675, pseudogene [Source:HGNC Symbol;Acc:HGNC:47638]"}, {"versioned_ensembl_gene_id":"ENSG00000200267.1","gene_symbol":"RNU6-66P","gene_name":"RNA, U6 small nuclear 66, pseudogene [Source:HGNC Symbol;Acc:HGNC:42556]","synonyms":"RNU6-66","biotype":"snRNA","ncbi_id":"100873770","summary":null,"start":73112915,"end":73113018,"strand":-1,"description":"RNA, U6 small nuclear 66, pseudogene [Source:HGNC Symbol;Acc:HGNC:42556]"}, {"versioned_ensembl_gene_id":"ENSG00000222385.1","gene_symbol":"RN7SKP158","gene_name":"RNA, 7SK small nuclear pseudogene 158 [Source:HGNC Symbol;Acc:HGNC:45882]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480883","summary":null,"start":28261194,"end":28261519,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 158 [Source:HGNC Symbol;Acc:HGNC:45882]"}, {"versioned_ensembl_gene_id":"ENSG00000201121.1","gene_symbol":"RNY1P12","gene_name":"RNA, Ro-associated Y1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:50875]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480309","summary":null,"start":101662060,"end":101662164,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:50875]"}, {"versioned_ensembl_gene_id":"ENSG00000199927.2","gene_symbol":"ACEA_U3","gene_name":"ACEA small nucleolar RNA U3 [Source:RFAM;Acc:RF01848]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30304320,"end":30304536,"strand":-1,"description":"ACEA small nucleolar RNA U3 [Source:RFAM;Acc:RF01848]"}, {"versioned_ensembl_gene_id":"ENSG00000272460.1","gene_symbol":"SNORD115-40","gene_name":"small nucleolar RNA, C/D box 115-40 [Source:HGNC Symbol;Acc:HGNC:33059]","synonyms":"HBII-52-40","biotype":"snoRNA","ncbi_id":"100033814","summary":null,"start":25243614,"end":25243695,"strand":1,"description":"small nucleolar RNA, C/D box 115-40 [Source:HGNC Symbol;Acc:HGNC:33059]"}, {"versioned_ensembl_gene_id":"ENSG00000263414.1","gene_symbol":"MIR3187","gene_name":"microRNA 3187 [Source:HGNC Symbol;Acc:HGNC:38319]","synonyms":"hsa-mir-3187","biotype":"miRNA","ncbi_id":"100422854","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":813584,"end":813653,"strand":1,"description":"microRNA 3187 [Source:HGNC Symbol;Acc:HGNC:38319]"}, {"versioned_ensembl_gene_id":"ENSG00000281552.1","gene_symbol":"AL035414.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":210303684,"end":210304540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000208022.1","gene_symbol":"MIR618","gene_name":"microRNA 618 [Source:HGNC Symbol;Acc:HGNC:32874]","synonyms":"MIRN618,hsa-mir-618","biotype":"miRNA","ncbi_id":"693203","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80935736,"end":80935833,"strand":-1,"description":"microRNA 618 [Source:HGNC Symbol;Acc:HGNC:32874]"}, {"versioned_ensembl_gene_id":"ENSG00000284259.1","gene_symbol":"MIR6773","gene_name":"microRNA 6773 [Source:HGNC Symbol;Acc:HGNC:50132]","synonyms":"hsa-mir-6773","biotype":"miRNA","ncbi_id":"102466194","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68233426,"end":68233499,"strand":-1,"description":"microRNA 6773 [Source:HGNC Symbol;Acc:HGNC:50132]"}, {"versioned_ensembl_gene_id":"ENSG00000263584.1","gene_symbol":"MIR4480","gene_name":"microRNA 4480 [Source:HGNC Symbol;Acc:HGNC:41716]","synonyms":"hsa-mir-4480","biotype":"miRNA","ncbi_id":"100616151","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12578753,"end":12578823,"strand":1,"description":"microRNA 4480 [Source:HGNC Symbol;Acc:HGNC:41716]"}, {"versioned_ensembl_gene_id":"ENSG00000251842.1","gene_symbol":"RNU6-732P","gene_name":"RNA, U6 small nuclear 732, pseudogene [Source:HGNC Symbol;Acc:HGNC:47695]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479890","summary":null,"start":149057554,"end":149057656,"strand":-1,"description":"RNA, U6 small nuclear 732, pseudogene [Source:HGNC Symbol;Acc:HGNC:47695]"}, {"versioned_ensembl_gene_id":"ENSG00000252772.1","gene_symbol":"RNU6-714P","gene_name":"RNA, U6 small nuclear 714, pseudogene [Source:HGNC Symbol;Acc:HGNC:47677]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480603","summary":null,"start":92820977,"end":92821079,"strand":1,"description":"RNA, U6 small nuclear 714, pseudogene [Source:HGNC Symbol;Acc:HGNC:47677]"}, {"versioned_ensembl_gene_id":"ENSG00000265048.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32360267,"end":32360373,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201342.1","gene_symbol":"RNU4-38P","gene_name":"RNA, U4 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46974]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479574","summary":null,"start":170057301,"end":170057429,"strand":1,"description":"RNA, U4 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46974]"}, {"versioned_ensembl_gene_id":"ENSG00000251893.2","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":75689152,"end":75689304,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000283584.1","gene_symbol":"snoMe28S-Am2634","gene_name":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":7431217,"end":7431296,"strand":1,"description":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]"}, {"versioned_ensembl_gene_id":"ENSG00000253043.1","gene_symbol":"RNU7-181P","gene_name":"RNA, U7 small nuclear 181 pseudogene [Source:HGNC Symbol;Acc:HGNC:45715]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479093","summary":null,"start":130004528,"end":130004601,"strand":-1,"description":"RNA, U7 small nuclear 181 pseudogene [Source:HGNC Symbol;Acc:HGNC:45715]"}, {"versioned_ensembl_gene_id":"ENSG00000222114.1","gene_symbol":"RNU6-985P","gene_name":"RNA, U6 small nuclear 985, pseudogene [Source:HGNC Symbol;Acc:HGNC:47948]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480001","summary":null,"start":137687891,"end":137687994,"strand":-1,"description":"RNA, U6 small nuclear 985, pseudogene [Source:HGNC Symbol;Acc:HGNC:47948]"}, {"versioned_ensembl_gene_id":"ENSG00000206999.1","gene_symbol":"RNU6-622P","gene_name":"RNA, U6 small nuclear 622, pseudogene [Source:HGNC Symbol;Acc:HGNC:47585]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479841","summary":null,"start":75183045,"end":75183147,"strand":1,"description":"RNA, U6 small nuclear 622, pseudogene [Source:HGNC Symbol;Acc:HGNC:47585]"}, {"versioned_ensembl_gene_id":"ENSG00000275133.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30050669,"end":30050772,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000240374.3","gene_symbol":"RN7SL503P","gene_name":"RNA, 7SL, cytoplasmic 503, pseudogene [Source:HGNC Symbol;Acc:HGNC:46519]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481060","summary":null,"start":35292196,"end":35292498,"strand":-1,"description":"RNA, 7SL, cytoplasmic 503, pseudogene [Source:HGNC Symbol;Acc:HGNC:46519]"}, {"versioned_ensembl_gene_id":"ENSG00000281917.2","gene_symbol":"SLC16A1","gene_name":"solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]","synonyms":"MCT1,MCT","biotype":"protein_coding","ncbi_id":"6566","summary":"The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]","start":112911847,"end":112957013,"strand":-1,"description":"solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]"}, {"versioned_ensembl_gene_id":"ENSG00000218227.3","gene_symbol":"AC136632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178055604,"end":178056194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273945.1","gene_symbol":"MIR6853","gene_name":"microRNA 6853 [Source:HGNC Symbol;Acc:HGNC:49945]","synonyms":"hsa-mir-6853","biotype":"miRNA","ncbi_id":"102466201","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35732922,"end":35732995,"strand":1,"description":"microRNA 6853 [Source:HGNC Symbol;Acc:HGNC:49945]"}, {"versioned_ensembl_gene_id":"ENSG00000283369.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":247607126,"end":247607201,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000253054.1","gene_symbol":"RNU7-77P","gene_name":"RNA, U7 small nuclear 77 pseudogene [Source:HGNC Symbol;Acc:HGNC:34173]","synonyms":"U7.77","biotype":"snRNA","ncbi_id":"100151674","summary":null,"start":35135443,"end":35135502,"strand":1,"description":"RNA, U7 small nuclear 77 pseudogene [Source:HGNC Symbol;Acc:HGNC:34173]"}, {"versioned_ensembl_gene_id":"ENSG00000251925.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":23423099,"end":23423236,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000264389.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32485042,"end":32485188,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000200794.1","gene_symbol":"RN7SKP250","gene_name":"RNA, 7SK small nuclear pseudogene 250 [Source:HGNC Symbol;Acc:HGNC:45974]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479206","summary":null,"start":109662863,"end":109663183,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 250 [Source:HGNC Symbol;Acc:HGNC:45974]"}, {"versioned_ensembl_gene_id":"ENSG00000201569.1","gene_symbol":"SNORD114-17","gene_name":"small nucleolar RNA, C/D box 114-17 [Source:HGNC Symbol;Acc:HGNC:33005]","synonyms":"14q(II-17)","biotype":"snoRNA","ncbi_id":"767595","summary":null,"start":100974806,"end":100974880,"strand":1,"description":"small nucleolar RNA, C/D box 114-17 [Source:HGNC Symbol;Acc:HGNC:33005]"}, {"versioned_ensembl_gene_id":"ENSG00000200152.1","gene_symbol":"RNU6-216P","gene_name":"RNA, U6 small nuclear 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:47179]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479662","summary":null,"start":74968189,"end":74968292,"strand":-1,"description":"RNA, U6 small nuclear 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:47179]"}, {"versioned_ensembl_gene_id":"ENSG00000200303.1","gene_symbol":"RNU6-940P","gene_name":"RNA, U6 small nuclear 940, pseudogene [Source:HGNC Symbol;Acc:HGNC:47903]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479982","summary":null,"start":48975543,"end":48975646,"strand":1,"description":"RNA, U6 small nuclear 940, pseudogene [Source:HGNC Symbol;Acc:HGNC:47903]"}, {"versioned_ensembl_gene_id":"ENSG00000199150.3","gene_symbol":"MIRLET7G","gene_name":"microRNA let-7g [Source:HGNC Symbol;Acc:HGNC:31485]","synonyms":"MIRNLET7G,hsa-let-7g","biotype":"miRNA","ncbi_id":"406890","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52268278,"end":52268361,"strand":-1,"description":"microRNA let-7g [Source:HGNC Symbol;Acc:HGNC:31485]"}, {"versioned_ensembl_gene_id":"ENSG00000253075.1","gene_symbol":"RN7SKP92","gene_name":"RNA, 7SK small nuclear pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:45816]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479135","summary":null,"start":100487544,"end":100487787,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:45816]"}, {"versioned_ensembl_gene_id":"ENSG00000273570.1","gene_symbol":"RMST_5","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 5 [Source:RFAM;Acc:RF01966]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97495932,"end":97496057,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 5 [Source:RFAM;Acc:RF01966]"}, {"versioned_ensembl_gene_id":"ENSG00000280968.1","gene_symbol":"MIR3653","gene_name":"microRNA 3653 [Source:HGNC Symbol;Acc:HGNC:38971]","synonyms":"hsa-mir-3653","biotype":"miRNA","ncbi_id":"100500833","summary":"This record was withdrawn by miRBase.","start":29333158,"end":29333267,"strand":-1,"description":"microRNA 3653 [Source:HGNC Symbol;Acc:HGNC:38971]"}, {"versioned_ensembl_gene_id":"ENSG00000207626.1","gene_symbol":"MIR562","gene_name":"microRNA 562 [Source:HGNC Symbol;Acc:HGNC:32818]","synonyms":"hsa-mir-562,MIRN562","biotype":"miRNA","ncbi_id":"693147","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":232172653,"end":232172747,"strand":1,"description":"microRNA 562 [Source:HGNC Symbol;Acc:HGNC:32818]"}, {"versioned_ensembl_gene_id":"ENSG00000222644.1","gene_symbol":"RNU2-16P","gene_name":"RNA, U2 small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:48509]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481639","summary":null,"start":75829454,"end":75829589,"strand":-1,"description":"RNA, U2 small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:48509]"}, {"versioned_ensembl_gene_id":"ENSG00000265156.1","gene_symbol":"SNORD52","gene_name":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]","synonyms":"U52,RNU52,U52,RNU52","biotype":"snoRNA","ncbi_id":"26797","summary":null,"start":31827320,"end":31827386,"strand":1,"description":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]"}, {"versioned_ensembl_gene_id":"ENSG00000263764.1","gene_symbol":"SNORD43","gene_name":"small nucleolar RNA, C/D box 43 [Source:HGNC Symbol;Acc:HGNC:10182]","synonyms":"U43,RNU43","biotype":"snoRNA","ncbi_id":"26807","summary":"Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD43, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD43, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]","start":39319050,"end":39319113,"strand":-1,"description":"small nucleolar RNA, C/D box 43 [Source:HGNC Symbol;Acc:HGNC:10182]"}, {"versioned_ensembl_gene_id":"ENSG00000239868.3","gene_symbol":"RN7SL34P","gene_name":"RNA, 7SL, cytoplasmic 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46050]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481824","summary":null,"start":41286424,"end":41286693,"strand":-1,"description":"RNA, 7SL, cytoplasmic 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46050]"}, {"versioned_ensembl_gene_id":"ENSG00000199525.1","gene_symbol":"RNA5SP295","gene_name":"RNA, 5S ribosomal pseudogene 295 [Source:HGNC Symbol;Acc:HGNC:43195]","synonyms":"RN5S295","biotype":"rRNA","ncbi_id":"100873548","summary":null,"start":112252258,"end":112252378,"strand":1,"description":"RNA, 5S ribosomal pseudogene 295 [Source:HGNC Symbol;Acc:HGNC:43195]"}, {"versioned_ensembl_gene_id":"ENSG00000222858.1","gene_symbol":"RNU6-920P","gene_name":"RNA, U6 small nuclear 920, pseudogene [Source:HGNC Symbol;Acc:HGNC:47883]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481470","summary":null,"start":29641611,"end":29641702,"strand":-1,"description":"RNA, U6 small nuclear 920, pseudogene [Source:HGNC Symbol;Acc:HGNC:47883]"}, {"versioned_ensembl_gene_id":"ENSG00000234428.2","gene_symbol":"AC023051.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26623369,"end":26649479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207620.1","gene_symbol":"MIR516A2","gene_name":"microRNA 516a-2 [Source:HGNC Symbol;Acc:HGNC:32131]","synonyms":"MIRN516A2,MIRN516-2,hsa-mir-516a-2,hsa-mir-516-2","biotype":"miRNA","ncbi_id":"574499","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53761133,"end":53761222,"strand":1,"description":"microRNA 516a-2 [Source:HGNC Symbol;Acc:HGNC:32131]"}, {"versioned_ensembl_gene_id":"ENSG00000252859.1","gene_symbol":"RNU6-375P","gene_name":"RNA, U6 small nuclear 375, pseudogene [Source:HGNC Symbol;Acc:HGNC:47338]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480575","summary":null,"start":41168217,"end":41168316,"strand":1,"description":"RNA, U6 small nuclear 375, pseudogene [Source:HGNC Symbol;Acc:HGNC:47338]"}, {"versioned_ensembl_gene_id":"ENSG00000252087.1","gene_symbol":"RN7SKP248","gene_name":"RNA, 7SK small nuclear pseudogene 248 [Source:HGNC Symbol;Acc:HGNC:45972]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480476","summary":null,"start":90370123,"end":90370427,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 248 [Source:HGNC Symbol;Acc:HGNC:45972]"}, {"versioned_ensembl_gene_id":"ENSG00000207730.3","gene_symbol":"MIR200B","gene_name":"microRNA 200b [Source:HGNC Symbol;Acc:HGNC:31579]","synonyms":"MIRN200B,hsa-mir-200b","biotype":"miRNA","ncbi_id":"406984","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1167104,"end":1167198,"strand":1,"description":"microRNA 200b [Source:HGNC Symbol;Acc:HGNC:31579]"}, {"versioned_ensembl_gene_id":"ENSG00000207868.1","gene_symbol":"MIR514A1","gene_name":"microRNA 514a-1 [Source:HGNC Symbol;Acc:HGNC:32148]","synonyms":"MIRN514-1,MIR514-1,hsa-mir-514-1","biotype":"miRNA","ncbi_id":"574516","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147279247,"end":147279344,"strand":-1,"description":"microRNA 514a-1 [Source:HGNC Symbol;Acc:HGNC:32148]"}, {"versioned_ensembl_gene_id":"ENSG00000240767.3","gene_symbol":"RN7SL288P","gene_name":"RNA, 7SL, cytoplasmic 288, pseudogene [Source:HGNC Symbol;Acc:HGNC:46304]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481000","summary":null,"start":46169458,"end":46169748,"strand":-1,"description":"RNA, 7SL, cytoplasmic 288, pseudogene [Source:HGNC Symbol;Acc:HGNC:46304]"}, {"versioned_ensembl_gene_id":"ENSG00000283210.1","gene_symbol":"MIR1322","gene_name":"microRNA 1322 [Source:HGNC Symbol;Acc:HGNC:35374]","synonyms":"MIRN1322,hsa-mir-1322","biotype":"miRNA","ncbi_id":"100302166","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10825373,"end":10825443,"strand":-1,"description":"microRNA 1322 [Source:HGNC Symbol;Acc:HGNC:35374]"}, {"versioned_ensembl_gene_id":"ENSG00000283289.1","gene_symbol":"MIR524","gene_name":"microRNA 524 [Source:HGNC Symbol;Acc:HGNC:32110]","synonyms":"MIRN524,hsa-mir-524","biotype":"miRNA","ncbi_id":"574478","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53711002,"end":53711088,"strand":1,"description":"microRNA 524 [Source:HGNC Symbol;Acc:HGNC:32110]"}, {"versioned_ensembl_gene_id":"ENSG00000264292.1","gene_symbol":"MIR2467","gene_name":"microRNA 2467 [Source:HGNC Symbol;Acc:HGNC:41881]","synonyms":"hsa-mir-2467","biotype":"miRNA","ncbi_id":"100616360","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":239351724,"end":239351804,"strand":-1,"description":"microRNA 2467 [Source:HGNC Symbol;Acc:HGNC:41881]"}, {"versioned_ensembl_gene_id":"ENSG00000256894.1","gene_symbol":"AC022509.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26125155,"end":26126617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284375.1","gene_symbol":"MIR19B1","gene_name":"microRNA 19b-1 [Source:HGNC Symbol;Acc:HGNC:31575]","synonyms":"MIRN19B1,hsa-mir-19b-1","biotype":"miRNA","ncbi_id":"406980","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91351192,"end":91351278,"strand":1,"description":"microRNA 19b-1 [Source:HGNC Symbol;Acc:HGNC:31575]"}, {"versioned_ensembl_gene_id":"ENSG00000283532.1","gene_symbol":"MIR4317","gene_name":"microRNA 4317 [Source:HGNC Symbol;Acc:HGNC:38260]","synonyms":"hsa-mir-4317","biotype":"miRNA","ncbi_id":"100422840","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6374361,"end":6374425,"strand":-1,"description":"microRNA 4317 [Source:HGNC Symbol;Acc:HGNC:38260]"}, {"versioned_ensembl_gene_id":"ENSG00000266370.1","gene_symbol":"MIR3657","gene_name":"microRNA 3657 [Source:HGNC Symbol;Acc:HGNC:38906]","synonyms":"hsa-mir-3657","biotype":"miRNA","ncbi_id":"100500889","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112037599,"end":112037715,"strand":-1,"description":"microRNA 3657 [Source:HGNC Symbol;Acc:HGNC:38906]"}, {"versioned_ensembl_gene_id":"ENSG00000200650.1","gene_symbol":"RNA5SP114","gene_name":"RNA, 5S ribosomal pseudogene 114 [Source:HGNC Symbol;Acc:HGNC:42912]","synonyms":"RN5S114","biotype":"rRNA","ncbi_id":"100873384","summary":null,"start":188276732,"end":188276844,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 114 [Source:HGNC Symbol;Acc:HGNC:42912]"}, {"versioned_ensembl_gene_id":"ENSG00000200714.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65592731,"end":65592820,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281185.1","gene_symbol":"GPX6","gene_name":"glutathione peroxidase 6 [Source:HGNC Symbol;Acc:HGNC:4558]","synonyms":"GPXP3,GPXP3","biotype":"protein_coding","ncbi_id":"257202","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. Expression of this gene has been observed in embryos and olfactory epithelium; however, the exact function of this gene is not known. This isozyme is a selenoprotein in humans, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. The orthologs of this gene in mouse and rat (and some other species) contain a cysteine (Cys) residue in place of the Sec residue, and their corresponding mRNAs lack SECIS element. [provided by RefSeq, Jul 2017]","start":28510773,"end":28515743,"strand":-1,"description":"glutathione peroxidase 6 [Source:HGNC Symbol;Acc:HGNC:4558]"}, {"versioned_ensembl_gene_id":"ENSG00000202445.1","gene_symbol":"RNU6-669P","gene_name":"RNA, U6 small nuclear 669, pseudogene [Source:HGNC Symbol;Acc:HGNC:47632]","synonyms":null,"biotype":"snRNA","ncbi_id":"107063537","summary":null,"start":94507738,"end":94507844,"strand":1,"description":"RNA, U6 small nuclear 669, pseudogene [Source:HGNC Symbol;Acc:HGNC:47632]"}, {"versioned_ensembl_gene_id":"ENSG00000238963.2","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":154905076,"end":154905206,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000252506.1","gene_symbol":"RNU6-180P","gene_name":"RNA, U6 small nuclear 180, pseudogene [Source:HGNC Symbol;Acc:HGNC:47143]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481233","summary":null,"start":229383128,"end":229383188,"strand":1,"description":"RNA, U6 small nuclear 180, pseudogene [Source:HGNC Symbol;Acc:HGNC:47143]"}, {"versioned_ensembl_gene_id":"ENSG00000277584.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":190019116,"end":190019233,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000222383.1","gene_symbol":"RNA5SP203","gene_name":"RNA, 5S ribosomal pseudogene 203 [Source:HGNC Symbol;Acc:HGNC:43103]","synonyms":"RN5S203","biotype":"rRNA","ncbi_id":"100873464","summary":null,"start":10752791,"end":10752926,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 203 [Source:HGNC Symbol;Acc:HGNC:43103]"}, {"versioned_ensembl_gene_id":"ENSG00000277678.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":145169519,"end":145169664,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000252222.1","gene_symbol":"RNU7-13P","gene_name":"RNA, U7 small nuclear 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:34109]","synonyms":"U7.13","biotype":"snRNA","ncbi_id":"100147761","summary":null,"start":184821428,"end":184821489,"strand":-1,"description":"RNA, U7 small nuclear 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:34109]"}, {"versioned_ensembl_gene_id":"ENSG00000264438.2","gene_symbol":"RN7SL560P","gene_name":"RNA, 7SL, cytoplasmic 560, pseudogene [Source:HGNC Symbol;Acc:HGNC:46576]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479426","summary":null,"start":128709780,"end":128710043,"strand":1,"description":"RNA, 7SL, cytoplasmic 560, pseudogene [Source:HGNC Symbol;Acc:HGNC:46576]"}, {"versioned_ensembl_gene_id":"ENSG00000251851.1","gene_symbol":"RNU6-772P","gene_name":"RNA, U6 small nuclear 772, pseudogene [Source:HGNC Symbol;Acc:HGNC:47735]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479908","summary":null,"start":20355748,"end":20355852,"strand":-1,"description":"RNA, U6 small nuclear 772, pseudogene [Source:HGNC Symbol;Acc:HGNC:47735]"}, {"versioned_ensembl_gene_id":"ENSG00000252452.1","gene_symbol":"RNU6-107P","gene_name":"RNA, U6 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:47070]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479614","summary":null,"start":232782665,"end":232782766,"strand":1,"description":"RNA, U6 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:47070]"}, {"versioned_ensembl_gene_id":"ENSG00000221719.1","gene_symbol":"SNORA3C","gene_name":"small nucleolar RNA, H/ACA box 3C [Source:HGNC Symbol;Acc:HGNC:52203]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616997","summary":null,"start":2796408,"end":2796532,"strand":-1,"description":"small nucleolar RNA, H/ACA box 3C [Source:HGNC Symbol;Acc:HGNC:52203]"}, {"versioned_ensembl_gene_id":"ENSG00000243801.3","gene_symbol":"RN7SL461P","gene_name":"RNA, 7SL, cytoplasmic 461, pseudogene [Source:HGNC Symbol;Acc:HGNC:46477]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481844","summary":null,"start":56824375,"end":56824656,"strand":-1,"description":"RNA, 7SL, cytoplasmic 461, pseudogene [Source:HGNC Symbol;Acc:HGNC:46477]"}, {"versioned_ensembl_gene_id":"ENSG00000223951.1","gene_symbol":"AL133244.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33056333,"end":33063113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276580.1","gene_symbol":"MIR8055","gene_name":"microRNA 8055 [Source:HGNC Symbol;Acc:HGNC:50241]","synonyms":"hsa-mir-8055","biotype":"miRNA","ncbi_id":"102465861","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6622124,"end":6622220,"strand":-1,"description":"microRNA 8055 [Source:HGNC Symbol;Acc:HGNC:50241]"}, {"versioned_ensembl_gene_id":"ENSG00000266750.1","gene_symbol":"MIR4645","gene_name":"microRNA 4645 [Source:HGNC Symbol;Acc:HGNC:41689]","synonyms":"hsa-mir-4645","biotype":"miRNA","ncbi_id":"100616285","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2854031,"end":2854107,"strand":-1,"description":"microRNA 4645 [Source:HGNC Symbol;Acc:HGNC:41689]"}, {"versioned_ensembl_gene_id":"ENSG00000200774.1","gene_symbol":"RNU6-478P","gene_name":"RNA, U6 small nuclear 478, pseudogene [Source:HGNC Symbol;Acc:HGNC:47441]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479778","summary":null,"start":83067962,"end":83068071,"strand":-1,"description":"RNA, U6 small nuclear 478, pseudogene [Source:HGNC Symbol;Acc:HGNC:47441]"}, {"versioned_ensembl_gene_id":"ENSG00000201487.1","gene_symbol":"SNORD45B","gene_name":"small nucleolar RNA, C/D box 45B [Source:HGNC Symbol;Acc:HGNC:10185]","synonyms":"U45b,RNU45B","biotype":"snoRNA","ncbi_id":"26804","summary":null,"start":75789477,"end":75789548,"strand":1,"description":"small nucleolar RNA, C/D box 45B [Source:HGNC Symbol;Acc:HGNC:10185]"}, {"versioned_ensembl_gene_id":"ENSG00000202368.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96979528,"end":96979629,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266119.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30726158,"end":30726268,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252137.1","gene_symbol":"RNU6-1338P","gene_name":"RNA, U6 small nuclear 1338, pseudogene [Source:HGNC Symbol;Acc:HGNC:48301]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480150","summary":null,"start":75593055,"end":75593145,"strand":1,"description":"RNA, U6 small nuclear 1338, pseudogene [Source:HGNC Symbol;Acc:HGNC:48301]"}, {"versioned_ensembl_gene_id":"ENSG00000199740.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50939927,"end":50940026,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276341.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":55049943,"end":55068836,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000274321.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88520000,"end":88520170,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000239180.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":70311607,"end":70311701,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265260.2","gene_symbol":"RN7SL74P","gene_name":"RNA, 7SL, cytoplasmic 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:46090]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480942","summary":null,"start":97341046,"end":97341344,"strand":1,"description":"RNA, 7SL, cytoplasmic 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:46090]"}, {"versioned_ensembl_gene_id":"ENSG00000264462.1","gene_symbol":"MIR3648-2","gene_name":"microRNA 3648-2 [Source:HGNC Symbol;Acc:HGNC:50843]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504731","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8986999,"end":8987178,"strand":1,"description":"microRNA 3648-2 [Source:HGNC Symbol;Acc:HGNC:50843]"}, {"versioned_ensembl_gene_id":"ENSG00000207815.1","gene_symbol":"MIR563","gene_name":"microRNA 563 [Source:HGNC Symbol;Acc:HGNC:32819]","synonyms":"MIRN563,hsa-mir-563","biotype":"miRNA","ncbi_id":"693148","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15873771,"end":15873849,"strand":1,"description":"microRNA 563 [Source:HGNC Symbol;Acc:HGNC:32819]"}, {"versioned_ensembl_gene_id":"ENSG00000277707.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"PRP31,PRP31,hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000200298.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72022407,"end":72022516,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240545.3","gene_symbol":"RN7SL492P","gene_name":"RNA, 7SL, cytoplasmic 492, pseudogene [Source:HGNC Symbol;Acc:HGNC:46508]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479402","summary":null,"start":56794348,"end":56794642,"strand":-1,"description":"RNA, 7SL, cytoplasmic 492, pseudogene [Source:HGNC Symbol;Acc:HGNC:46508]"}, {"versioned_ensembl_gene_id":"ENSG00000232058.1","gene_symbol":"AC005772.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15014805,"end":15052276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276169.1","gene_symbol":"MIR6871","gene_name":"microRNA 6871 [Source:HGNC Symbol;Acc:HGNC:49964]","synonyms":"hsa-mir-6871","biotype":"miRNA","ncbi_id":"102466912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41169023,"end":41169078,"strand":1,"description":"microRNA 6871 [Source:HGNC Symbol;Acc:HGNC:49964]"}, {"versioned_ensembl_gene_id":"ENSG00000199458.1","gene_symbol":"RNU4-35P","gene_name":"RNA, U4 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46971]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481182","summary":null,"start":121453981,"end":121454121,"strand":-1,"description":"RNA, U4 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46971]"}, {"versioned_ensembl_gene_id":"ENSG00000199839.1","gene_symbol":"RNA5SP150","gene_name":"RNA, 5S ribosomal pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:43050]","synonyms":"RN5S150","biotype":"rRNA","ncbi_id":"100873416","summary":null,"start":181822872,"end":181822990,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:43050]"}, {"versioned_ensembl_gene_id":"ENSG00000265537.1","gene_symbol":"MIR3180-1","gene_name":"microRNA 3180-1 [Source:HGNC Symbol;Acc:HGNC:38382]","synonyms":"hsa-mir-3180-1","biotype":"miRNA","ncbi_id":"100422870","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14911220,"end":14911313,"strand":1,"description":"microRNA 3180-1 [Source:HGNC Symbol;Acc:HGNC:38382]"}, {"versioned_ensembl_gene_id":"ENSG00000252411.1","gene_symbol":"RNU6-1087P","gene_name":"RNA, U6 small nuclear 1087, pseudogene [Source:HGNC Symbol;Acc:HGNC:48050]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481522","summary":null,"start":35594173,"end":35594273,"strand":1,"description":"RNA, U6 small nuclear 1087, pseudogene [Source:HGNC Symbol;Acc:HGNC:48050]"}, {"versioned_ensembl_gene_id":"ENSG00000277391.1","gene_symbol":"MIR6881","gene_name":"microRNA 6881 [Source:HGNC Symbol;Acc:HGNC:50098]","synonyms":"hsa-mir-6881","biotype":"miRNA","ncbi_id":"102465530","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74411357,"end":74411432,"strand":-1,"description":"microRNA 6881 [Source:HGNC Symbol;Acc:HGNC:50098]"}, {"versioned_ensembl_gene_id":"ENSG00000265612.1","gene_symbol":"MIR4539","gene_name":"microRNA 4539 [Source:HGNC Symbol;Acc:HGNC:41546]","synonyms":"hsa-mir-4539","biotype":"miRNA","ncbi_id":"100616374","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105857513,"end":105857572,"strand":-1,"description":"microRNA 4539 [Source:HGNC Symbol;Acc:HGNC:41546]"}, {"versioned_ensembl_gene_id":"ENSG00000252824.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":102194076,"end":102194164,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000265768.1","gene_symbol":"MIR4506","gene_name":"microRNA 4506 [Source:HGNC Symbol;Acc:HGNC:41663]","synonyms":"hsa-mir-4506","biotype":"miRNA","ncbi_id":"100616140","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93948226,"end":93948302,"strand":-1,"description":"microRNA 4506 [Source:HGNC Symbol;Acc:HGNC:41663]"}, {"versioned_ensembl_gene_id":"ENSG00000277739.1","gene_symbol":"RNA5-8SN1","gene_name":"RNA, 5.8S ribosomal N1 [Source:HGNC Symbol;Acc:HGNC:53517]","synonyms":null,"biotype":"rRNA","ncbi_id":"106632260","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units, that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. Gene and RefSeq, in collaboration with HGNC, currently describe one 45S rDNA cluster, and one set of 45S precursor and product rRNAs, for each of the five human chromosomes to which these loci are localized. This gene is a representative copy of the 5.8S ribosomal RNA on chromosome 21. [provided by RefSeq, Feb 2017]","start":8256781,"end":8256933,"strand":1,"description":"RNA, 5.8S ribosomal N1 [Source:HGNC Symbol;Acc:HGNC:53517]"}, {"versioned_ensembl_gene_id":"ENSG00000229012.1","gene_symbol":"AC003685.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8863861,"end":8867601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237594.2","gene_symbol":"AP000251.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31559245,"end":31560487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283699.1","gene_symbol":"MIR4481","gene_name":"microRNA 4481 [Source:HGNC Symbol;Acc:HGNC:41781]","synonyms":"hsa-mir-4481","biotype":"miRNA","ncbi_id":"100616320","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12653138,"end":12653197,"strand":-1,"description":"microRNA 4481 [Source:HGNC Symbol;Acc:HGNC:41781]"}, {"versioned_ensembl_gene_id":"ENSG00000222747.1","gene_symbol":"RNA5SP25","gene_name":"RNA, 5S ribosomal pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42601]","synonyms":"RN5S25","biotype":"rRNA","ncbi_id":"100873357","summary":null,"start":21369790,"end":21369899,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42601]"}, {"versioned_ensembl_gene_id":"ENSG00000206797.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":450663,"end":450762,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264553.1","gene_symbol":"MIR4257","gene_name":"microRNA 4257 [Source:HGNC Symbol;Acc:HGNC:38312]","synonyms":"hsa-mir-4257","biotype":"miRNA","ncbi_id":"100422997","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":150551929,"end":150552014,"strand":1,"description":"microRNA 4257 [Source:HGNC Symbol;Acc:HGNC:38312]"}, {"versioned_ensembl_gene_id":"ENSG00000202386.1","gene_symbol":"RNA5SP211","gene_name":"RNA, 5S ribosomal pseudogene 211 [Source:HGNC Symbol;Acc:HGNC:43111]","synonyms":"RN5S211","biotype":"rRNA","ncbi_id":"100873471","summary":null,"start":106449381,"end":106449497,"strand":1,"description":"RNA, 5S ribosomal pseudogene 211 [Source:HGNC Symbol;Acc:HGNC:43111]"}, {"versioned_ensembl_gene_id":"ENSG00000265815.1","gene_symbol":"MIR1273G","gene_name":"microRNA 1273g [Source:HGNC Symbol;Acc:HGNC:41684]","synonyms":"hsa-mir-1273g","biotype":"miRNA","ncbi_id":"100616145","summary":"This record was withdrawn by miRBase.","start":52940314,"end":52940413,"strand":1,"description":"microRNA 1273g [Source:HGNC Symbol;Acc:HGNC:41684]"}, {"versioned_ensembl_gene_id":"ENSG00000283477.1","gene_symbol":"MIR6079","gene_name":"microRNA 6079 [Source:HGNC Symbol;Acc:HGNC:50114]","synonyms":"hsa-mir-6079","biotype":"miRNA","ncbi_id":"102464830","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43838622,"end":43838683,"strand":1,"description":"microRNA 6079 [Source:HGNC Symbol;Acc:HGNC:50114]"}, {"versioned_ensembl_gene_id":"ENSG00000199594.1","gene_symbol":"RNU6-1301P","gene_name":"RNA, U6 small nuclear 1301, pseudogene [Source:HGNC Symbol;Acc:HGNC:48264]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481591","summary":null,"start":37140327,"end":37140430,"strand":1,"description":"RNA, U6 small nuclear 1301, pseudogene [Source:HGNC Symbol;Acc:HGNC:48264]"}, {"versioned_ensembl_gene_id":"ENSG00000252587.1","gene_symbol":"RNA5SP422","gene_name":"RNA, 5S ribosomal pseudogene 422 [Source:HGNC Symbol;Acc:HGNC:43322]","synonyms":"RN5S422","biotype":"rRNA","ncbi_id":"100873673","summary":null,"start":35754923,"end":35755033,"strand":1,"description":"RNA, 5S ribosomal pseudogene 422 [Source:HGNC Symbol;Acc:HGNC:43322]"}, {"versioned_ensembl_gene_id":"ENSG00000221206.1","gene_symbol":"RNU6ATAC15P","gene_name":"RNA, U6atac small nuclear 15, 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{"versioned_ensembl_gene_id":"ENSG00000277637.1","gene_symbol":"RN7SL469P","gene_name":"RNA, 7SL, cytoplasmic 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:46485]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480512","summary":null,"start":30143733,"end":30143969,"strand":1,"description":"RNA, 7SL, cytoplasmic 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:46485]"}, {"versioned_ensembl_gene_id":"ENSG00000283509.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":129819777,"end":129819876,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000199668.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11315067,"end":11315178,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278457.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":380608,"end":380726,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000252147.1","gene_symbol":"RNY3P16","gene_name":"RNA, Ro-associated Y3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:50891]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480686","summary":null,"start":119456558,"end":119456658,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:50891]"}, {"versioned_ensembl_gene_id":"ENSG00000274408.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":146539541,"end":146539663,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000201660.1","gene_symbol":"SNORA20","gene_name":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]","synonyms":"ACA20","biotype":"snoRNA","ncbi_id":"677806","summary":null,"start":5410122,"end":5410251,"strand":1,"description":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]"}, {"versioned_ensembl_gene_id":"ENSG00000283675.1","gene_symbol":"snoMe28S-Am2634","gene_name":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":19420279,"end":19420342,"strand":1,"description":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]"}, {"versioned_ensembl_gene_id":"ENSG00000199855.1","gene_symbol":"RNU6-490P","gene_name":"RNA, U6 small nuclear 490, pseudogene [Source:HGNC Symbol;Acc:HGNC:47453]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479783","summary":null,"start":27088321,"end":27088427,"strand":-1,"description":"RNA, U6 small nuclear 490, pseudogene [Source:HGNC Symbol;Acc:HGNC:47453]"}, {"versioned_ensembl_gene_id":"ENSG00000252530.1","gene_symbol":"RNU6-965P","gene_name":"RNA, U6 small nuclear 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:47928]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481484","summary":null,"start":101728642,"end":101728737,"strand":-1,"description":"RNA, U6 small nuclear 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:47928]"}, {"versioned_ensembl_gene_id":"ENSG00000238457.1","gene_symbol":"RNU7-169P","gene_name":"RNA, U7 small nuclear 169 pseudogene [Source:HGNC Symbol;Acc:HGNC:45703]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480827","summary":null,"start":108668448,"end":108668508,"strand":1,"description":"RNA, U7 small nuclear 169 pseudogene [Source:HGNC Symbol;Acc:HGNC:45703]"}, {"versioned_ensembl_gene_id":"ENSG00000237325.3","gene_symbol":"AP000563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31452466,"end":31453223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200105.1","gene_symbol":"RNU6-251P","gene_name":"RNA, U6 small nuclear 251, pseudogene [Source:HGNC Symbol;Acc:HGNC:47214]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481257","summary":null,"start":15671707,"end":15671810,"strand":-1,"description":"RNA, U6 small nuclear 251, pseudogene [Source:HGNC Symbol;Acc:HGNC:47214]"}, {"versioned_ensembl_gene_id":"ENSG00000212445.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":68189287,"end":68189421,"strand":1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000265584.1","gene_symbol":"MIR3978","gene_name":"microRNA 3978 [Source:HGNC Symbol;Acc:HGNC:41630]","synonyms":"hsa-mir-3978","biotype":"miRNA","ncbi_id":"100616491","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110082118,"end":110082218,"strand":1,"description":"microRNA 3978 [Source:HGNC Symbol;Acc:HGNC:41630]"}, {"versioned_ensembl_gene_id":"ENSG00000238884.1","gene_symbol":"RNU7-85P","gene_name":"RNA, U7 small nuclear 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:34181]","synonyms":"U7.85","biotype":"snRNA","ncbi_id":"100151682","summary":null,"start":79800133,"end":79800195,"strand":-1,"description":"RNA, U7 small nuclear 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:34181]"}, {"versioned_ensembl_gene_id":"ENSG00000284139.1","gene_symbol":"MIR1234","gene_name":"microRNA 1234 [Source:HGNC Symbol;Acc:HGNC:33926]","synonyms":"MIRN1234,hsa-mir-1234","biotype":"miRNA","ncbi_id":"100302196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144400086,"end":144400165,"strand":-1,"description":"microRNA 1234 [Source:HGNC Symbol;Acc:HGNC:33926]"}, {"versioned_ensembl_gene_id":"ENSG00000283622.1","gene_symbol":"MIR4328","gene_name":"microRNA 4328 [Source:HGNC Symbol;Acc:HGNC:38280]","synonyms":"hsa-mir-4328","biotype":"miRNA","ncbi_id":"100422932","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":78901194,"end":78901249,"strand":-1,"description":"microRNA 4328 [Source:HGNC Symbol;Acc:HGNC:38280]"}, {"versioned_ensembl_gene_id":"ENSG00000266168.1","gene_symbol":"MIR3147","gene_name":"microRNA 3147 [Source:HGNC Symbol;Acc:HGNC:38300]","synonyms":"hsa-mir-3147","biotype":"miRNA","ncbi_id":"100422939","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57405025,"end":57405090,"strand":1,"description":"microRNA 3147 [Source:HGNC Symbol;Acc:HGNC:38300]"}, {"versioned_ensembl_gene_id":"ENSG00000207701.1","gene_symbol":"MIR597","gene_name":"microRNA 597 [Source:HGNC Symbol;Acc:HGNC:32853]","synonyms":"MIRN597,hsa-mir-597","biotype":"miRNA","ncbi_id":"693182","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9741672,"end":9741768,"strand":1,"description":"microRNA 597 [Source:HGNC Symbol;Acc:HGNC:32853]"}, {"versioned_ensembl_gene_id":"ENSG00000199023.3","gene_symbol":"MIR339","gene_name":"microRNA 339 [Source:HGNC Symbol;Acc:HGNC:31776]","synonyms":"MIRN339,hsa-mir-339","biotype":"miRNA","ncbi_id":"442907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1022933,"end":1023026,"strand":-1,"description":"microRNA 339 [Source:HGNC Symbol;Acc:HGNC:31776]"}, {"versioned_ensembl_gene_id":"ENSG00000222457.1","gene_symbol":"RNU6-121P","gene_name":"RNA, U6 small nuclear 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:47084]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481215","summary":null,"start":154297650,"end":154297748,"strand":1,"description":"RNA, U6 small nuclear 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:47084]"}, {"versioned_ensembl_gene_id":"ENSG00000264585.1","gene_symbol":"MIR4449","gene_name":"microRNA 4449 [Source:HGNC Symbol;Acc:HGNC:41864]","synonyms":"hsa-mir-4449","biotype":"miRNA","ncbi_id":"100616436","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52712682,"end":52712747,"strand":1,"description":"microRNA 4449 [Source:HGNC Symbol;Acc:HGNC:41864]"}, {"versioned_ensembl_gene_id":"ENSG00000207779.1","gene_symbol":"MIR15B","gene_name":"microRNA 15b [Source:HGNC Symbol;Acc:HGNC:31544]","synonyms":"MIRN15B,hsa-mir-15b","biotype":"miRNA","ncbi_id":"406949","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160404588,"end":160404685,"strand":1,"description":"microRNA 15b [Source:HGNC Symbol;Acc:HGNC:31544]"}, {"versioned_ensembl_gene_id":"ENSG00000284134.1","gene_symbol":"MIR568","gene_name":"microRNA 568 [Source:HGNC Symbol;Acc:HGNC:32824]","synonyms":"MIRN568,hsa-mir-568","biotype":"miRNA","ncbi_id":"693153","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114316475,"end":114316569,"strand":-1,"description":"microRNA 568 [Source:HGNC Symbol;Acc:HGNC:32824]"}, {"versioned_ensembl_gene_id":"ENSG00000199571.1","gene_symbol":"SNORA22","gene_name":"Small nucleolar RNA SNORA22 [Source:RFAM;Acc:RF00414]","synonyms":"SNORA22A,ACA22","biotype":"snoRNA","ncbi_id":"677807","summary":null,"start":39819750,"end":39819883,"strand":-1,"description":"Small nucleolar RNA SNORA22 [Source:RFAM;Acc:RF00414]"}, {"versioned_ensembl_gene_id":"ENSG00000211590.1","gene_symbol":"MIR802","gene_name":"microRNA 802 [Source:HGNC Symbol;Acc:HGNC:33140]","synonyms":"MIRN802,hsa-mir-802","biotype":"miRNA","ncbi_id":"768219","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35720715,"end":35720808,"strand":1,"description":"microRNA 802 [Source:HGNC Symbol;Acc:HGNC:33140]"}, {"versioned_ensembl_gene_id":"ENSG00000274323.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54264323,"end":54264425,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207168.1","gene_symbol":"SNORA15","gene_name":"small nucleolar RNA, H/ACA box 15 [Source:HGNC Symbol;Acc:HGNC:32604]","synonyms":"SNORA15A,ACA15","biotype":"snoRNA","ncbi_id":"677803","summary":null,"start":56060470,"end":56060602,"strand":1,"description":"small nucleolar RNA, H/ACA box 15 [Source:HGNC Symbol;Acc:HGNC:32604]"}, {"versioned_ensembl_gene_id":"ENSG00000284079.1","gene_symbol":"MIR4775","gene_name":"microRNA 4775 [Source:HGNC Symbol;Acc:HGNC:41885]","synonyms":"hsa-mir-4775","biotype":"miRNA","ncbi_id":"100616361","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207754807,"end":207754881,"strand":1,"description":"microRNA 4775 [Source:HGNC Symbol;Acc:HGNC:41885]"}, {"versioned_ensembl_gene_id":"ENSG00000275587.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45538099,"end":45538379,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276229.1","gene_symbol":"Six3os1_3","gene_name":"Six3os1 conserved region 3 [Source:RFAM;Acc:RF02248]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44935294,"end":44935368,"strand":1,"description":"Six3os1 conserved region 3 [Source:RFAM;Acc:RF02248]"}, {"versioned_ensembl_gene_id":"ENSG00000251751.1","gene_symbol":"RN7SKP46","gene_name":"RNA, 7SK small nuclear pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:45770]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480847","summary":null,"start":157930492,"end":157930725,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:45770]"}, {"versioned_ensembl_gene_id":"ENSG00000201558.1","gene_symbol":"RNVU1-6","gene_name":"RNA, variant U1 small nuclear 6 [Source:HGNC Symbol;Acc:HGNC:48314]","synonyms":"vU1.6,RNU1-99","biotype":"snRNA","ncbi_id":"101954276","summary":null,"start":146052081,"end":146052244,"strand":-1,"description":"RNA, variant U1 small nuclear 6 [Source:HGNC Symbol;Acc:HGNC:48314]"}, {"versioned_ensembl_gene_id":"ENSG00000199715.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18273165,"end":18273266,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273788.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":72726122,"end":72726337,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000223040.1","gene_symbol":"RN7SKP144","gene_name":"RNA, 7SK small nuclear pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:45868]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479159","summary":null,"start":2088933,"end":2089211,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:45868]"}, {"versioned_ensembl_gene_id":"ENSG00000242999.3","gene_symbol":"RN7SL239P","gene_name":"RNA, 7SL, cytoplasmic 239, pseudogene [Source:HGNC Symbol;Acc:HGNC:46255]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479309","summary":null,"start":74845910,"end":74846209,"strand":1,"description":"RNA, 7SL, cytoplasmic 239, pseudogene [Source:HGNC Symbol;Acc:HGNC:46255]"}, {"versioned_ensembl_gene_id":"ENSG00000209582.1","gene_symbol":"SNORA48","gene_name":"small nucleolar RNA, H/ACA box 48 [Source:HGNC Symbol;Acc:HGNC:32641]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":7574713,"end":7574847,"strand":1,"description":"small nucleolar RNA, H/ACA box 48 [Source:HGNC Symbol;Acc:HGNC:32641]"}, {"versioned_ensembl_gene_id":"ENSG00000252268.1","gene_symbol":"RNA5SP417","gene_name":"RNA, 5S ribosomal pseudogene 417 [Source:HGNC Symbol;Acc:HGNC:43317]","synonyms":"RN5S417","biotype":"rRNA","ncbi_id":"100873668","summary":null,"start":35751828,"end":35751935,"strand":1,"description":"RNA, 5S ribosomal pseudogene 417 [Source:HGNC Symbol;Acc:HGNC:43317]"}, {"versioned_ensembl_gene_id":"ENSG00000244372.3","gene_symbol":"RN7SL423P","gene_name":"RNA, 7SL, cytoplasmic 423, pseudogene [Source:HGNC Symbol;Acc:HGNC:46439]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479378","summary":null,"start":160877547,"end":160877850,"strand":1,"description":"RNA, 7SL, cytoplasmic 423, pseudogene [Source:HGNC Symbol;Acc:HGNC:46439]"}, {"versioned_ensembl_gene_id":"ENSG00000284284.1","gene_symbol":"MIR4712","gene_name":"microRNA 4712 [Source:HGNC Symbol;Acc:HGNC:41732]","synonyms":"hsa-mir-4712","biotype":"miRNA","ncbi_id":"100616396","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50360329,"end":50360410,"strand":1,"description":"microRNA 4712 [Source:HGNC Symbol;Acc:HGNC:41732]"}, {"versioned_ensembl_gene_id":"ENSG00000207714.3","gene_symbol":"MIR584","gene_name":"microRNA 584 [Source:HGNC Symbol;Acc:HGNC:32840]","synonyms":"MIRN584,hsa-mir-584","biotype":"miRNA","ncbi_id":"693169","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149062313,"end":149062409,"strand":-1,"description":"microRNA 584 [Source:HGNC Symbol;Acc:HGNC:32840]"}, {"versioned_ensembl_gene_id":"ENSG00000274693.1","gene_symbol":"HTT-AS1_2","gene_name":"HTT antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02135]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3069977,"end":3070151,"strand":1,"description":"HTT antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02135]"}, {"versioned_ensembl_gene_id":"ENSG00000264915.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31702742,"end":31702855,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221760.1","gene_symbol":"MIR548J","gene_name":"microRNA 548j [Source:HGNC Symbol;Acc:HGNC:35276]","synonyms":"MIRN548J,hsa-mir-548j","biotype":"miRNA","ncbi_id":"100313914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26555212,"end":26555323,"strand":-1,"description":"microRNA 548j [Source:HGNC Symbol;Acc:HGNC:35276]"}, {"versioned_ensembl_gene_id":"ENSG00000264591.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31523278,"end":31523355,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000284329.1","gene_symbol":"MIR9-3","gene_name":"microRNA 9-3 [Source:HGNC Symbol;Acc:HGNC:31646]","synonyms":"MIRN9-3,hsa-mir-9-3","biotype":"miRNA","ncbi_id":"407051","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89368017,"end":89368106,"strand":1,"description":"microRNA 9-3 [Source:HGNC Symbol;Acc:HGNC:31646]"}, {"versioned_ensembl_gene_id":"ENSG00000278517.1","gene_symbol":"MIR6865","gene_name":"microRNA 6865 [Source:HGNC Symbol;Acc:HGNC:50182]","synonyms":"hsa-mir-6865","biotype":"miRNA","ncbi_id":"102465522","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4970086,"end":4970150,"strand":-1,"description":"microRNA 6865 [Source:HGNC Symbol;Acc:HGNC:50182]"}, {"versioned_ensembl_gene_id":"ENSG00000199460.2","gene_symbol":"RNU6-1216P","gene_name":"RNA, U6 small nuclear 1216, pseudogene [Source:HGNC Symbol;Acc:HGNC:48179]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480098","summary":null,"start":69182877,"end":69182983,"strand":1,"description":"RNA, U6 small nuclear 1216, pseudogene [Source:HGNC Symbol;Acc:HGNC:48179]"}, {"versioned_ensembl_gene_id":"ENSG00000206922.1","gene_symbol":"RNU6-80P","gene_name":"RNA, U6 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:42570]","synonyms":"RNU6-80","biotype":"snRNA","ncbi_id":"106478990","summary":null,"start":72706017,"end":72706123,"strand":-1,"description":"RNA, U6 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:42570]"}, {"versioned_ensembl_gene_id":"ENSG00000199805.1","gene_symbol":"RNU1-134P","gene_name":"RNA, U1 small nuclear 134, pseudogene [Source:HGNC Symbol;Acc:HGNC:48476]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480194","summary":null,"start":63908955,"end":63909119,"strand":1,"description":"RNA, U1 small nuclear 134, pseudogene [Source:HGNC Symbol;Acc:HGNC:48476]"}, {"versioned_ensembl_gene_id":"ENSG00000252839.1","gene_symbol":"RNU6-419P","gene_name":"RNA, U6 small nuclear 419, pseudogene [Source:HGNC Symbol;Acc:HGNC:47382]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479751","summary":null,"start":73246818,"end":73246880,"strand":-1,"description":"RNA, U6 small nuclear 419, pseudogene [Source:HGNC Symbol;Acc:HGNC:47382]"}, {"versioned_ensembl_gene_id":"ENSG00000207248.1","gene_symbol":"RNU6-1005P","gene_name":"RNA, U6 small nuclear 1005, pseudogene [Source:HGNC Symbol;Acc:HGNC:47968]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481497","summary":null,"start":21642054,"end":21642160,"strand":1,"description":"RNA, U6 small nuclear 1005, pseudogene [Source:HGNC Symbol;Acc:HGNC:47968]"}, {"versioned_ensembl_gene_id":"ENSG00000251908.1","gene_symbol":"RNU6-491P","gene_name":"RNA, U6 small nuclear 491, pseudogene [Source:HGNC Symbol;Acc:HGNC:47454]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479784","summary":null,"start":14250232,"end":14250341,"strand":-1,"description":"RNA, U6 small nuclear 491, pseudogene [Source:HGNC Symbol;Acc:HGNC:47454]"}, {"versioned_ensembl_gene_id":"ENSG00000238597.1","gene_symbol":"SNORD4B","gene_name":"small nucleolar RNA, C/D box 4B [Source:HGNC Symbol;Acc:HGNC:10098]","synonyms":"Z17B,RNU101B","biotype":"snoRNA","ncbi_id":"26772","summary":null,"start":28723682,"end":28723753,"strand":1,"description":"small nucleolar RNA, C/D box 4B [Source:HGNC Symbol;Acc:HGNC:10098]"}, {"versioned_ensembl_gene_id":"ENSG00000265878.2","gene_symbol":"MIR3914-1","gene_name":"microRNA 3914-1 [Source:HGNC Symbol;Acc:HGNC:38993]","synonyms":"hsa-mir-3914-1","biotype":"miRNA","ncbi_id":"100500836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71307672,"end":71307770,"strand":-1,"description":"microRNA 3914-1 [Source:HGNC Symbol;Acc:HGNC:38993]"}, {"versioned_ensembl_gene_id":"ENSG00000148700.14","gene_symbol":"ADD3","gene_name":"adducin 3 [Source:HGNC Symbol;Acc:HGNC:245]","synonyms":"ADDL","biotype":"protein_coding","ncbi_id":"120","summary":"Adducins are heteromeric proteins composed of different subunits referred to as adducin alpha, beta and gamma. The three subunits are encoded by distinct genes and belong to a family of membrane skeletal proteins involved in the assembly of spectrin-actin network in erythrocytes and at sites of cell-cell contact in epithelial tissues. While adducins alpha and gamma are ubiquitously expressed, the expression of adducin beta is restricted to brain and hematopoietic tissues. Adducin, originally purified from human erythrocytes, was found to be a heterodimer of adducins alpha and beta. Polymorphisms resulting in amino acid substitutions in these two subunits have been associated with the regulation of blood pressure in an animal model of hypertension. Heterodimers consisting of alpha and gamma subunits have also been described. Structurally, each subunit is comprised of two distinct domains. The amino-terminal region is protease resistant and globular in shape, while the carboxy-terminal region is protease sensitive. The latter contains multiple phosphorylation sites for protein kinase C, the binding site for calmodulin, and is required for association with spectrin and actin. Alternatively spliced adducin gamma transcripts encoding different isoforms have been described. The functions of the different isoforms are not known. [provided by RefSeq, Jul 2008]","start":109996368,"end":110135565,"strand":1,"description":"adducin 3 [Source:HGNC Symbol;Acc:HGNC:245]"}, {"versioned_ensembl_gene_id":"ENSG00000267634.1","gene_symbol":"RPL7L1P5","gene_name":"ribosomal protein L7 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390800","summary":null,"start":44365014,"end":44365751,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39487]"}, {"versioned_ensembl_gene_id":"ENSG00000229312.2","gene_symbol":"AL353693.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69472466,"end":69494513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126453.9","gene_symbol":"BCL2L12","gene_name":"BCL2 like 12 [Source:HGNC Symbol;Acc:HGNC:13787]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83596","summary":"This gene encodes a member of a family of proteins containing a Bcl-2 homology domain 2 (BH2). The encoded protein is an anti-apoptotic factor that acts as an inhibitor of caspases 3 and 7 in the cytoplasm. In the nucleus, it binds to the p53 tumor suppressor protein, preventing its association with target genes. Overexpression of this gene has been detected in a number of different cancers. There is a pseudogene for this gene on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":49665142,"end":49673916,"strand":1,"description":"BCL2 like 12 [Source:HGNC Symbol;Acc:HGNC:13787]"}, {"versioned_ensembl_gene_id":"ENSG00000280758.1","gene_symbol":"AL356481.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128630328,"end":128631685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108309.13","gene_symbol":"RUNDC3A","gene_name":"RUN domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16984]","synonyms":"RPIP8,RAP2IP","biotype":"protein_coding","ncbi_id":"10900","summary":null,"start":44308413,"end":44318671,"strand":1,"description":"RUN domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16984]"}, {"versioned_ensembl_gene_id":"ENSG00000119333.11","gene_symbol":"WDR34","gene_name":"WD repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:28296]","synonyms":"MGC20486,FAP133,DIC5,bA216B9.3","biotype":"protein_coding","ncbi_id":"89891","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Defects in this gene are a cause of short-rib thoracic dysplasia 11 with or without polydactyly. [provided by RefSeq, Mar 2014]","start":128633661,"end":128656787,"strand":-1,"description":"WD repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:28296]"}, {"versioned_ensembl_gene_id":"ENSG00000254462.1","gene_symbol":"TMX2-CTNND1","gene_name":"TMX2-CTNND1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528016","summary":"This locus represents naturally occurring read-through transcription between the neighboring TMX2 (thioredoxin-related transmembrane protein 2) and CTNND1 (catenin, cadherin-associated protein, delta 1) genes on chromosome 11. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":57712605,"end":57791586,"strand":1,"description":"TMX2-CTNND1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41992]"}, {"versioned_ensembl_gene_id":"ENSG00000216906.2","gene_symbol":"AL355312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149904243,"end":149906418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239317.1","gene_symbol":"AC091959.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146138771,"end":146139008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126773.12","gene_symbol":"PCNX4","gene_name":"pecanex homolog 4 [Source:HGNC Symbol;Acc:HGNC:20349]","synonyms":"PCNXL4,C14orf135","biotype":"protein_coding","ncbi_id":"64430","summary":null,"start":60091911,"end":60169133,"strand":1,"description":"pecanex homolog 4 [Source:HGNC Symbol;Acc:HGNC:20349]"}, {"versioned_ensembl_gene_id":"ENSG00000224907.1","gene_symbol":"RPL21P91","gene_name":"ribosomal protein L21 pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:36450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271424","summary":null,"start":109807651,"end":109808129,"strand":1,"description":"ribosomal protein L21 pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:36450]"}, {"versioned_ensembl_gene_id":"ENSG00000185813.10","gene_symbol":"PCYT2","gene_name":"phosphate cytidylyltransferase 2, ethanolamine [Source:HGNC Symbol;Acc:HGNC:8756]","synonyms":"ET","biotype":"protein_coding","ncbi_id":"5833","summary":"This gene encodes an enzyme that catalyzes the formation of CDP-ethanolamine from CTP and phosphoethanolamine in the Kennedy pathway of phospholipid synthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":81900965,"end":81911464,"strand":-1,"description":"phosphate cytidylyltransferase 2, ethanolamine [Source:HGNC Symbol;Acc:HGNC:8756]"}, {"versioned_ensembl_gene_id":"ENSG00000249149.2","gene_symbol":"AC099522.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":73382384,"end":73410509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157637.12","gene_symbol":"SLC38A10","gene_name":"solute carrier family 38 member 10 [Source:HGNC Symbol;Acc:HGNC:28237]","synonyms":"PP1744,MGC15523","biotype":"protein_coding","ncbi_id":"124565","summary":null,"start":81245000,"end":81295547,"strand":-1,"description":"solute carrier family 38 member 10 [Source:HGNC Symbol;Acc:HGNC:28237]"}, {"versioned_ensembl_gene_id":"ENSG00000167302.10","gene_symbol":"TEPSIN","gene_name":"TEPSIN, adaptor related protein complex 4 accessory protein [Source:HGNC Symbol;Acc:HGNC:26458]","synonyms":"FLJ31528,ENTHD2,C17orf56","biotype":"protein_coding","ncbi_id":"146705","summary":null,"start":81228277,"end":81239091,"strand":-1,"description":"TEPSIN, adaptor related protein complex 4 accessory protein [Source:HGNC Symbol;Acc:HGNC:26458]"}, {"versioned_ensembl_gene_id":"ENSG00000251599.1","gene_symbol":"AC116345.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73132008,"end":73150592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270236.1","gene_symbol":"AL162730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69107926,"end":69108217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141577.13","gene_symbol":"CEP131","gene_name":"centrosomal protein 131 [Source:HGNC Symbol;Acc:HGNC:29511]","synonyms":"KIAA1118,AZI1,AZ1","biotype":"protein_coding","ncbi_id":"22994","summary":null,"start":81189593,"end":81222999,"strand":-1,"description":"centrosomal protein 131 [Source:HGNC Symbol;Acc:HGNC:29511]"}, {"versioned_ensembl_gene_id":"ENSG00000176681.14","gene_symbol":"LRRC37A","gene_name":"leucine rich repeat containing 37A [Source:HGNC Symbol;Acc:HGNC:29069]","synonyms":"KIAA0563,KIAA0563","biotype":"protein_coding","ncbi_id":"9884","summary":null,"start":46292733,"end":46337794,"strand":1,"description":"leucine rich repeat containing 37A [Source:HGNC Symbol;Acc:HGNC:29069]"}, {"versioned_ensembl_gene_id":"ENSG00000113073.14","gene_symbol":"SLC4A9","gene_name":"solute carrier family 4 member 9 [Source:HGNC Symbol;Acc:HGNC:11035]","synonyms":"AE4","biotype":"protein_coding","ncbi_id":"83697","summary":"The protein encoded by this gene is a membrane protein involved in anion exchange. Expression of this gene is mostly limited to the kidney. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":140360202,"end":140375143,"strand":1,"description":"solute carrier family 4 member 9 [Source:HGNC Symbol;Acc:HGNC:11035]"}, {"versioned_ensembl_gene_id":"ENSG00000236504.2","gene_symbol":"AC087499.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20647287,"end":20681799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235785.1","gene_symbol":"AL109767.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99262948,"end":99264735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262539.1","gene_symbol":"AC005829.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46259551,"end":46260606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261575.2","gene_symbol":"AC005829.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46267037,"end":46268694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125319.14","gene_symbol":"C17orf53","gene_name":"chromosome 17 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:28460]","synonyms":"MGC3130","biotype":"protein_coding","ncbi_id":"78995","summary":null,"start":44141906,"end":44162476,"strand":1,"description":"chromosome 17 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:28460]"}, {"versioned_ensembl_gene_id":"ENSG00000198393.7","gene_symbol":"ZNF26","gene_name":"zinc finger protein 26 [Source:HGNC Symbol;Acc:HGNC:13053]","synonyms":"KOX20,FLJ20755","biotype":"protein_coding","ncbi_id":"7574","summary":null,"start":132986365,"end":133032952,"strand":1,"description":"zinc finger protein 26 [Source:HGNC Symbol;Acc:HGNC:13053]"}, {"versioned_ensembl_gene_id":"ENSG00000236714.1","gene_symbol":"LINC01844","gene_name":"long intergenic non-protein coding RNA 1844 [Source:HGNC Symbol;Acc:HGNC:52660]","synonyms":"LOC101926975","biotype":"lincRNA","ncbi_id":"101926975","summary":null,"start":142745600,"end":142760998,"strand":1,"description":"long intergenic non-protein coding RNA 1844 [Source:HGNC Symbol;Acc:HGNC:52660]"}, {"versioned_ensembl_gene_id":"ENSG00000261757.1","gene_symbol":"AC005592.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142703782,"end":142705421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259775.1","gene_symbol":"AL138976.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103331674,"end":103332367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257900.2","gene_symbol":"AL162632.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45377268,"end":45389286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258608.1","gene_symbol":"DNAJC19P9","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:45072]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644589","summary":null,"start":45290036,"end":45290386,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:45072]"}, {"versioned_ensembl_gene_id":"ENSG00000263278.2","gene_symbol":"AC233701.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79598032,"end":79603921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146005.3","gene_symbol":"PSD2","gene_name":"pleckstrin and Sec7 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19092]","synonyms":"EFA6C,DKFZp761B0514","biotype":"protein_coding","ncbi_id":"84249","summary":null,"start":139795821,"end":139844466,"strand":1,"description":"pleckstrin and Sec7 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19092]"}, {"versioned_ensembl_gene_id":"ENSG00000148082.9","gene_symbol":"SHC3","gene_name":"SHC adaptor protein 3 [Source:HGNC Symbol;Acc:HGNC:18181]","synonyms":"SHCC,NSHC,N-Shc","biotype":"protein_coding","ncbi_id":"53358","summary":null,"start":89005771,"end":89178767,"strand":-1,"description":"SHC adaptor protein 3 [Source:HGNC Symbol;Acc:HGNC:18181]"}, {"versioned_ensembl_gene_id":"ENSG00000249131.1","gene_symbol":"PSD2-AS1","gene_name":"PSD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52765]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929696","summary":null,"start":139741349,"end":139746223,"strand":-1,"description":"PSD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52765]"}, {"versioned_ensembl_gene_id":"ENSG00000248729.1","gene_symbol":"MTCO1P30","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52095]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075170","summary":null,"start":5395378,"end":5395957,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52095]"}, {"versioned_ensembl_gene_id":"ENSG00000228658.1","gene_symbol":"AL772202.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88971638,"end":88976298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197617.7","gene_symbol":"VN1R5","gene_name":"vomeronasal 1 receptor 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19870]","synonyms":"V1RL5","biotype":"polymorphic_pseudogene","ncbi_id":"317705","summary":null,"start":247255972,"end":247257210,"strand":1,"description":"vomeronasal 1 receptor 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19870]"}, {"versioned_ensembl_gene_id":"ENSG00000150782.11","gene_symbol":"IL18","gene_name":"interleukin 18 [Source:HGNC Symbol;Acc:HGNC:5986]","synonyms":"IL1F4,IL-1g,IL-18,IGIF","biotype":"protein_coding","ncbi_id":"3606","summary":"The protein encoded by this gene is a proinflammatory cytokine of the IL-1 family that is constitutively found as a precursor within the cytoplasm of a variety of cells including macrophages and keratinocytes. The inactive IL-18 precursor is processed to its active form by caspase-1, and is capable of stimulating interferon gamma production, and of regulating both T helper (Th) 1 and Th2 responses. This cytokine has been implicated in the injury of different organs, and in potentially fatal conditions characterized by a cytokine storm. In humans, IL-18 gene is located on chromosome 11. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2020]","start":112143251,"end":112164117,"strand":-1,"description":"interleukin 18 [Source:HGNC Symbol;Acc:HGNC:5986]"}, {"versioned_ensembl_gene_id":"ENSG00000143033.17","gene_symbol":"MTF2","gene_name":"metal response element binding transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:29535]","synonyms":"TDRD19A,PCL2,M96","biotype":"protein_coding","ncbi_id":"22823","summary":null,"start":93079235,"end":93139081,"strand":1,"description":"metal response element binding transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:29535]"}, {"versioned_ensembl_gene_id":"ENSG00000279339.1","gene_symbol":"AC100788.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78897264,"end":78900152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129197.14","gene_symbol":"RPAIN","gene_name":"RPA interacting protein [Source:HGNC Symbol;Acc:HGNC:28641]","synonyms":"RIP,MGC4189,hRIP","biotype":"protein_coding","ncbi_id":"84268","summary":null,"start":5419641,"end":5432876,"strand":1,"description":"RPA interacting protein [Source:HGNC Symbol;Acc:HGNC:28641]"}, {"versioned_ensembl_gene_id":"ENSG00000263220.1","gene_symbol":"AC015727.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5364315,"end":5371626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198752.10","gene_symbol":"CDC42BPB","gene_name":"CDC42 binding protein kinase beta [Source:HGNC Symbol;Acc:HGNC:1738]","synonyms":"MRCKB,KIAA1124","biotype":"protein_coding","ncbi_id":"9578","summary":"This gene encodes a member of the serine/threonine protein kinase family. The encoded protein contains a Cdc42/Rac-binding p21 binding domain resembling that of PAK kinase. The kinase domain of this protein is most closely related to that of myotonic dystrophy kinase-related ROK. Studies of the similar gene in rat suggested that this kinase may act as a downstream effector of Cdc42 in cytoskeletal reorganization. [provided by RefSeq, Jul 2008]","start":102932379,"end":103057462,"strand":-1,"description":"CDC42 binding protein kinase beta [Source:HGNC Symbol;Acc:HGNC:1738]"}, {"versioned_ensembl_gene_id":"ENSG00000150776.17","gene_symbol":"C11orf57","gene_name":"chromosome 11 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:25569]","synonyms":"FLJ10726","biotype":"protein_coding","ncbi_id":"55216","summary":null,"start":112074086,"end":112085150,"strand":1,"description":"chromosome 11 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:25569]"}, {"versioned_ensembl_gene_id":"ENSG00000230911.1","gene_symbol":"AP000907.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112029858,"end":112030367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242595.1","gene_symbol":"RPL26P26","gene_name":"ribosomal protein L26 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:35693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270967","summary":null,"start":58113189,"end":58113622,"strand":-1,"description":"ribosomal protein L26 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:35693]"}, {"versioned_ensembl_gene_id":"ENSG00000227438.1","gene_symbol":"AP001471.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46093264,"end":46097530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274297.1","gene_symbol":"AC009269.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70758269,"end":70758856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140471.16","gene_symbol":"LINS1","gene_name":"lines homolog 1 [Source:HGNC Symbol;Acc:HGNC:30922]","synonyms":"WINS1,LINS","biotype":"protein_coding","ncbi_id":"55180","summary":"The Drosophila segment polarity gene lin encodes a protein, lines, which plays important roles in development of the epidermis and hindgut. This gene encodes a protein containing a lines-like domain. This gene is located on chromosome 15 and clustered with the gene encoding ankyrin repeat and SOCS box-containing protein 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2017]","start":100559369,"end":100603230,"strand":-1,"description":"lines homolog 1 [Source:HGNC Symbol;Acc:HGNC:30922]"}, {"versioned_ensembl_gene_id":"ENSG00000029725.16","gene_symbol":"RABEP1","gene_name":"rabaptin, RAB GTPase binding effector protein 1 [Source:HGNC Symbol;Acc:HGNC:17677]","synonyms":"RABPT5,rabaptin-5,RAB5EP,neurocrescin","biotype":"protein_coding","ncbi_id":"9135","summary":null,"start":5282265,"end":5385812,"strand":1,"description":"rabaptin, RAB GTPase binding effector protein 1 [Source:HGNC Symbol;Acc:HGNC:17677]"}, {"versioned_ensembl_gene_id":"ENSG00000259540.1","gene_symbol":"AC027020.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100558677,"end":100559798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253886.1","gene_symbol":"AC026688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154493576,"end":154494743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113196.2","gene_symbol":"HAND1","gene_name":"heart and neural crest derivatives expressed 1 [Source:HGNC Symbol;Acc:HGNC:4807]","synonyms":"Thing1,Hxt,eHand,bHLHa27","biotype":"protein_coding","ncbi_id":"9421","summary":"The protein encoded by this gene belongs to the basic helix-loop-helix family of transcription factors. This gene product is one of two closely related family members, the HAND proteins, which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle and aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, it has been suggested that this transcription factor may be required for early trophoblast differentiation. [provided by RefSeq, Jul 2008]","start":154474972,"end":154478264,"strand":-1,"description":"heart and neural crest derivatives expressed 1 [Source:HGNC Symbol;Acc:HGNC:4807]"}, {"versioned_ensembl_gene_id":"ENSG00000279913.1","gene_symbol":"AP001962.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":99844138,"end":99844696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055483.19","gene_symbol":"USP36","gene_name":"ubiquitin specific peptidase 36 [Source:HGNC Symbol;Acc:HGNC:20062]","synonyms":"KIAA1453,FLJ12851","biotype":"protein_coding","ncbi_id":"57602","summary":"This gene encodes a member of the peptidase C19 or ubiquitin-specific protease family of cysteine proteases. Members of this family remove ubiquitin molecules from polyubiquitinated proteins. The encoded protein may deubiquitinate and stabilize the transcription factor c-Myc, also known as MYC, an important oncoprotein known to be upregulated in most human cancers. The encoded protease may also regulate the activation of autophagy. This gene exhibits elevated expression in some breast and lung cancers. [provided by RefSeq, Mar 2016]","start":78787381,"end":78841441,"strand":-1,"description":"ubiquitin specific peptidase 36 [Source:HGNC Symbol;Acc:HGNC:20062]"}, {"versioned_ensembl_gene_id":"ENSG00000100784.10","gene_symbol":"RPS6KA5","gene_name":"ribosomal protein S6 kinase A5 [Source:HGNC Symbol;Acc:HGNC:10434]","synonyms":"RLPK,MSK1","biotype":"protein_coding","ncbi_id":"9252","summary":null,"start":90847862,"end":91060636,"strand":-1,"description":"ribosomal protein S6 kinase A5 [Source:HGNC Symbol;Acc:HGNC:10434]"}, {"versioned_ensembl_gene_id":"ENSG00000266963.1","gene_symbol":"AC005625.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38361795,"end":38362484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081791.8","gene_symbol":"KIAA0141","gene_name":"KIAA0141 [Source:HGNC Symbol;Acc:HGNC:28969]","synonyms":"DELE","biotype":"protein_coding","ncbi_id":"9812","summary":null,"start":141923808,"end":141942047,"strand":1,"description":"KIAA0141 [Source:HGNC Symbol;Acc:HGNC:28969]"}, {"versioned_ensembl_gene_id":"ENSG00000130560.8","gene_symbol":"UBAC1","gene_name":"UBA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30221]","synonyms":"UBADC1,KPC2,GBDR1","biotype":"protein_coding","ncbi_id":"10422","summary":null,"start":135932969,"end":135961380,"strand":-1,"description":"UBA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30221]"}, {"versioned_ensembl_gene_id":"ENSG00000236703.1","gene_symbol":"MYB-AS1","gene_name":"MYB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37457]","synonyms":"NCRNA00209,MYBAS,MYB-AS,RP1-32B1.3","biotype":"antisense_RNA","ncbi_id":"100873904","summary":null,"start":135195083,"end":135195995,"strand":-1,"description":"MYB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37457]"}, {"versioned_ensembl_gene_id":"ENSG00000238058.1","gene_symbol":"AL355574.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135907812,"end":135913513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179058.6","gene_symbol":"C9orf50","gene_name":"chromosome 9 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:23677]","synonyms":"FLJ35803","biotype":"protein_coding","ncbi_id":"375759","summary":null,"start":129612225,"end":129620776,"strand":-1,"description":"chromosome 9 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:23677]"}, {"versioned_ensembl_gene_id":"ENSG00000254590.1","gene_symbol":"AP003396.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119402792,"end":119404088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267463.1","gene_symbol":"UBE2V2P2","gene_name":"ubiquitin conjugating enzyme E2 V2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44887]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"104548970","summary":null,"start":78066258,"end":78066761,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44887]"}, {"versioned_ensembl_gene_id":"ENSG00000279600.1","gene_symbol":"AC015804.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78008421,"end":78008855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258884.1","gene_symbol":"LINC02321","gene_name":"long intergenic non-protein coding RNA 2321 [Source:HGNC Symbol;Acc:HGNC:53240]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370623","summary":null,"start":90822365,"end":90828128,"strand":-1,"description":"long intergenic non-protein coding RNA 2321 [Source:HGNC Symbol;Acc:HGNC:53240]"}, {"versioned_ensembl_gene_id":"ENSG00000255415.1","gene_symbol":"AP000867.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71629045,"end":71629421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226164.2","gene_symbol":"FGFR3P6","gene_name":"fibroblast growth factor receptor 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420881","summary":null,"start":247119669,"end":247120278,"strand":1,"description":"fibroblast growth factor receptor 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37951]"}, {"versioned_ensembl_gene_id":"ENSG00000250602.5","gene_symbol":"AC093535.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126433505,"end":126490371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037749.11","gene_symbol":"MFAP3","gene_name":"microfibril associated protein 3 [Source:HGNC Symbol;Acc:HGNC:7034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4238","summary":null,"start":154038906,"end":154220478,"strand":1,"description":"microfibril associated protein 3 [Source:HGNC Symbol;Acc:HGNC:7034]"}, {"versioned_ensembl_gene_id":"ENSG00000134480.13","gene_symbol":"CCNH","gene_name":"cyclin H [Source:HGNC Symbol;Acc:HGNC:1594]","synonyms":"p37,p34,CycH","biotype":"protein_coding","ncbi_id":"902","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with CDK7 kinase and ring finger protein MAT1. The kinase complex is able to phosphorylate CDK2 and CDC2 kinases, thus functions as a CDK-activating kinase (CAK). This cyclin and its kinase partner are components of TFIIH, as well as RNA polymerase II protein complexes. They participate in two different transcriptional regulation processes, suggesting an important link between basal transcription control and the cell cycle machinery. A pseudogene of this gene is found on chromosome 4. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Nov 2010]","start":87391494,"end":87413019,"strand":-1,"description":"cyclin H [Source:HGNC Symbol;Acc:HGNC:1594]"}, {"versioned_ensembl_gene_id":"ENSG00000110274.15","gene_symbol":"CEP164","gene_name":"centrosomal protein 164 [Source:HGNC Symbol;Acc:HGNC:29182]","synonyms":"NPHP15,KIAA1052","biotype":"protein_coding","ncbi_id":"22897","summary":"This gene encodes a centrosomal protein involved in microtubule organization, DNA damage response, and chromosome segregation. The encoded protein is required for assembly of primary cilia and localizes to mature centrioles. Defects in this gene are a cause of nephronophthisis-related ciliopathies. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":117314557,"end":117413268,"strand":1,"description":"centrosomal protein 164 [Source:HGNC Symbol;Acc:HGNC:29182]"}, {"versioned_ensembl_gene_id":"ENSG00000255301.1","gene_symbol":"AP002893.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57476493,"end":57477534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186907.7","gene_symbol":"RTN4RL2","gene_name":"reticulon 4 receptor like 2 [Source:HGNC Symbol;Acc:HGNC:23053]","synonyms":"NGRH1,NgR2","biotype":"protein_coding","ncbi_id":"349667","summary":null,"start":57460549,"end":57477534,"strand":1,"description":"reticulon 4 receptor like 2 [Source:HGNC Symbol;Acc:HGNC:23053]"}, {"versioned_ensembl_gene_id":"ENSG00000189068.9","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040825,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000142408.4","gene_symbol":"CACNG8","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:13628]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59283","summary":"The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type II TARP and a calcium channel gamma subunit. The mRNA for this gene is believed to initiate translation from a non-AUG (CUG) start codon. [provided by RefSeq, Dec 2010]","start":53963040,"end":53990215,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:13628]"}, {"versioned_ensembl_gene_id":"ENSG00000245385.2","gene_symbol":"AP003396.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119336249,"end":119337309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231759.7","gene_symbol":"CYP21A1P","gene_name":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]","synonyms":"CYP21P,CYP21A,P450c21A","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1590","summary":null,"start":31987818,"end":31990633,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]"}, {"versioned_ensembl_gene_id":"ENSG00000198648.10","gene_symbol":"STK39","gene_name":"serine/threonine kinase 39 [Source:HGNC Symbol;Acc:HGNC:17717]","synonyms":"DCHT,SPAK","biotype":"protein_coding","ncbi_id":"27347","summary":"This gene encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The catalytically active kinase specifically activates the p38 MAP kinase pathway, and its interaction with p38 decreases upon cellular stress, suggesting that this kinase may serve as an intermediate in the response to cellular stress. [provided by RefSeq, Jul 2008]","start":167954020,"end":168248141,"strand":-1,"description":"serine/threonine kinase 39 [Source:HGNC Symbol;Acc:HGNC:17717]"}, {"versioned_ensembl_gene_id":"ENSG00000228095.3","gene_symbol":"AL354692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84604111,"end":84604425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248352.1","gene_symbol":"TNXA","gene_name":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]","synonyms":"XA,TNX,HXBL,D6S103E","biotype":"unprocessed_pseudogene","ncbi_id":"7146","summary":null,"start":31990796,"end":31994654,"strand":-1,"description":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]"}, {"versioned_ensembl_gene_id":"ENSG00000173456.4","gene_symbol":"RNF26","gene_name":"ring finger protein 26 [Source:HGNC Symbol;Acc:HGNC:14646]","synonyms":"MGC2642","biotype":"protein_coding","ncbi_id":"79102","summary":"The protein encoded by this intronless gene contains a C3HC5 type of RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. The expression of this gene was found to be upregulated in cancer cell lines derived from different types of cancer. [provided by RefSeq, Jul 2008]","start":119334527,"end":119337313,"strand":1,"description":"ring finger protein 26 [Source:HGNC Symbol;Acc:HGNC:14646]"}, {"versioned_ensembl_gene_id":"ENSG00000149212.11","gene_symbol":"SESN3","gene_name":"sestrin 3 [Source:HGNC Symbol;Acc:HGNC:23060]","synonyms":"SEST3,MGC29667","biotype":"protein_coding","ncbi_id":"143686","summary":"This gene encodes a member of the sestrin family of stress-induced proteins. The encoded protein reduces the levels of intracellular reactive oxygen species induced by activated Ras downstream of RAC-alpha serine/threonine-protein kinase (Akt) and FoxO transcription factor. The protein is required for normal regulation of blood glucose, insulin resistance and plays a role in lipid storage in obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":95165513,"end":95232541,"strand":-1,"description":"sestrin 3 [Source:HGNC Symbol;Acc:HGNC:23060]"}, {"versioned_ensembl_gene_id":"ENSG00000251183.1","gene_symbol":"LINC01861","gene_name":"long intergenic non-protein coding RNA 1861 [Source:HGNC Symbol;Acc:HGNC:52680]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378238","summary":null,"start":153887428,"end":153898987,"strand":-1,"description":"long intergenic non-protein coding RNA 1861 [Source:HGNC Symbol;Acc:HGNC:52680]"}, {"versioned_ensembl_gene_id":"ENSG00000240198.5","gene_symbol":"ARHGEF3-AS1","gene_name":"ARHGEF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40083]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874200","summary":null,"start":56940040,"end":56960854,"strand":1,"description":"ARHGEF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40083]"}, {"versioned_ensembl_gene_id":"ENSG00000110665.11","gene_symbol":"C11orf21","gene_name":"chromosome 11 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:13231]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29125","summary":null,"start":2295645,"end":2303049,"strand":-1,"description":"chromosome 11 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:13231]"}, {"versioned_ensembl_gene_id":"ENSG00000223649.1","gene_symbol":"AC105275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":211492255,"end":211492917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112531.16","gene_symbol":"QKI","gene_name":"QKI, KH domain containing RNA binding [Source:HGNC Symbol;Acc:HGNC:21100]","synonyms":"QK3","biotype":"protein_coding","ncbi_id":"9444","summary":"The protein encoded by this gene is an RNA-binding protein that regulates pre-mRNA splicing, export of mRNAs from the nucleus, protein translation, and mRNA stability. The encoded protein is involved in myelinization and oligodendrocyte differentiation and may play a role in schizophrenia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":163414000,"end":163578596,"strand":1,"description":"QKI, KH domain containing RNA binding [Source:HGNC Symbol;Acc:HGNC:21100]"}, {"versioned_ensembl_gene_id":"ENSG00000244411.3","gene_symbol":"KRTAP5-7","gene_name":"keratin associated protein 5-7 [Source:HGNC Symbol;Acc:HGNC:23602]","synonyms":"KRTAP5.7,KRTAP5-3","biotype":"protein_coding","ncbi_id":"440050","summary":null,"start":71527267,"end":71528674,"strand":1,"description":"keratin associated protein 5-7 [Source:HGNC Symbol;Acc:HGNC:23602]"}, {"versioned_ensembl_gene_id":"ENSG00000135723.13","gene_symbol":"FHOD1","gene_name":"formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17905]","synonyms":"FHOS","biotype":"protein_coding","ncbi_id":"29109","summary":"This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":67229387,"end":67247658,"strand":-1,"description":"formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17905]"}, {"versioned_ensembl_gene_id":"ENSG00000253203.6","gene_symbol":"GUSBP3","gene_name":"glucuronidase, beta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37301]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653188","summary":null,"start":69639459,"end":69679259,"strand":-1,"description":"glucuronidase, beta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37301]"}, {"versioned_ensembl_gene_id":"ENSG00000236591.1","gene_symbol":"AL357992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149027700,"end":149032573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229311.1","gene_symbol":"BX088651.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42579414,"end":42586534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250716.1","gene_symbol":"LINC01017","gene_name":"long intergenic non-protein coding RNA 1017 [Source:HGNC Symbol;Acc:HGNC:50641]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467075","summary":null,"start":3496229,"end":3504004,"strand":-1,"description":"long intergenic non-protein coding RNA 1017 [Source:HGNC Symbol;Acc:HGNC:50641]"}, {"versioned_ensembl_gene_id":"ENSG00000258776.1","gene_symbol":"AL161757.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56817570,"end":56893710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236809.2","gene_symbol":"SNX25P1","gene_name":"sorting nexin 25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41509]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419028","summary":null,"start":211417025,"end":211417934,"strand":1,"description":"sorting nexin 25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41509]"}, {"versioned_ensembl_gene_id":"ENSG00000226864.2","gene_symbol":"ATE1-AS1","gene_name":"ATE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49496]","synonyms":"ENST00000437593","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100130887","summary":null,"start":121928312,"end":121951965,"strand":1,"description":"ATE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49496]"}, {"versioned_ensembl_gene_id":"ENSG00000248648.1","gene_symbol":"AC113410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133003119,"end":133003365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119899.12","gene_symbol":"SLC17A5","gene_name":"solute carrier family 17 member 5 [Source:HGNC Symbol;Acc:HGNC:10933]","synonyms":"SLD,SIASD,SIALIN,SD,NSD,ISSD,AST","biotype":"protein_coding","ncbi_id":"26503","summary":"This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]","start":73593379,"end":73654155,"strand":-1,"description":"solute carrier family 17 member 5 [Source:HGNC Symbol;Acc:HGNC:10933]"}, {"versioned_ensembl_gene_id":"ENSG00000149485.18","gene_symbol":"FADS1","gene_name":"fatty acid desaturase 1 [Source:HGNC Symbol;Acc:HGNC:3574]","synonyms":"D5D,TU12,LLCDL1,FADSD5,FADS6","biotype":"protein_coding","ncbi_id":"3992","summary":"The protein encoded by this gene is a member of the fatty acid desaturase (FADS) gene family. Desaturase enzymes regulate unsaturation of fatty acids through the introduction of double bonds between defined carbons of the fatty acyl chain. FADS family members are considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal multiple membrane-spanning desaturase portion, both of which are characterized by conserved histidine motifs. This gene is clustered with family members FADS1 and FADS2 at 11q12-q13.1; this cluster is thought to have arisen evolutionarily from gene duplication based on its similar exon/intron organization. [provided by RefSeq, Jul 2008]","start":61799625,"end":61829318,"strand":-1,"description":"fatty acid desaturase 1 [Source:HGNC Symbol;Acc:HGNC:3574]"}, {"versioned_ensembl_gene_id":"ENSG00000228323.2","gene_symbol":"AC008440.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53854581,"end":53869107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230205.1","gene_symbol":"AL359382.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148133809,"end":148137404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248994.1","gene_symbol":"AC126768.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1933863,"end":1959176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132704.15","gene_symbol":"FCRL2","gene_name":"Fc receptor like 2 [Source:HGNC Symbol;Acc:HGNC:14875]","synonyms":"SPAP1,IRTA4,FCRH2,CD307b","biotype":"protein_coding","ncbi_id":"79368","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein has four extracellular C2-type immunoglobulin domains, a transmembrane domain and a cytoplasmic domain that contains one immunoreceptor-tyrosine activation motif and two immunoreceptor-tyrosine inhibitory motifs. This protein may be a prognostic marker for chronic lymphocytic leukemia. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Apr 2009]","start":157745733,"end":157777132,"strand":-1,"description":"Fc receptor like 2 [Source:HGNC Symbol;Acc:HGNC:14875]"}, {"versioned_ensembl_gene_id":"ENSG00000258803.1","gene_symbol":"AL355103.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56514331,"end":56551309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119715.14","gene_symbol":"ESRRB","gene_name":"estrogen related receptor beta [Source:HGNC Symbol;Acc:HGNC:3473]","synonyms":"NR3B2,ESRL2,ERRbeta,ERRb,ERR2,DFNB35","biotype":"protein_coding","ncbi_id":"2103","summary":"This gene encodes a protein with similarity to the estrogen receptor. Its function is unknown; however, a similar protein in mouse plays an essential role in placental development. [provided by RefSeq, Jul 2008]","start":76310614,"end":76501841,"strand":1,"description":"estrogen related receptor beta [Source:HGNC Symbol;Acc:HGNC:3473]"}, {"versioned_ensembl_gene_id":"ENSG00000259124.1","gene_symbol":"AC008050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76495363,"end":76726712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275734.1","gene_symbol":"AC010538.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89684642,"end":89685304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074855.10","gene_symbol":"ANO8","gene_name":"anoctamin 8 [Source:HGNC Symbol;Acc:HGNC:29329]","synonyms":"TMEM16H,KIAA1623","biotype":"protein_coding","ncbi_id":"57719","summary":null,"start":17323223,"end":17334829,"strand":-1,"description":"anoctamin 8 [Source:HGNC Symbol;Acc:HGNC:29329]"}, {"versioned_ensembl_gene_id":"ENSG00000254171.1","gene_symbol":"AC114321.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166128498,"end":166155439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264388.1","gene_symbol":"AC090312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71588537,"end":71588884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220494.4","gene_symbol":"YAP1P1","gene_name":"Yes associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442266","summary":null,"start":147406889,"end":147408281,"strand":1,"description":"Yes associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38016]"}, {"versioned_ensembl_gene_id":"ENSG00000248195.1","gene_symbol":"AC016550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86335024,"end":86335808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090971.4","gene_symbol":"NAT14","gene_name":"N-acetyltransferase 14 (putative) [Source:HGNC Symbol;Acc:HGNC:28918]","synonyms":"KLP1","biotype":"protein_coding","ncbi_id":"57106","summary":null,"start":55485004,"end":55487568,"strand":1,"description":"N-acetyltransferase 14 (putative) [Source:HGNC Symbol;Acc:HGNC:28918]"}, {"versioned_ensembl_gene_id":"ENSG00000109118.13","gene_symbol":"PHF12","gene_name":"PHD finger protein 12 [Source:HGNC Symbol;Acc:HGNC:20816]","synonyms":"PF1,KIAA1523","biotype":"protein_coding","ncbi_id":"57649","summary":null,"start":28905250,"end":28951771,"strand":-1,"description":"PHD finger protein 12 [Source:HGNC Symbol;Acc:HGNC:20816]"}, {"versioned_ensembl_gene_id":"ENSG00000258516.1","gene_symbol":"AL133167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95855548,"end":95866464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153820.12","gene_symbol":"SPHKAP","gene_name":"SPHK1 interactor, AKAP domain containing [Source:HGNC Symbol;Acc:HGNC:30619]","synonyms":"SKIP","biotype":"protein_coding","ncbi_id":"80309","summary":null,"start":227979950,"end":228181645,"strand":-1,"description":"SPHK1 interactor, AKAP domain containing [Source:HGNC Symbol;Acc:HGNC:30619]"}, {"versioned_ensembl_gene_id":"ENSG00000241888.2","gene_symbol":"RPSAP37","gene_name":"ribosomal protein SA pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35844]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270915","summary":null,"start":125966777,"end":125968085,"strand":-1,"description":"ribosomal protein SA pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35844]"}, {"versioned_ensembl_gene_id":"ENSG00000248752.1","gene_symbol":"AC010235.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126076800,"end":126279801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176761.7","gene_symbol":"ZNF285B","gene_name":"zinc finger protein 285B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33262]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"147711","summary":null,"start":44467641,"end":44473227,"strand":1,"description":"zinc finger protein 285B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33262]"}, {"versioned_ensembl_gene_id":"ENSG00000183474.15","gene_symbol":"GTF2H2C","gene_name":"GTF2H2 family member C [Source:HGNC Symbol;Acc:HGNC:31394]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728340","summary":null,"start":69560208,"end":69594723,"strand":1,"description":"GTF2H2 family member C [Source:HGNC Symbol;Acc:HGNC:31394]"}, {"versioned_ensembl_gene_id":"ENSG00000173660.11","gene_symbol":"UQCRH","gene_name":"ubiquinol-cytochrome c reductase hinge protein [Source:HGNC Symbol;Acc:HGNC:12590]","synonyms":"UQCR8,QCR6","biotype":"protein_coding","ncbi_id":"7388","summary":null,"start":46303631,"end":46316776,"strand":1,"description":"ubiquinol-cytochrome c reductase hinge protein [Source:HGNC Symbol;Acc:HGNC:12590]"}, {"versioned_ensembl_gene_id":"ENSG00000167113.10","gene_symbol":"COQ4","gene_name":"coenzyme Q4 [Source:HGNC Symbol;Acc:HGNC:19693]","synonyms":"CGI-92","biotype":"protein_coding","ncbi_id":"51117","summary":"This gene encodes a component of the coenzyme Q biosynthesis pathway. Coenzyme Q, an essential component of the electron transport chain, shuttles electrons between complexes I or II to complex III of the mitochondrial transport chain. This protein appears to play a structural role in stabilizing a complex that contains most of the coenzyme Q biosynthesis enzymes. Mutations in this gene are associated with mitochondrial disorders linked to coenzyme Q deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":128322536,"end":128334072,"strand":1,"description":"coenzyme Q4 [Source:HGNC Symbol;Acc:HGNC:19693]"}, {"versioned_ensembl_gene_id":"ENSG00000162039.14","gene_symbol":"MEIOB","gene_name":"meiosis specific with OB domains [Source:HGNC Symbol;Acc:HGNC:28569]","synonyms":"MGC35212,C16orf73","biotype":"protein_coding","ncbi_id":"254528","summary":null,"start":1833983,"end":1884294,"strand":-1,"description":"meiosis specific with OB domains [Source:HGNC Symbol;Acc:HGNC:28569]"}, {"versioned_ensembl_gene_id":"ENSG00000197948.10","gene_symbol":"FCHSD1","gene_name":"FCH and double SH3 domains 1 [Source:HGNC Symbol;Acc:HGNC:25463]","synonyms":"FLJ00007","biotype":"protein_coding","ncbi_id":"89848","summary":null,"start":141639302,"end":141651419,"strand":-1,"description":"FCH and double SH3 domains 1 [Source:HGNC Symbol;Acc:HGNC:25463]"}, {"versioned_ensembl_gene_id":"ENSG00000167112.9","gene_symbol":"TRUB2","gene_name":"TruB pseudouridine synthase family member 2 [Source:HGNC Symbol;Acc:HGNC:17170]","synonyms":"CLONE24922","biotype":"protein_coding","ncbi_id":"26995","summary":"Pseudouridine is an abundant component of rRNAs and tRNAs and is enzymatically generated by isomerization of uridine by pseudouridine synthase (Zucchini et al., 2003 [PubMed 12736709]).[supplied by OMIM, Mar 2008]","start":128305161,"end":128322742,"strand":-1,"description":"TruB pseudouridine synthase family member 2 [Source:HGNC Symbol;Acc:HGNC:17170]"}, {"versioned_ensembl_gene_id":"ENSG00000270876.1","gene_symbol":"ZNF30-AS1","gene_name":"ZNF30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51179]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723513","summary":null,"start":34923299,"end":34926812,"strand":-1,"description":"ZNF30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51179]"}, {"versioned_ensembl_gene_id":"ENSG00000245680.9","gene_symbol":"ZNF585B","gene_name":"zinc finger protein 585B [Source:HGNC Symbol;Acc:HGNC:30948]","synonyms":"SZFP41,FLJ14928","biotype":"protein_coding","ncbi_id":"92285","summary":null,"start":37181579,"end":37218153,"strand":-1,"description":"zinc finger protein 585B [Source:HGNC Symbol;Acc:HGNC:30948]"}, {"versioned_ensembl_gene_id":"ENSG00000232366.1","gene_symbol":"VDAC1P9","gene_name":"voltage dependent anion channel 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37484]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391106","summary":null,"start":157724180,"end":157725020,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37484]"}, {"versioned_ensembl_gene_id":"ENSG00000280367.1","gene_symbol":"AP002364.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90223153,"end":90226538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244564.1","gene_symbol":"AC096888.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64445231,"end":64454832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168658.18","gene_symbol":"VWA3B","gene_name":"von Willebrand factor A domain containing 3B [Source:HGNC Symbol;Acc:HGNC:28385]","synonyms":"DKFZp686F2227,MGC26733","biotype":"protein_coding","ncbi_id":"200403","summary":"This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017]","start":98087116,"end":98313299,"strand":1,"description":"von Willebrand factor A domain containing 3B [Source:HGNC Symbol;Acc:HGNC:28385]"}, {"versioned_ensembl_gene_id":"ENSG00000225698.3","gene_symbol":"IGHV3-72","gene_name":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28410","summary":null,"start":106790691,"end":106791233,"strand":-1,"description":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]"}, {"versioned_ensembl_gene_id":"ENSG00000171421.12","gene_symbol":"MRPL36","gene_name":"mitochondrial ribosomal protein L36 [Source:HGNC Symbol;Acc:HGNC:14490]","synonyms":"RPMJ,PRPL36,MRP-L36,L36mt,BRIP1","biotype":"protein_coding","ncbi_id":"64979","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. A pseudogene corresponding to this gene is found on chromosome 2p. [provided by RefSeq, Jul 2008]","start":1798386,"end":1801366,"strand":-1,"description":"mitochondrial ribosomal protein L36 [Source:HGNC Symbol;Acc:HGNC:14490]"}, {"versioned_ensembl_gene_id":"ENSG00000188176.11","gene_symbol":"SMTNL2","gene_name":"smoothelin like 2 [Source:HGNC Symbol;Acc:HGNC:24764]","synonyms":"FLJ42461","biotype":"protein_coding","ncbi_id":"342527","summary":null,"start":4583999,"end":4608319,"strand":1,"description":"smoothelin like 2 [Source:HGNC Symbol;Acc:HGNC:24764]"}, {"versioned_ensembl_gene_id":"ENSG00000263733.1","gene_symbol":"AC091691.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71225704,"end":71226721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273361.1","gene_symbol":"AC021016.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":218398743,"end":218399219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105287.12","gene_symbol":"PRKD2","gene_name":"protein kinase D2 [Source:HGNC Symbol;Acc:HGNC:17293]","synonyms":"PKD2,HSPC187,DKFZP586E0820","biotype":"protein_coding","ncbi_id":"25865","summary":"The protein encoded by this gene belongs to the protein kinase D (PKD) family of serine/threonine protein kinases. This kinase can be activated by phorbol esters as well as by gastrin via the cholecystokinin B receptor (CCKBR) in gastric cancer cells. It can bind to diacylglycerol (DAG) in the trans-Golgi network (TGN) and may regulate basolateral membrane protein exit from TGN. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":46674275,"end":46717127,"strand":-1,"description":"protein kinase D2 [Source:HGNC Symbol;Acc:HGNC:17293]"}, {"versioned_ensembl_gene_id":"ENSG00000116748.21","gene_symbol":"AMPD1","gene_name":"adenosine monophosphate deaminase 1 [Source:HGNC Symbol;Acc:HGNC:468]","synonyms":"MADA,MAD","biotype":"protein_coding","ncbi_id":"270","summary":"Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]","start":114673090,"end":114695618,"strand":-1,"description":"adenosine monophosphate deaminase 1 [Source:HGNC Symbol;Acc:HGNC:468]"}, {"versioned_ensembl_gene_id":"ENSG00000163597.14","gene_symbol":"SNHG16","gene_name":"small nucleolar RNA host gene 16 [Source:HGNC Symbol;Acc:HGNC:44352]","synonyms":"ncRAN,Nbla12061,Nbla10727","biotype":"processed_transcript","ncbi_id":"100507246","summary":null,"start":76557766,"end":76565348,"strand":1,"description":"small nucleolar RNA host gene 16 [Source:HGNC Symbol;Acc:HGNC:44352]"}, {"versioned_ensembl_gene_id":"ENSG00000153896.17","gene_symbol":"ZNF599","gene_name":"zinc finger protein 599 [Source:HGNC Symbol;Acc:HGNC:26408]","synonyms":"FLJ30663","biotype":"protein_coding","ncbi_id":"148103","summary":null,"start":34758076,"end":34773229,"strand":-1,"description":"zinc finger protein 599 [Source:HGNC Symbol;Acc:HGNC:26408]"}, {"versioned_ensembl_gene_id":"ENSG00000276329.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54861173,"end":54875478,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000160613.12","gene_symbol":"PCSK7","gene_name":"proprotein convertase subtilisin/kexin type 7 [Source:HGNC Symbol;Acc:HGNC:8748]","synonyms":"PC8,PC7,LPC,SPC7","biotype":"protein_coding","ncbi_id":"9159","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. It encodes a type 1 membrane bound protease that is expressed in many tissues, including neuroendocrine, liver, gut, and brain. The encoded protein undergoes an initial autocatalytic processing event in the ER and then sorts to the trans-Golgi network through endosomes where a second autocatalytic event takes place and the catalytic activity is acquired. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It can process proalbumin and is thought to be responsible for the activation of HIV envelope glycoproteins gp160 and gp140. This gene has been implicated in the transcriptional regulation of housekeeping genes and plays a role in the regulation of iron metabolism. A t(11;14)(q23;q32) chromosome translocation associated with B-cell lymphoma occurs between this gene and its inverted counterpart. [provided by RefSeq, Feb 2014]","start":117204337,"end":117232525,"strand":-1,"description":"proprotein convertase subtilisin/kexin type 7 [Source:HGNC Symbol;Acc:HGNC:8748]"}, {"versioned_ensembl_gene_id":"ENSG00000228486.10","gene_symbol":"LINC01125","gene_name":"long intergenic non-protein coding RNA 1125 [Source:HGNC Symbol;Acc:HGNC:49272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728537","summary":null,"start":97664217,"end":97703064,"strand":1,"description":"long intergenic non-protein coding RNA 1125 [Source:HGNC Symbol;Acc:HGNC:49272]"}, {"versioned_ensembl_gene_id":"ENSG00000267142.1","gene_symbol":"AC092296.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36421536,"end":36422534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227857.2","gene_symbol":"AL358075.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46134531,"end":46139081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262303.1","gene_symbol":"AL021878.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42124281,"end":42127775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277345.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54877376,"end":54892982,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000276676.5","gene_symbol":"GU182345.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54782658,"end":54797195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240298.3","gene_symbol":"AC015820.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25588475,"end":25588795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255454.1","gene_symbol":"AC100770.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25630720,"end":25631041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196415.9","gene_symbol":"PRTN3","gene_name":"proteinase 3 [Source:HGNC Symbol;Acc:HGNC:9495]","synonyms":"PR-3,P29,MBT,C-ANCA,AGP7,ACPA","biotype":"protein_coding","ncbi_id":"5657","summary":null,"start":840960,"end":848175,"strand":1,"description":"proteinase 3 [Source:HGNC Symbol;Acc:HGNC:9495]"}, {"versioned_ensembl_gene_id":"ENSG00000197665.7","gene_symbol":"AC007952.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19155727,"end":19159111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261070.1","gene_symbol":"AP003071.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69147228,"end":69171564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259084.6","gene_symbol":"AL133467.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":95663256,"end":95692630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120029.12","gene_symbol":"C10orf76","gene_name":"chromosome 10 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:25788]","synonyms":"FLJ13114","biotype":"protein_coding","ncbi_id":"79591","summary":null,"start":101845599,"end":102056193,"strand":-1,"description":"chromosome 10 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:25788]"}, {"versioned_ensembl_gene_id":"ENSG00000144736.13","gene_symbol":"SHQ1","gene_name":"SHQ1, H/ACA ribonucleoprotein assembly factor [Source:HGNC Symbol;Acc:HGNC:25543]","synonyms":"Shq1p,FLJ10539","biotype":"protein_coding","ncbi_id":"55164","summary":"SHQ1 assists in the assembly of H/ACA-box ribonucleoproteins that function in the processing of ribosomal RNAs, modification of spliceosomal small nuclear RNAs, and stabilization of telomerase (see MIM 602322) (Grozdanov et al., 2009 [PubMed 19383767]).[supplied by OMIM, Dec 2010]","start":72749277,"end":72861914,"strand":-1,"description":"SHQ1, H/ACA ribonucleoprotein assembly factor [Source:HGNC Symbol;Acc:HGNC:25543]"}, {"versioned_ensembl_gene_id":"ENSG00000260249.2","gene_symbol":"AC007608.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50666211,"end":50671639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108106.13","gene_symbol":"UBE2S","gene_name":"ubiquitin conjugating enzyme E2 S [Source:HGNC Symbol;Acc:HGNC:17895]","synonyms":"E2-EPF","biotype":"protein_coding","ncbi_id":"27338","summary":"This gene encodes a member of the ubiquitin-conjugating enzyme family. The encoded protein is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme-dependent manner, a characteristic property of ubiquitin carrier proteins. [provided by RefSeq, Jul 2008]","start":55399745,"end":55407777,"strand":-1,"description":"ubiquitin conjugating enzyme E2 S [Source:HGNC Symbol;Acc:HGNC:17895]"}, {"versioned_ensembl_gene_id":"ENSG00000162852.13","gene_symbol":"CNST","gene_name":"consortin, connexin sorting protein [Source:HGNC Symbol;Acc:HGNC:26486]","synonyms":"PPP1R64,FLJ32001,C1orf71","biotype":"protein_coding","ncbi_id":"163882","summary":"Targeting of numerous transmembrane proteins to the cell surface is thought to depend on their recognition by cargo receptors that interact with the adaptor machinery for anterograde traffic at the distal end of the Golgi complex. Consortin (CNST) is an integral membrane protein that acts as a binding partner of connexins, the building blocks of gap junctions, and acts as a trans-Golgi network (TGN) receptor involved in connexin targeting to the plasma membrane and recycling from the cell surface (del Castillo et al., 2010 [PubMed 19864490]).[supplied by OMIM, Jun 2010]","start":246566444,"end":246668584,"strand":1,"description":"consortin, connexin sorting protein [Source:HGNC Symbol;Acc:HGNC:26486]"}, {"versioned_ensembl_gene_id":"ENSG00000170819.4","gene_symbol":"BFSP2","gene_name":"beaded filament structural protein 2 [Source:HGNC Symbol;Acc:HGNC:1041]","synonyms":"phakinin,LIFL-L,CP49,CP47","biotype":"protein_coding","ncbi_id":"8419","summary":"More than 99% of the vertebrate ocular lens is comprised of terminally differentiated lens fiber cells. Two lens-specific intermediate filament-like proteins, the protein product of this gene (phakinin), and filensin, are expressed only after fiber cell differentiation has begun. Both proteins are found in a structurally unique cytoskeletal element that is referred to as the beaded filament (BF). Mutations in this gene have been associated with juvenile-onset, progressive cataracts and Dowling-Meara epidermolysis bullosa simplex. [provided by RefSeq, Jun 2009]","start":133399995,"end":133475222,"strand":1,"description":"beaded filament structural protein 2 [Source:HGNC Symbol;Acc:HGNC:1041]"}, {"versioned_ensembl_gene_id":"ENSG00000144868.13","gene_symbol":"TMEM108","gene_name":"transmembrane protein 108 [Source:HGNC Symbol;Acc:HGNC:28451]","synonyms":"MGC3040,CT124","biotype":"protein_coding","ncbi_id":"66000","summary":null,"start":133038391,"end":133397792,"strand":1,"description":"transmembrane protein 108 [Source:HGNC Symbol;Acc:HGNC:28451]"}, {"versioned_ensembl_gene_id":"ENSG00000176438.12","gene_symbol":"SYNE3","gene_name":"spectrin repeat containing nuclear envelope family member 3 [Source:HGNC Symbol;Acc:HGNC:19861]","synonyms":"LINC00341,FLJ25605,C14orf49,C14orf139,NET53,Nesprin-3,Nesp3,NCRNA00341","biotype":"protein_coding","ncbi_id":"161176","summary":null,"start":95407266,"end":95475836,"strand":-1,"description":"spectrin repeat containing nuclear envelope family member 3 [Source:HGNC Symbol;Acc:HGNC:19861]"}, {"versioned_ensembl_gene_id":"ENSG00000276412.1","gene_symbol":"AL591926.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41651935,"end":41652172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072571.19","gene_symbol":"HMMR","gene_name":"hyaluronan mediated motility receptor [Source:HGNC Symbol;Acc:HGNC:5012]","synonyms":"RHAMM,CD168","biotype":"protein_coding","ncbi_id":"3161","summary":"The protein encoded by this gene is involved in cell motility. It is expressed in breast tissue and together with other proteins, it forms a complex with BRCA1 and BRCA2, thus is potentially associated with higher risk of breast cancer. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Dec 2008]","start":163460203,"end":163491945,"strand":1,"description":"hyaluronan mediated motility receptor [Source:HGNC Symbol;Acc:HGNC:5012]"}, {"versioned_ensembl_gene_id":"ENSG00000170788.13","gene_symbol":"DYDC1","gene_name":"DPY30 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23460]","synonyms":"DPY30D1,bA36D19.5","biotype":"protein_coding","ncbi_id":"143241","summary":"This gene encodes a member of a family of proteins that contains a DPY30 domain. The encoded protein is involved in acrosome formation during spermatid development. This gene locus overlaps with a closely related gene on the opposite strand. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":80336105,"end":80356755,"strand":-1,"description":"DPY30 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23460]"}, {"versioned_ensembl_gene_id":"ENSG00000253132.1","gene_symbol":"IGHV3-62","gene_name":"immunoglobulin heavy variable 3-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5615]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28416","summary":null,"start":106643142,"end":106643585,"strand":-1,"description":"immunoglobulin heavy variable 3-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5615]"}, {"versioned_ensembl_gene_id":"ENSG00000255903.2","gene_symbol":"RPL12P46","gene_name":"ribosomal protein L12 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:51938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075251","summary":null,"start":115578049,"end":115578243,"strand":1,"description":"ribosomal protein L12 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:51938]"}, {"versioned_ensembl_gene_id":"ENSG00000259650.1","gene_symbol":"AC068397.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73335260,"end":73342387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229334.1","gene_symbol":"AC046143.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":194632923,"end":194645401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261066.1","gene_symbol":"AC074052.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8526549,"end":8532013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206512.6","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29587374,"end":29588957,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000151332.18","gene_symbol":"MBIP","gene_name":"MAP3K12 binding inhibitory protein 1 [Source:HGNC Symbol;Acc:HGNC:20427]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51562","summary":null,"start":36298558,"end":36320676,"strand":-1,"description":"MAP3K12 binding inhibitory protein 1 [Source:HGNC Symbol;Acc:HGNC:20427]"}, {"versioned_ensembl_gene_id":"ENSG00000281692.1","gene_symbol":"PACRG-AS1","gene_name":"PACRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27772]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285796","summary":null,"start":163309985,"end":163324530,"strand":-1,"description":"PACRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27772]"}, {"versioned_ensembl_gene_id":"ENSG00000188611.14","gene_symbol":"ASAH2","gene_name":"N-acylsphingosine amidohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:18860]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56624","summary":"Ceramidases (EC 3.5.1.23), such as ASAH2, catalyze hydrolysis of the N-acyl linkage of ceramide, a second messenger in a variety of cellular events, to produce sphingosine. Sphingosine exerts both mitogenic and apoptosis-inducing activities, and its phosphorylated form functions as an intra- and intercellular second messenger (see MIM 603730) (Mitsutake et al., 2001 [PubMed 11328816]).[supplied by OMIM, Mar 2008]","start":50182778,"end":50248610,"strand":-1,"description":"N-acylsphingosine amidohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:18860]"}, {"versioned_ensembl_gene_id":"ENSG00000225683.5","gene_symbol":"PACRG-AS3","gene_name":"PACRG antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:52053]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729658","summary":null,"start":163165414,"end":163192002,"strand":-1,"description":"PACRG antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:52053]"}, {"versioned_ensembl_gene_id":"ENSG00000240974.1","gene_symbol":"RPS27AP10","gene_name":"ribosomal protein S27a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36570]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271377","summary":null,"start":141588935,"end":141589142,"strand":1,"description":"ribosomal protein S27a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36570]"}, {"versioned_ensembl_gene_id":"ENSG00000133247.13","gene_symbol":"KMT5C","gene_name":"lysine methyltransferase 5C [Source:HGNC Symbol;Acc:HGNC:28405]","synonyms":"SUV420H2,MGC2705","biotype":"protein_coding","ncbi_id":"84787","summary":"SUV420H2 and the related enzyme SUV420H1 (MIM 610881) function as histone methyltransferases that specifically trimethylate nucleosomal histone H4 (see MIM 602822) on lysine-20 (K20) (Schotta et al., 2004 [PubMed 15145825]).[supplied by OMIM, Dec 2009]","start":55339853,"end":55348120,"strand":1,"description":"lysine methyltransferase 5C [Source:HGNC Symbol;Acc:HGNC:28405]"}, {"versioned_ensembl_gene_id":"ENSG00000132128.16","gene_symbol":"LRRC41","gene_name":"leucine rich repeat containing 41 [Source:HGNC Symbol;Acc:HGNC:16917]","synonyms":"MUF1","biotype":"protein_coding","ncbi_id":"10489","summary":null,"start":46261196,"end":46303608,"strand":-1,"description":"leucine rich repeat containing 41 [Source:HGNC Symbol;Acc:HGNC:16917]"}, {"versioned_ensembl_gene_id":"ENSG00000224542.7","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30102946,"end":30105603,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000166426.7","gene_symbol":"CRABP1","gene_name":"cellular retinoic acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2338]","synonyms":"RBP5,CRABPI,CRABP-I,CRABP","biotype":"protein_coding","ncbi_id":"1381","summary":"This gene encodes a specific binding protein for a vitamin A family member and is thought to play an important role in retinoic acid-mediated differentiation and proliferation processes. It is structurally similar to the cellular retinol-binding proteins, but binds only retinoic acid at specific sites within the nucleus, which may contribute to vitamin A-directed differentiation in epithelial tissue. [provided by RefSeq, Jul 2008]","start":78340324,"end":78348230,"strand":1,"description":"cellular retinoic acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2338]"}, {"versioned_ensembl_gene_id":"ENSG00000246422.2","gene_symbol":"AC008781.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141558311,"end":141565263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239736.2","gene_symbol":"CEACAMP3","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1825]","synonyms":"CGM10,CEACAM24P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1092","summary":null,"start":41599735,"end":41605984,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1825]"}, {"versioned_ensembl_gene_id":"ENSG00000109339.20","gene_symbol":"MAPK10","gene_name":"mitogen-activated protein kinase 10 [Source:HGNC Symbol;Acc:HGNC:6872]","synonyms":"PRKM10,p54bSAPK,p493F12,JNK3","biotype":"protein_coding","ncbi_id":"5602","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as integration points for multiple biochemical signals, and thus are involved in a wide variety of cellular processes, such as proliferation, differentiation, transcription regulation and development. This kinase is specifically expressed in a subset of neurons in the nervous system, and is activated by threonine and tyrosine phosphorylation. Targeted deletion of this gene in mice suggests that it may have a role in stress-induced neuronal apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Dec 2017]","start":85990007,"end":86594625,"strand":-1,"description":"mitogen-activated protein kinase 10 [Source:HGNC Symbol;Acc:HGNC:6872]"}, {"versioned_ensembl_gene_id":"ENSG00000205363.5","gene_symbol":"C15orf59","gene_name":"chromosome 15 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:33753]","synonyms":"MGC131524,LOC388135,INSYN1","biotype":"protein_coding","ncbi_id":"388135","summary":null,"start":73735431,"end":73752747,"strand":-1,"description":"chromosome 15 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:33753]"}, {"versioned_ensembl_gene_id":"ENSG00000278473.1","gene_symbol":"IGHV3-41","gene_name":"immunoglobulin heavy variable 3-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5602]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28428","summary":null,"start":106443133,"end":106443583,"strand":-1,"description":"immunoglobulin heavy variable 3-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5602]"}, {"versioned_ensembl_gene_id":"ENSG00000235618.7","gene_symbol":"FAM21EP","gene_name":"family with sequence similarity 21 member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:45010]","synonyms":"FLJ31813","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421577","summary":null,"start":50021182,"end":50067803,"strand":-1,"description":"family with sequence similarity 21 member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:45010]"}, {"versioned_ensembl_gene_id":"ENSG00000180061.9","gene_symbol":"TMEM150B","gene_name":"transmembrane protein 150B [Source:HGNC Symbol;Acc:HGNC:34415]","synonyms":"TTN2,TMEM224","biotype":"protein_coding","ncbi_id":"284417","summary":"This gene encodes a protein that belongs to the DRAM (damage-regulated autophagy modulator) family of membrane-spanning proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":55312801,"end":55334048,"strand":-1,"description":"transmembrane protein 150B [Source:HGNC Symbol;Acc:HGNC:34415]"}, {"versioned_ensembl_gene_id":"ENSG00000138639.17","gene_symbol":"ARHGAP24","gene_name":"Rho GTPase activating protein 24 [Source:HGNC Symbol;Acc:HGNC:25361]","synonyms":"FLJ33877,FilGAP,DKFZP564B1162","biotype":"protein_coding","ncbi_id":"83478","summary":"This gene encodes a Rho-GTPase activating protein, which is specific for the small GTPase family member Rac. Binding of the encoded protein by filamin A targets it to sites of membrane protrusion, where it antognizes Rac. This results in suppression of lamellae formation and promotion of retraction to regulate cell polarity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":85475114,"end":86002670,"strand":1,"description":"Rho GTPase activating protein 24 [Source:HGNC Symbol;Acc:HGNC:25361]"}, {"versioned_ensembl_gene_id":"ENSG00000138623.9","gene_symbol":"SEMA7A","gene_name":"semaphorin 7A (John Milton Hagen blood group) [Source:HGNC Symbol;Acc:HGNC:10741]","synonyms":"SEMAL,H-Sema-L,CD108","biotype":"protein_coding","ncbi_id":"8482","summary":"This gene encodes a member of the semaphorin family of proteins. The encoded preproprotein is proteolytically processed to generate the mature glycosylphosphatidylinositol (GPI)-anchored membrane glycoprotein. The encoded protein is found on activated lymphocytes and erythrocytes and may be involved in immunomodulatory and neuronal processes. The encoded protein carries the John Milton Hagen (JMH) blood group antigens. Mutations in this gene may be associated with reduced bone mineral density (BMD). Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":74409289,"end":74434467,"strand":-1,"description":"semaphorin 7A (John Milton Hagen blood group) [Source:HGNC Symbol;Acc:HGNC:10741]"}, {"versioned_ensembl_gene_id":"ENSG00000277362.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803533,"end":54814482,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000261092.1","gene_symbol":"LINC02178","gene_name":"long intergenic non-protein coding RNA 2178 [Source:HGNC Symbol;Acc:HGNC:53040]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371248","summary":null,"start":50390916,"end":50395133,"strand":-1,"description":"long intergenic non-protein coding RNA 2178 [Source:HGNC Symbol;Acc:HGNC:53040]"}, {"versioned_ensembl_gene_id":"ENSG00000230813.1","gene_symbol":"AL356583.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":246527030,"end":246528155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255418.5","gene_symbol":"AC090092.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23164900,"end":23203161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237470.3","gene_symbol":"DCLRE1CP1","gene_name":"DNA cross-link repair 1C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44877]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105376432","summary":null,"start":15015370,"end":15021863,"strand":-1,"description":"DNA cross-link repair 1C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44877]"}, {"versioned_ensembl_gene_id":"ENSG00000274912.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754924,"end":54767305,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000253240.1","gene_symbol":"IGHV3-36","gene_name":"immunoglobulin heavy variable 3-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5599]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28431","summary":null,"start":106392774,"end":106393231,"strand":-1,"description":"immunoglobulin heavy variable 3-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5599]"}, {"versioned_ensembl_gene_id":"ENSG00000204851.6","gene_symbol":"PNMA8B","gene_name":"paraneoplastic Ma antigen family member 8B [Source:HGNC Symbol;Acc:HGNC:29206]","synonyms":"PNMAL2,KIAA1183","biotype":"protein_coding","ncbi_id":"57469","summary":null,"start":46486906,"end":46496498,"strand":-1,"description":"paraneoplastic Ma antigen family member 8B [Source:HGNC Symbol;Acc:HGNC:29206]"}, {"versioned_ensembl_gene_id":"ENSG00000253325.1","gene_symbol":"IGHV7-34-1","gene_name":"immunoglobulin heavy variable 7-34-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5664]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28382","summary":null,"start":106377300,"end":106377733,"strand":-1,"description":"immunoglobulin heavy variable 7-34-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5664]"}, {"versioned_ensembl_gene_id":"ENSG00000270750.1","gene_symbol":"AC080078.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152320544,"end":152321044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254825.1","gene_symbol":"OR9G2P","gene_name":"olfactory receptor family 9 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15320]","synonyms":"OR9G6","biotype":"unprocessed_pseudogene","ncbi_id":"81160","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56751023,"end":56751902,"strand":-1,"description":"olfactory receptor family 9 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15320]"}, {"versioned_ensembl_gene_id":"ENSG00000038427.15","gene_symbol":"VCAN","gene_name":"versican [Source:HGNC Symbol;Acc:HGNC:2464]","synonyms":"PG-M,CSPG2","biotype":"protein_coding","ncbi_id":"1462","summary":"This gene is a member of the aggrecan/versican proteoglycan family. The protein encoded is a large chondroitin sulfate proteoglycan and is a major component of the extracellular matrix. This protein is involved in cell adhesion, proliferation, proliferation, migration and angiogenesis and plays a central role in tissue morphogenesis and maintenance. Mutations in this gene are the cause of Wagner syndrome type 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":83471465,"end":83582303,"strand":1,"description":"versican [Source:HGNC Symbol;Acc:HGNC:2464]"}, {"versioned_ensembl_gene_id":"ENSG00000100462.15","gene_symbol":"PRMT5","gene_name":"protein arginine methyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:10894]","synonyms":"SKB1Hs,SKB1,HRMT1L5","biotype":"protein_coding","ncbi_id":"10419","summary":"This gene encodes an enzyme that belongs to the methyltransferase family. The encoded protein catalyzes the transfer of methyl groups to the amino acid arginine, in target proteins that include histones, transcriptional elongation factors and the tumor suppressor p53. This gene plays a role in several cellular processes, including transcriptional regulation, and the assembly of small nuclear ribonucleoproteins. A pseudogene of this gene has been defined on chromosome 4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":22920511,"end":22929585,"strand":-1,"description":"protein arginine methyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:10894]"}, {"versioned_ensembl_gene_id":"ENSG00000248830.1","gene_symbol":"ZNF807","gene_name":"zinc finger protein 807 [Source:HGNC Symbol;Acc:HGNC:33229]","synonyms":"ZNF807P,ZNF181P1","biotype":"unprocessed_pseudogene","ncbi_id":"100129800","summary":null,"start":34542462,"end":34545395,"strand":-1,"description":"zinc finger protein 807 [Source:HGNC Symbol;Acc:HGNC:33229]"}, {"versioned_ensembl_gene_id":"ENSG00000249835.2","gene_symbol":"VCAN-AS1","gene_name":"VCAN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40163]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105379054","summary":null,"start":83531352,"end":83581320,"strand":-1,"description":"VCAN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40163]"}, {"versioned_ensembl_gene_id":"ENSG00000271034.1","gene_symbol":"AC139700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70125070,"end":70126609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114779.19","gene_symbol":"ABHD14B","gene_name":"abhydrolase domain containing 14B [Source:HGNC Symbol;Acc:HGNC:28235]","synonyms":"MGC15429,CIB","biotype":"protein_coding","ncbi_id":"84836","summary":null,"start":51968510,"end":51983409,"strand":-1,"description":"abhydrolase domain containing 14B [Source:HGNC Symbol;Acc:HGNC:28235]"}, {"versioned_ensembl_gene_id":"ENSG00000181325.7","gene_symbol":"OR9G3P","gene_name":"olfactory receptor family 9 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15321]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81159","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56740179,"end":56741096,"strand":1,"description":"olfactory receptor family 9 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15321]"}, {"versioned_ensembl_gene_id":"ENSG00000270437.1","gene_symbol":"AC009501.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63083008,"end":63087322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254953.1","gene_symbol":"AP001803.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56736316,"end":56736462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142279.12","gene_symbol":"WTIP","gene_name":"WT1 interacting protein [Source:HGNC Symbol;Acc:HGNC:20964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126374","summary":null,"start":34481638,"end":34512304,"strand":1,"description":"WT1 interacting protein [Source:HGNC Symbol;Acc:HGNC:20964]"}, {"versioned_ensembl_gene_id":"ENSG00000131748.15","gene_symbol":"STARD3","gene_name":"StAR related lipid transfer domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17579]","synonyms":"MLN64,es64","biotype":"protein_coding","ncbi_id":"10948","summary":"This gene encodes a member of a subfamily of lipid trafficking proteins that are characterized by a C-terminal steroidogenic acute regulatory domain and an N-terminal metastatic lymph node 64 domain. The encoded protein localizes to the membranes of late endosomes and may be involved in exporting cholesterol. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":39637065,"end":39663484,"strand":1,"description":"StAR related lipid transfer domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17579]"}, {"versioned_ensembl_gene_id":"ENSG00000253482.1","gene_symbol":"IGHVII-26-2","gene_name":"immunoglobulin heavy variable (II)-26-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5674]","synonyms":"IGHV(II)-26-2","biotype":"IG_V_pseudogene","ncbi_id":"28373","summary":null,"start":106314651,"end":106314975,"strand":-1,"description":"immunoglobulin heavy variable (II)-26-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5674]"}, {"versioned_ensembl_gene_id":"ENSG00000239415.1","gene_symbol":"AP001469.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46251549,"end":46254133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234746.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"dJ80I19.4,OR6-8,hs6M1-6","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173300,"end":29174571,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000119685.19","gene_symbol":"TTLL5","gene_name":"tubulin tyrosine ligase like 5 [Source:HGNC Symbol;Acc:HGNC:19963]","synonyms":"KIAA0998","biotype":"protein_coding","ncbi_id":"23093","summary":"This gene encodes a member of the tubulin tyrosine ligase like protein family. This protein interacts with two glucocorticoid receptor coactivators, transcriptional intermediary factor 2 and steroid receptor coactivator 1. This protein may function as a coregulator of glucocorticoid receptor mediated gene induction and repression. This protein may also function as an alpha tubulin polyglutamylase.[provided by RefSeq, Feb 2010]","start":75633625,"end":75955078,"strand":1,"description":"tubulin tyrosine ligase like 5 [Source:HGNC Symbol;Acc:HGNC:19963]"}, {"versioned_ensembl_gene_id":"ENSG00000070748.18","gene_symbol":"CHAT","gene_name":"choline O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:1912]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1103","summary":"This gene encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform. [provided by RefSeq, May 2010]","start":49609095,"end":49665104,"strand":1,"description":"choline O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:1912]"}, {"versioned_ensembl_gene_id":"ENSG00000241351.3","gene_symbol":"IGKV3-11","gene_name":"immunoglobulin kappa variable 3-11 [Source:HGNC Symbol;Acc:HGNC:5815]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28914","summary":null,"start":89027171,"end":89027731,"strand":-1,"description":"immunoglobulin kappa variable 3-11 [Source:HGNC Symbol;Acc:HGNC:5815]"}, {"versioned_ensembl_gene_id":"ENSG00000276545.1","gene_symbol":"AC005618.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":141439853,"end":141442449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253278.1","gene_symbol":"IGKV2-10","gene_name":"immunoglobulin kappa variable 2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5776]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28928","summary":null,"start":89019992,"end":89020686,"strand":-1,"description":"immunoglobulin kappa variable 2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5776]"}, {"versioned_ensembl_gene_id":"ENSG00000262576.2","gene_symbol":"PCDHGA4","gene_name":"protocadherin gamma subfamily A, 4 [Source:HGNC Symbol;Acc:HGNC:8702]","synonyms":"PCDH-GAMMA-A4","biotype":"protein_coding","ncbi_id":"56111","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141355025,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 4 [Source:HGNC Symbol;Acc:HGNC:8702]"}, {"versioned_ensembl_gene_id":"ENSG00000189348.6","gene_symbol":"FAM90A27P","gene_name":"family with sequence similarity 90 member A27, pseudogene [Source:HGNC Symbol;Acc:HGNC:43617]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646508","summary":null,"start":53281559,"end":53284944,"strand":1,"description":"family with sequence similarity 90 member A27, pseudogene [Source:HGNC Symbol;Acc:HGNC:43617]"}, {"versioned_ensembl_gene_id":"ENSG00000253233.1","gene_symbol":"AP005902.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39867436,"end":39867812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271635.1","gene_symbol":"AC017002.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111558413,"end":111559937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230499.1","gene_symbol":"AC108463.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111195963,"end":111206494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227992.1","gene_symbol":"AC108463.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111203964,"end":111206215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284690.1","gene_symbol":"AC079325.2","gene_name":null,"synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":null,"summary":null,"start":74560701,"end":74567343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215812.5","gene_symbol":"ZNF847P","gene_name":"zinc finger protein 847, pseudogene [Source:HGNC Symbol;Acc:HGNC:34384]","synonyms":"gm127","biotype":"unprocessed_pseudogene","ncbi_id":"401983","summary":null,"start":227696892,"end":227706699,"strand":-1,"description":"zinc finger protein 847, pseudogene [Source:HGNC Symbol;Acc:HGNC:34384]"}, {"versioned_ensembl_gene_id":"ENSG00000223570.2","gene_symbol":"AL592045.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":226188870,"end":226189221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155090.14","gene_symbol":"KLF10","gene_name":"Kruppel like factor 10 [Source:HGNC Symbol;Acc:HGNC:11810]","synonyms":"TIEG1,TIEG,EGRA","biotype":"protein_coding","ncbi_id":"7071","summary":"This gene encodes a member of a family of proteins that feature C2H2-type zinc finger domains. The encoded protein is a transcriptional repressor that acts as an effector of transforming growth factor beta signaling. Activity of this protein may inhibit the growth of cancers, particularly pancreatic cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":102648779,"end":102655902,"strand":-1,"description":"Kruppel like factor 10 [Source:HGNC Symbol;Acc:HGNC:11810]"}, {"versioned_ensembl_gene_id":"ENSG00000119699.7","gene_symbol":"TGFB3","gene_name":"transforming growth factor beta 3 [Source:HGNC Symbol;Acc:HGNC:11769]","synonyms":"ARVD1,ARVD","biotype":"protein_coding","ncbi_id":"7043","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGF-beta family members. This protein is involved in embryogenesis and cell differentiation, and may play a role in wound healing. Mutations in this gene are a cause of aortic aneurysms and dissections, as well as familial arrhythmogenic right ventricular dysplasia 1. [provided by RefSeq, Aug 2016]","start":75958099,"end":75982991,"strand":-1,"description":"transforming growth factor beta 3 [Source:HGNC Symbol;Acc:HGNC:11769]"}, {"versioned_ensembl_gene_id":"ENSG00000259103.1","gene_symbol":"AF107885.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75814502,"end":75847698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177291.3","gene_symbol":"GJD4","gene_name":"gap junction protein delta 4 [Source:HGNC Symbol;Acc:HGNC:23296]","synonyms":"FLJ90023,CX40.1","biotype":"protein_coding","ncbi_id":"219770","summary":"Connexins, such as GJD4, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]","start":35605410,"end":35608935,"strand":1,"description":"gap junction protein delta 4 [Source:HGNC Symbol;Acc:HGNC:23296]"}, {"versioned_ensembl_gene_id":"ENSG00000253831.1","gene_symbol":"ETV3L","gene_name":"ETS variant 3 like [Source:HGNC Symbol;Acc:HGNC:33834]","synonyms":"FLJ16478","biotype":"protein_coding","ncbi_id":"440695","summary":null,"start":157092044,"end":157099808,"strand":-1,"description":"ETS variant 3 like [Source:HGNC Symbol;Acc:HGNC:33834]"}, {"versioned_ensembl_gene_id":"ENSG00000224520.2","gene_symbol":"KRT8P45","gene_name":"keratin 8 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:39879]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"149501","summary":null,"start":157073257,"end":157074703,"strand":1,"description":"keratin 8 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:39879]"}, {"versioned_ensembl_gene_id":"ENSG00000242511.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29724363,"end":29724833,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000159882.12","gene_symbol":"ZNF230","gene_name":"zinc finger protein 230 [Source:HGNC Symbol;Acc:HGNC:13024]","synonyms":"FDZF2","biotype":"protein_coding","ncbi_id":"7773","summary":null,"start":44002948,"end":44013926,"strand":1,"description":"zinc finger protein 230 [Source:HGNC Symbol;Acc:HGNC:13024]"}, {"versioned_ensembl_gene_id":"ENSG00000230805.6","gene_symbol":"AL132709.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101073869,"end":101077910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213030.5","gene_symbol":"CGB8","gene_name":"chorionic gonadotropin beta subunit 8 [Source:HGNC Symbol;Acc:HGNC:16453]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94115","summary":"This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 8 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [provided by RefSeq, Jul 2008]","start":49047638,"end":49049106,"strand":-1,"description":"chorionic gonadotropin beta subunit 8 [Source:HGNC Symbol;Acc:HGNC:16453]"}, {"versioned_ensembl_gene_id":"ENSG00000277806.1","gene_symbol":"AC006213.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":43976815,"end":43977448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186185.13","gene_symbol":"KIF18B","gene_name":"kinesin family member 18B [Source:HGNC Symbol;Acc:HGNC:27102]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146909","summary":null,"start":44924709,"end":44947711,"strand":-1,"description":"kinesin family member 18B [Source:HGNC Symbol;Acc:HGNC:27102]"}, {"versioned_ensembl_gene_id":"ENSG00000019186.9","gene_symbol":"CYP24A1","gene_name":"cytochrome P450 family 24 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2602]","synonyms":"P450-CC24,CYP24,CP24","biotype":"protein_coding","ncbi_id":"1591","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein initiates the degradation of 1,25-dihydroxyvitamin D3, the physiologically active form of vitamin D3, by hydroxylation of the side chain. In regulating the level of vitamin D3, this enzyme plays a role in calcium homeostasis and the vitamin D endocrine system. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54153449,"end":54173973,"strand":-1,"description":"cytochrome P450 family 24 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2602]"}, {"versioned_ensembl_gene_id":"ENSG00000223615.2","gene_symbol":"AL807761.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107115784,"end":107115954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249633.1","gene_symbol":"OR52V1P","gene_name":"olfactory receptor family 52 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15238]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81242","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5527277,"end":5528174,"strand":-1,"description":"olfactory receptor family 52 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15238]"}, {"versioned_ensembl_gene_id":"ENSG00000165533.18","gene_symbol":"TTC8","gene_name":"tetratricopeptide repeat domain 8 [Source:HGNC Symbol;Acc:HGNC:20087]","synonyms":"RP51,BBS8","biotype":"protein_coding","ncbi_id":"123016","summary":"This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":88824153,"end":88881078,"strand":1,"description":"tetratricopeptide repeat domain 8 [Source:HGNC Symbol;Acc:HGNC:20087]"}, {"versioned_ensembl_gene_id":"ENSG00000119660.4","gene_symbol":"DPPA5P4","gene_name":"developmental pluripotency associated 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49665]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646701","summary":null,"start":75292131,"end":75292495,"strand":-1,"description":"developmental pluripotency associated 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49665]"}, {"versioned_ensembl_gene_id":"ENSG00000226645.1","gene_symbol":"AP006216.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116773389,"end":116774205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105427.9","gene_symbol":"CNFN","gene_name":"cornifelin [Source:HGNC Symbol;Acc:HGNC:30183]","synonyms":"PLAC8L2","biotype":"protein_coding","ncbi_id":"84518","summary":null,"start":42387019,"end":42390287,"strand":-1,"description":"cornifelin [Source:HGNC Symbol;Acc:HGNC:30183]"}, {"versioned_ensembl_gene_id":"ENSG00000138622.3","gene_symbol":"HCN4","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium channel 4 [Source:HGNC Symbol;Acc:HGNC:16882]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10021","summary":"This gene encodes a member of the hyperpolarization-activated cyclic nucleotide-gated potassium channels. The encoded protein shows slow kinetics of activation and inactivation, and is necessary for the cardiac pacemaking process. This channel may also mediate responses to sour stimuli. Mutations in this gene have been linked to sick sinus syndrome 2, also known as atrial fibrillation with bradyarrhythmia or familial sinus bradycardia. Two pseudogenes have been identified on chromosome 15. [provided by RefSeq, Oct 2008]","start":73319859,"end":73369264,"strand":-1,"description":"hyperpolarization activated cyclic nucleotide gated potassium channel 4 [Source:HGNC Symbol;Acc:HGNC:16882]"}, {"versioned_ensembl_gene_id":"ENSG00000215417.12","gene_symbol":"MIR17HG","gene_name":"miR-17-92a-1 cluster host gene [Source:HGNC Symbol;Acc:HGNC:23564]","synonyms":"FLJ14178,C13orf25,NCRNA00048,MIRHG1,MIRH1,miR-17-92,MIHG1,LINC00048","biotype":"processed_transcript","ncbi_id":"407975","summary":"This gene is the host gene for the MIR17-92 cluster, a group of at least six microRNAs (miRNAs) that may be involved in cell survival, proliferation, differentiation, and angiogenesis. Amplification of this gene has been found in several lymphomas and solid tumors. Two non-protein coding transcript variants have been found for this host gene, but only the longest is a polycistronic transcript containing the MIR17-92 cluster. [provided by RefSeq, May 2012]","start":91347820,"end":91354579,"strand":1,"description":"miR-17-92a-1 cluster host gene [Source:HGNC Symbol;Acc:HGNC:23564]"}, {"versioned_ensembl_gene_id":"ENSG00000268879.1","gene_symbol":"IGFL1P1","gene_name":"IGF like family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32956]","synonyms":"IGFL-5P","biotype":"unprocessed_pseudogene","ncbi_id":"727703","summary":null,"start":46196238,"end":46197323,"strand":1,"description":"IGF like family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32956]"}, {"versioned_ensembl_gene_id":"ENSG00000221974.11","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFIIH,TFB2,P52","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30897757,"end":30903679,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000250838.1","gene_symbol":"AC091133.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48995266,"end":48997492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251550.1","gene_symbol":"AC091133.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49037122,"end":49037429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224371.5","gene_symbol":"AL391361.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160872888,"end":160918649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226629.1","gene_symbol":"LINC00974","gene_name":"long intergenic non-protein coding RNA 974 [Source:HGNC Symbol;Acc:HGNC:27105]","synonyms":null,"biotype":"lincRNA","ncbi_id":"147093","summary":null,"start":41549606,"end":41554495,"strand":-1,"description":"long intergenic non-protein coding RNA 974 [Source:HGNC Symbol;Acc:HGNC:27105]"}, {"versioned_ensembl_gene_id":"ENSG00000274903.1","gene_symbol":"AL109933.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160773988,"end":160783214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197937.12","gene_symbol":"ZNF347","gene_name":"zinc finger protein 347 [Source:HGNC Symbol;Acc:HGNC:16447]","synonyms":"ZNF1111","biotype":"protein_coding","ncbi_id":"84671","summary":null,"start":53124072,"end":53159075,"strand":-1,"description":"zinc finger protein 347 [Source:HGNC Symbol;Acc:HGNC:16447]"}, {"versioned_ensembl_gene_id":"ENSG00000148143.12","gene_symbol":"ZNF462","gene_name":"zinc finger protein 462 [Source:HGNC Symbol;Acc:HGNC:21684]","synonyms":"DKFZP762N2316,Zfp462,KIAA1803","biotype":"protein_coding","ncbi_id":"58499","summary":"The protein encoded by this gene belongs to C2H2-type zinc finger family of proteins. It contains multiple C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":106863097,"end":107013634,"strand":1,"description":"zinc finger protein 462 [Source:HGNC Symbol;Acc:HGNC:21684]"}, {"versioned_ensembl_gene_id":"ENSG00000230782.1","gene_symbol":"AL807761.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106974833,"end":107102988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227983.1","gene_symbol":"BRK1P2","gene_name":"BRICK1, SCAR/WAVE actin-nucleating complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874492","summary":null,"start":91023732,"end":91023954,"strand":-1,"description":"BRICK1, SCAR/WAVE actin-nucleating complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42021]"}, {"versioned_ensembl_gene_id":"ENSG00000274898.1","gene_symbol":"AC001226.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77027944,"end":77028482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214593.3","gene_symbol":"AL354710.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125263845,"end":125264090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125875.13","gene_symbol":"TBC1D20","gene_name":"TBC1 domain family member 20 [Source:HGNC Symbol;Acc:HGNC:16133]","synonyms":"dJ852M4.2,C20orf140","biotype":"protein_coding","ncbi_id":"128637","summary":"This gene encodes a protein that belongs to a family of GTPase activator proteins of Rab-like small GTPases. The encoded protein and its cognate GTPase, Rab1, bind the nonstructural protein 5A (NS5A) of the hepatitis C virus (HCV) to mediate viral replication. Depletion of this protein inhibits replication of the virus and HCV infection. Mutations in this gene are associated with Warburg micro syndrome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":435480,"end":462553,"strand":-1,"description":"TBC1 domain family member 20 [Source:HGNC Symbol;Acc:HGNC:16133]"}, {"versioned_ensembl_gene_id":"ENSG00000234202.2","gene_symbol":"AC104332.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92749175,"end":92749330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231674.1","gene_symbol":"LINC00410","gene_name":"long intergenic non-protein coding RNA 410 [Source:HGNC Symbol;Acc:HGNC:42742]","synonyms":null,"biotype":"lincRNA","ncbi_id":"144776","summary":null,"start":90890954,"end":90926597,"strand":-1,"description":"long intergenic non-protein coding RNA 410 [Source:HGNC Symbol;Acc:HGNC:42742]"}, {"versioned_ensembl_gene_id":"ENSG00000235317.4","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCG4P10,HCGIV.9,HCGIV-10","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29789145,"end":29790142,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000149599.15","gene_symbol":"DUSP15","gene_name":"dual specificity phosphatase 15 [Source:HGNC Symbol;Acc:HGNC:16236]","synonyms":"VHY,FLJ20645,C20orf57,bA243J16.6,bA243J16.5","biotype":"protein_coding","ncbi_id":"128853","summary":"The protein encoded by this gene has both protein-tyrosine phophatase activity and serine/threonine-specific phosphatase activity, and therefore is known as a dual specificity phosphatase. This protein may function in the differentiation of oligodendrocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":31847637,"end":31870747,"strand":-1,"description":"dual specificity phosphatase 15 [Source:HGNC Symbol;Acc:HGNC:16236]"}, {"versioned_ensembl_gene_id":"ENSG00000167740.9","gene_symbol":"CYB5D2","gene_name":"cytochrome b5 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28471]","synonyms":"MGC32124","biotype":"protein_coding","ncbi_id":"124936","summary":null,"start":4143168,"end":4187310,"strand":1,"description":"cytochrome b5 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28471]"}, {"versioned_ensembl_gene_id":"ENSG00000139330.5","gene_symbol":"KERA","gene_name":"keratocan [Source:HGNC Symbol;Acc:HGNC:6309]","synonyms":"SLRR2B,CNA2","biotype":"protein_coding","ncbi_id":"11081","summary":"The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).[provided by RefSeq, May 2010]","start":91050491,"end":91057983,"strand":-1,"description":"keratocan [Source:HGNC Symbol;Acc:HGNC:6309]"}, {"versioned_ensembl_gene_id":"ENSG00000185722.16","gene_symbol":"ANKFY1","gene_name":"ankyrin repeat and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20763]","synonyms":"BTBD23,ANKHZN,ZFYVE14,RANK-5,KIAA1255","biotype":"protein_coding","ncbi_id":"51479","summary":"This gene encodes a cytoplasmic protein that contains a coiled-coil structure and a BTB/POZ domain at its N-terminus, ankyrin repeats in the middle portion, and a FYVE-finger motif at its C-terminus. This protein belongs to a subgroup of double zinc finger proteins which may be involved in vesicle or protein transport. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Apr 2012]","start":4163907,"end":4263977,"strand":-1,"description":"ankyrin repeat and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20763]"}, {"versioned_ensembl_gene_id":"ENSG00000240237.1","gene_symbol":"AF305872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133002605,"end":133003075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224419.1","gene_symbol":"KRT18P27","gene_name":"keratin 18 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:33396]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390418","summary":null,"start":90230384,"end":90231682,"strand":1,"description":"keratin 18 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:33396]"}, {"versioned_ensembl_gene_id":"ENSG00000275549.1","gene_symbol":"STPG3-AS1","gene_name":"STPG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51176]","synonyms":"C9orf173-AS1","biotype":"antisense_RNA","ncbi_id":"100129722","summary":null,"start":137250219,"end":137253497,"strand":-1,"description":"STPG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51176]"}, {"versioned_ensembl_gene_id":"ENSG00000223465.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"B144,LST-1,D6S49E","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31568266,"end":31571053,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000066923.17","gene_symbol":"STAG3","gene_name":"stromal antigen 3 [Source:HGNC Symbol;Acc:HGNC:11356]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10734","summary":"The protein encoded by this gene is expressed in the nucleus and is a subunit of the cohesin complex which regulates the cohesion of sister chromatids during cell division. A mutation in this gene is associated with premature ovarian failure. Alternate splicing results in multiple transcript variants encoding distinct isoforms. This gene has multiple pseudogenes. [provided by RefSeq, Apr 2014]","start":100177563,"end":100221488,"strand":1,"description":"stromal antigen 3 [Source:HGNC Symbol;Acc:HGNC:11356]"}, {"versioned_ensembl_gene_id":"ENSG00000251395.1","gene_symbol":"FTH1P9","gene_name":"ferritin heavy chain 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39089]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478936","summary":null,"start":83426676,"end":83427030,"strand":1,"description":"ferritin heavy chain 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39089]"}, {"versioned_ensembl_gene_id":"ENSG00000237468.2","gene_symbol":"AL359547.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146594516,"end":146598931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213736.2","gene_symbol":"AC026310.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24967127,"end":24967504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131738.10","gene_symbol":"KRT33B","gene_name":"keratin 33B [Source:HGNC Symbol;Acc:HGNC:6451]","synonyms":"KRTHA3B,Ha-3II","biotype":"protein_coding","ncbi_id":"3884","summary":"This gene encodes a member of the keratin gene family. This gene is one of multiple type I hair keratin genes that are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. As a type I hair keratin, the encoded protein is an acidic protein which heterodimerizes with type II keratins to form hair and nails. There are two isoforms of this protein, encoded by two separate genes, keratin 33A and keratin 33B. [provided by RefSeq, May 2012]","start":41363494,"end":41369800,"strand":-1,"description":"keratin 33B [Source:HGNC Symbol;Acc:HGNC:6451]"}, {"versioned_ensembl_gene_id":"ENSG00000275828.1","gene_symbol":"AC134879.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11412548,"end":11418716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270242.1","gene_symbol":"ACTR3BP1","gene_name":"ACTR3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643050","summary":null,"start":11395699,"end":11397076,"strand":1,"description":"ACTR3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37724]"}, {"versioned_ensembl_gene_id":"ENSG00000182938.4","gene_symbol":"OTOP3","gene_name":"otopetrin 3 [Source:HGNC Symbol;Acc:HGNC:19658]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347741","summary":null,"start":74935719,"end":74949992,"strand":1,"description":"otopetrin 3 [Source:HGNC Symbol;Acc:HGNC:19658]"}, {"versioned_ensembl_gene_id":"ENSG00000039650.11","gene_symbol":"PNKP","gene_name":"polynucleotide kinase 3'-phosphatase [Source:HGNC Symbol;Acc:HGNC:9154]","synonyms":"PNK","biotype":"protein_coding","ncbi_id":"11284","summary":"This locus represents a gene involved in DNA repair. In response to ionizing radiation or oxidative damage, the protein encoded by this locus catalyzes 5' phosphorylation and 3' dephosphorylation of nucleic acids. Mutations at this locus have been associated with microcephaly, seizures, and developmental delay.[provided by RefSeq, Sep 2010]","start":49859882,"end":49878351,"strand":-1,"description":"polynucleotide kinase 3'-phosphatase [Source:HGNC Symbol;Acc:HGNC:9154]"}, {"versioned_ensembl_gene_id":"ENSG00000162947.4","gene_symbol":"LINC01931","gene_name":"long intergenic non-protein coding RNA 1931 [Source:HGNC Symbol;Acc:HGNC:52743]","synonyms":null,"biotype":"lincRNA","ncbi_id":"150596","summary":null,"start":149767506,"end":149859191,"strand":-1,"description":"long intergenic non-protein coding RNA 1931 [Source:HGNC Symbol;Acc:HGNC:52743]"}, {"versioned_ensembl_gene_id":"ENSG00000171793.13","gene_symbol":"CTPS1","gene_name":"CTP synthase 1 [Source:HGNC Symbol;Acc:HGNC:2519]","synonyms":"GATD5,CTPS","biotype":"protein_coding","ncbi_id":"1503","summary":"This gene encodes an enzyme responsible for the catalytic conversion of UTP (uridine triphosphate) to CTP (cytidine triphospate). This reaction is an important step in the biosynthesis of phospholipids and nucleic acids. Activity of this proten is important in the immune system, and loss of function of this gene has been associated with immunodeficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":40979335,"end":41012565,"strand":1,"description":"CTP synthase 1 [Source:HGNC Symbol;Acc:HGNC:2519]"}, {"versioned_ensembl_gene_id":"ENSG00000283101.1","gene_symbol":"BMS1P21","gene_name":"BMS1, ribosome biogenesis factor pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51604]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288974","summary":null,"start":79906605,"end":79907856,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51604]"}, {"versioned_ensembl_gene_id":"ENSG00000133661.15","gene_symbol":"SFTPD","gene_name":"surfactant protein D [Source:HGNC Symbol;Acc:HGNC:10803]","synonyms":"SP-D,SFTP4,COLEC7","biotype":"protein_coding","ncbi_id":"6441","summary":"The protein encoded by this gene is part of the innate immune response, protecting the lungs against inhaled microorganisms and chemicals. The encoded protein may also be involved in surfactant metabolism. [provided by RefSeq, Jul 2015]","start":79937740,"end":79982614,"strand":-1,"description":"surfactant protein D [Source:HGNC Symbol;Acc:HGNC:10803]"}, {"versioned_ensembl_gene_id":"ENSG00000223496.2","gene_symbol":"EXOSC6","gene_name":"exosome component 6 [Source:HGNC Symbol;Acc:HGNC:19055]","synonyms":"p11,Mtr3p,MTR3,hMtr3p,EAP4","biotype":"protein_coding","ncbi_id":"118460","summary":"This gene product constitutes one of the subunits of the multisubunit particle called exosome, which mediates mRNA degradation. The composition of human exosome is similar to its yeast counterpart. This protein is homologous to the yeast Mtr3 protein. Its exact function is not known, however, it has been shown using a cell-free RNA decay system that the exosome is required for rapid degradation of unstable mRNAs containing AU-rich elements (AREs), but not for poly(A) shortening. The exosome does not recognize ARE-containing mRNAs on its own, but requires ARE-binding proteins that could interact with the exosome and recruit it to unstable mRNAs, thereby promoting their rapid degradation. [provided by RefSeq, Jul 2008]","start":70246778,"end":70251930,"strand":-1,"description":"exosome component 6 [Source:HGNC Symbol;Acc:HGNC:19055]"}, {"versioned_ensembl_gene_id":"ENSG00000113296.14","gene_symbol":"THBS4","gene_name":"thrombospondin 4 [Source:HGNC Symbol;Acc:HGNC:11788]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7060","summary":"The protein encoded by this gene belongs to the thrombospondin protein family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentamer and can bind to heparin and calcium. It is involved in local signaling in the developing and adult nervous system, and it contributes to spinal sensitization and neuropathic pain states. This gene is activated during the stromal response to invasive breast cancer. It may also play a role in inflammatory responses in Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":79991311,"end":80083287,"strand":1,"description":"thrombospondin 4 [Source:HGNC Symbol;Acc:HGNC:11788]"}, {"versioned_ensembl_gene_id":"ENSG00000259399.1","gene_symbol":"TGIF2-C20orf24","gene_name":"TGIF2-C20orf24 readthrough [Source:HGNC Symbol;Acc:HGNC:44664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527943","summary":"This locus represents naturally occurring read-through transcription between the neighboring TGIF2 (TGFB-induced factor homeobox 2) and C20orf24 (chromosome 20 open reading frame 24) genes. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Dec 2010]","start":36574553,"end":36612384,"strand":1,"description":"TGIF2-C20orf24 readthrough [Source:HGNC Symbol;Acc:HGNC:44664]"}, {"versioned_ensembl_gene_id":"ENSG00000249825.5","gene_symbol":"CTD-2201I18.1","gene_name":"uncharacterized LOC101929215 [Source:NCBI gene;Acc:101929215]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929215","summary":null,"start":80052374,"end":80083654,"strand":-1,"description":"uncharacterized LOC101929215 [Source:NCBI gene;Acc:101929215]"}, {"versioned_ensembl_gene_id":"ENSG00000242779.6","gene_symbol":"ZNF702P","gene_name":"zinc finger protein 702, pseudogene [Source:HGNC Symbol;Acc:HGNC:25775]","synonyms":"ZNF702,FLJ12985","biotype":"transcribed_processed_pseudogene","ncbi_id":"79986","summary":null,"start":52968251,"end":53037898,"strand":-1,"description":"zinc finger protein 702, pseudogene [Source:HGNC Symbol;Acc:HGNC:25775]"}, {"versioned_ensembl_gene_id":"ENSG00000253726.1","gene_symbol":"AC013562.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":72732045,"end":72751843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254705.1","gene_symbol":"AP000722.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92400191,"end":92408176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179772.7","gene_symbol":"FOXS1","gene_name":"forkhead box S1 [Source:HGNC Symbol;Acc:HGNC:3735]","synonyms":"FREAC10,FKHL18","biotype":"protein_coding","ncbi_id":"2307","summary":"The forkhead family of transcription factors belongs to the winged helix class of DNA-binding proteins. The protein encoded by this intronless gene contains a forkhead domain and is found predominantly in aorta and kidney. The function of the encoded protein is unknown. [provided by RefSeq, Jul 2008]","start":31844301,"end":31845619,"strand":-1,"description":"forkhead box S1 [Source:HGNC Symbol;Acc:HGNC:3735]"}, {"versioned_ensembl_gene_id":"ENSG00000227963.1","gene_symbol":"AL355488.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110286375,"end":110339171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240845.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29724152,"end":29724622,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000233617.1","gene_symbol":"CR753818.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720462,"end":29721452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263923.1","gene_symbol":"AC019131.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98928897,"end":98994994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179546.4","gene_symbol":"HTR1D","gene_name":"5-hydroxytryptamine receptor 1D [Source:HGNC Symbol;Acc:HGNC:5289]","synonyms":"RDC4,HTRL,HT1DA,5-HT1D","biotype":"protein_coding","ncbi_id":"3352","summary":null,"start":23191895,"end":23194729,"strand":-1,"description":"5-hydroxytryptamine receptor 1D [Source:HGNC Symbol;Acc:HGNC:5289]"}, {"versioned_ensembl_gene_id":"ENSG00000118322.12","gene_symbol":"ATP10B","gene_name":"ATPase phospholipid transporting 10B (putative) [Source:HGNC Symbol;Acc:HGNC:13543]","synonyms":"KIAA0715,FLJ21477,ATPVB","biotype":"protein_coding","ncbi_id":"23120","summary":null,"start":160563120,"end":160852214,"strand":-1,"description":"ATPase phospholipid transporting 10B (putative) [Source:HGNC Symbol;Acc:HGNC:13543]"}, {"versioned_ensembl_gene_id":"ENSG00000253796.1","gene_symbol":"AC104248.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108895029,"end":109063417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196119.7","gene_symbol":"OR8A1","gene_name":"olfactory receptor family 8 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8469]","synonyms":"OST025","biotype":"protein_coding","ncbi_id":"390275","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124566660,"end":124582942,"strand":1,"description":"olfactory receptor family 8 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8469]"}, {"versioned_ensembl_gene_id":"ENSG00000170953.3","gene_symbol":"OR8B12","gene_name":"olfactory receptor family 8 subfamily B member 12 [Source:HGNC Symbol;Acc:HGNC:15307]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219858","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124539635,"end":124545333,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 12 [Source:HGNC Symbol;Acc:HGNC:15307]"}, {"versioned_ensembl_gene_id":"ENSG00000271503.5","gene_symbol":"CCL5","gene_name":"C-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10632]","synonyms":"TCP228,SISd,SCYA5,RANTES,MGC17164,D17S136E","biotype":"protein_coding","ncbi_id":"6352","summary":"This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, functions as a chemoattractant for blood monocytes, memory T helper cells and eosinophils. It causes the release of histamine from basophils and activates eosinophils. This cytokine is one of the major HIV-suppressive factors produced by CD8+ cells. It functions as one of the natural ligands for the chemokine receptor chemokine (C-C motif) receptor 5 (CCR5), and it suppresses in vitro replication of the R5 strains of HIV-1, which use CCR5 as a coreceptor. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":35871491,"end":35880793,"strand":-1,"description":"C-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10632]"}, {"versioned_ensembl_gene_id":"ENSG00000229503.1","gene_symbol":"AC092155.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62532583,"end":62533059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069493.14","gene_symbol":"CLEC2D","gene_name":"C-type lectin domain family 2 member D [Source:HGNC Symbol;Acc:HGNC:14351]","synonyms":"LLT1,CLAX,OCIL","biotype":"protein_coding","ncbi_id":"29121","summary":"This gene encodes a member of the natural killer cell receptor C-type lectin family. The encoded protein inhibits osteoclast formation and contains a transmembrane domain near the N-terminus as well as the C-type lectin-like extracellular domain. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Oct 2010]","start":9664969,"end":9699555,"strand":1,"description":"C-type lectin domain family 2 member D [Source:HGNC Symbol;Acc:HGNC:14351]"}, {"versioned_ensembl_gene_id":"ENSG00000240156.1","gene_symbol":"COX6CP6","gene_name":"cytochrome c oxidase subunit 6C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:47037]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289131","summary":null,"start":70751123,"end":70751350,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:47037]"}, {"versioned_ensembl_gene_id":"ENSG00000227091.1","gene_symbol":"AL355990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110166186,"end":110172489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235526.1","gene_symbol":"AL355990.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110177643,"end":110178719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268218.1","gene_symbol":"AC137932.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89268104,"end":89273044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270832.1","gene_symbol":"AC092120.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89458870,"end":89459437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129566.12","gene_symbol":"TEP1","gene_name":"telomerase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:11726]","synonyms":"VAULT2,TROVE1,TP1,TLP1,p240","biotype":"protein_coding","ncbi_id":"7011","summary":"This gene product is a component of the ribonucleoprotein complex responsible for telomerase activity which catalyzes the addition of new telomeres on the chromosome ends. The telomerase-associated proteins are conserved from ciliates to humans. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":20365667,"end":20413429,"strand":-1,"description":"telomerase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:11726]"}, {"versioned_ensembl_gene_id":"ENSG00000259056.1","gene_symbol":"DUXAP1","gene_name":"double homeobox A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32180]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"503630","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":84750769,"end":84751231,"strand":1,"description":"double homeobox A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32180]"}, {"versioned_ensembl_gene_id":"ENSG00000231150.5","gene_symbol":"AL034345.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38923029,"end":38953099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196912.12","gene_symbol":"ANKRD36B","gene_name":"ankyrin repeat domain 36B [Source:HGNC Symbol;Acc:HGNC:29333]","synonyms":"KIAA1641,FLJ21281","biotype":"protein_coding","ncbi_id":"57730","summary":null,"start":97492663,"end":97589965,"strand":-1,"description":"ankyrin repeat domain 36B [Source:HGNC Symbol;Acc:HGNC:29333]"}, {"versioned_ensembl_gene_id":"ENSG00000227825.4","gene_symbol":"SLC9A7P1","gene_name":"solute carrier family 9 member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32679]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"121456","summary":null,"start":98453835,"end":98457145,"strand":-1,"description":"solute carrier family 9 member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32679]"}, {"versioned_ensembl_gene_id":"ENSG00000258312.1","gene_symbol":"AC016152.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98113014,"end":98292445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170100.13","gene_symbol":"ZNF778","gene_name":"zinc finger protein 778 [Source:HGNC Symbol;Acc:HGNC:26479]","synonyms":"FLJ31875","biotype":"protein_coding","ncbi_id":"197320","summary":"The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]","start":89217703,"end":89237071,"strand":1,"description":"zinc finger protein 778 [Source:HGNC Symbol;Acc:HGNC:26479]"}, {"versioned_ensembl_gene_id":"ENSG00000254796.1","gene_symbol":"AC134684.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7601004,"end":7601267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255557.1","gene_symbol":"AP001266.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65745729,"end":65771585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225302.2","gene_symbol":"AC023283.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":116828761,"end":116850205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223442.1","gene_symbol":"TH2LCRR","gene_name":"T helper type 2 locus control region associated RNA [Source:HGNC Symbol;Acc:HGNC:40495]","synonyms":"TH2-LCR","biotype":"antisense_RNA","ncbi_id":"101927761","summary":null,"start":132630589,"end":132664272,"strand":-1,"description":"T helper type 2 locus control region associated RNA [Source:HGNC Symbol;Acc:HGNC:40495]"}, {"versioned_ensembl_gene_id":"ENSG00000104447.12","gene_symbol":"TRPS1","gene_name":"transcriptional repressor GATA binding 1 [Source:HGNC Symbol;Acc:HGNC:12340]","synonyms":"LGCR,GC79","biotype":"protein_coding","ncbi_id":"7227","summary":"This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [provided by RefSeq, Jul 2008]","start":115408496,"end":115809673,"strand":-1,"description":"transcriptional repressor GATA binding 1 [Source:HGNC Symbol;Acc:HGNC:12340]"}, {"versioned_ensembl_gene_id":"ENSG00000212721.3","gene_symbol":"KRTAP4-11","gene_name":"keratin associated protein 4-11 [Source:HGNC Symbol;Acc:HGNC:18911]","synonyms":"KAP4.11,KRTAP4-14,KAP4.14","biotype":"protein_coding","ncbi_id":"653240","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Mar 2009]","start":41117181,"end":41118360,"strand":-1,"description":"keratin associated protein 4-11 [Source:HGNC Symbol;Acc:HGNC:18911]"}, {"versioned_ensembl_gene_id":"ENSG00000112306.7","gene_symbol":"RPS12","gene_name":"ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10385]","synonyms":"S12","biotype":"protein_coding","ncbi_id":"6206","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S12E family of ribosomal proteins. It is located in the cytoplasm. Increased expression of this gene in colorectal cancers compared to matched normal colonic mucosa has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":132814441,"end":132817564,"strand":1,"description":"ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10385]"}, {"versioned_ensembl_gene_id":"ENSG00000167554.14","gene_symbol":"ZNF610","gene_name":"zinc finger protein 610 [Source:HGNC Symbol;Acc:HGNC:26687]","synonyms":"FLJ36040","biotype":"protein_coding","ncbi_id":"162963","summary":null,"start":52336245,"end":52367778,"strand":1,"description":"zinc finger protein 610 [Source:HGNC Symbol;Acc:HGNC:26687]"}, {"versioned_ensembl_gene_id":"ENSG00000269535.1","gene_symbol":"AC010320.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52300693,"end":52345229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270612.1","gene_symbol":"AC112191.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160326693,"end":160326969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172794.19","gene_symbol":"RAB37","gene_name":"RAB37, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30268]","synonyms":null,"biotype":"protein_coding","ncbi_id":"326624","summary":"Rab proteins are low molecular mass GTPases that are critical regulators of vesicle trafficking. For additional background information on Rab proteins, see MIM 179508.[supplied by OMIM, Apr 2006]","start":74670578,"end":74747335,"strand":1,"description":"RAB37, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30268]"}, {"versioned_ensembl_gene_id":"ENSG00000283246.1","gene_symbol":"MEP1AP1","gene_name":"meprin A subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7016]","synonyms":"MEP1AL1","biotype":"unprocessed_pseudogene","ncbi_id":"642840","summary":null,"start":40187792,"end":40193921,"strand":-1,"description":"meprin A subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7016]"}, {"versioned_ensembl_gene_id":"ENSG00000100906.10","gene_symbol":"NFKBIA","gene_name":"NFKB inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:7797]","synonyms":"NFKBI,MAD-3,IKBA,IkappaBalpha","biotype":"protein_coding","ncbi_id":"4792","summary":"This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011]","start":35401511,"end":35404749,"strand":-1,"description":"NFKB inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:7797]"}, {"versioned_ensembl_gene_id":"ENSG00000268536.1","gene_symbol":"AC005523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4785120,"end":4791207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214518.3","gene_symbol":"KRTAP2-2","gene_name":"keratin associated protein 2-2 [Source:HGNC Symbol;Acc:HGNC:18905]","synonyms":"KAP2.2","biotype":"protein_coding","ncbi_id":"728279","summary":null,"start":41054498,"end":41055230,"strand":-1,"description":"keratin associated protein 2-2 [Source:HGNC Symbol;Acc:HGNC:18905]"}, {"versioned_ensembl_gene_id":"ENSG00000176857.5","gene_symbol":"GJA1P1","gene_name":"gap junction protein alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4275]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"2698","summary":null,"start":109051315,"end":109052457,"strand":-1,"description":"gap junction protein alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4275]"}, {"versioned_ensembl_gene_id":"ENSG00000180422.3","gene_symbol":"LINC00304","gene_name":"long intergenic non-protein coding RNA 304 [Source:HGNC Symbol;Acc:HGNC:26713]","synonyms":"C16orf81,NCRNA00304,FLJ36701","biotype":"lincRNA","ncbi_id":"283860","summary":null,"start":89159146,"end":89164245,"strand":1,"description":"long intergenic non-protein coding RNA 304 [Source:HGNC Symbol;Acc:HGNC:26713]"}, {"versioned_ensembl_gene_id":"ENSG00000236966.1","gene_symbol":"AL773545.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40131747,"end":40132218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248654.1","gene_symbol":"MTCO3P44","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52147]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075289","summary":null,"start":25720516,"end":25721056,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52147]"}, {"versioned_ensembl_gene_id":"ENSG00000267024.1","gene_symbol":"AC008747.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34426112,"end":34428273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251353.1","gene_symbol":"MTND3P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42154]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873186","summary":null,"start":25720099,"end":25720431,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42154]"}, {"versioned_ensembl_gene_id":"ENSG00000248133.1","gene_symbol":"MTND4LP22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42256]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075102","summary":null,"start":25719755,"end":25720030,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42256]"}, {"versioned_ensembl_gene_id":"ENSG00000266953.6","gene_symbol":"AC092073.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":34396315,"end":34409364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108262.15","gene_symbol":"GIT1","gene_name":"GIT ArfGAP 1 [Source:HGNC Symbol;Acc:HGNC:4272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"28964","summary":null,"start":29573469,"end":29594054,"strand":-1,"description":"GIT ArfGAP 1 [Source:HGNC Symbol;Acc:HGNC:4272]"}, {"versioned_ensembl_gene_id":"ENSG00000198711.5","gene_symbol":"SSBP3-AS1","gene_name":"SSBP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32328]","synonyms":"MSTP128,C1orf191","biotype":"antisense_RNA","ncbi_id":"619518","summary":null,"start":54236440,"end":54239063,"strand":1,"description":"SSBP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32328]"}, {"versioned_ensembl_gene_id":"ENSG00000113312.10","gene_symbol":"TTC1","gene_name":"tetratricopeptide repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:12391]","synonyms":"TPR1","biotype":"protein_coding","ncbi_id":"7265","summary":"This gene encodes a protein that belongs to the tetratrico peptide repeat superfamily of proteins. The encoded protein plays a role in protein-protein interactions, and binds to the Galpha subunit of G protein-coupled receptors to activate the Ras signaling pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":160009113,"end":160065543,"strand":1,"description":"tetratricopeptide repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:12391]"}, {"versioned_ensembl_gene_id":"ENSG00000165973.18","gene_symbol":"NELL1","gene_name":"neural EGFL like 1 [Source:HGNC Symbol;Acc:HGNC:7750]","synonyms":"IDH3GL,FLJ45906","biotype":"protein_coding","ncbi_id":"4745","summary":"This gene encodes a cytoplasmic protein that contains epidermal growth factor (EGF)-like repeats. The encoded heterotrimeric protein may be involved in cell growth regulation and differentiation. A similar protein in rodents is involved in craniosynostosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":20669551,"end":21575681,"strand":1,"description":"neural EGFL like 1 [Source:HGNC Symbol;Acc:HGNC:7750]"}, {"versioned_ensembl_gene_id":"ENSG00000196099.4","gene_symbol":"OR6M1","gene_name":"olfactory receptor family 6 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14711]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390261","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123805335,"end":123806387,"strand":-1,"description":"olfactory receptor family 6 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14711]"}, {"versioned_ensembl_gene_id":"ENSG00000267274.1","gene_symbol":"AC008770.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":11939959,"end":11953381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120068.6","gene_symbol":"HOXB8","gene_name":"homeobox B8 [Source:HGNC Symbol;Acc:HGNC:5119]","synonyms":"HOX2D,HOX2","biotype":"protein_coding","ncbi_id":"3218","summary":"This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with colorectal cancer. Mice that have had the murine ortholog of this gene knocked out exhibit an excessive pathologic grooming behavior. This behavior is similar to the behavior of humans suffering from the obsessive-compulsive spectrum disorder trichotillomania. [provided by RefSeq, Jul 2008]","start":48611377,"end":48614939,"strand":-1,"description":"homeobox B8 [Source:HGNC Symbol;Acc:HGNC:5119]"}, {"versioned_ensembl_gene_id":"ENSG00000227962.1","gene_symbol":"AL391994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235336806,"end":235337087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235025.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"RFB30,HERF1,RNF9","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30197074,"end":30206062,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000234442.4","gene_symbol":"BX276092.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71760764,"end":71763075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158457.5","gene_symbol":"TSPAN33","gene_name":"tetraspanin 33 [Source:HGNC Symbol;Acc:HGNC:28743]","synonyms":"Penumbra,MGC50844","biotype":"protein_coding","ncbi_id":"340348","summary":null,"start":129144892,"end":129169697,"strand":1,"description":"tetraspanin 33 [Source:HGNC Symbol;Acc:HGNC:28743]"}, {"versioned_ensembl_gene_id":"ENSG00000261845.2","gene_symbol":"AC124283.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82602989,"end":82604178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101977.19","gene_symbol":"MCF2","gene_name":"MCF.2 cell line derived transforming sequence [Source:HGNC Symbol;Acc:HGNC:6940]","synonyms":"DBL,ARHGEF21","biotype":"protein_coding","ncbi_id":"4168","summary":"The oncogenic protein encoded by this gene is a guanine nucleotide exchange factor (GEF) that exerts control over some members of the Rho family of small GTPases. Several transcript variants encoding different isoforms have been found for this gene. These isoforms exhibit different expression patterns and varying levels of GEF activity.[provided by RefSeq, Jan 2010]","start":139581770,"end":139708227,"strand":-1,"description":"MCF.2 cell line derived transforming sequence [Source:HGNC Symbol;Acc:HGNC:6940]"}, {"versioned_ensembl_gene_id":"ENSG00000120738.7","gene_symbol":"EGR1","gene_name":"early growth response 1 [Source:HGNC Symbol;Acc:HGNC:3238]","synonyms":"ZNF225,ZIF-268,TIS8,NGFI-A,KROX-24,G0S30,AT225","biotype":"protein_coding","ncbi_id":"1958","summary":"The protein encoded by this gene belongs to the EGR family of C2H2-type zinc-finger proteins. It is a nuclear protein and functions as a transcriptional regulator. The products of target genes it activates are required for differentitation and mitogenesis. Studies suggest this is a cancer suppressor gene. [provided by RefSeq, Dec 2014]","start":138465490,"end":138469315,"strand":1,"description":"early growth response 1 [Source:HGNC Symbol;Acc:HGNC:3238]"}, {"versioned_ensembl_gene_id":"ENSG00000215115.6","gene_symbol":"CXorf49","gene_name":"chromosome X open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:30891]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130361","summary":null,"start":71714371,"end":71718151,"strand":-1,"description":"chromosome X open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:30891]"}, {"versioned_ensembl_gene_id":"ENSG00000253638.1","gene_symbol":"AF186190.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133392211,"end":133392690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284601.1","gene_symbol":"AL590440.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":54974900,"end":54980464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237447.1","gene_symbol":"CDC27P2","gene_name":"cell division cycle 27 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38092]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130277","summary":null,"start":10190377,"end":10192298,"strand":-1,"description":"cell division cycle 27 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38092]"}, {"versioned_ensembl_gene_id":"ENSG00000141568.20","gene_symbol":"FOXK2","gene_name":"forkhead box K2 [Source:HGNC Symbol;Acc:HGNC:6036]","synonyms":"ILF1,ILF","biotype":"protein_coding","ncbi_id":"3607","summary":"The protein encoded by this gene contains a fork head DNA binding domain. This protein can bind to the purine-rich motifs of the HIV long terminal repeat (LTR), and to the similar purine-rich motif in the interleukin 2 (IL2) promoter. It may be involved in the regulation of viral and cellular promoter elements. [provided by RefSeq, Jul 2008]","start":82519713,"end":82644662,"strand":1,"description":"forkhead box K2 [Source:HGNC Symbol;Acc:HGNC:6036]"}, {"versioned_ensembl_gene_id":"ENSG00000136802.11","gene_symbol":"LRRC8A","gene_name":"leucine rich repeat containing 8 family member A [Source:HGNC Symbol;Acc:HGNC:19027]","synonyms":"SWELL1,LRRC8,KIAA1437,FLJ10337","biotype":"protein_coding","ncbi_id":"56262","summary":"This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":128882112,"end":128918039,"strand":1,"description":"leucine rich repeat containing 8 family member A [Source:HGNC Symbol;Acc:HGNC:19027]"}, {"versioned_ensembl_gene_id":"ENSG00000283376.1","gene_symbol":"AC011591.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":68691809,"end":68716064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266222.1","gene_symbol":"AC036222.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48377262,"end":48380370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216516.1","gene_symbol":"AL645733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160163539,"end":160163755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256195.2","gene_symbol":"AP002518.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114360635,"end":114380045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141753.6","gene_symbol":"IGFBP4","gene_name":"insulin like growth factor binding protein 4 [Source:HGNC Symbol;Acc:HGNC:5473]","synonyms":"HT29-IGFBP,BP-4,IGFBP-4,IBP4","biotype":"protein_coding","ncbi_id":"3487","summary":"This gene is a member of the insulin-like growth factor binding protein (IGFBP) family and encodes a protein with an IGFBP domain and a thyroglobulin type-I domain. The protein binds both insulin-like growth factors (IGFs) I and II and circulates in the plasma in both glycosylated and non-glycosylated forms. Binding of this protein prolongs the half-life of the IGFs and alters their interaction with cell surface receptors. [provided by RefSeq, Jul 2008]","start":40443461,"end":40457731,"strand":1,"description":"insulin like growth factor binding protein 4 [Source:HGNC Symbol;Acc:HGNC:5473]"}, {"versioned_ensembl_gene_id":"ENSG00000204897.6","gene_symbol":"KRT25","gene_name":"keratin 25 [Source:HGNC Symbol;Acc:HGNC:30839]","synonyms":"KRT25A","biotype":"protein_coding","ncbi_id":"147183","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40748021,"end":40755332,"strand":-1,"description":"keratin 25 [Source:HGNC Symbol;Acc:HGNC:30839]"}, {"versioned_ensembl_gene_id":"ENSG00000255184.1","gene_symbol":"AP004607.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90017611,"end":90024511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278338.4","gene_symbol":"VWA8-AS1","gene_name":"VWA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44270]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507240","summary":null,"start":41955808,"end":41981565,"strand":1,"description":"VWA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44270]"}, {"versioned_ensembl_gene_id":"ENSG00000223546.6","gene_symbol":"LINC00630","gene_name":"long intergenic non-protein coding RNA 630 [Source:HGNC Symbol;Acc:HGNC:44263]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287765","summary":null,"start":102769161,"end":102885406,"strand":1,"description":"long intergenic non-protein coding RNA 630 [Source:HGNC Symbol;Acc:HGNC:44263]"}, {"versioned_ensembl_gene_id":"ENSG00000232282.1","gene_symbol":"MTND1P32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100856881","summary":null,"start":102785667,"end":102786604,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42081]"}, {"versioned_ensembl_gene_id":"ENSG00000235138.1","gene_symbol":"AL445931.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134054290,"end":134058805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280093.1","gene_symbol":"AP002791.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91382909,"end":91383289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250126.1","gene_symbol":"AC116563.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137645265,"end":137655174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251632.1","gene_symbol":"LINC02172","gene_name":"long intergenic non-protein coding RNA 2172 [Source:HGNC Symbol;Acc:HGNC:53034]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377443","summary":null,"start":137545731,"end":137603430,"strand":1,"description":"long intergenic non-protein coding RNA 2172 [Source:HGNC Symbol;Acc:HGNC:53034]"}, {"versioned_ensembl_gene_id":"ENSG00000225826.1","gene_symbol":"LINC00626","gene_name":"long intergenic non-protein coding RNA 626 [Source:HGNC Symbol;Acc:HGNC:44257]","synonyms":"MGC4473","biotype":"lincRNA","ncbi_id":"79100","summary":null,"start":168786939,"end":168792886,"strand":1,"description":"long intergenic non-protein coding RNA 626 [Source:HGNC Symbol;Acc:HGNC:44257]"}, {"versioned_ensembl_gene_id":"ENSG00000230702.1","gene_symbol":"AC107081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61856695,"end":61857055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108946.14","gene_symbol":"PRKAR1A","gene_name":"protein kinase cAMP-dependent type I regulatory subunit alpha [Source:HGNC Symbol;Acc:HGNC:9388]","synonyms":"TSE1,PRKAR1,CNC1","biotype":"protein_coding","ncbi_id":"5573","summary":"cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. This gene encodes one of the regulatory subunits. This protein was found to be a tissue-specific extinguisher that down-regulates the expression of seven liver genes in hepatoma x fibroblast hybrids. Mutations in this gene cause Carney complex (CNC). This gene can fuse to the RET protooncogene by gene rearrangement and form the thyroid tumor-specific chimeric oncogene known as PTC2. A nonconventional nuclear localization sequence (NLS) has been found for this protein which suggests a role in DNA replication via the protein serving as a nuclear transport protein for the second subunit of the Replication Factor C (RFC40). Several alternatively spliced transcript variants encoding two different isoforms have been observed. [provided by RefSeq, Jan 2013]","start":68511780,"end":68551319,"strand":1,"description":"protein kinase cAMP-dependent type I regulatory subunit alpha [Source:HGNC Symbol;Acc:HGNC:9388]"}, {"versioned_ensembl_gene_id":"ENSG00000002919.14","gene_symbol":"SNX11","gene_name":"sorting nexin 11 [Source:HGNC Symbol;Acc:HGNC:14975]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29916","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. This gene encodes a protein of unknown function. This gene results in two transcript variants differing in the 5' UTR, but encoding the same protein. [provided by RefSeq, Jul 2008]","start":48103357,"end":48123074,"strand":1,"description":"sorting nexin 11 [Source:HGNC Symbol;Acc:HGNC:14975]"}, {"versioned_ensembl_gene_id":"ENSG00000159199.13","gene_symbol":"ATP5G1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:841]","synonyms":"ATP5G","biotype":"protein_coding","ncbi_id":"516","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":48892765,"end":48895871,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:841]"}, {"versioned_ensembl_gene_id":"ENSG00000258823.1","gene_symbol":"AL160314.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22723476,"end":22726572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111788.10","gene_symbol":"AC009533.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9277235,"end":9313241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147416.10","gene_symbol":"ATP6V1B2","gene_name":"ATPase H+ transporting V1 subunit B2 [Source:HGNC Symbol;Acc:HGNC:854]","synonyms":"ATP6B2,VPP3,Vma2,VATB,HO57","biotype":"protein_coding","ncbi_id":"526","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A, three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. The protein encoded by this gene is one of two V1 domain B subunit isoforms and is the only B isoform highly expressed in osteoclasts. [provided by RefSeq, Jul 2008]","start":20197367,"end":20226819,"strand":1,"description":"ATPase H+ transporting V1 subunit B2 [Source:HGNC Symbol;Acc:HGNC:854]"}, {"versioned_ensembl_gene_id":"ENSG00000230415.1","gene_symbol":"LINC01786","gene_name":"long intergenic non-protein coding RNA 1786 [Source:HGNC Symbol;Acc:HGNC:52575]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928895","summary":null,"start":1275223,"end":1280420,"strand":1,"description":"long intergenic non-protein coding RNA 1786 [Source:HGNC Symbol;Acc:HGNC:52575]"}, {"versioned_ensembl_gene_id":"ENSG00000255804.2","gene_symbol":"OR6J1","gene_name":"olfactory receptor family 6 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14707]","synonyms":"OR6J2,OR6J1P","biotype":"polymorphic_pseudogene","ncbi_id":"79549","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":22630929,"end":22644352,"strand":-1,"description":"olfactory receptor family 6 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14707]"}, {"versioned_ensembl_gene_id":"ENSG00000265664.1","gene_symbol":"AC005544.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67032409,"end":67033290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259715.1","gene_symbol":"AC022087.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50359450,"end":50360194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203733.5","gene_symbol":"GJE1","gene_name":"gap junction protein epsilon 1 [Source:HGNC Symbol;Acc:HGNC:33251]","synonyms":"CX23","biotype":"protein_coding","ncbi_id":"100126572","summary":null,"start":142133090,"end":142135151,"strand":1,"description":"gap junction protein epsilon 1 [Source:HGNC Symbol;Acc:HGNC:33251]"}, {"versioned_ensembl_gene_id":"ENSG00000224729.5","gene_symbol":"PCOLCE-AS1","gene_name":"PCOLCE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40430]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129845","summary":null,"start":100589402,"end":100604206,"strand":-1,"description":"PCOLCE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40430]"}, {"versioned_ensembl_gene_id":"ENSG00000246067.7","gene_symbol":"RAB30-AS1","gene_name":"RAB30 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48672]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506233","summary":null,"start":83072066,"end":83106719,"strand":1,"description":"RAB30 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48672]"}, {"versioned_ensembl_gene_id":"ENSG00000180613.10","gene_symbol":"GSX2","gene_name":"GS homeobox 2 [Source:HGNC Symbol;Acc:HGNC:24959]","synonyms":"Gsh2","biotype":"protein_coding","ncbi_id":"170825","summary":null,"start":54099523,"end":54102505,"strand":1,"description":"GS homeobox 2 [Source:HGNC Symbol;Acc:HGNC:24959]"}, {"versioned_ensembl_gene_id":"ENSG00000255503.1","gene_symbol":"AP001767.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83072402,"end":83097196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183122.5","gene_symbol":"OR2A3P","gene_name":"olfactory receptor family 2 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8231]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"202861","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144153486,"end":144158905,"strand":1,"description":"olfactory receptor family 2 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8231]"}, {"versioned_ensembl_gene_id":"ENSG00000221938.5","gene_symbol":"OR2A14","gene_name":"olfactory receptor family 2 subfamily A member 14 [Source:HGNC Symbol;Acc:HGNC:15084]","synonyms":"OST182,OR2A6,OR2A14P","biotype":"protein_coding","ncbi_id":"135941","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144123176,"end":144131188,"strand":1,"description":"olfactory receptor family 2 subfamily A member 14 [Source:HGNC Symbol;Acc:HGNC:15084]"}, {"versioned_ensembl_gene_id":"ENSG00000243303.1","gene_symbol":"AC103987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21854640,"end":21854987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277426.1","gene_symbol":"AC006441.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39023394,"end":39026742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136930.12","gene_symbol":"PSMB7","gene_name":"proteasome subunit beta 7 [Source:HGNC Symbol;Acc:HGNC:9544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5695","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. The encoded protein is a member of the proteasome B-type family, also known as the T1B family, and is a 20S core beta subunit in the proteasome. Expression of this catalytic subunit is downregulated by gamma interferon, and proteolytic processing is required to generate a mature subunit. A pseudogene of this gene is located on the long arm of chromosome 14. [provided by RefSeq, Jul 2012]","start":124353466,"end":124415444,"strand":-1,"description":"proteasome subunit beta 7 [Source:HGNC Symbol;Acc:HGNC:9544]"}, {"versioned_ensembl_gene_id":"ENSG00000002834.17","gene_symbol":"LASP1","gene_name":"LIM and SH3 protein 1 [Source:HGNC Symbol;Acc:HGNC:6513]","synonyms":"MLN50,Lasp-1","biotype":"protein_coding","ncbi_id":"3927","summary":"This gene encodes a member of a subfamily of LIM proteins, characterized by a LIM motif and a domain of Src homology region 3, and also a member of the nebulin family of actin-binding proteins. The encoded protein is a cAMP and cGMP dependent signaling protein and binds to the actin cytoskeleton at extensions of the cell membrane. The encoded protein has been linked to metastatic breast cancer, hematopoetic tumors such as B-cell lymphomas, and colorectal cancer. [provided by RefSeq, Oct 2012]","start":38869859,"end":38921770,"strand":1,"description":"LIM and SH3 protein 1 [Source:HGNC Symbol;Acc:HGNC:6513]"}, {"versioned_ensembl_gene_id":"ENSG00000235128.1","gene_symbol":"AC013474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126679622,"end":126680420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234397.3","gene_symbol":"AL591122.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22322840,"end":22323331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253422.1","gene_symbol":"AC008677.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158078099,"end":158078764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223427.1","gene_symbol":"AC016716.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80162428,"end":80163135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213414.3","gene_symbol":"AC008677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157986146,"end":157987706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188001.9","gene_symbol":"TPRG1","gene_name":"tumor protein p63 regulated 1 [Source:HGNC Symbol;Acc:HGNC:24759]","synonyms":"FAM79B,FLJ43694,FLJ41238","biotype":"protein_coding","ncbi_id":"285386","summary":null,"start":188947214,"end":189325304,"strand":1,"description":"tumor protein p63 regulated 1 [Source:HGNC Symbol;Acc:HGNC:24759]"}, {"versioned_ensembl_gene_id":"ENSG00000236182.1","gene_symbol":"AC009319.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188989382,"end":188990135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143155.12","gene_symbol":"TIPRL","gene_name":"TOR signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:30231]","synonyms":"TIPRL1,TIP41,MGC3794,dJ69E11.3","biotype":"protein_coding","ncbi_id":"261726","summary":"TIPRL is an inhibitory regulator of protein phosphatase-2A (PP2A) (see PPP2CA; MIM 176915), PP4 (see PPP4C; MIM 602035), and PP6 (see PPP6C; MIM 612725) (McConnell et al., 2007 [PubMed 17384681]).[supplied by OMIM, Nov 2010]","start":168178933,"end":168202114,"strand":1,"description":"TOR signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:30231]"}, {"versioned_ensembl_gene_id":"ENSG00000258830.1","gene_symbol":"AC137834.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57249609,"end":57296484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282760.1","gene_symbol":"TRBV12-1","gene_name":"T-cell receptor beta variable 12-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12183]","synonyms":"TCRBV8S4P,TCRBV12S1,TRBV121","biotype":"TR_V_pseudogene","ncbi_id":"28579","summary":null,"start":142436931,"end":142437373,"strand":1,"description":"T-cell receptor beta variable 12-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12183]"}, {"versioned_ensembl_gene_id":"ENSG00000249840.2","gene_symbol":"GAPDHP76","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:50649]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287725","summary":null,"start":11585246,"end":11587135,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:50649]"}, {"versioned_ensembl_gene_id":"ENSG00000242255.1","gene_symbol":"RPL39P34","gene_name":"ribosomal protein L39 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36528]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100271523","summary":null,"start":52564076,"end":52564231,"strand":1,"description":"ribosomal protein L39 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36528]"}, {"versioned_ensembl_gene_id":"ENSG00000145425.9","gene_symbol":"RPS3A","gene_name":"ribosomal protein S3A [Source:HGNC Symbol;Acc:HGNC:10421]","synonyms":"S3A,MFTL","biotype":"protein_coding","ncbi_id":"6189","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S3AE family of ribosomal proteins. It is located in the cytoplasm. Disruption of the gene encoding rat ribosomal protein S3a, also named v-fos transformation effector protein, in v-fos-transformed rat cells results in reversion of the transformed phenotype. This gene is co-transcribed with the U73A and U73B small nucleolar RNA genes, which are located in its fourth and third introns, respectively. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]","start":151099573,"end":151104652,"strand":1,"description":"ribosomal protein S3A [Source:HGNC Symbol;Acc:HGNC:10421]"}, {"versioned_ensembl_gene_id":"ENSG00000226497.1","gene_symbol":"LINC02549","gene_name":"long intergenic non-protein coding RNA 2549 [Source:HGNC Symbol;Acc:HGNC:53584]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928280","summary":null,"start":68226972,"end":68329899,"strand":-1,"description":"long intergenic non-protein coding RNA 2549 [Source:HGNC Symbol;Acc:HGNC:53584]"}, {"versioned_ensembl_gene_id":"ENSG00000229385.1","gene_symbol":"AC010975.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79493716,"end":79500844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250350.1","gene_symbol":"AC104819.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151279030,"end":151279192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230237.1","gene_symbol":"AC010975.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79573764,"end":79575593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224023.10","gene_symbol":"FLJ37035","gene_name":"uncharacterized LOC399821 [Source:NCBI gene;Acc:399821]","synonyms":null,"biotype":"lincRNA","ncbi_id":"399821","summary":null,"start":125700436,"end":125719566,"strand":-1,"description":"uncharacterized LOC399821 [Source:NCBI gene;Acc:399821]"}, {"versioned_ensembl_gene_id":"ENSG00000162337.11","gene_symbol":"LRP5","gene_name":"LDL receptor related protein 5 [Source:HGNC Symbol;Acc:HGNC:6697]","synonyms":"EVR4,EVR1,BMND1,VBCH2,OPTA1,OPS,OPPG,LRP7,LR3,HBM","biotype":"protein_coding","ncbi_id":"4041","summary":"This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":68312609,"end":68449275,"strand":1,"description":"LDL receptor related protein 5 [Source:HGNC Symbol;Acc:HGNC:6697]"}, {"versioned_ensembl_gene_id":"ENSG00000276033.4","gene_symbol":"KIR3DX1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]","synonyms":"FLJ00060,LENG12","biotype":"protein_coding","ncbi_id":"90011","summary":null,"start":54463149,"end":54476118,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]"}, {"versioned_ensembl_gene_id":"ENSG00000253541.1","gene_symbol":"SEPT10P1","gene_name":"septin 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:40018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389662","summary":null,"start":56476826,"end":56477987,"strand":-1,"description":"septin 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:40018]"}, {"versioned_ensembl_gene_id":"ENSG00000230408.3","gene_symbol":"AC007163.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":200780495,"end":200812170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203805.10","gene_symbol":"PLPP4","gene_name":"phospholipid phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:23531]","synonyms":"PPAPDC1A,PPAPDC1,DPPL2","biotype":"protein_coding","ncbi_id":"196051","summary":null,"start":120456954,"end":120589855,"strand":1,"description":"phospholipid phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:23531]"}, {"versioned_ensembl_gene_id":"ENSG00000127585.11","gene_symbol":"FBXL16","gene_name":"F-box and leucine rich repeat protein 16 [Source:HGNC Symbol;Acc:HGNC:14150]","synonyms":"MGC33974,Fbl16,C16orf22","biotype":"protein_coding","ncbi_id":"146330","summary":"Members of the F-box protein family, such as FBXL16, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":692498,"end":705829,"strand":-1,"description":"F-box and leucine rich repeat protein 16 [Source:HGNC Symbol;Acc:HGNC:14150]"}, {"versioned_ensembl_gene_id":"ENSG00000211886.1","gene_symbol":"TRAJ3","gene_name":"T-cell receptor alpha joining 3 [Source:HGNC Symbol;Acc:HGNC:12059]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28752","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22543179,"end":22543240,"strand":1,"description":"T-cell receptor alpha joining 3 [Source:HGNC Symbol;Acc:HGNC:12059]"}, {"versioned_ensembl_gene_id":"ENSG00000283428.1","gene_symbol":"CCDC195","gene_name":"coiled-coil domain containing 195 [Source:HGNC Symbol;Acc:HGNC:53441]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":224703764,"end":224716365,"strand":-1,"description":"coiled-coil domain containing 195 [Source:HGNC Symbol;Acc:HGNC:53441]"}, {"versioned_ensembl_gene_id":"ENSG00000231491.2","gene_symbol":"JKAMPP1","gene_name":"JNK1/MAPK8-associated membrane protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49759]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100049717","summary":null,"start":12287320,"end":12288238,"strand":1,"description":"JNK1/MAPK8-associated membrane protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49759]"}, {"versioned_ensembl_gene_id":"ENSG00000251440.2","gene_symbol":"STMN1P2","gene_name":"stathmin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44063]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289663","summary":null,"start":137425426,"end":137425864,"strand":-1,"description":"stathmin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44063]"}, {"versioned_ensembl_gene_id":"ENSG00000211884.1","gene_symbol":"TRAJ5","gene_name":"T-cell receptor alpha joining 5 [Source:HGNC Symbol;Acc:HGNC:12081]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28750","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22540247,"end":22540306,"strand":1,"description":"T-cell receptor alpha joining 5 [Source:HGNC Symbol;Acc:HGNC:12081]"}, {"versioned_ensembl_gene_id":"ENSG00000211883.1","gene_symbol":"TRAJ6","gene_name":"T-cell receptor alpha joining 6 [Source:HGNC Symbol;Acc:HGNC:12092]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28749","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22539073,"end":22539134,"strand":1,"description":"T-cell receptor alpha joining 6 [Source:HGNC Symbol;Acc:HGNC:12092]"}, {"versioned_ensembl_gene_id":"ENSG00000224342.1","gene_symbol":"AC007879.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207173634,"end":207222790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180230.6","gene_symbol":"NACAP2","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49489]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651144","summary":null,"start":119997086,"end":119997709,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49489]"}, {"versioned_ensembl_gene_id":"ENSG00000282493.1","gene_symbol":"AC100810.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1757770,"end":1760009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211872.1","gene_symbol":"TRAJ17","gene_name":"T-cell receptor alpha joining 17 [Source:HGNC Symbol;Acc:HGNC:12045]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28738","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22526844,"end":22526906,"strand":1,"description":"T-cell receptor alpha joining 17 [Source:HGNC Symbol;Acc:HGNC:12045]"}, {"versioned_ensembl_gene_id":"ENSG00000129116.17","gene_symbol":"PALLD","gene_name":"palladin, cytoskeletal associated protein [Source:HGNC Symbol;Acc:HGNC:17068]","synonyms":"SIH002,KIAA0992,CGI-151","biotype":"protein_coding","ncbi_id":"23022","summary":"This gene encodes a cytoskeletal protein that is required for organizing the actin cytoskeleton. The protein is a component of actin-containing microfilaments, and it is involved in the control of cell shape, adhesion, and contraction. Polymorphisms in this gene are associated with a susceptibility to pancreatic cancer type 1, and also with a risk for myocardial infarction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":168497066,"end":168928457,"strand":1,"description":"palladin, cytoskeletal associated protein [Source:HGNC Symbol;Acc:HGNC:17068]"}, {"versioned_ensembl_gene_id":"ENSG00000166922.8","gene_symbol":"SCG5","gene_name":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]","synonyms":"7B2,SgV,SGNE1,7B2,SgV,SGNE1","biotype":"protein_coding","ncbi_id":"6447","summary":"This gene encodes a secreted chaperone protein that prevents the aggregation of other secreted proteins, including proteins that are associated with neurodegenerative and metabolic disease. The encoded protein may be best known for its role in the trafficking and activation of prohormone convertase PC2 (encoded by Gene ID: 5126). Phosphorylation of the encoded protein has been shown to have an inhibitory effect on its chaperone function. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32641676,"end":32697098,"strand":1,"description":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]"}, {"versioned_ensembl_gene_id":"ENSG00000162552.14","gene_symbol":"WNT4","gene_name":"Wnt family member 4 [Source:HGNC Symbol;Acc:HGNC:12783]","synonyms":"WNT-4","biotype":"protein_coding","ncbi_id":"54361","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family, and is the first signaling molecule shown to influence the sex-determination cascade. It encodes a protein which shows 98% amino acid identity to the Wnt4 protein of mouse and rat. This gene and a nuclear receptor known to antagonize the testis-determining factor play a concerted role in both the control of female development and the prevention of testes formation. This gene and another two family members, WNT2 and WNT7B, may be associated with abnormal proliferation in breast tissue. Mutations in this gene can result in Rokitansky-Kuster-Hauser syndrome and in SERKAL syndrome. [provided by RefSeq, Jul 2008]","start":22117305,"end":22143969,"strand":-1,"description":"Wnt family member 4 [Source:HGNC Symbol;Acc:HGNC:12783]"}, {"versioned_ensembl_gene_id":"ENSG00000211861.1","gene_symbol":"TRAJ28","gene_name":"T-cell receptor alpha joining 28 [Source:HGNC Symbol;Acc:HGNC:12057]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28727","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22515623,"end":22515688,"strand":1,"description":"T-cell receptor alpha joining 28 [Source:HGNC Symbol;Acc:HGNC:12057]"}, {"versioned_ensembl_gene_id":"ENSG00000249875.1","gene_symbol":"AC116616.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174354854,"end":174376445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268289.1","gene_symbol":"AC020908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17051994,"end":17055087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104044.15","gene_symbol":"OCA2","gene_name":"OCA2 melanosomal transmembrane protein [Source:HGNC Symbol;Acc:HGNC:8101]","synonyms":"EYCL,D15S12,BEY2,BEY1,BEY,P,EYCL3,EYCL2","biotype":"protein_coding","ncbi_id":"4948","summary":"This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":27754875,"end":28099358,"strand":-1,"description":"OCA2 melanosomal transmembrane protein [Source:HGNC Symbol;Acc:HGNC:8101]"}, {"versioned_ensembl_gene_id":"ENSG00000103852.12","gene_symbol":"TTC23","gene_name":"tetratricopeptide repeat domain 23 [Source:HGNC Symbol;Acc:HGNC:25730]","synonyms":"HCC-8,FLJ12572","biotype":"protein_coding","ncbi_id":"64927","summary":null,"start":99136323,"end":99251223,"strand":-1,"description":"tetratricopeptide repeat domain 23 [Source:HGNC Symbol;Acc:HGNC:25730]"}, {"versioned_ensembl_gene_id":"ENSG00000214297.3","gene_symbol":"ALDOAP2","gene_name":"aldolase, fructose-bisphosphate A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:416]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"228","summary":null,"start":125666875,"end":125667950,"strand":-1,"description":"aldolase, fructose-bisphosphate A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:416]"}, {"versioned_ensembl_gene_id":"ENSG00000211856.1","gene_symbol":"TRAJ33","gene_name":"T-cell receptor alpha joining 33 [Source:HGNC Symbol;Acc:HGNC:12063]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28722","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22508602,"end":22508658,"strand":1,"description":"T-cell receptor alpha joining 33 [Source:HGNC Symbol;Acc:HGNC:12063]"}, {"versioned_ensembl_gene_id":"ENSG00000255295.1","gene_symbol":"AP002404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89498748,"end":89499198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261078.1","gene_symbol":"AC009118.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58382989,"end":58383798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012124.16","gene_symbol":"CD22","gene_name":"CD22 molecule [Source:HGNC Symbol;Acc:HGNC:1643]","synonyms":"SIGLEC2,SIGLEC-2","biotype":"protein_coding","ncbi_id":"933","summary":null,"start":35319261,"end":35347355,"strand":1,"description":"CD22 molecule [Source:HGNC Symbol;Acc:HGNC:1643]"}, {"versioned_ensembl_gene_id":"ENSG00000132718.8","gene_symbol":"SYT11","gene_name":"synaptotagmin 11 [Source:HGNC Symbol;Acc:HGNC:19239]","synonyms":"MGC17226,MGC10881,KIAA0080,DKFZp781D015","biotype":"protein_coding","ncbi_id":"23208","summary":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that are known calcium sensors and mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. The encoded protein is also a substrate for ubiquitin-E3-ligase parkin. The gene has previously been referred to as synaptotagmin XII but has been renamed synaptotagmin XI to be consistent with mouse and rat official nomenclature. [provided by RefSeq, Apr 2010]","start":155859509,"end":155885199,"strand":1,"description":"synaptotagmin 11 [Source:HGNC Symbol;Acc:HGNC:19239]"}, {"versioned_ensembl_gene_id":"ENSG00000183260.7","gene_symbol":"ABHD16B","gene_name":"abhydrolase domain containing 16B [Source:HGNC Symbol;Acc:HGNC:16128]","synonyms":"dJ591C20.1,C20orf135","biotype":"protein_coding","ncbi_id":"140701","summary":null,"start":63861498,"end":63862988,"strand":1,"description":"abhydrolase domain containing 16B [Source:HGNC Symbol;Acc:HGNC:16128]"}, {"versioned_ensembl_gene_id":"ENSG00000206140.10","gene_symbol":"TMEM191C","gene_name":"transmembrane protein 191C [Source:HGNC Symbol;Acc:HGNC:33601]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645426","summary":null,"start":21466423,"end":21471269,"strand":1,"description":"transmembrane protein 191C [Source:HGNC Symbol;Acc:HGNC:33601]"}, {"versioned_ensembl_gene_id":"ENSG00000217684.2","gene_symbol":"RPS3AP24","gene_name":"ribosomal protein S3a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36267]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271253","summary":null,"start":140761529,"end":140762262,"strand":1,"description":"ribosomal protein S3a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36267]"}, {"versioned_ensembl_gene_id":"ENSG00000236031.1","gene_symbol":"AL591721.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":243545532,"end":243548329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269814.1","gene_symbol":"AC008403.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48513207,"end":48513660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108825.17","gene_symbol":"PTGES3L-AARSD1","gene_name":"PTGES3L-AARSD1 readthrough [Source:HGNC Symbol;Acc:HGNC:43946]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100885850","summary":"This locus represents naturally occurring readthrough transcription between the neighboring PTGES3L (prostaglandin E synthase 3 (cytosolic)-like) and AARSD1(alanyl-tRNA synthetase domain containing 1) genes on chromosome 17. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, May 2012]","start":42950526,"end":42980528,"strand":-1,"description":"PTGES3L-AARSD1 readthrough [Source:HGNC Symbol;Acc:HGNC:43946]"}, {"versioned_ensembl_gene_id":"ENSG00000211837.1","gene_symbol":"TRAJ53","gene_name":"T-cell receptor alpha joining 53 [Source:HGNC Symbol;Acc:HGNC:12085]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28702","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22483004,"end":22483069,"strand":1,"description":"T-cell receptor alpha joining 53 [Source:HGNC Symbol;Acc:HGNC:12085]"}, {"versioned_ensembl_gene_id":"ENSG00000104419.14","gene_symbol":"NDRG1","gene_name":"N-myc downstream regulated 1 [Source:HGNC Symbol;Acc:HGNC:7679]","synonyms":"TDD5,RTP,NDR1,DRG1,CAP43","biotype":"protein_coding","ncbi_id":"10397","summary":"This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. The encoded protein is necessary for p53-mediated caspase activation and apoptosis. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4D, and expression of this gene may be a prognostic indicator for several types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":133237171,"end":133302022,"strand":-1,"description":"N-myc downstream regulated 1 [Source:HGNC Symbol;Acc:HGNC:7679]"}, {"versioned_ensembl_gene_id":"ENSG00000254277.1","gene_symbol":"AC009446.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71675300,"end":71702786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235962.5","gene_symbol":"RPL7AP53","gene_name":"ribosomal protein L7a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36392]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401640","summary":null,"start":33057615,"end":33058407,"strand":-1,"description":"ribosomal protein L7a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36392]"}, {"versioned_ensembl_gene_id":"ENSG00000127955.15","gene_symbol":"GNAI1","gene_name":"G protein subunit alpha i1 [Source:HGNC Symbol;Acc:HGNC:4384]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2770","summary":"Guanine nucleotide binding proteins are heterotrimeric signal-transducing molecules consisting of alpha, beta, and gamma subunits. The alpha subunit binds guanine nucleotide, can hydrolyze GTP, and can interact with other proteins. The protein encoded by this gene represents the alpha subunit of an inhibitory complex. The encoded protein is part of a complex that responds to beta-adrenergic signals by inhibiting adenylate cyclase. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":80133955,"end":80219402,"strand":1,"description":"G protein subunit alpha i1 [Source:HGNC Symbol;Acc:HGNC:4384]"}, {"versioned_ensembl_gene_id":"ENSG00000235077.1","gene_symbol":"AC073842.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100130964,"end":100140439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229496.10","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"D6S81E,BAT1,UAP56","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31606569,"end":31622924,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000211812.1","gene_symbol":"TRAV26-2","gene_name":"T-cell receptor alpha variable 26-2 [Source:HGNC Symbol;Acc:HGNC:12124]","synonyms":"TRAV262,TCRAV4S1,TCRAV26S2","biotype":"TR_V_gene","ncbi_id":"28656","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22202583,"end":22203368,"strand":1,"description":"T-cell receptor alpha variable 26-2 [Source:HGNC Symbol;Acc:HGNC:12124]"}, {"versioned_ensembl_gene_id":"ENSG00000254859.1","gene_symbol":"AC067930.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143541973,"end":143549729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166401.14","gene_symbol":"SERPINB8","gene_name":"serpin family B member 8 [Source:HGNC Symbol;Acc:HGNC:8952]","synonyms":"PI8,CAP2","biotype":"protein_coding","ncbi_id":"5271","summary":"The protein encoded by this gene is a member of the ov-serpin family of serine protease inhibitors. The encoded protein is produced by platelets and can bind to and inhibit the function of furin, a serine protease involved in platelet functions. In addition, this protein has been found to enhance the mechanical stability of cell-cell adhesion in the skin, and defects in this gene have been associated with an autosomal-recessive form of exfoliative ichthyosis. [provided by RefSeq, Jan 2017]","start":63969925,"end":64019779,"strand":1,"description":"serpin family B member 8 [Source:HGNC Symbol;Acc:HGNC:8952]"}, {"versioned_ensembl_gene_id":"ENSG00000176563.9","gene_symbol":"CNTD1","gene_name":"cyclin N-terminal domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26847]","synonyms":"FLJ40137,CNTD","biotype":"protein_coding","ncbi_id":"124817","summary":null,"start":42798792,"end":42811587,"strand":1,"description":"cyclin N-terminal domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26847]"}, {"versioned_ensembl_gene_id":"ENSG00000176986.15","gene_symbol":"SEC24C","gene_name":"SEC24 homolog C, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10705]","synonyms":"KIAA0079","biotype":"protein_coding","ncbi_id":"9632","summary":"The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec24p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The product of this gene may play a role in shaping the vesicle, as well as in cargo selection and concentration. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":73744384,"end":73772161,"strand":1,"description":"SEC24 homolog C, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10705]"}, {"versioned_ensembl_gene_id":"ENSG00000090975.12","gene_symbol":"PITPNM2","gene_name":"phosphatidylinositol transfer protein membrane associated 2 [Source:HGNC Symbol;Acc:HGNC:21044]","synonyms":"RDGBA2,RDGB2,NIR3","biotype":"protein_coding","ncbi_id":"57605","summary":"PITPNM2 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]","start":122983480,"end":123150015,"strand":-1,"description":"phosphatidylinositol transfer protein membrane associated 2 [Source:HGNC Symbol;Acc:HGNC:21044]"}, {"versioned_ensembl_gene_id":"ENSG00000255239.1","gene_symbol":"TREHP1","gene_name":"trehalase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51907]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"768086","summary":null,"start":118688039,"end":118690600,"strand":-1,"description":"trehalase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51907]"}, {"versioned_ensembl_gene_id":"ENSG00000128272.14","gene_symbol":"ATF4","gene_name":"activating transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:786]","synonyms":"TXREB,TAXREB67,CREB-2","biotype":"protein_coding","ncbi_id":"468","summary":"This gene encodes a transcription factor that was originally identified as a widely expressed mammalian DNA binding protein that could bind a tax-responsive enhancer element in the LTR of HTLV-1. The encoded protein was also isolated and characterized as the cAMP-response element binding protein 2 (CREB-2). The protein encoded by this gene belongs to a family of DNA-binding proteins that includes the AP-1 family of transcription factors, cAMP-response element binding proteins (CREBs) and CREB-like proteins. These transcription factors share a leucine zipper region that is involved in protein-protein interactions, located C-terminal to a stretch of basic amino acids that functions as a DNA binding domain. Two alternative transcripts encoding the same protein have been described. Two pseudogenes are located on the X chromosome at q28 in a region containing a large inverted duplication. [provided by RefSeq, Sep 2011]","start":39519695,"end":39522685,"strand":1,"description":"activating transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:786]"}, {"versioned_ensembl_gene_id":"ENSG00000270808.1","gene_symbol":"AC022400.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73740538,"end":73740823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108592.16","gene_symbol":"FTSJ3","gene_name":"FtsJ homolog 3 [Source:HGNC Symbol;Acc:HGNC:17136]","synonyms":"SPB1","biotype":"protein_coding","ncbi_id":"117246","summary":"Although the function of this gene is not known, the existence of this gene is supported by mRNA and EST data. A possible function of the encoded protein can be inferred from amino acid sequence similarity to the E.coli FtsJ protein and to a mouse protein possibly involved in embryogenesis. [provided by RefSeq, Jul 2008]","start":63819433,"end":63830012,"strand":-1,"description":"FtsJ homolog 3 [Source:HGNC Symbol;Acc:HGNC:17136]"}, {"versioned_ensembl_gene_id":"ENSG00000271321.1","gene_symbol":"CTAGE6","gene_name":"CTAGE family member 6 [Source:HGNC Symbol;Acc:HGNC:28644]","synonyms":"MGC41943,CTAGE6P","biotype":"protein_coding","ncbi_id":"340307","summary":null,"start":143755089,"end":143757696,"strand":-1,"description":"CTAGE family member 6 [Source:HGNC Symbol;Acc:HGNC:28644]"}, {"versioned_ensembl_gene_id":"ENSG00000274270.1","gene_symbol":"AL137060.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50125816,"end":50128463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279162.1","gene_symbol":"AC141586.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2592514,"end":2594563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261140.1","gene_symbol":"AC093525.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2569043,"end":2571936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100567.12","gene_symbol":"PSMA3","gene_name":"proteasome subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:9532]","synonyms":"HC8","biotype":"protein_coding","ncbi_id":"5684","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. Two alternative transcripts encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":58244831,"end":58272012,"strand":1,"description":"proteasome subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:9532]"}, {"versioned_ensembl_gene_id":"ENSG00000258682.1","gene_symbol":"AL132989.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":58264662,"end":58269681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260296.1","gene_symbol":"AC095057.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":40166675,"end":40167831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230941.1","gene_symbol":"AC002386.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109322320,"end":109326315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279043.1","gene_symbol":"AC004014.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108900105,"end":108905226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232164.1","gene_symbol":"LINC01873","gene_name":"long intergenic non-protein coding RNA 1873 [Source:HGNC Symbol;Acc:HGNC:52692]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729348","summary":null,"start":66383306,"end":66392450,"strand":1,"description":"long intergenic non-protein coding RNA 1873 [Source:HGNC Symbol;Acc:HGNC:52692]"}, {"versioned_ensembl_gene_id":"ENSG00000243378.1","gene_symbol":"AC083801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182691928,"end":182692285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262681.2","gene_symbol":"AC005722.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19719059,"end":19722428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131467.10","gene_symbol":"PSME3","gene_name":"proteasome activator subunit 3 [Source:HGNC Symbol;Acc:HGNC:9570]","synonyms":"REG-GAMMA,PA28G,PA28-gamma,Ki","biotype":"protein_coding","ncbi_id":"10197","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. The immunoproteasome contains an alternate regulator, referred to as the 11S regulator or PA28, that replaces the 19S regulator. Three subunits (alpha, beta and gamma) of the 11S regulator have been identified. This gene encodes the gamma subunit of the 11S regulator. Six gamma subunits combine to form a homohexameric ring. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":42824385,"end":42843758,"strand":1,"description":"proteasome activator subunit 3 [Source:HGNC Symbol;Acc:HGNC:9570]"}, {"versioned_ensembl_gene_id":"ENSG00000274699.4","gene_symbol":"TAS2R30","gene_name":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]","synonyms":"TAS2R47,T2R30","biotype":"protein_coding","ncbi_id":"259293","summary":null,"start":11129613,"end":11130572,"strand":-1,"description":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]"}, {"versioned_ensembl_gene_id":"ENSG00000282256.1","gene_symbol":"TAS2R31","gene_name":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]","synonyms":"TAS2R44,T2R53,T2R31","biotype":"protein_coding","ncbi_id":"259290","summary":"TAS2R44 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11030686,"end":11031706,"strand":-1,"description":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]"}, {"versioned_ensembl_gene_id":"ENSG00000278111.4","gene_symbol":"TAS2R46","gene_name":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]","synonyms":"T2R54","biotype":"protein_coding","ncbi_id":"259292","summary":"TAS2R46 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Sep 2009]","start":11063523,"end":11064452,"strand":-1,"description":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]"}, {"versioned_ensembl_gene_id":"ENSG00000188227.12","gene_symbol":"ZNF793","gene_name":"zinc finger protein 793 [Source:HGNC Symbol;Acc:HGNC:33115]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390927","summary":null,"start":37506939,"end":37548762,"strand":1,"description":"zinc finger protein 793 [Source:HGNC Symbol;Acc:HGNC:33115]"}, {"versioned_ensembl_gene_id":"ENSG00000283162.1","gene_symbol":"AL390726.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38433696,"end":38543880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205794.4","gene_symbol":"AC098591.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":40042917,"end":40057199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178752.15","gene_symbol":"ERFE","gene_name":"erythroferrone [Source:HGNC Symbol;Acc:HGNC:26727]","synonyms":"FLJ37034,FAM132B,CTRP15,C1QTNF15","biotype":"protein_coding","ncbi_id":"151176","summary":null,"start":238158982,"end":238168900,"strand":1,"description":"erythroferrone [Source:HGNC Symbol;Acc:HGNC:26727]"}, {"versioned_ensembl_gene_id":"ENSG00000270820.5","gene_symbol":"AC016727.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61471188,"end":61484130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243220.1","gene_symbol":"AC006159.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116563594,"end":116571234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254227.1","gene_symbol":"AC024681.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125998994,"end":126001001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268711.1","gene_symbol":"AC008750.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51426347,"end":51426668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258593.2","gene_symbol":"AL583810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104857792,"end":104858836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282014.1","gene_symbol":"TRBV4-1","gene_name":"T-cell receptor beta variable 4-1 [Source:HGNC Symbol;Acc:HGNC:12215]","synonyms":"TCRBV4S1,BV07S1J2.7,TRBV41,TCRBV7S1A1N2T","biotype":"TR_V_gene","ncbi_id":"28617","summary":null,"start":142313207,"end":142313689,"strand":1,"description":"T-cell receptor beta variable 4-1 [Source:HGNC Symbol;Acc:HGNC:12215]"}, {"versioned_ensembl_gene_id":"ENSG00000228589.3","gene_symbol":"SPCS2P4","gene_name":"signal peptidase complex subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45237]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653566","summary":null,"start":28095742,"end":28096422,"strand":-1,"description":"signal peptidase complex subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45237]"}, {"versioned_ensembl_gene_id":"ENSG00000234203.1","gene_symbol":"AC004771.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4972851,"end":4974681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224004.2","gene_symbol":"ATP5C1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:834]","synonyms":"ATP5CL2,ATP5C2","biotype":"processed_pseudogene","ncbi_id":"645560","summary":null,"start":53991101,"end":53991995,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:834]"}, {"versioned_ensembl_gene_id":"ENSG00000261970.1","gene_symbol":"AL391840.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79552794,"end":79553160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186687.15","gene_symbol":"LYRM7","gene_name":"LYR motif containing 7 [Source:HGNC Symbol;Acc:HGNC:28072]","synonyms":"MZM1L,FLJ20796,C5orf31","biotype":"protein_coding","ncbi_id":"90624","summary":"Inner mitochondrial membrane complex III (CIII) is the main enzyme complex in the mitochondrial respiratory chain, and Rieske Fe-S protein (UQCRFS1) is the last catalytic subunit added to the complex. The protein encoded by this gene is a nuclear-encoded mitochondrial matrix protein that stabilizes UQCRFS1 and chaperones it to the CIII complex. Defects in this gene are a cause of mitochondrial complex III deficiency, nuclear type 8. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":131170810,"end":131205426,"strand":1,"description":"LYR motif containing 7 [Source:HGNC Symbol;Acc:HGNC:28072]"}, {"versioned_ensembl_gene_id":"ENSG00000228209.1","gene_symbol":"AC073091.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76258034,"end":76258897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100335.13","gene_symbol":"MIEF1","gene_name":"mitochondrial elongation factor 1 [Source:HGNC Symbol;Acc:HGNC:25979]","synonyms":"SMCR7L,MiD51,FLJ20232","biotype":"protein_coding","ncbi_id":"54471","summary":null,"start":39499432,"end":39518132,"strand":1,"description":"mitochondrial elongation factor 1 [Source:HGNC Symbol;Acc:HGNC:25979]"}, {"versioned_ensembl_gene_id":"ENSG00000226950.6","gene_symbol":"DANCR","gene_name":"differentiation antagonizing non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:28964]","synonyms":"SNHG13,lncRNA-ANCR,KIAA0114,ANCR,AGU2","biotype":"processed_transcript","ncbi_id":"57291","summary":"This gene produces a long non-coding RNA that functions as a negative regulator of cell differentiation. This transcript associates with enhancer of zeste homolog 2 to repress expression of the runt related transcription factor 2 gene. Increased expression of this transcript may be associated with cancer. Alternatively spliced transcript variants have been observed. [provided by RefSeq, Dec 2016]","start":52712404,"end":52720351,"strand":1,"description":"differentiation antagonizing non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:28964]"}, {"versioned_ensembl_gene_id":"ENSG00000227157.1","gene_symbol":"AC068535.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104411201,"end":104415612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260165.1","gene_symbol":"AC105036.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75480661,"end":75480836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271816.1","gene_symbol":"BMS1P4","gene_name":"BMS1, ribosome biogenesis factor pseudogene 4 [Source:NCBI gene;Acc:729096]","synonyms":"OTTHUMG00000018478,BMS1LP4,BMS1LP4","biotype":"processed_transcript","ncbi_id":"729096","summary":null,"start":73699151,"end":73730487,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 4 [Source:NCBI gene;Acc:729096]"}, {"versioned_ensembl_gene_id":"ENSG00000260235.1","gene_symbol":"AC105020.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75624793,"end":75625690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237801.6","gene_symbol":"AMD1P2","gene_name":"adenosylmethionine decarboxylase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:460]","synonyms":"AMDPY,AMDPX,AMDP1,AMD2,AMD","biotype":"processed_pseudogene","ncbi_id":"263","summary":null,"start":155828585,"end":155829576,"strand":-1,"description":"adenosylmethionine decarboxylase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:460]"}, {"versioned_ensembl_gene_id":"ENSG00000213304.3","gene_symbol":"AC008481.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11521968,"end":11522498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217483.1","gene_symbol":"FO393414.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72522641,"end":72523238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235226.1","gene_symbol":"AL445528.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159759170,"end":159759589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228836.8","gene_symbol":"CT45A5","gene_name":"cancer/testis antigen family 45 member A5 [Source:HGNC Symbol;Acc:HGNC:33270]","synonyms":"CT45.5,CT45-5","biotype":"protein_coding","ncbi_id":"441521","summary":"This gene represents one of a cluster of several similar genes located on the q arm of chromosome X. The genes in this cluster encode members of the cancer/testis (CT) family of antigens, and are distinct from other CT antigens. These antigens are thought to be novel therapeutic targets for human cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":135777130,"end":135785298,"strand":-1,"description":"cancer/testis antigen family 45 member A5 [Source:HGNC Symbol;Acc:HGNC:33270]"}, {"versioned_ensembl_gene_id":"ENSG00000274312.1","gene_symbol":"AC015722.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98319687,"end":98320237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240069.1","gene_symbol":"GPAA1P1","gene_name":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4447]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"22945","summary":null,"start":109984058,"end":109984988,"strand":1,"description":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4447]"}, {"versioned_ensembl_gene_id":"ENSG00000250568.1","gene_symbol":"AC098591.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39973128,"end":39973442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226532.1","gene_symbol":"AL022718.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124326175,"end":124326258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272347.1","gene_symbol":"AC116351.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1005039,"end":1006623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254541.1","gene_symbol":"AC023078.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18886933,"end":18887920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179776.17","gene_symbol":"CDH5","gene_name":"cadherin 5 [Source:HGNC Symbol;Acc:HGNC:1764]","synonyms":"CD144,7B4","biotype":"protein_coding","ncbi_id":"1003","summary":"This gene encodes a classical cadherin of the cadherin superfamily. The encoded preproprotein is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion molecule is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Functioning as a classical cadherin by imparting to cells the ability to adhere in a homophilic manner, this protein plays a role in endothelial adherens junction assembly and maintenance. This gene is located in a gene cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. [provided by RefSeq, Nov 2015]","start":66366622,"end":66404786,"strand":1,"description":"cadherin 5 [Source:HGNC Symbol;Acc:HGNC:1764]"}, {"versioned_ensembl_gene_id":"ENSG00000149531.15","gene_symbol":"FRG1BP","gene_name":"FSHD region gene 1 family member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:15792]","synonyms":"FRG1B,C20orf80,bA348I14.2","biotype":"unprocessed_pseudogene","ncbi_id":"284802","summary":null,"start":30377372,"end":30399257,"strand":1,"description":"FSHD region gene 1 family member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:15792]"}, {"versioned_ensembl_gene_id":"ENSG00000230598.2","gene_symbol":"AL645937.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29212886,"end":29216933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162378.12","gene_symbol":"ZYG11B","gene_name":"zyg-11 family member B, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:25820]","synonyms":"ZYG11,FLJ13456","biotype":"protein_coding","ncbi_id":"79699","summary":null,"start":52726467,"end":52827342,"strand":1,"description":"zyg-11 family member B, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:25820]"}, {"versioned_ensembl_gene_id":"ENSG00000223711.1","gene_symbol":"AC069213.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":195544048,"end":195550581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284614.1","gene_symbol":"AF228730.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7221713,"end":7221930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251345.2","gene_symbol":"AC093826.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129133106,"end":129134098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213604.4","gene_symbol":"AC022882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56205125,"end":56205625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280117.1","gene_symbol":"AC122688.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125160525,"end":125164918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282423.1","gene_symbol":"TRBV1","gene_name":"T-cell receptor beta variable 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12176]","synonyms":"TCRBV27S1P,TCRBV1S1P","biotype":"TR_V_pseudogene","ncbi_id":"28621","summary":null,"start":142299217,"end":142299500,"strand":1,"description":"T-cell receptor beta variable 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12176]"}, {"versioned_ensembl_gene_id":"ENSG00000228968.1","gene_symbol":"AC096554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104125268,"end":104147229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232307.1","gene_symbol":"DAOA-AS1","gene_name":"DAOA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30243]","synonyms":"G30,DAOAAS,DAOA-AS","biotype":"antisense_RNA","ncbi_id":"282706","summary":null,"start":105459055,"end":105505681,"strand":-1,"description":"DAOA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30243]"}, {"versioned_ensembl_gene_id":"ENSG00000225792.1","gene_symbol":"AC004540.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26372144,"end":26376701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145041.15","gene_symbol":"DCAF1","gene_name":"DDB1 and CUL4 associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30911]","synonyms":"VPRBP,MGC102804,KIAA0800","biotype":"protein_coding","ncbi_id":"9730","summary":null,"start":51395867,"end":51500002,"strand":-1,"description":"DDB1 and CUL4 associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30911]"}, {"versioned_ensembl_gene_id":"ENSG00000081248.10","gene_symbol":"CACNA1S","gene_name":"calcium voltage-gated channel subunit alpha1 S [Source:HGNC Symbol;Acc:HGNC:1397]","synonyms":"MHS5,hypoPP,HOKPP,Cav1.1,CACNL1A3","biotype":"protein_coding","ncbi_id":"779","summary":"This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility. [provided by RefSeq, Jul 2008]","start":201039512,"end":201112566,"strand":-1,"description":"calcium voltage-gated channel subunit alpha1 S [Source:HGNC Symbol;Acc:HGNC:1397]"}, {"versioned_ensembl_gene_id":"ENSG00000232469.1","gene_symbol":"CR753509.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29290747,"end":29291689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231930.1","gene_symbol":"AF228730.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7200756,"end":7200857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214268.2","gene_symbol":"AF228730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7190901,"end":7191563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229347.1","gene_symbol":"AL596268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35058927,"end":35059974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259167.2","gene_symbol":"NMNAT1P1","gene_name":"NMNAT1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20024]","synonyms":"NMNATP","biotype":"processed_pseudogene","ncbi_id":"326607","summary":null,"start":81032529,"end":81033404,"strand":1,"description":"NMNAT1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20024]"}, {"versioned_ensembl_gene_id":"ENSG00000233861.1","gene_symbol":"MGAT2P1","gene_name":"MGAT2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51244]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422588","summary":null,"start":135730733,"end":135732197,"strand":-1,"description":"MGAT2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51244]"}, {"versioned_ensembl_gene_id":"ENSG00000097046.12","gene_symbol":"CDC7","gene_name":"cell division cycle 7 [Source:HGNC Symbol;Acc:HGNC:1745]","synonyms":"huCdc7,Hsk1,HsCdc7,CDC7L1","biotype":"protein_coding","ncbi_id":"8317","summary":"This gene encodes a cell division cycle protein with kinase activity that is critical for the G1/S transition. The yeast homolog is also essential for initiation of DNA replication as cell division occurs. Overexpression of this gene product may be associated with neoplastic transformation for some tumors. Multiple alternatively spliced transcript variants that encode the same protein have been detected. [provided by RefSeq, Aug 2008]","start":91500893,"end":91525764,"strand":1,"description":"cell division cycle 7 [Source:HGNC Symbol;Acc:HGNC:1745]"}, {"versioned_ensembl_gene_id":"ENSG00000229892.1","gene_symbol":"AL035666.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42606694,"end":42607559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263343.1","gene_symbol":"AC009088.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31165648,"end":31165927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273704.1","gene_symbol":"AL596245.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34768327,"end":34768688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231138.1","gene_symbol":"AC009987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123776670,"end":123777749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234351.1","gene_symbol":"CR753509.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29268481,"end":29269440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260902.1","gene_symbol":"LINC02011","gene_name":"long intergenic non-protein coding RNA 2011 [Source:HGNC Symbol;Acc:HGNC:27191]","synonyms":"FLJ31836","biotype":"lincRNA","ncbi_id":"152274","summary":null,"start":14799331,"end":14811414,"strand":-1,"description":"long intergenic non-protein coding RNA 2011 [Source:HGNC Symbol;Acc:HGNC:27191]"}, {"versioned_ensembl_gene_id":"ENSG00000171105.13","gene_symbol":"INSR","gene_name":"insulin receptor [Source:HGNC Symbol;Acc:HGNC:6091]","synonyms":"CD220","biotype":"protein_coding","ncbi_id":"3643","summary":"This gene encodes a member of the receptor tyrosine kinase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form a heterotetrameric receptor. Binding of insulin or other ligands to this receptor activates the insulin signaling pathway, which regulates glucose uptake and release, as well as the synthesis and storage of carbohydrates, lipids and protein. Mutations in this gene underlie the inherited severe insulin resistance syndromes including type A insulin resistance syndrome, Donohue syndrome and Rabson-Mendenhall syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":7112255,"end":7294034,"strand":-1,"description":"insulin receptor [Source:HGNC Symbol;Acc:HGNC:6091]"}, {"versioned_ensembl_gene_id":"ENSG00000236880.1","gene_symbol":"Z85995.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124688504,"end":124688838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182346.18","gene_symbol":"DAOA","gene_name":"D-amino acid oxidase activator [Source:HGNC Symbol;Acc:HGNC:21191]","synonyms":"G72","biotype":"protein_coding","ncbi_id":"267012","summary":"This gene encodes a protein that may function as an activator of D-amino acid oxidase, which degrades the gliotransmitter D-serine, a potent activator of N-methyl-D-aspartate (NMDA) type glutamate receptors. Studies also suggest that one encoded isoform may play a role in mitochondrial function and dendritic arborization. Polymorphisms in this gene have been implicated in susceptibility to schizophrenia and bipolar affective disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Mar 2011]","start":105465867,"end":105491034,"strand":1,"description":"D-amino acid oxidase activator [Source:HGNC Symbol;Acc:HGNC:21191]"}, {"versioned_ensembl_gene_id":"ENSG00000257940.1","gene_symbol":"AC079598.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87816486,"end":87817831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227209.1","gene_symbol":"WARS2P1","gene_name":"tryptophanyl tRNA synthetase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421633","summary":null,"start":80940665,"end":80941201,"strand":-1,"description":"tryptophanyl tRNA synthetase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45116]"}, {"versioned_ensembl_gene_id":"ENSG00000099377.13","gene_symbol":"HSD3B7","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 [Source:HGNC Symbol;Acc:HGNC:18324]","synonyms":"SDR11E3,C(27)-3BETA-HSD","biotype":"protein_coding","ncbi_id":"80270","summary":"This gene encodes an enzyme which is involved in the initial stages of the synthesis of bile acids from cholesterol and a member of the short-chain dehydrogenase/reductase superfamily. The encoded protein is a membrane-associated endoplasmic reticulum protein which is active against 7-alpha hydrosylated sterol substrates. Mutations in this gene are associated with a congenital bile acid synthesis defect which leads to neonatal cholestasis, a form of progressive liver disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":30985207,"end":30989152,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 [Source:HGNC Symbol;Acc:HGNC:18324]"}, {"versioned_ensembl_gene_id":"ENSG00000169087.10","gene_symbol":"HSPBAP1","gene_name":"HSPB1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16389]","synonyms":"PASS1,FLJ22623","biotype":"protein_coding","ncbi_id":"79663","summary":"This gene encodes a protein that binds to one of the small heat shock proteins, specifically hsp27. Hsp27 is involved with cell growth and differentiation. This encoded protein was found to be abnormally expressed in patients with intractable epilepsy, although how brain function is affected remains unknown. [provided by RefSeq, Sep 2011]","start":122740003,"end":122793824,"strand":-1,"description":"HSPB1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16389]"}, {"versioned_ensembl_gene_id":"ENSG00000268940.5","gene_symbol":"CT45A1","gene_name":"cancer/testis antigen family 45 member A1 [Source:HGNC Symbol;Acc:HGNC:33267]","synonyms":"CT45.1,CT45-1","biotype":"protein_coding","ncbi_id":"541466","summary":null,"start":135713453,"end":135723539,"strand":1,"description":"cancer/testis antigen family 45 member A1 [Source:HGNC Symbol;Acc:HGNC:33267]"}, {"versioned_ensembl_gene_id":"ENSG00000255217.1","gene_symbol":"AP003034.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56165500,"end":56165921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225823.1","gene_symbol":"RPL7P45","gene_name":"ribosomal protein L7 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35522]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271225","summary":null,"start":104814327,"end":104815069,"strand":1,"description":"ribosomal protein L7 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35522]"}, {"versioned_ensembl_gene_id":"ENSG00000223603.1","gene_symbol":"CRPP1","gene_name":"C-reactive protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2368]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"171422","summary":null,"start":159704983,"end":159705607,"strand":-1,"description":"C-reactive protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2368]"}, {"versioned_ensembl_gene_id":"ENSG00000198022.6","gene_symbol":"SAGE2P","gene_name":"sarcoma antigen 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:51337]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644717","summary":null,"start":135673591,"end":135686151,"strand":-1,"description":"sarcoma antigen 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:51337]"}, {"versioned_ensembl_gene_id":"ENSG00000181752.3","gene_symbol":"OR8K5","gene_name":"olfactory receptor family 8 subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:15315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219453","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56159394,"end":56160317,"strand":-1,"description":"olfactory receptor family 8 subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:15315]"}, {"versioned_ensembl_gene_id":"ENSG00000235257.8","gene_symbol":"ITGA9-AS1","gene_name":"ITGA9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49668]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101928153","summary":null,"start":37745432,"end":37861780,"strand":-1,"description":"ITGA9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49668]"}, {"versioned_ensembl_gene_id":"ENSG00000162377.5","gene_symbol":"COA7","gene_name":"cytochrome c oxidase assembly factor 7 (putative) [Source:HGNC Symbol;Acc:HGNC:25716]","synonyms":"SELRC1,RESA1,FLJ12439,C1orf163","biotype":"protein_coding","ncbi_id":"65260","summary":null,"start":52684451,"end":52698366,"strand":-1,"description":"cytochrome c oxidase assembly factor 7 (putative) [Source:HGNC Symbol;Acc:HGNC:25716]"}, {"versioned_ensembl_gene_id":"ENSG00000236411.1","gene_symbol":"NDUFAF4P3","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422532","summary":null,"start":37789921,"end":37790445,"strand":-1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44542]"}, {"versioned_ensembl_gene_id":"ENSG00000158731.2","gene_symbol":"OR10J6P","gene_name":"olfactory receptor family 10 subfamily J member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14994]","synonyms":"OR10J6","biotype":"unprocessed_pseudogene","ncbi_id":"401973","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159598298,"end":159599227,"strand":1,"description":"olfactory receptor family 10 subfamily J member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14994]"}, {"versioned_ensembl_gene_id":"ENSG00000230474.1","gene_symbol":"ATP6V1G1P7","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39852]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874514","summary":null,"start":103444620,"end":103444968,"strand":-1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39852]"}, {"versioned_ensembl_gene_id":"ENSG00000224978.1","gene_symbol":"BX682237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155212921,"end":155213638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132692.18","gene_symbol":"BCAN","gene_name":"brevican [Source:HGNC Symbol;Acc:HGNC:23059]","synonyms":"MGC13038,CSPG7,BEHAB","biotype":"protein_coding","ncbi_id":"63827","summary":"This gene encodes a member of the lectican family of chondroitin sulfate proteoglycans that is specifically expressed in the central nervous system. This protein is developmentally regulated and may function in the formation of the brain extracellular matrix. This protein is highly expressed in gliomas and may promote the growth and cell motility of brain tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":156641390,"end":156659532,"strand":1,"description":"brevican [Source:HGNC Symbol;Acc:HGNC:23059]"}, {"versioned_ensembl_gene_id":"ENSG00000282264.1","gene_symbol":"AC231381.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142285779,"end":142288898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079931.14","gene_symbol":"MOXD1","gene_name":"monooxygenase DBH like 1 [Source:HGNC Symbol;Acc:HGNC:21063]","synonyms":"MOX,DKFZP564G202,dJ248E1.1","biotype":"protein_coding","ncbi_id":"26002","summary":null,"start":132296055,"end":132401545,"strand":-1,"description":"monooxygenase DBH like 1 [Source:HGNC Symbol;Acc:HGNC:21063]"}, {"versioned_ensembl_gene_id":"ENSG00000234551.1","gene_symbol":"LINC01309","gene_name":"long intergenic non-protein coding RNA 1309 [Source:HGNC Symbol;Acc:HGNC:50497]","synonyms":"TCONS_l2_00007459","biotype":"lincRNA","ncbi_id":"104326190","summary":null,"start":103425200,"end":103427685,"strand":1,"description":"long intergenic non-protein coding RNA 1309 [Source:HGNC Symbol;Acc:HGNC:50497]"}, {"versioned_ensembl_gene_id":"ENSG00000272405.1","gene_symbol":"AL365181.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156641666,"end":156644887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227286.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33020794,"end":33026336,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000236141.1","gene_symbol":"AC013727.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103865746,"end":103869688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155714.13","gene_symbol":"PDZD9","gene_name":"PDZ domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28740]","synonyms":"C16orf65,MGC50721","biotype":"protein_coding","ncbi_id":"255762","summary":null,"start":21983865,"end":22001110,"strand":-1,"description":"PDZ domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28740]"}, {"versioned_ensembl_gene_id":"ENSG00000227994.1","gene_symbol":"AL035417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44172506,"end":44172719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254863.1","gene_symbol":"AP001360.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119987954,"end":119995037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145050.15","gene_symbol":"MANF","gene_name":"mesencephalic astrocyte derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:15461]","synonyms":"ARP,ARMET","biotype":"protein_coding","ncbi_id":"7873","summary":"The protein encoded by this gene is localized in the endoplasmic reticulum (ER) and golgi, and is also secreted. Reducing expression of this gene increases susceptibility to ER stress-induced death and results in cell proliferation. Activity of this protein is important in promoting the survival of dopaminergic neurons. The presence of polymorphisms in the N-terminal arginine-rich region, including a specific mutation that changes an ATG start codon to AGG, have been reported in a variety of solid tumors; however, these polymorphisms were later shown to exist in normal tissues and are thus no longer thought to be tumor-related. [provided by RefSeq, Apr 2014]","start":51385047,"end":51389397,"strand":1,"description":"mesencephalic astrocyte derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:15461]"}, {"versioned_ensembl_gene_id":"ENSG00000282303.1","gene_symbol":"PRSS3P3","gene_name":"protease, serine 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43790]","synonyms":"TRY3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"136540","summary":null,"start":142287280,"end":142289809,"strand":-1,"description":"protease, serine 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43790]"}, {"versioned_ensembl_gene_id":"ENSG00000256637.6","gene_symbol":"LINC01965","gene_name":"long intergenic non-protein coding RNA 1965 [Source:HGNC Symbol;Acc:HGNC:52790]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985928","summary":null,"start":103874310,"end":104077778,"strand":1,"description":"long intergenic non-protein coding RNA 1965 [Source:HGNC Symbol;Acc:HGNC:52790]"}, {"versioned_ensembl_gene_id":"ENSG00000121898.12","gene_symbol":"CPXM2","gene_name":"carboxypeptidase X, M14 family member 2 [Source:HGNC Symbol;Acc:HGNC:26977]","synonyms":"UNQ676,CPX2","biotype":"protein_coding","ncbi_id":"119587","summary":null,"start":123706207,"end":123940267,"strand":-1,"description":"carboxypeptidase X, M14 family member 2 [Source:HGNC Symbol;Acc:HGNC:26977]"}, {"versioned_ensembl_gene_id":"ENSG00000234677.1","gene_symbol":"AC068058.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123913574,"end":123931597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110492.15","gene_symbol":"MDK","gene_name":"midkine (neurite growth-promoting factor 2) [Source:HGNC Symbol;Acc:HGNC:6972]","synonyms":"NEGF2,MK,FLJ27379","biotype":"protein_coding","ncbi_id":"4192","summary":"This gene encodes a member of a small family of secreted growth factors that binds heparin and responds to retinoic acid. The encoded protein promotes cell growth, migration, and angiogenesis, in particular during tumorigenesis. This gene has been targeted as a therapeutic for a variety of different disorders. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2012]","start":46380756,"end":46383837,"strand":1,"description":"midkine (neurite growth-promoting factor 2) [Source:HGNC Symbol;Acc:HGNC:6972]"}, {"versioned_ensembl_gene_id":"ENSG00000261634.3","gene_symbol":"AC026992.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69278328,"end":69298763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259074.1","gene_symbol":"PSMB7P1","gene_name":"PSMB7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49192]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422289","summary":null,"start":20149232,"end":20149745,"strand":1,"description":"PSMB7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49192]"}, {"versioned_ensembl_gene_id":"ENSG00000225733.5","gene_symbol":"FGD5-AS1","gene_name":"FGD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40410]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505641","summary":null,"start":14920347,"end":14948424,"strand":-1,"description":"FGD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40410]"}, {"versioned_ensembl_gene_id":"ENSG00000189325.6","gene_symbol":"C6orf222","gene_name":"chromosome 6 open reading frame 222 [Source:HGNC Symbol;Acc:HGNC:33769]","synonyms":"DKFZp779B1540","biotype":"protein_coding","ncbi_id":"389384","summary":null,"start":36315757,"end":36336885,"strand":-1,"description":"chromosome 6 open reading frame 222 [Source:HGNC Symbol;Acc:HGNC:33769]"}, {"versioned_ensembl_gene_id":"ENSG00000259504.2","gene_symbol":"AC026992.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69278675,"end":69295322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165752.16","gene_symbol":"STK32C","gene_name":"serine/threonine kinase 32C [Source:HGNC Symbol;Acc:HGNC:21332]","synonyms":"YANK3,PKE,MGC23665","biotype":"protein_coding","ncbi_id":"282974","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. It is thought that this family member is functional in brain due to its high expression levels there. DNA methylation differences have been found in this gene in monozygotic twins that are discordant for adolescent depression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":132207492,"end":132331847,"strand":-1,"description":"serine/threonine kinase 32C [Source:HGNC Symbol;Acc:HGNC:21332]"}, {"versioned_ensembl_gene_id":"ENSG00000266899.2","gene_symbol":"AKR1B1P7","gene_name":"aldo-keto reductase family 1 member B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33497]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126242","summary":null,"start":33360497,"end":33361448,"strand":-1,"description":"aldo-keto reductase family 1 member B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33497]"}, {"versioned_ensembl_gene_id":"ENSG00000277486.1","gene_symbol":"SAGE3P","gene_name":"sarcoma antigen 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:51338]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419054","summary":null,"start":135637623,"end":135642756,"strand":-1,"description":"sarcoma antigen 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:51338]"}, {"versioned_ensembl_gene_id":"ENSG00000215802.3","gene_symbol":"RFKP1","gene_name":"riboflavin kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39181]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100313962","summary":null,"start":240823006,"end":240823433,"strand":-1,"description":"riboflavin kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39181]"}, {"versioned_ensembl_gene_id":"ENSG00000139637.13","gene_symbol":"C12orf10","gene_name":"chromosome 12 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:17590]","synonyms":"MYG1,MYG,Gamm1","biotype":"protein_coding","ncbi_id":"60314","summary":null,"start":53299686,"end":53307177,"strand":1,"description":"chromosome 12 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:17590]"}, {"versioned_ensembl_gene_id":"ENSG00000238085.1","gene_symbol":"AL590682.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240998451,"end":240998794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233615.1","gene_symbol":"HNRNPA1P42","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:48771]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287266","summary":null,"start":240919653,"end":240920609,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:48771]"}, {"versioned_ensembl_gene_id":"ENSG00000235589.4","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28994750,"end":29005281,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000243864.1","gene_symbol":"RPS3AP50","gene_name":"ribosomal protein S3a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:37018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271601","summary":null,"start":33340686,"end":33341984,"strand":1,"description":"ribosomal protein S3a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:37018]"}, {"versioned_ensembl_gene_id":"ENSG00000267130.1","gene_symbol":"AC008738.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33305036,"end":33309387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159377.10","gene_symbol":"PSMB4","gene_name":"proteasome subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:9541]","synonyms":"PROS26,HN3","biotype":"protein_coding","ncbi_id":"5692","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. [provided by RefSeq, Jul 2008]","start":151399534,"end":151401944,"strand":1,"description":"proteasome subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:9541]"}, {"versioned_ensembl_gene_id":"ENSG00000177791.11","gene_symbol":"MYOZ1","gene_name":"myozenin 1 [Source:HGNC Symbol;Acc:HGNC:13752]","synonyms":"MYOZ,FATZ,CS-2","biotype":"protein_coding","ncbi_id":"58529","summary":"The protein encoded by this gene is primarily expressed in the skeletal muscle, and belongs to the myozenin family. Members of this family function as calcineurin-interacting proteins that help tether calcineurin to the sarcomere of cardiac and skeletal muscle. They play an important role in modulation of calcineurin signaling. [provided by RefSeq, Apr 2012]","start":73631654,"end":73641757,"strand":-1,"description":"myozenin 1 [Source:HGNC Symbol;Acc:HGNC:13752]"}, {"versioned_ensembl_gene_id":"ENSG00000254633.1","gene_symbol":"AL512590.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":97276566,"end":97295759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228495.1","gene_symbol":"LINC01013","gene_name":"long intergenic non-protein coding RNA 1013 [Source:HGNC Symbol;Acc:HGNC:48987]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507254","summary":null,"start":132131915,"end":132169374,"strand":1,"description":"long intergenic non-protein coding RNA 1013 [Source:HGNC Symbol;Acc:HGNC:48987]"}, {"versioned_ensembl_gene_id":"ENSG00000147485.12","gene_symbol":"PXDNL","gene_name":"peroxidasin like [Source:HGNC Symbol;Acc:HGNC:26359]","synonyms":"PMR1,FLJ25471","biotype":"protein_coding","ncbi_id":"137902","summary":null,"start":51319578,"end":51809445,"strand":-1,"description":"peroxidasin like [Source:HGNC Symbol;Acc:HGNC:26359]"}, {"versioned_ensembl_gene_id":"ENSG00000254848.1","gene_symbol":"OR5BN1P","gene_name":"olfactory receptor family 5 subfamily BN member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15276]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81204","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56132666,"end":56133494,"strand":-1,"description":"olfactory receptor family 5 subfamily BN member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15276]"}, {"versioned_ensembl_gene_id":"ENSG00000206281.11","gene_symbol":"TAPBP","gene_name":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]","synonyms":"TAPA","biotype":"protein_coding","ncbi_id":"6892","summary":"This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33228522,"end":33243221,"strand":-1,"description":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]"}, {"versioned_ensembl_gene_id":"ENSG00000256977.12","gene_symbol":"LIMS3","gene_name":"LIM zinc finger domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30047]","synonyms":null,"biotype":"protein_coding","ncbi_id":"96626","summary":null,"start":109898428,"end":109924868,"strand":1,"description":"LIM zinc finger domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30047]"}, {"versioned_ensembl_gene_id":"ENSG00000255040.1","gene_symbol":"MORF4L1P3","gene_name":"mortality factor 4 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20402]","synonyms":"MRG11,MORF4LP3","biotype":"processed_pseudogene","ncbi_id":"326593","summary":null,"start":14673606,"end":14674555,"strand":-1,"description":"mortality factor 4 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20402]"}, {"versioned_ensembl_gene_id":"ENSG00000235494.1","gene_symbol":"AL590705.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97233201,"end":97235014,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260394.2","gene_symbol":"Z92544.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":678504,"end":679777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185219.16","gene_symbol":"ZNF445","gene_name":"zinc finger protein 445 [Source:HGNC Symbol;Acc:HGNC:21018]","synonyms":"ZSCAN47,ZNF168,ZKSCAN15","biotype":"protein_coding","ncbi_id":"353274","summary":null,"start":44431720,"end":44477670,"strand":-1,"description":"zinc finger protein 445 [Source:HGNC Symbol;Acc:HGNC:21018]"}, {"versioned_ensembl_gene_id":"ENSG00000109534.16","gene_symbol":"GAR1","gene_name":"GAR1 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14264]","synonyms":"NOLA1","biotype":"protein_coding","ncbi_id":"54433","summary":"This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the DKC1, NOLA2 and NOLA3 proteins. These four H/ACA snoRNP proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. These four H/ACA snoRNP proteins are also components of the telomerase complex. The encoded protein of this gene contains two glycine- and arginine-rich domains and is related to Saccharomyces cerevisiae Gar1p. Two splice variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":109815510,"end":109824740,"strand":1,"description":"GAR1 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14264]"}, {"versioned_ensembl_gene_id":"ENSG00000225873.3","gene_symbol":"LINC00694","gene_name":"long intergenic non-protein coding RNA 694 [Source:HGNC Symbol;Acc:HGNC:44570]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724231","summary":null,"start":44421127,"end":44439946,"strand":-1,"description":"long intergenic non-protein coding RNA 694 [Source:HGNC Symbol;Acc:HGNC:44570]"}, {"versioned_ensembl_gene_id":"ENSG00000167513.8","gene_symbol":"CDT1","gene_name":"chromatin licensing and DNA replication factor 1 [Source:HGNC Symbol;Acc:HGNC:24576]","synonyms":"RIS2,DUP","biotype":"protein_coding","ncbi_id":"81620","summary":"The protein encoded by this gene is involved in the formation of the pre-replication complex that is necessary for DNA replication. The encoded protein can bind geminin, which prevents replication and may function to prevent this protein from initiating replication at inappropriate origins. Phosphorylation of this protein by cyclin A-dependent kinases results in degradation of the protein. [provided by RefSeq, Mar 2011]","start":88803213,"end":88809258,"strand":1,"description":"chromatin licensing and DNA replication factor 1 [Source:HGNC Symbol;Acc:HGNC:24576]"}, {"versioned_ensembl_gene_id":"ENSG00000178150.9","gene_symbol":"ZNF114","gene_name":"zinc finger protein 114 [Source:HGNC Symbol;Acc:HGNC:12894]","synonyms":"MGC17986","biotype":"protein_coding","ncbi_id":"163071","summary":null,"start":48270102,"end":48287608,"strand":1,"description":"zinc finger protein 114 [Source:HGNC Symbol;Acc:HGNC:12894]"}, {"versioned_ensembl_gene_id":"ENSG00000229189.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31601313,"end":31601586,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000268186.1","gene_symbol":"AC008392.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48262900,"end":48271283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237426.1","gene_symbol":"ZIK1P1","gene_name":"zinc finger protein interacting with K protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38031]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131493","summary":null,"start":124173001,"end":124174459,"strand":-1,"description":"zinc finger protein interacting with K protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38031]"}, {"versioned_ensembl_gene_id":"ENSG00000280155.1","gene_symbol":"AL021408.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132130252,"end":132131795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267580.1","gene_symbol":"AC008738.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33299934,"end":33301168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176349.11","gene_symbol":"AC104129.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1838586,"end":1849931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102243.12","gene_symbol":"VGLL1","gene_name":"vestigial like family member 1 [Source:HGNC Symbol;Acc:HGNC:20985]","synonyms":"TONDU,TDU","biotype":"protein_coding","ncbi_id":"51442","summary":"The protein encoded by this gene binds proteins of the TEA domain family of transcription factors (TEFs) through the Vg (vestigial) homology region found in its N-terminus. It may thus function as a specific coactivator for the mammalian TEFs. [provided by RefSeq, Sep 2009]","start":136532152,"end":136556807,"strand":1,"description":"vestigial like family member 1 [Source:HGNC Symbol;Acc:HGNC:20985]"}, {"versioned_ensembl_gene_id":"ENSG00000245848.2","gene_symbol":"CEBPA","gene_name":"CCAAT/enhancer binding protein alpha [Source:HGNC Symbol;Acc:HGNC:1833]","synonyms":"CEBP,C/EBP-alpha","biotype":"protein_coding","ncbi_id":"1050","summary":"This intronless gene encodes a transcription factor that contains a basic leucine zipper (bZIP) domain and recognizes the CCAAT motif in the promoters of target genes. The encoded protein functions in homodimers and also heterodimers with CCAAT/enhancer-binding proteins beta and gamma. Activity of this protein can modulate the expression of genes involved in cell cycle regulation as well as in body weight homeostasis. Mutation of this gene is associated with acute myeloid leukemia. The use of alternative in-frame non-AUG (GUG) and AUG start codons results in protein isoforms with different lengths. Differential translation initiation is mediated by an out-of-frame, upstream open reading frame which is located between the GUG and the first AUG start codons. [provided by RefSeq, Dec 2013]","start":33299934,"end":33302564,"strand":-1,"description":"CCAAT/enhancer binding protein alpha [Source:HGNC Symbol;Acc:HGNC:1833]"}, {"versioned_ensembl_gene_id":"ENSG00000237723.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33386065,"end":33386688,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000282393.1","gene_symbol":"AC016588.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":248551,"end":251571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211810.3","gene_symbol":"TRAV29DV5","gene_name":"T-cell receptor alpha variable 29/delta variable 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12127]","synonyms":"TRAV29/DV5","biotype":"TR_V_gene","ncbi_id":"28653","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22163238,"end":22163870,"strand":1,"description":"T-cell receptor alpha variable 29/delta variable 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12127]"}, {"versioned_ensembl_gene_id":"ENSG00000258128.2","gene_symbol":"AC079598.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":87782163,"end":87784568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272795.1","gene_symbol":"AC126283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109815047,"end":109815410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214558.4","gene_symbol":"AL365217.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65302522,"end":65304957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254821.1","gene_symbol":"AL136309.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4135423,"end":4146053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243828.2","gene_symbol":"AL355357.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64728837,"end":64733837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110925.6","gene_symbol":"CSRNP2","gene_name":"cysteine and serine rich nuclear protein 2 [Source:HGNC Symbol;Acc:HGNC:16006]","synonyms":"TAIP-12,PPP1R72,FAM130A1,C12orf22,C12ORF2","biotype":"protein_coding","ncbi_id":"81566","summary":"The protein encoded by this gene belongs to the CSRNP family of nuclear proteins that share conserved regions, including cysteine- and serine- rich regions, a basic domain, a transcriptional activation domain, and bind the sequence 'AGAGTG', thus have the hallmark of transcription factors. Studies in mice suggest that these genes may have redundant functions. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]","start":51061205,"end":51083664,"strand":-1,"description":"cysteine and serine rich nuclear protein 2 [Source:HGNC Symbol;Acc:HGNC:16006]"}, {"versioned_ensembl_gene_id":"ENSG00000231115.3","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33378855,"end":33383082,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000241103.1","gene_symbol":"AC109925.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94369833,"end":94370163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154783.11","gene_symbol":"FGD5","gene_name":"FYVE, RhoGEF and PH domain containing 5 [Source:HGNC Symbol;Acc:HGNC:19117]","synonyms":"ZFYVE23,FLJ39957,FLJ00274","biotype":"protein_coding","ncbi_id":"152273","summary":null,"start":14810853,"end":14934565,"strand":1,"description":"FYVE, RhoGEF and PH domain containing 5 [Source:HGNC Symbol;Acc:HGNC:19117]"}, {"versioned_ensembl_gene_id":"ENSG00000283175.1","gene_symbol":"AC007920.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":187291272,"end":187297933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166396.12","gene_symbol":"SERPINB7","gene_name":"serpin family B member 7 [Source:HGNC Symbol;Acc:HGNC:13902]","synonyms":"MEGSIN","biotype":"protein_coding","ncbi_id":"8710","summary":"This gene encodes a member of a family of proteins which function as protease inhibitors. Expression of this gene is upregulated in IgA nephropathy and mutations have been found to cause palmoplantar keratoderma, Nagashima type. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":63752935,"end":63805376,"strand":1,"description":"serpin family B member 7 [Source:HGNC Symbol;Acc:HGNC:13902]"}, {"versioned_ensembl_gene_id":"ENSG00000085224.21","gene_symbol":"ATRX","gene_name":"ATRX, chromatin remodeler [Source:HGNC Symbol;Acc:HGNC:886]","synonyms":"XNP,XH2,RAD54,MRX52,JMS","biotype":"protein_coding","ncbi_id":"546","summary":"The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with X-linked syndromes exhibiting cognitive disabilities as well as alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2017]","start":77504878,"end":77786269,"strand":-1,"description":"ATRX, chromatin remodeler [Source:HGNC Symbol;Acc:HGNC:886]"}, {"versioned_ensembl_gene_id":"ENSG00000184394.2","gene_symbol":"OR4N5","gene_name":"olfactory receptor family 4 subfamily N member 5 [Source:HGNC Symbol;Acc:HGNC:15358]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390437","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20138820,"end":20145471,"strand":1,"description":"olfactory receptor family 4 subfamily N member 5 [Source:HGNC Symbol;Acc:HGNC:15358]"}, {"versioned_ensembl_gene_id":"ENSG00000176246.1","gene_symbol":"OR4L1","gene_name":"olfactory receptor family 4 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:15356]","synonyms":"OR4L2P","biotype":"protein_coding","ncbi_id":"122742","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20060045,"end":20060983,"strand":1,"description":"olfactory receptor family 4 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:15356]"}, {"versioned_ensembl_gene_id":"ENSG00000167280.16","gene_symbol":"ENGASE","gene_name":"endo-beta-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:24622]","synonyms":"FLJ21865","biotype":"protein_coding","ncbi_id":"64772","summary":"This gene encodes a cytosolic enzyme which catalyzes the hydrolysis of peptides and proteins with mannose modifications to produce free oligosaccharides. [provided by RefSeq, Feb 2012]","start":79074939,"end":79088599,"strand":1,"description":"endo-beta-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:24622]"}, {"versioned_ensembl_gene_id":"ENSG00000163106.10","gene_symbol":"HPGDS","gene_name":"hematopoietic prostaglandin D synthase [Source:HGNC Symbol;Acc:HGNC:17890]","synonyms":"PGDS,PGD2,H-PGDS,GSTS1-1,GSTS1,GSTS","biotype":"protein_coding","ncbi_id":"27306","summary":"Prostaglandin-D synthase is a sigma class glutathione-S-transferase family member. The enzyme catalyzes the conversion of PGH2 to PGD2 and plays a role in the production of prostanoids in the immune system and mast cells. The presence of this enzyme can be used to identify the differentiation stage of human megakaryocytes. [provided by RefSeq, Jul 2008]","start":94298535,"end":94342876,"strand":-1,"description":"hematopoietic prostaglandin D synthase [Source:HGNC Symbol;Acc:HGNC:17890]"}, {"versioned_ensembl_gene_id":"ENSG00000249531.2","gene_symbol":"AC098799.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68300325,"end":68302459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241484.9","gene_symbol":"ARHGAP8","gene_name":"Rho GTPase activating protein 8 [Source:HGNC Symbol;Acc:HGNC:677]","synonyms":"FLJ20185,BPGAP1","biotype":"protein_coding","ncbi_id":"23779","summary":"This gene encodes a member of the RHOGAP family. GAP (GTPase-activating) family proteins participate in signaling pathways that regulate cell processes involved in cytoskeletal changes. GAP proteins alternate between an active (GTP-bound) and inactive (GDP-bound) state based on the GTP:GDP ratio in the cell. This family member is a multidomain protein that functions to promote Erk activation and cell motility. Alternative splicing results in multiple transcript variants. Read-through transcripts from the upstream proline rich 5, renal (PRR5) gene into this gene also exist, which led to the original description of PRR5 and ARHGAP8 being a single gene. [provided by RefSeq, Nov 2010]","start":44752558,"end":44862788,"strand":1,"description":"Rho GTPase activating protein 8 [Source:HGNC Symbol;Acc:HGNC:677]"}, {"versioned_ensembl_gene_id":"ENSG00000224348.2","gene_symbol":"AL592076.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":241305580,"end":241305882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140090.17","gene_symbol":"SLC24A4","gene_name":"solute carrier family 24 member 4 [Source:HGNC Symbol;Acc:HGNC:10978]","synonyms":"NCKX4","biotype":"protein_coding","ncbi_id":"123041","summary":"This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jul 2010]","start":92322581,"end":92501483,"strand":1,"description":"solute carrier family 24 member 4 [Source:HGNC Symbol;Acc:HGNC:10978]"}, {"versioned_ensembl_gene_id":"ENSG00000250642.3","gene_symbol":"AC098799.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68282461,"end":68285959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112130.16","gene_symbol":"RNF8","gene_name":"ring finger protein 8 [Source:HGNC Symbol;Acc:HGNC:10071]","synonyms":"KIAA0646","biotype":"protein_coding","ncbi_id":"9025","summary":"The protein encoded by this gene contains a RING finger motif and an FHA domain. This protein has been shown to interact with several class II ubiquitin-conjugating enzymes (E2), including UBE2E1/UBCH6, UBE2E2, and UBE2E3, and may act as an ubiquitin ligase (E3) in the ubiquitination of certain nuclear proteins. This protein is also known to play a role in the DNA damage response and depletion of this protein causes cell growth inhibition and cell cycle arrest. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":37353972,"end":37394738,"strand":1,"description":"ring finger protein 8 [Source:HGNC Symbol;Acc:HGNC:10071]"}, {"versioned_ensembl_gene_id":"ENSG00000235545.1","gene_symbol":"AC103923.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62688482,"end":62710694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232357.2","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"KE6,FABGL,SDR30C1,HKE6,D6S2245E,RING2,H2-KE6","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33375002,"end":33377191,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000166226.12","gene_symbol":"CCT2","gene_name":"chaperonin containing TCP1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:1615]","synonyms":"Cctb","biotype":"protein_coding","ncbi_id":"10576","summary":"The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":69585334,"end":69601570,"strand":1,"description":"chaperonin containing TCP1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:1615]"}, {"versioned_ensembl_gene_id":"ENSG00000137875.4","gene_symbol":"BCL2L10","gene_name":"BCL2 like 10 [Source:HGNC Symbol;Acc:HGNC:993]","synonyms":"Diva,Boo,BCL-B","biotype":"protein_coding","ncbi_id":"10017","summary":"The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The protein encoded by this gene contains conserved BH4, BH1 and BH2 domains. This protein can interact with other members of BCL-2 protein family including BCL2, BCL2L1/BCL-X(L), and BAX. Overexpression of this gene has been shown to suppress cell apoptosis possibly through the prevention of cytochrome C release from the mitochondria, and thus activating caspase-3 activation. The mouse counterpart of this protein is found to interact with Apaf1 and forms a protein complex with Caspase 9, which suggests the involvement of this protein in APAF1 and CASPASE 9 related apoptotic pathway. [provided by RefSeq, Jul 2008]","start":52109263,"end":52112775,"strand":-1,"description":"BCL2 like 10 [Source:HGNC Symbol;Acc:HGNC:993]"}, {"versioned_ensembl_gene_id":"ENSG00000253395.1","gene_symbol":"AP003469.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101122145,"end":101126158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253664.1","gene_symbol":"AC012413.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51257688,"end":51321118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166860.2","gene_symbol":"ZBTB39","gene_name":"zinc finger and BTB domain containing 39 [Source:HGNC Symbol;Acc:HGNC:29014]","synonyms":"ZNF922,KIAA0352","biotype":"protein_coding","ncbi_id":"9880","summary":null,"start":56998834,"end":57006446,"strand":-1,"description":"zinc finger and BTB domain containing 39 [Source:HGNC Symbol;Acc:HGNC:29014]"}, {"versioned_ensembl_gene_id":"ENSG00000142512.14","gene_symbol":"SIGLEC10","gene_name":"sialic acid binding Ig like lectin 10 [Source:HGNC Symbol;Acc:HGNC:15620]","synonyms":"SLG2,SIGLEC-10,PRO940,MGC126774","biotype":"protein_coding","ncbi_id":"89790","summary":"SIGLECs are members of the immunoglobulin superfamily that are expressed on the cell surface. Most SIGLECs have 1 or more cytoplasmic immune receptor tyrosine-based inhibitory motifs, or ITIMs. SIGLECs are typically expressed on cells of the innate immune system, with the exception of the B-cell expressed SIGLEC6 (MIM 604405).[supplied by OMIM, Jul 2002]","start":51410021,"end":51417803,"strand":-1,"description":"sialic acid binding Ig like lectin 10 [Source:HGNC Symbol;Acc:HGNC:15620]"}, {"versioned_ensembl_gene_id":"ENSG00000279179.1","gene_symbol":"AL662907.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33162851,"end":33166298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230522.5","gene_symbol":"MBD3L2","gene_name":"methyl-CpG binding domain protein 3 like 2 [Source:HGNC Symbol;Acc:HGNC:18532]","synonyms":null,"biotype":"protein_coding","ncbi_id":"125997","summary":"This gene encodes a protein that is related to methyl-CpG-binding proteins but lacks the methyl-CpG binding domain. The protein has been found in germ cell tumors and some somatic tissues. [provided by RefSeq, Jul 2008]","start":7049321,"end":7051735,"strand":1,"description":"methyl-CpG binding domain protein 3 like 2 [Source:HGNC Symbol;Acc:HGNC:18532]"}, {"versioned_ensembl_gene_id":"ENSG00000234079.2","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31191499,"end":31197704,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000228469.1","gene_symbol":"CR388229.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31193904,"end":31195656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282053.1","gene_symbol":"AC019257.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1972570,"end":1974637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125629.14","gene_symbol":"INSIG2","gene_name":"insulin induced gene 2 [Source:HGNC Symbol;Acc:HGNC:20452]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51141","summary":"The protein encoded by this gene is highly similar to the protein product encoded by gene INSIG1. Both INSIG1 protein and this protein are endoplasmic reticulum proteins that block the processing of sterol regulatory element binding proteins (SREBPs) by binding to SREBP cleavage-activating protein (SCAP), and thus prevent SCAP from escorting SREBPs to the Golgi. [provided by RefSeq, Jul 2008]","start":118088452,"end":118110997,"strand":1,"description":"insulin induced gene 2 [Source:HGNC Symbol;Acc:HGNC:20452]"}, {"versioned_ensembl_gene_id":"ENSG00000228962.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"antisense_RNA","ncbi_id":"414764","summary":null,"start":32390510,"end":32393686,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000272791.1","gene_symbol":"AC073389.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73630556,"end":73631490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232346.1","gene_symbol":"Z74021.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32039490,"end":32039896,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228321.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31615015,"end":31617784,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000229209.1","gene_symbol":"AC073987.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103109759,"end":103176260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253340.1","gene_symbol":"AC087272.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50859530,"end":50860062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269761.1","gene_symbol":"AC025278.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7005012,"end":7006074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226462.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28969099,"end":28970429,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000278495.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769810,"end":54784323,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000242375.1","gene_symbol":"AL590705.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97195351,"end":97197687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204290.10","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II,HSBLMHC1","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32393963,"end":32407128,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000255160.5","gene_symbol":"AC009652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19299883,"end":19308358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254483.1","gene_symbol":"AL590705.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97238645,"end":97246184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227623.1","gene_symbol":"AC010881.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103275904,"end":103276138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137757.10","gene_symbol":"CASP5","gene_name":"caspase 5 [Source:HGNC Symbol;Acc:HGNC:1506]","synonyms":"ICE(rel)III","biotype":"protein_coding","ncbi_id":"838","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. Overexpression of the active form of this enzyme induces apoptosis in fibroblasts. Max, a central component of the Myc/Max/Mad transcription regulation network important for cell growth, differentiation, and apoptosis, is cleaved by this protein; this process requires Fas-mediated dephosphorylation of Max. The expression of this gene is regulated by interferon-gamma and lipopolysaccharide. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]","start":104994235,"end":105023168,"strand":-1,"description":"caspase 5 [Source:HGNC Symbol;Acc:HGNC:1506]"}, {"versioned_ensembl_gene_id":"ENSG00000188801.9","gene_symbol":"ZNF322P1","gene_name":"zinc finger protein 322 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14003]","synonyms":"ZNF322B,ZNF322","biotype":"processed_pseudogene","ncbi_id":"387328","summary":null,"start":97198303,"end":97199511,"strand":-1,"description":"zinc finger protein 322 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14003]"}, {"versioned_ensembl_gene_id":"ENSG00000265626.1","gene_symbol":"AC139085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76759685,"end":76759866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278445.1","gene_symbol":"AL137246.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102903339,"end":102904000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255036.6","gene_symbol":"AL512590.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":97238497,"end":97377287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278997.1","gene_symbol":"AL662907.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33141871,"end":33143230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283679.1","gene_symbol":"AC025278.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7011884,"end":7012679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264278.1","gene_symbol":"AC027575.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76794732,"end":76822295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277117.4","gene_symbol":"FP565260.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5022493,"end":5040666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278107.1","gene_symbol":"AC027575.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76805151,"end":76805736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248713.1","gene_symbol":"AC083902.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99636529,"end":99654648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175832.12","gene_symbol":"ETV4","gene_name":"ETS variant 4 [Source:HGNC Symbol;Acc:HGNC:3493]","synonyms":"PEA3,E1AF,E1A-F","biotype":"protein_coding","ncbi_id":"2118","summary":null,"start":43527844,"end":43579620,"strand":-1,"description":"ETS variant 4 [Source:HGNC Symbol;Acc:HGNC:3493]"}, {"versioned_ensembl_gene_id":"ENSG00000235242.1","gene_symbol":"AC010982.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114122274,"end":114123293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174125.7","gene_symbol":"TLR1","gene_name":"toll like receptor 1 [Source:HGNC Symbol;Acc:HGNC:11847]","synonyms":"rsc786,KIAA0012,CD281","biotype":"protein_coding","ncbi_id":"7096","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is ubiquitously expressed, and at higher levels than other TLR genes. Different length transcripts presumably resulting from use of alternative polyadenylation site, and/or from alternative splicing, have been noted for this gene. [provided by RefSeq, Jul 2008]","start":38790677,"end":38856817,"strand":-1,"description":"toll like receptor 1 [Source:HGNC Symbol;Acc:HGNC:11847]"}, {"versioned_ensembl_gene_id":"ENSG00000153266.12","gene_symbol":"FEZF2","gene_name":"FEZ family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13506]","synonyms":"TOF,FLJ10142,FKSG36,FEZL,ZNF312,Zfp312","biotype":"protein_coding","ncbi_id":"55079","summary":null,"start":62369681,"end":62374324,"strand":-1,"description":"FEZ family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13506]"}, {"versioned_ensembl_gene_id":"ENSG00000196589.6","gene_symbol":"MBD3L2B","gene_name":"methyl-CpG binding domain protein 3 like 2B [Source:HGNC Symbol;Acc:HGNC:53435]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729458","summary":null,"start":7018969,"end":7021450,"strand":-1,"description":"methyl-CpG binding domain protein 3 like 2B [Source:HGNC Symbol;Acc:HGNC:53435]"}, {"versioned_ensembl_gene_id":"ENSG00000283039.1","gene_symbol":"KLF18","gene_name":"Kruppel like factor 18 [Source:HGNC Symbol;Acc:HGNC:51793]","synonyms":null,"biotype":"protein_coding","ncbi_id":"105378952","summary":null,"start":44137821,"end":44141631,"strand":-1,"description":"Kruppel like factor 18 [Source:HGNC Symbol;Acc:HGNC:51793]"}, {"versioned_ensembl_gene_id":"ENSG00000100170.9","gene_symbol":"SLC5A1","gene_name":"solute carrier family 5 member 1 [Source:HGNC Symbol;Acc:HGNC:11036]","synonyms":"SGLT1,NAGT,D22S675","biotype":"protein_coding","ncbi_id":"6523","summary":"This gene encodes a member of the sodium-dependent glucose transporter (SGLT) family. The encoded integral membrane protein is the primary mediator of dietary glucose and galactose uptake from the intestinal lumen. Mutations in this gene have been associated with glucose-galactose malabsorption. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":32043032,"end":32113029,"strand":1,"description":"solute carrier family 5 member 1 [Source:HGNC Symbol;Acc:HGNC:11036]"}, {"versioned_ensembl_gene_id":"ENSG00000116525.13","gene_symbol":"TRIM62","gene_name":"tripartite motif containing 62 [Source:HGNC Symbol;Acc:HGNC:25574]","synonyms":"FLJ10759,DEAR1","biotype":"protein_coding","ncbi_id":"55223","summary":null,"start":33145402,"end":33182059,"strand":-1,"description":"tripartite motif containing 62 [Source:HGNC Symbol;Acc:HGNC:25574]"}, {"versioned_ensembl_gene_id":"ENSG00000109861.15","gene_symbol":"CTSC","gene_name":"cathepsin C [Source:HGNC Symbol;Acc:HGNC:2528]","synonyms":"PALS,DPP1,PLS","biotype":"protein_coding","ncbi_id":"1075","summary":"This gene encodes a member of the peptidase C1 family and lysosomal cysteine proteinase that appears to be a central coordinator for activation of many serine proteinases in cells of the immune system. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer. A portion of the propeptide acts as an intramolecular chaperone for the folding and stabilization of the mature enzyme. This enzyme requires chloride ions for activity and can degrade glucagon. Defects in the encoded protein have been shown to be a cause of Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis. [provided by RefSeq, Nov 2015]","start":88293592,"end":88337787,"strand":-1,"description":"cathepsin C [Source:HGNC Symbol;Acc:HGNC:2528]"}, {"versioned_ensembl_gene_id":"ENSG00000254225.1","gene_symbol":"BTF3P1","gene_name":"basic transcription factor 3, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1129]","synonyms":"HUMBTFA","biotype":"processed_pseudogene","ncbi_id":"693","summary":null,"start":51721670,"end":51722164,"strand":-1,"description":"basic transcription factor 3, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1129]"}, {"versioned_ensembl_gene_id":"ENSG00000226804.4","gene_symbol":"AL359839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44150594,"end":44151753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254025.1","gene_symbol":"BRIX1P1","gene_name":"BRX1, biogenesis of ribosomes pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51527]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422268","summary":null,"start":51435602,"end":51436509,"strand":1,"description":"BRX1, biogenesis of ribosomes pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51527]"}, {"versioned_ensembl_gene_id":"ENSG00000201778.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":157153548,"end":157153640,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241395.3","gene_symbol":"RN7SL344P","gene_name":"RNA, 7SL, cytoplasmic 344, pseudogene [Source:HGNC Symbol;Acc:HGNC:46360]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480503","summary":null,"start":211792111,"end":211792406,"strand":-1,"description":"RNA, 7SL, cytoplasmic 344, pseudogene [Source:HGNC Symbol;Acc:HGNC:46360]"}, {"versioned_ensembl_gene_id":"ENSG00000199132.1","gene_symbol":"MIR450A1","gene_name":"microRNA 450a-1 [Source:HGNC Symbol;Acc:HGNC:28008]","synonyms":"MIRN450,hsa-mir-450a-1,hsa-mir-450-1,hsa-mir-450,MIRN450A1,MIRN450-1","biotype":"miRNA","ncbi_id":"554214","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134540341,"end":134540431,"strand":-1,"description":"microRNA 450a-1 [Source:HGNC Symbol;Acc:HGNC:28008]"}, {"versioned_ensembl_gene_id":"ENSG00000283751.1","gene_symbol":"MIR452","gene_name":"microRNA 452 [Source:HGNC Symbol;Acc:HGNC:32054]","synonyms":"MIRN452,hsa-mir-452","biotype":"miRNA","ncbi_id":"574412","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151959628,"end":151959712,"strand":-1,"description":"microRNA 452 [Source:HGNC Symbol;Acc:HGNC:32054]"}, {"versioned_ensembl_gene_id":"ENSG00000005884.17","gene_symbol":"ITGA3","gene_name":"integrin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6139]","synonyms":"VLA3a,VCA-2,MSK18,GAP-B3,CD49c","biotype":"protein_coding","ncbi_id":"3675","summary":"The gene encodes a member of the integrin alpha chain family of proteins. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain that function as cell surface adhesion molecules. The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha 3 subunit. This subunit joins with a beta 1 subunit to form an integrin that interacts with extracellular matrix proteins including members of the laminin family. Expression of this gene may be correlated with breast cancer metastasis. [provided by RefSeq, Oct 2015]","start":50055968,"end":50090481,"strand":1,"description":"integrin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6139]"}, {"versioned_ensembl_gene_id":"ENSG00000235168.1","gene_symbol":"AL078581.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149561152,"end":149563949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284064.1","gene_symbol":"MIR6834","gene_name":"microRNA 6834 [Source:HGNC Symbol;Acc:HGNC:50108]","synonyms":"hsa-mir-6834","biotype":"miRNA","ncbi_id":"102465501","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33290245,"end":33290325,"strand":1,"description":"microRNA 6834 [Source:HGNC Symbol;Acc:HGNC:50108]"}, {"versioned_ensembl_gene_id":"ENSG00000216069.1","gene_symbol":"MIR875","gene_name":"microRNA 875 [Source:HGNC Symbol;Acc:HGNC:33652]","synonyms":"MIRN875,hsa-mir-875","biotype":"miRNA","ncbi_id":"100126309","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99536786,"end":99536861,"strand":-1,"description":"microRNA 875 [Source:HGNC Symbol;Acc:HGNC:33652]"}, {"versioned_ensembl_gene_id":"ENSG00000276494.1","gene_symbol":"KCNQ1OT1_3","gene_name":"KCNQ1 overlapping transcript 1 conserved region 3 [Source:RFAM;Acc:RF01948]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2674625,"end":2674740,"strand":1,"description":"KCNQ1 overlapping transcript 1 conserved region 3 [Source:RFAM;Acc:RF01948]"}, {"versioned_ensembl_gene_id":"ENSG00000201875.1","gene_symbol":"RN7SKP178","gene_name":"RNA, 7SK small nuclear pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:45902]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479175","summary":null,"start":205900630,"end":205900958,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:45902]"}, {"versioned_ensembl_gene_id":"ENSG00000206738.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2615124,"end":2615224,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278789.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"PYPAF2,NBS1,CLR19.9,NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54909282,"end":54945138,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000200879.1","gene_symbol":"SNORD14E","gene_name":"small nucleolar RNA, C/D box 14E [Source:HGNC Symbol;Acc:HGNC:30354]","synonyms":null,"biotype":"snoRNA","ncbi_id":"85391","summary":null,"start":123058077,"end":123058161,"strand":-1,"description":"small nucleolar RNA, C/D box 14E [Source:HGNC Symbol;Acc:HGNC:30354]"}, {"versioned_ensembl_gene_id":"ENSG00000274118.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":146311720,"end":146311822,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199716.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22867818,"end":22867917,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207180.1","gene_symbol":"RNU6-411P","gene_name":"RNA, U6 small nuclear 411, pseudogene [Source:HGNC Symbol;Acc:HGNC:47374]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479747","summary":null,"start":71182612,"end":71182718,"strand":1,"description":"RNA, U6 small nuclear 411, pseudogene [Source:HGNC Symbol;Acc:HGNC:47374]"}, {"versioned_ensembl_gene_id":"ENSG00000238731.1","gene_symbol":"RNU7-90P","gene_name":"RNA, U7 small nuclear 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:45624]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479060","summary":null,"start":72673503,"end":72673564,"strand":1,"description":"RNA, U7 small nuclear 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:45624]"}, {"versioned_ensembl_gene_id":"ENSG00000277572.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":14075950,"end":14076038,"strand":-1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000199629.1","gene_symbol":"RNU1-14P","gene_name":"RNA, U1 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:10139]","synonyms":"RNU1P7,U1P17","biotype":"snRNA","ncbi_id":"26859","summary":null,"start":53366058,"end":53366209,"strand":1,"description":"RNA, U1 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:10139]"}, {"versioned_ensembl_gene_id":"ENSG00000251766.1","gene_symbol":"RNA5SP518","gene_name":"RNA, 5S ribosomal pseudogene 518 [Source:HGNC Symbol;Acc:HGNC:43418]","synonyms":"RN5S518","biotype":"rRNA","ncbi_id":"100873569","summary":null,"start":10090410,"end":10090528,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 518 [Source:HGNC Symbol;Acc:HGNC:43418]"}, {"versioned_ensembl_gene_id":"ENSG00000253094.1","gene_symbol":"SNORD36","gene_name":"Small nucleolar RNA SNORD36 [Source:RFAM;Acc:RF00049]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":22803145,"end":22803224,"strand":1,"description":"Small nucleolar RNA SNORD36 [Source:RFAM;Acc:RF00049]"}, {"versioned_ensembl_gene_id":"ENSG00000251803.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17403508,"end":17403620,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200246.1","gene_symbol":"RNA5SP263","gene_name":"RNA, 5S ribosomal pseudogene 263 [Source:HGNC Symbol;Acc:HGNC:43163]","synonyms":"RN5S263","biotype":"rRNA","ncbi_id":"106479002","summary":null,"start":32256496,"end":32256623,"strand":1,"description":"RNA, 5S ribosomal pseudogene 263 [Source:HGNC Symbol;Acc:HGNC:43163]"}, {"versioned_ensembl_gene_id":"ENSG00000243539.3","gene_symbol":"RN7SL649P","gene_name":"RNA, 7SL, cytoplasmic 649, pseudogene [Source:HGNC Symbol;Acc:HGNC:46665]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481100","summary":null,"start":12036740,"end":12037014,"strand":-1,"description":"RNA, 7SL, cytoplasmic 649, pseudogene [Source:HGNC Symbol;Acc:HGNC:46665]"}, {"versioned_ensembl_gene_id":"ENSG00000200554.1","gene_symbol":"RNU6-1020P","gene_name":"RNA, U6 small nuclear 1020, pseudogene [Source:HGNC Symbol;Acc:HGNC:47983]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481503","summary":null,"start":125303920,"end":125304026,"strand":-1,"description":"RNA, U6 small nuclear 1020, pseudogene [Source:HGNC Symbol;Acc:HGNC:47983]"}, {"versioned_ensembl_gene_id":"ENSG00000167281.18","gene_symbol":"RBFOX3","gene_name":"RNA binding protein, fox-1 homolog 3 [Source:HGNC Symbol;Acc:HGNC:27097]","synonyms":"NeuN,HRNBP3,FOX-3","biotype":"protein_coding","ncbi_id":"146713","summary":"This gene encodes a member of the RNA-binding FOX protein family which is involved in the regulation of alternative splicing of pre-mRNA. The protein has an N-terminal proline-rich region, an RNA recognition motif (RRM) domain, and a C-terminal alanine-rich region. This gene produces the neuronal nuclei (NeuN) antigen that has been widely used as a marker for post-mitotic neurons. This gene has its highest expression in the central nervous system and plays a prominent role in neural tissue development and regulation of adult brain function. Mutations in this gene have been associated with numerous neurological disorders. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2017]","start":79089345,"end":79516148,"strand":-1,"description":"RNA binding protein, fox-1 homolog 3 [Source:HGNC Symbol;Acc:HGNC:27097]"}, {"versioned_ensembl_gene_id":"ENSG00000267137.1","gene_symbol":"AC005901.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61460224,"end":61463384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265433.1","gene_symbol":"MIR4447","gene_name":"microRNA 4447 [Source:HGNC Symbol;Acc:HGNC:41850]","synonyms":"hsa-mir-4447","biotype":"miRNA","ncbi_id":"100616485","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116850277,"end":116850367,"strand":-1,"description":"microRNA 4447 [Source:HGNC Symbol;Acc:HGNC:41850]"}, {"versioned_ensembl_gene_id":"ENSG00000221240.1","gene_symbol":"MIR1258","gene_name":"microRNA 1258 [Source:HGNC Symbol;Acc:HGNC:35323]","synonyms":"MIRN1258,hsa-mir-1258","biotype":"miRNA","ncbi_id":"100302172","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":179860836,"end":179860908,"strand":-1,"description":"microRNA 1258 [Source:HGNC Symbol;Acc:HGNC:35323]"}, {"versioned_ensembl_gene_id":"ENSG00000212161.1","gene_symbol":"SNORD64","gene_name":"Small Nucleolar RNA SNORD64 [Source:RFAM;Acc:RF00570]","synonyms":"HBII-13","biotype":"snoRNA","ncbi_id":"347686","summary":"This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]","start":159851906,"end":159851972,"strand":-1,"description":"Small Nucleolar RNA SNORD64 [Source:RFAM;Acc:RF00570]"}, {"versioned_ensembl_gene_id":"ENSG00000275411.1","gene_symbol":"MIR6882","gene_name":"microRNA 6882 [Source:HGNC Symbol;Acc:HGNC:49928]","synonyms":"hsa-mir-6882","biotype":"miRNA","ncbi_id":"102465531","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74840642,"end":74840707,"strand":-1,"description":"microRNA 6882 [Source:HGNC Symbol;Acc:HGNC:49928]"}, {"versioned_ensembl_gene_id":"ENSG00000264201.1","gene_symbol":"MIR4701","gene_name":"microRNA 4701 [Source:HGNC Symbol;Acc:HGNC:41627]","synonyms":"hsa-mir-4701","biotype":"miRNA","ncbi_id":"100616262","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48771975,"end":48772037,"strand":-1,"description":"microRNA 4701 [Source:HGNC Symbol;Acc:HGNC:41627]"}, {"versioned_ensembl_gene_id":"ENSG00000222636.1","gene_symbol":"RN7SKP54","gene_name":"RNA, 7SK small nuclear pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:45778]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080626","summary":null,"start":101058299,"end":101058567,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:45778]"}, {"versioned_ensembl_gene_id":"ENSG00000252850.1","gene_symbol":"RNU1-117P","gene_name":"RNA, U1 small nuclear 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:48459]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480189","summary":null,"start":88581639,"end":88581796,"strand":1,"description":"RNA, U1 small nuclear 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:48459]"}, {"versioned_ensembl_gene_id":"ENSG00000206731.1","gene_symbol":"SNORA36","gene_name":"Small nucleolar RNA SNORA36 family [Source:RFAM;Acc:RF00340]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":27642043,"end":27642169,"strand":-1,"description":"Small nucleolar RNA SNORA36 family [Source:RFAM;Acc:RF00340]"}, {"versioned_ensembl_gene_id":"ENSG00000202473.1","gene_symbol":"RN7SKP81","gene_name":"RNA, 7SK small nuclear pseudogene 81 [Source:HGNC Symbol;Acc:HGNC:45805]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480858","summary":null,"start":143090347,"end":143090677,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 81 [Source:HGNC Symbol;Acc:HGNC:45805]"}, {"versioned_ensembl_gene_id":"ENSG00000207397.1","gene_symbol":"RNU6-1179P","gene_name":"RNA, U6 small nuclear 1179, pseudogene [Source:HGNC Symbol;Acc:HGNC:48142]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480084","summary":null,"start":22555261,"end":22555367,"strand":1,"description":"RNA, U6 small nuclear 1179, pseudogene [Source:HGNC Symbol;Acc:HGNC:48142]"}, {"versioned_ensembl_gene_id":"ENSG00000222941.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":151916331,"end":151916418,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000258465.6","gene_symbol":"AL139011.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":160217464,"end":160285130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228606.2","gene_symbol":"AL139011.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160261744,"end":160262778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260046.1","gene_symbol":"AL162632.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45369215,"end":45370839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251108.1","gene_symbol":"YBX1P5","gene_name":"Y-box binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42426]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861569","summary":null,"start":72417489,"end":72418335,"strand":1,"description":"Y-box binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42426]"}, {"versioned_ensembl_gene_id":"ENSG00000261269.1","gene_symbol":"AC093278.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":72439903,"end":72442387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244061.1","gene_symbol":"AC093278.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72381794,"end":72382393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239257.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29726669,"end":29727139,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000091947.9","gene_symbol":"TMEM101","gene_name":"transmembrane protein 101 [Source:HGNC Symbol;Acc:HGNC:28653]","synonyms":"MGC4251,FLJ23987","biotype":"protein_coding","ncbi_id":"84336","summary":null,"start":44011188,"end":44023946,"strand":-1,"description":"transmembrane protein 101 [Source:HGNC Symbol;Acc:HGNC:28653]"}, {"versioned_ensembl_gene_id":"ENSG00000266711.1","gene_symbol":"AC021534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79132722,"end":79136402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178404.9","gene_symbol":"CEP295NL","gene_name":"CEP295 N-terminal like [Source:HGNC Symbol;Acc:HGNC:44659]","synonyms":"KIAA1731NL,DDC8","biotype":"protein_coding","ncbi_id":"100653515","summary":null,"start":78870910,"end":78903217,"strand":-1,"description":"CEP295 N-terminal like [Source:HGNC Symbol;Acc:HGNC:44659]"}, {"versioned_ensembl_gene_id":"ENSG00000254469.7","gene_symbol":"AP002495.1","gene_name":"Putative short transient receptor potential channel 2-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6ZNB5]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":71865509,"end":71928654,"strand":-1,"description":"Putative short transient receptor potential channel 2-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6ZNB5]"}, {"versioned_ensembl_gene_id":"ENSG00000219553.2","gene_symbol":"AL031133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149491567,"end":149492289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204584.1","gene_symbol":"AC027801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49845910,"end":49848837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148335.14","gene_symbol":"NTMT1","gene_name":"N-terminal Xaa-Pro-Lys N-methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23373]","synonyms":"NRMT,METTL11A,HOMT1A,C9orf32,AD-003,NRMT1","biotype":"protein_coding","ncbi_id":"28989","summary":"The METTL11A gene encodes an N-terminal methyltransferase for the RAN (MIM 601179) guanine nucleotide exchange factor regulator of chromosome condensation 1 (RCC1; MIM 179710). METTL11A enzyme alpha-N-methylates other protein targets such as SET (MIM 600960) and RB (MIM 180200).[supplied by OMIM, Nov 2010]","start":129608884,"end":129636131,"strand":1,"description":"N-terminal Xaa-Pro-Lys N-methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23373]"}, {"versioned_ensembl_gene_id":"ENSG00000235142.7","gene_symbol":"LINC02532","gene_name":"long intergenic non-protein coding RNA 2532 [Source:HGNC Symbol;Acc:HGNC:53549]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100422737","summary":null,"start":106717452,"end":106787541,"strand":-1,"description":"long intergenic non-protein coding RNA 2532 [Source:HGNC Symbol;Acc:HGNC:53549]"}, {"versioned_ensembl_gene_id":"ENSG00000233985.1","gene_symbol":"LINC01681","gene_name":"long intergenic non-protein coding RNA 1681 [Source:HGNC Symbol;Acc:HGNC:52468]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371609","summary":null,"start":170174403,"end":170241287,"strand":1,"description":"long intergenic non-protein coding RNA 1681 [Source:HGNC Symbol;Acc:HGNC:52468]"}, {"versioned_ensembl_gene_id":"ENSG00000238051.1","gene_symbol":"ISCUP1","gene_name":"iron-sulfur cluster assembly enzyme pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462833","summary":null,"start":170211010,"end":170211457,"strand":-1,"description":"iron-sulfur cluster assembly enzyme pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38021]"}, {"versioned_ensembl_gene_id":"ENSG00000228692.2","gene_symbol":"AL445307.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163586583,"end":163588165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226868.1","gene_symbol":"AC096637.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":211715928,"end":211725402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164187.6","gene_symbol":"LMBRD2","gene_name":"LMBR1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25287]","synonyms":"DKFZp434H2226","biotype":"protein_coding","ncbi_id":"92255","summary":null,"start":36098412,"end":36151961,"strand":-1,"description":"LMBR1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25287]"}, {"versioned_ensembl_gene_id":"ENSG00000156381.8","gene_symbol":"ANKRD9","gene_name":"ankyrin repeat domain 9 [Source:HGNC Symbol;Acc:HGNC:20096]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122416","summary":null,"start":102501760,"end":102509799,"strand":-1,"description":"ankyrin repeat domain 9 [Source:HGNC Symbol;Acc:HGNC:20096]"}, {"versioned_ensembl_gene_id":"ENSG00000237017.1","gene_symbol":"AC245052.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54119511,"end":54125343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105619.13","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"FB1,INO80F,INO80F,amida,amida,FB1","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107013,"end":54115675,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000196663.15","gene_symbol":"TECPR2","gene_name":"tectonin beta-propeller repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:19957]","synonyms":"KIAA0329","biotype":"protein_coding","ncbi_id":"9895","summary":"The protein encoded by this gene is a member of the tectonin beta-propeller repeat-containing (TECPR) family, and contains both TECPR and tryptophan-aspartic acid repeat (WD repeat) domains. This gene has been implicated in autophagy, as reduced expression levels of this gene have been associated with impaired autophagy. Recessive mutations in this gene have been associated with a hereditary form of spastic paraparesis (HSP). HSP is characterized by progressive spasticity and paralysis of the legs. There is also some evidence linking mutations in this gene with birdshot chorioretinopathy (BSCR), which results in inflammation of the choroid and retina. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":102362963,"end":102502481,"strand":1,"description":"tectonin beta-propeller repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:19957]"}, {"versioned_ensembl_gene_id":"ENSG00000278925.1","gene_symbol":"AC005753.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141825708,"end":141826325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254972.1","gene_symbol":"AP003498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71701268,"end":71705404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245248.7","gene_symbol":"USP2-AS1","gene_name":"USP2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48673]","synonyms":"THY1-AS1","biotype":"antisense_RNA","ncbi_id":"100499227","summary":null,"start":119381778,"end":119526664,"strand":1,"description":"USP2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48673]"}, {"versioned_ensembl_gene_id":"ENSG00000230676.1","gene_symbol":"AL353803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129430652,"end":129451422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233273.1","gene_symbol":"AMMECR1LP1","gene_name":"AMMECR1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39809]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420921","summary":null,"start":96573659,"end":96574499,"strand":1,"description":"AMMECR1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39809]"}, {"versioned_ensembl_gene_id":"ENSG00000216265.1","gene_symbol":"FABP12P1","gene_name":"fatty acid binding protein 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479057","summary":null,"start":149304107,"end":149304428,"strand":-1,"description":"fatty acid binding protein 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45176]"}, {"versioned_ensembl_gene_id":"ENSG00000249480.1","gene_symbol":"STK19B","gene_name":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]","synonyms":"bPG116M5.10,STK19P,RP2","biotype":"unprocessed_pseudogene","ncbi_id":"373159","summary":null,"start":31995452,"end":31995969,"strand":1,"description":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]"}, {"versioned_ensembl_gene_id":"ENSG00000219409.2","gene_symbol":"AL590704.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144397959,"end":144398752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220739.2","gene_symbol":"AL513475.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144708106,"end":144708497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253972.5","gene_symbol":"MAL2","gene_name":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]","synonyms":null,"biotype":"lincRNA","ncbi_id":"114569","summary":"This gene encodes a multispan transmembrane protein belonging to the MAL proteolipid family. The protein is a component of lipid rafts and, in polarized cells, it primarily localizes to endosomal structures beneath the apical membrane. It is required for transcytosis, an intracellular transport pathway used to deliver membrane-bound proteins and exogenous cargos from the basolateral to the apical surface. [provided by RefSeq, Jul 2008]","start":119215111,"end":119246848,"strand":-1,"description":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]"}, {"versioned_ensembl_gene_id":"ENSG00000225311.1","gene_symbol":"AL024474.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144311699,"end":144333301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238110.1","gene_symbol":"AL353572.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87944276,"end":87945023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170385.9","gene_symbol":"SLC30A1","gene_name":"solute carrier family 30 member 1 [Source:HGNC Symbol;Acc:HGNC:11012]","synonyms":"ZRC1,ZNT1","biotype":"protein_coding","ncbi_id":"7779","summary":null,"start":211571568,"end":211578742,"strand":-1,"description":"solute carrier family 30 member 1 [Source:HGNC Symbol;Acc:HGNC:11012]"}, {"versioned_ensembl_gene_id":"ENSG00000204572.9","gene_symbol":"KRTAP5-10","gene_name":"keratin associated protein 5-10 [Source:HGNC Symbol;Acc:HGNC:23605]","synonyms":"KRTAP5.10","biotype":"protein_coding","ncbi_id":"387273","summary":null,"start":71565563,"end":71566738,"strand":1,"description":"keratin associated protein 5-10 [Source:HGNC Symbol;Acc:HGNC:23605]"}, {"versioned_ensembl_gene_id":"ENSG00000055147.18","gene_symbol":"FAM114A2","gene_name":"family with sequence similarity 114 member A2 [Source:HGNC Symbol;Acc:HGNC:1333]","synonyms":"C5orf3,133K02","biotype":"protein_coding","ncbi_id":"10827","summary":null,"start":153990128,"end":154038936,"strand":-1,"description":"family with sequence similarity 114 member A2 [Source:HGNC Symbol;Acc:HGNC:1333]"}, {"versioned_ensembl_gene_id":"ENSG00000250529.1","gene_symbol":"LINC02121","gene_name":"long intergenic non-protein coding RNA 2121 [Source:HGNC Symbol;Acc:HGNC:52977]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374631","summary":null,"start":5069192,"end":5078311,"strand":-1,"description":"long intergenic non-protein coding RNA 2121 [Source:HGNC Symbol;Acc:HGNC:52977]"}, {"versioned_ensembl_gene_id":"ENSG00000284237.1","gene_symbol":"AL356275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207959292,"end":207969329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251426.1","gene_symbol":"AC010451.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5046796,"end":5049497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250481.1","gene_symbol":"AC010451.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4974690,"end":5034267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251506.1","gene_symbol":"AC010451.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4967764,"end":4970425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134825.15","gene_symbol":"TMEM258","gene_name":"transmembrane protein 258 [Source:HGNC Symbol;Acc:HGNC:1164]","synonyms":"C11orf10","biotype":"protein_coding","ncbi_id":"746","summary":null,"start":61768501,"end":61792802,"strand":-1,"description":"transmembrane protein 258 [Source:HGNC Symbol;Acc:HGNC:1164]"}, {"versioned_ensembl_gene_id":"ENSG00000243199.1","gene_symbol":"AC115223.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65573459,"end":65574328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165632.7","gene_symbol":"TAF3","gene_name":"TATA-box binding protein associated factor 3 [Source:HGNC Symbol;Acc:HGNC:17303]","synonyms":"TAFII140,TAF140","biotype":"protein_coding","ncbi_id":"83860","summary":"The highly conserved RNA polymerase II transcription factor TFIID (see TAF1; MIM 313650) comprises the TATA box-binding protein (TBP; MIM 600075) and a set of TBP-associated factors (TAFs), including TAF3. TAFs contribute to promoter recognition and selectivity and act as antiapoptotic factors (Gangloff et al., 2001 [PubMed 11438666]).[supplied by OMIM, May 2009]","start":7818504,"end":8016627,"strand":1,"description":"TATA-box binding protein associated factor 3 [Source:HGNC Symbol;Acc:HGNC:17303]"}, {"versioned_ensembl_gene_id":"ENSG00000251371.1","gene_symbol":"AC010634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4640731,"end":4648254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248311.1","gene_symbol":"AC026719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4775476,"end":4805769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267682.1","gene_symbol":"AC016590.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37337236,"end":37337743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248467.1","gene_symbol":"AC026719.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4831699,"end":4849800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249521.1","gene_symbol":"LINC02114","gene_name":"long intergenic non-protein coding RNA 2114 [Source:HGNC Symbol;Acc:HGNC:52968]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929153","summary":null,"start":4773481,"end":4774865,"strand":1,"description":"long intergenic non-protein coding RNA 2114 [Source:HGNC Symbol;Acc:HGNC:52968]"}, {"versioned_ensembl_gene_id":"ENSG00000243444.7","gene_symbol":"PALM2","gene_name":"paralemmin 2 [Source:HGNC Symbol;Acc:HGNC:15845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114299","summary":null,"start":109640788,"end":109946703,"strand":1,"description":"paralemmin 2 [Source:HGNC Symbol;Acc:HGNC:15845]"}, {"versioned_ensembl_gene_id":"ENSG00000251616.1","gene_symbol":"AC113410.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133111055,"end":133114475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127831.10","gene_symbol":"VIL1","gene_name":"villin 1 [Source:HGNC Symbol;Acc:HGNC:12690]","synonyms":"VIL,D2S1471","biotype":"protein_coding","ncbi_id":"7429","summary":"This gene encodes a member of a family of calcium-regulated actin-binding proteins. This protein represents a dominant part of the brush border cytoskeleton which functions in the capping, severing, and bundling of actin filaments. Two mRNAs of 2.7 kb and 3.5 kb have been observed; they result from utilization of alternate poly-adenylation signals present in the terminal exon. [provided by RefSeq, Jul 2008]","start":218419092,"end":218453295,"strand":1,"description":"villin 1 [Source:HGNC Symbol;Acc:HGNC:12690]"}, {"versioned_ensembl_gene_id":"ENSG00000082512.14","gene_symbol":"TRAF5","gene_name":"TNF receptor associated factor 5 [Source:HGNC Symbol;Acc:HGNC:12035]","synonyms":"RNF84","biotype":"protein_coding","ncbi_id":"7188","summary":"The scaffold protein encoded by this gene is a member of the tumor necrosis factor receptor-associated factor (TRAF) protein family and contains a meprin and TRAF homology (MATH) domain, a RING-type zinc finger, and two TRAF-type zinc fingers. TRAF proteins are associated with, and mediate signal transduction from members of the TNF receptor superfamily. This protein is one of the components of a multiple protein complex which binds to tumor necrosis factor (TNF) receptor cytoplasmic domains and mediates TNF-induced activation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":211326615,"end":211374946,"strand":1,"description":"TNF receptor associated factor 5 [Source:HGNC Symbol;Acc:HGNC:12035]"}, {"versioned_ensembl_gene_id":"ENSG00000247572.7","gene_symbol":"CKMT2-AS1","gene_name":"CKMT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48997]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131067","summary":null,"start":81204084,"end":81301560,"strand":-1,"description":"CKMT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48997]"}, {"versioned_ensembl_gene_id":"ENSG00000248794.1","gene_symbol":"AC026436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81242330,"end":81242599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222000.7","gene_symbol":"AC092675.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98331389,"end":98356005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215223.3","gene_symbol":"CYP51A1P3","gene_name":"cytochrome P450 family 51 subfamily A member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41991]","synonyms":"CYP51P3","biotype":"processed_pseudogene","ncbi_id":"100422264","summary":null,"start":148478693,"end":148480763,"strand":1,"description":"cytochrome P450 family 51 subfamily A member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41991]"}, {"versioned_ensembl_gene_id":"ENSG00000248597.1","gene_symbol":"AC126768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1963609,"end":1967154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249731.1","gene_symbol":"AC126768.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1968094,"end":1969013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168496.3","gene_symbol":"FEN1","gene_name":"flap structure-specific endonuclease 1 [Source:HGNC Symbol;Acc:HGNC:3650]","synonyms":"RAD2,MF1,FEN-1","biotype":"protein_coding","ncbi_id":"2237","summary":"The protein encoded by this gene removes 5' overhanging flaps in DNA repair and processes the 5' ends of Okazaki fragments in lagging strand DNA synthesis. Direct physical interaction between this protein and AP endonuclease 1 during long-patch base excision repair provides coordinated loading of the proteins onto the substrate, thus passing the substrate from one enzyme to another. The protein is a member of the XPG/RAD2 endonuclease family and is one of ten proteins essential for cell-free DNA replication. DNA secondary structure can inhibit flap processing at certain trinucleotide repeats in a length-dependent manner by concealing the 5' end of the flap that is necessary for both binding and cleavage by the protein encoded by this gene. Therefore, secondary structure can deter the protective function of this protein, leading to site-specific trinucleotide expansions. [provided by RefSeq, Jul 2008]","start":61792637,"end":61797244,"strand":1,"description":"flap structure-specific endonuclease 1 [Source:HGNC Symbol;Acc:HGNC:3650]"}, {"versioned_ensembl_gene_id":"ENSG00000217027.1","gene_symbol":"TPT1P4","gene_name":"tumor protein, translationally-controlled 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49298]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285741","summary":null,"start":144200447,"end":144200965,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49298]"}, {"versioned_ensembl_gene_id":"ENSG00000277060.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"CLR19.9,NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54894717,"end":54929555,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000170464.9","gene_symbol":"DNAJC18","gene_name":"DnaJ heat shock protein family (Hsp40) member C18 [Source:HGNC Symbol;Acc:HGNC:28429]","synonyms":"MGC29463","biotype":"protein_coding","ncbi_id":"202052","summary":null,"start":139408588,"end":139444491,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C18 [Source:HGNC Symbol;Acc:HGNC:28429]"}, {"versioned_ensembl_gene_id":"ENSG00000127184.12","gene_symbol":"COX7C","gene_name":"cytochrome c oxidase subunit 7C [Source:HGNC Symbol;Acc:HGNC:2292]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1350","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes subunit VIIc, which shares 87% and 85% amino acid sequence identity with mouse and bovine COX VIIc, respectively, and is found in all tissues. A pseudogene COX7CP1 has been found on chromosome 13. [provided by RefSeq, Jul 2008]","start":86617904,"end":86620962,"strand":1,"description":"cytochrome c oxidase subunit 7C [Source:HGNC Symbol;Acc:HGNC:2292]"}, {"versioned_ensembl_gene_id":"ENSG00000275198.1","gene_symbol":"AL512791.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90383365,"end":90387973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266809.1","gene_symbol":"AC022884.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24689914,"end":24690161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118515.11","gene_symbol":"SGK1","gene_name":"serum/glucocorticoid regulated kinase 1 [Source:HGNC Symbol;Acc:HGNC:10810]","synonyms":"SGK","biotype":"protein_coding","ncbi_id":"6446","summary":"This gene encodes a serine/threonine protein kinase that plays an important role in cellular stress response. This kinase activates certain potassium, sodium, and chloride channels, suggesting an involvement in the regulation of processes such as cell survival, neuronal excitability, and renal sodium excretion. High levels of expression of this gene may contribute to conditions such as hypertension and diabetic nephropathy. Several alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]","start":134169246,"end":134318112,"strand":-1,"description":"serum/glucocorticoid regulated kinase 1 [Source:HGNC Symbol;Acc:HGNC:10810]"}, {"versioned_ensembl_gene_id":"ENSG00000213397.10","gene_symbol":"HAUS7","gene_name":"HAUS augmin like complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:32979]","synonyms":"UIP1,UCHL5IP","biotype":"protein_coding","ncbi_id":"55559","summary":"This gene encodes a subunit of the augmin complex, which regulates centrosome and mitotic spindle integrity, and is necessary for the completion of cytokinesis. The encoded protein was identified by interaction with ubiquitin C-terminal hydrolase 37. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":153447666,"end":153495516,"strand":-1,"description":"HAUS augmin like complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:32979]"}, {"versioned_ensembl_gene_id":"ENSG00000249349.1","gene_symbol":"AC114928.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85112342,"end":85112756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182224.11","gene_symbol":"CYB5D1","gene_name":"cytochrome b5 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26516]","synonyms":"FLJ32499","biotype":"protein_coding","ncbi_id":"124637","summary":null,"start":7857746,"end":7862282,"strand":1,"description":"cytochrome b5 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26516]"}, {"versioned_ensembl_gene_id":"ENSG00000226986.4","gene_symbol":"AC092017.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211207239,"end":211207897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067221.13","gene_symbol":"STOML1","gene_name":"stomatin like 1 [Source:HGNC Symbol;Acc:HGNC:14560]","synonyms":"STORP,SLP-1,hUNC-24,FLJ36370","biotype":"protein_coding","ncbi_id":"9399","summary":null,"start":73978923,"end":73994622,"strand":-1,"description":"stomatin like 1 [Source:HGNC Symbol;Acc:HGNC:14560]"}, {"versioned_ensembl_gene_id":"ENSG00000214897.4","gene_symbol":"PNMA6E","gene_name":"paraneoplastic Ma antigen family member 6E [Source:HGNC Symbol;Acc:HGNC:50767]","synonyms":null,"biotype":"protein_coding","ncbi_id":"649238","summary":null,"start":153395640,"end":153401420,"strand":-1,"description":"paraneoplastic Ma antigen family member 6E [Source:HGNC Symbol;Acc:HGNC:50767]"}, {"versioned_ensembl_gene_id":"ENSG00000070159.13","gene_symbol":"PTPN3","gene_name":"protein tyrosine phosphatase, non-receptor type 3 [Source:HGNC Symbol;Acc:HGNC:9655]","synonyms":"PTPH1","biotype":"protein_coding","ncbi_id":"5774","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This protein contains a C-terminal PTP domain and an N-terminal domain homologous to the band 4.1 superfamily of cytoskeletal-associated proteins. P97, a cell cycle regulator involved in a variety of membrane related functions, has been shown to be a substrate of this PTP. This PTP was also found to interact with, and be regulated by adaptor protein 14-3-3 beta. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":109375466,"end":109498313,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 3 [Source:HGNC Symbol;Acc:HGNC:9655]"}, {"versioned_ensembl_gene_id":"ENSG00000255552.7","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31711771,"end":31714065,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000236022.6","gene_symbol":"AC106017.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19203825,"end":19214045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261335.1","gene_symbol":"AC005837.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76671942,"end":76673658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253274.1","gene_symbol":"IGHV1-67","gene_name":"immunoglobulin heavy variable 1-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5556]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28463","summary":null,"start":106680603,"end":106681042,"strand":-1,"description":"immunoglobulin heavy variable 1-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5556]"}, {"versioned_ensembl_gene_id":"ENSG00000230541.1","gene_symbol":"HCG21","gene_name":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]","synonyms":"NCRNA00150,AB023048.2","biotype":"processed_transcript","ncbi_id":"102723346","summary":null,"start":30935539,"end":30944421,"strand":-1,"description":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]"}, {"versioned_ensembl_gene_id":"ENSG00000265639.1","gene_symbol":"AC090415.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71028770,"end":71033056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265781.1","gene_symbol":"AC090415.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71000477,"end":71011490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229284.4","gene_symbol":"DPCR1","gene_name":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]","synonyms":"C6orf37,bCX105N19.6,PBLT","biotype":"protein_coding","ncbi_id":"135656","summary":null,"start":30930561,"end":30943780,"strand":1,"description":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]"}, {"versioned_ensembl_gene_id":"ENSG00000270909.1","gene_symbol":"CR788268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41979352,"end":41983753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278803.1","gene_symbol":"AC236972.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153276841,"end":153277803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231600.1","gene_symbol":"AC236972.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153249115,"end":153249691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132510.10","gene_symbol":"KDM6B","gene_name":"lysine demethylase 6B [Source:HGNC Symbol;Acc:HGNC:29012]","synonyms":"KIAA0346,JMJD3","biotype":"protein_coding","ncbi_id":"23135","summary":"The protein encoded by this gene is a lysine-specific demethylase that specifically demethylates di- or tri-methylated lysine 27 of histone H3 (H3K27me2 or H3K27me3). H3K27 trimethylation is a repressive epigenetic mark controlling chromatin organization and gene silencing. This protein can also demethylate non-histone proteins such as retinoblastoma protein. Through its demethylation actvity this gene influences cellular differentiation and development, tumorigenesis, inflammatory diseases, and neurodegenerative diseases. This protein has two classical nuclear localization signals at its N-terminus. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]","start":7839904,"end":7854796,"strand":1,"description":"lysine demethylase 6B [Source:HGNC Symbol;Acc:HGNC:29012]"}, {"versioned_ensembl_gene_id":"ENSG00000198681.6","gene_symbol":"MAGEA1","gene_name":"MAGE family member A1 [Source:HGNC Symbol;Acc:HGNC:6796]","synonyms":"MGC9326,MAGE1,CT1.1","biotype":"protein_coding","ncbi_id":"4100","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]","start":153179285,"end":153183880,"strand":1,"description":"MAGE family member A1 [Source:HGNC Symbol;Acc:HGNC:6796]"}, {"versioned_ensembl_gene_id":"ENSG00000161544.9","gene_symbol":"CYGB","gene_name":"cytoglobin [Source:HGNC Symbol;Acc:HGNC:16505]","synonyms":"STAP,HGB","biotype":"protein_coding","ncbi_id":"114757","summary":"This gene encodes a globin protein found in vertebrate cells. The encoded protein is described as a hexacoordinate hemoglobin which binds ligand differently from the pentacoordinate hemoglobins involved in oxygen transport, and may be involved in protection during oxidative stress. This gene is located on chromosome 17 in the same region as a retinal gene which is mutated in progressive rod-cone degeneration, but in the opposite orientation. [provided by RefSeq, Jan 2012]","start":76527356,"end":76551175,"strand":-1,"description":"cytoglobin [Source:HGNC Symbol;Acc:HGNC:16505]"}, {"versioned_ensembl_gene_id":"ENSG00000267033.1","gene_symbol":"AC020911.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16186276,"end":16189458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115009.11","gene_symbol":"CCL20","gene_name":"C-C motif chemokine ligand 20 [Source:HGNC Symbol;Acc:HGNC:10619]","synonyms":"MIP-3a,LARC,exodus-1,CKb4,ST38,SCYA20","biotype":"protein_coding","ncbi_id":"6364","summary":"This antimicrobial gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The protein encoded by this gene displays chemotactic activity for lymphocytes and can repress proliferation of myeloid progenitors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":227813842,"end":227817564,"strand":1,"description":"C-C motif chemokine ligand 20 [Source:HGNC Symbol;Acc:HGNC:10619]"}, {"versioned_ensembl_gene_id":"ENSG00000233308.1","gene_symbol":"OSTN-AS1","gene_name":"OSTN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41250]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480738","summary":null,"start":191213291,"end":191234605,"strand":-1,"description":"OSTN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41250]"}, {"versioned_ensembl_gene_id":"ENSG00000229172.1","gene_symbol":"AC073065.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227801840,"end":227804705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230310.1","gene_symbol":"AC010422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12552597,"end":12553644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141698.16","gene_symbol":"NT5C3B","gene_name":"5'-nucleotidase, cytosolic IIIB [Source:HGNC Symbol;Acc:HGNC:28300]","synonyms":"cN-IIIB,NT5C3L,MGC20781","biotype":"protein_coding","ncbi_id":"115024","summary":null,"start":41825181,"end":41836263,"strand":-1,"description":"5'-nucleotidase, cytosolic IIIB [Source:HGNC Symbol;Acc:HGNC:28300]"}, {"versioned_ensembl_gene_id":"ENSG00000235275.3","gene_symbol":"KRT18P16","gene_name":"keratin 18 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:33384]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391827","summary":null,"start":123636110,"end":123637403,"strand":1,"description":"keratin 18 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:33384]"}, {"versioned_ensembl_gene_id":"ENSG00000251018.2","gene_symbol":"HMMR-AS1","gene_name":"HMMR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49149]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927813","summary":null,"start":163483065,"end":163494058,"strand":-1,"description":"HMMR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49149]"}, {"versioned_ensembl_gene_id":"ENSG00000275297.1","gene_symbol":"AL162731.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":41760088,"end":41764175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274104.1","gene_symbol":"AC020910.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34733298,"end":34733837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140153.17","gene_symbol":"WDR20","gene_name":"WD repeat domain 20 [Source:HGNC Symbol;Acc:HGNC:19667]","synonyms":"MGC33177,FLJ33659,DMR","biotype":"protein_coding","ncbi_id":"91833","summary":"This gene encodes a WD repeat-containing protein that functions to preserve and regulate the activity of the USP12-UAF1 deubiquitinating enzyme complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011]","start":102139503,"end":102224847,"strand":1,"description":"WD repeat domain 20 [Source:HGNC Symbol;Acc:HGNC:19667]"}, {"versioned_ensembl_gene_id":"ENSG00000188613.6","gene_symbol":"NANOS1","gene_name":"nanos C2HC-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:23044]","synonyms":"ZC2HC12A,NOS1","biotype":"protein_coding","ncbi_id":"340719","summary":"This gene encodes a CCHC-type zinc finger protein that is a member of the nanos family. This protein co-localizes with the RNA-binding protein pumilio RNA-binding family member 2 and may be involved in regulating translation as a post-transcriptional repressor. Mutations in this gene are associated with spermatogenic impairment. [provided by RefSeq, Sep 2015]","start":119029716,"end":119033732,"strand":1,"description":"nanos C2HC-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:23044]"}, {"versioned_ensembl_gene_id":"ENSG00000132341.11","gene_symbol":"RAN","gene_name":"RAN, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9846]","synonyms":"Gsp1,ARA24,TC4","biotype":"protein_coding","ncbi_id":"5901","summary":"RAN (ras-related nuclear protein) is a small GTP binding protein belonging to the RAS superfamily that is essential for the translocation of RNA and proteins through the nuclear pore complex. The RAN protein is also involved in control of DNA synthesis and cell cycle progression. Nuclear localization of RAN requires the presence of regulator of chromosome condensation 1 (RCC1). Mutations in RAN disrupt DNA synthesis. Because of its many functions, it is likely that RAN interacts with several other proteins. RAN regulates formation and organization of the microtubule network independently of its role in the nucleus-cytosol exchange of macromolecules. RAN could be a key signaling molecule regulating microtubule polymerization during mitosis. RCC1 generates a high local concentration of RAN-GTP around chromatin which, in turn, induces the local nucleation of microtubules. RAN is an androgen receptor (AR) coactivator that binds differentially with different lengths of polyglutamine within the androgen receptor. Polyglutamine repeat expansion in the AR is linked to Kennedy's disease (X-linked spinal and bulbar muscular atrophy). RAN coactivation of the AR diminishes with polyglutamine expansion within the AR, and this weak coactivation may lead to partial androgen insensitivity during the development of Kennedy's disease. [provided by RefSeq, Jul 2008]","start":130871879,"end":130877678,"strand":1,"description":"RAN, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9846]"}, {"versioned_ensembl_gene_id":"ENSG00000269919.1","gene_symbol":"AL022067.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":106100140,"end":106100593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136828.18","gene_symbol":"RALGPS1","gene_name":"Ral GEF with PH domain and SH3 binding motif 1 [Source:HGNC Symbol;Acc:HGNC:16851]","synonyms":"RALGPS1A,RALGEF2,KIAA0351","biotype":"protein_coding","ncbi_id":"9649","summary":null,"start":126914774,"end":127223166,"strand":1,"description":"Ral GEF with PH domain and SH3 binding motif 1 [Source:HGNC Symbol;Acc:HGNC:16851]"}, {"versioned_ensembl_gene_id":"ENSG00000226197.2","gene_symbol":"AL583785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13446491,"end":13487511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225437.5","gene_symbol":"PACRG-AS2","gene_name":"PACRG antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40871]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929239","summary":null,"start":163042557,"end":163054161,"strand":-1,"description":"PACRG antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40871]"}, {"versioned_ensembl_gene_id":"ENSG00000275475.1","gene_symbol":"IGHV3-54","gene_name":"immunoglobulin heavy variable 3-54 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5611]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28419","summary":null,"start":106601346,"end":106601792,"strand":-1,"description":"immunoglobulin heavy variable 3-54 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5611]"}, {"versioned_ensembl_gene_id":"ENSG00000253714.1","gene_symbol":"IGHVII-53-1","gene_name":"immunoglobulin heavy variable (II)-53-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5685]","synonyms":"IGHV(II)-53-1","biotype":"IG_V_pseudogene","ncbi_id":"28362","summary":null,"start":106599670,"end":106599924,"strand":-1,"description":"immunoglobulin heavy variable (II)-53-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5685]"}, {"versioned_ensembl_gene_id":"ENSG00000167644.11","gene_symbol":"C19orf33","gene_name":"chromosome 19 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:16668]","synonyms":"IMUP-2,IMUP-1,IMUP,H2RSP","biotype":"protein_coding","ncbi_id":"64073","summary":"The protein encoded by this gene has been shown to be upregulated in SV40-immortalized fibroblasts as well as in endometrial carcinoma cells. The encoded protein is found primarily in the nucleus. This protein may play a role in placental development and diseases such as pre-eclampsia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":38304161,"end":38305009,"strand":1,"description":"chromosome 19 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:16668]"}, {"versioned_ensembl_gene_id":"ENSG00000253941.1","gene_symbol":"IGHVII-51-2","gene_name":"immunoglobulin heavy variable (II)-51-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5684]","synonyms":"IGHV(II)-51-2","biotype":"IG_V_pseudogene","ncbi_id":"28363","summary":null,"start":106584718,"end":106584976,"strand":-1,"description":"immunoglobulin heavy variable (II)-51-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5684]"}, {"versioned_ensembl_gene_id":"ENSG00000253545.1","gene_symbol":"IGHV3-52","gene_name":"immunoglobulin heavy variable 3-52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5609]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28421","summary":null,"start":106586376,"end":106586826,"strand":-1,"description":"immunoglobulin heavy variable 3-52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5609]"}, {"versioned_ensembl_gene_id":"ENSG00000176915.14","gene_symbol":"ANKLE2","gene_name":"ankyrin repeat and LEM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29101]","synonyms":"KIAA0692,LEMD7,Lem4","biotype":"protein_coding","ncbi_id":"23141","summary":"This gene encodes a member of the LEM family of inner nuclear membrane proteins. The encoded protein functions as a mitotic regulator through postmitotic formation of the nuclear envelope. Mutations in this gene cause morphology defects in the nuclear envelope and BAF hyperphosphorylation. [provided by RefSeq, Mar 2014]","start":132725503,"end":132761888,"strand":-1,"description":"ankyrin repeat and LEM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29101]"}, {"versioned_ensembl_gene_id":"ENSG00000253241.1","gene_symbol":"IGHV3-50","gene_name":"immunoglobulin heavy variable 3-50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5608]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28422","summary":null,"start":106566117,"end":106566555,"strand":-1,"description":"immunoglobulin heavy variable 3-50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5608]"}, {"versioned_ensembl_gene_id":"ENSG00000229092.2","gene_symbol":"IGHV3-47","gene_name":"immunoglobulin heavy variable 3-47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5605]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28425","summary":null,"start":106518582,"end":106519027,"strand":-1,"description":"immunoglobulin heavy variable 3-47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5605]"}, {"versioned_ensembl_gene_id":"ENSG00000228546.2","gene_symbol":"AC091390.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102337316,"end":102339115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253895.1","gene_symbol":"IGHVII-44-2","gene_name":"immunoglobulin heavy variable (II)-44-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5681]","synonyms":"IGHV(II)-44-2","biotype":"IG_V_pseudogene","ncbi_id":"28366","summary":null,"start":106494134,"end":106494383,"strand":-1,"description":"immunoglobulin heavy variable (II)-44-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5681]"}, {"versioned_ensembl_gene_id":"ENSG00000089335.20","gene_symbol":"ZNF302","gene_name":"zinc finger protein 302 [Source:HGNC Symbol;Acc:HGNC:13848]","synonyms":"ZNF327,ZNF140L,ZNF135L","biotype":"protein_coding","ncbi_id":"55900","summary":"This gene encodes a member of the zinc-finger protein family. The encoded protein contains seven C2H2-type zinc fingers and a KRAB domain, but its function has yet to be determined. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2014]","start":34677639,"end":34686397,"strand":1,"description":"zinc finger protein 302 [Source:HGNC Symbol;Acc:HGNC:13848]"}, {"versioned_ensembl_gene_id":"ENSG00000228737.2","gene_symbol":"AC008781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141618414,"end":141626481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254383.1","gene_symbol":"AC048387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40900016,"end":40901854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171202.6","gene_symbol":"TMEM126A","gene_name":"transmembrane protein 126A [Source:HGNC Symbol;Acc:HGNC:25382]","synonyms":"OPA7,DKFZp586C1924","biotype":"protein_coding","ncbi_id":"84233","summary":"The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":85647967,"end":85656547,"strand":1,"description":"transmembrane protein 126A [Source:HGNC Symbol;Acc:HGNC:25382]"}, {"versioned_ensembl_gene_id":"ENSG00000145907.14","gene_symbol":"G3BP1","gene_name":"G3BP stress granule assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:30292]","synonyms":"HDH-VIII,G3BP","biotype":"protein_coding","ncbi_id":"10146","summary":"This gene encodes one of the DNA-unwinding enzymes which prefers partially unwound 3'-tailed substrates and can also unwind partial RNA/DNA and RNA/RNA duplexes in an ATP-dependent fashion. This enzyme is a member of the heterogeneous nuclear RNA-binding proteins and is also an element of the Ras signal transduction pathway. It binds specifically to the Ras-GTPase-activating protein by associating with its SH3 domain. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":151771045,"end":151812785,"strand":1,"description":"G3BP stress granule assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:30292]"}, {"versioned_ensembl_gene_id":"ENSG00000139540.11","gene_symbol":"SLC39A5","gene_name":"solute carrier family 39 member 5 [Source:HGNC Symbol;Acc:HGNC:20502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283375","summary":"The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":56230049,"end":56237846,"strand":1,"description":"solute carrier family 39 member 5 [Source:HGNC Symbol;Acc:HGNC:20502]"}, {"versioned_ensembl_gene_id":"ENSG00000254228.2","gene_symbol":"IGHV3-42","gene_name":"immunoglobulin heavy variable 3-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5603]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28427","summary":null,"start":106463256,"end":106463691,"strand":-1,"description":"immunoglobulin heavy variable 3-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5603]"}, {"versioned_ensembl_gene_id":"ENSG00000273228.1","gene_symbol":"AP002826.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57029408,"end":57029722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227625.2","gene_symbol":"AL359510.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":228134785,"end":228134992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155890.3","gene_symbol":"TRIM42","gene_name":"tripartite motif containing 42 [Source:HGNC Symbol;Acc:HGNC:19014]","synonyms":"T4A1,PPP1R40,FLJ40097","biotype":"protein_coding","ncbi_id":"287015","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, namely a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. [provided by RefSeq, Jul 2008]","start":140678039,"end":140701150,"strand":1,"description":"tripartite motif containing 42 [Source:HGNC Symbol;Acc:HGNC:19014]"}, {"versioned_ensembl_gene_id":"ENSG00000165782.10","gene_symbol":"TMEM55B","gene_name":"transmembrane protein 55B [Source:HGNC Symbol;Acc:HGNC:19299]","synonyms":"MGC26684,C14orf9","biotype":"protein_coding","ncbi_id":"90809","summary":"TMEM55B catalyzes the degradation of phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) by removing the 4-phosphate (Ungewickell et al., 2005 [PubMed 16365287]).[supplied by OMIM, Mar 2008]","start":20457719,"end":20461612,"strand":-1,"description":"transmembrane protein 55B [Source:HGNC Symbol;Acc:HGNC:19299]"}, {"versioned_ensembl_gene_id":"ENSG00000226876.2","gene_symbol":"AC092801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":246108626,"end":246113866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147724.11","gene_symbol":"FAM135B","gene_name":"family with sequence similarity 135 member B [Source:HGNC Symbol;Acc:HGNC:28029]","synonyms":"C8ORFK32","biotype":"protein_coding","ncbi_id":"51059","summary":null,"start":138130023,"end":138496822,"strand":-1,"description":"family with sequence similarity 135 member B [Source:HGNC Symbol;Acc:HGNC:28029]"}, {"versioned_ensembl_gene_id":"ENSG00000204316.12","gene_symbol":"MRPL38","gene_name":"mitochondrial ribosomal protein L38 [Source:HGNC Symbol;Acc:HGNC:14033]","synonyms":"HSPC262,RPML3,MRP-L3,MGC4810","biotype":"protein_coding","ncbi_id":"64978","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":75898643,"end":75905413,"strand":-1,"description":"mitochondrial ribosomal protein L38 [Source:HGNC Symbol;Acc:HGNC:14033]"}, {"versioned_ensembl_gene_id":"ENSG00000236116.1","gene_symbol":"AC064853.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":227616998,"end":227617790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284704.1","gene_symbol":"AC064853.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227614538,"end":227614840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231099.1","gene_symbol":"BMS1P19","gene_name":"BMS1, ribosome biogenesis factor pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49163]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131577","summary":null,"start":109667128,"end":109668002,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49163]"}, {"versioned_ensembl_gene_id":"ENSG00000274658.1","gene_symbol":"TBC1D3J","gene_name":"TBC1 domain family member 3J [Source:HGNC Symbol;Acc:HGNC:51247]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100510707","summary":null,"start":36450146,"end":36457535,"strand":-1,"description":"TBC1 domain family member 3J [Source:HGNC Symbol;Acc:HGNC:51247]"}, {"versioned_ensembl_gene_id":"ENSG00000111361.12","gene_symbol":"EIF2B1","gene_name":"eukaryotic translation initiation factor 2B subunit alpha [Source:HGNC Symbol;Acc:HGNC:3257]","synonyms":"EIF2BA,EIF2B,EIF-2Balpha,EIF-2B","biotype":"protein_coding","ncbi_id":"1967","summary":"This gene encodes one of five subunits of eukaryotic translation initiation factor 2B (EIF2B), a GTP exchange factor for eukaryotic initiation factor 2 and an essential regulator for protein synthesis. Mutations in this gene and the genes encoding other EIF2B subunits have been associated with leukoencephalopathy with vanishing white matter. [provided by RefSeq, Oct 2009]","start":123620406,"end":123633766,"strand":-1,"description":"eukaryotic translation initiation factor 2B subunit alpha [Source:HGNC Symbol;Acc:HGNC:3257]"}, {"versioned_ensembl_gene_id":"ENSG00000231199.2","gene_symbol":"MTND5P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42301]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873270","summary":null,"start":235538052,"end":235539845,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42301]"}, {"versioned_ensembl_gene_id":"ENSG00000253669.3","gene_symbol":"AP003356.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102805517,"end":102809971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278850.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"cl-5,nkat4b,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54849551,"end":54866326,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000197070.13","gene_symbol":"ARRDC1","gene_name":"arrestin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28633]","synonyms":"MGC40555","biotype":"protein_coding","ncbi_id":"92714","summary":null,"start":137605654,"end":137615360,"strand":1,"description":"arrestin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28633]"}, {"versioned_ensembl_gene_id":"ENSG00000233483.2","gene_symbol":"AC008105.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45245186,"end":45248836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230958.1","gene_symbol":"AC093166.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111865798,"end":111866405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235042.1","gene_symbol":"AC098820.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216385288,"end":216412696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241520.1","gene_symbol":"AC098820.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216483032,"end":216487196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163412.12","gene_symbol":"EIF4E3","gene_name":"eukaryotic translation initiation factor 4E family member 3 [Source:HGNC Symbol;Acc:HGNC:31837]","synonyms":"MGC39820","biotype":"protein_coding","ncbi_id":"317649","summary":"EIF4E3 belongs to the EIF4E family of translational initiation factors that interact with the 5-prime cap structure of mRNA and recruit mRNA to the ribosome (Joshi et al., 2004 [PubMed 15153109]).[supplied by OMIM, Mar 2008]","start":71675416,"end":71754773,"strand":-1,"description":"eukaryotic translation initiation factor 4E family member 3 [Source:HGNC Symbol;Acc:HGNC:31837]"}, {"versioned_ensembl_gene_id":"ENSG00000112658.7","gene_symbol":"SRF","gene_name":"serum response factor [Source:HGNC Symbol;Acc:HGNC:11291]","synonyms":"MCM1","biotype":"protein_coding","ncbi_id":"6722","summary":"This gene encodes a ubiquitous nuclear protein that stimulates both cell proliferation and differentiation. It is a member of the MADS (MCM1, Agamous, Deficiens, and SRF) box superfamily of transcription factors. This protein binds to the serum response element (SRE) in the promoter region of target genes. This protein regulates the activity of many immediate-early genes, for example c-fos, and thereby participates in cell cycle regulation, apoptosis, cell growth, and cell differentiation. This gene is the downstream target of many pathways; for example, the mitogen-activated protein kinase pathway (MAPK) that acts through the ternary complex factors (TCFs). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":43171299,"end":43181507,"strand":1,"description":"serum response factor [Source:HGNC Symbol;Acc:HGNC:11291]"}, {"versioned_ensembl_gene_id":"ENSG00000157045.8","gene_symbol":"NTAN1","gene_name":"N-terminal asparagine amidase [Source:HGNC Symbol;Acc:HGNC:29909]","synonyms":null,"biotype":"protein_coding","ncbi_id":"123803","summary":"The protein encoded by this gene functions in a step-wise process of protein degradation through the N-end rule pathway. This protein acts as a tertiary destabilizing enzyme that deamidates N-terminal L-Asn residues on proteins to produce N-terminal L-Asp. L-Asp substrates are subsequently conjugated to L-Arg, which is recognized by specific E3 ubiquitin ligases and targeted to the proteasome. Pseudogenes of this gene are located on the long arms of chromosomes 8, 10 and 12. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":15037853,"end":15056079,"strand":-1,"description":"N-terminal asparagine amidase [Source:HGNC Symbol;Acc:HGNC:29909]"}, {"versioned_ensembl_gene_id":"ENSG00000253625.1","gene_symbol":"IGKV2-23","gene_name":"immunoglobulin kappa variable 2-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5780]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28924","summary":null,"start":89172022,"end":89172553,"strand":-1,"description":"immunoglobulin kappa variable 2-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5780]"}, {"versioned_ensembl_gene_id":"ENSG00000223840.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"TRIM26P,Em:AB023053.1,TRIM26P1","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30228173,"end":30232162,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000253578.1","gene_symbol":"IGKV1-22","gene_name":"immunoglobulin kappa variable 1-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5734]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28936","summary":null,"start":89170775,"end":89171212,"strand":-1,"description":"immunoglobulin kappa variable 1-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5734]"}, {"versioned_ensembl_gene_id":"ENSG00000167081.16","gene_symbol":"PBX3","gene_name":"PBX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:8634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5090","summary":null,"start":125747345,"end":125967377,"strand":1,"description":"PBX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:8634]"}, {"versioned_ensembl_gene_id":"ENSG00000163378.13","gene_symbol":"EOGT","gene_name":"EGF domain specific O-linked N-acetylglucosamine transferase [Source:HGNC Symbol;Acc:HGNC:28526]","synonyms":"FLJ33770,C3orf64,AER61","biotype":"protein_coding","ncbi_id":"285203","summary":"This gene encodes an enzyme that acts in the lumen of the endoplasmic reticulum to catalyze the transfer of N-acetylglucosamine to serine or threonine residues of extracellular-targeted proteins. This enzyme modifies proteins containing eukaryotic growth factor (EGF)-like domains, including the Notch receptor, thereby regulating developmental signalling. Mutations in this gene have been observed in individuals with Adams-Oliver syndrome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":68975214,"end":69013961,"strand":-1,"description":"EGF domain specific O-linked N-acetylglucosamine transferase [Source:HGNC Symbol;Acc:HGNC:28526]"}, {"versioned_ensembl_gene_id":"ENSG00000139567.12","gene_symbol":"ACVRL1","gene_name":"activin A receptor like type 1 [Source:HGNC Symbol;Acc:HGNC:175]","synonyms":"ORW2,HHT2,HHT,ALK1,ACVRLK1","biotype":"protein_coding","ncbi_id":"94","summary":"This gene encodes a type I cell-surface receptor for the TGF-beta superfamily of ligands. It shares with other type I receptors a high degree of similarity in serine-threonine kinase subdomains, a glycine- and serine-rich region (called the GS domain) preceding the kinase domain, and a short C-terminal tail. The encoded protein, sometimes termed ALK1, shares similar domain structures with other closely related ALK or activin receptor-like kinase proteins that form a subfamily of receptor serine/threonine kinases. Mutations in this gene are associated with hemorrhagic telangiectasia type 2, also known as Rendu-Osler-Weber syndrome 2. [provided by RefSeq, Jul 2008]","start":51906908,"end":51923361,"strand":1,"description":"activin A receptor like type 1 [Source:HGNC Symbol;Acc:HGNC:175]"}, {"versioned_ensembl_gene_id":"ENSG00000214653.4","gene_symbol":"HNRNPA3P3","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643689","summary":null,"start":140032344,"end":140033480,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39772]"}, {"versioned_ensembl_gene_id":"ENSG00000164040.16","gene_symbol":"PGRMC2","gene_name":"progesterone receptor membrane component 2 [Source:HGNC Symbol;Acc:HGNC:16089]","synonyms":"PMBP,DG6","biotype":"protein_coding","ncbi_id":"10424","summary":null,"start":128269237,"end":128288829,"strand":-1,"description":"progesterone receptor membrane component 2 [Source:HGNC Symbol;Acc:HGNC:16089]"}, {"versioned_ensembl_gene_id":"ENSG00000238111.1","gene_symbol":"AC066692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23900693,"end":23901149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132698.14","gene_symbol":"RAB25","gene_name":"RAB25, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18238]","synonyms":"CATX-8","biotype":"protein_coding","ncbi_id":"57111","summary":"The protein encoded by this gene is a member of the RAS superfamily of small GTPases. The encoded protein is involved in membrane trafficking and cell survival. This gene has been found to be a tumor suppressor and an oncogene, depending on the context. Two variants, one protein-coding and the other not, have been found for this gene. [provided by RefSeq, Nov 2015]","start":156061160,"end":156070514,"strand":1,"description":"RAB25, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18238]"}, {"versioned_ensembl_gene_id":"ENSG00000211898.7","gene_symbol":"IGHD","gene_name":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]","synonyms":"MGC29633,FLJ46727,FLJ00382","biotype":"IG_C_gene","ncbi_id":"3495","summary":null,"start":105836765,"end":105845678,"strand":-1,"description":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]"}, {"versioned_ensembl_gene_id":"ENSG00000283959.1","gene_symbol":"AP002851.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":102656464,"end":102687118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206522.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29111883,"end":29112818,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000187720.14","gene_symbol":"THSD4","gene_name":"thrombospondin type 1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25835]","synonyms":"ADAMTSL6,PRO34005,FVSY9334,FLJ13710","biotype":"protein_coding","ncbi_id":"79875","summary":null,"start":71096952,"end":71783383,"strand":1,"description":"thrombospondin type 1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25835]"}, {"versioned_ensembl_gene_id":"ENSG00000254028.1","gene_symbol":"AC083843.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134832747,"end":134834482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073803.13","gene_symbol":"MAP3K13","gene_name":"mitogen-activated protein kinase kinase kinase 13 [Source:HGNC Symbol;Acc:HGNC:6852]","synonyms":"MEKK13,LZK","biotype":"protein_coding","ncbi_id":"9175","summary":"The protein encoded by this gene is a member of serine/threonine protein kinase family. This kinase contains a dual leucine-zipper motif, and has been shown to form dimers/oligomers through its leucine-zipper motif. This kinase can phosphorylate and activate MAPK8/JNK, MAP2K7/MKK7, which suggests a role in the JNK signaling pathway. [provided by RefSeq, Jul 2008]","start":185282941,"end":185489097,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 13 [Source:HGNC Symbol;Acc:HGNC:6852]"}, {"versioned_ensembl_gene_id":"ENSG00000157388.15","gene_symbol":"CACNA1D","gene_name":"calcium voltage-gated channel subunit alpha1 D [Source:HGNC Symbol;Acc:HGNC:1391]","synonyms":"CCHL1A2,Cav1.3,CACNL1A2,CACN4,CACH3","biotype":"protein_coding","ncbi_id":"776","summary":"Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, namely alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1D subunit. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":53328963,"end":53813733,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 D [Source:HGNC Symbol;Acc:HGNC:1391]"}, {"versioned_ensembl_gene_id":"ENSG00000254287.1","gene_symbol":"AC007991.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39918076,"end":39920890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000016391.10","gene_symbol":"CHDH","gene_name":"choline dehydrogenase [Source:HGNC Symbol;Acc:HGNC:24288]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55349","summary":"The protein encoded by this gene is a choline dehydrogenase that localizes to the mitochondrion. Variations in this gene can affect susceptibility to choline deficiency. A few transcript variants have been found for this gene, but the full-length nature of only one has been characterized to date. [provided by RefSeq, Dec 2010]","start":53812335,"end":53846390,"strand":-1,"description":"choline dehydrogenase [Source:HGNC Symbol;Acc:HGNC:24288]"}, {"versioned_ensembl_gene_id":"ENSG00000253364.2","gene_symbol":"AL928742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105647924,"end":105649057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231104.8","gene_symbol":"AC022395.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118017487,"end":118045810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279478.1","gene_symbol":"AC127071.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130383364,"end":130383890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124196.5","gene_symbol":"GTSF1L","gene_name":"gametocyte specific factor 1 like [Source:HGNC Symbol;Acc:HGNC:16198]","synonyms":"FAM112A,dJ1028D15.4,C20orf65","biotype":"protein_coding","ncbi_id":"149699","summary":null,"start":43726164,"end":43726998,"strand":-1,"description":"gametocyte specific factor 1 like [Source:HGNC Symbol;Acc:HGNC:16198]"}, {"versioned_ensembl_gene_id":"ENSG00000226795.1","gene_symbol":"AL929561.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29076560,"end":29077155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254185.1","gene_symbol":"AC021001.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109470131,"end":109471117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206525.2","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044198,"end":29045225,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000272777.1","gene_symbol":"AC019131.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99067256,"end":99068125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143450.16","gene_symbol":"OAZ3","gene_name":"ornithine decarboxylase antizyme 3 [Source:HGNC Symbol;Acc:HGNC:8097]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51686","summary":"The protein encoded by this gene belongs to the ornithine decarboxylase antizyme family, which plays a role in cell growth and proliferation by regulating intracellular polyamine levels. Expression of antizymes requires +1 ribosomal frameshifting, which is enhanced by high levels of polyamines. Antizymes in turn bind to and inhibit ornithine decarboxylase (ODC), the key enzyme in polyamine biosynthesis; thus, completing the auto-regulatory circuit. This gene encodes antizyme 3, the third member of the antizyme family. Like antizymes 1 and 2, antizyme 3 inhibits ODC activity and polyamine uptake; however, it does not stimulate ODC degradation. Also, while antizymes 1 and 2 have broad tissue distribution, expression of antizyme 3 is restricted to haploid germ cells in testis, suggesting a distinct role for this antizyme in spermiogenesis. Antizyme 3 gene knockout studies showed that homozygous mutant male mice were infertile, and indicated the likely role of this antizyme in the formation of a rigid connection between the sperm head and tail during spermatogenesis. Alternatively spliced transcript variants encoding different isoforms, including one resulting from the use of non-AUG (CUG) translation initiation codon, have been found for this gene. [provided by RefSeq, Dec 2014]","start":151762899,"end":151771334,"strand":1,"description":"ornithine decarboxylase antizyme 3 [Source:HGNC Symbol;Acc:HGNC:8097]"}, {"versioned_ensembl_gene_id":"ENSG00000176101.11","gene_symbol":"SSNA1","gene_name":"SS nuclear autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:11321]","synonyms":"NA14,N14","biotype":"protein_coding","ncbi_id":"8636","summary":null,"start":137188647,"end":137190370,"strand":1,"description":"SS nuclear autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:11321]"}, {"versioned_ensembl_gene_id":"ENSG00000182173.12","gene_symbol":"TSEN54","gene_name":"tRNA splicing endonuclease subunit 54 [Source:HGNC Symbol;Acc:HGNC:27561]","synonyms":"SEN54L,SEN54","biotype":"protein_coding","ncbi_id":"283989","summary":"This gene encodes a subunit of the tRNA splicing endonuclease complex, which catalyzes the removal of introns from precursor tRNAs. The complex is also implicated in pre-mRNA 3-prime end processing. Mutations in this gene result in pontocerebellar hypoplasia type 2.[provided by RefSeq, Oct 2009]","start":75516060,"end":75524739,"strand":1,"description":"tRNA splicing endonuclease subunit 54 [Source:HGNC Symbol;Acc:HGNC:27561]"}, {"versioned_ensembl_gene_id":"ENSG00000188396.3","gene_symbol":"TCTEX1D4","gene_name":"Tctex1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343521","summary":null,"start":44805913,"end":44806675,"strand":-1,"description":"Tctex1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32315]"}, {"versioned_ensembl_gene_id":"ENSG00000259015.1","gene_symbol":"AL442663.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72960595,"end":72961993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137714.2","gene_symbol":"FDX1","gene_name":"ferredoxin 1 [Source:HGNC Symbol;Acc:HGNC:3638]","synonyms":"FDX,ADX","biotype":"protein_coding","ncbi_id":"2230","summary":"This gene encodes a small iron-sulfur protein that transfers electrons from NADPH through ferredoxin reductase to mitochondrial cytochrome P450, involved in steroid, vitamin D, and bile acid metabolism. Pseudogenes of this functional gene are found on chromosomes 20 and 21. [provided by RefSeq, Aug 2011]","start":110429883,"end":110464881,"strand":1,"description":"ferredoxin 1 [Source:HGNC Symbol;Acc:HGNC:3638]"}, {"versioned_ensembl_gene_id":"ENSG00000275944.1","gene_symbol":"AC244100.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36001419,"end":36011618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188833.9","gene_symbol":"ENTPD8","gene_name":"ectonucleoside triphosphate diphosphohydrolase 8 [Source:HGNC Symbol;Acc:HGNC:24860]","synonyms":"UNQ2492,NTPDase-8","biotype":"protein_coding","ncbi_id":"377841","summary":null,"start":137434364,"end":137441816,"strand":-1,"description":"ectonucleoside triphosphate diphosphohydrolase 8 [Source:HGNC Symbol;Acc:HGNC:24860]"}, {"versioned_ensembl_gene_id":"ENSG00000258210.1","gene_symbol":"AC144548.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":110387463,"end":110445548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258861.1","gene_symbol":"MIR381HG","gene_name":"MIR381 host gene [Source:HGNC Symbol;Acc:HGNC:20136]","synonyms":"NCRNA00225,C14orf89","biotype":"lincRNA","ncbi_id":"378881","summary":null,"start":101045157,"end":101051795,"strand":1,"description":"MIR381 host gene [Source:HGNC Symbol;Acc:HGNC:20136]"}, {"versioned_ensembl_gene_id":"ENSG00000176239.7","gene_symbol":"OR51B6","gene_name":"olfactory receptor family 51 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:19600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390058","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5351508,"end":5352446,"strand":1,"description":"olfactory receptor family 51 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:19600]"}, {"versioned_ensembl_gene_id":"ENSG00000117479.12","gene_symbol":"SLC19A2","gene_name":"solute carrier family 19 member 2 [Source:HGNC Symbol;Acc:HGNC:10938]","synonyms":"TRMA,THTR1","biotype":"protein_coding","ncbi_id":"10560","summary":"This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":169463909,"end":169486003,"strand":-1,"description":"solute carrier family 19 member 2 [Source:HGNC Symbol;Acc:HGNC:10938]"}, {"versioned_ensembl_gene_id":"ENSG00000282048.1","gene_symbol":"AL591742.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":114032393,"end":114034511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265987.1","gene_symbol":"AC011933.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75344405,"end":75373662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253809.1","gene_symbol":"AL160262.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70222758,"end":70242156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236520.2","gene_symbol":"GPC6-AS1","gene_name":"GPC6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39909]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873972","summary":null,"start":94154193,"end":94187991,"strand":-1,"description":"GPC6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39909]"}, {"versioned_ensembl_gene_id":"ENSG00000260970.1","gene_symbol":"AC006288.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119495375,"end":119524125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120322.3","gene_symbol":"PCDHB8","gene_name":"protocadherin beta 8 [Source:HGNC Symbol;Acc:HGNC:8693]","synonyms":"PCDH3I,PCDH-BETA8","biotype":"protein_coding","ncbi_id":"56128","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141177790,"end":141180529,"strand":1,"description":"protocadherin beta 8 [Source:HGNC Symbol;Acc:HGNC:8693]"}, {"versioned_ensembl_gene_id":"ENSG00000159023.19","gene_symbol":"EPB41","gene_name":"erythrocyte membrane protein band 4.1 [Source:HGNC Symbol;Acc:HGNC:3377]","synonyms":"EL1,4.1R","biotype":"protein_coding","ncbi_id":"2035","summary":"The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009]","start":28887091,"end":29120046,"strand":1,"description":"erythrocyte membrane protein band 4.1 [Source:HGNC Symbol;Acc:HGNC:3377]"}, {"versioned_ensembl_gene_id":"ENSG00000254897.1","gene_symbol":"AP003035.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85452282,"end":85453698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275152.4","gene_symbol":"CCL16","gene_name":"C-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:10614]","synonyms":"Mtn-1,LMC,LEC,LCC-1,HCC-4,CKb12,SCYL4,SCYA16,NCC-4","biotype":"protein_coding","ncbi_id":"6360","summary":"This gene is one of several cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for lymphocytes and monocytes but not for neutrophils. This cytokine also shows a potent myelosuppressive activity and suppresses proliferation of myeloid progenitor cells. The expression of this gene is upregulated by IL-10. [provided by RefSeq, Jul 2008]","start":35976493,"end":35981496,"strand":-1,"description":"C-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:10614]"}, {"versioned_ensembl_gene_id":"ENSG00000069482.6","gene_symbol":"GAL","gene_name":"galanin and GMAP prepropeptide [Source:HGNC Symbol;Acc:HGNC:4114]","synonyms":"GMAP,GLNN,GALN,GAL-GMAP","biotype":"protein_coding","ncbi_id":"51083","summary":"This gene encodes a neuroendocrine peptide that is widely expressed in the central and peripheral nervous systems and also the gastrointestinal tract, pancreas, adrenal gland and urogenital tract. The encoded protein is a precursor that is proteolytically processed to generate two mature peptides: galanin and galanin message-associated peptide (GMAP). Galanin has diverse physiological functions including nociception, feeding and energy homeostasis, osmotic regulation and water balance. GMAP has been demonstrated to possess antifungal activity and hypothesized to be part of the innate immune system. [provided by RefSeq, Jul 2015]","start":68683779,"end":68691175,"strand":1,"description":"galanin and GMAP prepropeptide [Source:HGNC Symbol;Acc:HGNC:4114]"}, {"versioned_ensembl_gene_id":"ENSG00000227824.1","gene_symbol":"AC122136.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215869923,"end":215870518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270682.1","gene_symbol":"AP003357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97788210,"end":97788357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112280.15","gene_symbol":"COL9A1","gene_name":"collagen type IX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2217]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1297","summary":"This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":70215061,"end":70303083,"strand":-1,"description":"collagen type IX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2217]"}, {"versioned_ensembl_gene_id":"ENSG00000225764.1","gene_symbol":"P3H2-AS1","gene_name":"P3H2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40886]","synonyms":"LEPREL1-AS1","biotype":"antisense_RNA","ncbi_id":"101929152","summary":null,"start":190120964,"end":190144846,"strand":1,"description":"P3H2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40886]"}, {"versioned_ensembl_gene_id":"ENSG00000227845.2","gene_symbol":"AL627223.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125372325,"end":125372766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257087.1","gene_symbol":"AP003174.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115538869,"end":115539384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112852.6","gene_symbol":"PCDHB2","gene_name":"protocadherin beta 2 [Source:HGNC Symbol;Acc:HGNC:8687]","synonyms":"PCDH-BETA2","biotype":"protein_coding","ncbi_id":"56133","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141094578,"end":141098703,"strand":1,"description":"protocadherin beta 2 [Source:HGNC Symbol;Acc:HGNC:8687]"}, {"versioned_ensembl_gene_id":"ENSG00000171815.5","gene_symbol":"PCDHB1","gene_name":"protocadherin beta 1 [Source:HGNC Symbol;Acc:HGNC:8680]","synonyms":"PCDH-BETA1","biotype":"protein_coding","ncbi_id":"29930","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141051135,"end":141059344,"strand":1,"description":"protocadherin beta 1 [Source:HGNC Symbol;Acc:HGNC:8680]"}, {"versioned_ensembl_gene_id":"ENSG00000110536.13","gene_symbol":"PTPMT1","gene_name":"protein tyrosine phosphatase, mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:26965]","synonyms":"PLIP,MOSP,DUSP23","biotype":"protein_coding","ncbi_id":"114971","summary":null,"start":47565430,"end":47573461,"strand":1,"description":"protein tyrosine phosphatase, mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:26965]"}, {"versioned_ensembl_gene_id":"ENSG00000162366.7","gene_symbol":"PDZK1IP1","gene_name":"PDZK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16887]","synonyms":"SPAP,MAP17,DD96","biotype":"protein_coding","ncbi_id":"10158","summary":null,"start":47183593,"end":47191044,"strand":-1,"description":"PDZK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16887]"}, {"versioned_ensembl_gene_id":"ENSG00000101162.3","gene_symbol":"TUBB1","gene_name":"tubulin beta 1 class VI [Source:HGNC Symbol;Acc:HGNC:16257]","synonyms":"dJ543J19.4","biotype":"protein_coding","ncbi_id":"81027","summary":"This gene encodes a member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is specifically expressed in platelets and megakaryocytes and may be involved in proplatelet production and platelet release. A mutations in this gene is associated with autosomal dominant macrothrombocytopenia. Two pseudogenes of this gene are found on chromosome Y.[provided by RefSeq, Jul 2010]","start":59019254,"end":59026654,"strand":1,"description":"tubulin beta 1 class VI [Source:HGNC Symbol;Acc:HGNC:16257]"}, {"versioned_ensembl_gene_id":"ENSG00000269095.1","gene_symbol":"AC010646.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17235940,"end":17255448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273806.1","gene_symbol":"AL137847.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83201957,"end":83202065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171345.13","gene_symbol":"KRT19","gene_name":"keratin 19 [Source:HGNC Symbol;Acc:HGNC:6436]","synonyms":"K1CS,K19,CK19,MGC15366","biotype":"protein_coding","ncbi_id":"3880","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. Unlike its related family members, this smallest known acidic cytokeratin is not paired with a basic cytokeratin in epithelial cells. It is specifically expressed in the periderm, the transiently superficial layer that envelopes the developing epidermis. The type I cytokeratins are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2008]","start":41523617,"end":41528308,"strand":-1,"description":"keratin 19 [Source:HGNC Symbol;Acc:HGNC:6436]"}, {"versioned_ensembl_gene_id":"ENSG00000149187.18","gene_symbol":"CELF1","gene_name":"CUGBP Elav-like family member 1 [Source:HGNC Symbol;Acc:HGNC:2549]","synonyms":"CUGBP,CUG-BP,BRUNOL2,NAPOR,NAB50,hNab50,EDEN-BP,CUGBP1","biotype":"protein_coding","ncbi_id":"10658","summary":"Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. This gene may play a role in myotonic dystrophy type 1 (DM1) via interactions with the dystrophia myotonica-protein kinase (DMPK) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":47465933,"end":47565569,"strand":-1,"description":"CUGBP Elav-like family member 1 [Source:HGNC Symbol;Acc:HGNC:2549]"}, {"versioned_ensembl_gene_id":"ENSG00000038219.12","gene_symbol":"BOD1L1","gene_name":"biorientation of chromosomes in cell division 1 like 1 [Source:HGNC Symbol;Acc:HGNC:31792]","synonyms":"KIAA1327,FLJ33215,FAM44A,BOD1L","biotype":"protein_coding","ncbi_id":"259282","summary":null,"start":13568738,"end":13627723,"strand":-1,"description":"biorientation of chromosomes in cell division 1 like 1 [Source:HGNC Symbol;Acc:HGNC:31792]"}, {"versioned_ensembl_gene_id":"ENSG00000231023.6","gene_symbol":"LINC00326","gene_name":"long intergenic non-protein coding RNA 326 [Source:HGNC Symbol;Acc:HGNC:41926]","synonyms":"NCRNA00326","biotype":"lincRNA","ncbi_id":"285735","summary":null,"start":133088080,"end":133106578,"strand":1,"description":"long intergenic non-protein coding RNA 326 [Source:HGNC Symbol;Acc:HGNC:41926]"}, {"versioned_ensembl_gene_id":"ENSG00000278941.1","gene_symbol":"SMG6-IT1","gene_name":"SMG6 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1220]","synonyms":"C17orf6","biotype":"TEC","ncbi_id":"53400","summary":null,"start":2235713,"end":2236086,"strand":-1,"description":"SMG6 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1220]"}, {"versioned_ensembl_gene_id":"ENSG00000236554.1","gene_symbol":"ASNSP3","gene_name":"asparagine synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39399]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100423061","summary":null,"start":100062296,"end":100063601,"strand":-1,"description":"asparagine synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39399]"}, {"versioned_ensembl_gene_id":"ENSG00000022355.16","gene_symbol":"GABRA1","gene_name":"gamma-aminobutyric acid type A receptor alpha1 subunit [Source:HGNC Symbol;Acc:HGNC:4075]","synonyms":"EJM5","biotype":"protein_coding","ncbi_id":"2554","summary":"This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene cause juvenile myoclonic epilepsy and childhood absence epilepsy type 4. Multiple transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":161847063,"end":161899981,"strand":1,"description":"gamma-aminobutyric acid type A receptor alpha1 subunit [Source:HGNC Symbol;Acc:HGNC:4075]"}, {"versioned_ensembl_gene_id":"ENSG00000229990.3","gene_symbol":"AC022400.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73841833,"end":73847115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256315.1","gene_symbol":"AP000462.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":115396756,"end":115397658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273373.1","gene_symbol":"AL355488.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110370154,"end":110373003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204011.4","gene_symbol":"COL5A1-AS1","gene_name":"COL5A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31368]","synonyms":"C9orf104,bA54A22.4","biotype":"antisense_RNA","ncbi_id":"414316","summary":null,"start":134649385,"end":134652843,"strand":-1,"description":"COL5A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31368]"}, {"versioned_ensembl_gene_id":"ENSG00000255210.1","gene_symbol":"AP001889.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110049528,"end":110050160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136104.19","gene_symbol":"RNASEH2B","gene_name":"ribonuclease H2 subunit B [Source:HGNC Symbol;Acc:HGNC:25671]","synonyms":"FLJ11712,DLEU8,AGS2","biotype":"protein_coding","ncbi_id":"79621","summary":"RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq, Nov 2008]","start":50909678,"end":50973745,"strand":1,"description":"ribonuclease H2 subunit B [Source:HGNC Symbol;Acc:HGNC:25671]"}, {"versioned_ensembl_gene_id":"ENSG00000224776.3","gene_symbol":"RPSAP50","gene_name":"ribosomal protein SA pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35896]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644109","summary":null,"start":109982192,"end":109983043,"strand":1,"description":"ribosomal protein SA pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35896]"}, {"versioned_ensembl_gene_id":"ENSG00000197079.8","gene_symbol":"KRT35","gene_name":"keratin 35 [Source:HGNC Symbol;Acc:HGNC:6453]","synonyms":"KRTHA5,Ha-5","biotype":"protein_coding","ncbi_id":"3886","summary":"The protein encoded by this gene is a member of the keratin gene family. This type I hair keratin is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41476689,"end":41481140,"strand":-1,"description":"keratin 35 [Source:HGNC Symbol;Acc:HGNC:6453]"}, {"versioned_ensembl_gene_id":"ENSG00000243572.1","gene_symbol":"LINC02017","gene_name":"long intergenic non-protein coding RNA 2017 [Source:HGNC Symbol;Acc:HGNC:52852]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377096","summary":null,"start":55178172,"end":55189214,"strand":1,"description":"long intergenic non-protein coding RNA 2017 [Source:HGNC Symbol;Acc:HGNC:52852]"}, {"versioned_ensembl_gene_id":"ENSG00000119703.13","gene_symbol":"ZC2HC1C","gene_name":"zinc finger C2HC-type containing 1C [Source:HGNC Symbol;Acc:HGNC:20354]","synonyms":"FAM164C,C14orf140","biotype":"protein_coding","ncbi_id":"79696","summary":null,"start":75064170,"end":75079987,"strand":1,"description":"zinc finger C2HC-type containing 1C [Source:HGNC Symbol;Acc:HGNC:20354]"}, {"versioned_ensembl_gene_id":"ENSG00000212864.3","gene_symbol":"RNF208","gene_name":"ring finger protein 208 [Source:HGNC Symbol;Acc:HGNC:25420]","synonyms":"DKFZP761H1710","biotype":"protein_coding","ncbi_id":"727800","summary":null,"start":137220247,"end":137221581,"strand":-1,"description":"ring finger protein 208 [Source:HGNC Symbol;Acc:HGNC:25420]"}, {"versioned_ensembl_gene_id":"ENSG00000258978.1","gene_symbol":"HIF1AP1","gene_name":"hypoxia inducible factor 1 alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874523","summary":null,"start":75116426,"end":75116600,"strand":-1,"description":"hypoxia inducible factor 1 alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43016]"}, {"versioned_ensembl_gene_id":"ENSG00000174437.16","gene_symbol":"ATP2A2","gene_name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:812]","synonyms":"SERCA2,DAR,ATP2B","biotype":"protein_coding","ncbi_id":"488","summary":"This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of the skeletal muscle. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol into the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Other types of mutations in this gene have been associated with various forms of muscular dystrophies. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2019]","start":110280756,"end":110351093,"strand":1,"description":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:812]"}, {"versioned_ensembl_gene_id":"ENSG00000118508.4","gene_symbol":"RAB32","gene_name":"RAB32, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9772]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10981","summary":"The protein encoded by this gene anchors the type II regulatory subunit of protein kinase A to the mitochondrion and aids in mitochondrial fission. The encoded protein also appears to be involved in autophagy and melanosome secretion. Variations in this gene may be linked to leprosy. [provided by RefSeq, Dec 2015]","start":146543693,"end":146554965,"strand":1,"description":"RAB32, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9772]"}, {"versioned_ensembl_gene_id":"ENSG00000176742.2","gene_symbol":"OR51V1","gene_name":"olfactory receptor family 51 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:19597]","synonyms":"OR51A12","biotype":"protein_coding","ncbi_id":"283111","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5199735,"end":5200700,"strand":-1,"description":"olfactory receptor family 51 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:19597]"}, {"versioned_ensembl_gene_id":"ENSG00000166004.14","gene_symbol":"CEP295","gene_name":"centrosomal protein 295 [Source:HGNC Symbol;Acc:HGNC:29366]","synonyms":"KIAA1731","biotype":"protein_coding","ncbi_id":"85459","summary":null,"start":93661639,"end":93730358,"strand":1,"description":"centrosomal protein 295 [Source:HGNC Symbol;Acc:HGNC:29366]"}, {"versioned_ensembl_gene_id":"ENSG00000228199.1","gene_symbol":"AL845450.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30176697,"end":30178517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138246.15","gene_symbol":"DNAJC13","gene_name":"DnaJ heat shock protein family (Hsp40) member C13 [Source:HGNC Symbol;Acc:HGNC:30343]","synonyms":"RME8,KIAA0678","biotype":"protein_coding","ncbi_id":"23317","summary":"This gene encodes a member of the Dnaj protein family whose members act as co-chaperones of a partner heat-shock protein by binding to the latter and stimulating ATP hydrolysis. The encoded protein associates with the heat-shock protein Hsc70 and plays a role in clathrin-mediated endocytosis. It may also be involved in post-endocytic transport mechanisms via its associations with other proteins, including the sorting nexin SNX1. Mutations in this gene are associated with Parkinson's disease. [provided by RefSeq, Jun 2016]","start":132417526,"end":132539032,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C13 [Source:HGNC Symbol;Acc:HGNC:30343]"}, {"versioned_ensembl_gene_id":"ENSG00000273969.1","gene_symbol":"AC138747.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28484946,"end":28485066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235887.2","gene_symbol":"AC239859.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143499187,"end":143500512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104951.15","gene_symbol":"IL4I1","gene_name":"interleukin 4 induced 1 [Source:HGNC Symbol;Acc:HGNC:19094]","synonyms":"FIG1","biotype":"protein_coding","ncbi_id":"259307","summary":"This gene encodes a secreted L-amino acid oxidase protein which primarily catabolizes L-phenylalanine and, to a lesser extent, L-arginine. The expression of this gene is induced by the cytokine interleukin 4 in B cells. This gene is also expressed in macrophages and dendritic cells. This protein may play a role immune system escape as it is expressed in tumor-associated macrophages and suppresses T-cell responses. This protein also contains domains thought to be involved in the binding of flavin adenine dinucleotide (FAD) cofactor. Multiple transcript variants encoding different isoforms have been found for this gene. Some transcripts of this gene share a promoter and exons of the 5' UTR with the overlapping NUP62 gene. [provided by RefSeq, Jul 2020]","start":49889654,"end":49929539,"strand":-1,"description":"interleukin 4 induced 1 [Source:HGNC Symbol;Acc:HGNC:19094]"}, {"versioned_ensembl_gene_id":"ENSG00000232508.1","gene_symbol":"MRPL45P1","gene_name":"mitochondrial ribosomal protein L45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359747","summary":null,"start":88364695,"end":88365608,"strand":-1,"description":"mitochondrial ribosomal protein L45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29715]"}, {"versioned_ensembl_gene_id":"ENSG00000282587.1","gene_symbol":"AC138747.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28455755,"end":28455878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095209.11","gene_symbol":"TMEM38B","gene_name":"transmembrane protein 38B [Source:HGNC Symbol;Acc:HGNC:25535]","synonyms":"TRIC-B,FLJ10493,D4Ertd89e,C9orf87,bA219P18.1","biotype":"protein_coding","ncbi_id":"55151","summary":"This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]","start":105694544,"end":105776612,"strand":1,"description":"transmembrane protein 38B [Source:HGNC Symbol;Acc:HGNC:25535]"}, {"versioned_ensembl_gene_id":"ENSG00000233025.1","gene_symbol":"CRYZP1","gene_name":"crystallin zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2421]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1430","summary":null,"start":103088664,"end":103089610,"strand":-1,"description":"crystallin zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2421]"}, {"versioned_ensembl_gene_id":"ENSG00000100281.13","gene_symbol":"HMGXB4","gene_name":"HMG-box containing 4 [Source:HGNC Symbol;Acc:HGNC:5003]","synonyms":"THC211630,HMG2L1","biotype":"protein_coding","ncbi_id":"10042","summary":"High mobility group (HMG) proteins are nonhistone chromosomal proteins. See HMG2 (MIM 163906) for additional information on HMG proteins.[supplied by OMIM, Nov 2010]","start":35257452,"end":35295807,"strand":1,"description":"HMG-box containing 4 [Source:HGNC Symbol;Acc:HGNC:5003]"}, {"versioned_ensembl_gene_id":"ENSG00000249068.1","gene_symbol":"AC008417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109840128,"end":109840692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261556.9","gene_symbol":"SMG1P7","gene_name":"SMG1P7, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49864]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100506060","summary":null,"start":70219574,"end":70246610,"strand":-1,"description":"SMG1P7, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49864]"}, {"versioned_ensembl_gene_id":"ENSG00000213024.11","gene_symbol":"NUP62","gene_name":"nucleoporin 62 [Source:HGNC Symbol;Acc:HGNC:8066]","synonyms":"SNDI,p62,MGC841,IBSN,FLJ43869,FLJ20822,DKFZp547L134","biotype":"protein_coding","ncbi_id":"23636","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a member of the FG-repeat containing nucleoporins and is localized to the nuclear pore central plug. This protein associates with the importin alpha/beta complex which is involved in the import of proteins containing nuclear localization signals. Multiple transcript variants of this gene encode a single protein isoform. [provided by RefSeq, Jul 2008]","start":49906825,"end":49929763,"strand":-1,"description":"nucleoporin 62 [Source:HGNC Symbol;Acc:HGNC:8066]"}, {"versioned_ensembl_gene_id":"ENSG00000228002.2","gene_symbol":"DHX9P1","gene_name":"DEAH-box helicase 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2751]","synonyms":"DHX9P,DDX9P","biotype":"processed_pseudogene","ncbi_id":"1661","summary":null,"start":76984868,"end":76987943,"strand":1,"description":"DEAH-box helicase 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2751]"}, {"versioned_ensembl_gene_id":"ENSG00000140470.13","gene_symbol":"ADAMTS17","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 17 [Source:HGNC Symbol;Acc:HGNC:17109]","synonyms":"FLJ32769,FLJ16363","biotype":"protein_coding","ncbi_id":"170691","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016]","start":99971589,"end":100342005,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 17 [Source:HGNC Symbol;Acc:HGNC:17109]"}, {"versioned_ensembl_gene_id":"ENSG00000257995.1","gene_symbol":"AC084365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90617759,"end":90622822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273323.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"dJ207F6.1,NOL5BP,NOL5B,NOP56-L","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28783631,"end":28784002,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000170632.13","gene_symbol":"ARMC10","gene_name":"armadillo repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:21706]","synonyms":"MGC3195,SVH","biotype":"protein_coding","ncbi_id":"83787","summary":"This gene encodes a protein that contains an armadillo repeat and transmembrane domain. The encoded protein decreases the transcriptional activity of the tumor suppressor protein p53 through direct interaction with the DNA-binding domain of p53, and may play a role in cell growth and survival. Upregulation of this gene may play a role in hepatocellular carcinoma. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 3. [provided by RefSeq, Sep 2011]","start":103074881,"end":103099764,"strand":1,"description":"armadillo repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:21706]"}, {"versioned_ensembl_gene_id":"ENSG00000154144.12","gene_symbol":"TBRG1","gene_name":"transforming growth factor beta regulator 1 [Source:HGNC Symbol;Acc:HGNC:29551]","synonyms":"TB-5,NIAM,FLJ14621","biotype":"protein_coding","ncbi_id":"84897","summary":null,"start":124622836,"end":124635398,"strand":1,"description":"transforming growth factor beta regulator 1 [Source:HGNC Symbol;Acc:HGNC:29551]"}, {"versioned_ensembl_gene_id":"ENSG00000251437.1","gene_symbol":"NDUFS5P4","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44042]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287817","summary":null,"start":98976800,"end":98977117,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44042]"}, {"versioned_ensembl_gene_id":"ENSG00000251367.1","gene_symbol":"AC091917.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109467353,"end":109467952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273068.1","gene_symbol":"Z99755.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35122661,"end":35127419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231090.1","gene_symbol":"MIR4422HG","gene_name":"MIR4422 host gene [Source:HGNC Symbol;Acc:HGNC:53113]","synonyms":"RP11-101C11.1","biotype":"lincRNA","ncbi_id":"109729135","summary":null,"start":55217861,"end":55234177,"strand":1,"description":"MIR4422 host gene [Source:HGNC Symbol;Acc:HGNC:53113]"}, {"versioned_ensembl_gene_id":"ENSG00000231095.1","gene_symbol":"GYG1P3","gene_name":"glycogenin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39711]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645506","summary":null,"start":55222379,"end":55223372,"strand":1,"description":"glycogenin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39711]"}, {"versioned_ensembl_gene_id":"ENSG00000238153.1","gene_symbol":"Z99755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35164304,"end":35165347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233080.3","gene_symbol":"LINC01399","gene_name":"long intergenic non-protein coding RNA 1399 [Source:HGNC Symbol;Acc:HGNC:50680]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"104310353","summary":null,"start":35119824,"end":35231056,"strand":-1,"description":"long intergenic non-protein coding RNA 1399 [Source:HGNC Symbol;Acc:HGNC:50680]"}, {"versioned_ensembl_gene_id":"ENSG00000251454.1","gene_symbol":"AC025244.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75341279,"end":75359024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272745.1","gene_symbol":"AC004948.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7619872,"end":7620543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163624.5","gene_symbol":"CDS1","gene_name":"CDP-diacylglycerol synthase 1 [Source:HGNC Symbol;Acc:HGNC:1800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1040","summary":"Breakdown products of phosphoinositides are ubiquitous second messengers that function downstream of many G protein-coupled receptors and tyrosine kinases regulating cell growth, calcium metabolism, and protein kinase C activity. This gene encodes an enzyme which regulates the amount of phosphatidylinositol available for signaling by catalyzing the conversion of phosphatidic acid to CDP-diacylglycerol. This enzyme is an integral membrane protein localized to two subcellular domains, the matrix side of the inner mitochondrial membrane where it is thought to be involved in the synthesis of phosphatidylglycerol and cardiolipin and the cytoplasmic side of the endoplasmic reticulum where it functions in phosphatidylinositol biosynthesis. Two genes encoding this enzyme have been identified in humans, one mapping to human chromosome 4q21 and a second to 20p13. [provided by RefSeq, Jul 2008]","start":84582979,"end":84651338,"strand":1,"description":"CDP-diacylglycerol synthase 1 [Source:HGNC Symbol;Acc:HGNC:1800]"}, {"versioned_ensembl_gene_id":"ENSG00000011677.12","gene_symbol":"GABRA3","gene_name":"gamma-aminobutyric acid type A receptor alpha3 subunit [Source:HGNC Symbol;Acc:HGNC:4077]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2556","summary":"GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. [provided by RefSeq, Jul 2008]","start":152166234,"end":152451358,"strand":-1,"description":"gamma-aminobutyric acid type A receptor alpha3 subunit [Source:HGNC Symbol;Acc:HGNC:4077]"}, {"versioned_ensembl_gene_id":"ENSG00000142945.12","gene_symbol":"KIF2C","gene_name":"kinesin family member 2C [Source:HGNC Symbol;Acc:HGNC:6393]","synonyms":"KNSL6,CT139,MCAK","biotype":"protein_coding","ncbi_id":"11004","summary":"This gene encodes a kinesin-like protein that functions as a microtubule-dependent molecular motor. The encoded protein can depolymerize microtubules at the plus end, thereby promoting mitotic chromosome segregation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":44739818,"end":44767767,"strand":1,"description":"kinesin family member 2C [Source:HGNC Symbol;Acc:HGNC:6393]"}, {"versioned_ensembl_gene_id":"ENSG00000228430.9","gene_symbol":"AL162726.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":81977614,"end":82780194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237316.1","gene_symbol":"Z82196.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34711908,"end":34724919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276423.6","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54802859,"end":54817155,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000261793.1","gene_symbol":"AL929554.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":137168854,"end":137171984,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170054.14","gene_symbol":"SERPINA9","gene_name":"serpin family A member 9 [Source:HGNC Symbol;Acc:HGNC:15995]","synonyms":"SERPINA11b,GCET1,CENTERIN","biotype":"protein_coding","ncbi_id":"327657","summary":null,"start":94462717,"end":94479689,"strand":-1,"description":"serpin family A member 9 [Source:HGNC Symbol;Acc:HGNC:15995]"}, {"versioned_ensembl_gene_id":"ENSG00000104973.16","gene_symbol":"MED25","gene_name":"mediator complex subunit 25 [Source:HGNC Symbol;Acc:HGNC:28845]","synonyms":"TCBAP0758,DKFZp434K0512,ARC92,ACID1","biotype":"protein_coding","ncbi_id":"81857","summary":"This gene encodes a component of the transcriptional coactivator complex termed the Mediator complex. This complex is required for transcription of most RNA polymerase II-dependent genes. The encoded protein plays a role in chromatin modification and in preinitiation complex assembly. Mutations in this gene are associated with Charcot-Marie-Tooth disease type 2B2. [provided by RefSeq, Apr 2010]","start":49818279,"end":49838816,"strand":1,"description":"mediator complex subunit 25 [Source:HGNC Symbol;Acc:HGNC:28845]"}, {"versioned_ensembl_gene_id":"ENSG00000240808.1","gene_symbol":"AC126389.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17137976,"end":17138265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272046.1","gene_symbol":"AL445647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87807634,"end":87811232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249917.2","gene_symbol":"LINC00536","gene_name":"long intergenic non-protein coding RNA 536 [Source:HGNC Symbol;Acc:HGNC:43645]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100859921","summary":null,"start":115950511,"end":116325059,"strand":-1,"description":"long intergenic non-protein coding RNA 536 [Source:HGNC Symbol;Acc:HGNC:43645]"}, {"versioned_ensembl_gene_id":"ENSG00000255921.1","gene_symbol":"AC026310.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24949163,"end":24960158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164077.13","gene_symbol":"MON1A","gene_name":"MON1 homolog A, secretory trafficking associated [Source:HGNC Symbol;Acc:HGNC:28207]","synonyms":"SAND1,MGC13272","biotype":"protein_coding","ncbi_id":"84315","summary":null,"start":49908862,"end":49930173,"strand":-1,"description":"MON1 homolog A, secretory trafficking associated [Source:HGNC Symbol;Acc:HGNC:28207]"}, {"versioned_ensembl_gene_id":"ENSG00000255028.5","gene_symbol":"AP003049.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109355085,"end":109583907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172818.9","gene_symbol":"OVOL1","gene_name":"ovo like transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:8525]","synonyms":"HOVO1","biotype":"protein_coding","ncbi_id":"5017","summary":"This gene encodes a putative zinc finger containing transcription factor that is highly similar to homologous protein in Drosophila and mouse. Based on known functions in these species, this protein is likely involved in hair formation and spermatogenesis in human as well. [provided by RefSeq, Aug 2011]","start":65787022,"end":65797219,"strand":1,"description":"ovo like transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:8525]"}, {"versioned_ensembl_gene_id":"ENSG00000221923.8","gene_symbol":"ZNF880","gene_name":"zinc finger protein 880 [Source:HGNC Symbol;Acc:HGNC:37249]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400713","summary":null,"start":52369917,"end":52385795,"strand":1,"description":"zinc finger protein 880 [Source:HGNC Symbol;Acc:HGNC:37249]"}, {"versioned_ensembl_gene_id":"ENSG00000226275.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31648357,"end":31650629,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000214659.4","gene_symbol":"KRT8P26","gene_name":"keratin 8 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:33378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390211","summary":null,"start":65726939,"end":65728214,"strand":1,"description":"keratin 8 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:33378]"}, {"versioned_ensembl_gene_id":"ENSG00000228923.1","gene_symbol":"AP000355.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24516508,"end":24518386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140932.9","gene_symbol":"CMTM2","gene_name":"CKLF like MARVEL transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19173]","synonyms":"MGC39436,FLJ25732,CKLFSF2","biotype":"protein_coding","ncbi_id":"146225","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that links the chemokine and the transmembrane 4 superfamilies of signaling molecules. The protein encoded by this gene may play an important role in testicular development. [provided by RefSeq, Jul 2008]","start":66579448,"end":66588275,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19173]"}, {"versioned_ensembl_gene_id":"ENSG00000198443.6","gene_symbol":"KRTAP4-1","gene_name":"keratin associated protein 4-1 [Source:HGNC Symbol;Acc:HGNC:18907]","synonyms":"KRTAP4-10,KAP4.10,KAP4.1","biotype":"protein_coding","ncbi_id":"85285","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41184102,"end":41185342,"strand":-1,"description":"keratin associated protein 4-1 [Source:HGNC Symbol;Acc:HGNC:18907]"}, {"versioned_ensembl_gene_id":"ENSG00000075415.12","gene_symbol":"SLC25A3","gene_name":"solute carrier family 25 member 3 [Source:HGNC Symbol;Acc:HGNC:10989]","synonyms":"PHC","biotype":"protein_coding","ncbi_id":"5250","summary":"The protein encoded by this gene catalyzes the transport of phosphate into the mitochondrial matrix, either by proton cotransport or in exchange for hydroxyl ions. The protein contains three related segments arranged in tandem which are related to those found in other characterized members of the mitochondrial carrier family. Both the N-terminal and C-terminal regions of this protein protrude toward the cytosol. Multiple alternatively spliced transcript variants have been isolated. [provided by RefSeq, Jul 2008]","start":98593591,"end":98606379,"strand":1,"description":"solute carrier family 25 member 3 [Source:HGNC Symbol;Acc:HGNC:10989]"}, {"versioned_ensembl_gene_id":"ENSG00000198464.13","gene_symbol":"ZNF480","gene_name":"zinc finger protein 480 [Source:HGNC Symbol;Acc:HGNC:23305]","synonyms":"MGC32104","biotype":"protein_coding","ncbi_id":"147657","summary":null,"start":52297177,"end":52325922,"strand":1,"description":"zinc finger protein 480 [Source:HGNC Symbol;Acc:HGNC:23305]"}, {"versioned_ensembl_gene_id":"ENSG00000234749.5","gene_symbol":"FAM90A21P","gene_name":"family with sequence similarity 90 member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32269]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"619418","summary":null,"start":7564350,"end":7567360,"strand":-1,"description":"family with sequence similarity 90 member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32269]"}, {"versioned_ensembl_gene_id":"ENSG00000212722.7","gene_symbol":"KRTAP4-9","gene_name":"keratin associated protein 4-9 [Source:HGNC Symbol;Acc:HGNC:18910]","synonyms":"KAP4.9","biotype":"protein_coding","ncbi_id":"100132386","summary":null,"start":41105332,"end":41106488,"strand":1,"description":"keratin associated protein 4-9 [Source:HGNC Symbol;Acc:HGNC:18910]"}, {"versioned_ensembl_gene_id":"ENSG00000273858.1","gene_symbol":"AC140113.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11042722,"end":11042943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277576.1","gene_symbol":"AC110741.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":133946677,"end":133947335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237943.6","gene_symbol":"PRKCQ-AS1","gene_name":"PRKCQ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44689]","synonyms":"ENST00000414894.1","biotype":"processed_transcript","ncbi_id":"439949","summary":null,"start":6580419,"end":6616452,"strand":1,"description":"PRKCQ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44689]"}, {"versioned_ensembl_gene_id":"ENSG00000064692.18","gene_symbol":"SNCAIP","gene_name":"synuclein alpha interacting protein [Source:HGNC Symbol;Acc:HGNC:11139]","synonyms":"SYPH1","biotype":"protein_coding","ncbi_id":"9627","summary":"This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":122311354,"end":122464219,"strand":1,"description":"synuclein alpha interacting protein [Source:HGNC Symbol;Acc:HGNC:11139]"}, {"versioned_ensembl_gene_id":"ENSG00000229408.8","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457659,"end":29464806,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000236660.6","gene_symbol":"FAM90A7P","gene_name":"family with sequence similarity 90 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:32255]","synonyms":"FAM90A7","biotype":"unprocessed_pseudogene","ncbi_id":"441317","summary":"FAM90A7 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7556700,"end":7559712,"strand":-1,"description":"family with sequence similarity 90 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:32255]"}, {"versioned_ensembl_gene_id":"ENSG00000273572.4","gene_symbol":"CDHR5","gene_name":"cadherin related family member 5 [Source:HGNC Symbol;Acc:HGNC:7521]","synonyms":"MUCDHL,MU-PCDH,FLJ20219,MUPCDH","biotype":"protein_coding","ncbi_id":"53841","summary":"This gene is a novel mucin-like gene that is a member of the cadherin superfamily. While encoding nonpolymorphic tandem repeats rich in proline, serine and threonine similar to mucin proteins, the gene also contains sequence encoding calcium-binding motifs found in all cadherins. The role of the hybrid extracellular region and the specific function of this protein have not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jan 2010]","start":616823,"end":626336,"strand":-1,"description":"cadherin related family member 5 [Source:HGNC Symbol;Acc:HGNC:7521]"}, {"versioned_ensembl_gene_id":"ENSG00000243746.1","gene_symbol":"EEF1A1P10","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:3205]","synonyms":"EEF1AL8","biotype":"processed_pseudogene","ncbi_id":"100421829","summary":null,"start":144647186,"end":144648575,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:3205]"}, {"versioned_ensembl_gene_id":"ENSG00000141258.12","gene_symbol":"SGSM2","gene_name":"small G protein signaling modulator 2 [Source:HGNC Symbol;Acc:HGNC:29026]","synonyms":"RUTBC1,KIAA0397","biotype":"protein_coding","ncbi_id":"9905","summary":"The protein encoded by this gene is a GTPase activator with activity towards RAB32 and RAB33B, which are regulators of membrane trafficking. The encoded protein inactivates RAB32 and can bind RAB9A-GTP, a protein required for RAB32 activation. [provided by RefSeq, Oct 2016]","start":2337498,"end":2381058,"strand":1,"description":"small G protein signaling modulator 2 [Source:HGNC Symbol;Acc:HGNC:29026]"}, {"versioned_ensembl_gene_id":"ENSG00000168785.7","gene_symbol":"TSPAN5","gene_name":"tetraspanin 5 [Source:HGNC Symbol;Acc:HGNC:17753]","synonyms":"Tspan-5,TM4SF9,NET-4","biotype":"protein_coding","ncbi_id":"10098","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. [provided by RefSeq, Jul 2008]","start":98470367,"end":98658629,"strand":-1,"description":"tetraspanin 5 [Source:HGNC Symbol;Acc:HGNC:17753]"}, {"versioned_ensembl_gene_id":"ENSG00000251523.1","gene_symbol":"AC108159.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98496364,"end":98509935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114786.16","gene_symbol":"ABHD14A-ACY1","gene_name":"ABHD14A-ACY1 readthrough [Source:HGNC Symbol;Acc:HGNC:38856]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526760","summary":"This locus represents naturally occurring read-through transcription between the neighboring abhydrolase domain containing 14A (ABHD14A) and aminoacylase 1 (ACY1) genes on chromosome 3. The read-through transcript encodes a protein that shares sequence identity with the downstream gene product but its N-terminal region is distinct due to the use of an alternate start codon relative to the upstream gene. [provided by RefSeq, Oct 2015]","start":51974706,"end":51989183,"strand":1,"description":"ABHD14A-ACY1 readthrough [Source:HGNC Symbol;Acc:HGNC:38856]"}, {"versioned_ensembl_gene_id":"ENSG00000115593.14","gene_symbol":"SMYD1","gene_name":"SET and MYND domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20986]","synonyms":"BOP,ZMYND22,KMT3D","biotype":"protein_coding","ncbi_id":"150572","summary":null,"start":88067780,"end":88113387,"strand":1,"description":"SET and MYND domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20986]"}, {"versioned_ensembl_gene_id":"ENSG00000230071.2","gene_symbol":"RPL4P6","gene_name":"ribosomal protein L4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271033","summary":null,"start":40586700,"end":40588003,"strand":-1,"description":"ribosomal protein L4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35611]"}, {"versioned_ensembl_gene_id":"ENSG00000283211.1","gene_symbol":"AL773545.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40167392,"end":40171329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258399.7","gene_symbol":"AL117190.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100836269,"end":100947194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249921.2","gene_symbol":"AC034207.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108784098,"end":108785552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258663.1","gene_symbol":"AL117190.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100834432,"end":100861026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176723.9","gene_symbol":"ZNF843","gene_name":"zinc finger protein 843 [Source:HGNC Symbol;Acc:HGNC:28710]","synonyms":"MGC46336","biotype":"protein_coding","ncbi_id":"283933","summary":null,"start":31432593,"end":31443160,"strand":-1,"description":"zinc finger protein 843 [Source:HGNC Symbol;Acc:HGNC:28710]"}, {"versioned_ensembl_gene_id":"ENSG00000242120.3","gene_symbol":"MDFIC2","gene_name":"MyoD family inhibitor domain containing 2 [Source:HGNC Symbol;Acc:HGNC:53442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"107986096","summary":null,"start":70196894,"end":70312726,"strand":-1,"description":"MyoD family inhibitor domain containing 2 [Source:HGNC Symbol;Acc:HGNC:53442]"}, {"versioned_ensembl_gene_id":"ENSG00000151422.12","gene_symbol":"FER","gene_name":"FER tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3655]","synonyms":"TYK3,PPP1R74","biotype":"protein_coding","ncbi_id":"2241","summary":"The protein encoded by this gene is a member of the FPS/FES family of non-transmembrane receptor tyrosine kinases. It regulates cell-cell adhesion and mediates signaling from the cell surface to the cytoskeleton via growth factor receptors. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Apr 2015]","start":108747822,"end":109196841,"strand":1,"description":"FER tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3655]"}, {"versioned_ensembl_gene_id":"ENSG00000250050.1","gene_symbol":"MTND4P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42226]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873193","summary":null,"start":25718082,"end":25719745,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42226]"}, {"versioned_ensembl_gene_id":"ENSG00000183060.15","gene_symbol":"LYSMD4","gene_name":"LysM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26571]","synonyms":"FLJ33008","biotype":"protein_coding","ncbi_id":"145748","summary":null,"start":99715697,"end":99733561,"strand":-1,"description":"LysM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26571]"}, {"versioned_ensembl_gene_id":"ENSG00000132646.10","gene_symbol":"PCNA","gene_name":"proliferating cell nuclear antigen [Source:HGNC Symbol;Acc:HGNC:8729]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5111","summary":"The protein encoded by this gene is found in the nucleus and is a cofactor of DNA polymerase delta. The encoded protein acts as a homotrimer and helps increase the processivity of leading strand synthesis during DNA replication. In response to DNA damage, this protein is ubiquitinated and is involved in the RAD6-dependent DNA repair pathway. Two transcript variants encoding the same protein have been found for this gene. Pseudogenes of this gene have been described on chromosome 4 and on the X chromosome. [provided by RefSeq, Jul 2008]","start":5114953,"end":5126626,"strand":-1,"description":"proliferating cell nuclear antigen [Source:HGNC Symbol;Acc:HGNC:8729]"}, {"versioned_ensembl_gene_id":"ENSG00000249277.1","gene_symbol":"AC092436.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25686202,"end":25686458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249959.5","gene_symbol":"AC024587.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107699835,"end":107716841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070366.13","gene_symbol":"SMG6","gene_name":"SMG6, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:17809]","synonyms":"SMG-6,KIAA0732,EST1A,C17orf31","biotype":"protein_coding","ncbi_id":"23293","summary":"This gene encodes a component of the telomerase ribonucleoprotein complex responsible for the replication and maintenance of chromosome ends. The encoded protein also plays a role in the nonsense-mediated mRNA decay (NMD) pathway, providing the endonuclease activity near the premature translation termination codon that is needed to initiate NMD. Alternatively spliced transcript variants encoding distinct protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":2059839,"end":2303771,"strand":-1,"description":"SMG6, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:17809]"}, {"versioned_ensembl_gene_id":"ENSG00000221852.4","gene_symbol":"KRTAP1-5","gene_name":"keratin associated protein 1-5 [Source:HGNC Symbol;Acc:HGNC:16777]","synonyms":"KAP1.5","biotype":"protein_coding","ncbi_id":"83895","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41026026,"end":41027202,"strand":-1,"description":"keratin associated protein 1-5 [Source:HGNC Symbol;Acc:HGNC:16777]"}, {"versioned_ensembl_gene_id":"ENSG00000108298.9","gene_symbol":"RPL19","gene_name":"ribosomal protein L19 [Source:HGNC Symbol;Acc:HGNC:10312]","synonyms":"MGC71997,L19,FLJ27452,DKFZp779D216","biotype":"protein_coding","ncbi_id":"6143","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L19E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":39200283,"end":39204727,"strand":1,"description":"ribosomal protein L19 [Source:HGNC Symbol;Acc:HGNC:10312]"}, {"versioned_ensembl_gene_id":"ENSG00000215522.11","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"NTRK4,RTK6,CD167,NEP,PTK3A,CAK,EDDR1","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30870550,"end":30889733,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000081692.12","gene_symbol":"JMJD4","gene_name":"jumonji domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25724]","synonyms":"FLJ12517","biotype":"protein_coding","ncbi_id":"65094","summary":null,"start":227730425,"end":227735411,"strand":-1,"description":"jumonji domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25724]"}, {"versioned_ensembl_gene_id":"ENSG00000230005.2","gene_symbol":"SNAP47-AS1","gene_name":"SNAP47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41501]","synonyms":"SNAP47-IT1","biotype":"antisense_RNA","ncbi_id":"100885800","summary":null,"start":227743831,"end":227747191,"strand":-1,"description":"SNAP47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41501]"}, {"versioned_ensembl_gene_id":"ENSG00000119414.11","gene_symbol":"PPP6C","gene_name":"protein phosphatase 6 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9323]","synonyms":"PP6","biotype":"protein_coding","ncbi_id":"5537","summary":"This gene encodes the catalytic subunit of protein phosphatase, a component of a signaling pathway regulating cell cycle progression. Splice variants encoding different protein isoforms exist. The pseudogene of this gene is located on chromosome X. [provided by RefSeq, Jul 2008]","start":125146573,"end":125189939,"strand":-1,"description":"protein phosphatase 6 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9323]"}, {"versioned_ensembl_gene_id":"ENSG00000126247.10","gene_symbol":"CAPNS1","gene_name":"calpain small subunit 1 [Source:HGNC Symbol;Acc:HGNC:1481]","synonyms":"CAPN4,CANPS,CANP,30K,CDPS","biotype":"protein_coding","ncbi_id":"826","summary":"This gene is a member of the calpain small subunit family. Calpains are calcium-dependent cysteine proteinases that are widely distributed in mammalian cells. Calpains operate as heterodimers, comprising a specific large catalytic subunit (calpain 1 subunit in Calpain I, and calpain 2 subunit in Calpain II), and a common small regulatory subunit encoded by this gene. This encoded protein is essential for the stability and function of both calpain heterodimers, whose proteolytic activities influence various cellular functions including apoptosis, proliferation, migration, adhesion, and autophagy. Calpains have been implicated in neurodegenerative processes, such as myotonic dystrophy. A pseudogene of this gene has been defined on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":36139575,"end":36150353,"strand":1,"description":"calpain small subunit 1 [Source:HGNC Symbol;Acc:HGNC:1481]"}, {"versioned_ensembl_gene_id":"ENSG00000234560.4","gene_symbol":"OR10G8","gene_name":"olfactory receptor family 10 subfamily G member 8 [Source:HGNC Symbol;Acc:HGNC:14845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219869","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124026798,"end":124030634,"strand":1,"description":"olfactory receptor family 10 subfamily G member 8 [Source:HGNC Symbol;Acc:HGNC:14845]"}, {"versioned_ensembl_gene_id":"ENSG00000236981.1","gene_symbol":"OR10G9","gene_name":"olfactory receptor family 10 subfamily G member 9 [Source:HGNC Symbol;Acc:HGNC:15129]","synonyms":"OR10G10P","biotype":"protein_coding","ncbi_id":"219870","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124023013,"end":124023948,"strand":1,"description":"olfactory receptor family 10 subfamily G member 9 [Source:HGNC Symbol;Acc:HGNC:15129]"}, {"versioned_ensembl_gene_id":"ENSG00000224223.1","gene_symbol":"VSTM2A-OT1","gene_name":"VSTM2A overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:50770]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"285878","summary":null,"start":54556970,"end":54571726,"strand":1,"description":"VSTM2A overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:50770]"}, {"versioned_ensembl_gene_id":"ENSG00000259924.1","gene_symbol":"AC011939.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65771176,"end":65772139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226174.6","gene_symbol":"TEX22","gene_name":"testis expressed 22 [Source:HGNC Symbol;Acc:HGNC:40026]","synonyms":null,"biotype":"protein_coding","ncbi_id":"647310","summary":null,"start":105398579,"end":105450106,"strand":1,"description":"testis expressed 22 [Source:HGNC Symbol;Acc:HGNC:40026]"}, {"versioned_ensembl_gene_id":"ENSG00000263098.1","gene_symbol":"AC068014.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82795486,"end":82796095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235939.1","gene_symbol":"AL138760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49419277,"end":49472903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265625.1","gene_symbol":"AC104564.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29644796,"end":29645847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074621.13","gene_symbol":"SLC24A1","gene_name":"solute carrier family 24 member 1 [Source:HGNC Symbol;Acc:HGNC:10975]","synonyms":"CSNB1D,RODX,NCKX1,NCKX,KIAA0702,HsT17412","biotype":"protein_coding","ncbi_id":"9187","summary":"This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. The encoded protein plays an important role in sodium/calcium exchange in retinal rod and cone photoreceptors by mediating the extrusion of one calcium ion and one potassium ion in exchange for four sodium ions. Mutations in this gene may play a role in congenital stationary night blindness. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":65611366,"end":65660995,"strand":1,"description":"solute carrier family 24 member 1 [Source:HGNC Symbol;Acc:HGNC:10975]"}, {"versioned_ensembl_gene_id":"ENSG00000107186.16","gene_symbol":"MPDZ","gene_name":"multiple PDZ domain crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:7208]","synonyms":"MUPP1","biotype":"protein_coding","ncbi_id":"8777","summary":"The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":13105704,"end":13279590,"strand":-1,"description":"multiple PDZ domain crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:7208]"}, {"versioned_ensembl_gene_id":"ENSG00000164332.7","gene_symbol":"UBLCP1","gene_name":"ubiquitin like domain containing CTD phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28110]","synonyms":"MGC10067,CPUB1","biotype":"protein_coding","ncbi_id":"134510","summary":null,"start":159263081,"end":159286040,"strand":1,"description":"ubiquitin like domain containing CTD phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28110]"}, {"versioned_ensembl_gene_id":"ENSG00000136631.12","gene_symbol":"VPS45","gene_name":"vacuolar protein sorting 45 homolog [Source:HGNC Symbol;Acc:HGNC:14579]","synonyms":"VPS45B,VPS45A,H1,h-vps45","biotype":"protein_coding","ncbi_id":"11311","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene is a member of the Sec1 domain family, and shows a high degree of sequence similarity to mouse, rat and yeast Vps45. The exact function of this gene is not known, but its high expression in peripheral blood mononuclear cells suggests a role in trafficking proteins, including inflammatory mediators. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2013]","start":150067293,"end":150145327,"strand":1,"description":"vacuolar protein sorting 45 homolog [Source:HGNC Symbol;Acc:HGNC:14579]"}, {"versioned_ensembl_gene_id":"ENSG00000228877.2","gene_symbol":"AL669970.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134527182,"end":134545244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223795.2","gene_symbol":"AL669970.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134505472,"end":134521442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235191.1","gene_symbol":"NUCB1-AS1","gene_name":"NUCB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40419]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874085","summary":null,"start":48910930,"end":48918891,"strand":-1,"description":"NUCB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40419]"}, {"versioned_ensembl_gene_id":"ENSG00000263321.1","gene_symbol":"AC024361.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82729164,"end":82734143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176840.11","gene_symbol":"MIR7-3HG","gene_name":"MIR7-3 host gene [Source:HGNC Symbol;Acc:HGNC:30049]","synonyms":"NCRNA00306,LINC00306,Huh7,C19orf30,uc002mbe.2,PGSF1b,PGSF1a,PGSF1","biotype":"lincRNA","ncbi_id":"284424","summary":null,"start":4769140,"end":4772533,"strand":1,"description":"MIR7-3 host gene [Source:HGNC Symbol;Acc:HGNC:30049]"}, {"versioned_ensembl_gene_id":"ENSG00000249610.1","gene_symbol":"AC010255.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122154496,"end":122156015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237717.1","gene_symbol":"BX276092.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71744828,"end":71745077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237182.1","gene_symbol":"BX276092.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71736454,"end":71736703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166257.8","gene_symbol":"SCN3B","gene_name":"sodium voltage-gated channel beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:20665]","synonyms":"HSA243396","biotype":"protein_coding","ncbi_id":"55800","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel beta subunit gene family, and influences the inactivation kinetics of the sodium channel. Two alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":123629187,"end":123655244,"strand":-1,"description":"sodium voltage-gated channel beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:20665]"}, {"versioned_ensembl_gene_id":"ENSG00000257838.5","gene_symbol":"AC106788.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22545698,"end":22576865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081148.11","gene_symbol":"IMPG2","gene_name":"interphotoreceptor matrix proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:18362]","synonyms":"RP56,IPM200","biotype":"protein_coding","ncbi_id":"50939","summary":"The protein encoded by this gene binds chondroitin sulfate and hyaluronan and is a proteoglycan. The encoded protein plays a role in the organization of the interphotoreceptor matrix and may promote the growth and maintenance of the light-sensitive photoreceptor outer segment. Defects in this gene are a cause of retinitis pigmentosa type 56 and maculopathy, IMPG2-related.[provided by RefSeq, Mar 2011]","start":101222546,"end":101320560,"strand":-1,"description":"interphotoreceptor matrix proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:18362]"}, {"versioned_ensembl_gene_id":"ENSG00000226705.1","gene_symbol":"SDCBPP1","gene_name":"syndecan binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128930","summary":null,"start":6293100,"end":6294684,"strand":-1,"description":"syndecan binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44684]"}, {"versioned_ensembl_gene_id":"ENSG00000109255.11","gene_symbol":"NMU","gene_name":"neuromedin U [Source:HGNC Symbol;Acc:HGNC:7859]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10874","summary":"This gene encodes a member of the neuromedin family of neuropeptides. The encoded protein is a precursor that is proteolytically processed to generate a biologically active neuropeptide that plays a role in pain, stress, immune-mediated inflammatory diseases and feeding regulation. Increased expression of this gene was observed in renal, pancreatic and lung cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. Some of these isoforms may undergo similar processing to generate the mature peptide. [provided by RefSeq, Jul 2015]","start":55595229,"end":55636698,"strand":-1,"description":"neuromedin U [Source:HGNC Symbol;Acc:HGNC:7859]"}, {"versioned_ensembl_gene_id":"ENSG00000120656.11","gene_symbol":"TAF12","gene_name":"TATA-box binding protein associated factor 12 [Source:HGNC Symbol;Acc:HGNC:11545]","synonyms":"TAFII20,TAF2J","biotype":"protein_coding","ncbi_id":"6883","summary":"Control of transcription by RNA polymerase II involves the basal transcription machinery which is a collection of proteins. These proteins with RNA polymerase II, assemble into complexes which are modulated by transactivator proteins that bind to cis-regulatory elements located adjacent to the transcription start site. Some modulators interact directly with the basal complex, whereas others may act as bridging proteins linking transactivators to the basal transcription factors. Some of these associated factors are weakly attached while others are tightly associated with TBP in the TFIID complex. Among the latter are the TAF proteins. Different TAFs are predicted to mediate the function of distinct transcriptional activators for a variety of gene promoters and RNA polymerases. TAF12 interacts directly with TBP as well as with TAF2I. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2008]","start":28589323,"end":28643085,"strand":-1,"description":"TATA-box binding protein associated factor 12 [Source:HGNC Symbol;Acc:HGNC:11545]"}, {"versioned_ensembl_gene_id":"ENSG00000242573.1","gene_symbol":"ACTR3P3","gene_name":"ACTR3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38679]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128020","summary":null,"start":101163094,"end":101163986,"strand":1,"description":"ACTR3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38679]"}, {"versioned_ensembl_gene_id":"ENSG00000281852.1","gene_symbol":"LINC00891","gene_name":"long intergenic non-protein coding RNA 891 [Source:HGNC Symbol;Acc:HGNC:48577]","synonyms":"FLJ46446","biotype":"lincRNA","ncbi_id":"441501","summary":null,"start":71697196,"end":71706455,"strand":1,"description":"long intergenic non-protein coding RNA 891 [Source:HGNC Symbol;Acc:HGNC:48577]"}, {"versioned_ensembl_gene_id":"ENSG00000278443.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29852167,"end":29852298,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000141580.15","gene_symbol":"WDR45B","gene_name":"WD repeat domain 45B [Source:HGNC Symbol;Acc:HGNC:25072]","synonyms":"WIPI3,WDR45L","biotype":"protein_coding","ncbi_id":"56270","summary":"This gene encodes a member of the WIPI or SVP1 family of WD40 repeat-containing proteins. The protein contains seven WD40 repeats that are thought to fold into a beta-propeller structure that mediates protein-protein interactions, and a conserved motif for interaction with phospholipids. The human genome contains several pseudogenes of this gene. [provided by RefSeq, Jul 2008]","start":82614562,"end":82648553,"strand":-1,"description":"WD repeat domain 45B [Source:HGNC Symbol;Acc:HGNC:25072]"}, {"versioned_ensembl_gene_id":"ENSG00000253207.3","gene_symbol":"AC103993.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113600310,"end":113616958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253164.5","gene_symbol":"AC023403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20350210,"end":20372769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249635.1","gene_symbol":"AC109361.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106003317,"end":106022478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232759.1","gene_symbol":"AC002480.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22563337,"end":22573996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228926.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31601835,"end":31602108,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000133195.11","gene_symbol":"SLC39A11","gene_name":"solute carrier family 39 member 11 [Source:HGNC Symbol;Acc:HGNC:14463]","synonyms":"C17orf26","biotype":"protein_coding","ncbi_id":"201266","summary":null,"start":72645949,"end":73092712,"strand":-1,"description":"solute carrier family 39 member 11 [Source:HGNC Symbol;Acc:HGNC:14463]"}, {"versioned_ensembl_gene_id":"ENSG00000204967.10","gene_symbol":"PCDHA4","gene_name":"protocadherin alpha 4 [Source:HGNC Symbol;Acc:HGNC:8670]","synonyms":"PCDH-ALPHA4,CRNR1,CNRN1,CNR1","biotype":"protein_coding","ncbi_id":"56144","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140806929,"end":141012344,"strand":1,"description":"protocadherin alpha 4 [Source:HGNC Symbol;Acc:HGNC:8670]"}, {"versioned_ensembl_gene_id":"ENSG00000141040.14","gene_symbol":"ZNF287","gene_name":"zinc finger protein 287 [Source:HGNC Symbol;Acc:HGNC:13502]","synonyms":"ZSCAN45,ZKSCAN13","biotype":"protein_coding","ncbi_id":"57336","summary":"This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":16551387,"end":16569206,"strand":-1,"description":"zinc finger protein 287 [Source:HGNC Symbol;Acc:HGNC:13502]"}, {"versioned_ensembl_gene_id":"ENSG00000271044.1","gene_symbol":"AC087468.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84940504,"end":84941133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153822.13","gene_symbol":"KCNJ16","gene_name":"potassium voltage-gated channel subfamily J member 16 [Source:HGNC Symbol;Acc:HGNC:6262]","synonyms":"Kir5.1,BIR9","biotype":"protein_coding","ncbi_id":"3773","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which tends to allow potassium to flow into rather than out of a cell, can form heterodimers with two other inward-rectifier type potassium channels. It may function in fluid and pH balance regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2014]","start":70053429,"end":70135608,"strand":1,"description":"potassium voltage-gated channel subfamily J member 16 [Source:HGNC Symbol;Acc:HGNC:6262]"}, {"versioned_ensembl_gene_id":"ENSG00000204970.9","gene_symbol":"PCDHA1","gene_name":"protocadherin alpha 1 [Source:HGNC Symbol;Acc:HGNC:8663]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56147","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140786136,"end":141012347,"strand":1,"description":"protocadherin alpha 1 [Source:HGNC Symbol;Acc:HGNC:8663]"}, {"versioned_ensembl_gene_id":"ENSG00000237265.6","gene_symbol":"BX276092.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71662998,"end":71666767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237560.5","gene_symbol":"LINC01497","gene_name":"long intergenic non-protein coding RNA 1497 [Source:HGNC Symbol;Acc:HGNC:51163]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723487","summary":null,"start":69961707,"end":69983538,"strand":1,"description":"long intergenic non-protein coding RNA 1497 [Source:HGNC Symbol;Acc:HGNC:51163]"}, {"versioned_ensembl_gene_id":"ENSG00000259760.1","gene_symbol":"AC015660.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99396613,"end":99401315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261523.1","gene_symbol":"AC009167.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14695567,"end":14707055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227711.3","gene_symbol":"AL451054.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":227509028,"end":227510618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152822.13","gene_symbol":"GRM1","gene_name":"glutamate metabotropic receptor 1 [Source:HGNC Symbol;Acc:HGNC:4593]","synonyms":"PPP1R85,MGLUR1,mGlu1,GPRC1A","biotype":"protein_coding","ncbi_id":"2911","summary":"This gene encodes a metabotropic glutamate receptor that functions by activating phospholipase C. L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The canonical alpha isoform of the encoded protein is a disulfide-linked homodimer whose activity is mediated by a G-protein-coupled phosphatidylinositol-calcium second messenger system. This gene may be associated with many disease states, including schizophrenia, bipolar disorder, depression, and breast cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":146027646,"end":146437598,"strand":1,"description":"glutamate metabotropic receptor 1 [Source:HGNC Symbol;Acc:HGNC:4593]"}, {"versioned_ensembl_gene_id":"ENSG00000216811.2","gene_symbol":"AL035698.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146364931,"end":146365494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116205.12","gene_symbol":"TCEANC2","gene_name":"transcription elongation factor A N-terminal and central domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26494]","synonyms":"FLJ32112,C1orf83","biotype":"protein_coding","ncbi_id":"127428","summary":null,"start":54053587,"end":54112519,"strand":1,"description":"transcription elongation factor A N-terminal and central domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26494]"}, {"versioned_ensembl_gene_id":"ENSG00000226798.1","gene_symbol":"AL138749.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80869758,"end":80871295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256269.7","gene_symbol":"HMBS","gene_name":"hydroxymethylbilane synthase [Source:HGNC Symbol;Acc:HGNC:4982]","synonyms":"UPS,PORC,PBGD","biotype":"protein_coding","ncbi_id":"3145","summary":"This gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":119084866,"end":119093549,"strand":1,"description":"hydroxymethylbilane synthase [Source:HGNC Symbol;Acc:HGNC:4982]"}, {"versioned_ensembl_gene_id":"ENSG00000254856.1","gene_symbol":"NDUFA3P2","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479051","summary":null,"start":68488609,"end":68488840,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45051]"}, {"versioned_ensembl_gene_id":"ENSG00000171552.12","gene_symbol":"BCL2L1","gene_name":"BCL2 like 1 [Source:HGNC Symbol;Acc:HGNC:992]","synonyms":"PPP1R52,BCLX,BCL2L,bcl-xS,bcl-xL,Bcl-X","biotype":"protein_coding","ncbi_id":"598","summary":"The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The proteins encoded by this gene are located at the outer mitochondrial membrane, and have been shown to regulate outer mitochondrial membrane channel (VDAC) opening. VDAC regulates mitochondrial membrane potential, and thus controls the production of reactive oxygen species and release of cytochrome C by mitochondria, both of which are the potent inducers of cell apoptosis. Alternative splicing results in multiple transcript variants encoding two different isoforms. The longer isoform acts as an apoptotic inhibitor and the shorter isoform acts as an apoptotic activator. [provided by RefSeq, Dec 2015]","start":31664452,"end":31723989,"strand":-1,"description":"BCL2 like 1 [Source:HGNC Symbol;Acc:HGNC:992]"}, {"versioned_ensembl_gene_id":"ENSG00000185304.14","gene_symbol":"RGPD2","gene_name":"RANBP2-like and GRIP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:32415]","synonyms":"RGP2,RANBP2L2","biotype":"protein_coding","ncbi_id":"729857","summary":null,"start":87755955,"end":87825952,"strand":-1,"description":"RANBP2-like and GRIP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:32415]"}, {"versioned_ensembl_gene_id":"ENSG00000184814.5","gene_symbol":"PRR23B","gene_name":"proline rich 23B [Source:HGNC Symbol;Acc:HGNC:33764]","synonyms":"FLJ46116","biotype":"protein_coding","ncbi_id":"389151","summary":null,"start":139019031,"end":139020926,"strand":-1,"description":"proline rich 23B [Source:HGNC Symbol;Acc:HGNC:33764]"}, {"versioned_ensembl_gene_id":"ENSG00000204611.6","gene_symbol":"ZNF616","gene_name":"zinc finger protein 616 [Source:HGNC Symbol;Acc:HGNC:28062]","synonyms":"MGC45556","biotype":"protein_coding","ncbi_id":"90317","summary":null,"start":52113091,"end":52139922,"strand":-1,"description":"zinc finger protein 616 [Source:HGNC Symbol;Acc:HGNC:28062]"}, {"versioned_ensembl_gene_id":"ENSG00000243680.1","gene_symbol":"RPL37P23","gene_name":"ribosomal protein L37 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37003]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648217","summary":null,"start":52143043,"end":52143336,"strand":1,"description":"ribosomal protein L37 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37003]"}, {"versioned_ensembl_gene_id":"ENSG00000279643.3","gene_symbol":"TAMM41","gene_name":"TAM41 mitochondrial translocator assembly and maintenance homolog [Source:HGNC Symbol;Acc:HGNC:25187]","synonyms":"MGC16471,DKFZp434E0519,C3orf31","biotype":"protein_coding","ncbi_id":"132001","summary":null,"start":11817080,"end":11846919,"strand":-1,"description":"TAM41 mitochondrial translocator assembly and maintenance homolog [Source:HGNC Symbol;Acc:HGNC:25187]"}, {"versioned_ensembl_gene_id":"ENSG00000187024.14","gene_symbol":"PTRH1","gene_name":"peptidyl-tRNA hydrolase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27039]","synonyms":"PTH1,C9orf115","biotype":"protein_coding","ncbi_id":"138428","summary":null,"start":127690348,"end":127724873,"strand":-1,"description":"peptidyl-tRNA hydrolase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27039]"}, {"versioned_ensembl_gene_id":"ENSG00000276858.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54874219,"end":54890443,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000241124.1","gene_symbol":"BX248109.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28987721,"end":28989460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163541.11","gene_symbol":"SUCLG1","gene_name":"succinate-CoA ligase alpha subunit [Source:HGNC Symbol;Acc:HGNC:11449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8802","summary":"This gene encodes the alpha subunit of the heterodimeric enzyme succinate coenzyme A ligase. This enzyme is targeted to the mitochondria and catalyzes the conversion of succinyl CoA and ADP or GDP to succinate and ATP or GTP. Mutations in this gene are the cause of the metabolic disorder fatal infantile lactic acidosis and mitochondrial DNA depletion. [provided by RefSeq, Feb 2010]","start":84423523,"end":84460045,"strand":-1,"description":"succinate-CoA ligase alpha subunit [Source:HGNC Symbol;Acc:HGNC:11449]"}, {"versioned_ensembl_gene_id":"ENSG00000121644.18","gene_symbol":"DESI2","gene_name":"desumoylating isopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:24264]","synonyms":"FAM152A,CGI-146,C1orf121,PPPDE1,PNAS-4,FLJ21998","biotype":"protein_coding","ncbi_id":"51029","summary":null,"start":244652935,"end":244709033,"strand":1,"description":"desumoylating isopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:24264]"}, {"versioned_ensembl_gene_id":"ENSG00000165916.8","gene_symbol":"PSMC3","gene_name":"proteasome 26S subunit, ATPase 3 [Source:HGNC Symbol;Acc:HGNC:9549]","synonyms":"TBP-1,TBP1","biotype":"protein_coding","ncbi_id":"5702","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases that have chaperone-like activity. This subunit may compete with PSMC2 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex. A pseudogene has been identified on chromosome 9. [provided by RefSeq, Jul 2008]","start":47418769,"end":47426473,"strand":-1,"description":"proteasome 26S subunit, ATPase 3 [Source:HGNC Symbol;Acc:HGNC:9549]"}, {"versioned_ensembl_gene_id":"ENSG00000206262.8","gene_symbol":"FOXL2NB","gene_name":"FOXL2 neighbor [Source:HGNC Symbol;Acc:HGNC:34428]","synonyms":"FLJ43329,C3orf72","biotype":"protein_coding","ncbi_id":"401089","summary":null,"start":138947234,"end":138953451,"strand":1,"description":"FOXL2 neighbor [Source:HGNC Symbol;Acc:HGNC:34428]"}, {"versioned_ensembl_gene_id":"ENSG00000259317.1","gene_symbol":"AC044860.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85272527,"end":85272974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216444.1","gene_symbol":"RAET1M","gene_name":"retinoic acid early transcript 1M pseudogene [Source:HGNC Symbol;Acc:HGNC:16799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"353094","summary":null,"start":150032769,"end":150033566,"strand":1,"description":"retinoic acid early transcript 1M pseudogene [Source:HGNC Symbol;Acc:HGNC:16799]"}, {"versioned_ensembl_gene_id":"ENSG00000226263.1","gene_symbol":"ISM1-AS1","gene_name":"ISM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44313]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505536","summary":null,"start":13237801,"end":13239674,"strand":-1,"description":"ISM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44313]"}, {"versioned_ensembl_gene_id":"ENSG00000132185.16","gene_symbol":"FCRLA","gene_name":"Fc receptor like A [Source:HGNC Symbol;Acc:HGNC:18504]","synonyms":"MGC4595,FREB,FCRLX,FCRLM1,FCRLe,FCRLd,FCRLc2,FCRLc1,FCRLb,FCRLa,FCRL","biotype":"protein_coding","ncbi_id":"84824","summary":"This gene encodes a protein similar to receptors for the Fc fragment of gamma immunoglobulin (IgG). These receptors, referred to as FCGRs, mediate the destruction of IgG-coated antigens and of cells induced by antibodies. This encoded protein is selectively expressed in B cells, and may be involved in their development. This protein may also be involved in the development of lymphomas. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":161706972,"end":161714352,"strand":1,"description":"Fc receptor like A [Source:HGNC Symbol;Acc:HGNC:18504]"}, {"versioned_ensembl_gene_id":"ENSG00000225230.1","gene_symbol":"AC008937.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56900041,"end":56910714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213075.7","gene_symbol":"RPL31P11","gene_name":"ribosomal protein L31 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35849]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"641311","summary":null,"start":161683695,"end":161685252,"strand":-1,"description":"ribosomal protein L31 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35849]"}, {"versioned_ensembl_gene_id":"ENSG00000259952.1","gene_symbol":"AC009133.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29806496,"end":29807732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163528.12","gene_symbol":"CHCHD4","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26467]","synonyms":"TIMM40,MIA40,FLJ31709","biotype":"protein_coding","ncbi_id":"131474","summary":"CHCHD4, a component of human mitochondria, belongs to a protein family whose members share 6 highly conserved cysteine residues constituting a -CXC-CX(9)C-CX(9)C- motif in the C terminus (Hofmann et al., 2005 [PubMed 16185709]).[supplied by OMIM, Mar 2008]","start":14112077,"end":14124870,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26467]"}, {"versioned_ensembl_gene_id":"ENSG00000224247.1","gene_symbol":"AJ009632.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15493932,"end":15496124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181191.11","gene_symbol":"PJA1","gene_name":"praja ring finger ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:16648]","synonyms":"RNF70,FLJ11830","biotype":"protein_coding","ncbi_id":"64219","summary":"This gene encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":69160851,"end":69165793,"strand":-1,"description":"praja ring finger ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:16648]"}, {"versioned_ensembl_gene_id":"ENSG00000188388.10","gene_symbol":"GOLGA6L3","gene_name":"golgin A6 family-like 3 [Source:HGNC Symbol;Acc:HGNC:37441]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100133220","summary":null,"start":85240472,"end":85247170,"strand":1,"description":"golgin A6 family-like 3 [Source:HGNC Symbol;Acc:HGNC:37441]"}, {"versioned_ensembl_gene_id":"ENSG00000271324.1","gene_symbol":"AC112220.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33793644,"end":33794145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228112.1","gene_symbol":"AC112220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33727250,"end":33727604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264365.1","gene_symbol":"AC023983.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24364787,"end":24367984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229212.7","gene_symbol":"AC044860.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85205440,"end":85234795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259270.1","gene_symbol":"AC044860.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85178628,"end":85178806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272900.1","gene_symbol":"AP000435.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58291826,"end":58292765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282904.1","gene_symbol":"AC107398.4","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":47463784,"end":47470477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267241.2","gene_symbol":"CYP4F10P","gene_name":"cytochrome P450 family 4 subfamily F member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:39943]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646575","summary":null,"start":15664106,"end":15669826,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:39943]"}, {"versioned_ensembl_gene_id":"ENSG00000141447.17","gene_symbol":"OSBPL1A","gene_name":"oxysterol binding protein like 1A [Source:HGNC Symbol;Acc:HGNC:16398]","synonyms":"OSBPL1B,ORP1,ORP-1","biotype":"protein_coding","ncbi_id":"114876","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain, although some members contain only the sterol-binding domain. Transcript variants derived from alternative promoter usage and/or alternative splicing exist; they encode different isoforms. [provided by RefSeq, Jul 2008]","start":24162044,"end":24397880,"strand":-1,"description":"oxysterol binding protein like 1A [Source:HGNC Symbol;Acc:HGNC:16398]"}, {"versioned_ensembl_gene_id":"ENSG00000216863.9","gene_symbol":"LY86-AS1","gene_name":"LY86 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26593]","synonyms":"LY86AS,FLJ33708,LY86-AS","biotype":"antisense_RNA","ncbi_id":"285780","summary":null,"start":6346465,"end":6622771,"strand":-1,"description":"LY86 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26593]"}, {"versioned_ensembl_gene_id":"ENSG00000214184.3","gene_symbol":"GCC2-AS1","gene_name":"GCC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28126]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644903","summary":null,"start":108507515,"end":108534196,"strand":-1,"description":"GCC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28126]"}, {"versioned_ensembl_gene_id":"ENSG00000265750.1","gene_symbol":"AC090772.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24159509,"end":24162211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258336.2","gene_symbol":"DUX4L52","gene_name":"double homeobox 4 like 52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480354","summary":null,"start":61600067,"end":61600843,"strand":-1,"description":"double homeobox 4 like 52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51811]"}, {"versioned_ensembl_gene_id":"ENSG00000279017.1","gene_symbol":"AC098476.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":45749627,"end":45750651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155034.18","gene_symbol":"FBXL18","gene_name":"F-box and leucine rich repeat protein 18 [Source:HGNC Symbol;Acc:HGNC:21874]","synonyms":"FLJ11467,Fbl18","biotype":"protein_coding","ncbi_id":"80028","summary":"The protein encoded by this gene is a member of a family of proteins that contain an approximately 40-amino acid F-box motif. This motif is important for interaction with SKP1 and for targeting some proteins for degradation. The encoded protein has been shown to control the cellular level of FBXL7, a protein that induces mitotic arrest, by targeting it for polyubiquitylation and proteasomal degradation. Members of the F-box protein family, such as FBXL18, are characterized by an approximately 40-amino acid F-box motif. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains. [provided by RefSeq, Mar 2016]","start":5431335,"end":5513798,"strand":-1,"description":"F-box and leucine rich repeat protein 18 [Source:HGNC Symbol;Acc:HGNC:21874]"}, {"versioned_ensembl_gene_id":"ENSG00000166984.11","gene_symbol":"TCP10L2","gene_name":"t-complex 10 like 2 [Source:HGNC Symbol;Acc:HGNC:21254]","synonyms":"bA517H2.3","biotype":"protein_coding","ncbi_id":"401285","summary":null,"start":167146414,"end":167196913,"strand":1,"description":"t-complex 10 like 2 [Source:HGNC Symbol;Acc:HGNC:21254]"}, {"versioned_ensembl_gene_id":"ENSG00000022840.15","gene_symbol":"RNF10","gene_name":"ring finger protein 10 [Source:HGNC Symbol;Acc:HGNC:10055]","synonyms":"RIE2,KIAA0262","biotype":"protein_coding","ncbi_id":"9921","summary":"The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [provided by RefSeq, Jul 2008]","start":120533480,"end":120577594,"strand":1,"description":"ring finger protein 10 [Source:HGNC Symbol;Acc:HGNC:10055]"}, {"versioned_ensembl_gene_id":"ENSG00000243517.1","gene_symbol":"AC024940.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31251992,"end":31252597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120436.3","gene_symbol":"GPR31","gene_name":"G protein-coupled receptor 31 [Source:HGNC Symbol;Acc:HGNC:4486]","synonyms":"HETER1,12-HETER","biotype":"protein_coding","ncbi_id":"2853","summary":null,"start":167156271,"end":167158329,"strand":-1,"description":"G protein-coupled receptor 31 [Source:HGNC Symbol;Acc:HGNC:4486]"}, {"versioned_ensembl_gene_id":"ENSG00000169811.8","gene_symbol":"RBMY1HP","gene_name":"RNA binding motif protein, Y-linked, family 1, member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:9916]","synonyms":"RBMY1H","biotype":"unprocessed_pseudogene","ncbi_id":"5944","summary":null,"start":21493519,"end":21501968,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:9916]"}, {"versioned_ensembl_gene_id":"ENSG00000215604.3","gene_symbol":"ZNF962P","gene_name":"zinc finger protein 962, pseudogene [Source:HGNC Symbol;Acc:HGNC:39250]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729501","summary":null,"start":18467172,"end":18485448,"strand":-1,"description":"zinc finger protein 962, pseudogene [Source:HGNC Symbol;Acc:HGNC:39250]"}, {"versioned_ensembl_gene_id":"ENSG00000182606.14","gene_symbol":"TRAK1","gene_name":"trafficking kinesin protein 1 [Source:HGNC Symbol;Acc:HGNC:29947]","synonyms":"OIP106,MILT1,KIAA1042","biotype":"protein_coding","ncbi_id":"22906","summary":null,"start":42013802,"end":42225889,"strand":1,"description":"trafficking kinesin protein 1 [Source:HGNC Symbol;Acc:HGNC:29947]"}, {"versioned_ensembl_gene_id":"ENSG00000223650.1","gene_symbol":"UHRF2P1","gene_name":"ubiquitin like with PHD and ring finger domains 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39565]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"260337","summary":null,"start":74105572,"end":74107958,"strand":1,"description":"ubiquitin like with PHD and ring finger domains 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39565]"}, {"versioned_ensembl_gene_id":"ENSG00000163217.1","gene_symbol":"BMP10","gene_name":"bone morphogenetic protein 10 [Source:HGNC Symbol;Acc:HGNC:20869]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27302","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which binds to the activin receptor-like kinase 1 (ALK1) and plays important roles in cardiovascular development including cardiomyocyte proliferation and regulation of heart size, closure of the ductus arteriosus, angiogenesis and ventricular trabeculation. [provided by RefSeq, Aug 2016]","start":68865481,"end":68871517,"strand":-1,"description":"bone morphogenetic protein 10 [Source:HGNC Symbol;Acc:HGNC:20869]"}, {"versioned_ensembl_gene_id":"ENSG00000232928.2","gene_symbol":"DDX3P1","gene_name":"DEAD-box helicase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42171]","synonyms":"DDX3YP1","biotype":"processed_pseudogene","ncbi_id":"100133180","summary":null,"start":74121012,"end":74131923,"strand":1,"description":"DEAD-box helicase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42171]"}, {"versioned_ensembl_gene_id":"ENSG00000198783.5","gene_symbol":"ZNF830","gene_name":"zinc finger protein 830 [Source:HGNC Symbol;Acc:HGNC:28291]","synonyms":"OMCG1,MGC20398,CCDC16","biotype":"protein_coding","ncbi_id":"91603","summary":null,"start":34961530,"end":34963775,"strand":1,"description":"zinc finger protein 830 [Source:HGNC Symbol;Acc:HGNC:28291]"}, {"versioned_ensembl_gene_id":"ENSG00000256513.1","gene_symbol":"AC022081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28821975,"end":28825831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214896.4","gene_symbol":"RPSAP55","gene_name":"ribosomal protein SA pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388122","summary":null,"start":52885595,"end":52886470,"strand":1,"description":"ribosomal protein SA pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36921]"}, {"versioned_ensembl_gene_id":"ENSG00000083544.13","gene_symbol":"TDRD3","gene_name":"tudor domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20612]","synonyms":"FLJ21007","biotype":"protein_coding","ncbi_id":"81550","summary":null,"start":60396457,"end":60573878,"strand":1,"description":"tudor domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20612]"}, {"versioned_ensembl_gene_id":"ENSG00000011143.16","gene_symbol":"MKS1","gene_name":"Meckel syndrome, type 1 [Source:HGNC Symbol;Acc:HGNC:7121]","synonyms":"POC12,MKS,FLJ20345,BBS13","biotype":"protein_coding","ncbi_id":"54903","summary":"The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":58205437,"end":58219605,"strand":-1,"description":"Meckel syndrome, type 1 [Source:HGNC Symbol;Acc:HGNC:7121]"}, {"versioned_ensembl_gene_id":"ENSG00000229536.2","gene_symbol":"AC079776.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129825126,"end":129877553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265933.5","gene_symbol":"LINC00668","gene_name":"long intergenic non-protein coding RNA 668 [Source:HGNC Symbol;Acc:HGNC:44328]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400643","summary":null,"start":6919496,"end":6929966,"strand":-1,"description":"long intergenic non-protein coding RNA 668 [Source:HGNC Symbol;Acc:HGNC:44328]"}, {"versioned_ensembl_gene_id":"ENSG00000248152.1","gene_symbol":"AC093879.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112979590,"end":113071962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160223.16","gene_symbol":"ICOSLG","gene_name":"inducible T-cell costimulator ligand [Source:HGNC Symbol;Acc:HGNC:17087]","synonyms":"ICOSL,ICOS-L,GL50,CD275,B7RP1,B7RP-1,B7H2,B7-H2,KIAA0653","biotype":"protein_coding","ncbi_id":"23308","summary":null,"start":44222991,"end":44240966,"strand":-1,"description":"inducible T-cell costimulator ligand [Source:HGNC Symbol;Acc:HGNC:17087]"}, {"versioned_ensembl_gene_id":"ENSG00000196218.12","gene_symbol":"RYR1","gene_name":"ryanodine receptor 1 [Source:HGNC Symbol;Acc:HGNC:10483]","synonyms":"RYR,PPP1R137,MHS1,MHS,CCO","biotype":"protein_coding","ncbi_id":"6261","summary":"This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":38433699,"end":38587564,"strand":1,"description":"ryanodine receptor 1 [Source:HGNC Symbol;Acc:HGNC:10483]"}, {"versioned_ensembl_gene_id":"ENSG00000273863.1","gene_symbol":"AC010678.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7905536,"end":7907303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000046889.18","gene_symbol":"PREX2","gene_name":"phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:22950]","synonyms":"PPP1R129,P-REX2,FLJ12987,DEPDC2,DEP.2","biotype":"protein_coding","ncbi_id":"80243","summary":"The protein encoded by this gene belongs to the phosphatidylinositol 3,4,5-trisphosphate (PIP3)-dependent Rac exchanger (PREX) family, which are Dbl-type guanine-nucleotide exchange factors for Rac family small G proteins. Structural domains of this protein include the catalytic diffuse B-cell lymphoma homology and pleckstrin homology (DHPH) domain, two disheveled, EGL-10, and pleckstrin homology (DEP) domains, two PDZ domains, and a C-terminal inositol polyphosphate-4 phosphatase (IP4P) domain that is found in one of the isoforms. This protein facilitates the exchange of GDP for GTP on Rac1, allowing the GTP-bound Rac1 to activate downstream effectors. Studies also show that the pleckstrin homology domain of this protein interacts with the phosphatase and tensin homolog (PTEN) gene product to inhibit PTEN phosphatase activity, thus activating the phosphoinositide-3 kinase (PI3K) signaling pathway. Conversely, the PTEN gene product has also been shown to inhibit the GEF activity of this protein. This gene plays a role in insulin-signaling pathways, and either mutations or overexpression of this gene have been observed in some cancers. [provided by RefSeq, Apr 2016]","start":67952118,"end":68237030,"strand":1,"description":"phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:22950]"}, {"versioned_ensembl_gene_id":"ENSG00000254051.1","gene_symbol":"AC011853.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68176768,"end":68177221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255206.1","gene_symbol":"AC011853.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68082204,"end":68095081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151498.11","gene_symbol":"ACAD8","gene_name":"acyl-CoA dehydrogenase family member 8 [Source:HGNC Symbol;Acc:HGNC:87]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27034","summary":"This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. The encoded protein is a mitochondrial enzyme that functions in catabolism of the branched-chain amino acid valine. Defects in this gene are the cause of isobutyryl-CoA dehydrogenase deficiency.[provided by RefSeq, Nov 2009]","start":134253495,"end":134265855,"strand":1,"description":"acyl-CoA dehydrogenase family member 8 [Source:HGNC Symbol;Acc:HGNC:87]"}, {"versioned_ensembl_gene_id":"ENSG00000259740.1","gene_symbol":"AC009558.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47525169,"end":47527756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258885.1","gene_symbol":"AL450267.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36856555,"end":36861375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272966.1","gene_symbol":"AC064836.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":202336739,"end":202337200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175449.13","gene_symbol":"RFESD","gene_name":"Rieske Fe-S domain containing [Source:HGNC Symbol;Acc:HGNC:29587]","synonyms":null,"biotype":"protein_coding","ncbi_id":"317671","summary":null,"start":95646754,"end":95684773,"strand":1,"description":"Rieske Fe-S domain containing [Source:HGNC Symbol;Acc:HGNC:29587]"}, {"versioned_ensembl_gene_id":"ENSG00000229968.1","gene_symbol":"AL022578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47776827,"end":47778697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257146.1","gene_symbol":"AC079905.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59719698,"end":59719944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228186.10","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"Em:AB014077.1,CAT56,Em:AB023052.2","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30546725,"end":30553562,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000258473.1","gene_symbol":"AC007686.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77048172,"end":77086446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000058056.8","gene_symbol":"USP13","gene_name":"ubiquitin specific peptidase 13 (isopeptidase T-3) [Source:HGNC Symbol;Acc:HGNC:12611]","synonyms":"IsoT-3","biotype":"protein_coding","ncbi_id":"8975","summary":null,"start":179652755,"end":179789401,"strand":1,"description":"ubiquitin specific peptidase 13 (isopeptidase T-3) [Source:HGNC Symbol;Acc:HGNC:12611]"}, {"versioned_ensembl_gene_id":"ENSG00000205832.7","gene_symbol":"C16orf96","gene_name":"chromosome 16 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:40031]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342346","summary":null,"start":4556490,"end":4600714,"strand":1,"description":"chromosome 16 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:40031]"}, {"versioned_ensembl_gene_id":"ENSG00000275243.1","gene_symbol":"AC244472.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142598016,"end":142598469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100911.15","gene_symbol":"PSME2","gene_name":"proteasome activator subunit 2 [Source:HGNC Symbol;Acc:HGNC:9569]","synonyms":"PA28beta","biotype":"protein_coding","ncbi_id":"5721","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. The immunoproteasome contains an alternate regulator, referred to as the 11S regulator or PA28, that replaces the 19S regulator. Three subunits (alpha, beta and gamma) of the 11S regulator have been identified. This gene encodes the beta subunit of the 11S regulator, one of the two 11S subunits that is induced by gamma-interferon. Three beta and three alpha subunits combine to form a heterohexameric ring. Six pseudogenes have been identified on chromosomes 4, 5, 8, 10 and 13. [provided by RefSeq, Jul 2008]","start":24143362,"end":24147570,"strand":-1,"description":"proteasome activator subunit 2 [Source:HGNC Symbol;Acc:HGNC:9569]"}, {"versioned_ensembl_gene_id":"ENSG00000229089.7","gene_symbol":"ANKRD20A8P","gene_name":"ankyrin repeat domain 20 family member A8, pseudogene [Source:HGNC Symbol;Acc:HGNC:23666]","synonyms":"ANKRD20B","biotype":"protein_coding","ncbi_id":"729171","summary":null,"start":94811046,"end":94857282,"strand":-1,"description":"ankyrin repeat domain 20 family member A8, pseudogene [Source:HGNC Symbol;Acc:HGNC:23666]"}, {"versioned_ensembl_gene_id":"ENSG00000234315.1","gene_symbol":"OSTCP5","gene_name":"oligosaccharyltransferase complex subunit pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874386","summary":null,"start":45069977,"end":45070429,"strand":-1,"description":"oligosaccharyltransferase complex subunit pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42867]"}, {"versioned_ensembl_gene_id":"ENSG00000138152.8","gene_symbol":"BTBD16","gene_name":"BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:26340]","synonyms":"FLJ25359,Em:AC061711.1,C10orf87","biotype":"protein_coding","ncbi_id":"118663","summary":"This gene encodes a protein that contains a BTB/POZ domain. This domain mediates protein-protein interactions. A mutation in this gene may be associated with bipolar disorder. [provided by RefSeq, Sep 2016]","start":122271306,"end":122338162,"strand":1,"description":"BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:26340]"}, {"versioned_ensembl_gene_id":"ENSG00000230331.1","gene_symbol":"AL160004.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":229425020,"end":229425650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259064.2","gene_symbol":"AC091544.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92627073,"end":92627414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243538.1","gene_symbol":"RPS26P28","gene_name":"ribosomal protein S26 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643003","summary":null,"start":16902294,"end":16902641,"strand":-1,"description":"ribosomal protein S26 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36149]"}, {"versioned_ensembl_gene_id":"ENSG00000244302.1","gene_symbol":"PEX5L-AS2","gene_name":"PEX5L antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41252]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928790","summary":null,"start":179898229,"end":179921895,"strand":1,"description":"PEX5L antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41252]"}, {"versioned_ensembl_gene_id":"ENSG00000047188.15","gene_symbol":"YTHDC2","gene_name":"YTH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24721]","synonyms":"FLJ2194,FLJ10053,DKFZp564A186","biotype":"protein_coding","ncbi_id":"64848","summary":"This gene encodes a member of the DEAH (Asp-Glu-Ala-His) subfamily of proteins, part of the DEAD (Asp-Glu-Ala-Asp) box family of RNA helicases. The encoded protein binds to N6-methyladenosine, a common modified RNA nucleotide that is enriched in the stop codons and 3' UTRs of eukaryotic messenger RNAs. Binding of proteins to this modified nucleotide may regulate mRNA translation and stability. This gene may be associated with susceptibility to pancreatic cancer in human patients, and knockdown of this gene resulted in reduced proliferation in a human liver cancer cell line. [provided by RefSeq, Sep 2016]","start":113513683,"end":113595285,"strand":1,"description":"YTH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24721]"}, {"versioned_ensembl_gene_id":"ENSG00000249230.1","gene_symbol":"CDH12P2","gene_name":"cadherin 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1752]","synonyms":"CDH12P,C41-CAD","biotype":"unprocessed_pseudogene","ncbi_id":"1011","summary":null,"start":69985204,"end":69985501,"strand":-1,"description":"cadherin 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1752]"}, {"versioned_ensembl_gene_id":"ENSG00000281184.1","gene_symbol":"PSMB1","gene_name":"proteasome subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9537]","synonyms":"HC5,PMSB1","biotype":"processed_transcript","ncbi_id":"5689","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is tightly linked to the TBP (TATA-binding protein) gene in human and in mouse, and is transcribed in the opposite orientation in both species. [provided by RefSeq, Jul 2008]","start":170544440,"end":170544544,"strand":-1,"description":"proteasome subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9537]"}, {"versioned_ensembl_gene_id":"ENSG00000280722.1","gene_symbol":"AL008628.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":170423462,"end":170428648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225624.1","gene_symbol":"TBL1YP1","gene_name":"transducin beta like 1, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23979]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"286555","summary":null,"start":20727254,"end":20742900,"strand":1,"description":"transducin beta like 1, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23979]"}, {"versioned_ensembl_gene_id":"ENSG00000063515.2","gene_symbol":"GSC2","gene_name":"goosecoid homeobox 2 [Source:HGNC Symbol;Acc:HGNC:4613]","synonyms":"GSCL","biotype":"protein_coding","ncbi_id":"2928","summary":"Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008]","start":19148576,"end":19150283,"strand":-1,"description":"goosecoid homeobox 2 [Source:HGNC Symbol;Acc:HGNC:4613]"}, {"versioned_ensembl_gene_id":"ENSG00000275158.1","gene_symbol":"AC244196.2","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142580917,"end":142581427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276953.1","gene_symbol":"AC244196.5","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142563740,"end":142564245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224764.1","gene_symbol":"AL353768.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94928551,"end":94934946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183643.4","gene_symbol":"C15orf32","gene_name":"chromosome 15 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:26549]","synonyms":"FLJ32831","biotype":"lincRNA","ncbi_id":"145858","summary":null,"start":92471654,"end":92501117,"strand":1,"description":"chromosome 15 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:26549]"}, {"versioned_ensembl_gene_id":"ENSG00000089351.14","gene_symbol":"GRAMD1A","gene_name":"GRAM domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29305]","synonyms":"FLJ90346,KIAA1533","biotype":"protein_coding","ncbi_id":"57655","summary":null,"start":34994784,"end":35026471,"strand":1,"description":"GRAM domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29305]"}, {"versioned_ensembl_gene_id":"ENSG00000276405.1","gene_symbol":"AC244196.3","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142535809,"end":142536292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268678.1","gene_symbol":"AC005261.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57350848,"end":57352012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278030.1","gene_symbol":"TRBV7-9","gene_name":"T-cell receptor beta variable 7-9 [Source:HGNC Symbol;Acc:HGNC:12243]","synonyms":"TCRBV6S4A1,TRBV79,TCRBV7S9","biotype":"TR_V_gene","ncbi_id":"28589","summary":null,"start":142529290,"end":142529762,"strand":1,"description":"T-cell receptor beta variable 7-9 [Source:HGNC Symbol;Acc:HGNC:12243]"}, {"versioned_ensembl_gene_id":"ENSG00000259443.1","gene_symbol":"AC012414.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20773084,"end":20774871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211731.1","gene_symbol":"TRBV5-7","gene_name":"T-cell receptor beta variable 5-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12224]","synonyms":"TCRBV5S7,TRBV57,TCRBV5S7P","biotype":"TR_V_gene","ncbi_id":"28608","summary":null,"start":142520090,"end":142520556,"strand":1,"description":"T-cell receptor beta variable 5-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12224]"}, {"versioned_ensembl_gene_id":"ENSG00000243014.1","gene_symbol":"PTMAP8","gene_name":"prothymosin, alpha pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42437]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728873","summary":null,"start":117026698,"end":117027039,"strand":1,"description":"prothymosin, alpha pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42437]"}, {"versioned_ensembl_gene_id":"ENSG00000108700.4","gene_symbol":"CCL8","gene_name":"C-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:10635]","synonyms":"SCYA8,MCP-2,HC14","biotype":"protein_coding","ncbi_id":"6355","summary":"This antimicrobial gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of N-terminal cysteine residues of the mature peptide. This chemokine is a member of the CC subfamily which is characterized by two adjacent cysteine residues. This cytokine displays chemotactic activity for monocytes, lymphocytes, basophils and eosinophils. By recruiting leukocytes to sites of inflammation this cytokine may contribute to tumor-associated leukocyte infiltration and to the antiviral state against HIV infection. [provided by RefSeq, Sep 2014]","start":34319036,"end":34321402,"strand":1,"description":"C-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:10635]"}, {"versioned_ensembl_gene_id":"ENSG00000250415.1","gene_symbol":"AC022113.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16617225,"end":16621276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241354.2","gene_symbol":"AL049874.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60602146,"end":60602533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175946.8","gene_symbol":"KLHL38","gene_name":"kelch like family member 38 [Source:HGNC Symbol;Acc:HGNC:34435]","synonyms":"C8ORFK36","biotype":"protein_coding","ncbi_id":"340359","summary":null,"start":123645527,"end":123652950,"strand":-1,"description":"kelch like family member 38 [Source:HGNC Symbol;Acc:HGNC:34435]"}, {"versioned_ensembl_gene_id":"ENSG00000267064.1","gene_symbol":"UXT-AS1","gene_name":"UXT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49239]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100133957","summary":null,"start":47658833,"end":47660377,"strand":1,"description":"UXT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49239]"}, {"versioned_ensembl_gene_id":"ENSG00000053371.12","gene_symbol":"AKR7A2","gene_name":"aldo-keto reductase family 7 member A2 [Source:HGNC Symbol;Acc:HGNC:389]","synonyms":"AFAR","biotype":"protein_coding","ncbi_id":"8574","summary":"The protein encoded by this gene belongs to the aldo/keto reductase (AKR) superfamily and AKR7 family, which are involved in the detoxification of aldehydes and ketones. The AKR7 family consists of 3 genes that are present in a cluster on the p arm of chromosome 1. This protein, thought to be localized in the golgi, catalyzes the NADPH-dependent reduction of succinic semialdehyde to the endogenous neuromodulator, gamma-hydroxybutyrate. It may also function as a detoxication enzyme in the reduction of aflatoxin B1 and 2-carboxybenzaldehyde. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":19303965,"end":19312146,"strand":-1,"description":"aldo-keto reductase family 7 member A2 [Source:HGNC Symbol;Acc:HGNC:389]"}, {"versioned_ensembl_gene_id":"ENSG00000218073.1","gene_symbol":"AL021407.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16160926,"end":16161411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241596.1","gene_symbol":"AC092468.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":115658533,"end":115661279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251383.1","gene_symbol":"LINC02483","gene_name":"long intergenic non-protein coding RNA 2483 [Source:HGNC Symbol;Acc:HGNC:53457]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441025","summary":null,"start":75354076,"end":75362566,"strand":1,"description":"long intergenic non-protein coding RNA 2483 [Source:HGNC Symbol;Acc:HGNC:53457]"}, {"versioned_ensembl_gene_id":"ENSG00000270790.1","gene_symbol":"AC025588.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57151587,"end":57151860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151276.23","gene_symbol":"MAGI1","gene_name":"membrane associated guanylate kinase, WW and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:946]","synonyms":"BAIAP1,AIP3,WWP3,TNRC19,MAGI-1,BAP1","biotype":"protein_coding","ncbi_id":"9223","summary":"The protein encoded by this gene is a member of the membrane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assembly of multiprotein complexes on the inner surface of the plasma membrane at regions of cell-cell contact. The product of this gene may play a role as scaffolding protein at cell-cell junctions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":65353525,"end":66038834,"strand":-1,"description":"membrane associated guanylate kinase, WW and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:946]"}, {"versioned_ensembl_gene_id":"ENSG00000278042.2","gene_symbol":"IGHV3-72","gene_name":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28410","summary":null,"start":106814867,"end":106815409,"strand":-1,"description":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]"}, {"versioned_ensembl_gene_id":"ENSG00000270285.1","gene_symbol":"AC124916.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48039267,"end":48039490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272610.1","gene_symbol":"MAGI1-IT1","gene_name":"MAGI1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42436]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"151877","summary":null,"start":65872815,"end":65954558,"strand":-1,"description":"MAGI1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42436]"}, {"versioned_ensembl_gene_id":"ENSG00000134352.19","gene_symbol":"IL6ST","gene_name":"interleukin 6 signal transducer [Source:HGNC Symbol;Acc:HGNC:6021]","synonyms":"GP130,CD130","biotype":"protein_coding","ncbi_id":"3572","summary":"The protein encoded by this gene is a signal transducer shared by many cytokines, including interleukin 6 (IL6), ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), and oncostatin M (OSM). This protein functions as a part of the cytokine receptor complex. The activation of this protein is dependent upon the binding of cytokines to their receptors. vIL6, a protein related to IL6 and encoded by the Kaposi sarcoma-associated herpesvirus, can bypass the interleukin 6 receptor (IL6R) and directly activate this protein. Knockout studies in mice suggest that this gene plays a critical role in regulating myocyte apoptosis. Alternatively spliced transcript variants have been described. A related pseudogene has been identified on chromosome 17. [provided by RefSeq, May 2014]","start":55935095,"end":55994993,"strand":-1,"description":"interleukin 6 signal transducer [Source:HGNC Symbol;Acc:HGNC:6021]"}, {"versioned_ensembl_gene_id":"ENSG00000255397.1","gene_symbol":"AC022182.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60937705,"end":60939871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235616.1","gene_symbol":"ST13P2","gene_name":"ST13, Hsp70 interacting protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38716]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344328","summary":null,"start":187825341,"end":187826449,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38716]"}, {"versioned_ensembl_gene_id":"ENSG00000223583.1","gene_symbol":"AL513365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26454653,"end":26455187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243910.7","gene_symbol":"TUBA4B","gene_name":"tubulin alpha 4b [Source:HGNC Symbol;Acc:HGNC:18637]","synonyms":"TUBA4,FLJ13940","biotype":"protein_coding","ncbi_id":"80086","summary":null,"start":219253243,"end":219272188,"strand":1,"description":"tubulin alpha 4b [Source:HGNC Symbol;Acc:HGNC:18637]"}, {"versioned_ensembl_gene_id":"ENSG00000173627.7","gene_symbol":"APOBEC4","gene_name":"apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4 [Source:HGNC Symbol;Acc:HGNC:32152]","synonyms":"FLJ25691,C1orf169,RP1-127C7.4,MGC26594","biotype":"protein_coding","ncbi_id":"403314","summary":"This gene encodes a member of the AID/APOBEC family of polynucleotide (deoxy)cytidine deaminases, which convert cytidine to uridine. Other AID/APOBEC family members are involved in mRNA editing, somatic hypermutation and recombination of immunoglobulin genes, and innate immunity to retroviral infection. [provided by RefSeq, Jul 2008]","start":183646404,"end":183653316,"strand":-1,"description":"apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4 [Source:HGNC Symbol;Acc:HGNC:32152]"}, {"versioned_ensembl_gene_id":"ENSG00000253647.1","gene_symbol":"CTD-2270F17.1","gene_name":"uncharacterized LOC101928033 [Source:NCBI gene;Acc:101928033]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928033","summary":null,"start":170389493,"end":170422844,"strand":1,"description":"uncharacterized LOC101928033 [Source:NCBI gene;Acc:101928033]"}, {"versioned_ensembl_gene_id":"ENSG00000236194.3","gene_symbol":"AC099811.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42270517,"end":42272683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119778.14","gene_symbol":"ATAD2B","gene_name":"ATPase family, AAA domain containing 2B [Source:HGNC Symbol;Acc:HGNC:29230]","synonyms":"KIAA1240","biotype":"protein_coding","ncbi_id":"54454","summary":"The protein encoded by this gene belongs to the AAA ATPase family. This family member includes an N-terminal bromodomain. It has been found to be localized to the nucleus, partly to replication sites, consistent with a chromatin-related function. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":23748664,"end":23927114,"strand":-1,"description":"ATPase family, AAA domain containing 2B [Source:HGNC Symbol;Acc:HGNC:29230]"}, {"versioned_ensembl_gene_id":"ENSG00000181201.3","gene_symbol":"HIST3H2BA","gene_name":"histone cluster 3 H2B family member a (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20515]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"337872","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 1. [provided by RefSeq, Oct 2015]","start":228464103,"end":228464626,"strand":-1,"description":"histone cluster 3 H2B family member a (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20515]"}, {"versioned_ensembl_gene_id":"ENSG00000235172.7","gene_symbol":"LINC01366","gene_name":"long intergenic non-protein coding RNA 1366 [Source:HGNC Symbol;Acc:HGNC:27416]","synonyms":null,"biotype":"lincRNA","ncbi_id":"257358","summary":null,"start":170331429,"end":170333879,"strand":1,"description":"long intergenic non-protein coding RNA 1366 [Source:HGNC Symbol;Acc:HGNC:27416]"}, {"versioned_ensembl_gene_id":"ENSG00000234303.2","gene_symbol":"CLYBL-AS1","gene_name":"CLYBL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39893]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927465","summary":null,"start":99726247,"end":99727491,"strand":-1,"description":"CLYBL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39893]"}, {"versioned_ensembl_gene_id":"ENSG00000260113.3","gene_symbol":"AC093249.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30626976,"end":30627178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203875.10","gene_symbol":"SNHG5","gene_name":"small nucleolar RNA host gene 5 [Source:HGNC Symbol;Acc:HGNC:21026]","synonyms":"bA33E24.2,U50HG,NCRNA00044,MGC16362,LINC00044,C6orf160","biotype":"processed_transcript","ncbi_id":"387066","summary":"This gene represent a snoRNA host gene and produces a long non-coding RNA. This RNA may regulate gene expression by acting as a sponge for microRNAs. This transcript may also stabilize mRNAs by blocking degradation by staufen double-stranded RNA binding protein 1. [provided by RefSeq, Dec 2017]","start":85660950,"end":85678736,"strand":-1,"description":"small nucleolar RNA host gene 5 [Source:HGNC Symbol;Acc:HGNC:21026]"}, {"versioned_ensembl_gene_id":"ENSG00000188133.5","gene_symbol":"TMEM215","gene_name":"transmembrane protein 215 [Source:HGNC Symbol;Acc:HGNC:33816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401498","summary":null,"start":32783499,"end":32787399,"strand":1,"description":"transmembrane protein 215 [Source:HGNC Symbol;Acc:HGNC:33816]"}, {"versioned_ensembl_gene_id":"ENSG00000067601.7","gene_symbol":"PMS2P4","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:9129]","synonyms":"PMS6,PMS2L4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5382","summary":null,"start":67295608,"end":67302907,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:9129]"}, {"versioned_ensembl_gene_id":"ENSG00000260835.1","gene_symbol":"AC007223.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6573767,"end":6577359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231563.1","gene_symbol":"AL670729.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":228407381,"end":228409694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155530.2","gene_symbol":"LRGUK","gene_name":"leucine rich repeats and guanylate kinase domain containing [Source:HGNC Symbol;Acc:HGNC:21964]","synonyms":"FLJ32786,CFAP246","biotype":"protein_coding","ncbi_id":"136332","summary":null,"start":134127299,"end":134264591,"strand":1,"description":"leucine rich repeats and guanylate kinase domain containing [Source:HGNC Symbol;Acc:HGNC:21964]"}, {"versioned_ensembl_gene_id":"ENSG00000270990.1","gene_symbol":"AC069304.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150676833,"end":150677918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239836.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32997896,"end":33033347,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000265618.1","gene_symbol":"AC002094.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28361601,"end":28362859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255443.1","gene_symbol":"CD44-AS1","gene_name":"CD44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40133]","synonyms":"RP1-68D18.4","biotype":"antisense_RNA","ncbi_id":"109729172","summary":null,"start":35210343,"end":35214985,"strand":-1,"description":"CD44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40133]"}, {"versioned_ensembl_gene_id":"ENSG00000277708.1","gene_symbol":"AL118522.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":44841925,"end":44842539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163285.7","gene_symbol":"GABRG1","gene_name":"gamma-aminobutyric acid type A receptor gamma1 subunit [Source:HGNC Symbol;Acc:HGNC:4086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2565","summary":"The protein encoded by this gene belongs to the ligand-gated ionic channel family. It is an integral membrane protein and plays an important role in inhibiting neurotransmission by binding to the benzodiazepine receptor and opening an integral chloride channel. This gene is clustered with three other family members on chromosome 4. [provided by RefSeq, Jul 2008]","start":46035769,"end":46124081,"strand":-1,"description":"gamma-aminobutyric acid type A receptor gamma1 subunit [Source:HGNC Symbol;Acc:HGNC:4086]"}, {"versioned_ensembl_gene_id":"ENSG00000211734.3","gene_symbol":"TRBV5-1","gene_name":"T-cell receptor beta variable 5-1 [Source:HGNC Symbol;Acc:HGNC:12218]","synonyms":"TRBV51,TCRBV5S1A1T,TCRBV5S1","biotype":"TR_V_gene","ncbi_id":"28614","summary":null,"start":142320677,"end":142321544,"strand":1,"description":"T-cell receptor beta variable 5-1 [Source:HGNC Symbol;Acc:HGNC:12218]"}, {"versioned_ensembl_gene_id":"ENSG00000271071.1","gene_symbol":"AL513548.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26611903,"end":26613109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122203.14","gene_symbol":"KIAA1191","gene_name":"KIAA1191 [Source:HGNC Symbol;Acc:HGNC:29209]","synonyms":"p60MONOX,p33MONOX,FLJ21022","biotype":"protein_coding","ncbi_id":"57179","summary":null,"start":176346061,"end":176361968,"strand":-1,"description":"KIAA1191 [Source:HGNC Symbol;Acc:HGNC:29209]"}, {"versioned_ensembl_gene_id":"ENSG00000237702.2","gene_symbol":"TRBV3-1","gene_name":"T-cell receptor beta variable 3-1 [Source:HGNC Symbol;Acc:HGNC:12212]","synonyms":"TRBV31,TCRBV9S1A1T,TCRBV3S1","biotype":"TR_V_gene","ncbi_id":"28619","summary":null,"start":142308542,"end":142309048,"strand":1,"description":"T-cell receptor beta variable 3-1 [Source:HGNC Symbol;Acc:HGNC:12212]"}, {"versioned_ensembl_gene_id":"ENSG00000229575.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30775289,"end":30776018,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000253361.1","gene_symbol":"AC069120.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38543652,"end":38552680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146109.4","gene_symbol":"ABT1","gene_name":"activator of basal transcription 1 [Source:HGNC Symbol;Acc:HGNC:17369]","synonyms":"Esf2","biotype":"protein_coding","ncbi_id":"29777","summary":"Basal transcription of genes by RNA polymerase II requires the interaction of TATA-binding protein (TBP) with the core region of class II promoters. Studies in mouse suggest that the protein encoded by this gene likely activates basal transcription from class II promoters by interaction with TBP and the class II promoter DNA. [provided by RefSeq, Jul 2008]","start":26596952,"end":26600744,"strand":1,"description":"activator of basal transcription 1 [Source:HGNC Symbol;Acc:HGNC:17369]"}, {"versioned_ensembl_gene_id":"ENSG00000125124.11","gene_symbol":"BBS2","gene_name":"Bardet-Biedl syndrome 2 [Source:HGNC Symbol;Acc:HGNC:967]","synonyms":"BBS","biotype":"protein_coding","ncbi_id":"583","summary":"This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014]","start":56466836,"end":56520283,"strand":-1,"description":"Bardet-Biedl syndrome 2 [Source:HGNC Symbol;Acc:HGNC:967]"}, {"versioned_ensembl_gene_id":"ENSG00000276054.1","gene_symbol":"AC243654.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37386886,"end":37387926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282781.1","gene_symbol":"AC093627.21","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164086,"end":167293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059377.16","gene_symbol":"TBXAS1","gene_name":"thromboxane A synthase 1 [Source:HGNC Symbol;Acc:HGNC:11609]","synonyms":"TS,THAS,CYP5A1,CYP5,TXS,TXAS","biotype":"protein_coding","ncbi_id":"6916","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic reticulum membrane protein catalyzes the conversion of prostglandin H2 to thromboxane A2, a potent vasoconstrictor and inducer of platelet aggregation. The enzyme plays a role in several pathophysiological processes including hemostasis, cardiovascular disease, and stroke. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":139777051,"end":140020325,"strand":1,"description":"thromboxane A synthase 1 [Source:HGNC Symbol;Acc:HGNC:11609]"}, {"versioned_ensembl_gene_id":"ENSG00000271711.1","gene_symbol":"AC069236.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150611262,"end":150611877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282385.1","gene_symbol":"AC240577.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72839039,"end":72839718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213398.7","gene_symbol":"LCAT","gene_name":"lecithin-cholesterol acyltransferase [Source:HGNC Symbol;Acc:HGNC:6522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3931","summary":"This gene encodes the extracellular cholesterol esterifying enzyme, lecithin-cholesterol acyltransferase. The esterification of cholesterol is required for cholesterol transport. Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency. [provided by RefSeq, Jul 2008]","start":67939750,"end":67944131,"strand":-1,"description":"lecithin-cholesterol acyltransferase [Source:HGNC Symbol;Acc:HGNC:6522]"}, {"versioned_ensembl_gene_id":"ENSG00000196867.7","gene_symbol":"ZFP28","gene_name":"ZFP28 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:17801]","synonyms":"mkr5,KIAA1431","biotype":"protein_coding","ncbi_id":"140612","summary":null,"start":56538948,"end":56556810,"strand":1,"description":"ZFP28 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:17801]"}, {"versioned_ensembl_gene_id":"ENSG00000269696.1","gene_symbol":"AC005498.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56545566,"end":56567411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172239.13","gene_symbol":"PAIP1","gene_name":"poly(A) binding protein interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16945]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10605","summary":"The protein encoded by this gene interacts with poly(A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":43526267,"end":43557758,"strand":-1,"description":"poly(A) binding protein interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16945]"}, {"versioned_ensembl_gene_id":"ENSG00000238073.1","gene_symbol":"RBMY2HP","gene_name":"RNA binding motif protein, Y-linked, family 2, member H pseudogene [Source:HGNC Symbol;Acc:HGNC:23893]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378953","summary":null,"start":7671743,"end":7676024,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member H pseudogene [Source:HGNC Symbol;Acc:HGNC:23893]"}, {"versioned_ensembl_gene_id":"ENSG00000274962.1","gene_symbol":"TEX28P1","gene_name":"testis expressed 28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33356]","synonyms":"pTEX","biotype":"unprocessed_pseudogene","ncbi_id":"728447","summary":null,"start":154196471,"end":154213487,"strand":-1,"description":"testis expressed 28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33356]"}, {"versioned_ensembl_gene_id":"ENSG00000283381.1","gene_symbol":"AC024614.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33692229,"end":33692484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279668.2","gene_symbol":"AC024610.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33827728,"end":34079100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233170.4","gene_symbol":"AC138356.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37747338,"end":37748004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227454.2","gene_symbol":"MTND4P30","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42217]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873251","summary":null,"start":202617983,"end":202618881,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42217]"}, {"versioned_ensembl_gene_id":"ENSG00000231398.1","gene_symbol":"AL359385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97275012,"end":97278097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213148.3","gene_symbol":"AC073465.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173431349,"end":173431812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230964.1","gene_symbol":"AC233266.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91578478,"end":91578573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270999.1","gene_symbol":"IGKV1OR2-118","gene_name":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]","synonyms":"IGKV1/OR2-118","biotype":"IG_V_pseudogene","ncbi_id":"339562","summary":null,"start":90315366,"end":90315836,"strand":-1,"description":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]"}, {"versioned_ensembl_gene_id":"ENSG00000233714.1","gene_symbol":"AC012506.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23347654,"end":23351864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101901.11","gene_symbol":"ALG13","gene_name":"ALG13, UDP-N-acetylglucosaminyltransferase subunit [Source:HGNC Symbol;Acc:HGNC:30881]","synonyms":"TDRD13,MDS031,GLT28D1,FLJ23018,CXorf45,CDG1S,YGL047W","biotype":"protein_coding","ncbi_id":"79868","summary":"The protein encoded by this gene is a subunit of a bipartite UDP-N-acetylglucosamine transferase. It heterodimerizes with asparagine-linked glycosylation 14 homolog to form a functional UDP-GlcNAc glycosyltransferase that catalyzes the second sugar addition of the highly conserved oligosaccharide precursor in endoplasmic reticulum N-linked glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":111665811,"end":111760649,"strand":1,"description":"ALG13, UDP-N-acetylglucosaminyltransferase subunit [Source:HGNC Symbol;Acc:HGNC:30881]"}, {"versioned_ensembl_gene_id":"ENSG00000268199.2","gene_symbol":"AC010335.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18441419,"end":18443597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258942.1","gene_symbol":"AL358332.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51344914,"end":51385603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148444.15","gene_symbol":"COMMD3","gene_name":"COMM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23332]","synonyms":"C10orf8,BUP","biotype":"protein_coding","ncbi_id":"23412","summary":null,"start":22315974,"end":22320308,"strand":1,"description":"COMM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23332]"}, {"versioned_ensembl_gene_id":"ENSG00000281566.2","gene_symbol":"AL157778.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98573859,"end":98864984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224893.5","gene_symbol":"AL160162.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152794496,"end":152831913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185518.11","gene_symbol":"SV2B","gene_name":"synaptic vesicle glycoprotein 2B [Source:HGNC Symbol;Acc:HGNC:16874]","synonyms":"KIAA0735,HsT19680","biotype":"protein_coding","ncbi_id":"9899","summary":"This gene encodes a member of the synaptic vesicle proteins 2 (SV2) family and major facilitator superfamily of proteins. This protein and other members of the family are localized to synaptic vesicles and may function in the regulation of vesicle trafficking and exocytosis. Studies in mice suggest that the encoded protein may act as a protein receptor for botulinum neurotoxin E in neurons, and that this protein may be important for the integrity of the glomerular filtration barrier. This gene shows reduced expression in areas of synaptic loss in the hippocampus of human temporal lobe epilepsy patients. [provided by RefSeq, Sep 2016]","start":91099950,"end":91301309,"strand":1,"description":"synaptic vesicle glycoprotein 2B [Source:HGNC Symbol;Acc:HGNC:16874]"}, {"versioned_ensembl_gene_id":"ENSG00000266282.1","gene_symbol":"UBL5P2","gene_name":"ubiquitin like 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287215","summary":null,"start":32227890,"end":32228108,"strand":-1,"description":"ubiquitin like 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44640]"}, {"versioned_ensembl_gene_id":"ENSG00000282691.1","gene_symbol":"IGHV4-59","gene_name":"immunoglobulin heavy variable 4-59 [Source:HGNC Symbol;Acc:HGNC:5654]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28392","summary":null,"start":106651930,"end":106652506,"strand":-1,"description":"immunoglobulin heavy variable 4-59 [Source:HGNC Symbol;Acc:HGNC:5654]"}, {"versioned_ensembl_gene_id":"ENSG00000282451.1","gene_symbol":"IGHV4-61","gene_name":"immunoglobulin heavy variable 4-61 [Source:HGNC Symbol;Acc:HGNC:5655]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28391","summary":null,"start":106663800,"end":106664338,"strand":-1,"description":"immunoglobulin heavy variable 4-61 [Source:HGNC Symbol;Acc:HGNC:5655]"}, {"versioned_ensembl_gene_id":"ENSG00000262381.1","gene_symbol":"MTATP6P24","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52180]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075232","summary":null,"start":10724620,"end":10725296,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52180]"}, {"versioned_ensembl_gene_id":"ENSG00000102098.17","gene_symbol":"SCML2","gene_name":"sex comb on midleg like 2 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:10581]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10389","summary":"This gene encodes a member of the Polycomb group proteins. These proteins form the Polycomb repressive complexes which are involved in transcriptional repression. The encoded protein binds histone peptides that are monomethylated at lysine residues and may be involved in regulating homeotic gene expression during development. [provided by RefSeq, Jun 2010]","start":18239314,"end":18354727,"strand":-1,"description":"sex comb on midleg like 2 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:10581]"}, {"versioned_ensembl_gene_id":"ENSG00000273972.1","gene_symbol":"AC068722.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45702640,"end":45703183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138640.14","gene_symbol":"FAM13A","gene_name":"family with sequence similarity 13 member A [Source:HGNC Symbol;Acc:HGNC:19367]","synonyms":"ARHGAP48,KIAA0914,FAM13A1","biotype":"protein_coding","ncbi_id":"10144","summary":null,"start":88725955,"end":89111398,"strand":-1,"description":"family with sequence similarity 13 member A [Source:HGNC Symbol;Acc:HGNC:19367]"}, {"versioned_ensembl_gene_id":"ENSG00000233448.2","gene_symbol":"PMS2P9","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9135]","synonyms":"PMSR5,PMS2LP1,PMS2L17","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132832","summary":null,"start":77039944,"end":77043776,"strand":1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9135]"}, {"versioned_ensembl_gene_id":"ENSG00000232817.1","gene_symbol":"AC073188.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63388808,"end":63393657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267775.1","gene_symbol":"OR7E16P","gene_name":"olfactory receptor family 7 subfamily E member 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:8387]","synonyms":"OR7E60P,OR7E17P,OR19-9,OR19-133","biotype":"unprocessed_pseudogene","ncbi_id":"26473","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9191286,"end":9192170,"strand":1,"description":"olfactory receptor family 7 subfamily E member 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:8387]"}, {"versioned_ensembl_gene_id":"ENSG00000140265.12","gene_symbol":"ZSCAN29","gene_name":"zinc finger and SCAN domain containing 29 [Source:HGNC Symbol;Acc:HGNC:26673]","synonyms":"ZNF690,Zfp690,FLJ35867","biotype":"protein_coding","ncbi_id":"146050","summary":null,"start":43358172,"end":43371025,"strand":-1,"description":"zinc finger and SCAN domain containing 29 [Source:HGNC Symbol;Acc:HGNC:26673]"}, {"versioned_ensembl_gene_id":"ENSG00000280420.1","gene_symbol":"AC005355.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134522613,"end":134523096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273244.1","gene_symbol":"AC005301.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":16676016,"end":16694648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149654.9","gene_symbol":"CDH22","gene_name":"cadherin 22 [Source:HGNC Symbol;Acc:HGNC:13251]","synonyms":"dJ998H6.1,C20orf25","biotype":"protein_coding","ncbi_id":"64405","summary":"This gene is a member of the cadherin superfamily. The gene product is composed of five cadherin repeat domains and a cytoplasmic tail similar to the highly conserved cytoplasmic region of classical cadherins. Expressed predominantly in the brain, this putative calcium-dependent cell adhesion protein may play an important role in morphogenesis and tissue formation in neural and non-neural cells during development and maintenance of the brain and neuroendocrine organs. [provided by RefSeq, Jul 2008]","start":46173733,"end":46308498,"strand":-1,"description":"cadherin 22 [Source:HGNC Symbol;Acc:HGNC:13251]"}, {"versioned_ensembl_gene_id":"ENSG00000243648.1","gene_symbol":"AC109454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134422838,"end":134423335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281975.1","gene_symbol":"AC243615.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16848984,"end":16850544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237190.3","gene_symbol":"CDKN2AIPNL","gene_name":"CDKN2A interacting protein N-terminal like [Source:HGNC Symbol;Acc:HGNC:30545]","synonyms":"MGC13017","biotype":"protein_coding","ncbi_id":"91368","summary":null,"start":134402087,"end":134411898,"strand":-1,"description":"CDKN2A interacting protein N-terminal like [Source:HGNC Symbol;Acc:HGNC:30545]"}, {"versioned_ensembl_gene_id":"ENSG00000267337.1","gene_symbol":"LINC01478","gene_name":"long intergenic non-protein coding RNA 1478 [Source:HGNC Symbol;Acc:HGNC:51121]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927921","summary":null,"start":44323436,"end":44531697,"strand":-1,"description":"long intergenic non-protein coding RNA 1478 [Source:HGNC Symbol;Acc:HGNC:51121]"}, {"versioned_ensembl_gene_id":"ENSG00000260325.1","gene_symbol":"HSPB9","gene_name":"heat shock protein family B (small) member 9 [Source:HGNC Symbol;Acc:HGNC:30589]","synonyms":"CT51","biotype":"protein_coding","ncbi_id":"94086","summary":null,"start":42121431,"end":42123352,"strand":1,"description":"heat shock protein family B (small) member 9 [Source:HGNC Symbol;Acc:HGNC:30589]"}, {"versioned_ensembl_gene_id":"ENSG00000197142.10","gene_symbol":"ACSL5","gene_name":"acyl-CoA synthetase long chain family member 5 [Source:HGNC Symbol;Acc:HGNC:16526]","synonyms":"FACL5,ACS5,ACS2","biotype":"protein_coding","ncbi_id":"51703","summary":"The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in uterus and spleen, and in trace amounts in normal brain, but has markedly increased levels in malignant gliomas. This gene functions in mediating fatty acid-induced glioma cell growth. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":112374018,"end":112428380,"strand":1,"description":"acyl-CoA synthetase long chain family member 5 [Source:HGNC Symbol;Acc:HGNC:16526]"}, {"versioned_ensembl_gene_id":"ENSG00000172594.12","gene_symbol":"SMPDL3A","gene_name":"sphingomyelin phosphodiesterase acid like 3A [Source:HGNC Symbol;Acc:HGNC:17389]","synonyms":"yR36GH4.1,FLJ20177,ASML3a,ASM3A","biotype":"protein_coding","ncbi_id":"10924","summary":null,"start":122789049,"end":122809720,"strand":1,"description":"sphingomyelin phosphodiesterase acid like 3A [Source:HGNC Symbol;Acc:HGNC:17389]"}, {"versioned_ensembl_gene_id":"ENSG00000234979.1","gene_symbol":"Z82185.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36816326,"end":36819736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273807.2","gene_symbol":"AC244489.1","gene_name":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16418201,"end":16436927,"strand":1,"description":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]"}, {"versioned_ensembl_gene_id":"ENSG00000111913.17","gene_symbol":"RIPOR2","gene_name":"RHO family interacting cell polarization regulator 2 [Source:HGNC Symbol;Acc:HGNC:13872]","synonyms":"MYONAP,KIAA0386,FAM65B,DIFF48,C6orf32","biotype":"protein_coding","ncbi_id":"9750","summary":"This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients. [provided by RefSeq, Sep 2016]","start":24804282,"end":25042018,"strand":-1,"description":"RHO family interacting cell polarization regulator 2 [Source:HGNC Symbol;Acc:HGNC:13872]"}, {"versioned_ensembl_gene_id":"ENSG00000279585.1","gene_symbol":"AL109653.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145797375,"end":145798439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211633.3","gene_symbol":"IGKV1D-42","gene_name":"immunoglobulin kappa variable 1D-42 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5757]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28892","summary":null,"start":90190193,"end":90190681,"strand":1,"description":"immunoglobulin kappa variable 1D-42 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5757]"}, {"versioned_ensembl_gene_id":"ENSG00000196943.12","gene_symbol":"NOP9","gene_name":"NOP9 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:19826]","synonyms":"C14orf21","biotype":"protein_coding","ncbi_id":"161424","summary":null,"start":24299862,"end":24309124,"strand":1,"description":"NOP9 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:19826]"}, {"versioned_ensembl_gene_id":"ENSG00000101911.12","gene_symbol":"PRPS2","gene_name":"phosphoribosyl pyrophosphate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:9465]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5634","summary":"This gene encodes a phosphoribosyl pyrophosphate synthetase that plays a central role in the synthesis of purines and pyrimidines. The encoded protein catalyzes the synthesis of 5-phosphoribosyl 1-pyrophosphate from ATP and D-ribose 5-phosphate. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":12791355,"end":12824222,"strand":1,"description":"phosphoribosyl pyrophosphate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:9465]"}, {"versioned_ensembl_gene_id":"ENSG00000157593.18","gene_symbol":"SLC35B2","gene_name":"solute carrier family 35 member B2 [Source:HGNC Symbol;Acc:HGNC:16872]","synonyms":"UGTrel4","biotype":"protein_coding","ncbi_id":"347734","summary":"Sulfotransferases (e.g., SULT4A1; MIM 608359) use an activated form of sulfate, 3-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS), as a common sulfate donor for sulfation of glycoproteins, proteoglycans, and glycolipids in the endoplasmic reticulum and Golgi apparatus. SLC35B2 is located in the microsomal membrane and transports PAPS from the cytosol, where it is synthesized, into the Golgi lumen (Kamiyama et al., 2003 [PubMed 12716889]).[supplied by OMIM, Mar 2008]","start":44254096,"end":44257890,"strand":-1,"description":"solute carrier family 35 member B2 [Source:HGNC Symbol;Acc:HGNC:16872]"}, {"versioned_ensembl_gene_id":"ENSG00000159904.11","gene_symbol":"ZNF890P","gene_name":"zinc finger protein 890, pseudogene [Source:HGNC Symbol;Acc:HGNC:38691]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645700","summary":null,"start":5121239,"end":5144546,"strand":-1,"description":"zinc finger protein 890, pseudogene [Source:HGNC Symbol;Acc:HGNC:38691]"}, {"versioned_ensembl_gene_id":"ENSG00000253138.5","gene_symbol":"LINC00967","gene_name":"long intergenic non-protein coding RNA 967 [Source:HGNC Symbol;Acc:HGNC:48725]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505659","summary":null,"start":66192093,"end":66197315,"strand":1,"description":"long intergenic non-protein coding RNA 967 [Source:HGNC Symbol;Acc:HGNC:48725]"}, {"versioned_ensembl_gene_id":"ENSG00000214281.3","gene_symbol":"HMGN2P39","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39410]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874483","summary":null,"start":59010332,"end":59010604,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39410]"}, {"versioned_ensembl_gene_id":"ENSG00000274413.1","gene_symbol":"AC011476.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55035708,"end":55062043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243550.2","gene_symbol":"LINC01214","gene_name":"long intergenic non-protein coding RNA 1214 [Source:HGNC Symbol;Acc:HGNC:49650]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928022","summary":null,"start":150265412,"end":150287373,"strand":-1,"description":"long intergenic non-protein coding RNA 1214 [Source:HGNC Symbol;Acc:HGNC:49650]"}, {"versioned_ensembl_gene_id":"ENSG00000240356.6","gene_symbol":"RPL23AP7","gene_name":"ribosomal protein L23a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:17336]","synonyms":"RPL23AL1,bA395L14.9","biotype":"transcribed_processed_pseudogene","ncbi_id":"118433","summary":null,"start":113610502,"end":113627090,"strand":-1,"description":"ribosomal protein L23a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:17336]"}, {"versioned_ensembl_gene_id":"ENSG00000283016.1","gene_symbol":"AL139353.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31320224,"end":31320634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259512.3","gene_symbol":"HNRNPA1P5","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:15787]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506712","summary":null,"start":67627852,"end":67629135,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:15787]"}, {"versioned_ensembl_gene_id":"ENSG00000225386.1","gene_symbol":"AC099754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26619330,"end":26622690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234751.1","gene_symbol":"AP002381.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72940498,"end":72941112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230709.1","gene_symbol":"AC104024.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16975999,"end":16981353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274782.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769765,"end":54784000,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000240951.1","gene_symbol":"MTCO2P6","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52022]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075266","summary":null,"start":89587886,"end":89588570,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52022]"}, {"versioned_ensembl_gene_id":"ENSG00000277292.2","gene_symbol":"PIP4K2B","gene_name":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]","synonyms":"PIP5KIIbeta,PIP5KIIB,PIP5K2B","biotype":"protein_coding","ncbi_id":"8396","summary":"The protein encoded by this gene catalyzes the phosphorylation of phosphatidylinositol-5-phosphate on the fourth hydroxyl of the myo-inositol ring to form phosphatidylinositol-5,4-bisphosphate. This gene is a member of the phosphatidylinositol-5-phosphate 4-kinase family. The encoded protein sequence does not show similarity to other kinases, but the protein does exhibit kinase activity. Additionally, the encoded protein interacts with p55 TNF receptor. [provided by RefSeq, Jul 2008]","start":38566476,"end":38600913,"strand":-1,"description":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]"}, {"versioned_ensembl_gene_id":"ENSG00000182652.2","gene_symbol":"OR4Q3","gene_name":"olfactory receptor family 4 subfamily Q member 3 [Source:HGNC Symbol;Acc:HGNC:15426]","synonyms":"OR4Q4,C14orf13","biotype":"protein_coding","ncbi_id":"441669","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19743571,"end":19749469,"strand":1,"description":"olfactory receptor family 4 subfamily Q member 3 [Source:HGNC Symbol;Acc:HGNC:15426]"}, {"versioned_ensembl_gene_id":"ENSG00000203546.7","gene_symbol":"AL139353.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31334312,"end":31457441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176312.4","gene_symbol":"OR4H12P","gene_name":"olfactory receptor family 4 subfamily H member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:19433]","synonyms":"OR4H12,C14orf14","biotype":"unprocessed_pseudogene","ncbi_id":"161271","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19759868,"end":19760774,"strand":1,"description":"olfactory receptor family 4 subfamily H member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:19433]"}, {"versioned_ensembl_gene_id":"ENSG00000175756.13","gene_symbol":"AURKAIP1","gene_name":"aurora kinase A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24114]","synonyms":"FLJ20608,AKIP,AIP","biotype":"protein_coding","ncbi_id":"54998","summary":null,"start":1373730,"end":1375495,"strand":-1,"description":"aurora kinase A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24114]"}, {"versioned_ensembl_gene_id":"ENSG00000272839.1","gene_symbol":"AC011899.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157868538,"end":157869154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258438.3","gene_symbol":"AL512310.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19733355,"end":19734302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257831.1","gene_symbol":"AL136418.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31248628,"end":31302739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101098.12","gene_symbol":"RIMS4","gene_name":"regulating synaptic membrane exocytosis 4 [Source:HGNC Symbol;Acc:HGNC:16183]","synonyms":"dJ781B1.3,C20orf190","biotype":"protein_coding","ncbi_id":"140730","summary":null,"start":44751808,"end":44810338,"strand":-1,"description":"regulating synaptic membrane exocytosis 4 [Source:HGNC Symbol;Acc:HGNC:16183]"}, {"versioned_ensembl_gene_id":"ENSG00000278540.4","gene_symbol":"ACACA","gene_name":"acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:HGNC:84]","synonyms":"ACC,ACAC,ACC1","biotype":"protein_coding","ncbi_id":"31","summary":"Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. There are two ACC forms, alpha and beta, encoded by two different genes. ACC-alpha is highly enriched in lipogenic tissues. The enzyme is under long term control at the transcriptional and translational levels and under short term regulation by the phosphorylation/dephosphorylation of targeted serine residues and by allosteric transformation by citrate or palmitoyl-CoA. Multiple alternatively spliced transcript variants divergent in the 5' sequence and encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":37084988,"end":37406818,"strand":-1,"description":"acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:HGNC:84]"}, {"versioned_ensembl_gene_id":"ENSG00000170923.3","gene_symbol":"OR7G2","gene_name":"olfactory receptor family 7 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:8466]","synonyms":"OST260","biotype":"protein_coding","ncbi_id":"390882","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9100407,"end":9107475,"strand":-1,"description":"olfactory receptor family 7 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:8466]"}, {"versioned_ensembl_gene_id":"ENSG00000145949.9","gene_symbol":"MYLK4","gene_name":"myosin light chain kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:27972]","synonyms":"SgK085","biotype":"protein_coding","ncbi_id":"340156","summary":null,"start":2663629,"end":2750966,"strand":-1,"description":"myosin light chain kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:27972]"}, {"versioned_ensembl_gene_id":"ENSG00000267796.7","gene_symbol":"LIN37","gene_name":"lin-37 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:33234]","synonyms":"ZK418.4,lin-37,F25965","biotype":"protein_coding","ncbi_id":"55957","summary":"This gene encodes a protein expressed in the eye. [provided by RefSeq, Jul 2008]","start":35748361,"end":35754519,"strand":1,"description":"lin-37 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:33234]"}, {"versioned_ensembl_gene_id":"ENSG00000170929.6","gene_symbol":"OR1M1","gene_name":"olfactory receptor family 1 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:8220]","synonyms":"OR19-6","biotype":"protein_coding","ncbi_id":"125963","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9087061,"end":9095669,"strand":1,"description":"olfactory receptor family 1 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:8220]"}, {"versioned_ensembl_gene_id":"ENSG00000267154.1","gene_symbol":"OR1M4P","gene_name":"olfactory receptor family 1 subfamily M member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:31244]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403232","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9083112,"end":9083398,"strand":-1,"description":"olfactory receptor family 1 subfamily M member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:31244]"}, {"versioned_ensembl_gene_id":"ENSG00000214708.4","gene_symbol":"AC116407.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32141226,"end":32143135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280033.1","gene_symbol":"AC116407.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32159311,"end":32160371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280020.1","gene_symbol":"AC116407.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32178946,"end":32180074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182585.9","gene_symbol":"EPGN","gene_name":"epithelial mitogen [Source:HGNC Symbol;Acc:HGNC:17470]","synonyms":"PRO9904,epigen,EPG,ALGV3072","biotype":"protein_coding","ncbi_id":"255324","summary":"The protein encoded by this gene is a member of the epidermal growth factor family. Members of this family are ligands for the epidermal growth factor receptor and play a role in cell survival, proliferation and migration. This protein has been reported to have high mitogenic activity but low affinity for its receptor. Expression of this transcript and protein have been reported in cancer specimens of the breast, bladder, and prostate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":74308473,"end":74315307,"strand":1,"description":"epithelial mitogen [Source:HGNC Symbol;Acc:HGNC:17470]"}, {"versioned_ensembl_gene_id":"ENSG00000279233.1","gene_symbol":"AC122688.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125138245,"end":125141711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282084.1","gene_symbol":"UBE2Q2P2","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37440]","synonyms":"UBE2QP2,UBE2Q2P3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100134869","summary":null,"start":82434179,"end":82499143,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37440]"}, {"versioned_ensembl_gene_id":"ENSG00000133317.14","gene_symbol":"LGALS12","gene_name":"galectin 12 [Source:HGNC Symbol;Acc:HGNC:15788]","synonyms":"GRIP1","biotype":"protein_coding","ncbi_id":"85329","summary":"This gene encodes a member of the galectin superfamily, a group of beta-galactoside-binding proteins with conserved carbohydrate recognition domains. The related mouse protein is a primary regulator of the early stages of adipose tissue development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, May 2010]","start":63506084,"end":63516774,"strand":1,"description":"galectin 12 [Source:HGNC Symbol;Acc:HGNC:15788]"}, {"versioned_ensembl_gene_id":"ENSG00000101017.13","gene_symbol":"CD40","gene_name":"CD40 molecule [Source:HGNC Symbol;Acc:HGNC:11919]","synonyms":"TNFRSF5,p50,Bp50","biotype":"protein_coding","ncbi_id":"958","summary":"This gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2014]","start":46118272,"end":46129863,"strand":1,"description":"CD40 molecule [Source:HGNC Symbol;Acc:HGNC:11919]"}, {"versioned_ensembl_gene_id":"ENSG00000198198.15","gene_symbol":"SZT2","gene_name":"SZT2, KICSTOR complex subunit [Source:HGNC Symbol;Acc:HGNC:29040]","synonyms":"FLJ10387,C1orf84,SZT2B,SZT2A,RP11-506B15.1,KIAA0467,FLJ34502","biotype":"protein_coding","ncbi_id":"23334","summary":"The protein encoded by this gene is expressed in the brain, predominantly in the parietal and frontal cortex as well as in dorsal root ganglia. It is localized to the peroxisome, and is implicated in resistance to oxidative stress. It likely functions by increasing superoxide dismutase (SOD) activity, but itself has no direct SOD activity. Studies in mice show that this gene confers low seizure threshold, and may also enhance epileptogenesis. [provided by RefSeq, Jun 2011]","start":43389882,"end":43454247,"strand":1,"description":"SZT2, KICSTOR complex subunit [Source:HGNC Symbol;Acc:HGNC:29040]"}, {"versioned_ensembl_gene_id":"ENSG00000257159.1","gene_symbol":"AC084033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57967058,"end":57968399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255857.5","gene_symbol":"PXN-AS1","gene_name":"PXN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44123]","synonyms":"EyeLinc4","biotype":"antisense_RNA","ncbi_id":"100506649","summary":null,"start":120201291,"end":120213138,"strand":1,"description":"PXN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44123]"}, {"versioned_ensembl_gene_id":"ENSG00000100181.22","gene_symbol":"TPTEP1","gene_name":"transmembrane phosphatase with tensin homology pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43648]","synonyms":"psiTPTE22","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387590","summary":null,"start":16601887,"end":16698742,"strand":1,"description":"transmembrane phosphatase with tensin homology pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43648]"}, {"versioned_ensembl_gene_id":"ENSG00000274320.2","gene_symbol":"GOLGA6L9","gene_name":"golgin A6 family-like 9 [Source:HGNC Symbol;Acc:HGNC:37229]","synonyms":"GOLGA6L20","biotype":"protein_coding","ncbi_id":"440295","summary":null,"start":82509086,"end":82518216,"strand":1,"description":"golgin A6 family-like 9 [Source:HGNC Symbol;Acc:HGNC:37229]"}, {"versioned_ensembl_gene_id":"ENSG00000235804.2","gene_symbol":"AL357078.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65077413,"end":65078131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274904.1","gene_symbol":"AC093512.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30064306,"end":30064825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163746.11","gene_symbol":"PLSCR2","gene_name":"phospholipid scramblase 2 [Source:HGNC Symbol;Acc:HGNC:16494]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57047","summary":"This gene encodes a member of the phospholipid scramblase family. Phospholipid scramblases are membrane proteins that mediate calcium-dependent, non-specific movement of plasma membrane phospholipids and phosphatidylserine exposure. The encoded protein contains a low affinity calcium binding motif and may play a role in blood coagulation and apoptosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":146391421,"end":146495991,"strand":-1,"description":"phospholipid scramblase 2 [Source:HGNC Symbol;Acc:HGNC:16494]"}, {"versioned_ensembl_gene_id":"ENSG00000241358.1","gene_symbol":"AC069528.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":146391363,"end":146416603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240668.1","gene_symbol":"KRT8P36","gene_name":"keratin 8 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39870]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418748","summary":null,"start":138101478,"end":138102917,"strand":-1,"description":"keratin 8 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39870]"}, {"versioned_ensembl_gene_id":"ENSG00000140379.7","gene_symbol":"BCL2A1","gene_name":"BCL2 related protein A1 [Source:HGNC Symbol;Acc:HGNC:991]","synonyms":"GRS,BFL1,BCL2L5,ACC2,ACC1,ACC-2,ACC-1,HBPA1","biotype":"protein_coding","ncbi_id":"597","summary":"This gene encodes a member of the BCL-2 protein family. The proteins of this family form hetero- or homodimers and act as anti- and pro-apoptotic regulators that are involved in a wide variety of cellular activities such as embryonic development, homeostasis and tumorigenesis. The protein encoded by this gene is able to reduce the release of pro-apoptotic cytochrome c from mitochondria and block caspase activation. This gene is a direct transcription target of NF-kappa B in response to inflammatory mediators, and is up-regulated by different extracellular signals, such as granulocyte-macrophage colony-stimulating factor (GM-CSF), CD40, phorbol ester and inflammatory cytokine TNF and IL-1, which suggests a cytoprotective function that is essential for lymphocyte activation as well as cell survival. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":79960889,"end":79971446,"strand":-1,"description":"BCL2 related protein A1 [Source:HGNC Symbol;Acc:HGNC:991]"}, {"versioned_ensembl_gene_id":"ENSG00000283866.1","gene_symbol":"AP000842.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125957900,"end":125958647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236409.2","gene_symbol":"NRADDP","gene_name":"neurotrophin receptor associated death domain, pseudogene [Source:HGNC Symbol;Acc:HGNC:19337]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"100129354","summary":"The neurotrophin receptor alike death domain proteins belong to the death domain superfamily and are involved in mediating apoptosis. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Oct 2008]","start":47010824,"end":47013465,"strand":1,"description":"neurotrophin receptor associated death domain, pseudogene [Source:HGNC Symbol;Acc:HGNC:19337]"}, {"versioned_ensembl_gene_id":"ENSG00000256504.2","gene_symbol":"AC009509.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27704568,"end":27708365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174236.3","gene_symbol":"REP15","gene_name":"RAB15 effector protein [Source:HGNC Symbol;Acc:HGNC:33748]","synonyms":"RAB15EP","biotype":"protein_coding","ncbi_id":"387849","summary":"The protein encoded by this intronless gene interacts with GTP-bound Rab15 and is involved in recycling of transferrin receptor from the endocytic recycling compartment to the cell surface. [provided by RefSeq, Sep 2016]","start":27696519,"end":27697596,"strand":1,"description":"RAB15 effector protein [Source:HGNC Symbol;Acc:HGNC:33748]"}, {"versioned_ensembl_gene_id":"ENSG00000169057.21","gene_symbol":"MECP2","gene_name":"methyl-CpG binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6990]","synonyms":"RTT,MRX79,MRX16","biotype":"protein_coding","ncbi_id":"4204","summary":"DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of cognitive disability in females. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]","start":154021573,"end":154137103,"strand":-1,"description":"methyl-CpG binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6990]"}, {"versioned_ensembl_gene_id":"ENSG00000205155.7","gene_symbol":"PSENEN","gene_name":"presenilin enhancer gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:30100]","synonyms":"PEN2","biotype":"protein_coding","ncbi_id":"55851","summary":"Presenilins, which are components of the gamma-secretase protein complex, are required for intramembranous processing of some type I transmembrane proteins, such as the Notch proteins and the beta-amyloid precursor protein. Signaling by Notch receptors mediates a wide range of developmental cell fates. Processing of the beta-amyloid precursor protein generates neurotoxic amyloid beta peptides, the major component of senile plaques associated with Alzheimer's disease. This gene encodes a protein that is required for Notch pathway signaling, and for the activity and accumulation of gamma-secretase. Mutations resulting in haploinsufficiency for this gene cause familial acne inversa-2 (ACNINV2). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":35745114,"end":35747519,"strand":1,"description":"presenilin enhancer gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:30100]"}, {"versioned_ensembl_gene_id":"ENSG00000275296.1","gene_symbol":"AC241377.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121058948,"end":121059353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281344.1","gene_symbol":"HELLPAR","gene_name":"HELLP associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:43984]","synonyms":"LINC-HELLP","biotype":"macro_lncRNA","ncbi_id":"101101692","summary":null,"start":102197585,"end":102402596,"strand":1,"description":"HELLP associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:43984]"}, {"versioned_ensembl_gene_id":"ENSG00000274129.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34L,LENG5,LENG5,SEN34,SEN34,SEN34L","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190535,"end":54195132,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000256463.8","gene_symbol":"SALL3","gene_name":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]","synonyms":"ZNF796","biotype":"protein_coding","ncbi_id":"27164","summary":"This gene encodes a sal-like C2H2-type zinc-finger protein, and belongs to a family of evolutionarily conserved genes found in species as diverse as Drosophila, C. elegans, and vertebrates. Mutations in some of these genes are associated with congenital disorders in human, suggesting their importance in embryonic development. This protein binds to DNA methyltransferase 3 alpha (DNMT3A), and reduces DNMT3A-mediated CpG island methylation. It is suggested that silencing of this gene, resulting in acceleration of DNA methylation, may have a role in oncogenesis. [provided by RefSeq, Oct 2011]","start":78980275,"end":79002677,"strand":1,"description":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]"}, {"versioned_ensembl_gene_id":"ENSG00000277511.1","gene_symbol":"AC116407.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32127595,"end":32128454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103257.8","gene_symbol":"SLC7A5","gene_name":"solute carrier family 7 member 5 [Source:HGNC Symbol;Acc:HGNC:11063]","synonyms":"CD98,MPE16,LAT1,E16,D16S469E","biotype":"protein_coding","ncbi_id":"8140","summary":null,"start":87830023,"end":87869488,"strand":-1,"description":"solute carrier family 7 member 5 [Source:HGNC Symbol;Acc:HGNC:11063]"}, {"versioned_ensembl_gene_id":"ENSG00000267549.5","gene_symbol":"AC006116.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56314703,"end":56341287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266932.1","gene_symbol":"AC006116.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":56342432,"end":56343419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132872.11","gene_symbol":"SYT4","gene_name":"synaptotagmin 4 [Source:HGNC Symbol;Acc:HGNC:11512]","synonyms":"KIAA1342,HsT1192","biotype":"protein_coding","ncbi_id":"6860","summary":null,"start":43267878,"end":43277650,"strand":-1,"description":"synaptotagmin 4 [Source:HGNC Symbol;Acc:HGNC:11512]"}, {"versioned_ensembl_gene_id":"ENSG00000280168.1","gene_symbol":"AC005274.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":12973033,"end":12973834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169933.13","gene_symbol":"FRMPD4","gene_name":"FERM and PDZ domain containing 4 [Source:HGNC Symbol;Acc:HGNC:29007]","synonyms":"PDZK10,PDZD10,KIAA0316","biotype":"protein_coding","ncbi_id":"9758","summary":"This gene encodes a multi-domain (WW, PDZ, FERM) containing protein. Through its interaction with other proteins (such as PSD-95), it functions as a positive regulator of dendritic spine morphogenesis and density, and is required for the maintenance of excitatory synaptic transmission. [provided by RefSeq, Jan 2010]","start":12138466,"end":12724523,"strand":1,"description":"FERM and PDZ domain containing 4 [Source:HGNC Symbol;Acc:HGNC:29007]"}, {"versioned_ensembl_gene_id":"ENSG00000250961.1","gene_symbol":"AC025470.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57395060,"end":57533424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234658.1","gene_symbol":"AC013429.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138645671,"end":138646448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234770.1","gene_symbol":"GULOP","gene_name":"gulonolactone (L-) oxidase, pseudogene [Source:HGNC Symbol;Acc:HGNC:4695]","synonyms":"scurvy,GULO","biotype":"unitary_pseudogene","ncbi_id":"2989","summary":"This gene is nonfunctional in humans and other primates. In most mammalian species the corresponding gene encodes L-gulono-gamma-lactone oxidase which catalyzes the last step of ascorbic acid biosynthesis. The human gene is a remnant that lacks five of twelve exons found in functional rodent genes. The loss of enzyme activity results in hypoascorbemia or the inability to synthesize vitamin C. [provided by RefSeq, Nov 2010]","start":27560274,"end":27589073,"strand":1,"description":"gulonolactone (L-) oxidase, pseudogene [Source:HGNC Symbol;Acc:HGNC:4695]"}, {"versioned_ensembl_gene_id":"ENSG00000154370.15","gene_symbol":"TRIM11","gene_name":"tripartite motif containing 11 [Source:HGNC Symbol;Acc:HGNC:16281]","synonyms":"RNF92,BIA1","biotype":"protein_coding","ncbi_id":"81559","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nucleus and the cytoplasm. Its function has not been identified. [provided by RefSeq, Jul 2008]","start":228393673,"end":228406840,"strand":-1,"description":"tripartite motif containing 11 [Source:HGNC Symbol;Acc:HGNC:16281]"}, {"versioned_ensembl_gene_id":"ENSG00000218980.2","gene_symbol":"FTH1P15","gene_name":"ferritin heavy chain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:3985]","synonyms":"FTHL15","biotype":"processed_pseudogene","ncbi_id":"2507","summary":null,"start":57004520,"end":57004799,"strand":1,"description":"ferritin heavy chain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:3985]"}, {"versioned_ensembl_gene_id":"ENSG00000240122.1","gene_symbol":"FABP5P11","gene_name":"fatty acid binding protein 5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19328]","synonyms":"FABP5P1,FABP5L11","biotype":"processed_pseudogene","ncbi_id":"266699","summary":null,"start":16595089,"end":16595485,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19328]"}, {"versioned_ensembl_gene_id":"ENSG00000155957.17","gene_symbol":"TMBIM4","gene_name":"transmembrane BAX inhibitor motif containing 4 [Source:HGNC Symbol;Acc:HGNC:24257]","synonyms":"S1R,LFG4,GAAP,CGI-119,ZPRO","biotype":"protein_coding","ncbi_id":"51643","summary":null,"start":66135846,"end":66170072,"strand":-1,"description":"transmembrane BAX inhibitor motif containing 4 [Source:HGNC Symbol;Acc:HGNC:24257]"}, {"versioned_ensembl_gene_id":"ENSG00000154319.14","gene_symbol":"FAM167A","gene_name":"family with sequence similarity 167 member A [Source:HGNC Symbol;Acc:HGNC:15549]","synonyms":"C8orf13","biotype":"protein_coding","ncbi_id":"83648","summary":null,"start":11421463,"end":11474715,"strand":-1,"description":"family with sequence similarity 167 member A [Source:HGNC Symbol;Acc:HGNC:15549]"}, {"versioned_ensembl_gene_id":"ENSG00000255020.1","gene_symbol":"AF131216.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11345748,"end":11347502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280182.1","gene_symbol":"AC131888.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81261924,"end":81264091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135697.9","gene_symbol":"BCO1","gene_name":"beta-carotene oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:13815]","synonyms":"FLJ10730,BCMO1,BCMO,BCDO1,BCDO","biotype":"protein_coding","ncbi_id":"53630","summary":"Vitamin A metabolism is important for vital processes such as vision, embryonic development, cell differentiation, and membrane and skin protection. The protein encoded by this gene is a key enzyme in beta-carotene metabolism to vitamin A. It catalyzes the oxidative cleavage of beta,beta-carotene into two retinal molecules. [provided by RefSeq, Jul 2008]","start":81238448,"end":81291142,"strand":1,"description":"beta-carotene oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:13815]"}, {"versioned_ensembl_gene_id":"ENSG00000031698.12","gene_symbol":"SARS","gene_name":"seryl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:10537]","synonyms":"SERS","biotype":"protein_coding","ncbi_id":"6301","summary":"This gene belongs to the class II amino-acyl tRNA family. The encoded enzyme catalyzes the transfer of L-serine to tRNA (Ser) and is related to bacterial and yeast counterparts. Multiple alternatively spliced transcript variants have been described but the biological validity of all variants is unknown. [provided by RefSeq, Jul 2010]","start":109213918,"end":109238169,"strand":1,"description":"seryl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:10537]"}, {"versioned_ensembl_gene_id":"ENSG00000258443.1","gene_symbol":"AC005225.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73517233,"end":73520648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250170.1","gene_symbol":"RASA2-IT1","gene_name":"RASA2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41376]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874298","summary":null,"start":141525133,"end":141526121,"strand":1,"description":"RASA2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41376]"}, {"versioned_ensembl_gene_id":"ENSG00000018869.16","gene_symbol":"ZNF582","gene_name":"zinc finger protein 582 [Source:HGNC Symbol;Acc:HGNC:26421]","synonyms":"FLJ30927","biotype":"protein_coding","ncbi_id":"147948","summary":"The protein encoded by this gene is a zing finger protein and putative transcription factor that is highly methylated in cervical cancers. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":56375846,"end":56393545,"strand":-1,"description":"zinc finger protein 582 [Source:HGNC Symbol;Acc:HGNC:26421]"}, {"versioned_ensembl_gene_id":"ENSG00000185031.6","gene_symbol":"SLC2A3P2","gene_name":"solute carrier family 2 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31074]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391045","summary":null,"start":64984608,"end":64986087,"strand":-1,"description":"solute carrier family 2 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31074]"}, {"versioned_ensembl_gene_id":"ENSG00000184227.7","gene_symbol":"ACOT1","gene_name":"acyl-CoA thioesterase 1 [Source:HGNC Symbol;Acc:HGNC:33128]","synonyms":"CTE-1,ACH2,LACH2","biotype":"protein_coding","ncbi_id":"641371","summary":null,"start":73537114,"end":73543794,"strand":1,"description":"acyl-CoA thioesterase 1 [Source:HGNC Symbol;Acc:HGNC:33128]"}, {"versioned_ensembl_gene_id":"ENSG00000158079.14","gene_symbol":"PTPDC1","gene_name":"protein tyrosine phosphatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30184]","synonyms":"PTP9Q22,FLJ37312","biotype":"protein_coding","ncbi_id":"138639","summary":"The protein encoded by this gene contains a characteristic motif of protein tyrosine phosphatases (PTPs). PTPs regulate activities of phosphoproteins through dephosphorylation. They are signaling molecules involved in the regulation of a wide variety of biological processes. The specific function of this protein has not yet been determined. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":94030794,"end":94109856,"strand":1,"description":"protein tyrosine phosphatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30184]"}, {"versioned_ensembl_gene_id":"ENSG00000255224.1","gene_symbol":"AC109322.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144078002,"end":144079265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263146.2","gene_symbol":"LINC01896","gene_name":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645321","summary":null,"start":78976555,"end":78979074,"strand":-1,"description":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]"}, {"versioned_ensembl_gene_id":"ENSG00000017427.15","gene_symbol":"IGF1","gene_name":"insulin like growth factor 1 [Source:HGNC Symbol;Acc:HGNC:5464]","synonyms":"IGFI,IGF1A,IGF-I","biotype":"protein_coding","ncbi_id":"3479","summary":"The protein encoded by this gene is similar to insulin in function and structure and is a member of a family of proteins involved in mediating growth and development. The encoded protein is processed from a precursor, bound by a specific receptor, and secreted. Defects in this gene are a cause of insulin-like growth factor I deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]","start":102395867,"end":102480645,"strand":-1,"description":"insulin like growth factor 1 [Source:HGNC Symbol;Acc:HGNC:5464]"}, {"versioned_ensembl_gene_id":"ENSG00000265101.1","gene_symbol":"AC091027.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78925064,"end":78927441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283052.1","gene_symbol":"LINC02456","gene_name":"long intergenic non-protein coding RNA 2456 [Source:HGNC Symbol;Acc:HGNC:53389]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369942","summary":null,"start":102304355,"end":102463491,"strand":1,"description":"long intergenic non-protein coding RNA 2456 [Source:HGNC Symbol;Acc:HGNC:53389]"}, {"versioned_ensembl_gene_id":"ENSG00000211626.2","gene_symbol":"IGKV6D-41","gene_name":"immunoglobulin kappa variable 6D-41 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5838]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28869","summary":null,"start":90069662,"end":90070238,"strand":1,"description":"immunoglobulin kappa variable 6D-41 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5838]"}, {"versioned_ensembl_gene_id":"ENSG00000279945.1","gene_symbol":"AC013489.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88477871,"end":88478387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242766.1","gene_symbol":"IGKV1D-17","gene_name":"immunoglobulin kappa variable 1D-17 [Source:HGNC Symbol;Acc:HGNC:5749]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28900","summary":null,"start":90082635,"end":90083291,"strand":1,"description":"immunoglobulin kappa variable 1D-17 [Source:HGNC Symbol;Acc:HGNC:5749]"}, {"versioned_ensembl_gene_id":"ENSG00000267710.6","gene_symbol":"EDDM13","gene_name":"epididymal protein 13 [Source:HGNC Symbol;Acc:HGNC:53168]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506374","summary":null,"start":56272769,"end":56310450,"strand":1,"description":"epididymal protein 13 [Source:HGNC Symbol;Acc:HGNC:53168]"}, {"versioned_ensembl_gene_id":"ENSG00000267776.1","gene_symbol":"AC006116.10","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56376704,"end":56377284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151490.13","gene_symbol":"PTPRO","gene_name":"protein tyrosine phosphatase, receptor type O [Source:HGNC Symbol;Acc:HGNC:9678]","synonyms":"PTPU2,PTP-U2,PTP-oc,NPHS6,GLEPP1","biotype":"protein_coding","ncbi_id":"5800","summary":"This gene encodes a member of the R3 subtype family of receptor-type protein tyrosine phosphatases. These proteins are localized to the apical surface of polarized cells and may have tissue-specific functions through activation of Src family kinases. This gene contains two distinct promoters, and alternatively spliced transcript variants encoding multiple isoforms have been observed. The encoded proteins may have multiple isoform-specific and tissue-specific functions, including the regulation of osteoclast production and activity, inhibition of cell proliferation and facilitation of apoptosis. This gene is a candidate tumor suppressor, and decreased expression of this gene has been observed in several types of cancer. [provided by RefSeq, May 2011]","start":15322397,"end":15597399,"strand":1,"description":"protein tyrosine phosphatase, receptor type O [Source:HGNC Symbol;Acc:HGNC:9678]"}, {"versioned_ensembl_gene_id":"ENSG00000255547.1","gene_symbol":"RPA2P3","gene_name":"replication protein A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45118]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420359","summary":null,"start":100336856,"end":100337625,"strand":1,"description":"replication protein A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45118]"}, {"versioned_ensembl_gene_id":"ENSG00000265574.1","gene_symbol":"WDR45BP1","gene_name":"WD repeat domain 45B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26605]","synonyms":"WDR45LP1","biotype":"processed_pseudogene","ncbi_id":"646086","summary":null,"start":32111562,"end":32112590,"strand":-1,"description":"WD repeat domain 45B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26605]"}, {"versioned_ensembl_gene_id":"ENSG00000161265.14","gene_symbol":"U2AF1L4","gene_name":"U2 small nuclear RNA auxiliary factor 1 like 4 [Source:HGNC Symbol;Acc:HGNC:23020]","synonyms":"U2af26,U2AF1L3,MGC33901","biotype":"protein_coding","ncbi_id":"199746","summary":null,"start":35742464,"end":35745445,"strand":-1,"description":"U2 small nuclear RNA auxiliary factor 1 like 4 [Source:HGNC Symbol;Acc:HGNC:23020]"}, {"versioned_ensembl_gene_id":"ENSG00000166159.10","gene_symbol":"LRTM2","gene_name":"leucine rich repeats and transmembrane domains 2 [Source:HGNC Symbol;Acc:HGNC:32443]","synonyms":null,"biotype":"protein_coding","ncbi_id":"654429","summary":null,"start":1820267,"end":1836752,"strand":1,"description":"leucine rich repeats and transmembrane domains 2 [Source:HGNC Symbol;Acc:HGNC:32443]"}, {"versioned_ensembl_gene_id":"ENSG00000242290.2","gene_symbol":"ZBTB20-AS5","gene_name":"ZBTB20 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:52841]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929754","summary":null,"start":114445521,"end":114529452,"strand":1,"description":"ZBTB20 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:52841]"}, {"versioned_ensembl_gene_id":"ENSG00000229774.1","gene_symbol":"AC018866.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120686635,"end":120710517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226550.1","gene_symbol":"CR759848.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32751146,"end":32751980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008056.13","gene_symbol":"SYN1","gene_name":"synapsin I [Source:HGNC Symbol;Acc:HGNC:11494]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6853","summary":"This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":47571898,"end":47619943,"strand":-1,"description":"synapsin I [Source:HGNC Symbol;Acc:HGNC:11494]"}, {"versioned_ensembl_gene_id":"ENSG00000241295.1","gene_symbol":"ZBTB20-AS2","gene_name":"ZBTB20 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42421]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506673","summary":null,"start":114684580,"end":114687609,"strand":1,"description":"ZBTB20 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42421]"}, {"versioned_ensembl_gene_id":"ENSG00000187688.14","gene_symbol":"TRPV2","gene_name":"transient receptor potential cation channel subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:18082]","synonyms":"VRL1,VRL-1,VRL","biotype":"protein_coding","ncbi_id":"51393","summary":"This gene encodes an ion channel that is activated by high temperatures above 52 degrees Celsius. The protein may be involved in transduction of high-temperature heat responses in sensory ganglia. It is thought that in other tissues the channel may be activated by stimuli other than heat. [provided by RefSeq, Jul 2008]","start":16415542,"end":16437003,"strand":1,"description":"transient receptor potential cation channel subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:18082]"}, {"versioned_ensembl_gene_id":"ENSG00000228025.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32739769,"end":32740601,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000216360.1","gene_symbol":"AL136968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5817421,"end":5818366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264739.1","gene_symbol":"AC093484.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16414524,"end":16416689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170468.7","gene_symbol":"RIOX1","gene_name":"ribosomal oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:20968]","synonyms":"NO66,MAPJD,JMJD9,FLJ21802,C14orf169","biotype":"protein_coding","ncbi_id":"79697","summary":null,"start":73490964,"end":73493392,"strand":1,"description":"ribosomal oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:20968]"}, {"versioned_ensembl_gene_id":"ENSG00000081760.16","gene_symbol":"AACS","gene_name":"acetoacetyl-CoA synthetase [Source:HGNC Symbol;Acc:HGNC:21298]","synonyms":"SUR-5,FLJ12389,ACSF1","biotype":"protein_coding","ncbi_id":"65985","summary":null,"start":125065379,"end":125143333,"strand":1,"description":"acetoacetyl-CoA synthetase [Source:HGNC Symbol;Acc:HGNC:21298]"}, {"versioned_ensembl_gene_id":"ENSG00000267439.1","gene_symbol":"AD000671.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35747057,"end":35753415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214823.3","gene_symbol":"NXT1P1","gene_name":"nuclear transport factor 2 like export factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39708]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652801","summary":null,"start":39169636,"end":39169951,"strand":-1,"description":"nuclear transport factor 2 like export factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39708]"}, {"versioned_ensembl_gene_id":"ENSG00000229255.1","gene_symbol":"AC138089.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":248484245,"end":248485484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257142.1","gene_symbol":"AL512310.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19700479,"end":19700650,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196539.3","gene_symbol":"OR2T3","gene_name":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343173","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248473351,"end":248474307,"strand":1,"description":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]"}, {"versioned_ensembl_gene_id":"ENSG00000112039.3","gene_symbol":"FANCE","gene_name":"Fanconi anemia complementation group E [Source:HGNC Symbol;Acc:HGNC:3586]","synonyms":"FAE,FACE","biotype":"protein_coding","ncbi_id":"2178","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group E. [provided by RefSeq, Jul 2008]","start":35452361,"end":35467103,"strand":1,"description":"Fanconi anemia complementation group E [Source:HGNC Symbol;Acc:HGNC:3586]"}, {"versioned_ensembl_gene_id":"ENSG00000258623.1","gene_symbol":"AL121820.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68683411,"end":68685565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241945.7","gene_symbol":"PWP2","gene_name":"PWP2, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:9711]","synonyms":"EHOC-17,UTP1,PWP2H","biotype":"protein_coding","ncbi_id":"5822","summary":null,"start":44107290,"end":44131181,"strand":1,"description":"PWP2, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:9711]"}, {"versioned_ensembl_gene_id":"ENSG00000274696.2","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724453,"end":54767462,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000162551.13","gene_symbol":"ALPL","gene_name":"alkaline phosphatase, liver/bone/kidney [Source:HGNC Symbol;Acc:HGNC:438]","synonyms":"TNSALP,HOPS","biotype":"protein_coding","ncbi_id":"249","summary":"This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015]","start":21509372,"end":21578412,"strand":1,"description":"alkaline phosphatase, liver/bone/kidney [Source:HGNC Symbol;Acc:HGNC:438]"}, {"versioned_ensembl_gene_id":"ENSG00000274851.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754976,"end":54767325,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000253605.1","gene_symbol":"HNRNPA1P38","gene_name":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:48767]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421384","summary":null,"start":141459075,"end":141460031,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:48767]"}, {"versioned_ensembl_gene_id":"ENSG00000213924.3","gene_symbol":"HNRNPH1P2","gene_name":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129368","summary":null,"start":143677153,"end":143678362,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48810]"}, {"versioned_ensembl_gene_id":"ENSG00000253388.1","gene_symbol":"AC124067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37480089,"end":37480809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254294.1","gene_symbol":"AC021305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123400582,"end":123402095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230750.1","gene_symbol":"SDAD1P2","gene_name":"SDA1 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400836","summary":null,"start":10385779,"end":10387806,"strand":1,"description":"SDA1 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31404]"}, {"versioned_ensembl_gene_id":"ENSG00000253365.1","gene_symbol":"IGKV1D-22","gene_name":"immunoglobulin kappa variable 1D-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5750]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28899","summary":null,"start":90010741,"end":90011184,"strand":1,"description":"immunoglobulin kappa variable 1D-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5750]"}, {"versioned_ensembl_gene_id":"ENSG00000257698.1","gene_symbol":"AC084033.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57931528,"end":57936175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228718.1","gene_symbol":"LINC02521","gene_name":"long intergenic non-protein coding RNA 2521 [Source:HGNC Symbol;Acc:HGNC:53560]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374885","summary":null,"start":2636936,"end":2640001,"strand":1,"description":"long intergenic non-protein coding RNA 2521 [Source:HGNC Symbol;Acc:HGNC:53560]"}, {"versioned_ensembl_gene_id":"ENSG00000253414.2","gene_symbol":"AC124067.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37516410,"end":37517021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103485.17","gene_symbol":"QPRT","gene_name":"quinolinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:9755]","synonyms":"QPRTase","biotype":"protein_coding","ncbi_id":"23475","summary":"This gene encodes a key enzyme in catabolism of quinolinate, an intermediate in the tryptophan-nicotinamide adenine dinucleotide pathway. Quinolinate acts as a most potent endogenous exitotoxin to neurons. Elevation of quinolinate levels in the brain has been linked to the pathogenesis of neurodegenerative disorders such as epilepsy, Alzheimer's disease, and Huntington's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":29679008,"end":29698699,"strand":1,"description":"quinolinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:9755]"}, {"versioned_ensembl_gene_id":"ENSG00000231823.3","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32895064,"end":32900625,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000131848.9","gene_symbol":"ZSCAN5A","gene_name":"zinc finger and SCAN domain containing 5A [Source:HGNC Symbol;Acc:HGNC:23710]","synonyms":"ZSCAN5,ZNF495,MGC4161","biotype":"protein_coding","ncbi_id":"79149","summary":null,"start":56219670,"end":56368383,"strand":-1,"description":"zinc finger and SCAN domain containing 5A [Source:HGNC Symbol;Acc:HGNC:23710]"}, {"versioned_ensembl_gene_id":"ENSG00000242767.1","gene_symbol":"ZBTB20-AS4","gene_name":"ZBTB20 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42423]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874131","summary":null,"start":115100423,"end":115103061,"strand":1,"description":"ZBTB20 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42423]"}, {"versioned_ensembl_gene_id":"ENSG00000213014.3","gene_symbol":"VN2R17P","gene_name":"vomeronasal 2 receptor 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:33223]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649186","summary":null,"start":56317177,"end":56318008,"strand":-1,"description":"vomeronasal 2 receptor 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:33223]"}, {"versioned_ensembl_gene_id":"ENSG00000282749.1","gene_symbol":"AC006449.10","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38550147,"end":38552244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265944.1","gene_symbol":"LINC01387","gene_name":"long intergenic non-protein coding RNA 1387 [Source:HGNC Symbol;Acc:HGNC:44660]","synonyms":"C18orf64","biotype":"lincRNA","ncbi_id":"100130480","summary":null,"start":6511416,"end":6590653,"strand":1,"description":"long intergenic non-protein coding RNA 1387 [Source:HGNC Symbol;Acc:HGNC:44660]"}, {"versioned_ensembl_gene_id":"ENSG00000120279.6","gene_symbol":"MYCT1","gene_name":"MYC target 1 [Source:HGNC Symbol;Acc:HGNC:23172]","synonyms":"MTLC,FLJ21269","biotype":"protein_coding","ncbi_id":"80177","summary":null,"start":152697895,"end":152724567,"strand":1,"description":"MYC target 1 [Source:HGNC Symbol;Acc:HGNC:23172]"}, {"versioned_ensembl_gene_id":"ENSG00000253730.1","gene_symbol":"AC015909.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50158333,"end":50161276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176476.8","gene_symbol":"SGF29","gene_name":"SAGA complex associated factor 29 [Source:HGNC Symbol;Acc:HGNC:25156]","synonyms":"TDRD29,FLJ32446,CCDC101","biotype":"protein_coding","ncbi_id":"112869","summary":"CCDC101 is a subunit of 2 histone acetyltransferase complexes: the ADA2A (TADA2A; MIM 602276)-containing (ATAC) complex and the SPT3 (SUPT3H; MIM 602947)-TAF9 (MIM 600822)-GCN5 (KAT2A; MIM 602301)/PCAF (KAT2B; MIM 602303) acetylase (STAGA) complex. Both of these complexes contain either GCN5 or PCAF, which are paralogous acetyltransferases (Wang et al., 2008 [PubMed 18838386]).[supplied by OMIM, Apr 2010]","start":28553915,"end":28591790,"strand":1,"description":"SAGA complex associated factor 29 [Source:HGNC Symbol;Acc:HGNC:25156]"}, {"versioned_ensembl_gene_id":"ENSG00000226205.1","gene_symbol":"AC007790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133732493,"end":133733595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235967.1","gene_symbol":"COX5BP3","gene_name":"cytochrome c oxidase subunit 5B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2272]","synonyms":"COX5BL3","biotype":"processed_pseudogene","ncbi_id":"1332","summary":null,"start":133727368,"end":133727734,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2272]"}, {"versioned_ensembl_gene_id":"ENSG00000277621.1","gene_symbol":"AC005277.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12982613,"end":12983002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077463.14","gene_symbol":"SIRT6","gene_name":"sirtuin 6 [Source:HGNC Symbol;Acc:HGNC:14934]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51548","summary":"This gene encodes a member of the sirtuin family of NAD-dependent enzymes that are implicated in cellular stress resistance, genomic stability, aging and energy homeostasis. The encoded protein is localized to the nucleus, exhibits ADP-ribosyl transferase and histone deacetylase activities, and plays a role in DNA repair, maintenance of telomeric chromatin, inflammation, lipid and glucose metabolism. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":4174109,"end":4182604,"strand":-1,"description":"sirtuin 6 [Source:HGNC Symbol;Acc:HGNC:14934]"}, {"versioned_ensembl_gene_id":"ENSG00000248854.1","gene_symbol":"HNRNPH1P3","gene_name":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402216","summary":null,"start":55838801,"end":55840025,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48811]"}, {"versioned_ensembl_gene_id":"ENSG00000198155.5","gene_symbol":"ZNF876P","gene_name":"zinc finger protein 876, pseudogene [Source:HGNC Symbol;Acc:HGNC:32472]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"642280","summary":null,"start":212610,"end":255985,"strand":1,"description":"zinc finger protein 876, pseudogene [Source:HGNC Symbol;Acc:HGNC:32472]"}, {"versioned_ensembl_gene_id":"ENSG00000255039.1","gene_symbol":"LINC02553","gene_name":"long intergenic non-protein coding RNA 2553 [Source:HGNC Symbol;Acc:HGNC:53588]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369449","summary":null,"start":97222644,"end":97259987,"strand":-1,"description":"long intergenic non-protein coding RNA 2553 [Source:HGNC Symbol;Acc:HGNC:53588]"}, {"versioned_ensembl_gene_id":"ENSG00000198128.4","gene_symbol":"OR2L3","gene_name":"olfactory receptor family 2 subfamily L member 3 [Source:HGNC Symbol;Acc:HGNC:15009]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391192","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248046836,"end":248063407,"strand":1,"description":"olfactory receptor family 2 subfamily L member 3 [Source:HGNC Symbol;Acc:HGNC:15009]"}, {"versioned_ensembl_gene_id":"ENSG00000107566.13","gene_symbol":"ERLIN1","gene_name":"ER lipid raft associated 1 [Source:HGNC Symbol;Acc:HGNC:16947]","synonyms":"SPG62,SPFH1,KE04,Erlin-1,C10orf69","biotype":"protein_coding","ncbi_id":"10613","summary":"The protein encoded by this gene is part of a protein complex that mediates degradation of inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum. The encoded protein also binds cholesterol and regulates the SREBP signaling pathway, which promotes cellular cholesterol homeostasis. Defects in this gene have been associated with spastic paraplegia 62. [provided by RefSeq, Dec 2016]","start":100150094,"end":100188334,"strand":-1,"description":"ER lipid raft associated 1 [Source:HGNC Symbol;Acc:HGNC:16947]"}, {"versioned_ensembl_gene_id":"ENSG00000128655.17","gene_symbol":"PDE11A","gene_name":"phosphodiesterase 11A [Source:HGNC Symbol;Acc:HGNC:8773]","synonyms":"PPNAD2","biotype":"protein_coding","ncbi_id":"50940","summary":"The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a member of the PDE protein superfamily. Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":177623252,"end":178072755,"strand":-1,"description":"phosphodiesterase 11A [Source:HGNC Symbol;Acc:HGNC:8773]"}, {"versioned_ensembl_gene_id":"ENSG00000067704.9","gene_symbol":"IARS2","gene_name":"isoleucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29685]","synonyms":"FLJ10326","biotype":"protein_coding","ncbi_id":"55699","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAS, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Two forms of isoleucine-tRNA synthetase exist, a cytoplasmic form and a mitochondrial form. This gene encodes the mitochondrial isoleucine-tRNA synthetase which belongs to the class-I aminoacyl-tRNA synthetase family. [provided by RefSeq, Dec 2014]","start":220094102,"end":220148041,"strand":1,"description":"isoleucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29685]"}, {"versioned_ensembl_gene_id":"ENSG00000232134.1","gene_symbol":"RPS15AP12","gene_name":"ribosomal protein S15a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36759]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129243","summary":null,"start":220143964,"end":220144351,"strand":-1,"description":"ribosomal protein S15a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36759]"}, {"versioned_ensembl_gene_id":"ENSG00000146707.14","gene_symbol":"POMZP3","gene_name":"POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:HGNC:9203]","synonyms":"POM121,POM-ZP3","biotype":"protein_coding","ncbi_id":"22932","summary":"This gene appears to have resulted from a fusion of DNA sequences derived from 2 distinct loci, specifically through the duplication of two internal exons from the POM121 gene and four 3' exons from the ZP3 gene. The 5' end of this gene is similar to the 5` coding region of the POM121 gene which encodes an integral nuclear pore membrane protein. However, the protein encoded by this gene lacks the nuclear pore localization motif. The 3' end of this gene is similar to the last 4 exons of the zona pellucida glycoprotein 3 (ZP3) gene and the encoded protein retains one zona pellucida domain. Multiple protein isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":76609986,"end":76627261,"strand":-1,"description":"POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:HGNC:9203]"}, {"versioned_ensembl_gene_id":"ENSG00000197454.2","gene_symbol":"OR2L5","gene_name":"olfactory receptor family 2 subfamily L member 5 [Source:HGNC Symbol;Acc:HGNC:15011]","synonyms":"OR2L5P,OR2L11","biotype":"protein_coding","ncbi_id":"81466","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248013660,"end":248024276,"strand":1,"description":"olfactory receptor family 2 subfamily L member 5 [Source:HGNC Symbol;Acc:HGNC:15011]"}, {"versioned_ensembl_gene_id":"ENSG00000261198.1","gene_symbol":"AC005774.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7614230,"end":7614992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282579.1","gene_symbol":"IGHV4-39","gene_name":"immunoglobulin heavy variable 4-39 [Source:HGNC Symbol;Acc:HGNC:5651]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28394","summary":null,"start":106446390,"end":106446899,"strand":-1,"description":"immunoglobulin heavy variable 4-39 [Source:HGNC Symbol;Acc:HGNC:5651]"}, {"versioned_ensembl_gene_id":"ENSG00000081800.8","gene_symbol":"SLC13A1","gene_name":"solute carrier family 13 member 1 [Source:HGNC Symbol;Acc:HGNC:10916]","synonyms":"NaSi-1,NAS1","biotype":"protein_coding","ncbi_id":"6561","summary":"The protein encoded by this gene is an apical membrane Na(+)-sulfate cotransporter involved in sulfate homeostasis in the kidney. Defects in this gene lead to many pathophysiologic problems. [provided by RefSeq, May 2016]","start":123113531,"end":123199986,"strand":-1,"description":"solute carrier family 13 member 1 [Source:HGNC Symbol;Acc:HGNC:10916]"}, {"versioned_ensembl_gene_id":"ENSG00000280224.1","gene_symbol":"AL008636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49500568,"end":49501585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212939.2","gene_symbol":"Z97192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49548681,"end":49556473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270001.1","gene_symbol":"AL121894.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23631826,"end":23632316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263353.3","gene_symbol":"PPIAL4A","gene_name":"peptidylprolyl isomerase A like 4A [Source:HGNC Symbol;Acc:HGNC:24369]","synonyms":"PPIAL4B,PPIAL4,COAS2","biotype":"protein_coding","ncbi_id":"653505","summary":null,"start":120889746,"end":120890405,"strand":1,"description":"peptidylprolyl isomerase A like 4A [Source:HGNC Symbol;Acc:HGNC:24369]"}, {"versioned_ensembl_gene_id":"ENSG00000226121.2","gene_symbol":"AC009487.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161500885,"end":161507705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184384.13","gene_symbol":"MAML2","gene_name":"mastermind like transcriptional coactivator 2 [Source:HGNC Symbol;Acc:HGNC:16259]","synonyms":"MAM3,KIAA1819","biotype":"protein_coding","ncbi_id":"84441","summary":"The protein encoded by this gene is a member of the Mastermind-like family of proteins. All family members are proline and glutamine-rich, and contain a conserved basic domain that binds the ankyrin repeat domain of the intracellular domain of the Notch receptors (ICN1-4) in their N-terminus, and a transcriptional activation domain in their C-terminus. This protein binds to an extended groove that is formed by the interaction of CBF1, Suppressor of Hairless, LAG-1 (CSL) with ICN, and positively regulates Notch signaling. High levels of expression of this gene have been observed in several B cell-derived lymphomas. Translocations resulting in fusion proteins with both CRTC1 and CRTC3 have been implicated in the development of mucoepidermoid carcinomas, while a translocation event with CXCR4 has been linked with chronic lymphocytic leukemia (CLL). Copy number variation in the polyglutamine tract has been observed. [provided by RefSeq, Jan 2015]","start":95976598,"end":96343180,"strand":-1,"description":"mastermind like transcriptional coactivator 2 [Source:HGNC Symbol;Acc:HGNC:16259]"}, {"versioned_ensembl_gene_id":"ENSG00000249047.2","gene_symbol":"COX6B1P5","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37675]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289662","summary":null,"start":2234251,"end":2234499,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37675]"}, {"versioned_ensembl_gene_id":"ENSG00000230576.1","gene_symbol":"OR6R1P","gene_name":"olfactory receptor family 6 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15037]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81440","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247833349,"end":247834288,"strand":-1,"description":"olfactory receptor family 6 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15037]"}, {"versioned_ensembl_gene_id":"ENSG00000228336.2","gene_symbol":"OR9H1P","gene_name":"olfactory receptor family 9 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15038]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"81439","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247770169,"end":247779524,"strand":1,"description":"olfactory receptor family 9 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15038]"}, {"versioned_ensembl_gene_id":"ENSG00000221888.4","gene_symbol":"OR1C1","gene_name":"olfactory receptor family 1 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8182]","synonyms":"TPCR27,HSTPCR27","biotype":"protein_coding","ncbi_id":"26188","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247754846,"end":247760556,"strand":-1,"description":"olfactory receptor family 1 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8182]"}, {"versioned_ensembl_gene_id":"ENSG00000220184.2","gene_symbol":"HMGB3P18","gene_name":"high mobility group box 3 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39310]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644502","summary":null,"start":121858179,"end":121858768,"strand":-1,"description":"high mobility group box 3 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39310]"}, {"versioned_ensembl_gene_id":"ENSG00000162959.13","gene_symbol":"MEMO1","gene_name":"mediator of cell motility 1 [Source:HGNC Symbol;Acc:HGNC:14014]","synonyms":"MEMO,CGI-27,C2orf4","biotype":"protein_coding","ncbi_id":"51072","summary":null,"start":31865060,"end":32011230,"strand":-1,"description":"mediator of cell motility 1 [Source:HGNC Symbol;Acc:HGNC:14014]"}, {"versioned_ensembl_gene_id":"ENSG00000271317.1","gene_symbol":"IGHD4OR15-4A","gene_name":"immunoglobulin heavy diversity 4/OR15-4A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5506]","synonyms":"IGHD4OR154A,IGHD4/OR15-4A","biotype":"IG_D_gene","ncbi_id":"28329","summary":null,"start":20004797,"end":20004815,"strand":-1,"description":"immunoglobulin heavy diversity 4/OR15-4A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5506]"}, {"versioned_ensembl_gene_id":"ENSG00000214628.3","gene_symbol":"NDUFB5P2","gene_name":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52268]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422431","summary":null,"start":96953630,"end":96954195,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52268]"}, {"versioned_ensembl_gene_id":"ENSG00000198445.4","gene_symbol":"CCT8L2","gene_name":"chaperonin containing TCP1 subunit 8 like 2 [Source:HGNC Symbol;Acc:HGNC:15553]","synonyms":"CESK1","biotype":"protein_coding","ncbi_id":"150160","summary":null,"start":16590751,"end":16592810,"strand":-1,"description":"chaperonin containing TCP1 subunit 8 like 2 [Source:HGNC Symbol;Acc:HGNC:15553]"}, {"versioned_ensembl_gene_id":"ENSG00000239435.2","gene_symbol":"KCNMB3P1","gene_name":"potassium calcium-activated channel subfamily M regulatory beta subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6288]","synonyms":"KCNMBLP,KCNMB3L1,KCNMB3L,KCNMB2L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"27093","summary":null,"start":16575363,"end":16582707,"strand":-1,"description":"potassium calcium-activated channel subfamily M regulatory beta subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6288]"}, {"versioned_ensembl_gene_id":"ENSG00000259490.2","gene_symbol":"IGHV3OR15-7","gene_name":"immunoglobulin heavy variable 3/OR15-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5633]","synonyms":"IGHV3/OR15-7","biotype":"IG_V_gene","ncbi_id":"28318","summary":null,"start":19987656,"end":19988117,"strand":-1,"description":"immunoglobulin heavy variable 3/OR15-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5633]"}, {"versioned_ensembl_gene_id":"ENSG00000266158.2","gene_symbol":"RN7SL785P","gene_name":"RNA, 7SL, cytoplasmic 785, pseudogene [Source:HGNC Symbol;Acc:HGNC:46801]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480532","summary":null,"start":47280811,"end":47281063,"strand":-1,"description":"RNA, 7SL, cytoplasmic 785, pseudogene [Source:HGNC Symbol;Acc:HGNC:46801]"}, {"versioned_ensembl_gene_id":"ENSG00000259337.4","gene_symbol":"IGHV1OR15-2","gene_name":"immunoglobulin heavy variable 1/OR15-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5564]","synonyms":"IGHV1/OR15-2","biotype":"IG_V_pseudogene","ncbi_id":"100287128","summary":null,"start":19972782,"end":19973218,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5564]"}, {"versioned_ensembl_gene_id":"ENSG00000171729.13","gene_symbol":"TMEM51","gene_name":"transmembrane protein 51 [Source:HGNC Symbol;Acc:HGNC:25488]","synonyms":"FLJ10199,C1orf72","biotype":"protein_coding","ncbi_id":"55092","summary":null,"start":15152532,"end":15220480,"strand":1,"description":"transmembrane protein 51 [Source:HGNC Symbol;Acc:HGNC:25488]"}, {"versioned_ensembl_gene_id":"ENSG00000163040.14","gene_symbol":"CCDC74A","gene_name":"coiled-coil domain containing 74A [Source:HGNC Symbol;Acc:HGNC:25197]","synonyms":"FLJ40345","biotype":"protein_coding","ncbi_id":"90557","summary":null,"start":131527675,"end":131533666,"strand":1,"description":"coiled-coil domain containing 74A [Source:HGNC Symbol;Acc:HGNC:25197]"}, {"versioned_ensembl_gene_id":"ENSG00000204464.7","gene_symbol":"C1orf195","gene_name":"chromosome 1 open reading frame 195 [Source:HGNC Symbol;Acc:HGNC:32332]","synonyms":null,"biotype":"lincRNA","ncbi_id":"727684","summary":null,"start":15164344,"end":15171317,"strand":-1,"description":"chromosome 1 open reading frame 195 [Source:HGNC Symbol;Acc:HGNC:32332]"}, {"versioned_ensembl_gene_id":"ENSG00000215720.4","gene_symbol":"AL035405.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15191828,"end":15192845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273391.1","gene_symbol":"AC083880.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139359032,"end":139359566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279388.1","gene_symbol":"AC073578.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131478844,"end":131483034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242070.1","gene_symbol":"NPM1P17","gene_name":"nucleophosmin 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:7919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10830","summary":null,"start":137723774,"end":137724543,"strand":1,"description":"nucleophosmin 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:7919]"}, {"versioned_ensembl_gene_id":"ENSG00000256209.1","gene_symbol":"AC073578.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131469311,"end":131492951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206013.2","gene_symbol":"IFITM5","gene_name":"interferon induced transmembrane protein 5 [Source:HGNC Symbol;Acc:HGNC:16644]","synonyms":"BRIL,Hrmp1,fragilis4","biotype":"protein_coding","ncbi_id":"387733","summary":"This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012]","start":298200,"end":299526,"strand":-1,"description":"interferon induced transmembrane protein 5 [Source:HGNC Symbol;Acc:HGNC:16644]"}, {"versioned_ensembl_gene_id":"ENSG00000280409.1","gene_symbol":"LINC01101","gene_name":"long intergenic non-protein coding RNA 1101 [Source:HGNC Symbol;Acc:HGNC:25923]","synonyms":"FLJ14816","biotype":"TEC","ncbi_id":"84931","summary":null,"start":120464335,"end":120466218,"strand":-1,"description":"long intergenic non-protein coding RNA 1101 [Source:HGNC Symbol;Acc:HGNC:25923]"}, {"versioned_ensembl_gene_id":"ENSG00000026508.17","gene_symbol":"CD44","gene_name":"CD44 molecule (Indian blood group) [Source:HGNC Symbol;Acc:HGNC:1681]","synonyms":"MIC4,MDU3,MDU2,MC56,IN,HCELL,CSPG8,CD44R,Pgp1","biotype":"protein_coding","ncbi_id":"960","summary":"The protein encoded by this gene is a cell-surface glycoprotein involved in cell-cell interactions, cell adhesion and migration. It is a receptor for hyaluronic acid (HA) and can also interact with other ligands, such as osteopontin, collagens, and matrix metalloproteinases (MMPs). This protein participates in a wide variety of cellular functions including lymphocyte activation, recirculation and homing, hematopoiesis, and tumor metastasis. Transcripts for this gene undergo complex alternative splicing that results in many functionally distinct isoforms, however, the full length nature of some of these variants has not been determined. Alternative splicing is the basis for the structural and functional diversity of this protein, and may be related to tumor metastasis. [provided by RefSeq, Jul 2008]","start":35138870,"end":35232402,"strand":1,"description":"CD44 molecule (Indian blood group) [Source:HGNC Symbol;Acc:HGNC:1681]"}, {"versioned_ensembl_gene_id":"ENSG00000234041.1","gene_symbol":"AL512326.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179137764,"end":179137934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282595.1","gene_symbol":"AC234301.4","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106380821,"end":106381287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278082.3","gene_symbol":"AC234301.1","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106373990,"end":106374420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243430.1","gene_symbol":"CR788234.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29742604,"end":29746182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257162.6","gene_symbol":"MED15P6","gene_name":"mediator complex subunit 15 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48655]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100996438","summary":null,"start":19485336,"end":19489148,"strand":1,"description":"mediator complex subunit 15 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48655]"}, {"versioned_ensembl_gene_id":"ENSG00000227484.1","gene_symbol":"CR559946.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50314631,"end":50316008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248703.2","gene_symbol":"LINC02415","gene_name":"long intergenic non-protein coding RNA 2415 [Source:HGNC Symbol;Acc:HGNC:53344]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107161159","summary":null,"start":131296110,"end":131297972,"strand":-1,"description":"long intergenic non-protein coding RNA 2415 [Source:HGNC Symbol;Acc:HGNC:53344]"}, {"versioned_ensembl_gene_id":"ENSG00000261147.1","gene_symbol":"AC091167.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":90249556,"end":90272208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275929.1","gene_symbol":"AC068831.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91031246,"end":91031691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182648.11","gene_symbol":"LINC01006","gene_name":"long intergenic non-protein coding RNA 1006 [Source:HGNC Symbol;Acc:HGNC:48971]","synonyms":"MY040,C7orf13","biotype":"lincRNA","ncbi_id":"100506380","summary":null,"start":156472196,"end":156640654,"strand":-1,"description":"long intergenic non-protein coding RNA 1006 [Source:HGNC Symbol;Acc:HGNC:48971]"}, {"versioned_ensembl_gene_id":"ENSG00000226938.1","gene_symbol":"AC119428.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53348488,"end":53349233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251017.1","gene_symbol":"AC093677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74085995,"end":74086672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050393.11","gene_symbol":"MCUR1","gene_name":"mitochondrial calcium uniporter regulator 1 [Source:HGNC Symbol;Acc:HGNC:21097]","synonyms":"FLJ20958,CCDC90A,C6orf79","biotype":"protein_coding","ncbi_id":"63933","summary":null,"start":13786557,"end":13814568,"strand":-1,"description":"mitochondrial calcium uniporter regulator 1 [Source:HGNC Symbol;Acc:HGNC:21097]"}, {"versioned_ensembl_gene_id":"ENSG00000111802.13","gene_symbol":"TDP2","gene_name":"tyrosyl-DNA phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:17768]","synonyms":"TTRAP","biotype":"protein_coding","ncbi_id":"51567","summary":"This gene encodes a member of a superfamily of divalent cation-dependent phosphodiesterases. The encoded protein associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor associated factors (TRAFs), and inhibits nuclear factor-kappa-B activation. This protein has sequence and structural similarities with APE1 endonuclease, which is involved in both DNA repair and the activation of transcription factors. [provided by RefSeq, Jul 2008]","start":24649977,"end":24667033,"strand":-1,"description":"tyrosyl-DNA phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:17768]"}, {"versioned_ensembl_gene_id":"ENSG00000218891.4","gene_symbol":"ZNF579","gene_name":"zinc finger protein 579 [Source:HGNC Symbol;Acc:HGNC:26646]","synonyms":"FLJ35453","biotype":"protein_coding","ncbi_id":"163033","summary":null,"start":55576770,"end":55580845,"strand":-1,"description":"zinc finger protein 579 [Source:HGNC Symbol;Acc:HGNC:26646]"}, {"versioned_ensembl_gene_id":"ENSG00000150991.14","gene_symbol":"UBC","gene_name":"ubiquitin C [Source:HGNC Symbol;Acc:HGNC:12468]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7316","summary":"This gene represents a ubiquitin gene, ubiquitin C. The encoded protein is a polyubiquitin precursor. Conjugation of ubiquitin monomers or polymers can lead to various effects within a cell, depending on the residues to which ubiquitin is conjugated. Ubiquitination has been associated with protein degradation, DNA repair, cell cycle regulation, kinase modification, endocytosis, and regulation of other cell signaling pathways. [provided by RefSeq, Aug 2010]","start":124911604,"end":124917368,"strand":-1,"description":"ubiquitin C [Source:HGNC Symbol;Acc:HGNC:12468]"}, {"versioned_ensembl_gene_id":"ENSG00000251429.1","gene_symbol":"AC098679.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":158270378,"end":158278676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253925.1","gene_symbol":"AC011369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168085329,"end":168187719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231274.5","gene_symbol":"SBK3","gene_name":"SH3 domain binding kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:44121]","synonyms":"SgK110","biotype":"protein_coding","ncbi_id":"100130827","summary":null,"start":55540656,"end":55545543,"strand":-1,"description":"SH3 domain binding kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:44121]"}, {"versioned_ensembl_gene_id":"ENSG00000176566.4","gene_symbol":"DCAF4L2","gene_name":"DDB1 and CUL4 associated factor 4 like 2 [Source:HGNC Symbol;Acc:HGNC:26657]","synonyms":"WDR21C","biotype":"protein_coding","ncbi_id":"138009","summary":null,"start":87870743,"end":87874068,"strand":-1,"description":"DDB1 and CUL4 associated factor 4 like 2 [Source:HGNC Symbol;Acc:HGNC:26657]"}, {"versioned_ensembl_gene_id":"ENSG00000181733.3","gene_symbol":"OR2Z1","gene_name":"olfactory receptor family 2 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:15391]","synonyms":"OR2Z2","biotype":"protein_coding","ncbi_id":"284383","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":8721634,"end":8732160,"strand":1,"description":"olfactory receptor family 2 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:15391]"}, {"versioned_ensembl_gene_id":"ENSG00000206492.11","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30530868,"end":30546666,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000230020.1","gene_symbol":"NHS-AS1","gene_name":"NHS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40403]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873920","summary":null,"start":17552349,"end":17557387,"strand":-1,"description":"NHS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40403]"}, {"versioned_ensembl_gene_id":"ENSG00000277252.1","gene_symbol":"AL589743.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19220796,"end":19220912,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143971.7","gene_symbol":"ETAA1","gene_name":"ETAA1, ATR kinase activator [Source:HGNC Symbol;Acc:HGNC:24648]","synonyms":"ETAA16","biotype":"protein_coding","ncbi_id":"54465","summary":null,"start":67397319,"end":67410545,"strand":1,"description":"ETAA1, ATR kinase activator [Source:HGNC Symbol;Acc:HGNC:24648]"}, {"versioned_ensembl_gene_id":"ENSG00000144369.12","gene_symbol":"FAM171B","gene_name":"family with sequence similarity 171 member B [Source:HGNC Symbol;Acc:HGNC:29412]","synonyms":"FLJ34104,KIAA1946","biotype":"protein_coding","ncbi_id":"165215","summary":null,"start":186693971,"end":186765965,"strand":1,"description":"family with sequence similarity 171 member B [Source:HGNC Symbol;Acc:HGNC:29412]"}, {"versioned_ensembl_gene_id":"ENSG00000159479.16","gene_symbol":"MED8","gene_name":"mediator complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:19971]","synonyms":"MGC19641,MGC17544,ARC32","biotype":"protein_coding","ncbi_id":"112950","summary":"This gene encodes a protein component of the mediator complex, which aids in transcriptional activation through interaction with RNA polymerase II and gene-specific transcription factors. The encoded protein may also function in ubiquitin ligation and protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013]","start":43383917,"end":43389808,"strand":-1,"description":"mediator complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:19971]"}, {"versioned_ensembl_gene_id":"ENSG00000223532.10","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31260536,"end":31347723,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000233231.1","gene_symbol":"HNRNPA1P49","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:48779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481663","summary":null,"start":166334568,"end":166335471,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:48779]"}, {"versioned_ensembl_gene_id":"ENSG00000276371.2","gene_symbol":"FAM60A","gene_name":"family with sequence similarity 60 member A [Source:HGNC Symbol;Acc:HGNC:30702]","synonyms":"TERA,C12orf14","biotype":"protein_coding","ncbi_id":"58516","summary":null,"start":31282857,"end":31329331,"strand":-1,"description":"family with sequence similarity 60 member A [Source:HGNC Symbol;Acc:HGNC:30702]"}, {"versioned_ensembl_gene_id":"ENSG00000257691.2","gene_symbol":"AC133555.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29475064,"end":29475355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229890.1","gene_symbol":"ACTP1","gene_name":"actin family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51621]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480335","summary":null,"start":108099110,"end":108099492,"strand":1,"description":"actin family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51621]"}, {"versioned_ensembl_gene_id":"ENSG00000145934.16","gene_symbol":"TENM2","gene_name":"teneurin transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:29943]","synonyms":"Ten-M2,ODZ2,KIAA1127","biotype":"protein_coding","ncbi_id":"57451","summary":null,"start":167284799,"end":168264157,"strand":1,"description":"teneurin transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:29943]"}, {"versioned_ensembl_gene_id":"ENSG00000253660.1","gene_symbol":"AC008464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167937717,"end":167953469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224557.7","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33112451,"end":33129084,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000256056.1","gene_symbol":"AC087257.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27592461,"end":27594039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282378.1","gene_symbol":"AC208188.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":451401,"end":453138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256557.1","gene_symbol":"AC009509.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27608733,"end":27609046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243215.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"RING6,D6S222E","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":33039313,"end":33061428,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000242562.1","gene_symbol":"DCAF13P1","gene_name":"DDB1 and CUL4 associated factor 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129009","summary":null,"start":106125371,"end":106126700,"strand":1,"description":"DDB1 and CUL4 associated factor 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43866]"}, {"versioned_ensembl_gene_id":"ENSG00000136250.11","gene_symbol":"AOAH","gene_name":"acyloxyacyl hydrolase [Source:HGNC Symbol;Acc:HGNC:548]","synonyms":null,"biotype":"protein_coding","ncbi_id":"313","summary":"This locus encodes both the light and heavy subunits of acyloxyacyl hydrolase. The encoded enzyme catalyzes the hydrolysis of acyloxylacyl-linked fatty acyl chains from bacterial lipopolysaccharides, effectively detoxifying these molecules. The encoded protein may play a role in modulating host inflammatory response to gram-negative bacteria. Alternatively spliced transcript variants have been described.[provided by RefSeq, Apr 2010]","start":36512949,"end":36724549,"strand":-1,"description":"acyloxyacyl hydrolase [Source:HGNC Symbol;Acc:HGNC:548]"}, {"versioned_ensembl_gene_id":"ENSG00000262210.1","gene_symbol":"PEBP1P3","gene_name":"phosphatidylethanolamine binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129570","summary":null,"start":198690621,"end":198691520,"strand":-1,"description":"phosphatidylethanolamine binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44345]"}, {"versioned_ensembl_gene_id":"ENSG00000187134.13","gene_symbol":"AKR1C1","gene_name":"aldo-keto reductase family 1 member C1 [Source:HGNC Symbol;Acc:HGNC:384]","synonyms":"MBAB,HAKRC,DDH1,DDH,DD1","biotype":"protein_coding","ncbi_id":"1645","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme catalyzes the reaction of progesterone to the inactive form 20-alpha-hydroxy-progesterone. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14. [provided by RefSeq, Jul 2008]","start":4963253,"end":4983283,"strand":1,"description":"aldo-keto reductase family 1 member C1 [Source:HGNC Symbol;Acc:HGNC:384]"}, {"versioned_ensembl_gene_id":"ENSG00000280978.1","gene_symbol":"AC106772.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":604294,"end":613884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272599.2","gene_symbol":"AC016394.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73124573,"end":73125532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257987.5","gene_symbol":"TEX49","gene_name":"testis expressed 49 [Source:HGNC Symbol;Acc:HGNC:48628]","synonyms":"LINC00935","biotype":"protein_coding","ncbi_id":"255411","summary":null,"start":48727435,"end":48765786,"strand":1,"description":"testis expressed 49 [Source:HGNC Symbol;Acc:HGNC:48628]"}, {"versioned_ensembl_gene_id":"ENSG00000174450.11","gene_symbol":"GOLGA6L2","gene_name":"golgin A6 family-like 2 [Source:HGNC Symbol;Acc:HGNC:26695]","synonyms":"FLJ36144,CT105","biotype":"protein_coding","ncbi_id":"283685","summary":null,"start":23439498,"end":23447234,"strand":-1,"description":"golgin A6 family-like 2 [Source:HGNC Symbol;Acc:HGNC:26695]"}, {"versioned_ensembl_gene_id":"ENSG00000244550.1","gene_symbol":"AC006455.8","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":63233115,"end":63241645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087095.12","gene_symbol":"NLK","gene_name":"nemo like kinase [Source:HGNC Symbol;Acc:HGNC:29858]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51701","summary":null,"start":28041737,"end":28196381,"strand":1,"description":"nemo like kinase [Source:HGNC Symbol;Acc:HGNC:29858]"}, {"versioned_ensembl_gene_id":"ENSG00000243302.3","gene_symbol":"AC018638.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128651185,"end":128652334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236957.7","gene_symbol":"AL139010.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157925065,"end":157949071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231389.7","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33064569,"end":33080775,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000146677.7","gene_symbol":"AC004453.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44467897,"end":44468304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282072.1","gene_symbol":"AC243657.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28904945,"end":28905656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280749.1","gene_symbol":"AC231647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197450327,"end":197456654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138286.14","gene_symbol":"FAM149B1","gene_name":"family with sequence similarity 149 member B1 [Source:HGNC Symbol;Acc:HGNC:29162]","synonyms":"KIAA0974","biotype":"protein_coding","ncbi_id":"317662","summary":null,"start":73168166,"end":73244504,"strand":1,"description":"family with sequence similarity 149 member B1 [Source:HGNC Symbol;Acc:HGNC:29162]"}, {"versioned_ensembl_gene_id":"ENSG00000111215.11","gene_symbol":"PRR4","gene_name":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]","synonyms":"PROL4,LPRP","biotype":"protein_coding","ncbi_id":"11272","summary":"This gene encodes a member of the proline-rich protein family that lacks a conserved repetitive domain. This protein may play a role in protective functions in the eye. Alternative splicing result in multiple transcript variants. Read-through transcription also exists between this gene and the upstream PRH1 (proline-rich protein HaeIII subfamily 1) gene. [provided by RefSeq, Feb 2011]","start":10845849,"end":11171613,"strand":-1,"description":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]"}, {"versioned_ensembl_gene_id":"ENSG00000213126.2","gene_symbol":"AC092642.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179814251,"end":179814675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230392.1","gene_symbol":"AC004835.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119291529,"end":119335610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184708.17","gene_symbol":"EIF4ENIF1","gene_name":"eukaryotic translation initiation factor 4E nuclear import factor 1 [Source:HGNC Symbol;Acc:HGNC:16687]","synonyms":"4E-T,2610509L04Rik,FLJ21601,Clast4","biotype":"protein_coding","ncbi_id":"56478","summary":"The protein encoded by this gene is a nucleocytoplasmic shuttle protein for the translation initiation factor eIF4E. This shuttle protein interacts with the importin alpha-beta complex to mediate nuclear import of eIF4E. It is predominantly cytoplasmic; its own nuclear import is regulated by a nuclear localization signal and nuclear export signals. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":31436977,"end":31496108,"strand":-1,"description":"eukaryotic translation initiation factor 4E nuclear import factor 1 [Source:HGNC Symbol;Acc:HGNC:16687]"}, {"versioned_ensembl_gene_id":"ENSG00000111142.13","gene_symbol":"METAP2","gene_name":"methionyl aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:16672]","synonyms":"p67,MNPEP,MAP2","biotype":"protein_coding","ncbi_id":"10988","summary":"The protein encoded by this gene is a member of the methionyl aminopeptidase family. The encoded protein functions both by protecting the alpha subunit of eukaryotic initiation factor 2 from inhibitory phosphorylation and by removing the amino-terminal methionine residue from nascent proteins. Increased expression of this gene is associated with various forms of cancer, and the anti-cancer drugs fumagillin and ovalicin inhibit the protein by irreversibly binding to its active site. Inhibitors of this gene have also been shown to be effective for the treatment of obesity. A pseudogene of this gene is located on chromosome 2. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":95473520,"end":95515839,"strand":1,"description":"methionyl aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:16672]"}, {"versioned_ensembl_gene_id":"ENSG00000283214.1","gene_symbol":"AC006453.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89662601,"end":89662977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226307.1","gene_symbol":"HNRNPDLP1","gene_name":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128595","summary":null,"start":95638375,"end":95638924,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48752]"}, {"versioned_ensembl_gene_id":"ENSG00000282284.1","gene_symbol":"IGHV1-24","gene_name":"immunoglobulin heavy variable 1-24 [Source:HGNC Symbol;Acc:HGNC:5551]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28467","summary":null,"start":106277317,"end":106277814,"strand":-1,"description":"immunoglobulin heavy variable 1-24 [Source:HGNC Symbol;Acc:HGNC:5551]"}, {"versioned_ensembl_gene_id":"ENSG00000229815.1","gene_symbol":"CCNB1IP1P1","gene_name":"cyclin B1 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728887","summary":null,"start":44958557,"end":44959395,"strand":1,"description":"cyclin B1 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37693]"}, {"versioned_ensembl_gene_id":"ENSG00000270601.4","gene_symbol":"PRAMEF5","gene_name":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]","synonyms":"PRAMEF5L,PRAMEF23","biotype":"protein_coding","ncbi_id":"343068","summary":null,"start":13254212,"end":13263314,"strand":1,"description":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]"}, {"versioned_ensembl_gene_id":"ENSG00000232867.1","gene_symbol":"AL355433.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27210327,"end":27210626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249606.1","gene_symbol":"TRAPPC2P7","gene_name":"trafficking protein particle complex 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:10716]","synonyms":"SEDLP7","biotype":"unprocessed_pseudogene","ncbi_id":"392597","summary":null,"start":18655520,"end":18656190,"strand":-1,"description":"trafficking protein particle complex 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:10716]"}, {"versioned_ensembl_gene_id":"ENSG00000196406.4","gene_symbol":"SPANXD","gene_name":"SPANX family member D [Source:HGNC Symbol;Acc:HGNC:14332]","synonyms":"CT11.4,SPANXE","biotype":"protein_coding","ncbi_id":"64648","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular gene encodes a sperm protein that is associated with the nucleus but, although a role in spermatogenesis is suggested, the specific function of this family member has not yet been determined. Polymorphisms in this gene may be associated with prostate cancer susceptibility. [provided by RefSeq, Apr 2014]","start":141697411,"end":141698739,"strand":-1,"description":"SPANX family member D [Source:HGNC Symbol;Acc:HGNC:14332]"}, {"versioned_ensembl_gene_id":"ENSG00000196600.12","gene_symbol":"SLC22A25","gene_name":"solute carrier family 22 member 25 [Source:HGNC Symbol;Acc:HGNC:32935]","synonyms":"UST6,MGC120420,HIMTP","biotype":"protein_coding","ncbi_id":"387601","summary":null,"start":63163776,"end":63229652,"strand":-1,"description":"solute carrier family 22 member 25 [Source:HGNC Symbol;Acc:HGNC:32935]"}, {"versioned_ensembl_gene_id":"ENSG00000146410.11","gene_symbol":"MTFR2","gene_name":"mitochondrial fission regulator 2 [Source:HGNC Symbol;Acc:HGNC:21115]","synonyms":"FAM54A,DUFD1","biotype":"protein_coding","ncbi_id":"113115","summary":null,"start":136231024,"end":136250335,"strand":-1,"description":"mitochondrial fission regulator 2 [Source:HGNC Symbol;Acc:HGNC:21115]"}, {"versioned_ensembl_gene_id":"ENSG00000253568.1","gene_symbol":"AC090572.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86776479,"end":86776638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214113.10","gene_symbol":"LYRM4","gene_name":"LYR motif containing 4 [Source:HGNC Symbol;Acc:HGNC:21365]","synonyms":"ISD11,CGI-203,C6orf149","biotype":"protein_coding","ncbi_id":"57128","summary":"The protein encoded by this gene is found in both mitochondria and the nucleus, where it binds cysteine desulfurase and helps free inorganic sulfur for Fe/S clusters. Disruption of this gene negatively impacts mitochondrial and cytosolic iron homeostasis. [provided by RefSeq, Sep 2016]","start":5102593,"end":5260939,"strand":-1,"description":"LYR motif containing 4 [Source:HGNC Symbol;Acc:HGNC:21365]"}, {"versioned_ensembl_gene_id":"ENSG00000204480.7","gene_symbol":"PRAMEF19","gene_name":"PRAME family member 19 [Source:HGNC Symbol;Acc:HGNC:24908]","synonyms":"OTTHUMG00000007919","biotype":"protein_coding","ncbi_id":"645414","summary":null,"start":13369067,"end":13371693,"strand":-1,"description":"PRAME family member 19 [Source:HGNC Symbol;Acc:HGNC:24908]"}, {"versioned_ensembl_gene_id":"ENSG00000225412.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II,HSBLMHC1","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32433363,"end":32446554,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000260335.1","gene_symbol":"AC133555.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29449191,"end":29449625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278638.1","gene_symbol":"AC244093.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37045462,"end":37052775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117222.13","gene_symbol":"RBBP5","gene_name":"RB binding protein 5, histone lysine methyltransferase complex subunit [Source:HGNC Symbol;Acc:HGNC:9888]","synonyms":"SWD1,RBQ3","biotype":"protein_coding","ncbi_id":"5929","summary":"This gene encodes a ubiquitously expressed nuclear protein which belongs to a highly conserved subfamily of WD-repeat proteins. The encoded protein binds directly to retinoblastoma protein, which regulates cell proliferation. It interacts preferentially with the underphosphorylated retinoblastoma protein via the E1A-binding pocket B. Three alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2010]","start":205086142,"end":205122015,"strand":-1,"description":"RB binding protein 5, histone lysine methyltransferase complex subunit [Source:HGNC Symbol;Acc:HGNC:9888]"}, {"versioned_ensembl_gene_id":"ENSG00000004399.12","gene_symbol":"PLXND1","gene_name":"plexin D1 [Source:HGNC Symbol;Acc:HGNC:9107]","synonyms":"KIAA0620","biotype":"protein_coding","ncbi_id":"23129","summary":null,"start":129555175,"end":129606818,"strand":-1,"description":"plexin D1 [Source:HGNC Symbol;Acc:HGNC:9107]"}, {"versioned_ensembl_gene_id":"ENSG00000132824.13","gene_symbol":"SERINC3","gene_name":"serine incorporator 3 [Source:HGNC Symbol;Acc:HGNC:11699]","synonyms":"TMS-1,TDE1,TDE,SBBI99,DIFF33,AIGP1","biotype":"protein_coding","ncbi_id":"10955","summary":null,"start":44496221,"end":44522109,"strand":-1,"description":"serine incorporator 3 [Source:HGNC Symbol;Acc:HGNC:11699]"}, {"versioned_ensembl_gene_id":"ENSG00000259351.1","gene_symbol":"AC015914.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63928274,"end":63935953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279307.2","gene_symbol":"AC012065.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20529467,"end":20529976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260302.1","gene_symbol":"AP005482.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12774651,"end":12775923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183454.16","gene_symbol":"GRIN2A","gene_name":"glutamate ionotropic receptor NMDA type subunit 2A [Source:HGNC Symbol;Acc:HGNC:4585]","synonyms":"NMDAR2A,GluN2A","biotype":"protein_coding","ncbi_id":"2903","summary":"This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":9753404,"end":10182754,"strand":-1,"description":"glutamate ionotropic receptor NMDA type subunit 2A [Source:HGNC Symbol;Acc:HGNC:4585]"}, {"versioned_ensembl_gene_id":"ENSG00000275499.2","gene_symbol":"ZNF280A","gene_name":"zinc finger protein 280A [Source:HGNC Symbol;Acc:HGNC:18597]","synonyms":"ZNF636,ZNF280,SUHW1,3'OY11.1","biotype":"protein_coding","ncbi_id":"129025","summary":"This gene encodes a zinc finger protein. The encoded protein contains 4 C2H2-type zinc fingers, which are commonly found in transcription factors. A variety of functions may be performed by this type of zinc finger protein, including the binding of DNA or RNA. [provided by RefSeq, Apr 2014]","start":22522841,"end":22529375,"strand":-1,"description":"zinc finger protein 280A [Source:HGNC Symbol;Acc:HGNC:18597]"}, {"versioned_ensembl_gene_id":"ENSG00000143878.9","gene_symbol":"RHOB","gene_name":"ras homolog family member B [Source:HGNC Symbol;Acc:HGNC:668]","synonyms":"RHOH6,RhoB,MST081,ARHB,ARH6","biotype":"protein_coding","ncbi_id":"388","summary":null,"start":20447074,"end":20449445,"strand":1,"description":"ras homolog family member B [Source:HGNC Symbol;Acc:HGNC:668]"}, {"versioned_ensembl_gene_id":"ENSG00000203684.5","gene_symbol":"IBA57-AS1","gene_name":"IBA57 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:32062]","synonyms":"FLJ32878,C1orf148","biotype":"lincRNA","ncbi_id":"574432","summary":null,"start":228164086,"end":228165512,"strand":-1,"description":"IBA57 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:32062]"}, {"versioned_ensembl_gene_id":"ENSG00000237399.7","gene_symbol":"PITRM1-AS1","gene_name":"PITRM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44675]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507034","summary":null,"start":3141632,"end":3167972,"strand":1,"description":"PITRM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44675]"}, {"versioned_ensembl_gene_id":"ENSG00000163701.18","gene_symbol":"IL17RE","gene_name":"interleukin 17 receptor E [Source:HGNC Symbol;Acc:HGNC:18439]","synonyms":"FLJ23658","biotype":"protein_coding","ncbi_id":"132014","summary":"This gene encodes a transmembrane protein that functions as the receptor for interleukin-17C. The encoded protein signals to downstream components of the mitogen activated protein kinase (MAPK) pathway. Activity of this protein is important in the immune response to bacterial pathogens. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013]","start":9902612,"end":9916402,"strand":1,"description":"interleukin 17 receptor E [Source:HGNC Symbol;Acc:HGNC:18439]"}, {"versioned_ensembl_gene_id":"ENSG00000166862.6","gene_symbol":"CACNG2","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:1406]","synonyms":"stargazin,MGC138504,MGC138502","biotype":"protein_coding","ncbi_id":"10369","summary":"The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. The AMPA subtype of ionotropic glutamate receptors are ligand gated ion channels that are typically activated by glutamate released from presynaptic neuron terminals and mediate fast neurotransmission in excitatory synapses. TARPs thus play an important role in synaptic plasticity, learning and memory. Mutations in this gene cause an autosomal dominant form of cognitive disability. [provided by RefSeq, Jul 2017]","start":36563921,"end":36703558,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:1406]"}, {"versioned_ensembl_gene_id":"ENSG00000070785.16","gene_symbol":"EIF2B3","gene_name":"eukaryotic translation initiation factor 2B subunit gamma [Source:HGNC Symbol;Acc:HGNC:3259]","synonyms":"EIF2Bgamma,EIF-2B","biotype":"protein_coding","ncbi_id":"8891","summary":"The protein encoded by this gene is one of the subunits of initiation factor eIF2B, which catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP. It has also been found to function as a cofactor of hepatitis C virus internal ribosome entry site-mediated translation. Mutations in this gene have been associated with leukodystrophy with vanishing white matter. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":44850522,"end":44986722,"strand":-1,"description":"eukaryotic translation initiation factor 2B subunit gamma [Source:HGNC Symbol;Acc:HGNC:3259]"}, {"versioned_ensembl_gene_id":"ENSG00000273976.1","gene_symbol":"GOLGA6L1","gene_name":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283767","summary":null,"start":23128268,"end":23136822,"strand":-1,"description":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]"}, {"versioned_ensembl_gene_id":"ENSG00000074590.13","gene_symbol":"NUAK1","gene_name":"NUAK family kinase 1 [Source:HGNC Symbol;Acc:HGNC:14311]","synonyms":"NuaK1,KIAA0537,ARK5","biotype":"protein_coding","ncbi_id":"9891","summary":null,"start":106063340,"end":106140033,"strand":-1,"description":"NUAK family kinase 1 [Source:HGNC Symbol;Acc:HGNC:14311]"}, {"versioned_ensembl_gene_id":"ENSG00000120156.20","gene_symbol":"TEK","gene_name":"TEK receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11724]","synonyms":"TIE-2,CD202b,VMCM1,VMCM,TIE2","biotype":"protein_coding","ncbi_id":"7010","summary":"This gene encodes a receptor that belongs to the protein tyrosine kinase Tie2 family. The encoded protein possesses a unique extracellular region that contains two immunoglobulin-like domains, three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats. The ligand angiopoietin-1 binds to this receptor and mediates a signaling pathway that functions in embryonic vascular development. Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2014]","start":27109141,"end":27230175,"strand":1,"description":"TEK receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11724]"}, {"versioned_ensembl_gene_id":"ENSG00000253548.1","gene_symbol":"PYDC2","gene_name":"pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33512]","synonyms":"POP2","biotype":"protein_coding","ncbi_id":"152138","summary":null,"start":191461163,"end":191461456,"strand":1,"description":"pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33512]"}, {"versioned_ensembl_gene_id":"ENSG00000223812.6","gene_symbol":"AC073365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191425526,"end":191591097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107959.15","gene_symbol":"PITRM1","gene_name":"pitrilysin metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:17663]","synonyms":"PreP,MP1,KIAA1104,hMP1","biotype":"protein_coding","ncbi_id":"10531","summary":"The protein encoded by this gene is an ATP-dependent metalloprotease that degrades post-cleavage mitochondrial transit peptides. The encoded protein binds zinc and can also degrade amyloid beta A4 protein, suggesting a possible role in Alzheimer's disease. [provided by RefSeq, Dec 2016]","start":3137728,"end":3172841,"strand":-1,"description":"pitrilysin metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:17663]"}, {"versioned_ensembl_gene_id":"ENSG00000144445.16","gene_symbol":"KANSL1L","gene_name":"KAT8 regulatory NSL complex subunit 1 like [Source:HGNC Symbol;Acc:HGNC:26310]","synonyms":"MSL1v2,KIAA1267L,FLJ32349,FLJ23861,C2orf67","biotype":"protein_coding","ncbi_id":"151050","summary":null,"start":210021423,"end":210171383,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 1 like [Source:HGNC Symbol;Acc:HGNC:26310]"}, {"versioned_ensembl_gene_id":"ENSG00000173198.5","gene_symbol":"CYSLTR1","gene_name":"cysteinyl leukotriene receptor 1 [Source:HGNC Symbol;Acc:HGNC:17451]","synonyms":"CYSLT1R,CysLT1,CysLT(1)","biotype":"protein_coding","ncbi_id":"10800","summary":"This gene encodes a member of the G-protein coupled receptor 1 family. The encoded protein is a receptor for cysteinyl leukotrienes, and is involved in mediating bronchoconstriction via activation of a phosphatidylinositol-calcium second messenger system. Activation of the encoded receptor results in contraction and proliferation of bronchial smooth muscle cells, eosinophil migration, and damage to the mucus layer in the lung. Upregulation of this gene is associated with asthma and dysregulation may also be implicated in cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":78271464,"end":78327691,"strand":-1,"description":"cysteinyl leukotriene receptor 1 [Source:HGNC Symbol;Acc:HGNC:17451]"}, {"versioned_ensembl_gene_id":"ENSG00000126934.13","gene_symbol":"MAP2K2","gene_name":"mitogen-activated protein kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6842]","synonyms":"MEK2,PRKMK2","biotype":"protein_coding","ncbi_id":"5605","summary":"The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase is known to play a critical role in mitogen growth factor signal transduction. It phosphorylates and thus activates MAPK1/ERK2 and MAPK2/ERK3. The activation of this kinase itself is dependent on the Ser/Thr phosphorylation by MAP kinase kinase kinases. Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome), a disease characterized by heart defects, cognitive disability, and distinctive facial features similar to those found in Noonan syndrome. The inhibition or degradation of this kinase is also found to be involved in the pathogenesis of Yersinia and anthrax. A pseudogene, which is located on chromosome 7, has been identified for this gene. [provided by RefSeq, Jul 2008]","start":4090321,"end":4124129,"strand":-1,"description":"mitogen-activated protein kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6842]"}, {"versioned_ensembl_gene_id":"ENSG00000249240.2","gene_symbol":"AC069368.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":64841883,"end":64930920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255497.1","gene_symbol":"AC022616.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43313948,"end":43314200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228935.1","gene_symbol":"AL353132.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22960534,"end":22966063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198121.13","gene_symbol":"LPAR1","gene_name":"lysophosphatidic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:3166]","synonyms":"vzg-1,rec.1.3,Mrec1.3,LPA1,GPR26,Gpcr26,EDG2,edg-2","biotype":"protein_coding","ncbi_id":"1902","summary":"The integral membrane protein encoded by this gene is a lysophosphatidic acid (LPA) receptor from a group known as EDG receptors. These receptors are members of the G protein-coupled receptor superfamily. Utilized by LPA for cell signaling, EDG receptors mediate diverse biologic functions, including proliferation, platelet aggregation, smooth muscle contraction, inhibition of neuroblastoma cell differentiation, chemotaxis, and tumor cell invasion. Many transcript variants encoding a few different isoforms have been identified for this gene. [provided by RefSeq, Oct 2020]","start":110873263,"end":111038458,"strand":-1,"description":"lysophosphatidic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:3166]"}, {"versioned_ensembl_gene_id":"ENSG00000188877.12","gene_symbol":"POTEA","gene_name":"POTE ankyrin domain family member A [Source:HGNC Symbol;Acc:HGNC:33893]","synonyms":"POTE8,POTE-8,CT104.3,A26A1","biotype":"polymorphic_pseudogene","ncbi_id":"340441","summary":null,"start":43292483,"end":43363518,"strand":1,"description":"POTE ankyrin domain family member A [Source:HGNC Symbol;Acc:HGNC:33893]"}, {"versioned_ensembl_gene_id":"ENSG00000230492.1","gene_symbol":"AL049651.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23010209,"end":23030785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232060.3","gene_symbol":"SLC4A1APP1","gene_name":"solute carrier family 4 member 1 adaptor protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288436","summary":null,"start":30558880,"end":30559481,"strand":-1,"description":"solute carrier family 4 member 1 adaptor protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49811]"}, {"versioned_ensembl_gene_id":"ENSG00000175556.16","gene_symbol":"LONRF3","gene_name":"LON peptidase N-terminal domain and ring finger 3 [Source:HGNC Symbol;Acc:HGNC:21152]","synonyms":"RNF127,FLJ22612","biotype":"protein_coding","ncbi_id":"79836","summary":"The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Multiple alternatively spliced transcript variants have been suggested, but their full length natures are not clear. [provided by RefSeq, Jul 2008]","start":118974614,"end":119018355,"strand":1,"description":"LON peptidase N-terminal domain and ring finger 3 [Source:HGNC Symbol;Acc:HGNC:21152]"}, {"versioned_ensembl_gene_id":"ENSG00000282069.1","gene_symbol":"LINC02124","gene_name":"long intergenic non-protein coding RNA 2124 [Source:HGNC Symbol;Acc:HGNC:52981]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371048","summary":null,"start":1891136,"end":1892455,"strand":1,"description":"long intergenic non-protein coding RNA 2124 [Source:HGNC Symbol;Acc:HGNC:52981]"}, {"versioned_ensembl_gene_id":"ENSG00000261675.1","gene_symbol":"AL022313.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":36560870,"end":36562915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166839.16","gene_symbol":"ANKDD1A","gene_name":"ankyrin repeat and death domain containing 1A [Source:HGNC Symbol;Acc:HGNC:28002]","synonyms":"FLJ25870","biotype":"protein_coding","ncbi_id":"348094","summary":null,"start":64911902,"end":64958700,"strand":1,"description":"ankyrin repeat and death domain containing 1A [Source:HGNC Symbol;Acc:HGNC:28002]"}, {"versioned_ensembl_gene_id":"ENSG00000232800.1","gene_symbol":"SLC7A15P","gene_name":"solute carrier family 7 member 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:32724]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100289450","summary":null,"start":20386386,"end":20396588,"strand":1,"description":"solute carrier family 7 member 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:32724]"}, {"versioned_ensembl_gene_id":"ENSG00000232161.1","gene_symbol":"AC023141.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57770966,"end":57771173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186678.7","gene_symbol":"AL590240.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55172717,"end":55176026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055118.14","gene_symbol":"KCNH2","gene_name":"potassium voltage-gated channel subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:6251]","synonyms":"HERG,erg1,LQT2,Kv11.1","biotype":"protein_coding","ncbi_id":"3757","summary":"This gene encodes a voltage-activated potassium channel belonging to the eag family. It shares sequence similarity with the Drosophila ether-a-go-go (eag) gene. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":150944961,"end":150978315,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:6251]"}, {"versioned_ensembl_gene_id":"ENSG00000215018.9","gene_symbol":"COL28A1","gene_name":"collagen type XXVIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340267","summary":"COL28A1 belongs to a class of collagens containing von Willebrand factor (VWF; MIM 613160) type A (VWFA) domains (Veit et al., 2006 [PubMed 16330543]).[supplied by OMIM, Nov 2010]","start":7356203,"end":7535853,"strand":-1,"description":"collagen type XXVIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22442]"}, {"versioned_ensembl_gene_id":"ENSG00000070476.14","gene_symbol":"ZXDC","gene_name":"ZXD family zinc finger C [Source:HGNC Symbol;Acc:HGNC:28160]","synonyms":"MGC11349,FLJ13861","biotype":"protein_coding","ncbi_id":"79364","summary":null,"start":126437601,"end":126475919,"strand":-1,"description":"ZXD family zinc finger C [Source:HGNC Symbol;Acc:HGNC:28160]"}, {"versioned_ensembl_gene_id":"ENSG00000213111.5","gene_symbol":"COX5BP2","gene_name":"cytochrome c oxidase subunit 5B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2271]","synonyms":"COX5BL2","biotype":"transcribed_processed_pseudogene","ncbi_id":"1331","summary":null,"start":136034553,"end":136034886,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2271]"}, {"versioned_ensembl_gene_id":"ENSG00000277973.1","gene_symbol":"AL138828.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136206478,"end":136206860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274296.3","gene_symbol":"DECR2","gene_name":"2,4-dienoyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:2754]","synonyms":"SDR17C1,PDCR","biotype":"protein_coding","ncbi_id":"26063","summary":null,"start":401826,"end":412487,"strand":1,"description":"2,4-dienoyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:2754]"}, {"versioned_ensembl_gene_id":"ENSG00000237596.6","gene_symbol":"AL138828.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135991936,"end":136225751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011426.10","gene_symbol":"ANLN","gene_name":"anillin actin binding protein [Source:HGNC Symbol;Acc:HGNC:14082]","synonyms":"scra,ANILLIN,Scraps","biotype":"protein_coding","ncbi_id":"54443","summary":"This gene encodes an actin-binding protein that plays a role in cell growth and migration, and in cytokinesis. The encoded protein is thought to regulate actin cytoskeletal dynamics in podocytes, components of the glomerulus. Mutations in this gene are associated with focal segmental glomerulosclerosis 8. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":36389806,"end":36453791,"strand":1,"description":"anillin actin binding protein [Source:HGNC Symbol;Acc:HGNC:14082]"}, {"versioned_ensembl_gene_id":"ENSG00000225808.1","gene_symbol":"DNAJC19P5","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45068]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861453","summary":null,"start":177229191,"end":177229506,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45068]"}, {"versioned_ensembl_gene_id":"ENSG00000271825.1","gene_symbol":"AC019080.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177300600,"end":177302006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115705.20","gene_symbol":"TPO","gene_name":"thyroid peroxidase [Source:HGNC Symbol;Acc:HGNC:12015]","synonyms":"TPX","biotype":"protein_coding","ncbi_id":"7173","summary":"This gene encodes a membrane-bound glycoprotein. The encoded protein acts as an enzyme and plays a central role in thyroid gland function. The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones, thyroxine and triiodothyronine. Mutations in this gene are associated with several disorders of thyroid hormonogenesis, including congenital hypothyroidism, congenital goiter, and thyroid hormone organification defect IIA. Multiple transcript variants encoding distinct isoforms have been identified for this gene, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2011]","start":1374223,"end":1543711,"strand":1,"description":"thyroid peroxidase [Source:HGNC Symbol;Acc:HGNC:12015]"}, {"versioned_ensembl_gene_id":"ENSG00000271996.1","gene_symbol":"AC019080.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177306373,"end":177310572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186188.10","gene_symbol":"FFAR4","gene_name":"free fatty acid receptor 4 [Source:HGNC Symbol;Acc:HGNC:19061]","synonyms":"PGR4,O3FAR1,GPR129,GPR120","biotype":"protein_coding","ncbi_id":"338557","summary":"This gene encodes a G protein-coupled receptor (GPR) which belongs to the rhodopsin family of GPRs. The encoded protein functions as a receptor for free fatty acids, including omega-3, and participates in suppressing anti-inflammatory responses and insulin sensitizing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":93566665,"end":93604480,"strand":1,"description":"free fatty acid receptor 4 [Source:HGNC Symbol;Acc:HGNC:19061]"}, {"versioned_ensembl_gene_id":"ENSG00000197860.9","gene_symbol":"SGTB","gene_name":"small glutamine rich tetratricopeptide repeat containing beta [Source:HGNC Symbol;Acc:HGNC:23567]","synonyms":"Sgt2,FLJ39002","biotype":"protein_coding","ncbi_id":"54557","summary":null,"start":65665928,"end":65723035,"strand":-1,"description":"small glutamine rich tetratricopeptide repeat containing beta [Source:HGNC Symbol;Acc:HGNC:23567]"}, {"versioned_ensembl_gene_id":"ENSG00000237178.2","gene_symbol":"AC019080.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177344443,"end":177344836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197321.14","gene_symbol":"SVIL","gene_name":"supervillin [Source:HGNC Symbol;Acc:HGNC:11480]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6840","summary":"This gene encodes a bipartite protein with distinct amino- and carboxy-terminal domains. The amino-terminus contains nuclear localization signals and the carboxy-terminus contains numerous consecutive sequences with extensive similarity to proteins in the gelsolin family of actin-binding proteins, which cap, nucleate, and/or sever actin filaments. The gene product is tightly associated with both actin filaments and plasma membranes, suggesting a role as a high-affinity link between the actin cytoskeleton and the membrane. The encoded protein appears to aid in both myosin II assembly during cell spreading and disassembly of focal adhesions. Several transcript variants encoding different isoforms of supervillin have been described. [provided by RefSeq, Apr 2016]","start":29457338,"end":29736781,"strand":-1,"description":"supervillin [Source:HGNC Symbol;Acc:HGNC:11480]"}, {"versioned_ensembl_gene_id":"ENSG00000184378.2","gene_symbol":"ACTRT3","gene_name":"actin related protein T3 [Source:HGNC Symbol;Acc:HGNC:24022]","synonyms":"ARPM1","biotype":"protein_coding","ncbi_id":"84517","summary":null,"start":169766921,"end":169769895,"strand":-1,"description":"actin related protein T3 [Source:HGNC Symbol;Acc:HGNC:24022]"}, {"versioned_ensembl_gene_id":"ENSG00000163359.15","gene_symbol":"COL6A3","gene_name":"collagen type VI alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2213]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1293","summary":"This gene encodes the alpha-3 chain, one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The alpha-3 chain of type VI collagen is much larger than the alpha-1 and -2 chains. This difference in size is largely due to an increase in the number of subdomains, similar to von Willebrand Factor type A domains, that are found in the amino terminal globular domain of all the alpha chains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in the type VI collagen genes are associated with Bethlem myopathy, a rare autosomal dominant proximal myopathy with early childhood onset. Mutations in this gene are also a cause of Ullrich congenital muscular dystrophy, also referred to as Ullrich scleroatonic muscular dystrophy, an autosomal recessive congenital myopathy that is more severe than Bethlem myopathy. Multiple transcript variants have been identified, but the full-length nature of only some of these variants has been described. [provided by RefSeq, Jun 2009]","start":237324003,"end":237414375,"strand":-1,"description":"collagen type VI alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2213]"}, {"versioned_ensembl_gene_id":"ENSG00000213963.6","gene_symbol":"AC019080.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":177283508,"end":177392691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234947.8","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31958721,"end":31968992,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000170509.11","gene_symbol":"HSD17B13","gene_name":"hydroxysteroid 17-beta dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:18685]","synonyms":"SDR16C3,SCDR9","biotype":"protein_coding","ncbi_id":"345275","summary":null,"start":87303789,"end":87322906,"strand":-1,"description":"hydroxysteroid 17-beta dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:18685]"}, {"versioned_ensembl_gene_id":"ENSG00000153037.13","gene_symbol":"SRP19","gene_name":"signal recognition particle 19 [Source:HGNC Symbol;Acc:HGNC:11300]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6728","summary":null,"start":112861222,"end":112869788,"strand":1,"description":"signal recognition particle 19 [Source:HGNC Symbol;Acc:HGNC:11300]"}, {"versioned_ensembl_gene_id":"ENSG00000166037.10","gene_symbol":"CEP57","gene_name":"centrosomal protein 57 [Source:HGNC Symbol;Acc:HGNC:30794]","synonyms":"TSP57,Translokin,KIAA0092","biotype":"protein_coding","ncbi_id":"9702","summary":"This gene encodes a cytoplasmic protein called Translokin. This protein localizes to the centrosome and has a function in microtubular stabilization. The N-terminal half of this protein is required for its centrosome localization and for its multimerization, and the C-terminal half is required for nucleating, bundling and anchoring microtubules to the centrosomes. This protein specifically interacts with fibroblast growth factor 2 (FGF2), sorting nexin 6, Ran-binding protein M and the kinesins KIF3A and KIF3B, and thus mediates the nuclear translocation and mitogenic activity of the FGF2. It also interacts with cyclin D1 and controls nucleocytoplasmic distribution of the cyclin D1 in quiescent cells. This protein is crucial for maintaining correct chromosomal number during cell division. Mutations in this gene cause mosaic variegated aneuploidy syndrome, a rare autosomal recessive disorder. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":95789965,"end":95832693,"strand":1,"description":"centrosomal protein 57 [Source:HGNC Symbol;Acc:HGNC:30794]"}, {"versioned_ensembl_gene_id":"ENSG00000273955.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754987,"end":54767361,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000270397.1","gene_symbol":"AL670379.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120952344,"end":120952595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228517.2","gene_symbol":"CT47A7","gene_name":"cancer/testis antigen family 47, member A7 [Source:HGNC Symbol;Acc:HGNC:33288]","synonyms":"CT47.7","biotype":"protein_coding","ncbi_id":"653282","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120953288,"end":120956600,"strand":-1,"description":"cancer/testis antigen family 47, member A7 [Source:HGNC Symbol;Acc:HGNC:33288]"}, {"versioned_ensembl_gene_id":"ENSG00000235444.2","gene_symbol":"PSMB3P2","gene_name":"proteasome subunit beta 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"130700","summary":null,"start":216610342,"end":216610959,"strand":-1,"description":"proteasome subunit beta 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30150]"}, {"versioned_ensembl_gene_id":"ENSG00000224391.1","gene_symbol":"LINC01280","gene_name":"long intergenic non-protein coding RNA 1280 [Source:HGNC Symbol;Acc:HGNC:50336]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928232","summary":null,"start":216590426,"end":216606938,"strand":-1,"description":"long intergenic non-protein coding RNA 1280 [Source:HGNC Symbol;Acc:HGNC:50336]"}, {"versioned_ensembl_gene_id":"ENSG00000280374.1","gene_symbol":"AC019080.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":177317715,"end":177318471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171408.13","gene_symbol":"PDE7B","gene_name":"phosphodiesterase 7B [Source:HGNC Symbol;Acc:HGNC:8792]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27115","summary":"The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a cAMP-specific phosphodiesterase, a member of the cyclic nucleotide phosphodiesterase family.[provided by RefSeq, Apr 2009]","start":135851696,"end":136195574,"strand":1,"description":"phosphodiesterase 7B [Source:HGNC Symbol;Acc:HGNC:8792]"}, {"versioned_ensembl_gene_id":"ENSG00000225794.1","gene_symbol":"AC073321.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":216604771,"end":216611202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228036.1","gene_symbol":"HSPD1P9","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35132]","synonyms":"HSPD1-14P","biotype":"processed_pseudogene","ncbi_id":"646910","summary":null,"start":37993085,"end":37994720,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35132]"}, {"versioned_ensembl_gene_id":"ENSG00000116044.15","gene_symbol":"NFE2L2","gene_name":"nuclear factor, erythroid 2 like 2 [Source:HGNC Symbol;Acc:HGNC:7782]","synonyms":"NRF2","biotype":"protein_coding","ncbi_id":"4780","summary":"This gene encodes a transcription factor which is a member of a small family of basic leucine zipper (bZIP) proteins. The encoded transcription factor regulates genes which contain antioxidant response elements (ARE) in their promoters; many of these genes encode proteins involved in response to injury and inflammation which includes the production of free radicals. Multiple transcript variants encoding different isoforms have been characterized for this gene. [provided by RefSeq, Sep 2015]","start":177227595,"end":177392697,"strand":-1,"description":"nuclear factor, erythroid 2 like 2 [Source:HGNC Symbol;Acc:HGNC:7782]"}, {"versioned_ensembl_gene_id":"ENSG00000237653.2","gene_symbol":"AC026320.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":191952349,"end":191952826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274317.1","gene_symbol":"LINC02334","gene_name":"long intergenic non-protein coding RNA 2334 [Source:HGNC Symbol;Acc:HGNC:53254]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929077","summary":null,"start":37934565,"end":38048169,"strand":1,"description":"long intergenic non-protein coding RNA 2334 [Source:HGNC Symbol;Acc:HGNC:53254]"}, {"versioned_ensembl_gene_id":"ENSG00000232353.5","gene_symbol":"AC026320.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":192029880,"end":192036557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219807.2","gene_symbol":"ARF1P1","gene_name":"ADP ribosylation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442334","summary":null,"start":94833904,"end":94834447,"strand":1,"description":"ADP ribosylation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22500]"}, {"versioned_ensembl_gene_id":"ENSG00000228521.2","gene_symbol":"AC099552.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155204147,"end":155205189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271502.1","gene_symbol":"AL670379.12","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120957227,"end":120957479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226023.6","gene_symbol":"CT47A6","gene_name":"cancer/testis antigen family 47, member A6 [Source:HGNC Symbol;Acc:HGNC:33287]","synonyms":"CT47.6","biotype":"protein_coding","ncbi_id":"728062","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120958165,"end":120961487,"strand":-1,"description":"cancer/testis antigen family 47, member A6 [Source:HGNC Symbol;Acc:HGNC:33287]"}, {"versioned_ensembl_gene_id":"ENSG00000239792.2","gene_symbol":"C2orf27AP2","gene_name":"chromosome 2 open reading frame 27A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49813]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100131855","summary":null,"start":30670964,"end":30671966,"strand":-1,"description":"chromosome 2 open reading frame 27A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49813]"}, {"versioned_ensembl_gene_id":"ENSG00000225612.1","gene_symbol":"AC099552.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155267299,"end":155268052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115457.9","gene_symbol":"IGFBP2","gene_name":"insulin like growth factor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5471]","synonyms":"IBP2","biotype":"protein_coding","ncbi_id":"3485","summary":"The protein encoded by this gene is one of six similar proteins that bind insulin-like growth factors I and II (IGF-I and IGF-II). The encoded protein can be secreted into the bloodstream, where it binds IGF-I and IGF-II with high affinity, or it can remain intracellular, interacting with many different ligands. High expression levels of this protein promote the growth of several types of tumors and may be predictive of the chances of recovery of the patient. Several transcript variants, one encoding a secreted isoform and the others encoding nonsecreted isoforms, have been found for this gene. [provided by RefSeq, Sep 2015]","start":216632828,"end":216664436,"strand":1,"description":"insulin like growth factor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5471]"}, {"versioned_ensembl_gene_id":"ENSG00000273481.1","gene_symbol":"AL391069.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151327949,"end":151328429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215210.3","gene_symbol":"RBMXP2","gene_name":"RNA binding motif protein, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23284]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441391","summary":null,"start":30689105,"end":30690272,"strand":1,"description":"RNA binding motif protein, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23284]"}, {"versioned_ensembl_gene_id":"ENSG00000273117.1","gene_symbol":"AC144652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155295918,"end":155297541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184945.13","gene_symbol":"AQP12A","gene_name":"aquaporin 12A [Source:HGNC Symbol;Acc:HGNC:19941]","synonyms":"AQP12","biotype":"protein_coding","ncbi_id":"375318","summary":null,"start":240691845,"end":240698483,"strand":1,"description":"aquaporin 12A [Source:HGNC Symbol;Acc:HGNC:19941]"}, {"versioned_ensembl_gene_id":"ENSG00000111052.7","gene_symbol":"LIN7A","gene_name":"lin-7 homolog A, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17787]","synonyms":"VELI1,TIP-33,MALS-1,LIN-7A","biotype":"protein_coding","ncbi_id":"8825","summary":"The protein encoded by this gene is involved in generating and maintaining the asymmetric distribution of channels and receptors at the cell membrane. The encoded protein also is required for the localization of some specific channels and can be part of a protein complex that couples synaptic vesicle exocytosis to cell adhesion in the brain. [provided by RefSeq, May 2016]","start":80792520,"end":80937925,"strand":-1,"description":"lin-7 homolog A, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17787]"}, {"versioned_ensembl_gene_id":"ENSG00000238216.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"NCRNA00149,AB023051.1","biotype":"processed_transcript","ncbi_id":"105375013","summary":null,"start":30780908,"end":30784476,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000276385.1","gene_symbol":"AL445567.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8934984,"end":8935481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259920.1","gene_symbol":"AC007938.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130481491,"end":130484392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130513.6","gene_symbol":"GDF15","gene_name":"growth differentiation factor 15 [Source:HGNC Symbol;Acc:HGNC:30142]","synonyms":"PLAB,PDF,NAG-1,MIC1,MIC-1,PTGFB","biotype":"protein_coding","ncbi_id":"9518","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. The protein is expressed in a broad range of cell types, acts as a pleiotropic cytokine and is involved in the stress response program of cells after cellular injury. Increased protein levels are associated with disease states such as tissue hypoxia, inflammation, acute injury and oxidative stress. [provided by RefSeq, Aug 2016]","start":18374731,"end":18389176,"strand":1,"description":"growth differentiation factor 15 [Source:HGNC Symbol;Acc:HGNC:30142]"}, {"versioned_ensembl_gene_id":"ENSG00000239314.1","gene_symbol":"MORC1-AS1","gene_name":"MORC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40377]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506506","summary":null,"start":109101456,"end":109110342,"strand":1,"description":"MORC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40377]"}, {"versioned_ensembl_gene_id":"ENSG00000114487.9","gene_symbol":"MORC1","gene_name":"MORC family CW-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:7198]","synonyms":"ZCW6,MORC,CT33","biotype":"protein_coding","ncbi_id":"27136","summary":"This gene encodes the human homolog of mouse morc and like the mouse protein it is testis-specific. Mouse studies support a testis-specific function since only male knockout mice are infertile; infertility is the only apparent defect. These studies further support a role for this protein early in spermatogenesis, possibly by affecting entry into apoptosis because testis from knockout mice show greatly increased numbers of apoptotic cells. [provided by RefSeq, Jan 2009]","start":108958239,"end":109118142,"strand":-1,"description":"MORC family CW-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:7198]"}, {"versioned_ensembl_gene_id":"ENSG00000224808.1","gene_symbol":"SRGAP3-AS1","gene_name":"SRGAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40898]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874103","summary":null,"start":9014123,"end":9015979,"strand":1,"description":"SRGAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40898]"}, {"versioned_ensembl_gene_id":"ENSG00000105401.8","gene_symbol":"CDC37","gene_name":"cell division cycle 37 [Source:HGNC Symbol;Acc:HGNC:1735]","synonyms":"P50CDC37","biotype":"protein_coding","ncbi_id":"11140","summary":"The protein encoded by this gene is highly similar to Cdc 37, a cell division cycle control protein of Sacchromyces cerevisiae. This protein is a molecular chaperone with specific function in cell signal transduction. It has been shown to form complex with Hsp90 and a variety of protein kinases including CDK4, CDK6, SRC, RAF-1, MOK, as well as eIF2 alpha kinases. It is thought to play a critical role in directing Hsp90 to its target kinases. [provided by RefSeq, Jul 2008]","start":10391134,"end":10420121,"strand":-1,"description":"cell division cycle 37 [Source:HGNC Symbol;Acc:HGNC:1735]"}, {"versioned_ensembl_gene_id":"ENSG00000235830.1","gene_symbol":"SRGAP3-AS4","gene_name":"SRGAP3 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42434]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927440","summary":null,"start":9256759,"end":9257507,"strand":1,"description":"SRGAP3 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42434]"}, {"versioned_ensembl_gene_id":"ENSG00000225773.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":31927103,"end":31934377,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000108442.2","gene_symbol":"TVP23BP2","gene_name":"TVP23B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38869]","synonyms":"FAM18B4P","biotype":"processed_pseudogene","ncbi_id":"100421473","summary":null,"start":74628328,"end":74628942,"strand":-1,"description":"TVP23B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38869]"}, {"versioned_ensembl_gene_id":"ENSG00000233877.2","gene_symbol":"AL606517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64941979,"end":64942365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159374.17","gene_symbol":"M1AP","gene_name":"meiosis 1 associated protein [Source:HGNC Symbol;Acc:HGNC:25183]","synonyms":"SPATA37,D6Mm5e,C2orf65","biotype":"protein_coding","ncbi_id":"130951","summary":"This gene encodes a protein that is likely to function in progression of meiosis. A similar protein in mouse plays a role in gametogenesis in both sexes. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":74557883,"end":74648338,"strand":-1,"description":"meiosis 1 associated protein [Source:HGNC Symbol;Acc:HGNC:25183]"}, {"versioned_ensembl_gene_id":"ENSG00000270426.1","gene_symbol":"AC099343.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":184471924,"end":184472609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240389.5","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"NG3,C6orf8","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32231591,"end":32235290,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000277535.2","gene_symbol":"AL772284.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":119073226,"end":119076373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183747.11","gene_symbol":"ACSM2A","gene_name":"acyl-CoA synthetase medium chain family member 2A [Source:HGNC Symbol;Acc:HGNC:32017]","synonyms":"MGC150530,ACSM2,A-923A4.1","biotype":"protein_coding","ncbi_id":"123876","summary":"This gene encodes a mitochondrial acyl-coenzyme A synthetase that is specific for medium chain fatty acids. These enzymes catalyze fatty acid activation, the first step of fatty acid metabolism, through the transfer of acyl-CoA. These enzymes also participate in the glycine conjugation pathway in the detoxification of xenobiotics such as benzoate and ibuprofen. Expression levels of this gene in the kidney may be correlated with kidney function. This gene and its paralog ACSM2B (Gene ID: 348158), both present on chromosome 16, likely arose from a chromosomal duplication event. [provided by RefSeq, May 2017]","start":20451461,"end":20487667,"strand":1,"description":"acyl-CoA synthetase medium chain family member 2A [Source:HGNC Symbol;Acc:HGNC:32017]"}, {"versioned_ensembl_gene_id":"ENSG00000237459.6","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"NG31,C6orf25,G6b-B,G6b","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31794876,"end":31802992,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000168310.10","gene_symbol":"IRF2","gene_name":"interferon regulatory factor 2 [Source:HGNC Symbol;Acc:HGNC:6117]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3660","summary":"IRF2 encodes interferon regulatory factor 2, a member of the interferon regulatory transcription factor (IRF) family. IRF2 competitively inhibits the IRF1-mediated transcriptional activation of interferons alpha and beta, and presumably other genes that employ IRF1 for transcription activation. However, IRF2 also functions as a transcriptional activator of histone H4. [provided by RefSeq, Jul 2008]","start":184387713,"end":184474580,"strand":-1,"description":"interferon regulatory factor 2 [Source:HGNC Symbol;Acc:HGNC:6117]"}, {"versioned_ensembl_gene_id":"ENSG00000235626.2","gene_symbol":"KRT18P66","gene_name":"keratin 18 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:48893]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442405","summary":null,"start":30773464,"end":30774732,"strand":1,"description":"keratin 18 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:48893]"}, {"versioned_ensembl_gene_id":"ENSG00000226246.1","gene_symbol":"KRT18P36","gene_name":"keratin 18 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:33405]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442406","summary":null,"start":30799471,"end":30800746,"strand":-1,"description":"keratin 18 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:33405]"}, {"versioned_ensembl_gene_id":"ENSG00000234784.2","gene_symbol":"AL606517.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64918443,"end":64918683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184624.4","gene_symbol":"ZNF72P","gene_name":"zinc finger protein 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:13142]","synonyms":"ZNF72,Cos8","biotype":"unprocessed_pseudogene","ncbi_id":"100287084","summary":null,"start":15326037,"end":15343065,"strand":-1,"description":"zinc finger protein 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:13142]"}, {"versioned_ensembl_gene_id":"ENSG00000171060.10","gene_symbol":"C8orf74","gene_name":"chromosome 8 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:32296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203076","summary":null,"start":10672637,"end":10700593,"strand":1,"description":"chromosome 8 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:32296]"}, {"versioned_ensembl_gene_id":"ENSG00000276411.1","gene_symbol":"AC106875.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11673964,"end":11676925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236097.1","gene_symbol":"BNIP3P2","gene_name":"BCL2 interacting protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39655]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421754","summary":null,"start":15349467,"end":15350043,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39655]"}, {"versioned_ensembl_gene_id":"ENSG00000242539.2","gene_symbol":"AC007620.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179396961,"end":179399191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236831.1","gene_symbol":"YME1L1P1","gene_name":"YME1L1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12844]","synonyms":"YME1L2","biotype":"unprocessed_pseudogene","ncbi_id":"23749","summary":null,"start":15489990,"end":15492564,"strand":1,"description":"YME1L1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12844]"}, {"versioned_ensembl_gene_id":"ENSG00000272699.1","gene_symbol":"AC007620.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179405448,"end":179405944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114450.9","gene_symbol":"GNB4","gene_name":"G protein subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:20731]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59345","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. [provided by RefSeq, Jul 2008]","start":179396089,"end":179451590,"strand":-1,"description":"G protein subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:20731]"}, {"versioned_ensembl_gene_id":"ENSG00000162434.11","gene_symbol":"JAK1","gene_name":"Janus kinase 1 [Source:HGNC Symbol;Acc:HGNC:6190]","synonyms":"JTK3,JAK1B,JAK1A","biotype":"protein_coding","ncbi_id":"3716","summary":"This gene encodes a membrane protein that is a member of a class of protein-tyrosine kinases (PTK) characterized by the presence of a second phosphotransferase-related domain immediately N-terminal to the PTK domain. The encoded kinase phosphorylates STAT proteins (signal transducers and activators of transcription) and plays a key role in interferon-alpha/beta, interferon-gamma, and cytokine signal transduction. This gene plays a crucial role in effecting the expression of genes that mediate inflammation, epithelial remodeling, and metastatic cancer progression. This gene is a key component of the interleukin-6 (IL-6)/JAK1/STAT3 immune and inflammation response and is a therapeutic target for alleviating cytokine storms. The kinase activity of this gene is directly inhibited by the suppressor of cytokine signalling 1 (SOCS1) protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":64833229,"end":64966504,"strand":-1,"description":"Janus kinase 1 [Source:HGNC Symbol;Acc:HGNC:6190]"}, {"versioned_ensembl_gene_id":"ENSG00000274092.1","gene_symbol":"AC106739.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27313387,"end":27314101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107554.16","gene_symbol":"DNMBP","gene_name":"dynamin binding protein [Source:HGNC Symbol;Acc:HGNC:30373]","synonyms":"KIAA1010,ARHGEF36,Tuba","biotype":"protein_coding","ncbi_id":"23268","summary":"This gene encodes a protein belonging to the guanine nucleotide exchange factor family, and which regulates the configuration of cell junctions. It contains multiple binding sites for dynamin and thus links dynamin to actin regulatory proteins. Polymorphisms in this gene have been linked to Alzheimer's disease in some populations, though there are conflicting reports of such linkages in other populations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":99875577,"end":100009919,"strand":-1,"description":"dynamin binding protein [Source:HGNC Symbol;Acc:HGNC:30373]"}, {"versioned_ensembl_gene_id":"ENSG00000130538.4","gene_symbol":"OR11H1","gene_name":"olfactory receptor family 11 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15404]","synonyms":"OR22-1","biotype":"protein_coding","ncbi_id":"81061","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15528158,"end":15529139,"strand":1,"description":"olfactory receptor family 11 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15404]"}, {"versioned_ensembl_gene_id":"ENSG00000272389.1","gene_symbol":"AC008536.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112898023,"end":112898371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256151.1","gene_symbol":"ADGRD1-AS1","gene_name":"ADGRD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53314]","synonyms":"LACAT8","biotype":"lincRNA","ncbi_id":"105755954","summary":null,"start":130990138,"end":130993976,"strand":-1,"description":"ADGRD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53314]"}, {"versioned_ensembl_gene_id":"ENSG00000149452.15","gene_symbol":"SLC22A8","gene_name":"solute carrier family 22 member 8 [Source:HGNC Symbol;Acc:HGNC:10972]","synonyms":"OAT3","biotype":"protein_coding","ncbi_id":"9376","summary":"This gene encodes a protein involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, May 2010]","start":62989154,"end":63015839,"strand":-1,"description":"solute carrier family 22 member 8 [Source:HGNC Symbol;Acc:HGNC:10972]"}, {"versioned_ensembl_gene_id":"ENSG00000258864.1","gene_symbol":"AC008575.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":112827213,"end":112867582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168917.8","gene_symbol":"SLC35G2","gene_name":"solute carrier family 35 member G2 [Source:HGNC Symbol;Acc:HGNC:28480]","synonyms":"MGC3295,DKFZp564K2464,TMEM22","biotype":"protein_coding","ncbi_id":"80723","summary":null,"start":136818647,"end":136855892,"strand":1,"description":"solute carrier family 35 member G2 [Source:HGNC Symbol;Acc:HGNC:28480]"}, {"versioned_ensembl_gene_id":"ENSG00000237299.1","gene_symbol":"AP000534.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15541436,"end":15578006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134982.16","gene_symbol":"APC","gene_name":"APC, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:583]","synonyms":"PPP1R46,DP3,DP2.5,DP2","biotype":"protein_coding","ncbi_id":"324","summary":"This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Mutations in the APC gene have been found to occur in most colorectal cancers. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq, Dec 2019]","start":112707498,"end":112846239,"strand":1,"description":"APC, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:583]"}, {"versioned_ensembl_gene_id":"ENSG00000257658.1","gene_symbol":"AC004217.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112321759,"end":112323089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111058.7","gene_symbol":"ACSS3","gene_name":"acyl-CoA synthetase short chain family member 3 [Source:HGNC Symbol;Acc:HGNC:24723]","synonyms":"FLJ21963","biotype":"protein_coding","ncbi_id":"79611","summary":null,"start":80936414,"end":81261205,"strand":1,"description":"acyl-CoA synthetase short chain family member 3 [Source:HGNC Symbol;Acc:HGNC:24723]"}, {"versioned_ensembl_gene_id":"ENSG00000213727.3","gene_symbol":"AP000533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15572089,"end":15573265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235759.1","gene_symbol":"ARHGAP42P3","gene_name":"Rho GTPase activating protein 42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19327]","synonyms":"OPHN1P1","biotype":"processed_pseudogene","ncbi_id":"266698","summary":null,"start":15550904,"end":15553838,"strand":-1,"description":"Rho GTPase activating protein 42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19327]"}, {"versioned_ensembl_gene_id":"ENSG00000239213.5","gene_symbol":"NCK1-AS1","gene_name":"NCK1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49645]","synonyms":"SLC35G2-AS1","biotype":"antisense_RNA","ncbi_id":"101927597","summary":null,"start":136841726,"end":136862054,"strand":-1,"description":"NCK1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49645]"}, {"versioned_ensembl_gene_id":"ENSG00000173064.12","gene_symbol":"HECTD4","gene_name":"HECT domain E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:26611]","synonyms":"FLJ34154,C12orf51,KIAA0614","biotype":"protein_coding","ncbi_id":"283450","summary":null,"start":112160188,"end":112382439,"strand":-1,"description":"HECT domain E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:26611]"}, {"versioned_ensembl_gene_id":"ENSG00000233408.1","gene_symbol":"AP000534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15557577,"end":15560694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183638.5","gene_symbol":"RP1L1","gene_name":"RP1 like 1 [Source:HGNC Symbol;Acc:HGNC:15946]","synonyms":"DCDC4B","biotype":"protein_coding","ncbi_id":"94137","summary":"This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, and two C-terminal large repetitive regions, both of which contain a high percentage of glutamine and glutamic acid residues. This protein is a retinal-specific protein. Its exact length varies among individuals due to the presence of a 16aa repeat in the first C-terminal repetitive region. The 16aa repeat is encoded by the highly polymorphic 48-bp repeat, and 1-6 copies of the 16aa repeat have been identified in normal individuals. The current reference sequence shown here has a single copy of the 16aa repeat. This protein and the RP1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Mutations in this gene cause occult macular dystrophy (OMD). [provided by RefSeq, Sep 2010]","start":10606349,"end":10712187,"strand":-1,"description":"RP1 like 1 [Source:HGNC Symbol;Acc:HGNC:15946]"}, {"versioned_ensembl_gene_id":"ENSG00000215268.3","gene_symbol":"AP000533.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15562017,"end":15564276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174529.7","gene_symbol":"TMEM81","gene_name":"transmembrane protein 81 [Source:HGNC Symbol;Acc:HGNC:32349]","synonyms":"UNQ2788,MGC75217,KVLA2788,HC3107","biotype":"protein_coding","ncbi_id":"388730","summary":null,"start":205083129,"end":205084460,"strand":-1,"description":"transmembrane protein 81 [Source:HGNC Symbol;Acc:HGNC:32349]"}, {"versioned_ensembl_gene_id":"ENSG00000254344.1","gene_symbol":"LINC01288","gene_name":"long intergenic non-protein coding RNA 1288 [Source:HGNC Symbol;Acc:HGNC:50353]","synonyms":"TCONS_00014671","biotype":"lincRNA","ncbi_id":"103689844","summary":null,"start":34784052,"end":34864798,"strand":1,"description":"long intergenic non-protein coding RNA 1288 [Source:HGNC Symbol;Acc:HGNC:50353]"}, {"versioned_ensembl_gene_id":"ENSG00000230274.1","gene_symbol":"PGAM1P3","gene_name":"phosphoglycerate mutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873887","summary":null,"start":40322715,"end":40323279,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42450]"}, {"versioned_ensembl_gene_id":"ENSG00000282145.1","gene_symbol":"AC243913.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28687420,"end":28691285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223797.5","gene_symbol":"ENTPD3-AS1","gene_name":"ENTPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26710]","synonyms":"FLJ36665","biotype":"antisense_RNA","ncbi_id":"285266","summary":null,"start":40313802,"end":40453329,"strand":-1,"description":"ENTPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26710]"}, {"versioned_ensembl_gene_id":"ENSG00000274870.1","gene_symbol":"OR2T4","gene_name":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]","synonyms":"OR2T4Q","biotype":"protein_coding","ncbi_id":"127074","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248361581,"end":248362627,"strand":1,"description":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]"}, {"versioned_ensembl_gene_id":"ENSG00000243181.2","gene_symbol":"AC087343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34874159,"end":34874633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235479.1","gene_symbol":"RAB9AP4","gene_name":"RAB9A, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38108]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288397","summary":null,"start":18649671,"end":18650279,"strand":1,"description":"RAB9A, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38108]"}, {"versioned_ensembl_gene_id":"ENSG00000284684.1","gene_symbol":"AC092442.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":6064977,"end":6070162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225682.6","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":31957356,"end":31959838,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000273486.1","gene_symbol":"AC096992.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136837338,"end":136839021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282444.1","gene_symbol":"AC243913.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28695142,"end":28702879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275785.1","gene_symbol":"AC015914.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63890030,"end":63890317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225569.1","gene_symbol":"CCT4P2","gene_name":"chaperonin containing TCP1 subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131638","summary":null,"start":65270913,"end":65273019,"strand":1,"description":"chaperonin containing TCP1 subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35141]"}, {"versioned_ensembl_gene_id":"ENSG00000249115.8","gene_symbol":"HAUS5","gene_name":"HAUS augmin like complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:29130]","synonyms":"KIAA0841,dgt5","biotype":"protein_coding","ncbi_id":"23354","summary":"HAUS5 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010]","start":35612744,"end":35625349,"strand":1,"description":"HAUS augmin like complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:29130]"}, {"versioned_ensembl_gene_id":"ENSG00000111452.12","gene_symbol":"ADGRD1","gene_name":"adhesion G protein-coupled receptor D1 [Source:HGNC Symbol;Acc:HGNC:19893]","synonyms":"PGR25,GPR133,DKFZp434B1272","biotype":"protein_coding","ncbi_id":"283383","summary":"The adhesion G-protein-coupled receptors (GPCRs), including GPR133, are membrane-bound proteins with long N termini containing multiple domains. GPCRs, or GPRs, contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins (summary by Bjarnadottir et al., 2004 [PubMed 15203201]).[supplied by OMIM, Nov 2010]","start":130953907,"end":131141469,"strand":1,"description":"adhesion G protein-coupled receptor D1 [Source:HGNC Symbol;Acc:HGNC:19893]"}, {"versioned_ensembl_gene_id":"ENSG00000254342.1","gene_symbol":"AC022616.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43372559,"end":43372677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233872.1","gene_symbol":"AC005033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74618856,"end":74620979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251322.7","gene_symbol":"SHANK3","gene_name":"SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:14294]","synonyms":"SPANK-2,PSAP2,prosap2,KIAA1650","biotype":"protein_coding","ncbi_id":"85358","summary":"This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]","start":50674415,"end":50733298,"strand":1,"description":"SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:14294]"}, {"versioned_ensembl_gene_id":"ENSG00000250637.2","gene_symbol":"AC134698.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43442902,"end":43452912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168907.13","gene_symbol":"PLA2G4F","gene_name":"phospholipase A2 group IVF [Source:HGNC Symbol;Acc:HGNC:27396]","synonyms":"PLA2G4F/Z","biotype":"protein_coding","ncbi_id":"255189","summary":null,"start":42139034,"end":42156636,"strand":-1,"description":"phospholipase A2 group IVF [Source:HGNC Symbol;Acc:HGNC:27396]"}, {"versioned_ensembl_gene_id":"ENSG00000223685.5","gene_symbol":"LINC00571","gene_name":"long intergenic non-protein coding RNA 571 [Source:HGNC Symbol;Acc:HGNC:43721]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874188","summary":null,"start":38050817,"end":38143232,"strand":-1,"description":"long intergenic non-protein coding RNA 571 [Source:HGNC Symbol;Acc:HGNC:43721]"}, {"versioned_ensembl_gene_id":"ENSG00000248573.1","gene_symbol":"PRYP6","gene_name":"PTPN13-like, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38786]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106480721","summary":null,"start":18790709,"end":18791051,"strand":-1,"description":"PTPN13-like, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38786]"}, {"versioned_ensembl_gene_id":"ENSG00000242153.7","gene_symbol":"OFD1P6Y","gene_name":"OFD1 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:13657]","synonyms":"OFDYP6,OFD1PY6,OFD1P6,OFD1P2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"386690","summary":null,"start":18674033,"end":18739197,"strand":1,"description":"OFD1 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:13657]"}, {"versioned_ensembl_gene_id":"ENSG00000252554.1","gene_symbol":"RNU6-861P","gene_name":"RNA, U6 small nuclear 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:47824]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479947","summary":null,"start":129436875,"end":129436980,"strand":-1,"description":"RNA, U6 small nuclear 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:47824]"}, {"versioned_ensembl_gene_id":"ENSG00000273727.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":120354987,"end":120355148,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000222942.1","gene_symbol":"RN7SKP58","gene_name":"RNA, 7SK small nuclear pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:45782]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480850","summary":null,"start":41766615,"end":41766919,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:45782]"}, {"versioned_ensembl_gene_id":"ENSG00000199985.1","gene_symbol":"RNA5SP264","gene_name":"RNA, 5S ribosomal pseudogene 264 [Source:HGNC Symbol;Acc:HGNC:43164]","synonyms":"RN5S264","biotype":"rRNA","ncbi_id":"100873517","summary":null,"start":36764445,"end":36764551,"strand":1,"description":"RNA, 5S ribosomal pseudogene 264 [Source:HGNC Symbol;Acc:HGNC:43164]"}, {"versioned_ensembl_gene_id":"ENSG00000200890.1","gene_symbol":"RNA5SP99","gene_name":"RNA, 5S ribosomal pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:42897]","synonyms":"RN5S99","biotype":"rRNA","ncbi_id":"106478993","summary":null,"start":81496214,"end":81496327,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:42897]"}, {"versioned_ensembl_gene_id":"ENSG00000206710.1","gene_symbol":"RNU6-147P","gene_name":"RNA, U6 small nuclear 147, pseudogene [Source:HGNC Symbol;Acc:HGNC:47110]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480556","summary":null,"start":49972106,"end":49972212,"strand":1,"description":"RNA, U6 small nuclear 147, pseudogene [Source:HGNC Symbol;Acc:HGNC:47110]"}, {"versioned_ensembl_gene_id":"ENSG00000252947.1","gene_symbol":"SCARNA1","gene_name":"small Cajal body-specific RNA 1 [Source:HGNC Symbol;Acc:HGNC:32555]","synonyms":"ACA35","biotype":"scaRNA","ncbi_id":"677774","summary":null,"start":27834401,"end":27834566,"strand":1,"description":"small Cajal body-specific RNA 1 [Source:HGNC Symbol;Acc:HGNC:32555]"}, {"versioned_ensembl_gene_id":"ENSG00000241785.3","gene_symbol":"RN7SL390P","gene_name":"RNA, 7SL, cytoplasmic 390, pseudogene [Source:HGNC Symbol;Acc:HGNC:46406]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479366","summary":null,"start":54255627,"end":54255910,"strand":-1,"description":"RNA, 7SL, cytoplasmic 390, pseudogene [Source:HGNC Symbol;Acc:HGNC:46406]"}, {"versioned_ensembl_gene_id":"ENSG00000222920.1","gene_symbol":"RNA5SP29","gene_name":"RNA, 5S ribosomal pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42605]","synonyms":"RN5S29","biotype":"rRNA","ncbi_id":"100873361","summary":null,"start":51027747,"end":51027852,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42605]"}, {"versioned_ensembl_gene_id":"ENSG00000264910.2","gene_symbol":"RN7SL525P","gene_name":"RNA, 7SL, cytoplasmic 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:46541]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480516","summary":null,"start":58543299,"end":58543578,"strand":-1,"description":"RNA, 7SL, cytoplasmic 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:46541]"}, {"versioned_ensembl_gene_id":"ENSG00000206921.1","gene_symbol":"RNU6-481P","gene_name":"RNA, U6 small nuclear 481, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000277965.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38711821,"end":38712103,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276601.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58785323,"end":58785608,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266747.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31445150,"end":31445248,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251936.1","gene_symbol":"RNA5SP249","gene_name":"RNA, 5S ribosomal pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:43149]","synonyms":"RN5S249","biotype":"rRNA","ncbi_id":"100873505","summary":null,"start":147849884,"end":147849982,"strand":1,"description":"RNA, 5S ribosomal pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:43149]"}, {"versioned_ensembl_gene_id":"ENSG00000206772.1","gene_symbol":"RNU6-44P","gene_name":"RNA, U6 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:34288]","synonyms":"RNU6-44","biotype":"snRNA","ncbi_id":"106478922","summary":null,"start":112352556,"end":112352662,"strand":-1,"description":"RNA, U6 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:34288]"}, {"versioned_ensembl_gene_id":"ENSG00000252297.1","gene_symbol":"RNU6-875P","gene_name":"RNA, U6 small nuclear 875, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000242559.3","gene_symbol":"RN7SL144P","gene_name":"RNA, 7SL, cytoplasmic 144, pseudogene [Source:HGNC Symbol;Acc:HGNC:46160]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480960","summary":null,"start":41683168,"end":41683462,"strand":-1,"description":"RNA, 7SL, cytoplasmic 144, pseudogene [Source:HGNC Symbol;Acc:HGNC:46160]"}, {"versioned_ensembl_gene_id":"ENSG00000265795.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28915634,"end":28915733,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200274.1","gene_symbol":"RNU4-32P","gene_name":"RNA, U4 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46968]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479572","summary":null,"start":109567975,"end":109568115,"strand":-1,"description":"RNA, U4 small nuclear 32, 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Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]","start":25041974,"end":25042040,"strand":1,"description":"small nucleolar RNA, C/D box 109A [Source:HGNC Symbol;Acc:HGNC:32773]"}, {"versioned_ensembl_gene_id":"ENSG00000252950.1","gene_symbol":"RNA5SP490","gene_name":"RNA, 5S ribosomal pseudogene 490 [Source:HGNC Symbol;Acc:HGNC:43390]","synonyms":"RN5S490","biotype":"rRNA","ncbi_id":"100873732","summary":null,"start":32563075,"end":32563210,"strand":1,"description":"RNA, 5S ribosomal pseudogene 490 [Source:HGNC Symbol;Acc:HGNC:43390]"}, {"versioned_ensembl_gene_id":"ENSG00000201048.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10674658,"end":10674768,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207013.1","gene_symbol":"RNU6-804P","gene_name":"RNA, U6 small nuclear 804, pseudogene [Source:HGNC Symbol;Acc:HGNC:47767]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479921","summary":null,"start":86663144,"end":86663250,"strand":-1,"description":"RNA, U6 small nuclear 804, pseudogene [Source:HGNC Symbol;Acc:HGNC:47767]"}, {"versioned_ensembl_gene_id":"ENSG00000252294.1","gene_symbol":"RNU6-589P","gene_name":"RNA, U6 small nuclear 589, pseudogene [Source:HGNC Symbol;Acc:HGNC:47552]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481367","summary":null,"start":102678707,"end":102678813,"strand":-1,"description":"RNA, U6 small nuclear 589, pseudogene [Source:HGNC Symbol;Acc:HGNC:47552]"}, {"versioned_ensembl_gene_id":"ENSG00000281766.2","gene_symbol":"RYBP","gene_name":"RING1 and YY1 binding protein [Source:NCBI gene;Acc:23429]","synonyms":"DEDAF,YEAF1,AAP1,DEDAF,APAP-1,AAP1,YEAF1","biotype":"protein_coding","ncbi_id":"23429","summary":null,"start":72378406,"end":72447301,"strand":-1,"description":"RING1 and YY1 binding protein [Source:NCBI gene;Acc:23429]"}, {"versioned_ensembl_gene_id":"ENSG00000265873.1","gene_symbol":"MIR4289","gene_name":"microRNA 4289 [Source:HGNC Symbol;Acc:HGNC:38278]","synonyms":"hsa-mir-4289","biotype":"miRNA","ncbi_id":"100423015","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88745836,"end":88745905,"strand":-1,"description":"microRNA 4289 [Source:HGNC Symbol;Acc:HGNC:38278]"}, {"versioned_ensembl_gene_id":"ENSG00000206602.1","gene_symbol":"SNORD58A","gene_name":"small nucleolar RNA, C/D box 58A [Source:HGNC Symbol;Acc:HGNC:10208]","synonyms":"U58a,RNU58A","biotype":"snoRNA","ncbi_id":"26791","summary":null,"start":49491283,"end":49491347,"strand":-1,"description":"small nucleolar RNA, C/D box 58A [Source:HGNC Symbol;Acc:HGNC:10208]"}, {"versioned_ensembl_gene_id":"ENSG00000221771.1","gene_symbol":"MIR1205","gene_name":"microRNA 1205 [Source:HGNC Symbol;Acc:HGNC:35271]","synonyms":"MIRN1205,hsa-mir-1205","biotype":"miRNA","ncbi_id":"100302161","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127960633,"end":127960695,"strand":1,"description":"microRNA 1205 [Source:HGNC Symbol;Acc:HGNC:35271]"}, {"versioned_ensembl_gene_id":"ENSG00000275069.1","gene_symbol":"GNAS-AS1_5","gene_name":"GNAS antisense RNA 1 conserved region 5 [Source:RFAM;Acc:RF02131]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58850783,"end":58850903,"strand":1,"description":"GNAS antisense RNA 1 conserved region 5 [Source:RFAM;Acc:RF02131]"}, {"versioned_ensembl_gene_id":"ENSG00000194717.4","gene_symbol":"MIR494","gene_name":"microRNA 494 [Source:HGNC Symbol;Acc:HGNC:32084]","synonyms":"MIRN494,hsa-mir-494","biotype":"miRNA","ncbi_id":"574452","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101029634,"end":101029714,"strand":1,"description":"microRNA 494 [Source:HGNC Symbol;Acc:HGNC:32084]"}, {"versioned_ensembl_gene_id":"ENSG00000263974.2","gene_symbol":"RN7SL121P","gene_name":"RNA, 7SL, cytoplasmic 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:46137]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479265","summary":null,"start":2595019,"end":2595291,"strand":-1,"description":"RNA, 7SL, cytoplasmic 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:46137]"}, {"versioned_ensembl_gene_id":"ENSG00000253119.1","gene_symbol":"HNRNPA3P7","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48496]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421357","summary":null,"start":154337471,"end":154338452,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48496]"}, {"versioned_ensembl_gene_id":"ENSG00000215372.6","gene_symbol":"ZNF705G","gene_name":"zinc finger protein 705G [Source:HGNC Symbol;Acc:HGNC:37134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131980","summary":null,"start":7355517,"end":7385558,"strand":-1,"description":"zinc finger protein 705G [Source:HGNC Symbol;Acc:HGNC:37134]"}, {"versioned_ensembl_gene_id":"ENSG00000264483.1","gene_symbol":"MIR5008","gene_name":"microRNA 5008 [Source:HGNC Symbol;Acc:HGNC:43546]","synonyms":"hsa-mir-5008","biotype":"miRNA","ncbi_id":"100847072","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":227941590,"end":227941683,"strand":-1,"description":"microRNA 5008 [Source:HGNC Symbol;Acc:HGNC:43546]"}, {"versioned_ensembl_gene_id":"ENSG00000264747.1","gene_symbol":"MIR3924","gene_name":"microRNA 3924 [Source:HGNC Symbol;Acc:HGNC:38984]","synonyms":"hsa-mir-3924","biotype":"miRNA","ncbi_id":"100500834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57304479,"end":57304559,"strand":-1,"description":"microRNA 3924 [Source:HGNC Symbol;Acc:HGNC:38984]"}, {"versioned_ensembl_gene_id":"ENSG00000200755.1","gene_symbol":"RNA5SP68","gene_name":"RNA, 5S ribosomal pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:42845]","synonyms":"RN5S68","biotype":"rRNA","ncbi_id":"100873303","summary":null,"start":173969318,"end":173969436,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:42845]"}, {"versioned_ensembl_gene_id":"ENSG00000206870.1","gene_symbol":"RNU6-398P","gene_name":"RNA, U6 small nuclear 398, pseudogene [Source:HGNC Symbol;Acc:HGNC:47361]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479742","summary":null,"start":60974327,"end":60974435,"strand":1,"description":"RNA, U6 small nuclear 398, pseudogene [Source:HGNC Symbol;Acc:HGNC:47361]"}, {"versioned_ensembl_gene_id":"ENSG00000212413.1","gene_symbol":"RNU11-3P","gene_name":"RNA, U11 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:46943]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479562","summary":null,"start":103312436,"end":103312568,"strand":-1,"description":"RNA, U11 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:46943]"}, {"versioned_ensembl_gene_id":"ENSG00000212219.1","gene_symbol":"RNU6-604P","gene_name":"RNA, U6 small nuclear 604, pseudogene [Source:HGNC Symbol;Acc:HGNC:47567]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479833","summary":null,"start":151900275,"end":151900374,"strand":1,"description":"RNA, U6 small nuclear 604, pseudogene [Source:HGNC Symbol;Acc:HGNC:47567]"}, {"versioned_ensembl_gene_id":"ENSG00000275283.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":14938852,"end":14938951,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201672.1","gene_symbol":"SNORD113-4","gene_name":"small nucleolar RNA, C/D box 113-4 [Source:HGNC Symbol;Acc:HGNC:32983]","synonyms":"14q(I-4)","biotype":"snoRNA","ncbi_id":"767564","summary":null,"start":100936491,"end":100936565,"strand":1,"description":"small nucleolar RNA, C/D box 113-4 [Source:HGNC Symbol;Acc:HGNC:32983]"}, {"versioned_ensembl_gene_id":"ENSG00000212409.1","gene_symbol":"RNY4P18","gene_name":"RNA, Ro-associated Y4 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:34068]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379298","summary":null,"start":111097325,"end":111097413,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:34068]"}, {"versioned_ensembl_gene_id":"ENSG00000202273.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6212638,"end":6212740,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201789.1","gene_symbol":"RNU6-1071P","gene_name":"RNA, U6 small nuclear 1071, pseudogene [Source:HGNC Symbol;Acc:HGNC:48034]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481517","summary":null,"start":146288596,"end":146288696,"strand":1,"description":"RNA, U6 small nuclear 1071, pseudogene [Source:HGNC Symbol;Acc:HGNC:48034]"}, {"versioned_ensembl_gene_id":"ENSG00000266751.1","gene_symbol":"MIR3661","gene_name":"microRNA 3661 [Source:HGNC Symbol;Acc:HGNC:38892]","synonyms":"hsa-mir-3661","biotype":"miRNA","ncbi_id":"100500905","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134225757,"end":134225852,"strand":1,"description":"microRNA 3661 [Source:HGNC Symbol;Acc:HGNC:38892]"}, {"versioned_ensembl_gene_id":"ENSG00000238750.1","gene_symbol":"RNU7-27P","gene_name":"RNA, U7 small nuclear 27 pseudogene [Source:HGNC Symbol;Acc:HGNC:34123]","synonyms":"U7.27","biotype":"snRNA","ncbi_id":"100147814","summary":null,"start":128344081,"end":128344142,"strand":1,"description":"RNA, U7 small nuclear 27 pseudogene [Source:HGNC Symbol;Acc:HGNC:34123]"}, {"versioned_ensembl_gene_id":"ENSG00000252660.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62935701,"end":62935802,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222686.1","gene_symbol":"RNU4-72P","gene_name":"RNA, U4 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:47008]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479591","summary":null,"start":85751581,"end":85751753,"strand":1,"description":"RNA, U4 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:47008]"}, {"versioned_ensembl_gene_id":"ENSG00000241789.3","gene_symbol":"RN7SL504P","gene_name":"RNA, 7SL, cytoplasmic 504, pseudogene [Source:HGNC Symbol;Acc:HGNC:46520]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480515","summary":null,"start":51872178,"end":51872464,"strand":1,"description":"RNA, 7SL, cytoplasmic 504, pseudogene [Source:HGNC Symbol;Acc:HGNC:46520]"}, {"versioned_ensembl_gene_id":"ENSG00000252417.1","gene_symbol":"RNU7-179P","gene_name":"RNA, U7 small nuclear 179 pseudogene [Source:HGNC Symbol;Acc:HGNC:45713]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479092","summary":null,"start":15608078,"end":15608145,"strand":-1,"description":"RNA, U7 small nuclear 179 pseudogene [Source:HGNC Symbol;Acc:HGNC:45713]"}, {"versioned_ensembl_gene_id":"ENSG00000266619.1","gene_symbol":"MIR4642","gene_name":"microRNA 4642 [Source:HGNC Symbol;Acc:HGNC:41865]","synonyms":"hsa-mir-4642","biotype":"miRNA","ncbi_id":"100616352","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44435641,"end":44435722,"strand":1,"description":"microRNA 4642 [Source:HGNC Symbol;Acc:HGNC:41865]"}, {"versioned_ensembl_gene_id":"ENSG00000199719.1","gene_symbol":"RN7SKP74","gene_name":"RNA, 7SK small nuclear pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:45798]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479127","summary":null,"start":18295143,"end":18295451,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:45798]"}, {"versioned_ensembl_gene_id":"ENSG00000263834.1","gene_symbol":"MIR4635","gene_name":"microRNA 4635 [Source:HGNC Symbol;Acc:HGNC:41748]","synonyms":"hsa-mir-4635","biotype":"miRNA","ncbi_id":"100616479","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1062896,"end":1062974,"strand":-1,"description":"microRNA 4635 [Source:HGNC Symbol;Acc:HGNC:41748]"}, {"versioned_ensembl_gene_id":"ENSG00000201544.1","gene_symbol":"SNORA16B","gene_name":"small nucleolar RNA, H/ACA box 16B [Source:HGNC Symbol;Acc:HGNC:32606]","synonyms":"U98b","biotype":"snoRNA","ncbi_id":"692157","summary":null,"start":212352816,"end":212352950,"strand":1,"description":"small nucleolar RNA, H/ACA box 16B [Source:HGNC Symbol;Acc:HGNC:32606]"}, {"versioned_ensembl_gene_id":"ENSG00000278333.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85613017,"end":85613186,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000284436.1","gene_symbol":"MIR6869","gene_name":"microRNA 6869 [Source:HGNC Symbol;Acc:HGNC:50056]","synonyms":"hsa-mir-6869","biotype":"miRNA","ncbi_id":"102465524","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1392900,"end":1392961,"strand":-1,"description":"microRNA 6869 [Source:HGNC Symbol;Acc:HGNC:50056]"}, {"versioned_ensembl_gene_id":"ENSG00000200108.1","gene_symbol":"RNU6-774P","gene_name":"RNA, U6 small nuclear 774, pseudogene [Source:HGNC Symbol;Acc:HGNC:47737]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481425","summary":null,"start":84233657,"end":84233763,"strand":1,"description":"RNA, U6 small nuclear 774, pseudogene [Source:HGNC Symbol;Acc:HGNC:47737]"}, {"versioned_ensembl_gene_id":"ENSG00000207734.1","gene_symbol":"MIR517A","gene_name":"microRNA 517a [Source:HGNC Symbol;Acc:HGNC:32111]","synonyms":"hsa-mir-517a,MIRN517A","biotype":"miRNA","ncbi_id":"574479","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53712268,"end":53712354,"strand":1,"description":"microRNA 517a [Source:HGNC Symbol;Acc:HGNC:32111]"}, {"versioned_ensembl_gene_id":"ENSG00000222663.1","gene_symbol":"RNU4-55P","gene_name":"RNA, U4 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:46991]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481189","summary":null,"start":105824634,"end":105824770,"strand":1,"description":"RNA, U4 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:46991]"}, {"versioned_ensembl_gene_id":"ENSG00000278670.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55019324,"end":55043883,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000252370.1","gene_symbol":"RNA5SP438","gene_name":"RNA, 5S ribosomal pseudogene 438 [Source:HGNC Symbol;Acc:HGNC:43338]","synonyms":"RN5S438","biotype":"rRNA","ncbi_id":"100873687","summary":null,"start":34120056,"end":34120167,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 438 [Source:HGNC Symbol;Acc:HGNC:43338]"}, {"versioned_ensembl_gene_id":"ENSG00000263638.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31747708,"end":31747810,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000266195.2","gene_symbol":"RN7SL163P","gene_name":"RNA, 7SL, cytoplasmic 163, pseudogene [Source:HGNC Symbol;Acc:HGNC:46179]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479280","summary":null,"start":17506453,"end":17506728,"strand":1,"description":"RNA, 7SL, cytoplasmic 163, pseudogene [Source:HGNC Symbol;Acc:HGNC:46179]"}, {"versioned_ensembl_gene_id":"ENSG00000242256.3","gene_symbol":"RN7SL57P","gene_name":"RNA, 7SL, cytoplasmic 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:46073]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480484","summary":null,"start":112242550,"end":112242839,"strand":-1,"description":"RNA, 7SL, cytoplasmic 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:46073]"}, {"versioned_ensembl_gene_id":"ENSG00000252758.1","gene_symbol":"RNU6-445P","gene_name":"RNA, U6 small nuclear 445, pseudogene [Source:HGNC Symbol;Acc:HGNC:47408]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479763","summary":null,"start":74857675,"end":74857781,"strand":1,"description":"RNA, U6 small nuclear 445, pseudogene [Source:HGNC Symbol;Acc:HGNC:47408]"}, {"versioned_ensembl_gene_id":"ENSG00000207775.1","gene_symbol":"MIR548A1","gene_name":"microRNA 548a-1 [Source:HGNC Symbol;Acc:HGNC:32796]","synonyms":"MIRN548A1,hsa-mir-548a-1","biotype":"miRNA","ncbi_id":"693125","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18571784,"end":18571880,"strand":1,"description":"microRNA 548a-1 [Source:HGNC Symbol;Acc:HGNC:32796]"}, {"versioned_ensembl_gene_id":"ENSG00000229005.2","gene_symbol":"HNF4A-AS1","gene_name":"HNF4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49505]","synonyms":"uc002xlx","biotype":"antisense_RNA","ncbi_id":"101927219","summary":null,"start":44372746,"end":44395706,"strand":-1,"description":"HNF4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49505]"}, {"versioned_ensembl_gene_id":"ENSG00000229415.9","gene_symbol":"SFTA3","gene_name":"surfactant associated 3 [Source:HGNC Symbol;Acc:HGNC:18387]","synonyms":"SP-H,SFTPH,NANCI,SFTPH,NANCI","biotype":"protein_coding","ncbi_id":"253970","summary":null,"start":36473288,"end":36513829,"strand":-1,"description":"surfactant associated 3 [Source:HGNC Symbol;Acc:HGNC:18387]"}, {"versioned_ensembl_gene_id":"ENSG00000207825.1","gene_symbol":"MIR519B","gene_name":"microRNA 519b [Source:HGNC Symbol;Acc:HGNC:32101]","synonyms":"MIRN519B,hsa-mir-519b","biotype":"miRNA","ncbi_id":"574469","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53695213,"end":53695293,"strand":1,"description":"microRNA 519b [Source:HGNC Symbol;Acc:HGNC:32101]"}, {"versioned_ensembl_gene_id":"ENSG00000207946.3","gene_symbol":"MIR516B1","gene_name":"microRNA 516b-1 [Source:HGNC Symbol;Acc:HGNC:32122]","synonyms":"MIRN516B1,MIRN516-4,hsa-mir-516b-1,hsa-mir-516-4","biotype":"miRNA","ncbi_id":"574490","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53736845,"end":53736934,"strand":1,"description":"microRNA 516b-1 [Source:HGNC Symbol;Acc:HGNC:32122]"}, {"versioned_ensembl_gene_id":"ENSG00000207942.2","gene_symbol":"MIR136","gene_name":"microRNA 136 [Source:HGNC Symbol;Acc:HGNC:31522]","synonyms":"MIRN136,hsa-mir-136","biotype":"miRNA","ncbi_id":"406927","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100884702,"end":100884783,"strand":1,"description":"microRNA 136 [Source:HGNC Symbol;Acc:HGNC:31522]"}, {"versioned_ensembl_gene_id":"ENSG00000207361.1","gene_symbol":"RNU6-178P","gene_name":"RNA, U6 small nuclear 178, pseudogene [Source:HGNC Symbol;Acc:HGNC:47141]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479645","summary":null,"start":28416448,"end":28416551,"strand":1,"description":"RNA, U6 small nuclear 178, pseudogene [Source:HGNC Symbol;Acc:HGNC:47141]"}, {"versioned_ensembl_gene_id":"ENSG00000252618.1","gene_symbol":"RNA5SP441","gene_name":"RNA, 5S ribosomal pseudogene 441 [Source:HGNC Symbol;Acc:HGNC:43341]","synonyms":"RN5S441","biotype":"rRNA","ncbi_id":"100873689","summary":null,"start":40374089,"end":40374176,"strand":1,"description":"RNA, 5S ribosomal pseudogene 441 [Source:HGNC Symbol;Acc:HGNC:43341]"}, {"versioned_ensembl_gene_id":"ENSG00000251748.1","gene_symbol":"RNU4ATAC11P","gene_name":"RNA, U4atac small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46897]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481158","summary":null,"start":33868540,"end":33868665,"strand":1,"description":"RNA, U4atac small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46897]"}, {"versioned_ensembl_gene_id":"ENSG00000239820.3","gene_symbol":"RN7SL213P","gene_name":"RNA, 7SL, cytoplasmic 213, pseudogene [Source:HGNC Symbol;Acc:HGNC:46229]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480979","summary":null,"start":67751228,"end":67751544,"strand":-1,"description":"RNA, 7SL, cytoplasmic 213, pseudogene [Source:HGNC Symbol;Acc:HGNC:46229]"}, {"versioned_ensembl_gene_id":"ENSG00000251952.1","gene_symbol":"RNU6-1219P","gene_name":"RNA, U6 small nuclear 1219, pseudogene [Source:HGNC Symbol;Acc:HGNC:48182]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480649","summary":null,"start":29191697,"end":29191808,"strand":-1,"description":"RNA, U6 small nuclear 1219, pseudogene [Source:HGNC Symbol;Acc:HGNC:48182]"}, {"versioned_ensembl_gene_id":"ENSG00000222428.1","gene_symbol":"RNA5SP231","gene_name":"RNA, 5S ribosomal pseudogene 231 [Source:HGNC Symbol;Acc:HGNC:43131]","synonyms":"RN5S231","biotype":"rRNA","ncbi_id":"100873489","summary":null,"start":68723911,"end":68724048,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 231 [Source:HGNC Symbol;Acc:HGNC:43131]"}, {"versioned_ensembl_gene_id":"ENSG00000200680.1","gene_symbol":"SNORD115-4","gene_name":"small nucleolar RNA, C/D box 115-4 [Source:HGNC Symbol;Acc:HGNC:33023]","synonyms":"HBII-52-4","biotype":"snoRNA","ncbi_id":"100033441","summary":null,"start":25176832,"end":25176913,"strand":1,"description":"small nucleolar RNA, C/D box 115-4 [Source:HGNC Symbol;Acc:HGNC:33023]"}, {"versioned_ensembl_gene_id":"ENSG00000212455.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":18040606,"end":18040733,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000199562.1","gene_symbol":"RNU6-37P","gene_name":"RNA, U6 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:34281]","synonyms":"RNU6-37","biotype":"snRNA","ncbi_id":"106478920","summary":null,"start":10298966,"end":10299072,"strand":1,"description":"RNA, U6 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:34281]"}, {"versioned_ensembl_gene_id":"ENSG00000277415.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30053279,"end":30053354,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000249020.1","gene_symbol":"SNORA58","gene_name":"small nucleolar RNA, H/ACA box 58 [Source:HGNC Symbol;Acc:HGNC:32652]","synonyms":"SNORA58B,ACA58","biotype":"snoRNA","ncbi_id":"677836","summary":null,"start":131479097,"end":131479233,"strand":-1,"description":"small nucleolar RNA, H/ACA box 58 [Source:HGNC Symbol;Acc:HGNC:32652]"}, {"versioned_ensembl_gene_id":"ENSG00000277771.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49846456,"end":49846720,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000221187.1","gene_symbol":"MIR548M","gene_name":"microRNA 548m [Source:HGNC Symbol;Acc:HGNC:35331]","synonyms":"MIRN548M,hsa-mir-548m","biotype":"miRNA","ncbi_id":"100313772","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95063141,"end":95063226,"strand":-1,"description":"microRNA 548m [Source:HGNC Symbol;Acc:HGNC:35331]"}, {"versioned_ensembl_gene_id":"ENSG00000275752.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54264578,"end":54264680,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000159915.12","gene_symbol":"ZNF233","gene_name":"zinc finger protein 233 [Source:HGNC Symbol;Acc:HGNC:30946]","synonyms":"FLJ38032","biotype":"protein_coding","ncbi_id":"353355","summary":null,"start":44259880,"end":44275317,"strand":1,"description":"zinc finger protein 233 [Source:HGNC Symbol;Acc:HGNC:30946]"}, {"versioned_ensembl_gene_id":"ENSG00000207816.1","gene_symbol":"MIR124-2","gene_name":"microRNA 124-2 [Source:HGNC Symbol;Acc:HGNC:31503]","synonyms":"MIRN124A2,MIRN124-2,hsa-mir-124a-2,hsa-mir-124-2","biotype":"miRNA","ncbi_id":"406908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64379149,"end":64379257,"strand":1,"description":"microRNA 124-2 [Source:HGNC Symbol;Acc:HGNC:31503]"}, {"versioned_ensembl_gene_id":"ENSG00000263575.1","gene_symbol":"MIR4665","gene_name":"microRNA 4665 [Source:HGNC Symbol;Acc:HGNC:41696]","synonyms":"hsa-mir-4665","biotype":"miRNA","ncbi_id":"100616288","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6007826,"end":6007904,"strand":1,"description":"microRNA 4665 [Source:HGNC Symbol;Acc:HGNC:41696]"}, {"versioned_ensembl_gene_id":"ENSG00000263573.1","gene_symbol":"MIR4270","gene_name":"microRNA 4270 [Source:HGNC Symbol;Acc:HGNC:38377]","synonyms":"hsa-mir-4270","biotype":"miRNA","ncbi_id":"100422868","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15496239,"end":15496308,"strand":-1,"description":"microRNA 4270 [Source:HGNC Symbol;Acc:HGNC:38377]"}, {"versioned_ensembl_gene_id":"ENSG00000275803.1","gene_symbol":"RN7SL736P","gene_name":"RNA, 7SL, cytoplasmic 736, pseudogene [Source:HGNC Symbol;Acc:HGNC:46752]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080652","summary":null,"start":90293939,"end":90294207,"strand":1,"description":"RNA, 7SL, cytoplasmic 736, pseudogene [Source:HGNC Symbol;Acc:HGNC:46752]"}, {"versioned_ensembl_gene_id":"ENSG00000207987.1","gene_symbol":"MIR518E","gene_name":"microRNA 518e [Source:HGNC Symbol;Acc:HGNC:32119]","synonyms":"MIRN518E,hsa-mir-518e","biotype":"miRNA","ncbi_id":"574487","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53729838,"end":53729925,"strand":1,"description":"microRNA 518e [Source:HGNC Symbol;Acc:HGNC:32119]"}, {"versioned_ensembl_gene_id":"ENSG00000264089.1","gene_symbol":"MIR3681","gene_name":"microRNA 3681 [Source:HGNC Symbol;Acc:HGNC:38994]","synonyms":"hsa-mir-3681","biotype":"miRNA","ncbi_id":"100500884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12199130,"end":12199201,"strand":1,"description":"microRNA 3681 [Source:HGNC Symbol;Acc:HGNC:38994]"}, {"versioned_ensembl_gene_id":"ENSG00000276181.1","gene_symbol":"MIR6794","gene_name":"microRNA 6794 [Source:HGNC Symbol;Acc:HGNC:50117]","synonyms":"hsa-mir-6794","biotype":"miRNA","ncbi_id":"102466196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12852260,"end":12852327,"strand":1,"description":"microRNA 6794 [Source:HGNC Symbol;Acc:HGNC:50117]"}, {"versioned_ensembl_gene_id":"ENSG00000230076.1","gene_symbol":"RPL10P6","gene_name":"ribosomal protein L10 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52343]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285176","summary":null,"start":214847128,"end":214847445,"strand":1,"description":"ribosomal protein L10 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52343]"}, {"versioned_ensembl_gene_id":"ENSG00000184659.5","gene_symbol":"FOXD4L4","gene_name":"forkhead box D4 like 4 [Source:HGNC Symbol;Acc:HGNC:23762]","synonyms":"OTTHUMG00000013337,FOXD4L2,bA460E7.2,OTTHUMG00000066752","biotype":"protein_coding","ncbi_id":"349334","summary":null,"start":65736555,"end":65738784,"strand":1,"description":"forkhead box D4 like 4 [Source:HGNC Symbol;Acc:HGNC:23762]"}, {"versioned_ensembl_gene_id":"ENSG00000280103.1","gene_symbol":"AC007792.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3355554,"end":3355955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278098.1","gene_symbol":"MIR7973-1","gene_name":"microRNA 7973-1 [Source:HGNC Symbol;Acc:HGNC:50040]","synonyms":"hsa-mir-7973-1","biotype":"miRNA","ncbi_id":"102466250","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51314034,"end":51314109,"strand":1,"description":"microRNA 7973-1 [Source:HGNC Symbol;Acc:HGNC:50040]"}, {"versioned_ensembl_gene_id":"ENSG00000258577.1","gene_symbol":"SNRPGP1","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20033]","synonyms":"SNRPGP","biotype":"processed_pseudogene","ncbi_id":"326272","summary":null,"start":50571919,"end":50572140,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20033]"}, {"versioned_ensembl_gene_id":"ENSG00000283879.1","gene_symbol":"AC132825.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22519195,"end":22519504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255870.1","gene_symbol":"AP003170.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113789242,"end":113790027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283045.1","gene_symbol":"AC103703.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44486153,"end":44486815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250668.1","gene_symbol":"LINC02123","gene_name":"long intergenic non-protein coding RNA 2123 [Source:HGNC Symbol;Acc:HGNC:52980]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929261","summary":null,"start":7346986,"end":7347977,"strand":-1,"description":"long intergenic non-protein coding RNA 2123 [Source:HGNC Symbol;Acc:HGNC:52980]"}, {"versioned_ensembl_gene_id":"ENSG00000248775.1","gene_symbol":"AC091951.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7287924,"end":7288477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090612.20","gene_symbol":"ZNF268","gene_name":"zinc finger protein 268 [Source:HGNC Symbol;Acc:HGNC:13061]","synonyms":"HZF3","biotype":"protein_coding","ncbi_id":"10795","summary":null,"start":133181409,"end":133214831,"strand":1,"description":"zinc finger protein 268 [Source:HGNC Symbol;Acc:HGNC:13061]"}, {"versioned_ensembl_gene_id":"ENSG00000256825.4","gene_symbol":"AC026786.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":133130984,"end":133202369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130720.12","gene_symbol":"FIBCD1","gene_name":"fibrinogen C domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25922]","synonyms":"FLJ14810","biotype":"protein_coding","ncbi_id":"84929","summary":"FIBCD1 is a conserved type II transmembrane endocytic receptor that binds chitin and is located primarily in the intestinal brush border (Schlosser et al., 2009 [PubMed 19710473]).[supplied by OMIM, Apr 2010]","start":130902438,"end":130939286,"strand":-1,"description":"fibrinogen C domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25922]"}, {"versioned_ensembl_gene_id":"ENSG00000173914.11","gene_symbol":"RBM4B","gene_name":"RNA binding motif protein 4B [Source:HGNC Symbol;Acc:HGNC:28842]","synonyms":"ZCRB3B,ZCCHC21B,ZCCHC15,RBM4L,RBM30,MGC10871","biotype":"protein_coding","ncbi_id":"83759","summary":null,"start":66664998,"end":66677921,"strand":-1,"description":"RNA binding motif protein 4B [Source:HGNC Symbol;Acc:HGNC:28842]"}, {"versioned_ensembl_gene_id":"ENSG00000066027.11","gene_symbol":"PPP2R5A","gene_name":"protein phosphatase 2 regulatory subunit B'alpha [Source:HGNC Symbol;Acc:HGNC:9309]","synonyms":"B56alpha,B56A,PR61A","biotype":"protein_coding","ncbi_id":"5525","summary":"The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes an alpha isoform of the regulatory subunit B56 subfamily. Alternative transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":212285537,"end":212361863,"strand":1,"description":"protein phosphatase 2 regulatory subunit B'alpha [Source:HGNC Symbol;Acc:HGNC:9309]"}, {"versioned_ensembl_gene_id":"ENSG00000184154.13","gene_symbol":"LRTOMT","gene_name":"leucine rich transmembrane and O-methyltransferase domain containing [Source:HGNC Symbol;Acc:HGNC:25033]","synonyms":"CFAP111,LRRC51,DFNB63,COMT2","biotype":"protein_coding","ncbi_id":"220074","summary":"This locus represents naturally occurring readthrough transcription between the neighboring LRRC51 (leucine-rich repeat containing 51) and TOMT (transmembrane O-methyltransferase) genes on chromosome 11. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. Multiple reports implicate mutations in this gene in nonsyndromic deafness.[provided by RefSeq, Feb 2021]","start":72080331,"end":72110782,"strand":1,"description":"leucine rich transmembrane and O-methyltransferase domain containing [Source:HGNC Symbol;Acc:HGNC:25033]"}, {"versioned_ensembl_gene_id":"ENSG00000165060.11","gene_symbol":"FXN","gene_name":"frataxin [Source:HGNC Symbol;Acc:HGNC:3951]","synonyms":"X25,FRDA,FARR,FA,CyaY","biotype":"protein_coding","ncbi_id":"2395","summary":"This nuclear gene encodes a mitochondrial protein which belongs to the FRATAXIN family. The protein functions in regulating mitochondrial iron transport and respiration. The expansion of intronic trinucleotide repeat GAA from 8-33 repeats to >90 repeats results in Friedreich ataxia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":69035259,"end":69100178,"strand":1,"description":"frataxin [Source:HGNC Symbol;Acc:HGNC:3951]"}, {"versioned_ensembl_gene_id":"ENSG00000127152.17","gene_symbol":"BCL11B","gene_name":"B-cell CLL/lymphoma 11B [Source:HGNC Symbol;Acc:HGNC:13222]","synonyms":"CTIP-2,ZNF856B,hRIT1-alpha,CTIP2","biotype":"protein_coding","ncbi_id":"64919","summary":"This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function of this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":99169287,"end":99271524,"strand":-1,"description":"B-cell CLL/lymphoma 11B [Source:HGNC Symbol;Acc:HGNC:13222]"}, {"versioned_ensembl_gene_id":"ENSG00000248930.1","gene_symbol":"AC020893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73020700,"end":73021279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251467.1","gene_symbol":"AC020893.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72996920,"end":72997642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265916.1","gene_symbol":"AC015818.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20532248,"end":20532881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278456.1","gene_symbol":"AC015712.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100888472,"end":100889106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273189.1","gene_symbol":"AC010619.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":49474586,"end":49487637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262098.1","gene_symbol":"AC127496.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81023545,"end":81025503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259579.1","gene_symbol":"AC087762.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100716249,"end":100828497,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242199.1","gene_symbol":"AC022336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124733418,"end":124733754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083097.14","gene_symbol":"DOPEY1","gene_name":"dopey family member 1 [Source:HGNC Symbol;Acc:HGNC:21194]","synonyms":"KIAA1117,dJ202D23.2","biotype":"protein_coding","ncbi_id":"23033","summary":null,"start":83067666,"end":83171350,"strand":1,"description":"dopey family member 1 [Source:HGNC Symbol;Acc:HGNC:21194]"}, {"versioned_ensembl_gene_id":"ENSG00000165501.16","gene_symbol":"LRR1","gene_name":"leucine rich repeat protein 1 [Source:HGNC Symbol;Acc:HGNC:19742]","synonyms":"PPIL5,MGC20689,LRR-1","biotype":"protein_coding","ncbi_id":"122769","summary":"The protein encoded by this gene contains a leucine-rich repeat (LRR). It specifically interacts with TNFRSF9/4-1BB, a member of the tumor necrosis factor receptor (TNFR) superfamily. Overexpression of this gene suppresses the activation of NF-kappa B induced by TNFRSF9 or TNF receptor-associated factor 2 (TRAF2), which suggests that this protein is a negative regulator of TNFRSF9-mediated signaling cascades. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011]","start":49598697,"end":49614672,"strand":1,"description":"leucine rich repeat protein 1 [Source:HGNC Symbol;Acc:HGNC:19742]"}, {"versioned_ensembl_gene_id":"ENSG00000281928.1","gene_symbol":"AC247036.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106207374,"end":106209342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013375.15","gene_symbol":"PGM3","gene_name":"phosphoglucomutase 3 [Source:HGNC Symbol;Acc:HGNC:8907]","synonyms":"PAGM,DKFZP434B187,AGM1","biotype":"protein_coding","ncbi_id":"5238","summary":"This gene encodes a member of the phosphohexose mutase family. The encoded protein mediates both glycogen formation and utilization by catalyzing the interconversion of glucose-1-phosphate and glucose-6-phosphate. A non-synonymous single nucleotide polymorphism in this gene may play a role in resistance to diabetic nephropathy and neuropathy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":83161150,"end":83193936,"strand":-1,"description":"phosphoglucomutase 3 [Source:HGNC Symbol;Acc:HGNC:8907]"}, {"versioned_ensembl_gene_id":"ENSG00000260369.2","gene_symbol":"AC120024.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80453735,"end":80454729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258868.1","gene_symbol":"AL110505.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49057713,"end":49077505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107130.9","gene_symbol":"NCS1","gene_name":"neuronal calcium sensor 1 [Source:HGNC Symbol;Acc:HGNC:3953]","synonyms":"NCS-1,FREQ","biotype":"protein_coding","ncbi_id":"23413","summary":"This gene is a member of the neuronal calcium sensor gene family, which encode calcium-binding proteins expressed predominantly in neurons. The protein encoded by this gene regulates G protein-coupled receptor phosphorylation in a calcium-dependent manner and can substitute for calmodulin. The protein is associated with secretory granules and modulates synaptic transmission and synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":130172578,"end":130237304,"strand":1,"description":"neuronal calcium sensor 1 [Source:HGNC Symbol;Acc:HGNC:3953]"}, {"versioned_ensembl_gene_id":"ENSG00000274137.2","gene_symbol":"MYOM2","gene_name":"myomesin 2 [Source:HGNC Symbol;Acc:HGNC:7614]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9172","summary":"The giant protein titin, together with its associated proteins, interconnects the major structure of sarcomeres, the M bands and Z discs. The C-terminal end of the titin string extends into the M line, where it binds tightly to M-band constituents of apparent molecular masses of 190 kD and 165 kD. The predicted MYOM2 protein contains 1,465 amino acids. Like MYOM1, MYOM2 has a unique N-terminal domain followed by 12 repeat domains with strong homology to either fibronectin type III or immunoglobulin C2 domains. Protein sequence comparisons suggested that the MYOM2 protein and bovine M protein are identical. [provided by RefSeq, Jul 2008]","start":2044989,"end":2165303,"strand":1,"description":"myomesin 2 [Source:HGNC Symbol;Acc:HGNC:7614]"}, {"versioned_ensembl_gene_id":"ENSG00000246394.7","gene_symbol":"AC073911.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133030389,"end":133037222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220804.8","gene_symbol":"LINC01881","gene_name":"long intergenic non-protein coding RNA 1881 [Source:HGNC Symbol;Acc:HGNC:52700]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728323","summary":null,"start":242088633,"end":242160153,"strand":1,"description":"long intergenic non-protein coding RNA 1881 [Source:HGNC Symbol;Acc:HGNC:52700]"}, {"versioned_ensembl_gene_id":"ENSG00000189423.11","gene_symbol":"USP32P3","gene_name":"ubiquitin specific peptidase 32 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43576]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"347716","summary":null,"start":20415547,"end":20431008,"strand":1,"description":"ubiquitin specific peptidase 32 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43576]"}, {"versioned_ensembl_gene_id":"ENSG00000224958.5","gene_symbol":"PGM5-AS1","gene_name":"PGM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44181]","synonyms":"FAM233A","biotype":"antisense_RNA","ncbi_id":"572558","summary":null,"start":68355189,"end":68357852,"strand":-1,"description":"PGM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44181]"}, {"versioned_ensembl_gene_id":"ENSG00000148358.19","gene_symbol":"GPR107","gene_name":"G protein-coupled receptor 107 [Source:HGNC Symbol;Acc:HGNC:17830]","synonyms":"RP11-88G17,LUSTR1,KIAA1624,FLJ20998","biotype":"protein_coding","ncbi_id":"57720","summary":null,"start":130053426,"end":130140169,"strand":1,"description":"G protein-coupled receptor 107 [Source:HGNC Symbol;Acc:HGNC:17830]"}, {"versioned_ensembl_gene_id":"ENSG00000233178.7","gene_symbol":"AL161457.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68393881,"end":68406500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273466.1","gene_symbol":"AC012510.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":218633256,"end":218634014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132716.18","gene_symbol":"DCAF8","gene_name":"DDB1 and CUL4 associated factor 8 [Source:HGNC Symbol;Acc:HGNC:24891]","synonyms":"WDR42A,H326,FLJ35857","biotype":"protein_coding","ncbi_id":"50717","summary":"This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddb1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2009]","start":160215715,"end":160262531,"strand":-1,"description":"DDB1 and CUL4 associated factor 8 [Source:HGNC Symbol;Acc:HGNC:24891]"}, {"versioned_ensembl_gene_id":"ENSG00000282191.1","gene_symbol":"AC125453.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2033484,"end":2039347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248371.5","gene_symbol":"LINC02056","gene_name":"long intergenic non-protein coding RNA 2056 [Source:HGNC Symbol;Acc:HGNC:52898]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102477328","summary":null,"start":72574120,"end":72660669,"strand":-1,"description":"long intergenic non-protein coding RNA 2056 [Source:HGNC Symbol;Acc:HGNC:52898]"}, {"versioned_ensembl_gene_id":"ENSG00000261120.1","gene_symbol":"AL133299.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59919423,"end":59920339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037757.13","gene_symbol":"MRI1","gene_name":"methylthioribose-1-phosphate isomerase 1 [Source:HGNC Symbol;Acc:HGNC:28469]","synonyms":"mtnA,MRDI,MGC3207,Ypr118w","biotype":"protein_coding","ncbi_id":"84245","summary":"This enzyme functions in the methionine salvage pathway by catalyzing the interconversion of methylthioribose-1-phosphate and methythioribulose-1-phosphate. Elevated expression of the encoded protein is associated with metastatic melanoma and this protein promotes melanoma cell invasion independent of its enzymatic activity. Mutations in this gene may be associated with vanishing white matter disease (VMWD). [provided by RefSeq, Jul 2016]","start":13764532,"end":13774282,"strand":1,"description":"methylthioribose-1-phosphate isomerase 1 [Source:HGNC Symbol;Acc:HGNC:28469]"}, {"versioned_ensembl_gene_id":"ENSG00000150779.11","gene_symbol":"TIMM8B","gene_name":"translocase of inner mitochondrial membrane 8 homolog B [Source:HGNC Symbol;Acc:HGNC:11818]","synonyms":"TIM8B,MGC117373,MGC102866,FLJ21744,DDP2","biotype":"protein_coding","ncbi_id":"26521","summary":"This gene encodes a member of a well-conserved family of proteins with similarity to yeast Tim mitochondrial import proteins. This gene is encoded by a nuclear gene and is transported into the intermembrane space of the mitochondrion. When formed into complexes, these proteins guide membrane-spanning proteins across the mitochondrial intermembrane space before they are added into the mitochondrial inner membrane. This gene is adjacent to succinate dehydrogenase, subunit D (SDHD), in which mutations have been found in affected members of families with hereditary paraganglioma.[provided by RefSeq, Aug 2009]","start":112084800,"end":112086798,"strand":-1,"description":"translocase of inner mitochondrial membrane 8 homolog B [Source:HGNC Symbol;Acc:HGNC:11818]"}, {"versioned_ensembl_gene_id":"ENSG00000099341.11","gene_symbol":"PSMD8","gene_name":"proteasome 26S subunit, non-ATPase 8 [Source:HGNC Symbol;Acc:HGNC:9566]","synonyms":"p31,Nin1p,HYPF,HIP6,S14,Rpn12","biotype":"protein_coding","ncbi_id":"5714","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. A pseudogene has been identified on chromosome 1. [provided by RefSeq, Jul 2008]","start":38374536,"end":38383824,"strand":1,"description":"proteasome 26S subunit, non-ATPase 8 [Source:HGNC Symbol;Acc:HGNC:9566]"}, {"versioned_ensembl_gene_id":"ENSG00000274305.4","gene_symbol":"LENG8","gene_name":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]","synonyms":"pp13842,MGC40108,KIAA1932","biotype":"protein_coding","ncbi_id":"114823","summary":null,"start":54379038,"end":54392337,"strand":1,"description":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]"}, {"versioned_ensembl_gene_id":"ENSG00000258605.1","gene_symbol":"DYNLL1P2","gene_name":"dynein light chain LC8-type 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20724]","synonyms":"DNCL1P2","biotype":"processed_pseudogene","ncbi_id":"731308","summary":null,"start":81412970,"end":81413239,"strand":1,"description":"dynein light chain LC8-type 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20724]"}, {"versioned_ensembl_gene_id":"ENSG00000204370.9","gene_symbol":"SDHD","gene_name":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]","synonyms":"cybS,PGL1,PGL","biotype":"protein_coding","ncbi_id":"6392","summary":"This gene encodes a member of complex II of the respiratory chain, which is responsible for the oxidation of succinate. The encoded protein is one of two integral membrane proteins anchoring the complex to the matrix side of the mitochondrial inner membrane. Mutations in this gene are associated with the formation of tumors, including hereditary paraganglioma. Transmission of disease occurs almost exclusively through the paternal allele, suggesting that this locus may be maternally imprinted. There are pseudogenes for this gene on chromosomes 1, 2, 3, 7, and 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]","start":112086773,"end":112120013,"strand":1,"description":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]"}, {"versioned_ensembl_gene_id":"ENSG00000214264.4","gene_symbol":"KCTD9P4","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422242","summary":null,"start":112180773,"end":112183191,"strand":1,"description":"potassium channel tetramerization domain containing 9 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49913]"}, {"versioned_ensembl_gene_id":"ENSG00000101331.15","gene_symbol":"CCM2L","gene_name":"CCM2 like scaffolding protein [Source:HGNC Symbol;Acc:HGNC:16153]","synonyms":"dJ310O13.5,C20orf160","biotype":"protein_coding","ncbi_id":"140706","summary":null,"start":32010450,"end":32032180,"strand":1,"description":"CCM2 like scaffolding protein [Source:HGNC Symbol;Acc:HGNC:16153]"}, {"versioned_ensembl_gene_id":"ENSG00000263494.1","gene_symbol":"AC004702.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20185082,"end":20322973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173918.14","gene_symbol":"C1QTNF1","gene_name":"C1q and TNF related 1 [Source:HGNC Symbol;Acc:HGNC:14324]","synonyms":"FLJ90694,CTRP1,ZSIG37,GIP","biotype":"protein_coding","ncbi_id":"114897","summary":null,"start":79022814,"end":79049788,"strand":1,"description":"C1q and TNF related 1 [Source:HGNC Symbol;Acc:HGNC:14324]"}, {"versioned_ensembl_gene_id":"ENSG00000254638.1","gene_symbol":"AP002884.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112165197,"end":112172606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136827.11","gene_symbol":"TOR1A","gene_name":"torsin family 1 member A [Source:HGNC Symbol;Acc:HGNC:3098]","synonyms":"DYT1,DQ2","biotype":"protein_coding","ncbi_id":"1861","summary":"The protein encoded by this gene is a member of the AAA family of adenosine triphosphatases (ATPases), is related to the Clp protease/heat shock family and is expressed prominently in the substantia nigra pars compacta. Mutations in this gene result in the autosomal dominant disorder, torsion dystonia 1. [provided by RefSeq, Jul 2008]","start":129812944,"end":129824134,"strand":-1,"description":"torsin family 1 member A [Source:HGNC Symbol;Acc:HGNC:3098]"}, {"versioned_ensembl_gene_id":"ENSG00000254293.1","gene_symbol":"AC026688.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154483917,"end":154486150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262075.3","gene_symbol":"DKFZP434A062","gene_name":"uncharacterized LOC26102 [Source:NCBI gene;Acc:26102]","synonyms":null,"biotype":"lincRNA","ncbi_id":"26102","summary":null,"start":136322303,"end":136327323,"strand":-1,"description":"uncharacterized LOC26102 [Source:NCBI gene;Acc:26102]"}, {"versioned_ensembl_gene_id":"ENSG00000259381.2","gene_symbol":"AC090695.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100645434,"end":100646655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156345.17","gene_symbol":"CDK20","gene_name":"cyclin dependent kinase 20 [Source:HGNC Symbol;Acc:HGNC:21420]","synonyms":"p42,CCRK","biotype":"protein_coding","ncbi_id":"23552","summary":"The protein encoded by this gene contains a kinase domain most closely related to the cyclin-dependent protein kinases. The encoded kinase may activate cyclin-dependent kinase 2 and is involved in cell growth. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Dec 2009]","start":87966441,"end":87974753,"strand":-1,"description":"cyclin dependent kinase 20 [Source:HGNC Symbol;Acc:HGNC:21420]"}, {"versioned_ensembl_gene_id":"ENSG00000226355.1","gene_symbol":"AL353803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129438216,"end":129439118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267624.1","gene_symbol":"AC087645.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78211618,"end":78211908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284625.1","gene_symbol":"AP000867.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71639551,"end":71639769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126790.11","gene_symbol":"L3HYPDH","gene_name":"trans-L-3-hydroxyproline dehydratase [Source:HGNC Symbol;Acc:HGNC:20488]","synonyms":"C14orf149,FLJ25436","biotype":"protein_coding","ncbi_id":"112849","summary":"The protein encoded by this gene is a dehydratase that converts trans-3-hydroxy-L-proline to delta(1)-pyrroline-2-carboxylate. This enzyme may function to degrade dietary proteins that contain trans-3-hydroxy-L-proline as well as other proteins such as collagen IV. The encoded protein can be converted to an epimerase by changing a threonine to a cysteine at a catalytic site. [provided by RefSeq, Sep 2016]","start":59460363,"end":59484430,"strand":-1,"description":"trans-L-3-hydroxyproline dehydratase [Source:HGNC Symbol;Acc:HGNC:20488]"}, {"versioned_ensembl_gene_id":"ENSG00000254975.1","gene_symbol":"AP001189.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76675079,"end":76703195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136856.17","gene_symbol":"SLC2A8","gene_name":"solute carrier family 2 member 8 [Source:HGNC Symbol;Acc:HGNC:13812]","synonyms":"GLUTX1,GLUT8","biotype":"protein_coding","ncbi_id":"29988","summary":"This gene belongs to the solute carrier 2A family, which includes intracellular glucose transporters. Based on sequence comparison, the glucose transporters are grouped into three classes and this gene is a member of class II. The encoded protein, like other members of the family, contains several conserved residues and motifs and 12 transmembrane domains with both amino and carboxyl ends being on the cytosolic side of the membrane. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]","start":127397138,"end":127408424,"strand":1,"description":"solute carrier family 2 member 8 [Source:HGNC Symbol;Acc:HGNC:13812]"}, {"versioned_ensembl_gene_id":"ENSG00000215795.2","gene_symbol":"AL390728.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247183813,"end":247185482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255605.1","gene_symbol":"AP000820.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95698086,"end":95700623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076356.6","gene_symbol":"PLXNA2","gene_name":"plexin A2 [Source:HGNC Symbol;Acc:HGNC:9100]","synonyms":"PLXN2,OCT,KIAA0463,FLJ30634,FLJ11751","biotype":"protein_coding","ncbi_id":"5362","summary":"This gene encodes a member of the plexin-A family of semaphorin co-receptors. Semaphorins are a large family of secreted or membrane-bound proteins that mediate repulsive effects on axon pathfinding during nervous system development. A subset of semaphorins are recognized by plexin-A/neuropilin transmembrane receptor complexes, triggering a cellular signal transduction cascade that leads to axon repulsion. This plexin-A family member is thought to transduce signals from semaphorin-3A and -3C. [provided by RefSeq, Jul 2008]","start":208022242,"end":208244320,"strand":-1,"description":"plexin A2 [Source:HGNC Symbol;Acc:HGNC:9100]"}, {"versioned_ensembl_gene_id":"ENSG00000261314.1","gene_symbol":"AC105275.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":211583015,"end":211583725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249387.1","gene_symbol":"KRTAP5-14P","gene_name":"keratin associated protein 5-14, pseudogene [Source:HGNC Symbol;Acc:HGNC:23608]","synonyms":"KRTAP5P2,KRTAP5.P2","biotype":"processed_pseudogene","ncbi_id":"387276","summary":null,"start":71579728,"end":71579848,"strand":-1,"description":"keratin associated protein 5-14, pseudogene [Source:HGNC Symbol;Acc:HGNC:23608]"}, {"versioned_ensembl_gene_id":"ENSG00000184055.4","gene_symbol":"OR7E87P","gene_name":"olfactory receptor family 7 subfamily E member 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:14709]","synonyms":"OR11-9,OR7F3P,OR7E3P","biotype":"unprocessed_pseudogene","ncbi_id":"8586","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71593454,"end":71594382,"strand":1,"description":"olfactory receptor family 7 subfamily E member 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:14709]"}, {"versioned_ensembl_gene_id":"ENSG00000283205.1","gene_symbol":"AL353572.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":87956214,"end":87956883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224366.1","gene_symbol":"AC243964.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":44570304,"end":44570564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248903.1","gene_symbol":"AP000867.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71568680,"end":71568934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236823.1","gene_symbol":"AL035691.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159899186,"end":159902510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258065.1","gene_symbol":"AL122126.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28857384,"end":28858701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167895.14","gene_symbol":"TMC8","gene_name":"transmembrane channel like 8 [Source:HGNC Symbol;Acc:HGNC:20474]","synonyms":"EVER2,EVIN2","biotype":"protein_coding","ncbi_id":"147138","summary":"Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 8 predicted transmembrane domains and 3 leucine zipper motifs. [provided by RefSeq, Jul 2008]","start":78130770,"end":78142968,"strand":1,"description":"transmembrane channel like 8 [Source:HGNC Symbol;Acc:HGNC:20474]"}, {"versioned_ensembl_gene_id":"ENSG00000266998.1","gene_symbol":"AC111182.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77373818,"end":77377236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267263.1","gene_symbol":"AC111170.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":77469068,"end":77471045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145715.14","gene_symbol":"RASA1","gene_name":"RAS p21 protein activator 1 [Source:HGNC Symbol;Acc:HGNC:9871]","synonyms":"p120,GAP,CM-AVM,RASA,p120RASGAP,p120GAP","biotype":"protein_coding","ncbi_id":"5921","summary":"The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues. [provided by RefSeq, May 2012]","start":87267888,"end":87391931,"strand":1,"description":"RAS p21 protein activator 1 [Source:HGNC Symbol;Acc:HGNC:9871]"}, {"versioned_ensembl_gene_id":"ENSG00000153363.12","gene_symbol":"LINC00467","gene_name":"long intergenic non-protein coding RNA 467 [Source:HGNC Symbol;Acc:HGNC:28227]","synonyms":"MGC14801,C1orf97","biotype":"lincRNA","ncbi_id":"84791","summary":null,"start":211382803,"end":211435333,"strand":1,"description":"long intergenic non-protein coding RNA 467 [Source:HGNC Symbol;Acc:HGNC:28227]"}, {"versioned_ensembl_gene_id":"ENSG00000180884.9","gene_symbol":"ZNF792","gene_name":"zinc finger protein 792 [Source:HGNC Symbol;Acc:HGNC:24751]","synonyms":"FLJ38451","biotype":"protein_coding","ncbi_id":"126375","summary":null,"start":34956354,"end":34964049,"strand":-1,"description":"zinc finger protein 792 [Source:HGNC Symbol;Acc:HGNC:24751]"}, {"versioned_ensembl_gene_id":"ENSG00000178464.6","gene_symbol":"RPL10P16","gene_name":"ribosomal protein L10 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36882]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284393","summary":null,"start":12643275,"end":12643919,"strand":-1,"description":"ribosomal protein L10 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36882]"}, {"versioned_ensembl_gene_id":"ENSG00000168701.18","gene_symbol":"TMEM208","gene_name":"transmembrane protein 208 [Source:HGNC Symbol;Acc:HGNC:25015]","synonyms":"HSPC171","biotype":"protein_coding","ncbi_id":"29100","summary":"This gene encodes a highly conserved protein which is localized in the endoplasmic reticulum (ER). The protein is linked to autophagy and ER stress. Knockdown of this gene increased autophagy and triggered ER stress. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":67227103,"end":67229278,"strand":1,"description":"transmembrane protein 208 [Source:HGNC Symbol;Acc:HGNC:25015]"}, {"versioned_ensembl_gene_id":"ENSG00000230114.1","gene_symbol":"AL590432.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49257411,"end":49269285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215887.5","gene_symbol":"ZNF859P","gene_name":"zinc finger protein 859, pseudogene [Source:HGNC Symbol;Acc:HGNC:34507]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100507490","summary":null,"start":49841821,"end":49846400,"strand":1,"description":"zinc finger protein 859, pseudogene [Source:HGNC Symbol;Acc:HGNC:34507]"}, {"versioned_ensembl_gene_id":"ENSG00000256779.2","gene_symbol":"AP002383.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":95037482,"end":95039811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138813.9","gene_symbol":"C4orf17","gene_name":"chromosome 4 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:25274]","synonyms":"DKFZP434G072","biotype":"protein_coding","ncbi_id":"84103","summary":null,"start":99511004,"end":99542303,"strand":1,"description":"chromosome 4 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:25274]"}, {"versioned_ensembl_gene_id":"ENSG00000265908.1","gene_symbol":"AC024267.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28944796,"end":28945394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258729.2","gene_symbol":"AL355102.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96275046,"end":96276723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223551.1","gene_symbol":"TMSB4XP4","gene_name":"thymosin beta 4, X-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:11886]","synonyms":"TMSL4","biotype":"processed_pseudogene","ncbi_id":"7118","summary":null,"start":128342153,"end":128342770,"strand":1,"description":"thymosin beta 4, X-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:11886]"}, {"versioned_ensembl_gene_id":"ENSG00000260877.2","gene_symbol":"AP005233.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69371463,"end":69372512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224012.3","gene_symbol":"AC116917.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163709210,"end":163709514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249153.1","gene_symbol":"AC026414.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85848502,"end":85849199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250359.1","gene_symbol":"PTP4A1P4","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129564","summary":null,"start":86087526,"end":86087847,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41931]"}, {"versioned_ensembl_gene_id":"ENSG00000241965.2","gene_symbol":"RPS2P25","gene_name":"ribosomal protein S2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36410]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270913","summary":null,"start":85762559,"end":85763138,"strand":1,"description":"ribosomal protein S2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36410]"}, {"versioned_ensembl_gene_id":"ENSG00000250874.1","gene_symbol":"AC010595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85663232,"end":85664684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170476.15","gene_symbol":"MZB1","gene_name":"marginal zone B and B1 cell specific protein [Source:HGNC Symbol;Acc:HGNC:30125]","synonyms":"pERp1,PACAP,MGC29506,MEDA-7,HSPC190","biotype":"protein_coding","ncbi_id":"51237","summary":null,"start":139387480,"end":139390081,"strand":-1,"description":"marginal zone B and B1 cell specific protein [Source:HGNC Symbol;Acc:HGNC:30125]"}, {"versioned_ensembl_gene_id":"ENSG00000267168.1","gene_symbol":"AC005837.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":76732978,"end":76738522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248667.1","gene_symbol":"AC010486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85420028,"end":85420451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275547.1","gene_symbol":"AC010632.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37024886,"end":37025254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231555.4","gene_symbol":"HSPA1B","gene_name":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]","synonyms":"HSP70-2","biotype":"protein_coding","ncbi_id":"3304","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31809921,"end":31812441,"strand":1,"description":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]"}, {"versioned_ensembl_gene_id":"ENSG00000076944.15","gene_symbol":"STXBP2","gene_name":"syntaxin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:11445]","synonyms":"UNC18B,Hunc18b","biotype":"protein_coding","ncbi_id":"6813","summary":"This gene encodes a member of the STXBP/unc-18/SEC1 family. The encoded protein is involved in intracellular trafficking, control of SNARE (soluble NSF attachment protein receptor) complex assembly, and the release of cytotoxic granules by natural killer cells. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2013]","start":7636881,"end":7647873,"strand":1,"description":"syntaxin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:11445]"}, {"versioned_ensembl_gene_id":"ENSG00000204547.7","gene_symbol":"DEFB122","gene_name":"defensin beta 122 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18102]","synonyms":"DEFB122P,DEFB-22","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"245935","summary":null,"start":31421436,"end":31429180,"strand":-1,"description":"defensin beta 122 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18102]"}, {"versioned_ensembl_gene_id":"ENSG00000110395.6","gene_symbol":"CBL","gene_name":"Cbl proto-oncogene [Source:HGNC Symbol;Acc:HGNC:1541]","synonyms":"RNF55,CBL2,c-Cbl","biotype":"protein_coding","ncbi_id":"867","summary":"This gene is a proto-oncogene that encodes a RING finger E3 ubiquitin ligase. The encoded protein is one of the enzymes required for targeting substrates for degradation by the proteasome. This protein mediates the transfer of ubiquitin from ubiquitin conjugating enzymes (E2) to specific substrates. This protein also contains an N-terminal phosphotyrosine binding domain that allows it to interact with numerous tyrosine-phosphorylated substrates and target them for proteasome degradation. As such it functions as a negative regulator of many signal transduction pathways. This gene has been found to be mutated or translocated in many cancers including acute myeloid leukaemia, and expansion of CGG repeats in the 5' UTR has been associated with Jacobsen syndrome. Mutations in this gene are also the cause of Noonan syndrome-like disorder. [provided by RefSeq, Jul 2016]","start":119206276,"end":119313926,"strand":1,"description":"Cbl proto-oncogene [Source:HGNC Symbol;Acc:HGNC:1541]"}, {"versioned_ensembl_gene_id":"ENSG00000260676.5","gene_symbol":"LINC01541","gene_name":"long intergenic non-protein coding RNA 1541 [Source:HGNC Symbol;Acc:HGNC:51309]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505776","summary":null,"start":71519962,"end":71578956,"strand":-1,"description":"long intergenic non-protein coding RNA 1541 [Source:HGNC Symbol;Acc:HGNC:51309]"}, {"versioned_ensembl_gene_id":"ENSG00000257057.2","gene_symbol":"C11orf97","gene_name":"chromosome 11 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:49544]","synonyms":"LINC01171","biotype":"protein_coding","ncbi_id":"643037","summary":null,"start":94512432,"end":94532123,"strand":1,"description":"chromosome 11 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:49544]"}, {"versioned_ensembl_gene_id":"ENSG00000270281.1","gene_symbol":"AC020910.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34779412,"end":34780021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144791.9","gene_symbol":"LIMD1","gene_name":"LIM domains containing 1 [Source:HGNC Symbol;Acc:HGNC:6612]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8994","summary":null,"start":45555394,"end":45686338,"strand":1,"description":"LIM domains containing 1 [Source:HGNC Symbol;Acc:HGNC:6612]"}, {"versioned_ensembl_gene_id":"ENSG00000177350.6","gene_symbol":"RPL13AP3","gene_name":"ribosomal protein L13a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23539]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"645683","summary":null,"start":55766177,"end":55767717,"strand":1,"description":"ribosomal protein L13a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23539]"}, {"versioned_ensembl_gene_id":"ENSG00000229000.1","gene_symbol":"SEPT7P8","gene_name":"septin 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38044]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418735","summary":null,"start":53772506,"end":53773280,"strand":-1,"description":"septin 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38044]"}, {"versioned_ensembl_gene_id":"ENSG00000134874.17","gene_symbol":"DZIP1","gene_name":"DAZ interacting zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:20908]","synonyms":"KIAA0996,DZIP","biotype":"protein_coding","ncbi_id":"22873","summary":null,"start":95578202,"end":95644703,"strand":-1,"description":"DAZ interacting zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:20908]"}, {"versioned_ensembl_gene_id":"ENSG00000281990.1","gene_symbol":"AC245369.4","gene_name":"Immunoglobulin heavy variable 1-69-2 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JMI3]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106737110,"end":106737547,"strand":-1,"description":"Immunoglobulin heavy variable 1-69-2 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JMI3]"}, {"versioned_ensembl_gene_id":"ENSG00000237589.1","gene_symbol":"HMGN1P32","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874465","summary":null,"start":53767971,"end":53768553,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39376]"}, {"versioned_ensembl_gene_id":"ENSG00000223506.2","gene_symbol":"SLC20A1P1","gene_name":"solute carrier family 20 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"192127","summary":null,"start":106683395,"end":106684350,"strand":-1,"description":"solute carrier family 20 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20051]"}, {"versioned_ensembl_gene_id":"ENSG00000234475.5","gene_symbol":"HSPA1A","gene_name":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]","synonyms":"HSPA1,HSP70-1","biotype":"protein_coding","ncbi_id":"3303","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31797650,"end":31800132,"strand":1,"description":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]"}, {"versioned_ensembl_gene_id":"ENSG00000154529.14","gene_symbol":"CNTNAP3B","gene_name":"contactin associated protein like 3B [Source:HGNC Symbol;Acc:HGNC:32035]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728577","summary":null,"start":41890314,"end":42129510,"strand":-1,"description":"contactin associated protein like 3B [Source:HGNC Symbol;Acc:HGNC:32035]"}, {"versioned_ensembl_gene_id":"ENSG00000276808.1","gene_symbol":"AC245128.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250013.1","gene_symbol":"AC093286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83875166,"end":83875821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269755.1","gene_symbol":"AC008758.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12433103,"end":12484816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272491.1","gene_symbol":"AL109659.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48227888,"end":48229561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278239.1","gene_symbol":"AC243967.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41833686,"end":41835950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249709.7","gene_symbol":"ZNF564","gene_name":"zinc finger protein 564 [Source:HGNC Symbol;Acc:HGNC:31106]","synonyms":"MGC26914","biotype":"protein_coding","ncbi_id":"163050","summary":null,"start":12525370,"end":12551542,"strand":-1,"description":"zinc finger protein 564 [Source:HGNC Symbol;Acc:HGNC:31106]"}, {"versioned_ensembl_gene_id":"ENSG00000234003.1","gene_symbol":"MTATP6P27","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52183]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075204","summary":null,"start":12506249,"end":12508030,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52183]"}, {"versioned_ensembl_gene_id":"ENSG00000168092.13","gene_symbol":"PAFAH1B2","gene_name":"platelet activating factor acetylhydrolase 1b catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:8575]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5049","summary":"Platelet-activating factor acetylhydrolase (PAFAH) inactivates platelet-activating factor (PAF) into acetate and LYSO-PAF. This gene encodes the beta subunit of PAFAH, the other subunits are alpha and gamma. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jan 2014]","start":117144267,"end":117176894,"strand":1,"description":"platelet activating factor acetylhydrolase 1b catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:8575]"}, {"versioned_ensembl_gene_id":"ENSG00000268744.1","gene_symbol":"AC008758.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12379189,"end":12401274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278318.4","gene_symbol":"ZNF229","gene_name":"zinc finger protein 229 [Source:HGNC Symbol;Acc:HGNC:13022]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7772","summary":null,"start":44417519,"end":44448578,"strand":-1,"description":"zinc finger protein 229 [Source:HGNC Symbol;Acc:HGNC:13022]"}, {"versioned_ensembl_gene_id":"ENSG00000261801.5","gene_symbol":"LOXL1-AS1","gene_name":"LOXL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44169]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287616","summary":null,"start":73908071,"end":73928248,"strand":-1,"description":"LOXL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44169]"}, {"versioned_ensembl_gene_id":"ENSG00000223568.1","gene_symbol":"RPL3P11","gene_name":"ribosomal protein L3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35521]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131893","summary":null,"start":14040716,"end":14041861,"strand":-1,"description":"ribosomal protein L3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35521]"}, {"versioned_ensembl_gene_id":"ENSG00000254678.1","gene_symbol":"AP005018.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117143891,"end":117144191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188033.9","gene_symbol":"ZNF490","gene_name":"zinc finger protein 490 [Source:HGNC Symbol;Acc:HGNC:23705]","synonyms":"KIAA1198","biotype":"protein_coding","ncbi_id":"57474","summary":null,"start":12577961,"end":12640098,"strand":-1,"description":"zinc finger protein 490 [Source:HGNC Symbol;Acc:HGNC:23705]"}, {"versioned_ensembl_gene_id":"ENSG00000261430.1","gene_symbol":"AL031600.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1467673,"end":1472684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175931.12","gene_symbol":"UBE2O","gene_name":"ubiquitin conjugating enzyme E2 O [Source:HGNC Symbol;Acc:HGNC:29554]","synonyms":"E2-230K","biotype":"protein_coding","ncbi_id":"63893","summary":null,"start":76389451,"end":76453206,"strand":-1,"description":"ubiquitin conjugating enzyme E2 O [Source:HGNC Symbol;Acc:HGNC:29554]"}, {"versioned_ensembl_gene_id":"ENSG00000231361.1","gene_symbol":"RPS29P23","gene_name":"ribosomal protein S29 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271588","summary":null,"start":12373609,"end":12373731,"strand":1,"description":"ribosomal protein S29 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35779]"}, {"versioned_ensembl_gene_id":"ENSG00000244468.1","gene_symbol":"AC093001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149284782,"end":149333653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107147.12","gene_symbol":"KCNT1","gene_name":"potassium sodium-activated channel subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:18865]","synonyms":"Slo2.2,SLACK,KIAA1422,KCa4.1","biotype":"protein_coding","ncbi_id":"57582","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":135702185,"end":135795508,"strand":1,"description":"potassium sodium-activated channel subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:18865]"}, {"versioned_ensembl_gene_id":"ENSG00000244345.1","gene_symbol":"AC104435.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72504806,"end":72550552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101280.7","gene_symbol":"ANGPT4","gene_name":"angiopoietin 4 [Source:HGNC Symbol;Acc:HGNC:487]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51378","summary":"Angiopoietins are proteins with important roles in vascular development and angiogenesis. All angiopoietins bind with similar affinity to an endothelial cell-specific tyrosine-protein kinase receptor. The mechanism by which they contribute to angiogenesis is thought to involve regulation of endothelial cell interactions with supporting perivascular cells. The protein encoded by this gene functions as an agonist and is an angiopoietin. [provided by RefSeq, Jul 2008]","start":869899,"end":916317,"strand":-1,"description":"angiopoietin 4 [Source:HGNC Symbol;Acc:HGNC:487]"}, {"versioned_ensembl_gene_id":"ENSG00000225137.1","gene_symbol":"DYNC1I2P1","gene_name":"dynein cytoplasmic 1 intermediate chain 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728532","summary":null,"start":50264978,"end":50266815,"strand":1,"description":"dynein cytoplasmic 1 intermediate chain 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45012]"}, {"versioned_ensembl_gene_id":"ENSG00000211972.2","gene_symbol":"IGHV3-66","gene_name":"immunoglobulin heavy variable 3-66 [Source:HGNC Symbol;Acc:HGNC:5619]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28412","summary":null,"start":106675017,"end":106675544,"strand":-1,"description":"immunoglobulin heavy variable 3-66 [Source:HGNC Symbol;Acc:HGNC:5619]"}, {"versioned_ensembl_gene_id":"ENSG00000086548.8","gene_symbol":"CEACAM6","gene_name":"carcinoembryonic antigen related cell adhesion molecule 6 [Source:HGNC Symbol;Acc:HGNC:1818]","synonyms":"NCA,CD66c","biotype":"protein_coding","ncbi_id":"4680","summary":"This gene encodes a protein that belongs to the carcinoembryonic antigen (CEA) family whose members are glycosyl phosphatidyl inositol (GPI) anchored cell surface glycoproteins. Members of this family play a role in cell adhesion and are widely used as tumor markers in serum immunoassay determinations of carcinoma. This gene affects the sensitivity of tumor cells to adenovirus infection. The protein encoded by this gene acts as a receptor for adherent-invasive E. coli adhesion to the surface of ileal epithelial cells in patients with Crohn's disease. This gene is clustered with genes and pseudogenes of the cell adhesion molecules subgroup of the CEA family on chromosome 19. [provided by RefSeq, Apr 2014]","start":41750977,"end":41772208,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 6 [Source:HGNC Symbol;Acc:HGNC:1818]"}, {"versioned_ensembl_gene_id":"ENSG00000279561.2","gene_symbol":"AL845472.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41269916,"end":41273997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158710.14","gene_symbol":"TAGLN2","gene_name":"transgelin 2 [Source:HGNC Symbol;Acc:HGNC:11554]","synonyms":"KIAA0120,HA1756","biotype":"protein_coding","ncbi_id":"8407","summary":"The protein encoded by this gene is similar to the protein transgelin, which is one of the earliest markers of differentiated smooth muscle. The specific function of this protein has not yet been determined, although it is thought to be a tumor suppressor. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2013]","start":159918107,"end":159925732,"strand":-1,"description":"transgelin 2 [Source:HGNC Symbol;Acc:HGNC:11554]"}, {"versioned_ensembl_gene_id":"ENSG00000196290.14","gene_symbol":"NIF3L1","gene_name":"NGG1 interacting factor 3 like 1 [Source:HGNC Symbol;Acc:HGNC:13390]","synonyms":"ALS2CR1,MDS015,CALS-7","biotype":"protein_coding","ncbi_id":"60491","summary":null,"start":200889327,"end":200903930,"strand":1,"description":"NGG1 interacting factor 3 like 1 [Source:HGNC Symbol;Acc:HGNC:13390]"}, {"versioned_ensembl_gene_id":"ENSG00000100302.6","gene_symbol":"RASD2","gene_name":"RASD family member 2 [Source:HGNC Symbol;Acc:HGNC:18229]","synonyms":"TEM2,Rhes,MGC:4834","biotype":"protein_coding","ncbi_id":"23551","summary":"This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the protein mutated in Huntington disease (HD). Sumoylation of mHTT by this protein may cause degeneration of the striatum. The protein functions as an activator of mechanistic target of rapamycin 1 (mTOR1), which in turn plays a role in myelination, axon growth and regeneration. Reduced levels of mRNA expressed by this gene were found in HD patients. [provided by RefSeq, Jan 2016]","start":35540868,"end":35554001,"strand":1,"description":"RASD family member 2 [Source:HGNC Symbol;Acc:HGNC:18229]"}, {"versioned_ensembl_gene_id":"ENSG00000273044.1","gene_symbol":"AL022334.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35526932,"end":35527415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233388.2","gene_symbol":"AL022334.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35501861,"end":35503586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276807.1","gene_symbol":"AC022188.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73730048,"end":73731711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229112.1","gene_symbol":"AL356583.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":246528562,"end":246528841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167110.17","gene_symbol":"GOLGA2","gene_name":"golgin A2 [Source:HGNC Symbol;Acc:HGNC:4425]","synonyms":"golgin-95,GM130","biotype":"protein_coding","ncbi_id":"2801","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This encoded protein has been postulated to play roles in the stacking of Golgi cisternae and in vesicular transport. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of these variants has not been determined. [provided by RefSeq, Feb 2010]","start":128255829,"end":128275995,"strand":-1,"description":"golgin A2 [Source:HGNC Symbol;Acc:HGNC:4425]"}, {"versioned_ensembl_gene_id":"ENSG00000279355.1","gene_symbol":"AGPAT4-IT1","gene_name":"AGPAT4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:20988]","synonyms":"NCRNA00241,FLJ23112,C6orf59","biotype":"TEC","ncbi_id":"79992","summary":null,"start":161160105,"end":161161982,"strand":-1,"description":"AGPAT4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:20988]"}, {"versioned_ensembl_gene_id":"ENSG00000241130.1","gene_symbol":"AC012100.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50798670,"end":50798951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232403.1","gene_symbol":"AC009501.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63108118,"end":63108429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277531.2","gene_symbol":"PNMA8C","gene_name":"paraneoplastic Ma antigen family member 8C [Source:HGNC Symbol;Acc:HGNC:53427]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46424697,"end":46428951,"strand":-1,"description":"paraneoplastic Ma antigen family member 8C [Source:HGNC Symbol;Acc:HGNC:53427]"}, {"versioned_ensembl_gene_id":"ENSG00000167880.7","gene_symbol":"EVPL","gene_name":"envoplakin [Source:HGNC Symbol;Acc:HGNC:3503]","synonyms":"EVPK","biotype":"protein_coding","ncbi_id":"2125","summary":"This gene encodes a member of the plakin family of proteins that forms a component of desmosomes and the epidermal cornified envelope. This gene is located in the tylosis oesophageal cancer locus on chromosome 17q25, and its deletion is associated with both familial and sporadic forms of oesophageal squamous cell carcinoma. Patients suffering from the autoimmune mucocutaneous disorder, paraneoplastic pemphigus, develop antibodies against the encoded protein. [provided by RefSeq, Jul 2016]","start":76004502,"end":76027452,"strand":-1,"description":"envoplakin [Source:HGNC Symbol;Acc:HGNC:3503]"}, {"versioned_ensembl_gene_id":"ENSG00000263045.1","gene_symbol":"AC090286.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18986148,"end":18986334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236451.2","gene_symbol":"AC067956.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220450679,"end":220704566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239498.1","gene_symbol":"AC019211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220105656,"end":220450778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136546.13","gene_symbol":"SCN7A","gene_name":"sodium voltage-gated channel alpha subunit 7 [Source:HGNC Symbol;Acc:HGNC:10594]","synonyms":"SCN6A,Nav2.2,Nav2.1,NaG","biotype":"protein_coding","ncbi_id":"6332","summary":"This gene encodes one of the many voltage-gated sodium channel proteins. For proper functioning of neurons and muscles during action potentials, voltage-gated sodium channels direct sodium ion diffusion for membrane depolarization. This sodium channel protein has some atypical characteristics; the similarity between the human and mouse proteins is lower compared to other orthologous sodium channel pairs. Also, the S4 segments, which sense voltage changes, have fewer positive charged residues that in other sodium channels; domain 4 has fewer arginine and lysine residues compared to other sodium channel proteins. Several alternatively spliced transcript variants exist, but the full-length natures of all of them remain unknown. [provided by RefSeq, Dec 2011]","start":166403573,"end":166494247,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 7 [Source:HGNC Symbol;Acc:HGNC:10594]"}, {"versioned_ensembl_gene_id":"ENSG00000283657.1","gene_symbol":"AC074101.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":166414489,"end":166414729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211951.2","gene_symbol":"IGHV2-26","gene_name":"immunoglobulin heavy variable 2-26 [Source:HGNC Symbol;Acc:HGNC:5575]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28455","summary":null,"start":106301396,"end":106301862,"strand":-1,"description":"immunoglobulin heavy variable 2-26 [Source:HGNC Symbol;Acc:HGNC:5575]"}, {"versioned_ensembl_gene_id":"ENSG00000279359.1","gene_symbol":"AL359195.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80249710,"end":80254121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181333.11","gene_symbol":"HEPHL1","gene_name":"hephaestin like 1 [Source:HGNC Symbol;Acc:HGNC:30477]","synonyms":"DKFZp686F22190","biotype":"protein_coding","ncbi_id":"341208","summary":null,"start":94021361,"end":94113751,"strand":1,"description":"hephaestin like 1 [Source:HGNC Symbol;Acc:HGNC:30477]"}, {"versioned_ensembl_gene_id":"ENSG00000151893.14","gene_symbol":"CACUL1","gene_name":"CDK2 associated cullin domain 1 [Source:HGNC Symbol;Acc:HGNC:23727]","synonyms":"MGC33215,FLJ40409,CAC1,C10orf46","biotype":"protein_coding","ncbi_id":"143384","summary":null,"start":118674167,"end":118755249,"strand":-1,"description":"CDK2 associated cullin domain 1 [Source:HGNC Symbol;Acc:HGNC:23727]"}, {"versioned_ensembl_gene_id":"ENSG00000234382.2","gene_symbol":"AL513174.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80233664,"end":80245367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224842.2","gene_symbol":"AL161908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126589594,"end":126613700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170837.2","gene_symbol":"GPR27","gene_name":"G protein-coupled receptor 27 [Source:HGNC Symbol;Acc:HGNC:4482]","synonyms":"SREB1","biotype":"protein_coding","ncbi_id":"2850","summary":"GPR27 is a member of the G protein-coupled receptors (GPCRs), a large family of receptors that have a similar structure characterized by 7 transmembrane domains. Activation of GPCRs by extracellular stimuli such as neurotransmitters, hormones, or light induces an intracellular signaling cascade mediated by heterotrimeric GTP-binding proteins, or G proteins.[supplied by OMIM, May 2010]","start":71754050,"end":71756496,"strand":1,"description":"G protein-coupled receptor 27 [Source:HGNC Symbol;Acc:HGNC:4482]"}, {"versioned_ensembl_gene_id":"ENSG00000247867.2","gene_symbol":"AP001922.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75758455,"end":75768647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152582.13","gene_symbol":"SPEF2","gene_name":"sperm flagellar 2 [Source:HGNC Symbol;Acc:HGNC:26293]","synonyms":"KPL2,FLJ23577,CT122","biotype":"protein_coding","ncbi_id":"79925","summary":null,"start":35617844,"end":35814611,"strand":1,"description":"sperm flagellar 2 [Source:HGNC Symbol;Acc:HGNC:26293]"}, {"versioned_ensembl_gene_id":"ENSG00000253248.5","gene_symbol":"AC079098.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136047021,"end":136166122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149636.15","gene_symbol":"DSN1","gene_name":"DSN1 homolog, MIS12 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:16165]","synonyms":"C20orf172,MIS13,KNL3,hKNL-3,dJ469A13.2","biotype":"protein_coding","ncbi_id":"79980","summary":"This gene encodes a kinetochore protein that functions as part of the minichromosome instability-12 centromere complex. The encoded protein is required for proper kinetochore assembly and progression through the cell cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009]","start":36751791,"end":36773818,"strand":-1,"description":"DSN1 homolog, MIS12 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:16165]"}, {"versioned_ensembl_gene_id":"ENSG00000272444.1","gene_symbol":"AL118558.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101952416,"end":101953063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267254.5","gene_symbol":"ZNF790-AS1","gene_name":"ZNF790 antisense RNA 1 [Source:NCBI gene;Acc:284408]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"284408","summary":null,"start":36797518,"end":36828115,"strand":1,"description":"ZNF790 antisense RNA 1 [Source:NCBI gene;Acc:284408]"}, {"versioned_ensembl_gene_id":"ENSG00000254150.1","gene_symbol":"AC087664.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59557528,"end":59557855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205057.4","gene_symbol":"CLLU1OS","gene_name":"chronic lymphocytic leukemia up-regulated 1 opposite strand [Source:HGNC Symbol;Acc:HGNC:24070]","synonyms":null,"biotype":"protein_coding","ncbi_id":"574016","summary":null,"start":92420094,"end":92428148,"strand":-1,"description":"chronic lymphocytic leukemia up-regulated 1 opposite strand [Source:HGNC Symbol;Acc:HGNC:24070]"}, {"versioned_ensembl_gene_id":"ENSG00000143125.5","gene_symbol":"PROK1","gene_name":"prokineticin 1 [Source:HGNC Symbol;Acc:HGNC:18454]","synonyms":"PRK1,PK1,EGVEGF","biotype":"protein_coding","ncbi_id":"84432","summary":"The protein encoded by this gene induces proliferation, migration, and fenestration (the formation of membrane discontinuities) in capillary endothelial cells derived from endocrine glands. It has little or no effect on a variety of other endothelial and non-endothelial cell types. Its expression is restricted to the steroidogenic glands (ovary, testis, adrenal, and placenta), is induced by hypoxia, and often complementary to the expression of vascular endothelial growth factor (VEGF), suggesting that these molecules function in a coordinated manner. [provided by RefSeq, Sep 2011]","start":110451200,"end":110457354,"strand":1,"description":"prokineticin 1 [Source:HGNC Symbol;Acc:HGNC:18454]"}, {"versioned_ensembl_gene_id":"ENSG00000138600.9","gene_symbol":"SPPL2A","gene_name":"signal peptide peptidase like 2A [Source:HGNC Symbol;Acc:HGNC:30227]","synonyms":"PSL2,IMP3","biotype":"protein_coding","ncbi_id":"84888","summary":"This gene encodes a member of the GXGD family of aspartic proteases, which are transmembrane proteins with two conserved catalytic motifs localized within the membrane-spanning regions, as well as a member of the signal peptide peptidase-like protease (SPPL) family. This protein is expressed in all major adult human tissues and localizes to late endosomal compartments and lysosomal membranes. A pseudogene of this gene also lies on chromosome 15. [provided by RefSeq, Feb 2012]","start":50702266,"end":50765808,"strand":-1,"description":"signal peptide peptidase like 2A [Source:HGNC Symbol;Acc:HGNC:30227]"}, {"versioned_ensembl_gene_id":"ENSG00000271201.1","gene_symbol":"AC247036.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106206603,"end":106208571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171806.11","gene_symbol":"METTL18","gene_name":"methyltransferase like 18 [Source:HGNC Symbol;Acc:HGNC:28793]","synonyms":"MGC9084,HPM1,C1orf156,AsTP2","biotype":"protein_coding","ncbi_id":"92342","summary":null,"start":169792529,"end":169794966,"strand":-1,"description":"methyltransferase like 18 [Source:HGNC Symbol;Acc:HGNC:28793]"}, {"versioned_ensembl_gene_id":"ENSG00000271795.1","gene_symbol":"AC011337.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151509453,"end":151512769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124089.4","gene_symbol":"MC3R","gene_name":"melanocortin 3 receptor [Source:HGNC Symbol;Acc:HGNC:6931]","synonyms":"MC3","biotype":"protein_coding","ncbi_id":"4159","summary":"This gene encodes a G-protein-coupled receptor for melanocyte-stimulating hormone and adrenocorticotropic hormone that is expressed in tissues other than the adrenal cortex and melanocytes. This gene maps to the same region as the locus for benign neonatal epilepsy. Mice deficient for this gene have increased fat mass despite decreased food intake, suggesting a role for this gene product in the regulation of energy homeostasis. Mutations in this gene are associated with a susceptibility to obesity in humans. [provided by RefSeq, Jul 2008]","start":56248732,"end":56249815,"strand":1,"description":"melanocortin 3 receptor [Source:HGNC Symbol;Acc:HGNC:6931]"}, {"versioned_ensembl_gene_id":"ENSG00000152380.9","gene_symbol":"FAM151B","gene_name":"family with sequence similarity 151 member B [Source:HGNC Symbol;Acc:HGNC:33716]","synonyms":"UNQ9217","biotype":"protein_coding","ncbi_id":"167555","summary":null,"start":80487969,"end":80542563,"strand":1,"description":"family with sequence similarity 151 member B [Source:HGNC Symbol;Acc:HGNC:33716]"}, {"versioned_ensembl_gene_id":"ENSG00000174677.4","gene_symbol":"VN1R6P","gene_name":"vomeronasal 1 receptor 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:13712]","synonyms":"ZVNR2,ZVNH2,VNR19I2","biotype":"unitary_pseudogene","ncbi_id":"653753","summary":null,"start":53315137,"end":53316043,"strand":1,"description":"vomeronasal 1 receptor 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:13712]"}, {"versioned_ensembl_gene_id":"ENSG00000269118.1","gene_symbol":"FAM90A28P","gene_name":"family with sequence similarity 90 member A28, pseudogene [Source:HGNC Symbol;Acc:HGNC:43747]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100128254","summary":null,"start":53299051,"end":53308644,"strand":-1,"description":"family with sequence similarity 90 member A28, pseudogene [Source:HGNC Symbol;Acc:HGNC:43747]"}, {"versioned_ensembl_gene_id":"ENSG00000132475.10","gene_symbol":"H3F3B","gene_name":"H3 histone family member 3B [Source:HGNC Symbol;Acc:HGNC:4765]","synonyms":"H3.3B","biotype":"protein_coding","ncbi_id":"3021","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene contains introns and its mRNA is polyadenylated, unlike most histone genes. The protein encoded by this gene is a replication-independent histone that is a member of the histone H3 family. Pseudogenes of this gene have been identified on the X chromosome, and on chromosomes 5, 13 and 17. [provided by RefSeq, Oct 2015]","start":75776434,"end":75785893,"strand":-1,"description":"H3 histone family member 3B [Source:HGNC Symbol;Acc:HGNC:4765]"}, {"versioned_ensembl_gene_id":"ENSG00000054803.3","gene_symbol":"CBLN4","gene_name":"cerebellin 4 precursor [Source:HGNC Symbol;Acc:HGNC:16231]","synonyms":"dJ885A10.1,CBLNL1","biotype":"protein_coding","ncbi_id":"140689","summary":"This gene encodes a member of a family of small secreted proteins containing C1Q domains. Members of this family are involved in regulation of neurexin signalling during synapse development. The mouse homolog of the protein encoded by this gene competes with netrin to bind to the deleted in colorectal cancer receptor. [provided by RefSeq, Aug 2012]","start":55997440,"end":56005472,"strand":-1,"description":"cerebellin 4 precursor [Source:HGNC Symbol;Acc:HGNC:16231]"}, {"versioned_ensembl_gene_id":"ENSG00000282639.1","gene_symbol":"AC247036.4","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106088122,"end":106088573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253387.1","gene_symbol":"IGHVIII-5-1","gene_name":"immunoglobulin heavy variable (III)-5-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5702]","synonyms":"IGHV(III)-5-1","biotype":"IG_V_pseudogene","ncbi_id":"28354","summary":null,"start":106039666,"end":106039764,"strand":-1,"description":"immunoglobulin heavy variable (III)-5-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5702]"}, {"versioned_ensembl_gene_id":"ENSG00000279036.1","gene_symbol":"AC015656.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49494223,"end":49497800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257458.1","gene_symbol":"AC069437.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98931682,"end":98976656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118137.9","gene_symbol":"APOA1","gene_name":"apolipoprotein A1 [Source:HGNC Symbol;Acc:HGNC:600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"335","summary":"This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The encoded preproprotein is proteolytically processed to generate the mature protein, which promotes cholesterol efflux from tissues to the liver for excretion, and is a cofactor for lecithin cholesterolacyltransferase (LCAT), an enzyme responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein. [provided by RefSeq, Dec 2015]","start":116835751,"end":116837950,"strand":-1,"description":"apolipoprotein A1 [Source:HGNC Symbol;Acc:HGNC:600]"}, {"versioned_ensembl_gene_id":"ENSG00000236341.1","gene_symbol":"AL161740.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56963886,"end":56996757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112276.13","gene_symbol":"BVES","gene_name":"blood vessel epicardial substance [Source:HGNC Symbol;Acc:HGNC:1152]","synonyms":"POPDC1,POP1,HBVES","biotype":"protein_coding","ncbi_id":"11149","summary":"This gene encodes a member of the POP family of proteins containing three putative transmembrane domains. This gene is expressed in cardiac and skeletal muscle and may play an important role in development of these tissues. The mouse ortholog may be involved in the regeneration of adult skeletal muscle and may act as a cell adhesion molecule in coronary vasculogenesis. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":105096822,"end":105137174,"strand":-1,"description":"blood vessel epicardial substance [Source:HGNC Symbol;Acc:HGNC:1152]"}, {"versioned_ensembl_gene_id":"ENSG00000284629.1","gene_symbol":"AC097662.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227387683,"end":227387949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226759.7","gene_symbol":"DAB1-AS1","gene_name":"DAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49443]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926890","summary":null,"start":57860532,"end":57880905,"strand":1,"description":"DAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49443]"}, {"versioned_ensembl_gene_id":"ENSG00000206516.10","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457053,"end":29464201,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000122359.17","gene_symbol":"ANXA11","gene_name":"annexin A11 [Source:HGNC Symbol;Acc:HGNC:535]","synonyms":"ANX11","biotype":"protein_coding","ncbi_id":"311","summary":"This gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains, which contain calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Several transcript variants encoding two different isoforms have been identified. [provided by RefSeq, Dec 2015]","start":80150889,"end":80205572,"strand":-1,"description":"annexin A11 [Source:HGNC Symbol;Acc:HGNC:535]"}, {"versioned_ensembl_gene_id":"ENSG00000275637.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54906192,"end":54910107,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000225884.2","gene_symbol":"AC098872.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":191793425,"end":191820250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174307.6","gene_symbol":"PHLDA3","gene_name":"pleckstrin homology like domain family A member 3 [Source:HGNC Symbol;Acc:HGNC:8934]","synonyms":"TIH1","biotype":"protein_coding","ncbi_id":"23612","summary":null,"start":201464383,"end":201469237,"strand":-1,"description":"pleckstrin homology like domain family A member 3 [Source:HGNC Symbol;Acc:HGNC:8934]"}, {"versioned_ensembl_gene_id":"ENSG00000168243.10","gene_symbol":"GNG4","gene_name":"G protein subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:4407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2786","summary":null,"start":235547687,"end":235650754,"strand":-1,"description":"G protein subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:4407]"}, {"versioned_ensembl_gene_id":"ENSG00000179889.18","gene_symbol":"PDXDC1","gene_name":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]","synonyms":"KIAA0251,KIAA0251","biotype":"protein_coding","ncbi_id":"23042","summary":null,"start":14974591,"end":15139339,"strand":1,"description":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]"}, {"versioned_ensembl_gene_id":"ENSG00000235700.1","gene_symbol":"CYCSP52","gene_name":"cytochrome c, somatic pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:24393]","synonyms":"HC6,HCP2","biotype":"processed_pseudogene","ncbi_id":"360155","summary":null,"start":157128362,"end":157128671,"strand":1,"description":"cytochrome c, somatic pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:24393]"}, {"versioned_ensembl_gene_id":"ENSG00000253838.1","gene_symbol":"AC007991.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":39914229,"end":39915721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242683.1","gene_symbol":"RPL12P21","gene_name":"ribosomal protein L12 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36845]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270921","summary":null,"start":139035148,"end":139035987,"strand":-1,"description":"ribosomal protein L12 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36845]"}, {"versioned_ensembl_gene_id":"ENSG00000109265.13","gene_symbol":"KIAA1211","gene_name":"KIAA1211 [Source:HGNC Symbol;Acc:HGNC:29219]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57482","summary":null,"start":56049073,"end":56328625,"strand":1,"description":"KIAA1211 [Source:HGNC Symbol;Acc:HGNC:29219]"}, {"versioned_ensembl_gene_id":"ENSG00000230773.6","gene_symbol":"AC092650.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47941696,"end":48240983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223973.2","gene_symbol":"AC068491.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":111383752,"end":111384992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233599.8","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"ZNF178,RNF93,ZNFB7","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30208315,"end":30217805,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000249087.6","gene_symbol":"ZNF436-AS1","gene_name":"ZNF436 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25122]","synonyms":"FLJ90508,C1orf213","biotype":"antisense_RNA","ncbi_id":"148898","summary":null,"start":23368997,"end":23371839,"strand":1,"description":"ZNF436 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25122]"}, {"versioned_ensembl_gene_id":"ENSG00000273312.2","gene_symbol":"AL121749.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35604485,"end":35608153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273880.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54716322,"end":54720285,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000186815.12","gene_symbol":"TPCN1","gene_name":"two pore segment channel 1 [Source:HGNC Symbol;Acc:HGNC:18182]","synonyms":"TPC1,KIAA1169,FLJ20612","biotype":"protein_coding","ncbi_id":"53373","summary":"Voltage-gated Ca(2+) and Na+ channels have 4 homologous domains, each containing 6 transmembrane segments, S1 to S6. TPCN1 is similar to these channels, but it has only 2 domains containing S1 to S6 (Ishibashi et al., 2000 [PubMed 10753632]).[supplied by OMIM, Mar 2008]","start":113221050,"end":113298585,"strand":1,"description":"two pore segment channel 1 [Source:HGNC Symbol;Acc:HGNC:18182]"}, {"versioned_ensembl_gene_id":"ENSG00000213558.3","gene_symbol":"HMGN2P32","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39403]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874473","summary":null,"start":107458038,"end":107458306,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39403]"}, {"versioned_ensembl_gene_id":"ENSG00000172269.18","gene_symbol":"DPAGT1","gene_name":"dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:2995]","synonyms":"CDG-Ij,ALG7,GPT,DPAGT2,DPAGT,DGPT,D11S366","biotype":"protein_coding","ncbi_id":"1798","summary":"The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme. [provided by RefSeq, Jul 2008]","start":119096503,"end":119108331,"strand":-1,"description":"dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:2995]"}, {"versioned_ensembl_gene_id":"ENSG00000185271.7","gene_symbol":"KLHL33","gene_name":"kelch like family member 33 [Source:HGNC Symbol;Acc:HGNC:31952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"123103","summary":null,"start":20425870,"end":20435811,"strand":-1,"description":"kelch like family member 33 [Source:HGNC Symbol;Acc:HGNC:31952]"}, {"versioned_ensembl_gene_id":"ENSG00000034693.14","gene_symbol":"PEX3","gene_name":"peroxisomal biogenesis factor 3 [Source:HGNC Symbol;Acc:HGNC:8858]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8504","summary":"The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]","start":143450807,"end":143490010,"strand":1,"description":"peroxisomal biogenesis factor 3 [Source:HGNC Symbol;Acc:HGNC:8858]"}, {"versioned_ensembl_gene_id":"ENSG00000268606.5","gene_symbol":"MAGEA2","gene_name":"MAGE family member A2 [Source:HGNC Symbol;Acc:HGNC:6800]","synonyms":"MAGEA2A,MAGE2,CT1.2","biotype":"protein_coding","ncbi_id":"4101","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci. Alternatively spliced transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":152749863,"end":152753884,"strand":-1,"description":"MAGE family member A2 [Source:HGNC Symbol;Acc:HGNC:6800]"}, {"versioned_ensembl_gene_id":"ENSG00000259140.2","gene_symbol":"AL049839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94674877,"end":94675829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235198.1","gene_symbol":"AC005871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117562084,"end":117572457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181513.14","gene_symbol":"ACBD4","gene_name":"acyl-CoA binding domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23337]","synonyms":"FLJ13322","biotype":"protein_coding","ncbi_id":"79777","summary":"This gene encodes a member of the acyl-coenzyme A binding domain containing protein family. All family members contain the conserved acyl-Coenzyme A binding domain, which binds acyl-CoA thiol esters. They are thought to play roles in acyl-CoA dependent lipid metabolism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":45132600,"end":45144181,"strand":1,"description":"acyl-CoA binding domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23337]"}, {"versioned_ensembl_gene_id":"ENSG00000225370.1","gene_symbol":"AC243962.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54671231,"end":54672591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250302.1","gene_symbol":"LINC01618","gene_name":"long intergenic non-protein coding RNA 1618 [Source:HGNC Symbol;Acc:HGNC:27195]","synonyms":"LOC152578","biotype":"lincRNA","ncbi_id":"152578","summary":null,"start":52789994,"end":52815464,"strand":1,"description":"long intergenic non-protein coding RNA 1618 [Source:HGNC Symbol;Acc:HGNC:27195]"}, {"versioned_ensembl_gene_id":"ENSG00000248423.1","gene_symbol":"AC100850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15688914,"end":15689562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254042.1","gene_symbol":"AC011365.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168706567,"end":168720884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073350.13","gene_symbol":"LLGL2","gene_name":"LLGL2, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6629]","synonyms":"Hugl-2,HGL","biotype":"protein_coding","ncbi_id":"3993","summary":"The lethal (2) giant larvae protein of Drosophila plays a role in asymmetric cell division, epithelial cell polarity, and cell migration. This human gene encodes a protein similar to lethal (2) giant larvae of Drosophila. In fly, the protein's ability to localize cell fate determinants is regulated by the atypical protein kinase C (aPKC). In human, this protein interacts with aPKC-containing complexes and is cortically localized in mitotic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":75525080,"end":75575208,"strand":1,"description":"LLGL2, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6629]"}, {"versioned_ensembl_gene_id":"ENSG00000181609.5","gene_symbol":"OR52D1","gene_name":"olfactory receptor family 52 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:15212]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5488685,"end":5489749,"strand":1,"description":"olfactory receptor family 52 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:15212]"}, {"versioned_ensembl_gene_id":"ENSG00000276409.4","gene_symbol":"CCL14","gene_name":"C-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10612]","synonyms":"NCC-2,MCIF,HCC-3,HCC-1,CKb1,SCYL2,SCYA14","biotype":"protein_coding","ncbi_id":"6358","summary":"This gene, chemokine (C-C motif) ligand 14, is one of several CC cytokine genes clustered on 17q11.2. The CC cytokines are secreted proteins characterized by two adjacent cysteines. The cytokine encoded by this gene induces changes in intracellular calcium concentration and enzyme release in monocytes. Multiple transcript variants encoding different isoforms have been found for this gene. Read-through transcripts are also expressed that include exons from the upstream cytokine gene, chemokine (C-C motif) ligand 15, and are represented as GeneID: 348249. [provided by RefSeq, Dec 2009]","start":35983291,"end":35987004,"strand":-1,"description":"C-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10612]"}, {"versioned_ensembl_gene_id":"ENSG00000175520.8","gene_symbol":"UBQLN3","gene_name":"ubiquilin 3 [Source:HGNC Symbol;Acc:HGNC:12510]","synonyms":"TUP-1","biotype":"protein_coding","ncbi_id":"50613","summary":"This gene encodes a ubiquitin-like protein (ubiquilin) that shares a high degree of similarity with related products in yeast, rat and frog. Ubiquilins contain an N-terminal ubiquitin-like domain and a C-terminal ubiquitin-associated domain. They physically associate with both proteasomes and ubiquitin ligases, and are thus thought to functionally link the ubiquitination machinery to the proteasome to affect in vivo protein degradation. This gene is specifically expressed in the testis. It has been suggested that this gene may regulate cell-cycle progression during spermatogenesis, however, it has been shown that the ortholgous mouse gene is dispensable for embryonic development and spermatogenesis. [provided by RefSeq, Nov 2016]","start":5507300,"end":5509985,"strand":-1,"description":"ubiquilin 3 [Source:HGNC Symbol;Acc:HGNC:12510]"}, {"versioned_ensembl_gene_id":"ENSG00000167359.8","gene_symbol":"OR51I1","gene_name":"olfactory receptor family 51 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:15200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390063","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5440570,"end":5441514,"strand":-1,"description":"olfactory receptor family 51 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:15200]"}, {"versioned_ensembl_gene_id":"ENSG00000279012.2","gene_symbol":"OR51B2","gene_name":"olfactory receptor family 51 subfamily B member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14703]","synonyms":"OR51B1P","biotype":"polymorphic_pseudogene","ncbi_id":"79345","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":5323359,"end":5324297,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14703]"}, {"versioned_ensembl_gene_id":"ENSG00000278492.1","gene_symbol":"AC006213.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":43978376,"end":43978663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008226.19","gene_symbol":"DLEC1","gene_name":"deleted in lung and esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:2899]","synonyms":"DLC1,CFAP81","biotype":"protein_coding","ncbi_id":"9940","summary":"The cytogenetic location of this gene is 3p21.3, and it is located in a region that is commonly deleted in a variety of malignancies. Down-regulation of this gene has been observed in several human cancers including lung, esophageal, renal tumors, and head and neck squamous cell carcinoma. In some cases, reduced expression of this gene in tumor cells is a result of aberrant promoter methylation. Several alternatively spliced transcripts have been observed that contain disrupted coding regions and likely encode nonfunctional proteins.[provided by RefSeq, Mar 2016]","start":38039205,"end":38124025,"strand":1,"description":"deleted in lung and esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:2899]"}, {"versioned_ensembl_gene_id":"ENSG00000168930.13","gene_symbol":"TRIM49","gene_name":"tripartite motif containing 49 [Source:HGNC Symbol;Acc:HGNC:13431]","synonyms":"TRIM49A,RNF18","biotype":"protein_coding","ncbi_id":"57093","summary":"The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This gene has been found to be preferentially expressed in testis. Related pseudogenes and gene duplicates have also been identified on chromosome 11. [provided by RefSeq, Aug 2010]","start":89797655,"end":89808575,"strand":-1,"description":"tripartite motif containing 49 [Source:HGNC Symbol;Acc:HGNC:13431]"}, {"versioned_ensembl_gene_id":"ENSG00000255162.1","gene_symbol":"AP004833.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89785945,"end":89787838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243716.10","gene_symbol":"NPIPB5","gene_name":"nuclear pore complex interacting protein family member B5 [Source:HGNC Symbol;Acc:HGNC:37233]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132247","summary":null,"start":22479121,"end":22536521,"strand":1,"description":"nuclear pore complex interacting protein family member B5 [Source:HGNC Symbol;Acc:HGNC:37233]"}, {"versioned_ensembl_gene_id":"ENSG00000275485.1","gene_symbol":"AL512652.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":20768876,"end":20769375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233835.1","gene_symbol":"AL132875.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79871873,"end":79874610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254411.1","gene_symbol":"AP002512.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56495760,"end":56496412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232034.1","gene_symbol":"AC092168.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":100822661,"end":100847220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273510.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769838,"end":54784324,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000278177.1","gene_symbol":"AL354811.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93226612,"end":93227317,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256995.6","gene_symbol":"AC084816.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22699859,"end":23174125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256923.1","gene_symbol":"AC084819.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22742582,"end":22743091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170356.9","gene_symbol":"OR2A20P","gene_name":"olfactory receptor family 2 subfamily A member 20 pseudogene [Source:NCBI gene;Acc:401428]","synonyms":"OR2A20","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401428","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144250045,"end":144256244,"strand":-1,"description":"olfactory receptor family 2 subfamily A member 20 pseudogene [Source:NCBI gene;Acc:401428]"}, {"versioned_ensembl_gene_id":"ENSG00000164399.4","gene_symbol":"IL3","gene_name":"interleukin 3 [Source:HGNC Symbol;Acc:HGNC:6011]","synonyms":"MULTI-CSF,MGC79399,MGC79398,MCGF,IL-3","biotype":"protein_coding","ncbi_id":"3562","summary":"The protein encoded by this gene is a potent growth promoting cytokine. This cytokine is capable of supporting the proliferation of a broad range of hematopoietic cell types. It is involved in a variety of cell activities such as cell growth, differentiation and apoptosis. This cytokine has been shown to also possess neurotrophic activity, and it may be associated with neurologic disorders. [provided by RefSeq, Jul 2008]","start":132060529,"end":132063204,"strand":1,"description":"interleukin 3 [Source:HGNC Symbol;Acc:HGNC:6011]"}, {"versioned_ensembl_gene_id":"ENSG00000257809.1","gene_symbol":"AC034102.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56150796,"end":56158220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226046.1","gene_symbol":"AP1S2P1","gene_name":"adaptor related protein complex 1 sigma 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480305","summary":null,"start":97437518,"end":97437896,"strand":1,"description":"adaptor related protein complex 1 sigma 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50752]"}, {"versioned_ensembl_gene_id":"ENSG00000131480.8","gene_symbol":"AOC2","gene_name":"amine oxidase, copper containing 2 [Source:HGNC Symbol;Acc:HGNC:549]","synonyms":"RAO,DAO2","biotype":"protein_coding","ncbi_id":"314","summary":"Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. This gene shows high sequence similarity to copper amine oxidases from various species ranging from bacteria to mammals. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. This gene may be a candidate gene for hereditary ocular diseases. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":42844600,"end":42850707,"strand":1,"description":"amine oxidase, copper containing 2 [Source:HGNC Symbol;Acc:HGNC:549]"}, {"versioned_ensembl_gene_id":"ENSG00000253424.1","gene_symbol":"AC025437.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158256137,"end":158258436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277556.1","gene_symbol":"OR13C5","gene_name":"olfactory receptor family 13 subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:15100]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138799","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104598457,"end":104599413,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:15100]"}, {"versioned_ensembl_gene_id":"ENSG00000277087.1","gene_symbol":"AL121890.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5045761,"end":5046276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259146.3","gene_symbol":"AC005476.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71292729,"end":71321814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275106.1","gene_symbol":"AC025594.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":128952527,"end":128953316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277490.1","gene_symbol":"BX664608.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66879454,"end":66879940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153485.5","gene_symbol":"TMEM251","gene_name":"transmembrane protein 251 [Source:HGNC Symbol;Acc:HGNC:20218]","synonyms":"DKFZP564F1123,C14orf109","biotype":"protein_coding","ncbi_id":"26175","summary":null,"start":93184951,"end":93187089,"strand":1,"description":"transmembrane protein 251 [Source:HGNC Symbol;Acc:HGNC:20218]"}, {"versioned_ensembl_gene_id":"ENSG00000228237.5","gene_symbol":"EFCAB14-AS1","gene_name":"EFCAB14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44108]","synonyms":"KIAA0494-AS1","biotype":"antisense_RNA","ncbi_id":"100130197","summary":null,"start":46674036,"end":46692098,"strand":1,"description":"EFCAB14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44108]"}, {"versioned_ensembl_gene_id":"ENSG00000229115.1","gene_symbol":"AL390774.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123759220,"end":123759775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230536.1","gene_symbol":"AL360268.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128090969,"end":128094457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234771.3","gene_symbol":"SLC25A25-AS1","gene_name":"SLC25A25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27844]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289019","summary":null,"start":128108581,"end":128118693,"strand":-1,"description":"SLC25A25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27844]"}, {"versioned_ensembl_gene_id":"ENSG00000265298.1","gene_symbol":"AC132812.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64750420,"end":64751311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130165.10","gene_symbol":"ELOF1","gene_name":"elongation factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:28691]","synonyms":"MGC4549,ELF1","biotype":"protein_coding","ncbi_id":"84337","summary":null,"start":11551147,"end":11559236,"strand":-1,"description":"elongation factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:28691]"}, {"versioned_ensembl_gene_id":"ENSG00000227706.3","gene_symbol":"AL713998.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67887646,"end":67889339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256551.1","gene_symbol":"LINC02369","gene_name":"long intergenic non-protein coding RNA 2369 [Source:HGNC Symbol;Acc:HGNC:53292]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996679","summary":null,"start":128086985,"end":128118132,"strand":-1,"description":"long intergenic non-protein coding RNA 2369 [Source:HGNC Symbol;Acc:HGNC:53292]"}, {"versioned_ensembl_gene_id":"ENSG00000186152.6","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000139613.11","gene_symbol":"SMARCC2","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2 [Source:HGNC Symbol;Acc:HGNC:11105]","synonyms":"BAF170,Rsc8,CRACC2","biotype":"protein_coding","ncbi_id":"6601","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and contains a predicted leucine zipper motif typical of many transcription factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56162983,"end":56189567,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2 [Source:HGNC Symbol;Acc:HGNC:11105]"}, {"versioned_ensembl_gene_id":"ENSG00000231128.5","gene_symbol":"AL137856.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113812379,"end":113829171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235448.1","gene_symbol":"LURAP1L-AS1","gene_name":"LURAP1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49761]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929467","summary":null,"start":12700100,"end":12814345,"strand":-1,"description":"LURAP1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49761]"}, {"versioned_ensembl_gene_id":"ENSG00000134852.14","gene_symbol":"CLOCK","gene_name":"clock circadian regulator [Source:HGNC Symbol;Acc:HGNC:2082]","synonyms":"KIAA0334,KAT13D,bHLHe8","biotype":"protein_coding","ncbi_id":"9575","summary":"The protein encoded by this gene plays a central role in the regulation of circadian rhythms. The protein encodes a transcription factor of the basic helix-loop-helix (bHLH) family and contains DNA binding histone acetyltransferase activity. The encoded protein forms a heterodimer with ARNTL (BMAL1) that binds E-box enhancer elements upstream of Period (PER1, PER2, PER3) and Cryptochrome (CRY1, CRY2) genes and activates transcription of these genes. PER and CRY proteins heterodimerize and repress their own transcription by interacting in a feedback loop with CLOCK/ARNTL complexes. Polymorphisms in this gene may be associated with behavioral changes in certain populations and with obesity and metabolic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":55427903,"end":55547138,"strand":-1,"description":"clock circadian regulator [Source:HGNC Symbol;Acc:HGNC:2082]"}, {"versioned_ensembl_gene_id":"ENSG00000140463.13","gene_symbol":"BBS4","gene_name":"Bardet-Biedl syndrome 4 [Source:HGNC Symbol;Acc:HGNC:969]","synonyms":null,"biotype":"protein_coding","ncbi_id":"585","summary":"This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein \"BBSome\" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":72686179,"end":72738476,"strand":1,"description":"Bardet-Biedl syndrome 4 [Source:HGNC Symbol;Acc:HGNC:969]"}, {"versioned_ensembl_gene_id":"ENSG00000237541.3","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32741342,"end":32747215,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000259881.1","gene_symbol":"AC092384.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88881038,"end":88887136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232748.3","gene_symbol":"AC135050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31056460,"end":31062803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169242.11","gene_symbol":"EFNA1","gene_name":"ephrin A1 [Source:HGNC Symbol;Acc:HGNC:3221]","synonyms":"TNFAIP4,LERK1,EPLG1,ECKLG","biotype":"protein_coding","ncbi_id":"1942","summary":"This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNA class ephrin which binds to the EPHA2, EPHA4, EPHA5, EPHA6, and EPHA7 receptors. Two transcript variants that encode different isoforms were identified through sequence analysis. [provided by RefSeq, Jul 2008]","start":155127460,"end":155134857,"strand":1,"description":"ephrin A1 [Source:HGNC Symbol;Acc:HGNC:3221]"}, {"versioned_ensembl_gene_id":"ENSG00000127418.14","gene_symbol":"FGFRL1","gene_name":"fibroblast growth factor receptor like 1 [Source:HGNC Symbol;Acc:HGNC:3693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53834","summary":"The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein would consist of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. A marked difference between this gene product and the other family members is its lack of a cytoplasmic tyrosine kinase domain. The result is a transmembrane receptor that could interact with other family members and potentially inhibit signaling. Multiple alternatively spliced transcript variants encoding the same isoform have been found for this gene. [provided by RefSeq, Jul 2008]","start":1009936,"end":1026897,"strand":1,"description":"fibroblast growth factor receptor like 1 [Source:HGNC Symbol;Acc:HGNC:3693]"}, {"versioned_ensembl_gene_id":"ENSG00000280500.1","gene_symbol":"ELMO2P1","gene_name":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729894","summary":null,"start":23086215,"end":23124800,"strand":1,"description":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]"}, {"versioned_ensembl_gene_id":"ENSG00000226721.2","gene_symbol":"EEF1DP2","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33523]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442429","summary":null,"start":92836826,"end":92837668,"strand":-1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33523]"}, {"versioned_ensembl_gene_id":"ENSG00000259912.1","gene_symbol":"AC023813.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48620319,"end":48622033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259565.2","gene_symbol":"KRT8P23","gene_name":"keratin 8 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:33375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390610","summary":null,"start":76979245,"end":76980451,"strand":-1,"description":"keratin 8 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:33375]"}, {"versioned_ensembl_gene_id":"ENSG00000186008.7","gene_symbol":"RPS4XP21","gene_name":"ribosomal protein S4X pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36228]","synonyms":"RPS4P21","biotype":"processed_pseudogene","ncbi_id":"126235","summary":null,"start":34092561,"end":34093310,"strand":-1,"description":"ribosomal protein S4X pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36228]"}, {"versioned_ensembl_gene_id":"ENSG00000261267.1","gene_symbol":"AC026470.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48559661,"end":48587403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243364.7","gene_symbol":"EFNA4","gene_name":"ephrin A4 [Source:HGNC Symbol;Acc:HGNC:3224]","synonyms":"LERK4,EPLG4","biotype":"protein_coding","ncbi_id":"1945","summary":"This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNA class ephrin. Three transcript variants that encode distinct proteins have been identified. [provided by RefSeq, Jul 2008]","start":155063731,"end":155069553,"strand":1,"description":"ephrin A4 [Source:HGNC Symbol;Acc:HGNC:3224]"}, {"versioned_ensembl_gene_id":"ENSG00000259153.1","gene_symbol":"AC004816.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70810205,"end":70815403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165168.7","gene_symbol":"CYBB","gene_name":"cytochrome b-245 beta chain [Source:HGNC Symbol;Acc:HGNC:2578]","synonyms":"NOX2,GP91-PHOX,CGD","biotype":"protein_coding","ncbi_id":"1536","summary":"Cytochrome b (-245) is composed of cytochrome b alpha (CYBA) and beta (CYBB) chain. It has been proposed as a primary component of the microbicidal oxidase system of phagocytes. CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD). In this disorder, there is decreased activity of phagocyte NADPH oxidase; neutrophils are able to phagocytize bacteria but cannot kill them in the phagocytic vacuoles. The cause of the killing defect is an inability to increase the cell's respiration and consequent failure to deliver activated oxygen into the phagocytic vacuole. [provided by RefSeq, Jul 2008]","start":37780011,"end":37813461,"strand":1,"description":"cytochrome b-245 beta chain [Source:HGNC Symbol;Acc:HGNC:2578]"}, {"versioned_ensembl_gene_id":"ENSG00000170290.3","gene_symbol":"SLN","gene_name":"sarcolipin [Source:HGNC Symbol;Acc:HGNC:11089]","synonyms":"MGC125855,MGC125854,MGC12301","biotype":"protein_coding","ncbi_id":"6588","summary":"Sarcoplasmic reticulum Ca(2+)-ATPases are transmembrane proteins that catalyze the ATP-dependent transport of Ca(2+) from the cytosol into the lumen of the sarcoplasmic reticulum in muscle cells. This gene encodes a small proteolipid that regulates several sarcoplasmic reticulum Ca(2+)-ATPases. The transmembrane protein interacts with Ca(2+)-ATPases and reduces the accumulation of Ca(2+) in the sarcoplasmic reticulum without affecting the rate of ATP hydrolysis. [provided by RefSeq, Jul 2008]","start":107707378,"end":107719693,"strand":-1,"description":"sarcolipin [Source:HGNC Symbol;Acc:HGNC:11089]"}, {"versioned_ensembl_gene_id":"ENSG00000258532.1","gene_symbol":"LINC02305","gene_name":"long intergenic non-protein coding RNA 2305 [Source:HGNC Symbol;Acc:HGNC:53224]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724338","summary":null,"start":83906872,"end":83915050,"strand":-1,"description":"long intergenic non-protein coding RNA 2305 [Source:HGNC Symbol;Acc:HGNC:53224]"}, {"versioned_ensembl_gene_id":"ENSG00000223766.10","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"Em:AB014077.1,CAT56,Em:AB023052.2","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30601522,"end":30608359,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000188394.6","gene_symbol":"GPR21","gene_name":"G protein-coupled receptor 21 [Source:HGNC Symbol;Acc:HGNC:4476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2844","summary":"This gene encodes a member of the G-protein-coupled receptor 1 family. G-protein coupled receptors are membrane proteins which activate signaling cascades as a response to extracellular stress. The encoded protein activates a Gq signal transduction pathway which mobilizes calcium. [provided by RefSeq, Nov 2012]","start":123034527,"end":123035696,"strand":1,"description":"G protein-coupled receptor 21 [Source:HGNC Symbol;Acc:HGNC:4476]"}, {"versioned_ensembl_gene_id":"ENSG00000136404.15","gene_symbol":"TM6SF1","gene_name":"transmembrane 6 superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:11860]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53346","summary":null,"start":83107407,"end":83144854,"strand":1,"description":"transmembrane 6 superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:11860]"}, {"versioned_ensembl_gene_id":"ENSG00000237314.2","gene_symbol":"RPL12P39","gene_name":"ribosomal protein L12 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:35976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271410","summary":null,"start":64072158,"end":64072653,"strand":1,"description":"ribosomal protein L12 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:35976]"}, {"versioned_ensembl_gene_id":"ENSG00000173276.13","gene_symbol":"ZBTB21","gene_name":"zinc finger and BTB domain containing 21 [Source:HGNC Symbol;Acc:HGNC:13083]","synonyms":"ZNF295,KIAA1227","biotype":"protein_coding","ncbi_id":"49854","summary":null,"start":41986831,"end":42010387,"strand":-1,"description":"zinc finger and BTB domain containing 21 [Source:HGNC Symbol;Acc:HGNC:13083]"}, {"versioned_ensembl_gene_id":"ENSG00000234062.7","gene_symbol":"AL390879.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":136909395,"end":137021630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225078.2","gene_symbol":"AL365338.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123061845,"end":123063312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235778.1","gene_symbol":"AC130360.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7341826,"end":7342942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205424.1","gene_symbol":"AL592528.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45827961,"end":45836419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249446.2","gene_symbol":"TRAJ60","gene_name":"T-cell receptor alpha joining 60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12093]","synonyms":null,"biotype":"TR_J_pseudogene","ncbi_id":"28695","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22476306,"end":22476362,"strand":1,"description":"T-cell receptor alpha joining 60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12093]"}, {"versioned_ensembl_gene_id":"ENSG00000274959.1","gene_symbol":"SPDYE13P","gene_name":"speedy/RINGO cell cycle regulator family member E13, pseudogene [Source:HGNC Symbol;Acc:HGNC:51509]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105180390","summary":null,"start":75281267,"end":75287118,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E13, pseudogene [Source:HGNC Symbol;Acc:HGNC:51509]"}, {"versioned_ensembl_gene_id":"ENSG00000270137.1","gene_symbol":"AF230666.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":132826179,"end":132826903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278313.1","gene_symbol":"AC100827.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72604399,"end":72605008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165355.7","gene_symbol":"FBXO33","gene_name":"F-box protein 33 [Source:HGNC Symbol;Acc:HGNC:19833]","synonyms":"Fbx33","biotype":"protein_coding","ncbi_id":"254170","summary":"This locus represents an member of the F-box gene family. The encoded protein contains an F-box motif and a domain that might form a structure similar to a leucine-rich repeat found in placental RNAse inhibitor. This locus may be associated with copy number variation of UGT2B17 (GeneID 7367), which has been associated with susceptibility to osteoporosis.[provided by RefSeq, Sep 2010]","start":39397669,"end":39432500,"strand":-1,"description":"F-box protein 33 [Source:HGNC Symbol;Acc:HGNC:19833]"}, {"versioned_ensembl_gene_id":"ENSG00000227329.2","gene_symbol":"AL139396.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53164391,"end":53164557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103319.11","gene_symbol":"EEF2K","gene_name":"eukaryotic elongation factor 2 kinase [Source:HGNC Symbol;Acc:HGNC:24615]","synonyms":"eEF-2K","biotype":"protein_coding","ncbi_id":"29904","summary":"This gene encodes a highly conserved protein kinase in the calmodulin-mediated signaling pathway that links activation of cell surface receptors to cell division. This kinase is involved in the regulation of protein synthesis. It phosphorylates eukaryotic elongation factor 2 (EEF2) and thus inhibits the EEF2 function. The activity of this kinase is increased in many cancers and may be a valid target for anti-cancer treatment. [provided by RefSeq, Jul 2008]","start":22206282,"end":22288732,"strand":1,"description":"eukaryotic elongation factor 2 kinase [Source:HGNC Symbol;Acc:HGNC:24615]"}, {"versioned_ensembl_gene_id":"ENSG00000211829.9","gene_symbol":"TRDC","gene_name":"T-cell receptor delta constant [Source:HGNC Symbol;Acc:HGNC:12253]","synonyms":null,"biotype":"TR_C_gene","ncbi_id":"28526","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22462932,"end":22465787,"strand":1,"description":"T-cell receptor delta constant [Source:HGNC Symbol;Acc:HGNC:12253]"}, {"versioned_ensembl_gene_id":"ENSG00000211827.1","gene_symbol":"TRDJ2","gene_name":"T-cell receptor delta joining 2 [Source:HGNC Symbol;Acc:HGNC:12258]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28521","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22456689,"end":22456742,"strand":1,"description":"T-cell receptor delta joining 2 [Source:HGNC Symbol;Acc:HGNC:12258]"}, {"versioned_ensembl_gene_id":"ENSG00000259042.2","gene_symbol":"AC244502.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22417836,"end":22418657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237444.1","gene_symbol":"AP001342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25031005,"end":25031529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237235.2","gene_symbol":"TRDD2","gene_name":"T-cell receptor delta diversity 2 [Source:HGNC Symbol;Acc:HGNC:12255]","synonyms":null,"biotype":"TR_D_gene","ncbi_id":"28524","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22439007,"end":22439015,"strand":1,"description":"T-cell receptor delta diversity 2 [Source:HGNC Symbol;Acc:HGNC:12255]"}, {"versioned_ensembl_gene_id":"ENSG00000184916.8","gene_symbol":"JAG2","gene_name":"jagged 2 [Source:HGNC Symbol;Acc:HGNC:6189]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3714","summary":"The Notch signaling pathway is an intercellular signaling mechanism that is essential for proper embryonic development. Members of the Notch gene family encode transmembrane receptors that are critical for various cell fate decisions. The protein encoded by this gene is one of several ligands that activate Notch and related receptors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":105140981,"end":105168824,"strand":-1,"description":"jagged 2 [Source:HGNC Symbol;Acc:HGNC:6189]"}, {"versioned_ensembl_gene_id":"ENSG00000251111.2","gene_symbol":"FCF1P8","gene_name":"FCF1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422531","summary":null,"start":55351812,"end":55352408,"strand":-1,"description":"FCF1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44620]"}, {"versioned_ensembl_gene_id":"ENSG00000117419.14","gene_symbol":"ERI3","gene_name":"ERI1 exoribonuclease family member 3 [Source:HGNC Symbol;Acc:HGNC:17276]","synonyms":"PRNPIP,PINT1,FLJ22943","biotype":"protein_coding","ncbi_id":"79033","summary":null,"start":44221070,"end":44355260,"strand":-1,"description":"ERI1 exoribonuclease family member 3 [Source:HGNC Symbol;Acc:HGNC:17276]"}, {"versioned_ensembl_gene_id":"ENSG00000271398.1","gene_symbol":"AL353622.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28247144,"end":28247568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279433.1","gene_symbol":"AC018529.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77108284,"end":77110537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197712.11","gene_symbol":"FAM114A1","gene_name":"family with sequence similarity 114 member A1 [Source:HGNC Symbol;Acc:HGNC:25087]","synonyms":"Noxp20","biotype":"protein_coding","ncbi_id":"92689","summary":"The protein encoded by this gene belongs to the FAM114 family and may play a role in neuronal cell development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":38867677,"end":38945739,"strand":1,"description":"family with sequence similarity 114 member A1 [Source:HGNC Symbol;Acc:HGNC:25087]"}, {"versioned_ensembl_gene_id":"ENSG00000274447.1","gene_symbol":"AC005790.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5294247,"end":5294696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198373.12","gene_symbol":"WWP2","gene_name":"WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16804]","synonyms":"AIP2","biotype":"protein_coding","ncbi_id":"11060","summary":"This gene encodes a member of the Nedd4 family of E3 ligases, which play an important role in protein ubiquitination. The encoded protein contains four WW domains and may play a role in multiple processes including chondrogenesis and the regulation of oncogenic signaling pathways via interactions with Smad proteins and the tumor suppressor PTEN. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 10. [provided by RefSeq, Jul 2012]","start":69762306,"end":69941741,"strand":1,"description":"WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16804]"}, {"versioned_ensembl_gene_id":"ENSG00000238035.8","gene_symbol":"AC138035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181306502,"end":181324685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279064.1","gene_symbol":"FP236315.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5707004,"end":5709456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183283.15","gene_symbol":"DAZAP2","gene_name":"DAZ associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2684]","synonyms":"KIAA0058","biotype":"protein_coding","ncbi_id":"9802","summary":"This gene encodes a proline-rich protein which interacts with the deleted in azoospermia (DAZ) and the deleted in azoospermia-like gene through the DAZ-like repeats. This protein also interacts with the transforming growth factor-beta signaling molecule SARA (Smad anchor for receptor activation), eukaryotic initiation factor 4G, and an E3 ubiquitinase that regulates its stability in splicing factor containing nuclear speckles. The encoded protein may function in various biological and pathological processes including spermatogenesis, cell signaling and transcription regulation, formation of stress granules during translation arrest, RNA splicing, and pathogenesis of multiple myeloma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":51238292,"end":51271362,"strand":1,"description":"DAZ associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2684]"}, {"versioned_ensembl_gene_id":"ENSG00000213073.4","gene_symbol":"AL353625.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":160093082,"end":160096212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183484.11","gene_symbol":"GPR132","gene_name":"G protein-coupled receptor 132 [Source:HGNC Symbol;Acc:HGNC:17482]","synonyms":"G2A","biotype":"protein_coding","ncbi_id":"29933","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor (GPCR) superfamily. The receptors are seven-pass transmembrane proteins that respond to extracellular cues and activate intracellular signal transduction pathways. This protein was reported to be a receptor for lysophosphatidylcholine action, but PubMedID: 15653487 retracts this finding and instead suggests this protein to be an effector of lysophosphatidylcholine action. This protein may have proton-sensing activity and may be a receptor for oxidized free fatty acids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":105049389,"end":105065445,"strand":-1,"description":"G protein-coupled receptor 132 [Source:HGNC Symbol;Acc:HGNC:17482]"}, {"versioned_ensembl_gene_id":"ENSG00000132581.9","gene_symbol":"SDF2","gene_name":"stromal cell derived factor 2 [Source:HGNC Symbol;Acc:HGNC:10675]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6388","summary":"The protein encoded by this gene is believed to be a secretory protein. It has regions of similarity to hydrophilic segments of yeast mannosyltransferases. Its expression is ubiquitous and the gene appears to be relatively conserved among mammals. Alternate splicing results in both coding and non-coding variants. A pseudogene of this gene is located on chromosome 15. [provided by RefSeq, Dec 2011]","start":28648356,"end":28662189,"strand":-1,"description":"stromal cell derived factor 2 [Source:HGNC Symbol;Acc:HGNC:10675]"}, {"versioned_ensembl_gene_id":"ENSG00000220744.1","gene_symbol":"RPL5P18","gene_name":"ribosomal protein L5 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389428","summary":null,"start":127362513,"end":127363403,"strand":1,"description":"ribosomal protein L5 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36640]"}, {"versioned_ensembl_gene_id":"ENSG00000230798.5","gene_symbol":"FOXD3-AS1","gene_name":"FOXD3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40241]","synonyms":"pasFOXD3","biotype":"antisense_RNA","ncbi_id":"100996301","summary":null,"start":63320884,"end":63324441,"strand":-1,"description":"FOXD3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40241]"}, {"versioned_ensembl_gene_id":"ENSG00000236467.8","gene_symbol":"KCNMA1-AS1","gene_name":"KCNMA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51213]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929328","summary":null,"start":76888044,"end":76980624,"strand":1,"description":"KCNMA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51213]"}, {"versioned_ensembl_gene_id":"ENSG00000215482.3","gene_symbol":"CALM2P3","gene_name":"calmodulin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1448]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"807","summary":null,"start":41170700,"end":41171148,"strand":-1,"description":"calmodulin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1448]"}, {"versioned_ensembl_gene_id":"ENSG00000137142.4","gene_symbol":"IGFBPL1","gene_name":"insulin like growth factor binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:20081]","synonyms":"bA113O24.1","biotype":"protein_coding","ncbi_id":"347252","summary":null,"start":38408994,"end":38424447,"strand":-1,"description":"insulin like growth factor binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:20081]"}, {"versioned_ensembl_gene_id":"ENSG00000266549.1","gene_symbol":"AC023575.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26952201,"end":26952558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184515.10","gene_symbol":"BEX5","gene_name":"brain expressed X-linked 5 [Source:HGNC Symbol;Acc:HGNC:27990]","synonyms":"NGFRAP1L1","biotype":"protein_coding","ncbi_id":"340542","summary":null,"start":102153708,"end":102156057,"strand":-1,"description":"brain expressed X-linked 5 [Source:HGNC Symbol;Acc:HGNC:27990]"}, {"versioned_ensembl_gene_id":"ENSG00000231683.6","gene_symbol":"AL033397.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53561289,"end":53617171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254063.2","gene_symbol":"DUXAP2","gene_name":"double homeobox A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32181]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"503631","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":101366417,"end":101367005,"strand":-1,"description":"double homeobox A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32181]"}, {"versioned_ensembl_gene_id":"ENSG00000251488.1","gene_symbol":"AC115622.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132836772,"end":132981677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143954.12","gene_symbol":"REG3G","gene_name":"regenerating family member 3 gamma [Source:HGNC Symbol;Acc:HGNC:29595]","synonyms":"UNQ429,PAP1B,LPPM429","biotype":"protein_coding","ncbi_id":"130120","summary":"This gene encodes a member of the regenerating islet-derived genes (REG)3 protein family. These proteins are secreted, C-type lectins with a carbohydrate recognition domain and N-terminal signal peptide. The protein encoded by this gene is an antimicrobial lectin with activity against Gram-positive bacteria. Alternative splicing results in multiple transcript variants encoding multiple isoforms. [provided by RefSeq, Nov 2014]","start":79025686,"end":79028505,"strand":1,"description":"regenerating family member 3 gamma [Source:HGNC Symbol;Acc:HGNC:29595]"}, {"versioned_ensembl_gene_id":"ENSG00000255336.1","gene_symbol":"AP003181.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":105246880,"end":105247060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253942.1","gene_symbol":"AP001330.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101223941,"end":101224573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279936.1","gene_symbol":"AC008806.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37401404,"end":37403846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129946.10","gene_symbol":"SHC2","gene_name":"SHC adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:29869]","synonyms":"SLI,SHCB,SCK","biotype":"protein_coding","ncbi_id":"25759","summary":null,"start":416583,"end":460996,"strand":-1,"description":"SHC adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:29869]"}, {"versioned_ensembl_gene_id":"ENSG00000232790.2","gene_symbol":"LINC01162","gene_name":"long intergenic non-protein coding RNA 1162 [Source:HGNC Symbol;Acc:HGNC:49528]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355138","summary":null,"start":20835431,"end":21023148,"strand":1,"description":"long intergenic non-protein coding RNA 1162 [Source:HGNC Symbol;Acc:HGNC:49528]"}, {"versioned_ensembl_gene_id":"ENSG00000234839.1","gene_symbol":"RPS26P30","gene_name":"ribosomal protein S26 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35574]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271111","summary":null,"start":20843627,"end":20843961,"strand":1,"description":"ribosomal protein S26 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35574]"}, {"versioned_ensembl_gene_id":"ENSG00000227411.1","gene_symbol":"BAATP1","gene_name":"bile acid-CoA: amino acid N-acyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34504]","synonyms":"ACNATP","biotype":"unitary_pseudogene","ncbi_id":"347275","summary":null,"start":101334084,"end":101339347,"strand":-1,"description":"bile acid-CoA: amino acid N-acyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34504]"}, {"versioned_ensembl_gene_id":"ENSG00000260517.3","gene_symbol":"AC009093.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29139661,"end":29216706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130368.5","gene_symbol":"MAS1","gene_name":"MAS1 proto-oncogene, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:6899]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4142","summary":"This gene encodes a class I seven-transmembrane G-protein-coupled receptor. The encoded protein is a receptor for angiotensin-(1-7) and preferentially couples to the Gq protein, activating the phospholipase C signaling pathway. The encoded protein may play a role in multiple processes including hypotension, smooth muscle relaxation and cardioprotection by mediating the effects of angiotensin-(1-7). [provided by RefSeq, May 2012]","start":159906690,"end":159916530,"strand":1,"description":"MAS1 proto-oncogene, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:6899]"}, {"versioned_ensembl_gene_id":"ENSG00000083457.11","gene_symbol":"ITGAE","gene_name":"integrin subunit alpha E [Source:HGNC Symbol;Acc:HGNC:6147]","synonyms":"HUMINAE,CD103","biotype":"protein_coding","ncbi_id":"3682","summary":"Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This gene encodes an I-domain-containing alpha integrin that undergoes post-translational cleavage in the extracellular domain, yielding disulfide-linked heavy and light chains. In combination with the beta 7 integrin, this protein forms the E-cadherin binding integrin known as the human mucosal lymphocyte-1 antigen. This protein is preferentially expressed in human intestinal intraepithelial lymphocytes (IEL), and in addition to a role in adhesion, it may serve as an accessory molecule for IEL activation. [provided by RefSeq, Jul 2008]","start":3714628,"end":3801243,"strand":-1,"description":"integrin subunit alpha E [Source:HGNC Symbol;Acc:HGNC:6147]"}, {"versioned_ensembl_gene_id":"ENSG00000280257.1","gene_symbol":"AC007741.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":65790039,"end":65793533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113300.11","gene_symbol":"CNOT6","gene_name":"CCR4-NOT transcription complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:14099]","synonyms":"KIAA1194,Ccr4a,CCR4","biotype":"protein_coding","ncbi_id":"57472","summary":"This gene encodes the catalytic component of the CCR4-NOT core transcriptional regulation complex. The encoded protein has a 3'-5' RNase activity and prefers polyadenylated substrates. The CCR4-NOT complex plays a role in many cellular processes, including miRNA-mediated repression, mRNA degradation, and transcriptional regulation. [provided by RefSeq, Dec 2014]","start":180494412,"end":180578405,"strand":1,"description":"CCR4-NOT transcription complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:14099]"}, {"versioned_ensembl_gene_id":"ENSG00000255172.2","gene_symbol":"OR5AM1P","gene_name":"olfactory receptor family 5 subfamily AM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15254]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81226","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56619779,"end":56620810,"strand":-1,"description":"olfactory receptor family 5 subfamily AM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15254]"}, {"versioned_ensembl_gene_id":"ENSG00000249463.1","gene_symbol":"AC096711.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132027175,"end":132028434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108439.10","gene_symbol":"PNPO","gene_name":"pyridoxamine 5'-phosphate oxidase [Source:HGNC Symbol;Acc:HGNC:30260]","synonyms":"PDXPO","biotype":"protein_coding","ncbi_id":"55163","summary":"The enzyme encoded by this gene catalyzes the terminal, rate-limiting step in the synthesis of pyridoxal 5'-phosphate, also known as vitamin B6. Vitamin B6 is a required co-factor for enzymes involved in both homocysteine metabolism and synthesis of neurotransmitters such as catecholamine. Mutations in this gene result in pyridoxamine 5'-phosphate oxidase (PNPO) deficiency, a form of neonatal epileptic encephalopathy. [provided by RefSeq, Oct 2008]","start":47941506,"end":47949308,"strand":1,"description":"pyridoxamine 5'-phosphate oxidase [Source:HGNC Symbol;Acc:HGNC:30260]"}, {"versioned_ensembl_gene_id":"ENSG00000251598.1","gene_symbol":"AC096711.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132004810,"end":132124031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238265.1","gene_symbol":"LINC00317","gene_name":"long intergenic non-protein coding RNA 317 [Source:HGNC Symbol;Acc:HGNC:23126]","synonyms":"NCRNA00317,C21orf117,PRED89","biotype":"lincRNA","ncbi_id":"378828","summary":null,"start":21723293,"end":21737319,"strand":-1,"description":"long intergenic non-protein coding RNA 317 [Source:HGNC Symbol;Acc:HGNC:23126]"}, {"versioned_ensembl_gene_id":"ENSG00000237527.1","gene_symbol":"AF241725.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21655038,"end":21686329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283000.1","gene_symbol":"AL392046.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34969909,"end":34975578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135241.16","gene_symbol":"PNPLA8","gene_name":"patatin like phospholipase domain containing 8 [Source:HGNC Symbol;Acc:HGNC:28900]","synonyms":"iPLA2gamma,IPLA2G,IPLA2-2","biotype":"protein_coding","ncbi_id":"50640","summary":"This gene encodes a member of the patatin-like phospholipase domain containing protein family. Members of this family are phospholipases which catalyze the cleavage of fatty acids from membrane phospholipids. The product of this gene is a calcium-independent phospholipase. Mutations in this gene have been associated with mitochondrial myopathy with lactic acidosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2015]","start":108470422,"end":108569666,"strand":-1,"description":"patatin like phospholipase domain containing 8 [Source:HGNC Symbol;Acc:HGNC:28900]"}, {"versioned_ensembl_gene_id":"ENSG00000204110.6","gene_symbol":"LINC02520","gene_name":"long intergenic non-protein coding RNA 2520 [Source:HGNC Symbol;Acc:HGNC:53511]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505530","summary":null,"start":37507348,"end":37535616,"strand":1,"description":"long intergenic non-protein coding RNA 2520 [Source:HGNC Symbol;Acc:HGNC:53511]"}, {"versioned_ensembl_gene_id":"ENSG00000225553.7","gene_symbol":"PHF1","gene_name":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]","synonyms":"MTF2L2,TDRD19C,PCL1","biotype":"protein_coding","ncbi_id":"5252","summary":"This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":33550562,"end":33556643,"strand":1,"description":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]"}, {"versioned_ensembl_gene_id":"ENSG00000231048.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"B144,LST-1,D6S49E","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31625572,"end":31628357,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000250844.2","gene_symbol":"USP17L18","gene_name":"ubiquitin specific peptidase 17-like family member 18 [Source:HGNC Symbol;Acc:HGNC:44446]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287364","summary":null,"start":9248630,"end":9250581,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 18 [Source:HGNC Symbol;Acc:HGNC:44446]"}, {"versioned_ensembl_gene_id":"ENSG00000140022.9","gene_symbol":"STON2","gene_name":"stonin 2 [Source:HGNC Symbol;Acc:HGNC:30652]","synonyms":"STN2,STNB2","biotype":"protein_coding","ncbi_id":"85439","summary":"This gene encodes a protein which is a membrane protein involved in regulating endocytotic complexes. The protein product is described as one of the clathrin-associated sorting proteins, adaptor molecules which ensure specific proteins are internalized. The encoded protein has also been shown to participate in synaptic vesicle recycling through interaction with synaptotagmin 1 required for neurotransmission. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":81260656,"end":81436465,"strand":-1,"description":"stonin 2 [Source:HGNC Symbol;Acc:HGNC:30652]"}, {"versioned_ensembl_gene_id":"ENSG00000251010.1","gene_symbol":"AC097372.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146241806,"end":146243669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253114.2","gene_symbol":"AC090151.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54696398,"end":54697127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177455.12","gene_symbol":"CD19","gene_name":"CD19 molecule [Source:HGNC Symbol;Acc:HGNC:1633]","synonyms":null,"biotype":"protein_coding","ncbi_id":"930","summary":"This gene encodes a member of the immunoglobulin gene superfamily. Expression of this cell surface protein is restricted to B cell lymphocytes. This protein is a reliable marker for pre-B cells but its expression diminishes during terminal B cell differentiation in antibody secreting plasma cells. The protein has two N-terminal extracellular Ig-like domains separated by a non-Ig-like domain, a hydrophobic transmembrane domain, and a large C-terminal cytoplasmic domain. This protein forms a complex with several membrane proteins including complement receptor type 2 (CD21) and tetraspanin (CD81) and this complex reduces the threshold for antigen-initiated B cell activation. Activation of this B-cell antigen receptor complex activates the phosphatidylinositol 3-kinase signalling pathway and the subsequent release of intracellular stores of calcium ions. This protein is a target of chimeric antigen receptor (CAR) T-cells used in the treatment of lymphoblastic leukemia. Mutations in this gene are associated with the disease common variable immunodeficiency 3 (CVID3) which results in a failure of B-cell differentiation and impaired secretion of immunoglobulins. CVID3 is characterized by hypogammaglobulinemia, an inability to mount an antibody response to antigen, and recurrent bacterial infections. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2020]","start":28931939,"end":28939346,"strand":1,"description":"CD19 molecule [Source:HGNC Symbol;Acc:HGNC:1633]"}, {"versioned_ensembl_gene_id":"ENSG00000260442.5","gene_symbol":"ATP2A1-AS1","gene_name":"ATP2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51370]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289092","summary":null,"start":28878957,"end":28879920,"strand":-1,"description":"ATP2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51370]"}, {"versioned_ensembl_gene_id":"ENSG00000143799.12","gene_symbol":"PARP1","gene_name":"poly(ADP-ribose) polymerase 1 [Source:HGNC Symbol;Acc:HGNC:270]","synonyms":"PARP,ADPRT,PPOL","biotype":"protein_coding","ncbi_id":"142","summary":"This gene encodes a chromatin-associated enzyme, poly(ADP-ribosyl)transferase, which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation, proliferation, and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition, this enzyme may be the site of mutation in Fanconi anemia, and may participate in the pathophysiology of type I diabetes. [provided by RefSeq, Jul 2008]","start":226360691,"end":226408079,"strand":-1,"description":"poly(ADP-ribose) polymerase 1 [Source:HGNC Symbol;Acc:HGNC:270]"}, {"versioned_ensembl_gene_id":"ENSG00000103742.11","gene_symbol":"IGDCC4","gene_name":"immunoglobulin superfamily DCC subclass member 4 [Source:HGNC Symbol;Acc:HGNC:13770]","synonyms":"NOPE,LOC57722","biotype":"protein_coding","ncbi_id":"57722","summary":null,"start":65381464,"end":65423072,"strand":-1,"description":"immunoglobulin superfamily DCC subclass member 4 [Source:HGNC Symbol;Acc:HGNC:13770]"}, {"versioned_ensembl_gene_id":"ENSG00000100599.15","gene_symbol":"RIN3","gene_name":"Ras and Rab interactor 3 [Source:HGNC Symbol;Acc:HGNC:18751]","synonyms":"FLJ22439","biotype":"protein_coding","ncbi_id":"79890","summary":"Summary: This protein encoded by this gene is a member of the RIN family of Ras interaction-interference proteins, which are binding partners to the RAB5 small GTPases. The protein functions as a guanine nucleotide exchange for RAB5B and RAB31. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":92513774,"end":92688994,"strand":1,"description":"Ras and Rab interactor 3 [Source:HGNC Symbol;Acc:HGNC:18751]"}, {"versioned_ensembl_gene_id":"ENSG00000204687.4","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"MAS-L,dJ994E9.2,MRG","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486697,"end":29487956,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000229867.1","gene_symbol":"STEAP3-AS1","gene_name":"STEAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41053]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874111","summary":null,"start":119244422,"end":119249071,"strand":-1,"description":"STEAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41053]"}, {"versioned_ensembl_gene_id":"ENSG00000275629.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"cl-5,nkat4b,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54849620,"end":54866390,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000249104.2","gene_symbol":"USP17L17","gene_name":"ubiquitin specific peptidase 17-like family member 17 [Source:HGNC Symbol;Acc:HGNC:44445]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287327","summary":null,"start":9243879,"end":9245830,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 17 [Source:HGNC Symbol;Acc:HGNC:44445]"}, {"versioned_ensembl_gene_id":"ENSG00000168765.16","gene_symbol":"GSTM4","gene_name":"glutathione S-transferase mu 4 [Source:HGNC Symbol;Acc:HGNC:4636]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2948","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. Multiple transcript variants, each encoding a distinct protein isoform, have been identified. [provided by RefSeq, Jul 2008]","start":109656081,"end":109674836,"strand":1,"description":"glutathione S-transferase mu 4 [Source:HGNC Symbol;Acc:HGNC:4636]"}, {"versioned_ensembl_gene_id":"ENSG00000178585.14","gene_symbol":"CTNNBIP1","gene_name":"catenin beta interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16913]","synonyms":"MGC15093,ICAT","biotype":"protein_coding","ncbi_id":"56998","summary":"The protein encoded by this gene binds CTNNB1 and prevents interaction between CTNNB1 and TCF family members. The encoded protein is a negative regulator of the Wnt signaling pathway. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":9848276,"end":9910336,"strand":-1,"description":"catenin beta interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16913]"}, {"versioned_ensembl_gene_id":"ENSG00000276631.1","gene_symbol":"AC007786.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29222542,"end":29223137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000026559.13","gene_symbol":"KCNG1","gene_name":"potassium voltage-gated channel modifier subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:6248]","synonyms":"KCNG,K13,Kv6.1,kH2","biotype":"protein_coding","ncbi_id":"3755","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This gene is abundantly expressed in skeletal muscle. Multiple alternatively spliced transcript variants have been found in normal and cancerous tissues. [provided by RefSeq, Jul 2008]","start":51003656,"end":51023129,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:6248]"}, {"versioned_ensembl_gene_id":"ENSG00000223569.6","gene_symbol":"USP17L15","gene_name":"ubiquitin specific peptidase 17-like family member 15 [Source:HGNC Symbol;Acc:HGNC:44443]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288520","summary":null,"start":9234385,"end":9236334,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 15 [Source:HGNC Symbol;Acc:HGNC:44443]"}, {"versioned_ensembl_gene_id":"ENSG00000256763.1","gene_symbol":"LINC02467","gene_name":"long intergenic non-protein coding RNA 2467 [Source:HGNC Symbol;Acc:HGNC:53404]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984446","summary":null,"start":126168235,"end":126171666,"strand":1,"description":"long intergenic non-protein coding RNA 2467 [Source:HGNC Symbol;Acc:HGNC:53404]"}, {"versioned_ensembl_gene_id":"ENSG00000223356.1","gene_symbol":"AL590666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156712212,"end":156713174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234877.2","gene_symbol":"AC092660.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78597911,"end":78599406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166349.9","gene_symbol":"RAG1","gene_name":"recombination activating 1 [Source:HGNC Symbol;Acc:HGNC:9831]","synonyms":"RNF74,MGC43321","biotype":"protein_coding","ncbi_id":"5896","summary":"The protein encoded by this gene is involved in activation of immunoglobulin V-D-J recombination. The encoded protein is involved in recognition of the DNA substrate, but stable binding and cleavage activity also requires RAG2. Defects in this gene can be the cause of several diseases. [provided by RefSeq, Jul 2008]","start":36510709,"end":36593156,"strand":1,"description":"recombination activating 1 [Source:HGNC Symbol;Acc:HGNC:9831]"}, {"versioned_ensembl_gene_id":"ENSG00000270470.1","gene_symbol":"AC064872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78437850,"end":78438921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226898.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555714,"end":29560028,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000203668.2","gene_symbol":"CHML","gene_name":"CHM like, Rab escort protein 2 [Source:HGNC Symbol;Acc:HGNC:1941]","synonyms":"REP-2","biotype":"protein_coding","ncbi_id":"1122","summary":"The product of the CHML gene supports geranylgeranylation of most Rab proteins and may substitute for REP-1 in tissues other than retina. CHML is localized close to the gene for Usher syndrome type II. [provided by RefSeq, Jul 2008]","start":241628853,"end":241640254,"strand":-1,"description":"CHM like, Rab escort protein 2 [Source:HGNC Symbol;Acc:HGNC:1941]"}, {"versioned_ensembl_gene_id":"ENSG00000270765.5","gene_symbol":"GAS2L2","gene_name":"growth arrest specific 2 like 2 [Source:HGNC Symbol;Acc:HGNC:24846]","synonyms":"GAR17","biotype":"protein_coding","ncbi_id":"246176","summary":"The protein encoded by this gene appears to crosslink microtubules and microfilaments and may be part of the cytoskeleton. This gene is mainly expressed in skeletal muscle. [provided by RefSeq, Jul 2011]","start":35744511,"end":35752878,"strand":-1,"description":"growth arrest specific 2 like 2 [Source:HGNC Symbol;Acc:HGNC:24846]"}, {"versioned_ensembl_gene_id":"ENSG00000232399.3","gene_symbol":"USP17L13","gene_name":"ubiquitin specific peptidase 17-like family member 13 [Source:HGNC Symbol;Acc:HGNC:44441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287238","summary":null,"start":9224896,"end":9226847,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 13 [Source:HGNC Symbol;Acc:HGNC:44441]"}, {"versioned_ensembl_gene_id":"ENSG00000227551.1","gene_symbol":"USP17L12","gene_name":"ubiquitin specific peptidase 17-like family member 12 [Source:HGNC Symbol;Acc:HGNC:44440]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287205","summary":null,"start":9220152,"end":9221744,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 12 [Source:HGNC Symbol;Acc:HGNC:44440]"}, {"versioned_ensembl_gene_id":"ENSG00000142227.10","gene_symbol":"EMP3","gene_name":"epithelial membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:3335]","synonyms":"YMP","biotype":"protein_coding","ncbi_id":"2014","summary":"The protein encoded by this gene belongs to the PMP-22/EMP/MP20 family of proteins. The protein contains four transmembrane domains and two N-linked glycosylation sites. It is thought to be involved in cell proliferation, cell-cell interactions and function as a tumor suppressor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":48321509,"end":48330553,"strand":1,"description":"epithelial membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:3335]"}, {"versioned_ensembl_gene_id":"ENSG00000214429.3","gene_symbol":"CYCSP6","gene_name":"cytochrome c, somatic pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24421]","synonyms":"HCP6","biotype":"processed_pseudogene","ncbi_id":"360159","summary":null,"start":78412793,"end":78413094,"strand":-1,"description":"cytochrome c, somatic pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24421]"}, {"versioned_ensembl_gene_id":"ENSG00000148019.12","gene_symbol":"CEP78","gene_name":"centrosomal protein 78 [Source:HGNC Symbol;Acc:HGNC:25740]","synonyms":"FLJ12643,C9orf81","biotype":"protein_coding","ncbi_id":"84131","summary":"This gene encodes a centrosomal protein that is both required for the regulation of centrosome-related events during the cell cycle, and required for ciliogenesis. The encoded protein has an N-terminal leucine-rich repeat (LRR) domain with six consecutive LRR repeats, and a C-terminal coiled-coil domain. It interacts with the N-terminal catalytic domain of polo-like kinase 4 (PLK4) and colocalizes with PLK4 to the distal end of the centriole. Naturally occurring mutations in this gene cause defects in primary cilia that result in retinal degeneration and sensorineural hearing loss which are associated with cone-rod degeneration disease as well as Usher syndrome. Low expression of this gene is associated with poor prognosis of colorectal cancer patients. [provided by RefSeq, Mar 2017]","start":78236062,"end":78279690,"strand":1,"description":"centrosomal protein 78 [Source:HGNC Symbol;Acc:HGNC:25740]"}, {"versioned_ensembl_gene_id":"ENSG00000233136.2","gene_symbol":"USP17L11","gene_name":"ubiquitin specific peptidase 17-like family member 11 [Source:HGNC Symbol;Acc:HGNC:44439]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287178","summary":null,"start":9215405,"end":9217356,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 11 [Source:HGNC Symbol;Acc:HGNC:44439]"}, {"versioned_ensembl_gene_id":"ENSG00000232376.4","gene_symbol":"LYPLA2P1","gene_name":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]","synonyms":"dJ570F3.6,APT,LYPLA2L","biotype":"processed_pseudogene","ncbi_id":"653639","summary":null,"start":33294377,"end":33295072,"strand":-1,"description":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]"}, {"versioned_ensembl_gene_id":"ENSG00000232653.8","gene_symbol":"GOLGA8N","gene_name":"golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643699","summary":null,"start":32593456,"end":32607310,"strand":1,"description":"golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]"}, {"versioned_ensembl_gene_id":"ENSG00000276724.1","gene_symbol":"AC123768.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32583612,"end":32584312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249416.2","gene_symbol":"AC107393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131768233,"end":131768578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250102.5","gene_symbol":"LINC02377","gene_name":"long intergenic non-protein coding RNA 2377 [Source:HGNC Symbol;Acc:HGNC:53300]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377424","summary":null,"start":131380013,"end":131541397,"strand":1,"description":"long intergenic non-protein coding RNA 2377 [Source:HGNC Symbol;Acc:HGNC:53300]"}, {"versioned_ensembl_gene_id":"ENSG00000225797.2","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464596,"end":29469806,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000223509.8","gene_symbol":"AC135983.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32519848,"end":32536926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272410.5","gene_symbol":"AC022384.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10249372,"end":10285796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271447.5","gene_symbol":"MMP28","gene_name":"matrix metallopeptidase 28 [Source:HGNC Symbol;Acc:HGNC:14366]","synonyms":"EPILYSIN,MMP-28,MMP-25,MM28","biotype":"protein_coding","ncbi_id":"79148","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction and tissue remodeling, and disease processes, such as asthma and metastasis. This gene encodes a secreted enzyme that degrades casein. Its expression pattern suggests that it plays a role in tissue homeostasis and in wound repair. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":35756249,"end":35795707,"strand":-1,"description":"matrix metallopeptidase 28 [Source:HGNC Symbol;Acc:HGNC:14366]"}, {"versioned_ensembl_gene_id":"ENSG00000088320.3","gene_symbol":"REM1","gene_name":"RRAD and GEM like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:15922]","synonyms":"REM,GES","biotype":"protein_coding","ncbi_id":"28954","summary":"The protein encoded by this gene is a GTPase and member of the RAS-like GTP-binding protein family. The encoded protein is expressed in endothelial cells, where it promotes reorganization of the actin cytoskeleton and morphological changes in the cells. [provided by RefSeq, Jul 2008]","start":31475293,"end":31484905,"strand":1,"description":"RRAD and GEM like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:15922]"}, {"versioned_ensembl_gene_id":"ENSG00000144061.12","gene_symbol":"NPHP1","gene_name":"nephrocystin 1 [Source:HGNC Symbol;Acc:HGNC:7905]","synonyms":"SLSN1,NPH1,JBTS4","biotype":"protein_coding","ncbi_id":"4867","summary":"This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell and cell-matrix adhesion signaling, likely as part of a multifunctional complex localized in actin- and microtubule-based structures. Mutations in this gene cause familial juvenile nephronophthisis type 1, a kidney disorder involving both tubules and glomeruli. Defects in this gene are also associated with Senior-Loken syndrome type 1, also referred to as juvenile nephronophthisis with Leber amaurosis, which is characterized by kidney and eye disease, and with Joubert syndrome type 4, which is characterized by cerebellar ataxia, oculomotor apraxia, psychomotor delay and neonatal breathing abnormalities, sometimes including retinal dystrophy and renal disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":110122311,"end":110205066,"strand":-1,"description":"nephrocystin 1 [Source:HGNC Symbol;Acc:HGNC:7905]"}, {"versioned_ensembl_gene_id":"ENSG00000082898.16","gene_symbol":"XPO1","gene_name":"exportin 1 [Source:HGNC Symbol;Acc:HGNC:12825]","synonyms":"emb,CRM1","biotype":"protein_coding","ncbi_id":"7514","summary":"This cell-cycle-regulated gene encodes a protein that mediates leucine-rich nuclear export signal (NES)-dependent protein transport. The protein specifically inhibits the nuclear export of Rev and U snRNAs. It is involved in the control of several cellular processes by controlling the localization of cyclin B, MPAK, and MAPKAP kinase 2. This protein also regulates NFAT and AP-1. [provided by RefSeq, Jan 2015]","start":61477849,"end":61538626,"strand":-1,"description":"exportin 1 [Source:HGNC Symbol;Acc:HGNC:12825]"}, {"versioned_ensembl_gene_id":"ENSG00000229143.1","gene_symbol":"AC009480.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147810346,"end":147810777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278613.4","gene_symbol":"NAIP","gene_name":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]","synonyms":"NLRB1,BIRC1","biotype":"protein_coding","ncbi_id":"4671","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length; additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1. The protein encoded by this gene contains regions of homology to two baculovirus inhibitor of apoptosis proteins, and it is able to suppress apoptosis induced by various signals. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":69602550,"end":69659159,"strand":1,"description":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]"}, {"versioned_ensembl_gene_id":"ENSG00000175097.7","gene_symbol":"RAG2","gene_name":"recombination activating 2 [Source:HGNC Symbol;Acc:HGNC:9832]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5897","summary":"This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms. [provided by RefSeq, Jul 2008]","start":36575574,"end":36598279,"strand":-1,"description":"recombination activating 2 [Source:HGNC Symbol;Acc:HGNC:9832]"}, {"versioned_ensembl_gene_id":"ENSG00000084710.13","gene_symbol":"EFR3B","gene_name":"EFR3 homolog B [Source:HGNC Symbol;Acc:HGNC:29155]","synonyms":"KIAA0953,FLJ37871","biotype":"protein_coding","ncbi_id":"22979","summary":null,"start":25042130,"end":25159137,"strand":1,"description":"EFR3 homolog B [Source:HGNC Symbol;Acc:HGNC:29155]"}, {"versioned_ensembl_gene_id":"ENSG00000180424.6","gene_symbol":"DEFB123","gene_name":"defensin beta 123 [Source:HGNC Symbol;Acc:HGNC:18103]","synonyms":"DEFB-23","biotype":"protein_coding","ncbi_id":"245936","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the host immunologic response to invading microorganisms. This antimicrobial protein is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20q11.1. Two transcript variants, one protein-coding and the other not, have been found for this gene. [provided by RefSeq, Nov 2014]","start":31440519,"end":31450257,"strand":1,"description":"defensin beta 123 [Source:HGNC Symbol;Acc:HGNC:18103]"}, {"versioned_ensembl_gene_id":"ENSG00000237440.8","gene_symbol":"ZNF737","gene_name":"zinc finger protein 737 [Source:HGNC Symbol;Acc:HGNC:32468]","synonyms":"ZNF102","biotype":"protein_coding","ncbi_id":"100129842","summary":null,"start":20535825,"end":20565809,"strand":-1,"description":"zinc finger protein 737 [Source:HGNC Symbol;Acc:HGNC:32468]"}, {"versioned_ensembl_gene_id":"ENSG00000103266.10","gene_symbol":"STUB1","gene_name":"STIP1 homology and U-box containing protein 1 [Source:HGNC Symbol;Acc:HGNC:11427]","synonyms":"UBOX1,SDCCAG7,NY-CO-7,HSPABP2,CHIP","biotype":"protein_coding","ncbi_id":"10273","summary":"This gene encodes a protein containing tetratricopeptide repeat and a U-box that functions as a ubiquitin ligase/cochaperone. The encoded protein binds to and ubiquitinates shock cognate 71 kDa protein (Hspa8) and DNA polymerase beta (Polb), among other targets. Mutations in this gene cause spinocerebellar ataxia, autosomal recessive 16. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 2. [provided by RefSeq, Jun 2014]","start":680224,"end":682870,"strand":1,"description":"STIP1 homology and U-box containing protein 1 [Source:HGNC Symbol;Acc:HGNC:11427]"}, {"versioned_ensembl_gene_id":"ENSG00000269043.1","gene_symbol":"AC008554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20432552,"end":20528615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268272.1","gene_symbol":"VN1R78P","gene_name":"vomeronasal 1 receptor 78 pseudogene [Source:HGNC Symbol;Acc:HGNC:37399]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312823","summary":null,"start":20583084,"end":20583647,"strand":-1,"description":"vomeronasal 1 receptor 78 pseudogene [Source:HGNC Symbol;Acc:HGNC:37399]"}, {"versioned_ensembl_gene_id":"ENSG00000214825.2","gene_symbol":"EI24P3","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131881","summary":null,"start":44524744,"end":44525805,"strand":-1,"description":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]"}, {"versioned_ensembl_gene_id":"ENSG00000092020.10","gene_symbol":"PPP2R3C","gene_name":"protein phosphatase 2 regulatory subunit B''gamma [Source:HGNC Symbol;Acc:HGNC:17485]","synonyms":"G5PR,G4-1,FLJ20644,C14orf10","biotype":"protein_coding","ncbi_id":"55012","summary":"This gene encodes a regulatory subunit of the serine/threonine phosphatase, protein phosphatase 2. This protein is localized to both nuclear and cytoplasmic regions depending on cell cycle phase. Homozygous conditional knockout mice for this gene exhibit reduced numbers and impaired proliferation of immune system B cells. This protein may regulate the expression of the P-glycoprotein ATP-binding cassette transporter through its phosphatase activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":35085467,"end":35122517,"strand":-1,"description":"protein phosphatase 2 regulatory subunit B''gamma [Source:HGNC Symbol;Acc:HGNC:17485]"}, {"versioned_ensembl_gene_id":"ENSG00000069966.18","gene_symbol":"GNB5","gene_name":"G protein subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:4401]","synonyms":"GB5","biotype":"protein_coding","ncbi_id":"10681","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. Alternatively spliced transcript variants encoding different isoforms exist. [provided by RefSeq, Jul 2008]","start":52115105,"end":52191369,"strand":-1,"description":"G protein subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:4401]"}, {"versioned_ensembl_gene_id":"ENSG00000280331.1","gene_symbol":"AC061999.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36510361,"end":36510537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239671.1","gene_symbol":"AC100793.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42714299,"end":42714643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259709.1","gene_symbol":"AC023906.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52124561,"end":52140246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259327.1","gene_symbol":"AC023906.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52116574,"end":52122131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117009.11","gene_symbol":"KMO","gene_name":"kynurenine 3-monooxygenase [Source:HGNC Symbol;Acc:HGNC:6381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8564","summary":"This gene encodes a mitochondrion outer membrane protein that catalyzes the hydroxylation of L-tryptophan metabolite, L-kynurenine, to form L-3-hydroxykynurenine. Studies in yeast identified this gene as a therapeutic target for Huntington disease. [provided by RefSeq, Oct 2011]","start":241532134,"end":241595642,"strand":1,"description":"kynurenine 3-monooxygenase [Source:HGNC Symbol;Acc:HGNC:6381]"}, {"versioned_ensembl_gene_id":"ENSG00000244527.1","gene_symbol":"AC022795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21119182,"end":21119661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229117.8","gene_symbol":"RPL41","gene_name":"ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:10354]","synonyms":"L41","biotype":"protein_coding","ncbi_id":"6171","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which shares sequence similarity with the yeast ribosomal protein YL41, belongs to the L41E family of ribosomal proteins. It is located in the cytoplasm. The protein can interact with the beta subunit of protein kinase CKII and can stimulate the phosphorylation of DNA topoisomerase II-alpha by CKII. Two alternative splice variants have been identified, both encoding the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":56116586,"end":56117943,"strand":1,"description":"ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:10354]"}, {"versioned_ensembl_gene_id":"ENSG00000225026.1","gene_symbol":"AC091492.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12328003,"end":12328274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233605.2","gene_symbol":"LINC01851","gene_name":"long intergenic non-protein coding RNA 1851 [Source:HGNC Symbol;Acc:HGNC:52667]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927926","summary":null,"start":77915934,"end":77918011,"strand":1,"description":"long intergenic non-protein coding RNA 1851 [Source:HGNC Symbol;Acc:HGNC:52667]"}, {"versioned_ensembl_gene_id":"ENSG00000260920.2","gene_symbol":"AL031985.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":40464319,"end":40466767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250456.1","gene_symbol":"LINC02260","gene_name":"long intergenic non-protein coding RNA 2260 [Source:HGNC Symbol;Acc:HGNC:27956]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339978","summary":null,"start":54603211,"end":54607131,"strand":-1,"description":"long intergenic non-protein coding RNA 2260 [Source:HGNC Symbol;Acc:HGNC:27956]"}, {"versioned_ensembl_gene_id":"ENSG00000251264.1","gene_symbol":"AC098868.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54440502,"end":54446723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229924.3","gene_symbol":"FAM90A26","gene_name":"family with sequence similarity 90 member A26 [Source:HGNC Symbol;Acc:HGNC:43746]","synonyms":"FAM90A26P","biotype":"protein_coding","ncbi_id":"100287045","summary":null,"start":9170409,"end":9176730,"strand":1,"description":"family with sequence similarity 90 member A26 [Source:HGNC Symbol;Acc:HGNC:43746]"}, {"versioned_ensembl_gene_id":"ENSG00000137878.16","gene_symbol":"GCOM1","gene_name":"GRINL1A complex locus 1 [Source:HGNC Symbol;Acc:HGNC:26424]","synonyms":"MYZAP-POLR2M,GRINL1A,FLJ30973","biotype":"protein_coding","ncbi_id":"145781","summary":"This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013]","start":57591908,"end":57714745,"strand":1,"description":"GRINL1A complex locus 1 [Source:HGNC Symbol;Acc:HGNC:26424]"}, {"versioned_ensembl_gene_id":"ENSG00000269885.1","gene_symbol":"VN1R79P","gene_name":"vomeronasal 1 receptor 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:37400]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312824","summary":null,"start":20758440,"end":20758952,"strand":1,"description":"vomeronasal 1 receptor 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:37400]"}, {"versioned_ensembl_gene_id":"ENSG00000237725.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"OR2I3P,HS6M1-14,OR2I2,OR2I4P,OR2I1","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29553169,"end":29554116,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000269110.1","gene_symbol":"AC010636.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20553792,"end":20661583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269040.1","gene_symbol":"BNIP3P24","gene_name":"BCL2 interacting protein 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49704]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421698","summary":null,"start":20784596,"end":20785152,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49704]"}, {"versioned_ensembl_gene_id":"ENSG00000233030.2","gene_symbol":"AC243772.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149785659,"end":149793020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164081.12","gene_symbol":"TEX264","gene_name":"testis expressed 264 [Source:HGNC Symbol;Acc:HGNC:30247]","synonyms":"ZSIG11,FLJ13935","biotype":"protein_coding","ncbi_id":"51368","summary":null,"start":51662693,"end":51704323,"strand":1,"description":"testis expressed 264 [Source:HGNC Symbol;Acc:HGNC:30247]"}, {"versioned_ensembl_gene_id":"ENSG00000083896.12","gene_symbol":"YTHDC1","gene_name":"YTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30626]","synonyms":"YT521-B,YT521,KIAA1966","biotype":"protein_coding","ncbi_id":"91746","summary":null,"start":68310387,"end":68350089,"strand":-1,"description":"YTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30626]"}, {"versioned_ensembl_gene_id":"ENSG00000253960.1","gene_symbol":"AC016885.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93215925,"end":93234878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269373.1","gene_symbol":"AC008739.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20838515,"end":20847417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251638.1","gene_symbol":"AC006390.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24768049,"end":24768331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280171.1","gene_symbol":"AC010329.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20674923,"end":20696533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177306.4","gene_symbol":"OR7E125P","gene_name":"olfactory receptor family 7 subfamily E member 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:15098]","synonyms":"PJCG6","biotype":"unprocessed_pseudogene","ncbi_id":"389616","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7246726,"end":7247571,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:15098]"}, {"versioned_ensembl_gene_id":"ENSG00000268461.2","gene_symbol":"AC078899.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20389658,"end":20390689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144119.3","gene_symbol":"C1QL2","gene_name":"complement C1q like 2 [Source:HGNC Symbol;Acc:HGNC:24181]","synonyms":"CTRP10,C1QTNF10","biotype":"protein_coding","ncbi_id":"165257","summary":null,"start":119156243,"end":119158889,"strand":-1,"description":"complement C1q like 2 [Source:HGNC Symbol;Acc:HGNC:24181]"}, {"versioned_ensembl_gene_id":"ENSG00000105974.11","gene_symbol":"CAV1","gene_name":"caveolin 1 [Source:HGNC Symbol;Acc:HGNC:1527]","synonyms":"CAV","biotype":"protein_coding","ncbi_id":"857","summary":"The scaffolding protein encoded by this gene is the main component of the caveolae plasma membranes found in most cell types. The protein links integrin subunits to the tyrosine kinase FYN, an initiating step in coupling integrins to the Ras-ERK pathway and promoting cell cycle progression. The gene is a tumor suppressor gene candidate and a negative regulator of the Ras-p42/44 mitogen-activated kinase cascade. Caveolin 1 and caveolin 2 are located next to each other on chromosome 7 and express colocalizing proteins that form a stable hetero-oligomeric complex. Mutations in this gene have been associated with Berardinelli-Seip congenital lipodystrophy. Alternatively spliced transcripts encode alpha and beta isoforms of caveolin 1.[provided by RefSeq, Mar 2010]","start":116524785,"end":116561184,"strand":1,"description":"caveolin 1 [Source:HGNC Symbol;Acc:HGNC:1527]"}, {"versioned_ensembl_gene_id":"ENSG00000150337.13","gene_symbol":"FCGR1A","gene_name":"Fc fragment of IgG receptor Ia [Source:HGNC Symbol;Acc:HGNC:3613]","synonyms":"CD64,CD64A","biotype":"protein_coding","ncbi_id":"2209","summary":"This gene encodes a protein that plays an important role in the immune response. This protein is a high-affinity Fc-gamma receptor. The gene is one of three related gene family members located on chromosome 1. [provided by RefSeq, Jul 2008]","start":149782671,"end":149792518,"strand":1,"description":"Fc fragment of IgG receptor Ia [Source:HGNC Symbol;Acc:HGNC:3613]"}, {"versioned_ensembl_gene_id":"ENSG00000116209.11","gene_symbol":"TMEM59","gene_name":"transmembrane protein 59 [Source:HGNC Symbol;Acc:HGNC:1239]","synonyms":"HSPC001,C1orf8","biotype":"protein_coding","ncbi_id":"9528","summary":"This gene encodes a protein shown to regulate autophagy in response to bacterial infection. This protein may also regulate the retention of amyloid precursor protein (APP) in the Golgi apparatus through its control of APP glycosylation. Overexpression of this protein has been found to promote apoptosis in a glioma cell line. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":54026681,"end":54053504,"strand":-1,"description":"transmembrane protein 59 [Source:HGNC Symbol;Acc:HGNC:1239]"}, {"versioned_ensembl_gene_id":"ENSG00000247911.3","gene_symbol":"HMGN1P12","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39356]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480725","summary":null,"start":71537652,"end":71537846,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39356]"}, {"versioned_ensembl_gene_id":"ENSG00000280378.1","gene_symbol":"AL353898.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":54033126,"end":54034880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257246.1","gene_symbol":"PHBP19","gene_name":"prohibitin pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"494150","summary":null,"start":51124628,"end":51125381,"strand":-1,"description":"prohibitin pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51552]"}, {"versioned_ensembl_gene_id":"ENSG00000100890.15","gene_symbol":"KIAA0391","gene_name":"KIAA0391 [Source:HGNC Symbol;Acc:HGNC:19958]","synonyms":"PRORP,MRPP3","biotype":"protein_coding","ncbi_id":"9692","summary":null,"start":35121846,"end":35277614,"strand":1,"description":"KIAA0391 [Source:HGNC Symbol;Acc:HGNC:19958]"}, {"versioned_ensembl_gene_id":"ENSG00000162843.17","gene_symbol":"WDR64","gene_name":"WD repeat domain 64 [Source:HGNC Symbol;Acc:HGNC:26570]","synonyms":"FLJ32978","biotype":"protein_coding","ncbi_id":"128025","summary":null,"start":241652278,"end":241802133,"strand":1,"description":"WD repeat domain 64 [Source:HGNC Symbol;Acc:HGNC:26570]"}, {"versioned_ensembl_gene_id":"ENSG00000262227.1","gene_symbol":"AC004771.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4987706,"end":4988446,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278595.1","gene_symbol":"AL133396.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4761300,"end":4761696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259090.1","gene_symbol":"AL121594.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35157904,"end":35159099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114948.12","gene_symbol":"ADAM23","gene_name":"ADAM metallopeptidase domain 23 [Source:HGNC Symbol;Acc:HGNC:202]","synonyms":"MDC3","biotype":"protein_coding","ncbi_id":"8745","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. It is reported that inactivation of this gene is associated with tumorigenesis in human cancers. [provided by RefSeq, May 2013]","start":206443539,"end":206621130,"strand":1,"description":"ADAM metallopeptidase domain 23 [Source:HGNC Symbol;Acc:HGNC:202]"}, {"versioned_ensembl_gene_id":"ENSG00000240392.1","gene_symbol":"AL121594.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35262462,"end":35263036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184905.8","gene_symbol":"TCEAL2","gene_name":"transcription elongation factor A like 2 [Source:HGNC Symbol;Acc:HGNC:29818]","synonyms":"WEX1,MY0876G05,my048","biotype":"protein_coding","ncbi_id":"140597","summary":"This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family contain TFA domains and may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. [provided by RefSeq, Jul 2008]","start":102125688,"end":102127711,"strand":1,"description":"transcription elongation factor A like 2 [Source:HGNC Symbol;Acc:HGNC:29818]"}, {"versioned_ensembl_gene_id":"ENSG00000262429.1","gene_symbol":"AC004771.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4967995,"end":4968822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234503.1","gene_symbol":"AP000550.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21177892,"end":21179875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125703.14","gene_symbol":"ATG4C","gene_name":"autophagy related 4C cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:16040]","synonyms":"FLJ14867,AUTL3,AUTL1,APG4C","biotype":"protein_coding","ncbi_id":"84938","summary":"Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. Alternate transcriptional splice variants, encoding the same protein, have been characterized. [provided by RefSeq, Jul 2008]","start":62784135,"end":62865513,"strand":1,"description":"autophagy related 4C cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:16040]"}, {"versioned_ensembl_gene_id":"ENSG00000205579.3","gene_symbol":"DYNLL1P1","gene_name":"dynein light chain LC8-type 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20723]","synonyms":"DNCL1P1","biotype":"processed_pseudogene","ncbi_id":"246720","summary":null,"start":81246295,"end":81246563,"strand":-1,"description":"dynein light chain LC8-type 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20723]"}, {"versioned_ensembl_gene_id":"ENSG00000197632.8","gene_symbol":"SERPINB2","gene_name":"serpin family B member 2 [Source:HGNC Symbol;Acc:HGNC:8584]","synonyms":"HsT1201,PLANH2,PAI2","biotype":"protein_coding","ncbi_id":"5055","summary":null,"start":63871692,"end":63903890,"strand":1,"description":"serpin family B member 2 [Source:HGNC Symbol;Acc:HGNC:8584]"}, {"versioned_ensembl_gene_id":"ENSG00000270871.1","gene_symbol":"AC015849.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35816717,"end":35830293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274082.1","gene_symbol":"AC245128.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254834.4","gene_symbol":"OR5M10","gene_name":"olfactory receptor family 5 subfamily M member 10 [Source:HGNC Symbol;Acc:HGNC:15290]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390167","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56576736,"end":56577787,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 10 [Source:HGNC Symbol;Acc:HGNC:15290]"}, {"versioned_ensembl_gene_id":"ENSG00000255223.4","gene_symbol":"OR5M11","gene_name":"olfactory receptor family 5 subfamily M member 11 [Source:HGNC Symbol;Acc:HGNC:15291]","synonyms":"OR11-199","biotype":"protein_coding","ncbi_id":"219487","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56542262,"end":56543281,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 11 [Source:HGNC Symbol;Acc:HGNC:15291]"}, {"versioned_ensembl_gene_id":"ENSG00000234502.2","gene_symbol":"FYTTD1P1","gene_name":"forty-two-three domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128665","summary":null,"start":101375344,"end":101376603,"strand":-1,"description":"forty-two-three domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38035]"}, {"versioned_ensembl_gene_id":"ENSG00000228400.1","gene_symbol":"AC079154.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124016858,"end":124025173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250503.1","gene_symbol":"AC093831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130881027,"end":130885641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280059.1","gene_symbol":"AC093831.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130808507,"end":130811933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188343.12","gene_symbol":"FAM92A","gene_name":"family with sequence similarity 92 member A [Source:HGNC Symbol;Acc:HGNC:30452]","synonyms":"FLJ38979,FAM92A1","biotype":"protein_coding","ncbi_id":"137392","summary":null,"start":93698561,"end":93731527,"strand":1,"description":"family with sequence similarity 92 member A [Source:HGNC Symbol;Acc:HGNC:30452]"}, {"versioned_ensembl_gene_id":"ENSG00000249018.2","gene_symbol":"GAPDHP56","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:38562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421232","summary":null,"start":130503357,"end":130504344,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:38562]"}, {"versioned_ensembl_gene_id":"ENSG00000253854.1","gene_symbol":"AC010834.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93719574,"end":93721167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269586.7","gene_symbol":"CT45A10","gene_name":"cancer/testis antigen family 45 member A10 [Source:HGNC Symbol;Acc:HGNC:51263]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723631","summary":null,"start":135881063,"end":135889086,"strand":-1,"description":"cancer/testis antigen family 45 member A10 [Source:HGNC Symbol;Acc:HGNC:51263]"}, {"versioned_ensembl_gene_id":"ENSG00000235020.4","gene_symbol":"AL390783.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18206127,"end":18261194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118402.5","gene_symbol":"ELOVL4","gene_name":"ELOVL fatty acid elongase 4 [Source:HGNC Symbol;Acc:HGNC:14415]","synonyms":"STGD3,STGD2,SCA34,CT118","biotype":"protein_coding","ncbi_id":"6785","summary":"This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul 2008]","start":79914812,"end":79947580,"strand":-1,"description":"ELOVL fatty acid elongase 4 [Source:HGNC Symbol;Acc:HGNC:14415]"}, {"versioned_ensembl_gene_id":"ENSG00000148053.15","gene_symbol":"NTRK2","gene_name":"neurotrophic receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:8032]","synonyms":"TRKB","biotype":"protein_coding","ncbi_id":"4915","summary":"This gene encodes a member of the neurotrophic tyrosine receptor kinase (NTRK) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. Signalling through this kinase leads to cell differentiation. Mutations in this gene have been associated with obesity and mood disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":84668551,"end":85027070,"strand":1,"description":"neurotrophic receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:8032]"}, {"versioned_ensembl_gene_id":"ENSG00000254603.1","gene_symbol":"OR5M6P","gene_name":"olfactory receptor family 5 subfamily M member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14814]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79512","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56512235,"end":56513171,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14814]"}, {"versioned_ensembl_gene_id":"ENSG00000110721.11","gene_symbol":"CHKA","gene_name":"choline kinase alpha [Source:HGNC Symbol;Acc:HGNC:1937]","synonyms":"CKI,CHK","biotype":"protein_coding","ncbi_id":"1119","summary":"The major pathway for the biosynthesis of phosphatidylcholine occurs via the CDP-choline pathway. The protein encoded by this gene is the initial enzyme in the sequence and may play a regulatory role. The encoded protein also catalyzes the phosphorylation of ethanolamine. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":68052859,"end":68121444,"strand":-1,"description":"choline kinase alpha [Source:HGNC Symbol;Acc:HGNC:1937]"}, {"versioned_ensembl_gene_id":"ENSG00000231071.1","gene_symbol":"AL133396.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4735669,"end":4736673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270946.5","gene_symbol":"CT45A9","gene_name":"cancer/testis antigen family 45 member A9 [Source:HGNC Symbol;Acc:HGNC:51262]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723680","summary":null,"start":135863776,"end":135871812,"strand":-1,"description":"cancer/testis antigen family 45 member A9 [Source:HGNC Symbol;Acc:HGNC:51262]"}, {"versioned_ensembl_gene_id":"ENSG00000255031.5","gene_symbol":"AP002807.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68050740,"end":68053762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188004.9","gene_symbol":"SNHG28","gene_name":"small nucleolar RNA host gene 28 [Source:HGNC Symbol;Acc:HGNC:27647]","synonyms":"VSIG8-OT1,FLJ39187,C1orf204","biotype":"protein_coding","ncbi_id":"284677","summary":null,"start":159834474,"end":159855347,"strand":-1,"description":"small nucleolar RNA host gene 28 [Source:HGNC Symbol;Acc:HGNC:27647]"}, {"versioned_ensembl_gene_id":"ENSG00000253722.1","gene_symbol":"AC010834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93733216,"end":93734022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253781.1","gene_symbol":"ZNF317P1","gene_name":"zinc finger protein 317 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288659","summary":null,"start":93646066,"end":93647092,"strand":1,"description":"zinc finger protein 317 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31062]"}, {"versioned_ensembl_gene_id":"ENSG00000056586.15","gene_symbol":"RC3H2","gene_name":"ring finger and CCCH-type domains 2 [Source:HGNC Symbol;Acc:HGNC:21461]","synonyms":"RNF164,MNAB,FLJ20713,FLJ20301","biotype":"protein_coding","ncbi_id":"54542","summary":null,"start":122844556,"end":122905341,"strand":-1,"description":"ring finger and CCCH-type domains 2 [Source:HGNC Symbol;Acc:HGNC:21461]"}, {"versioned_ensembl_gene_id":"ENSG00000276074.1","gene_symbol":"SOX2OT_exon1","gene_name":"SOX2 overlapping transcript exon 1 [Source:RFAM;Acc:RF01951]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":181610498,"end":181610729,"strand":1,"description":"SOX2 overlapping transcript exon 1 [Source:RFAM;Acc:RF01951]"}, {"versioned_ensembl_gene_id":"ENSG00000108799.12","gene_symbol":"EZH1","gene_name":"enhancer of zeste 1 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:3526]","synonyms":"KMT6B,KIAA0388","biotype":"protein_coding","ncbi_id":"2145","summary":"EZH1 is a component of a noncanonical Polycomb repressive complex-2 (PRC2) that mediates methylation of histone H3 (see MIM 602812) lys27 (H3K27) and functions in the maintenance of embryonic stem cell pluripotency and plasticity (Shen et al., 2008 [PubMed 19026780]).[supplied by OMIM, Mar 2009]","start":42700275,"end":42745049,"strand":-1,"description":"enhancer of zeste 1 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:3526]"}, {"versioned_ensembl_gene_id":"ENSG00000241058.3","gene_symbol":"NSUN6","gene_name":"NOP2/Sun RNA methyltransferase family member 6 [Source:HGNC Symbol;Acc:HGNC:23529]","synonyms":"NOPD1,FLJ23743,ARL5B-AS1","biotype":"protein_coding","ncbi_id":"221078","summary":null,"start":18545561,"end":18659285,"strand":-1,"description":"NOP2/Sun RNA methyltransferase family member 6 [Source:HGNC Symbol;Acc:HGNC:23529]"}, {"versioned_ensembl_gene_id":"ENSG00000163380.15","gene_symbol":"LMOD3","gene_name":"leiomodin 3 [Source:HGNC Symbol;Acc:HGNC:6649]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56203","summary":"The protein encoded by this gene is a member of the leiomodin family of proteins. This protein contains three actin-binding domains, a tropomyosin domain, a leucine-rich repeat domain, and a Wiskott-Aldrich syndrome protein homology 2 domain (WH2). Localization of this protein to the pointed ends of thin filaments has been observed, and there is evidence that this protein acts as a catalyst of actin nucleation, and is important to the organization of sarcomeric thin filaments in skeletal muscles. Mutations in this gene have been associated as one cause of Nemaline myopathy, as other genes have also been linked to this disorder. Nemaline myopathy is a disorder characterized by nonprogressive generalized muscle weakness and protein inclusions (nemaline bodies) in skeletal myofibers. Patients with mutations in this gene often present with a severe congenital form of the disorder. [provided by RefSeq, Jan 2015]","start":69106872,"end":69123032,"strand":-1,"description":"leiomodin 3 [Source:HGNC Symbol;Acc:HGNC:6649]"}, {"versioned_ensembl_gene_id":"ENSG00000273696.4","gene_symbol":"CT45A7","gene_name":"cancer/testis antigen family 45 member A7 [Source:HGNC Symbol;Acc:HGNC:51260]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060211","summary":null,"start":135829247,"end":135837268,"strand":-1,"description":"cancer/testis antigen family 45 member A7 [Source:HGNC Symbol;Acc:HGNC:51260]"}, {"versioned_ensembl_gene_id":"ENSG00000254902.1","gene_symbol":"ANO1-AS1","gene_name":"ANO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40016]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873981","summary":null,"start":70187788,"end":70188509,"strand":-1,"description":"ANO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40016]"}, {"versioned_ensembl_gene_id":"ENSG00000227738.1","gene_symbol":"AC092646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123762171,"end":123763071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260851.6","gene_symbol":"AC010542.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":66469812,"end":66517312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267868.1","gene_symbol":"AL356740.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112964835,"end":112966131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225313.5","gene_symbol":"AL513327.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33307348,"end":33349245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271449.7","gene_symbol":"CT45A2","gene_name":"cancer/testis antigen family 45 member A2 [Source:HGNC Symbol;Acc:HGNC:28400]","synonyms":"CT45.2,CT45-2","biotype":"protein_coding","ncbi_id":"728911","summary":"This gene represents one of a cluster of several similar genes located on the q arm of chromosome X. The genes in this cluster encode members of the cancer/testis (CT) family of antigens, and are distinct from other CT antigens. These antigens are thought to be novel therapeutic targets for human cancers. [provided by RefSeq, Apr 2014]","start":135811668,"end":135820012,"strand":-1,"description":"cancer/testis antigen family 45 member A2 [Source:HGNC Symbol;Acc:HGNC:28400]"}, {"versioned_ensembl_gene_id":"ENSG00000171864.4","gene_symbol":"PRND","gene_name":"prion like protein doppel [Source:HGNC Symbol;Acc:HGNC:15748]","synonyms":"PrPLP,DPL,DOPPEL,dJ1068H6.4","biotype":"protein_coding","ncbi_id":"23627","summary":"This gene is found on chromosome 20, approximately 20 kbp downstream of the gene encoding cellular prion protein, to which it is biochemically and structurally similar. The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that is found predominantly in testis. Mutations in this gene may lead to neurological disorders. [provided by RefSeq, Jul 2008]","start":4721910,"end":4728460,"strand":1,"description":"prion like protein doppel [Source:HGNC Symbol;Acc:HGNC:15748]"}, {"versioned_ensembl_gene_id":"ENSG00000125877.12","gene_symbol":"ITPA","gene_name":"inosine triphosphatase [Source:HGNC Symbol;Acc:HGNC:6176]","synonyms":"HLC14-06-P,dJ794I6.3,C20orf37","biotype":"protein_coding","ncbi_id":"3704","summary":"This gene encodes an inosine triphosphate pyrophosphohydrolase. The encoded protein hydrolyzes inosine triphosphate and deoxyinosine triphosphate to the monophosphate nucleotide and diphosphate. This protein, which is a member of the HAM1 NTPase protein family, is found in the cytoplasm and acts as a homodimer. Defects in the encoded protein can result in inosine triphosphate pyrophosphorylase deficiency which causes an accumulation of ITP in red blood cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":3208868,"end":3223870,"strand":1,"description":"inosine triphosphatase [Source:HGNC Symbol;Acc:HGNC:6176]"}, {"versioned_ensembl_gene_id":"ENSG00000257524.5","gene_symbol":"AL157935.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":127867864,"end":127886787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254912.2","gene_symbol":"AC135983.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32494003,"end":32500346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277147.4","gene_symbol":"LINC00869","gene_name":"long intergenic non-protein coding RNA 869 [Source:HGNC Symbol;Acc:HGNC:29050]","synonyms":"KIAA0493","biotype":"lincRNA","ncbi_id":"57234","summary":null,"start":149606334,"end":149679523,"strand":1,"description":"long intergenic non-protein coding RNA 869 [Source:HGNC Symbol;Acc:HGNC:29050]"}, {"versioned_ensembl_gene_id":"ENSG00000261375.1","gene_symbol":"AC135983.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32489267,"end":32491586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261519.3","gene_symbol":"AC010542.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66549280,"end":66551189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280113.2","gene_symbol":"AL357140.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":9826289,"end":9828271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283787.1","gene_symbol":"AC051649.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1888577,"end":1891895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158985.13","gene_symbol":"CDC42SE2","gene_name":"CDC42 small effector 2 [Source:HGNC Symbol;Acc:HGNC:18547]","synonyms":"SPEC2,FLJ21967","biotype":"protein_coding","ncbi_id":"56990","summary":null,"start":131245493,"end":131398447,"strand":1,"description":"CDC42 small effector 2 [Source:HGNC Symbol;Acc:HGNC:18547]"}, {"versioned_ensembl_gene_id":"ENSG00000279370.1","gene_symbol":"AC004777.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131261321,"end":131261607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270789.1","gene_symbol":"AC135983.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32461666,"end":32461809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100902.10","gene_symbol":"PSMA6","gene_name":"proteasome subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:9535]","synonyms":"PROS27,p27K,MGC23846,MGC2333,MGC22756,IOTA","biotype":"protein_coding","ncbi_id":"5687","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. Multiple transcript variants encoding several different isoforms have been found for this gene. A pseudogene has been identified on the Y chromosome. [provided by RefSeq, Aug 2013]","start":35278633,"end":35317493,"strand":1,"description":"proteasome subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:9535]"}, {"versioned_ensembl_gene_id":"ENSG00000261656.5","gene_symbol":"BEAN1-AS1","gene_name":"BEAN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51114]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927726","summary":null,"start":66469796,"end":66481230,"strand":-1,"description":"BEAN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51114]"}, {"versioned_ensembl_gene_id":"ENSG00000174498.13","gene_symbol":"IGDCC3","gene_name":"immunoglobulin superfamily DCC subclass member 3 [Source:HGNC Symbol;Acc:HGNC:9700]","synonyms":"PUNC,HsT18880","biotype":"protein_coding","ncbi_id":"9543","summary":null,"start":65327127,"end":65378040,"strand":-1,"description":"immunoglobulin superfamily DCC subclass member 3 [Source:HGNC Symbol;Acc:HGNC:9700]"}, {"versioned_ensembl_gene_id":"ENSG00000220918.1","gene_symbol":"AL132875.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79854684,"end":79855632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257337.6","gene_symbol":"AC068888.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53014596,"end":53054438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270115.1","gene_symbol":"AL513327.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33261212,"end":33261680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264023.1","gene_symbol":"AC068418.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21457434,"end":21458989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165178.9","gene_symbol":"NCF1C","gene_name":"neutrophil cytosolic factor 1C pseudogene [Source:HGNC Symbol;Acc:HGNC:32523]","synonyms":"SH3PXD1C","biotype":"unprocessed_pseudogene","ncbi_id":"654817","summary":"The neutrophil cytosolic factor 1 (NCF1) gene encodes the 47 kDa cytosolic subunit of neutrophil NADPH oxidase, which produces superoxide anion. The NCF1 gene is located in close proximity to two highly similar, multi-exon pseudogenes at chromosome 7q11.23, corresponding to this gene record and GeneID:654816. The two pseudogenes contain a dinucleotide deletion (delta-GT) in exon 2 that results in a frameshift and truncation of the open reading frame, and neither pseudogene is likely to express a protein. Recombination events between the pseudogenes and the functional NCF1 gene can inactivate the NCF1 gene and result in chronic granulomatous disease. [provided by RefSeq, Nov 2009]","start":75156639,"end":75172044,"strand":-1,"description":"neutrophil cytosolic factor 1C pseudogene [Source:HGNC Symbol;Acc:HGNC:32523]"}, {"versioned_ensembl_gene_id":"ENSG00000250268.3","gene_symbol":"ALG1L14P","gene_name":"asparagine-linked glycosylation 1-like 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44383]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996649","summary":null,"start":9166297,"end":9170270,"strand":-1,"description":"asparagine-linked glycosylation 1-like 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44383]"}, {"versioned_ensembl_gene_id":"ENSG00000230968.1","gene_symbol":"AC084149.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77672215,"end":77673792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263464.2","gene_symbol":"PPIAL4C","gene_name":"peptidylprolyl isomerase A like 4C [Source:HGNC Symbol;Acc:HGNC:33995]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653598","summary":null,"start":149583865,"end":149584464,"strand":1,"description":"peptidylprolyl isomerase A like 4C [Source:HGNC Symbol;Acc:HGNC:33995]"}, {"versioned_ensembl_gene_id":"ENSG00000271392.1","gene_symbol":"AC006237.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35757199,"end":35758325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238100.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"processed_transcript","ncbi_id":"414768","summary":null,"start":33073573,"end":33076557,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000050748.17","gene_symbol":"MAPK9","gene_name":"mitogen-activated protein kinase 9 [Source:HGNC Symbol;Acc:HGNC:6886]","synonyms":"SAPK,PRKM9,p54a,JNK2","biotype":"protein_coding","ncbi_id":"5601","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase targets specific transcription factors, and thus mediates immediate-early gene expression in response to various cell stimuli. It is most closely related to MAPK8, both of which are involved in UV radiation induced apoptosis, thought to be related to the cytochrome c-mediated cell death pathway. This gene and MAPK8 are also known as c-Jun N-terminal kinases. This kinase blocks the ubiquitination of tumor suppressor p53, and thus it increases the stability of p53 in nonstressed cells. Studies of this gene's mouse counterpart suggest a key role in T-cell differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Sep 2008]","start":180233143,"end":180292099,"strand":-1,"description":"mitogen-activated protein kinase 9 [Source:HGNC Symbol;Acc:HGNC:6886]"}, {"versioned_ensembl_gene_id":"ENSG00000237856.1","gene_symbol":"AC062020.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123065321,"end":123067722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171236.9","gene_symbol":"LRG1","gene_name":"leucine rich alpha-2-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:29480]","synonyms":"LRG","biotype":"protein_coding","ncbi_id":"116844","summary":"The leucine-rich repeat (LRR) family of proteins, including LRG1, have been shown to be involved in protein-protein interaction, signal transduction, and cell adhesion and development. LRG1 is expressed during granulocyte differentiation (O'Donnell et al., 2002 [PubMed 12223515]).[supplied by OMIM, Mar 2008]","start":4536409,"end":4540474,"strand":-1,"description":"leucine rich alpha-2-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:29480]"}, {"versioned_ensembl_gene_id":"ENSG00000162517.12","gene_symbol":"PEF1","gene_name":"penta-EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30009]","synonyms":"PEF1A","biotype":"protein_coding","ncbi_id":"553115","summary":"This gene encodes a calcium-binding protein belonging to the penta-EF-hand protein family. The encoded protein has been shown to form a heterodimer with the programmed cell death 6 gene product and may modulate its function in Ca(2+) signaling. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 1.[provided by RefSeq, May 2010]","start":31629862,"end":31644896,"strand":-1,"description":"penta-EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30009]"}, {"versioned_ensembl_gene_id":"ENSG00000213431.4","gene_symbol":"AC080014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100910975,"end":100912175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158714.10","gene_symbol":"SLAMF8","gene_name":"SLAM family member 8 [Source:HGNC Symbol;Acc:HGNC:21391]","synonyms":"CD353,BLAME,SBBI42","biotype":"protein_coding","ncbi_id":"56833","summary":"This gene encodes a member of the CD2 family of cell surface proteins involved in lymphocyte activation. These proteins are characterized by Ig domains. This protein is expressed in lymphoid tissues, and studies of a similar protein in mouse suggest that it may function during B cell lineage commitment. The gene is found in a region of chromosome 1 containing many CD2 genes. [provided by RefSeq, Jul 2008]","start":159826750,"end":159837249,"strand":1,"description":"SLAM family member 8 [Source:HGNC Symbol;Acc:HGNC:21391]"}, {"versioned_ensembl_gene_id":"ENSG00000259621.1","gene_symbol":"AC069029.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98880659,"end":98893535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279067.1","gene_symbol":"AC002540.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96118647,"end":96119995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279135.1","gene_symbol":"AL512652.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20712431,"end":20714146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229721.3","gene_symbol":"AC104115.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180226378,"end":180227000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284677.1","gene_symbol":"AL031985.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40436199,"end":40450039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278291.1","gene_symbol":"AL161772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20699307,"end":20703718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235790.7","gene_symbol":"AC114488.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31644049,"end":31660162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267385.1","gene_symbol":"AC011498.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4528427,"end":4540067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183571.10","gene_symbol":"PGPEP1L","gene_name":"pyroglutamyl-peptidase I-like [Source:HGNC Symbol;Acc:HGNC:27080]","synonyms":null,"biotype":"protein_coding","ncbi_id":"145814","summary":null,"start":98968230,"end":99007795,"strand":-1,"description":"pyroglutamyl-peptidase I-like [Source:HGNC Symbol;Acc:HGNC:27080]"}, {"versioned_ensembl_gene_id":"ENSG00000150456.10","gene_symbol":"EEF1AKMT1","gene_name":"EEF1A lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:27351]","synonyms":"N6AMT2","biotype":"protein_coding","ncbi_id":"221143","summary":null,"start":20728731,"end":20773958,"strand":-1,"description":"EEF1A lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:27351]"}, {"versioned_ensembl_gene_id":"ENSG00000256342.1","gene_symbol":"LINC02359","gene_name":"long intergenic non-protein coding RNA 2359 [Source:HGNC Symbol;Acc:HGNC:53280]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927464","summary":null,"start":126095992,"end":126103935,"strand":1,"description":"long intergenic non-protein coding RNA 2359 [Source:HGNC Symbol;Acc:HGNC:53280]"}, {"versioned_ensembl_gene_id":"ENSG00000121764.11","gene_symbol":"HCRTR1","gene_name":"hypocretin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4848]","synonyms":"OX1R","biotype":"protein_coding","ncbi_id":"3061","summary":"The protein encoded by this gene is a G-protein coupled receptor involved in the regulation of feeding behavior. The encoded protein selectively binds the hypothalamic neuropeptide orexin A. A related gene (HCRTR2) encodes a G-protein coupled receptor that binds orexin A and orexin B. [provided by RefSeq, Jan 2009]","start":31617686,"end":31632518,"strand":1,"description":"hypocretin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4848]"}, {"versioned_ensembl_gene_id":"ENSG00000220515.2","gene_symbol":"PGAM1P10","gene_name":"phosphoglycerate mutase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42457]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420633","summary":null,"start":73055097,"end":73055857,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42457]"}, {"versioned_ensembl_gene_id":"ENSG00000172458.4","gene_symbol":"IL17D","gene_name":"interleukin 17D [Source:HGNC Symbol;Acc:HGNC:5984]","synonyms":"IL27,IL-27,IL-22,IL-17D,FLJ30846","biotype":"protein_coding","ncbi_id":"53342","summary":"The protein encoded by this gene is a cytokine that shares the sequence similarity with IL17. The treatment of endothelial cells with this cytokine has been shown to stimulate the production of other cytokines including IL6, IL8 and CSF2/ GM-CSF. The increased expression of IL8 induced by this cytokine was found to be NF-kappa B-dependent. [provided by RefSeq, Jul 2008]","start":20702127,"end":20723098,"strand":1,"description":"interleukin 17D [Source:HGNC Symbol;Acc:HGNC:5984]"}, {"versioned_ensembl_gene_id":"ENSG00000176268.5","gene_symbol":"CYCSP34","gene_name":"cytochrome c, somatic pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:24408]","synonyms":"HCP34","biotype":"processed_pseudogene","ncbi_id":"360182","summary":null,"start":40863599,"end":40863902,"strand":-1,"description":"cytochrome c, somatic pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:24408]"}, {"versioned_ensembl_gene_id":"ENSG00000089280.18","gene_symbol":"FUS","gene_name":"FUS RNA binding protein [Source:HGNC Symbol;Acc:HGNC:4010]","synonyms":"HNRNPP2,hnRNP-P2,FUS1,ALS6,TLS","biotype":"protein_coding","ncbi_id":"2521","summary":"This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6. [provided by RefSeq, Sep 2009]","start":31180110,"end":31194871,"strand":1,"description":"FUS RNA binding protein [Source:HGNC Symbol;Acc:HGNC:4010]"}, {"versioned_ensembl_gene_id":"ENSG00000233425.1","gene_symbol":"KRT18P67","gene_name":"keratin 18 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:48894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631239","summary":null,"start":122837557,"end":122838820,"strand":1,"description":"keratin 18 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:48894]"}, {"versioned_ensembl_gene_id":"ENSG00000168852.12","gene_symbol":"TPTE2P5","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42356]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100616668","summary":null,"start":40822296,"end":40921749,"strand":-1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42356]"}, {"versioned_ensembl_gene_id":"ENSG00000106992.17","gene_symbol":"AK1","gene_name":"adenylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:361]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203","summary":"This gene encodes an adenylate kinase enzyme involved in energy metabolism and homeostasis of cellular adenine nucleotide ratios in different intracellular compartments. This gene is highly expressed in skeletal muscle, brain and erythrocytes. Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":127866480,"end":127877743,"strand":-1,"description":"adenylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:361]"}, {"versioned_ensembl_gene_id":"ENSG00000226887.7","gene_symbol":"ERVMER34-1","gene_name":"endogenous retrovirus group MER34 member 1, envelope [Source:HGNC Symbol;Acc:HGNC:42970]","synonyms":"envMER34","biotype":"protein_coding","ncbi_id":"100288413","summary":null,"start":52722618,"end":52751640,"strand":-1,"description":"endogenous retrovirus group MER34 member 1, envelope [Source:HGNC Symbol;Acc:HGNC:42970]"}, {"versioned_ensembl_gene_id":"ENSG00000164363.9","gene_symbol":"SLC6A18","gene_name":"solute carrier family 6 member 18 [Source:HGNC Symbol;Acc:HGNC:26441]","synonyms":"Xtrp2,FLJ31236","biotype":"protein_coding","ncbi_id":"348932","summary":"The SLC6 family of proteins, which includes SLC6A18, act as specific transporters for neurotransmitters, amino acids, and osmolytes like betaine, taurine, and creatine. SLC6 proteins are sodium cotransporters that derive the energy for solute transport from the electrochemical gradient for sodium ions (Hoglund et al., 2005 [PubMed 16125675]).[supplied by OMIM, Apr 2010]","start":1225355,"end":1246189,"strand":1,"description":"solute carrier family 6 member 18 [Source:HGNC Symbol;Acc:HGNC:26441]"}, {"versioned_ensembl_gene_id":"ENSG00000249238.1","gene_symbol":"BCL9P1","gene_name":"B-cell CLL/lymphoma 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51328]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419324","summary":null,"start":67636382,"end":67638942,"strand":1,"description":"B-cell CLL/lymphoma 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51328]"}, {"versioned_ensembl_gene_id":"ENSG00000104043.14","gene_symbol":"ATP8B4","gene_name":"ATPase phospholipid transporting 8B4 (putative) [Source:HGNC Symbol;Acc:HGNC:13536]","synonyms":"KIAA1939,ATPIM","biotype":"protein_coding","ncbi_id":"79895","summary":"This gene encodes a member of the cation transport ATPase (P-type) family and type IV subfamily. The encoded protein is involved in phospholipid transport in the cell membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":49858238,"end":50182817,"strand":-1,"description":"ATPase phospholipid transporting 8B4 (putative) [Source:HGNC Symbol;Acc:HGNC:13536]"}, {"versioned_ensembl_gene_id":"ENSG00000146090.15","gene_symbol":"RASGEF1C","gene_name":"RasGEF domain family member 1C [Source:HGNC Symbol;Acc:HGNC:27400]","synonyms":"FLJ35841","biotype":"protein_coding","ncbi_id":"255426","summary":null,"start":180100791,"end":180209153,"strand":-1,"description":"RasGEF domain family member 1C [Source:HGNC Symbol;Acc:HGNC:27400]"}, {"versioned_ensembl_gene_id":"ENSG00000254752.2","gene_symbol":"OR5M2P","gene_name":"olfactory receptor family 5 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14803]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79523","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56476287,"end":56484839,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14803]"}, {"versioned_ensembl_gene_id":"ENSG00000249364.5","gene_symbol":"AC112206.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67379378,"end":67805238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223769.3","gene_symbol":"CR388393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489201,"end":29489606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249767.1","gene_symbol":"ENPP7P10","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48693]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421805","summary":null,"start":9079023,"end":9141608,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48693]"}, {"versioned_ensembl_gene_id":"ENSG00000248877.2","gene_symbol":"PGBD4P4","gene_name":"piggyBac transposable element derived 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421146","summary":null,"start":130494673,"end":130495285,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44076]"}, {"versioned_ensembl_gene_id":"ENSG00000251326.1","gene_symbol":"LINC02479","gene_name":"long intergenic non-protein coding RNA 2479 [Source:HGNC Symbol;Acc:HGNC:53453]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377420","summary":null,"start":130376229,"end":130386371,"strand":1,"description":"long intergenic non-protein coding RNA 2479 [Source:HGNC Symbol;Acc:HGNC:53453]"}, {"versioned_ensembl_gene_id":"ENSG00000279311.1","gene_symbol":"AC092999.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":158869898,"end":158871821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167778.8","gene_symbol":"SPRYD3","gene_name":"SPRY domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25920]","synonyms":"FLJ14800","biotype":"protein_coding","ncbi_id":"84926","summary":null,"start":53064316,"end":53079420,"strand":-1,"description":"SPRY domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25920]"}, {"versioned_ensembl_gene_id":"ENSG00000250342.1","gene_symbol":"SNRPCP16","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49831]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480291","summary":null,"start":9051842,"end":9052051,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49831]"}, {"versioned_ensembl_gene_id":"ENSG00000278965.1","gene_symbol":"AC122713.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":180078357,"end":180081691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239870.1","gene_symbol":"AC112206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67608654,"end":67609130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242979.1","gene_symbol":"AC010285.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179933805,"end":179934196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278022.1","gene_symbol":"AC118658.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":98660210,"end":98660668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284636.1","gene_symbol":"AC073648.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9000841,"end":9001058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259475.1","gene_symbol":"AC036108.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98954149,"end":99105824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140006.11","gene_symbol":"WDR89","gene_name":"WD repeat domain 89 [Source:HGNC Symbol;Acc:HGNC:20489]","synonyms":"MGC9907,C14orf150","biotype":"protein_coding","ncbi_id":"112840","summary":null,"start":63597039,"end":63641861,"strand":-1,"description":"WD repeat domain 89 [Source:HGNC Symbol;Acc:HGNC:20489]"}, {"versioned_ensembl_gene_id":"ENSG00000166275.15","gene_symbol":"BORCS7","gene_name":"BLOC-1 related complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:23516]","synonyms":"FLJ40752,C10orf32","biotype":"protein_coding","ncbi_id":"119032","summary":null,"start":102854223,"end":102864961,"strand":1,"description":"BLOC-1 related complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:23516]"}, {"versioned_ensembl_gene_id":"ENSG00000136940.13","gene_symbol":"PDCL","gene_name":"phosducin like [Source:HGNC Symbol;Acc:HGNC:8770]","synonyms":"PhLP,DKFZp564M1863","biotype":"protein_coding","ncbi_id":"5082","summary":"Phosducin-like protein is a putative modulator of heterotrimeric G proteins. The protein shares extensive amino acid sequence homology with phosducin, a phosphoprotein expressed in retina and pineal gland. Both phosducin-like protein and phosphoducin have been shown to regulate G-protein signaling by binding to the beta-gamma subunits of G proteins. [provided by RefSeq, Jul 2008]","start":122798389,"end":122828631,"strand":-1,"description":"phosducin like [Source:HGNC Symbol;Acc:HGNC:8770]"}, {"versioned_ensembl_gene_id":"ENSG00000169668.11","gene_symbol":"BCRP2","gene_name":"breakpoint cluster region pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1015]","synonyms":"BCR2,BCR-2,BCRL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400892","summary":null,"start":21103016,"end":21122285,"strand":1,"description":"breakpoint cluster region pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1015]"}, {"versioned_ensembl_gene_id":"ENSG00000282367.1","gene_symbol":"PTDSS2","gene_name":"phosphatidylserine synthase 2 [Source:HGNC Symbol;Acc:HGNC:15463]","synonyms":"PSS2","biotype":"protein_coding","ncbi_id":"81490","summary":"The protein encoded by this gene catalyzes the conversion of phosphatidylethanolamine to phosphatidylserine, a structural membrane phospholipid that functions in cell signaling, blood coagulation, and apoptosis. The encoded enzyme also has a high affinity for docosahexaenoic acid (DHA) and can use it to make DHA-containing phosphatidylserine. [provided by RefSeq, Jul 2016]","start":473895,"end":491399,"strand":1,"description":"phosphatidylserine synthase 2 [Source:HGNC Symbol;Acc:HGNC:15463]"}, {"versioned_ensembl_gene_id":"ENSG00000173334.3","gene_symbol":"TRIB1","gene_name":"tribbles pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:16891]","synonyms":"C8FW,TRB1,GIG2","biotype":"protein_coding","ncbi_id":"10221","summary":null,"start":125430321,"end":125438405,"strand":1,"description":"tribbles pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:16891]"}, {"versioned_ensembl_gene_id":"ENSG00000250405.2","gene_symbol":"AC113367.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130994253,"end":130996164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112078.13","gene_symbol":"KCTD20","gene_name":"potassium channel tetramerization domain containing 20 [Source:HGNC Symbol;Acc:HGNC:21052]","synonyms":"MGC14254,dJ108K11.3,C6orf69","biotype":"protein_coding","ncbi_id":"222658","summary":null,"start":36442767,"end":36491143,"strand":1,"description":"potassium channel tetramerization domain containing 20 [Source:HGNC Symbol;Acc:HGNC:21052]"}, {"versioned_ensembl_gene_id":"ENSG00000282669.1","gene_symbol":"AK3P2","gene_name":"adenylate kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31099]","synonyms":"HsT26053","biotype":"processed_pseudogene","ncbi_id":"100419074","summary":null,"start":143057059,"end":143057816,"strand":-1,"description":"adenylate kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31099]"}, {"versioned_ensembl_gene_id":"ENSG00000165202.3","gene_symbol":"OR1Q1","gene_name":"olfactory receptor family 1 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:8223]","synonyms":"OR1Q3,OR1Q2,HSTPCR106,TPCR106,OST226OR9-A,OST226,OR9-A","biotype":"protein_coding","ncbi_id":"158131","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122614738,"end":122615682,"strand":1,"description":"olfactory receptor family 1 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:8223]"}, {"versioned_ensembl_gene_id":"ENSG00000148814.17","gene_symbol":"LRRC27","gene_name":"leucine rich repeat containing 27 [Source:HGNC Symbol;Acc:HGNC:29346]","synonyms":"KIAA1674","biotype":"protein_coding","ncbi_id":"80313","summary":null,"start":132332154,"end":132379918,"strand":1,"description":"leucine rich repeat containing 27 [Source:HGNC Symbol;Acc:HGNC:29346]"}, {"versioned_ensembl_gene_id":"ENSG00000231919.1","gene_symbol":"BX908738.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215243,"end":29216186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231626.1","gene_symbol":"AC013402.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104580821,"end":104581890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136319.11","gene_symbol":"TTC5","gene_name":"tetratricopeptide repeat domain 5 [Source:HGNC Symbol;Acc:HGNC:19274]","synonyms":"Strap","biotype":"protein_coding","ncbi_id":"91875","summary":null,"start":20256558,"end":20305994,"strand":-1,"description":"tetratricopeptide repeat domain 5 [Source:HGNC Symbol;Acc:HGNC:19274]"}, {"versioned_ensembl_gene_id":"ENSG00000225441.1","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"dJ80I19.2,OR2J1P,hs6M1-4,OR6-5","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100915,"end":29101853,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000251195.1","gene_symbol":"AC105417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129177386,"end":129179094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259931.2","gene_symbol":"AC105036.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75512770,"end":75513040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162391.11","gene_symbol":"FAM151A","gene_name":"family with sequence similarity 151 member A [Source:HGNC Symbol;Acc:HGNC:25032]","synonyms":"MGC27169,C1orf179","biotype":"protein_coding","ncbi_id":"338094","summary":null,"start":54609182,"end":54623556,"strand":-1,"description":"family with sequence similarity 151 member A [Source:HGNC Symbol;Acc:HGNC:25032]"}, {"versioned_ensembl_gene_id":"ENSG00000261708.1","gene_symbol":"DNM1P32","gene_name":"dynamin 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:35179]","synonyms":"DNM1DN4@,DNM1DN4-5","biotype":"unprocessed_pseudogene","ncbi_id":"100132100","summary":null,"start":32436503,"end":32439767,"strand":1,"description":"dynamin 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:35179]"}, {"versioned_ensembl_gene_id":"ENSG00000248866.1","gene_symbol":"USP46-AS1","gene_name":"USP46 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43991]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643783","summary":null,"start":52659406,"end":52661668,"strand":1,"description":"USP46 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43991]"}, {"versioned_ensembl_gene_id":"ENSG00000154874.15","gene_symbol":"CCDC144B","gene_name":"coiled-coil domain containing 144B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26704]","synonyms":"FLJ36492","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284047","summary":null,"start":18537800,"end":18625617,"strand":-1,"description":"coiled-coil domain containing 144B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26704]"}, {"versioned_ensembl_gene_id":"ENSG00000227077.3","gene_symbol":"AC107983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18572752,"end":18572961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243925.1","gene_symbol":"AC091021.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26098839,"end":26099226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198369.9","gene_symbol":"SPRED2","gene_name":"sprouty related EVH1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17722]","synonyms":"Spred-2,FLJ31917,FLJ21897","biotype":"protein_coding","ncbi_id":"200734","summary":"SPRED2 is a member of the Sprouty (see SPRY1; MIM 602465)/SPRED family of proteins that regulate growth factor-induced activation of the MAP kinase cascade (see MAPK1; MIM 176948) (Nonami et al., 2004 [PubMed 15465815]).[supplied by OMIM, Mar 2008]","start":65310851,"end":65432637,"strand":-1,"description":"sprouty related EVH1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17722]"}, {"versioned_ensembl_gene_id":"ENSG00000212717.3","gene_symbol":"DEFB117","gene_name":"defensin beta 117 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18098]","synonyms":"DEFB-17","biotype":"processed_pseudogene","ncbi_id":"245931","summary":null,"start":31360790,"end":31360930,"strand":1,"description":"defensin beta 117 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18098]"}, {"versioned_ensembl_gene_id":"ENSG00000277881.1","gene_symbol":"AL645927.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29450210,"end":29450558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000054965.10","gene_symbol":"FAM168A","gene_name":"family with sequence similarity 168 member A [Source:HGNC Symbol;Acc:HGNC:28999]","synonyms":"TCRP1,KIAA0280","biotype":"protein_coding","ncbi_id":"23201","summary":null,"start":73400487,"end":73598189,"strand":-1,"description":"family with sequence similarity 168 member A [Source:HGNC Symbol;Acc:HGNC:28999]"}, {"versioned_ensembl_gene_id":"ENSG00000256148.1","gene_symbol":"AP000763.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73510658,"end":73510820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130592.15","gene_symbol":"LSP1","gene_name":"lymphocyte-specific protein 1 [Source:HGNC Symbol;Acc:HGNC:6707]","synonyms":"WP34","biotype":"protein_coding","ncbi_id":"4046","summary":"This gene encodes an intracellular F-actin binding protein. The protein is expressed in lymphocytes, neutrophils, macrophages, and endothelium and may regulate neutrophil motility, adhesion to fibrinogen matrix proteins, and transendothelial migration. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":1852970,"end":1892267,"strand":1,"description":"lymphocyte-specific protein 1 [Source:HGNC Symbol;Acc:HGNC:6707]"}, {"versioned_ensembl_gene_id":"ENSG00000254619.1","gene_symbol":"AC113192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33810145,"end":33811178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255169.1","gene_symbol":"AC113192.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33804768,"end":33805641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254102.1","gene_symbol":"AC090136.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64574306,"end":64581888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255161.1","gene_symbol":"AC113192.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33787054,"end":33787795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255272.1","gene_symbol":"AC113192.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33776188,"end":33779495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262011.1","gene_symbol":"AC003009.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13331368,"end":13332583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130159.13","gene_symbol":"ECSIT","gene_name":"ECSIT signalling integrator [Source:HGNC Symbol;Acc:HGNC:29548]","synonyms":"SITPEC","biotype":"protein_coding","ncbi_id":"51295","summary":null,"start":11505916,"end":11529174,"strand":-1,"description":"ECSIT signalling integrator [Source:HGNC Symbol;Acc:HGNC:29548]"}, {"versioned_ensembl_gene_id":"ENSG00000180316.12","gene_symbol":"PNPLA1","gene_name":"patatin like phospholipase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21246]","synonyms":"FLJ38755,dJ50J22.1","biotype":"protein_coding","ncbi_id":"285848","summary":"The protein encoded by this gene belongs to the patatin-like phospholipase (PNPLA) family, which is characterized by the presence of a highly conserved patatin domain. PNPLA family members have diverse lipolytic and acyltransferase activities, and are key elements in lipid metabolism. While other members of this family have been well characterized, the function of this gene remained an enigma. However, recent studies show that this gene is expressed in the skin epidermal keratinocytes, and has a role in glycerophospholipid metabolism in the cutaneous barrier. Consistent with these observations, mutations in this gene are associated with ichthyosis in human (autosomal recessive congenital ichthyoses, ARCI) and dog. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":36243203,"end":36312229,"strand":1,"description":"patatin like phospholipase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21246]"}, {"versioned_ensembl_gene_id":"ENSG00000279083.1","gene_symbol":"AL160274.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35360540,"end":35362054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130811.11","gene_symbol":"EIF3G","gene_name":"eukaryotic translation initiation factor 3 subunit G [Source:HGNC Symbol;Acc:HGNC:3274]","synonyms":"EIF3S4,eIF3g,eIF3-p44,eIF3-delta","biotype":"protein_coding","ncbi_id":"8666","summary":"This gene encodes a core subunit of the eukaryotic translation initiation factor 3 (eIF3) complex, which is required for initiation of protein translation. An N-terminal caspase cleavage product of the encoded protein may stimulate degradation of DNA. A mutation in this gene is associated with narcolepsy. [provided by RefSeq, Jul 2016]","start":10115017,"end":10119918,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit G [Source:HGNC Symbol;Acc:HGNC:3274]"}, {"versioned_ensembl_gene_id":"ENSG00000232383.1","gene_symbol":"AC010677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26276195,"end":26276606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237462.10","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RNF76,RFP","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28914742,"end":28923955,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000273200.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859590,"end":28863315,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000226979.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31572054,"end":31574324,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000262651.1","gene_symbol":"AL513043.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63612761,"end":63612903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235812.4","gene_symbol":"ADAM21P1","gene_name":"ADAM metallopeptidase domain 21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19822]","synonyms":"ADAM21P","biotype":"transcribed_processed_pseudogene","ncbi_id":"145241","summary":null,"start":70245491,"end":70247801,"strand":-1,"description":"ADAM metallopeptidase domain 21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19822]"}, {"versioned_ensembl_gene_id":"ENSG00000223708.1","gene_symbol":"AL645935.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29931616,"end":29932608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255063.1","gene_symbol":"AP001646.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82805354,"end":82806509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215246.5","gene_symbol":"AC116351.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":987180,"end":997308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267359.1","gene_symbol":"AC015911.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35553205,"end":35554767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230172.1","gene_symbol":"AC090957.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14764952,"end":14767440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079277.19","gene_symbol":"MKNK1","gene_name":"MAP kinase interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:7110]","synonyms":"MNK1","biotype":"protein_coding","ncbi_id":"8569","summary":"This gene encodes a Ser/Thr protein kinase that interacts with, and is activated by ERK1 and p38 mitogen-activated protein kinases, and thus may play a role in the response to environmental stress and cytokines. This kinase may also regulate transcription by phosphorylating eIF4E via interaction with the C-terminal region of eIF4G. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2012]","start":46557408,"end":46616843,"strand":-1,"description":"MAP kinase interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:7110]"}, {"versioned_ensembl_gene_id":"ENSG00000132254.12","gene_symbol":"ARFIP2","gene_name":"ADP ribosylation factor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17160]","synonyms":"POR1","biotype":"protein_coding","ncbi_id":"23647","summary":null,"start":6474683,"end":6481479,"strand":-1,"description":"ADP ribosylation factor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17160]"}, {"versioned_ensembl_gene_id":"ENSG00000177776.8","gene_symbol":"AC005519.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74377818,"end":74378418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269956.1","gene_symbol":"MKNK1-AS1","gene_name":"MKNK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44129]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507423","summary":null,"start":46538696,"end":46570255,"strand":1,"description":"MKNK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44129]"}, {"versioned_ensembl_gene_id":"ENSG00000248647.2","gene_symbol":"AC012613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149163955,"end":149276776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276110.1","gene_symbol":"AC242988.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150255095,"end":150257286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213262.3","gene_symbol":"VDAC2P3","gene_name":"voltage dependent anion channel 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401959","summary":null,"start":117640812,"end":117641639,"strand":-1,"description":"voltage dependent anion channel 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51931]"}, {"versioned_ensembl_gene_id":"ENSG00000249494.5","gene_symbol":"AC008629.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119006347,"end":119070890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229995.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"352967","summary":null,"start":29806254,"end":29806385,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000224253.1","gene_symbol":"AL669813.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29742254,"end":29742478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237395.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29960309,"end":29961971,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000274105.1","gene_symbol":"AC084824.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32728169,"end":32729024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170426.1","gene_symbol":"SDR9C7","gene_name":"short chain dehydrogenase/reductase family 9C member 7 [Source:HGNC Symbol;Acc:HGNC:29958]","synonyms":"SDR-O,RDHS","biotype":"protein_coding","ncbi_id":"121214","summary":"This gene encodes a protein with similarity to the short-chain dehydrogenase/reductase (SDR) family but has not been shown to have retinoid or dehydrogenase activities. [provided by RefSeq, Apr 2010]","start":56923154,"end":56934405,"strand":-1,"description":"short chain dehydrogenase/reductase family 9C member 7 [Source:HGNC Symbol;Acc:HGNC:29958]"}, {"versioned_ensembl_gene_id":"ENSG00000226755.2","gene_symbol":"VPS25P1","gene_name":"VPS25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44250]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441899","summary":null,"start":117549415,"end":117549922,"strand":1,"description":"VPS25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44250]"}, {"versioned_ensembl_gene_id":"ENSG00000269296.1","gene_symbol":"AC005614.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40090754,"end":40094406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260293.2","gene_symbol":"AC106820.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2476558,"end":2482173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273326.1","gene_symbol":"TAS2R7","gene_name":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]","synonyms":"TRB4,T2R7","biotype":"protein_coding","ncbi_id":"50837","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10801532,"end":10802627,"strand":-1,"description":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]"}, {"versioned_ensembl_gene_id":"ENSG00000238022.1","gene_symbol":"AL390730.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165215980,"end":165219104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225032.5","gene_symbol":"AL162586.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127816066,"end":127822520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219992.2","gene_symbol":"AL391422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3754099,"end":3754840,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261532.1","gene_symbol":"AC009065.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2211997,"end":2212863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259320.1","gene_symbol":"AC022523.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98122563,"end":98131607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259199.1","gene_symbol":"AC022523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98046667,"end":98293177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206291.10","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":32993608,"end":33009820,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000203618.5","gene_symbol":"GP1BB","gene_name":"glycoprotein Ib platelet beta subunit [Source:HGNC Symbol;Acc:HGNC:4440]","synonyms":"GPIbbeta,CD42c","biotype":"protein_coding","ncbi_id":"2812","summary":"Platelet glycoprotein Ib (GPIb) is a heterodimeric transmembrane protein consisting of a disulfide-linked 140 kD alpha chain and 22 kD beta chain. It is part of the GPIb-V-IX system that constitutes the receptor for von Willebrand factor (VWF), and mediates platelet adhesion in the arterial circulation. GPIb alpha chain provides the VWF binding site, and GPIb beta contributes to surface expression of the receptor and participates in transmembrane signaling through phosphorylation of its intracellular domain. Mutations in the GPIb beta subunit have been associated with Bernard-Soulier syndrome, velocardiofacial syndrome and giant platelet disorder. The 206 amino acid precursor of GPIb beta is synthesized from a 1.0 kb mRNA expressed in plateletes and megakaryocytes. A 411 amino acid protein arising from a longer, unspliced transcript in endothelial cells has been described; however, the authenticity of this product has been questioned. Yet another less abundant GPIb beta mRNA species of 3.5 kb, expressed in nonhematopoietic tissues such as endothelium, brain and heart, was shown to result from inefficient usage of a non-consensus polyA signal in the neighboring upstream gene (SEPT5, septin 5). In the absence of polyadenylation from its own imperfect site, the SEPT5 gene produces read-through transcripts that use the consensus polyA signal of this gene. [provided by RefSeq, Dec 2010]","start":19722945,"end":19724771,"strand":1,"description":"glycoprotein Ib platelet beta subunit [Source:HGNC Symbol;Acc:HGNC:4440]"}, {"versioned_ensembl_gene_id":"ENSG00000249547.1","gene_symbol":"AC092440.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23234625,"end":23285573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279642.1","gene_symbol":"AL023973.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44486295,"end":44486914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196312.12","gene_symbol":"MFSD14C","gene_name":"major facilitator superfamily domain containing 14C [Source:HGNC Symbol;Acc:HGNC:23672]","synonyms":"MGC12945,HIATL2","biotype":"protein_coding","ncbi_id":"84278","summary":null,"start":96897917,"end":97013708,"strand":-1,"description":"major facilitator superfamily domain containing 14C [Source:HGNC Symbol;Acc:HGNC:23672]"}, {"versioned_ensembl_gene_id":"ENSG00000233519.1","gene_symbol":"AL590490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":240400671,"end":240401123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186124.4","gene_symbol":"OR9M1P","gene_name":"olfactory receptor family 9 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15327]","synonyms":"OR5BG1P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81153","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55850347,"end":55858547,"strand":1,"description":"olfactory receptor family 9 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15327]"}, {"versioned_ensembl_gene_id":"ENSG00000256966.6","gene_symbol":"AL513165.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37512547,"end":37592469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234123.1","gene_symbol":"RHBDF1P1","gene_name":"RHBDF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44499]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"131973","summary":null,"start":14572852,"end":14574792,"strand":-1,"description":"RHBDF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44499]"}, {"versioned_ensembl_gene_id":"ENSG00000279240.1","gene_symbol":"AC063980.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136376348,"end":136397042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260991.2","gene_symbol":"AC120498.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1280161,"end":1280544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231755.1","gene_symbol":"CHODL-AS1","gene_name":"CHODL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1279]","synonyms":"NCRNA00157,C21orf39","biotype":"lincRNA","ncbi_id":"54075","summary":null,"start":17835016,"end":17885608,"strand":-1,"description":"CHODL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1279]"}, {"versioned_ensembl_gene_id":"ENSG00000254457.2","gene_symbol":"OR5D2P","gene_name":"olfactory receptor family 5 subfamily D member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8335]","synonyms":"OR11-7a,OR8-125,OR5D9P,OR5D8P,OR5D7P,OR5D6P,OR5D5P,OR5D1P,OR5D12P,OR5D12,OR5D11P,OR5D11,OR5D10P,R5D9P,OR18-44,OR912-94,OR18-43,OR912-91,OR18-42,OR912-47,OR18-17,OR8-127","biotype":"unprocessed_pseudogene","ncbi_id":"8595","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55714799,"end":55715709,"strand":1,"description":"olfactory receptor family 5 subfamily D member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8335]"}, {"versioned_ensembl_gene_id":"ENSG00000279704.1","gene_symbol":"AC148477.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132351855,"end":132352322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126264.9","gene_symbol":"HCST","gene_name":"hematopoietic cell signal transducer [Source:HGNC Symbol;Acc:HGNC:16977]","synonyms":"DAP10,PIK3AP,KAP10,DKFZP586C1522","biotype":"protein_coding","ncbi_id":"10870","summary":"This gene encodes a transmembrane signaling adaptor that contains a YxxM motif in its cytoplasmic domain. The encoded protein may form part of the immune recognition receptor complex with the C-type lectin-like receptor NKG2D. As part of this receptor complex, this protein may activate phosphatidylinositol 3-kinase dependent signaling pathways through its intracytoplasmic YxxM motif. This receptor complex may have a role in cell survival and proliferation by activation of NK and T cell responses. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":35902480,"end":35904377,"strand":1,"description":"hematopoietic cell signal transducer [Source:HGNC Symbol;Acc:HGNC:16977]"}, {"versioned_ensembl_gene_id":"ENSG00000188385.11","gene_symbol":"JAKMIP3","gene_name":"Janus kinase and microtubule interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:23523]","synonyms":"NECC2,KIAA4091,FLJ37857,C10orf39,C10orf14,bA140A10.5","biotype":"protein_coding","ncbi_id":"282973","summary":null,"start":132104671,"end":132184809,"strand":1,"description":"Janus kinase and microtubule interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:23523]"}, {"versioned_ensembl_gene_id":"ENSG00000244327.1","gene_symbol":"AC109992.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":142465315,"end":142472337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230266.1","gene_symbol":"XXYLT1-AS2","gene_name":"XXYLT1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41154]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410543","summary":null,"start":195147871,"end":195152790,"strand":1,"description":"XXYLT1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41154]"}, {"versioned_ensembl_gene_id":"ENSG00000218713.1","gene_symbol":"AL512378.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53206598,"end":53208697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224083.1","gene_symbol":"MTCO1P11","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52013]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075264","summary":null,"start":5096666,"end":5098193,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52013]"}, {"versioned_ensembl_gene_id":"ENSG00000267711.1","gene_symbol":"AC060766.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35400878,"end":35403006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267315.1","gene_symbol":"AC060766.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35377416,"end":35377678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159640.15","gene_symbol":"ACE","gene_name":"angiotensin I converting enzyme [Source:HGNC Symbol;Acc:HGNC:2707]","synonyms":"DCP1,CD143,ACE1","biotype":"protein_coding","ncbi_id":"1636","summary":"This gene encodes an enzyme involved in blood pressure regulation and electrolyte balance. It catalyzes the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance. This angiotensin converting enzyme (ACE) also inactivates the vasodilator protein, bradykinin. Accordingly, the encoded enzyme increases blood pressure and is a drug target of ACE inhibitors, which are often prescribed to reduce blood pressure. This enzyme additionally plays a role in fertility through its ability to cleave and release GPI-anchored membrane proteins in spermatozoa. Many studies have associated the presence or absence of a 287 bp Alu repeat element in this gene with the levels of circulating enzyme. This polymorphism, as well as mutations in this gene, have been implicated in a wide variety of diseases including cardiovascular pathophysiologies, psoriasis, renal disease, stroke, and Alzheimer's disease. Regulation of the homologous ACE2 gene may be involved in progression of disease caused by several human coronaviruses, including SARS-CoV and SARS-CoV-2. Alternative splicing results in multiple transcript variants encoding both somatic (sACE) and male-specific testicular (tACE) isoforms. [provided by RefSeq, Sep 2020]","start":63477061,"end":63498380,"strand":1,"description":"angiotensin I converting enzyme [Source:HGNC Symbol;Acc:HGNC:2707]"}, {"versioned_ensembl_gene_id":"ENSG00000128699.13","gene_symbol":"ORMDL1","gene_name":"ORMDL sphingolipid biosynthesis regulator 1 [Source:HGNC Symbol;Acc:HGNC:16036]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94101","summary":null,"start":189770323,"end":189784371,"strand":-1,"description":"ORMDL sphingolipid biosynthesis regulator 1 [Source:HGNC Symbol;Acc:HGNC:16036]"}, {"versioned_ensembl_gene_id":"ENSG00000109189.12","gene_symbol":"USP46","gene_name":"ubiquitin specific peptidase 46 [Source:HGNC Symbol;Acc:HGNC:20075]","synonyms":"FLJ12552","biotype":"protein_coding","ncbi_id":"64854","summary":"Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP46 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Jun 2009]","start":52590972,"end":52659335,"strand":-1,"description":"ubiquitin specific peptidase 46 [Source:HGNC Symbol;Acc:HGNC:20075]"}, {"versioned_ensembl_gene_id":"ENSG00000228979.4","gene_symbol":"AC113554.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63471604,"end":63472093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237281.1","gene_symbol":"CATIP-AS2","gene_name":"CATIP antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41079]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103689911","summary":null,"start":218326889,"end":218357966,"strand":-1,"description":"CATIP antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41079]"}, {"versioned_ensembl_gene_id":"ENSG00000270673.1","gene_symbol":"YTHDF3-AS1","gene_name":"YTHDF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48728]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101410533","summary":null,"start":63167725,"end":63168442,"strand":-1,"description":"YTHDF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48728]"}, {"versioned_ensembl_gene_id":"ENSG00000158560.14","gene_symbol":"DYNC1I1","gene_name":"dynein cytoplasmic 1 intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:2963]","synonyms":"DNCIC1,DNCI1","biotype":"protein_coding","ncbi_id":"1780","summary":null,"start":95772506,"end":96110322,"strand":1,"description":"dynein cytoplasmic 1 intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:2963]"}, {"versioned_ensembl_gene_id":"ENSG00000266718.1","gene_symbol":"AC079336.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32495536,"end":32499333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105483.17","gene_symbol":"CARD8","gene_name":"caspase recruitment domain family member 8 [Source:HGNC Symbol;Acc:HGNC:17057]","synonyms":"CARDINAL,TUCAN,NDPP,KIAA0955,Dakar","biotype":"protein_coding","ncbi_id":"22900","summary":"The protein encoded by this gene belongs to the caspase recruitment domain (CARD)-containing family of proteins, which are involved in pathways leading to activation of caspases or nuclear factor kappa-B (NFKB). This protein may be a component of the inflammasome, a protein complex that plays a role in the activation of proinflammatory caspases. It is thought that this protein acts as an adaptor molecule that negatively regulates NFKB activation, CASP1-dependent IL1B secretion, and apoptosis. Polymorphisms in this gene may be associated with a susceptibility to rheumatoid arthritis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]","start":48180770,"end":48255946,"strand":-1,"description":"caspase recruitment domain family member 8 [Source:HGNC Symbol;Acc:HGNC:17057]"}, {"versioned_ensembl_gene_id":"ENSG00000228245.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31533053,"end":31533887,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000227632.2","gene_symbol":"AC018804.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130202312,"end":130212628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248351.1","gene_symbol":"HSPD1P18","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35136]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100359397","summary":null,"start":136381268,"end":136381511,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35136]"}, {"versioned_ensembl_gene_id":"ENSG00000226758.1","gene_symbol":"DISC1-IT1","gene_name":"DISC1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41325]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"104472714","summary":null,"start":231925834,"end":231945233,"strand":1,"description":"DISC1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41325]"}, {"versioned_ensembl_gene_id":"ENSG00000179840.5","gene_symbol":"PIK3CD-AS1","gene_name":"PIK3CD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32346]","synonyms":"C1orf200","biotype":"antisense_RNA","ncbi_id":"644997","summary":null,"start":9652610,"end":9654586,"strand":-1,"description":"PIK3CD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32346]"}, {"versioned_ensembl_gene_id":"ENSG00000107815.7","gene_symbol":"TWNK","gene_name":"twinkle mtDNA helicase [Source:HGNC Symbol;Acc:HGNC:1160]","synonyms":"TWINL,TWINKLE,PEO1,PEO,IOSCA,FLJ21832,C10orf2","biotype":"protein_coding","ncbi_id":"56652","summary":"This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009]","start":100987367,"end":100994401,"strand":1,"description":"twinkle mtDNA helicase [Source:HGNC Symbol;Acc:HGNC:1160]"}, {"versioned_ensembl_gene_id":"ENSG00000224070.1","gene_symbol":"HMGN1P6","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874430","summary":null,"start":206259628,"end":206259918,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39349]"}, {"versioned_ensembl_gene_id":"ENSG00000104892.16","gene_symbol":"KLC3","gene_name":"kinesin light chain 3 [Source:HGNC Symbol;Acc:HGNC:20717]","synonyms":"KNS2B,KLCt,KLC2L","biotype":"protein_coding","ncbi_id":"147700","summary":"This gene encodes a member of the kinesin light chain gene family. Kinesins are molecular motors involved in the transport of cargo along microtubules, and are composed of two kinesin heavy chain (KHC) and two kinesin light chain (KLC) molecules. KLCs are thought to typically be involved in binding cargo and regulating kinesin activity. In the rat, a protein similar to this gene product is expressed in post-meiotic spermatids, where it associates with structural components of sperm tails and mitochondria. [provided by RefSeq, Jul 2008]","start":45333434,"end":45351520,"strand":1,"description":"kinesin light chain 3 [Source:HGNC Symbol;Acc:HGNC:20717]"}, {"versioned_ensembl_gene_id":"ENSG00000155269.11","gene_symbol":"GPR78","gene_name":"G protein-coupled receptor 78 [Source:HGNC Symbol;Acc:HGNC:4528]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27201","summary":"The protein encoded by this gene belongs to the G protein-coupled receptor family, which contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. This is an orphan receptor, which displays significant level of constitutive activity. Association analysis shows preliminary evidence for the involvement of this gene in susceptibility to bipolar affective disorder and schizophrenia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2011]","start":8558725,"end":8619761,"strand":1,"description":"G protein-coupled receptor 78 [Source:HGNC Symbol;Acc:HGNC:4528]"}, {"versioned_ensembl_gene_id":"ENSG00000176658.16","gene_symbol":"MYO1D","gene_name":"myosin ID [Source:HGNC Symbol;Acc:HGNC:7598]","synonyms":"PPP1R108,myr4,KIAA0727","biotype":"protein_coding","ncbi_id":"4642","summary":null,"start":32492522,"end":32877177,"strand":-1,"description":"myosin ID [Source:HGNC Symbol;Acc:HGNC:7598]"}, {"versioned_ensembl_gene_id":"ENSG00000281379.2","gene_symbol":"SEPT14P19","gene_name":"septin 14 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51707]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107105271","summary":null,"start":186373,"end":195696,"strand":-1,"description":"septin 14 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51707]"}, {"versioned_ensembl_gene_id":"ENSG00000235683.1","gene_symbol":"AC018442.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99695957,"end":99698017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268222.1","gene_symbol":"EEF1A1P7","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:3202]","synonyms":"EEF1AL5","biotype":"processed_pseudogene","ncbi_id":"390924","summary":null,"start":35382172,"end":35384052,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:3202]"}, {"versioned_ensembl_gene_id":"ENSG00000276993.1","gene_symbol":"AC116003.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75387056,"end":75387596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232332.1","gene_symbol":"AC233982.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76029895,"end":76030330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231924.9","gene_symbol":"PSG1","gene_name":"pregnancy specific beta-1-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:9514]","synonyms":"PBG1,CD66f,PSGGA,PSBG1","biotype":"protein_coding","ncbi_id":"5669","summary":"The human placenta is a multihormonal endocrine organ that produces hormones, enzymes, and other molecules that support fetal survival and development. Pregnancy-specific beta-1-glycoprotein (PSBG, PSG) is a major product of the syncytiotrophoblast, reaching concentrations of 100 to 290 mg/l at term in the serum of pregnant women (Horne et al., 1976 [PubMed 971765]). PSG is a member of the immunoglobulin (Ig) superfamily (Watanabe and Chou, 1988 [PubMed 3257488]; Streydio et al., 1988 [PubMed 3260773]).[supplied by OMIM, Oct 2009]","start":42866464,"end":42879822,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:9514]"}, {"versioned_ensembl_gene_id":"ENSG00000223753.2","gene_symbol":"AC234775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101683780,"end":101684449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267641.1","gene_symbol":"BNIP3P16","gene_name":"BCL2 interacting protein 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480418","summary":null,"start":20175013,"end":20177063,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49696]"}, {"versioned_ensembl_gene_id":"ENSG00000272848.1","gene_symbol":"AL009176.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169426420,"end":169427069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236778.7","gene_symbol":"INTS6-AS1","gene_name":"INTS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42691]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507398","summary":null,"start":51452367,"end":51552364,"strand":1,"description":"INTS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42691]"}, {"versioned_ensembl_gene_id":"ENSG00000255345.1","gene_symbol":"AP002957.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79092848,"end":79098003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095917.13","gene_symbol":"TPSD1","gene_name":"tryptase delta 1 [Source:HGNC Symbol;Acc:HGNC:14118]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23430","summary":"Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. Although this gene may be an exception, most of the tryptase genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. This gene was once considered to be a pseudogene, although it is now believed to be a functional gene that encodes a protein. [provided by RefSeq, Jul 2008]","start":1256059,"end":1258998,"strand":1,"description":"tryptase delta 1 [Source:HGNC Symbol;Acc:HGNC:14118]"}, {"versioned_ensembl_gene_id":"ENSG00000260182.1","gene_symbol":"AC120498.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1257339,"end":1258074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234572.1","gene_symbol":"LINC01800","gene_name":"long intergenic non-protein coding RNA 1800 [Source:HGNC Symbol;Acc:HGNC:52590]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927438","summary":null,"start":64846130,"end":64863626,"strand":-1,"description":"long intergenic non-protein coding RNA 1800 [Source:HGNC Symbol;Acc:HGNC:52590]"}, {"versioned_ensembl_gene_id":"ENSG00000231697.3","gene_symbol":"NANOGP5","gene_name":"Nanog homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23103]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"414133","summary":null,"start":100175178,"end":100176054,"strand":1,"description":"Nanog homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23103]"}, {"versioned_ensembl_gene_id":"ENSG00000216687.2","gene_symbol":"AL390237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58071720,"end":58073134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226794.1","gene_symbol":"MTND1P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42069]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873339","summary":null,"start":69595487,"end":69596436,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42069]"}, {"versioned_ensembl_gene_id":"ENSG00000229659.1","gene_symbol":"RPL26P6","gene_name":"ribosomal protein L26 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131526","summary":null,"start":73422259,"end":73422696,"strand":-1,"description":"ribosomal protein L26 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34023]"}, {"versioned_ensembl_gene_id":"ENSG00000253297.1","gene_symbol":"AC008627.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":148644687,"end":148646390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254686.2","gene_symbol":"AL138812.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35656694,"end":35661339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128656.13","gene_symbol":"CHN1","gene_name":"chimerin 1 [Source:HGNC Symbol;Acc:HGNC:1943]","synonyms":"CHN,ARHGAP2,RhoGAP2,n-chimerin,DURS2","biotype":"protein_coding","ncbi_id":"1123","summary":"This gene encodes GTPase-activating protein for ras-related p21-rac and a phorbol ester receptor. It is predominantly expressed in neurons, and plays an important role in neuronal signal-transduction mechanisms. Mutations in this gene are associated with Duane's retraction syndrome 2 (DURS2). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011]","start":174799363,"end":175005369,"strand":-1,"description":"chimerin 1 [Source:HGNC Symbol;Acc:HGNC:1943]"}, {"versioned_ensembl_gene_id":"ENSG00000166343.9","gene_symbol":"MSS51","gene_name":"MSS51 mitochondrial translational activator [Source:HGNC Symbol;Acc:HGNC:21000]","synonyms":"ZMYND17,FLJ39565","biotype":"protein_coding","ncbi_id":"118490","summary":null,"start":73423579,"end":73433561,"strand":-1,"description":"MSS51 mitochondrial translational activator [Source:HGNC Symbol;Acc:HGNC:21000]"}, {"versioned_ensembl_gene_id":"ENSG00000117450.13","gene_symbol":"PRDX1","gene_name":"peroxiredoxin 1 [Source:HGNC Symbol;Acc:HGNC:9352]","synonyms":"PAGA,NKEFA","biotype":"protein_coding","ncbi_id":"5052","summary":"This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in cells, and may contribute to the antiviral activity of CD8(+) T-cells. This protein may have a proliferative effect and play a role in cancer development or progression. Four transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jan 2011]","start":45511036,"end":45523047,"strand":-1,"description":"peroxiredoxin 1 [Source:HGNC Symbol;Acc:HGNC:9352]"}, {"versioned_ensembl_gene_id":"ENSG00000235294.1","gene_symbol":"RPL7AP25","gene_name":"ribosomal protein L7a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271042","summary":null,"start":181505075,"end":181505879,"strand":-1,"description":"ribosomal protein L7a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36714]"}, {"versioned_ensembl_gene_id":"ENSG00000171224.8","gene_symbol":"C10orf35","gene_name":"chromosome 10 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:23519]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219738","summary":null,"start":69630251,"end":69633599,"strand":1,"description":"chromosome 10 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:23519]"}, {"versioned_ensembl_gene_id":"ENSG00000237806.1","gene_symbol":"FAUP2","gene_name":"FAU, ubiquitin like and ribosomal protein S30 fusion pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36535]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271125","summary":null,"start":181242345,"end":181242901,"strand":-1,"description":"FAU, ubiquitin like and ribosomal protein S30 fusion pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36535]"}, {"versioned_ensembl_gene_id":"ENSG00000185897.6","gene_symbol":"FFAR3","gene_name":"free fatty acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:4499]","synonyms":"GPR41,FFA3R","biotype":"protein_coding","ncbi_id":"2865","summary":null,"start":35358460,"end":35360485,"strand":1,"description":"free fatty acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:4499]"}, {"versioned_ensembl_gene_id":"ENSG00000251261.4","gene_symbol":"OR7H2P","gene_name":"olfactory receptor family 7 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31314]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403301","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101816475,"end":101816780,"strand":-1,"description":"olfactory receptor family 7 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31314]"}, {"versioned_ensembl_gene_id":"ENSG00000150907.7","gene_symbol":"FOXO1","gene_name":"forkhead box O1 [Source:HGNC Symbol;Acc:HGNC:3819]","synonyms":"FOXO1A,FKHR,FKH1","biotype":"protein_coding","ncbi_id":"2308","summary":"This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma. [provided by RefSeq, Jul 2008]","start":40469953,"end":40666597,"strand":-1,"description":"forkhead box O1 [Source:HGNC Symbol;Acc:HGNC:3819]"}, {"versioned_ensembl_gene_id":"ENSG00000241231.1","gene_symbol":"AC022294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181421058,"end":181442486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267364.1","gene_symbol":"AC022706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35313502,"end":35324900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230570.1","gene_symbol":"AL139095.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7340854,"end":7342056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249495.1","gene_symbol":"AC117525.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101976296,"end":101976798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242808.7","gene_symbol":"SOX2-OT","gene_name":"SOX2 overlapping transcript [Source:HGNC Symbol;Acc:HGNC:20209]","synonyms":"SOX2OT,NCRNA00043,DKFZp761J1324","biotype":"sense_overlapping","ncbi_id":"347689","summary":"This gene produces alternatively spliced long non-coding RNAs. These RNAs were observed to be upregulated in tumor cells and positively correlated to expression of the SRY-box 2 gene. Overexpression of these transcripts may promote cell proliferation. [provided by RefSeq, Dec 2017]","start":180989770,"end":181836880,"strand":1,"description":"SOX2 overlapping transcript [Source:HGNC Symbol;Acc:HGNC:20209]"}, {"versioned_ensembl_gene_id":"ENSG00000267271.1","gene_symbol":"AC060766.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35344231,"end":35344564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166326.6","gene_symbol":"TRIM44","gene_name":"tripartite motif containing 44 [Source:HGNC Symbol;Acc:HGNC:19016]","synonyms":"MC7,DIPB","biotype":"protein_coding","ncbi_id":"54765","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, namely a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. [provided by RefSeq, Jul 2008]","start":35662805,"end":35818007,"strand":1,"description":"tripartite motif containing 44 [Source:HGNC Symbol;Acc:HGNC:19016]"}, {"versioned_ensembl_gene_id":"ENSG00000169040.14","gene_symbol":"PMCHL2","gene_name":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5370","summary":null,"start":71375786,"end":71385993,"strand":1,"description":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]"}, {"versioned_ensembl_gene_id":"ENSG00000206190.11","gene_symbol":"ATP10A","gene_name":"ATPase phospholipid transporting 10A (putative) [Source:HGNC Symbol;Acc:HGNC:13542]","synonyms":"KIAA0566,ATPVC,ATPVA,ATP10C","biotype":"protein_coding","ncbi_id":"57194","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene is maternally expressed. It maps within the most common interval of deletion responsible for Angelman syndrome, also known as 'happy puppet syndrome'. [provided by RefSeq, Jul 2008]","start":25677273,"end":25865172,"strand":-1,"description":"ATPase phospholipid transporting 10A (putative) [Source:HGNC Symbol;Acc:HGNC:13542]"}, {"versioned_ensembl_gene_id":"ENSG00000110046.12","gene_symbol":"ATG2A","gene_name":"autophagy related 2A [Source:HGNC Symbol;Acc:HGNC:29028]","synonyms":"KIAA0404","biotype":"protein_coding","ncbi_id":"23130","summary":null,"start":64894546,"end":64917248,"strand":-1,"description":"autophagy related 2A [Source:HGNC Symbol;Acc:HGNC:29028]"}, {"versioned_ensembl_gene_id":"ENSG00000164074.14","gene_symbol":"ABHD18","gene_name":"abhydrolase domain containing 18 [Source:HGNC Symbol;Acc:HGNC:26111]","synonyms":"FLJ21106,C4orf29","biotype":"protein_coding","ncbi_id":"80167","summary":null,"start":127965306,"end":128039711,"strand":1,"description":"abhydrolase domain containing 18 [Source:HGNC Symbol;Acc:HGNC:26111]"}, {"versioned_ensembl_gene_id":"ENSG00000230710.1","gene_symbol":"LINC00332","gene_name":"long intergenic non-protein coding RNA 332 [Source:HGNC Symbol;Acc:HGNC:42049]","synonyms":"NCRNA00332","biotype":"lincRNA","ncbi_id":"100874127","summary":null,"start":40181809,"end":40189028,"strand":1,"description":"long intergenic non-protein coding RNA 332 [Source:HGNC Symbol;Acc:HGNC:42049]"}, {"versioned_ensembl_gene_id":"ENSG00000165410.14","gene_symbol":"CFL2","gene_name":"cofilin 2 [Source:HGNC Symbol;Acc:HGNC:1875]","synonyms":"NEM7","biotype":"protein_coding","ncbi_id":"1073","summary":"This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. This protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH-dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":34706769,"end":34714823,"strand":-1,"description":"cofilin 2 [Source:HGNC Symbol;Acc:HGNC:1875]"}, {"versioned_ensembl_gene_id":"ENSG00000229456.1","gene_symbol":"RLIMP1","gene_name":"ring finger protein, LIM domain interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39682]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533695","summary":null,"start":40618738,"end":40621348,"strand":1,"description":"ring finger protein, LIM domain interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39682]"}, {"versioned_ensembl_gene_id":"ENSG00000227791.3","gene_symbol":"AC007365.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64665607,"end":64666064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280332.1","gene_symbol":"AC020917.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16356329,"end":16358327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143502.14","gene_symbol":"SUSD4","gene_name":"sushi domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25470]","synonyms":"FLJ10052","biotype":"protein_coding","ncbi_id":"55061","summary":null,"start":223220819,"end":223364202,"strand":-1,"description":"sushi domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25470]"}, {"versioned_ensembl_gene_id":"ENSG00000179833.4","gene_symbol":"SERTAD2","gene_name":"SERTA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30784]","synonyms":"TRIP-Br2,Sei-2,KIAA0127","biotype":"protein_coding","ncbi_id":"9792","summary":null,"start":64631621,"end":64751005,"strand":-1,"description":"SERTA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30784]"}, {"versioned_ensembl_gene_id":"ENSG00000253985.1","gene_symbol":"AC145141.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71372676,"end":71374898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249981.1","gene_symbol":"AC145141.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71445616,"end":71446569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225048.1","gene_symbol":"CR759835.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026690,"end":29027617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127527.13","gene_symbol":"EPS15L1","gene_name":"epidermal growth factor receptor pathway substrate 15 like 1 [Source:HGNC Symbol;Acc:HGNC:24634]","synonyms":"eps15R","biotype":"protein_coding","ncbi_id":"58513","summary":null,"start":16355239,"end":16472085,"strand":-1,"description":"epidermal growth factor receptor pathway substrate 15 like 1 [Source:HGNC Symbol;Acc:HGNC:24634]"}, {"versioned_ensembl_gene_id":"ENSG00000250387.2","gene_symbol":"LINC02197","gene_name":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724392","summary":null,"start":71351855,"end":71446342,"strand":-1,"description":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]"}, {"versioned_ensembl_gene_id":"ENSG00000260172.1","gene_symbol":"LINC01413","gene_name":"long intergenic non-protein coding RNA 1413 [Source:HGNC Symbol;Acc:HGNC:50705]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928611","summary":null,"start":57319138,"end":57323908,"strand":1,"description":"long intergenic non-protein coding RNA 1413 [Source:HGNC Symbol;Acc:HGNC:50705]"}, {"versioned_ensembl_gene_id":"ENSG00000280670.2","gene_symbol":"CCDC163","gene_name":"coiled-coil domain containing 163 [Source:HGNC Symbol;Acc:HGNC:27003]","synonyms":"LOC126661,CCDC163P,C1orf231","biotype":"protein_coding","ncbi_id":"126661","summary":null,"start":45493866,"end":45500079,"strand":-1,"description":"coiled-coil domain containing 163 [Source:HGNC Symbol;Acc:HGNC:27003]"}, {"versioned_ensembl_gene_id":"ENSG00000224272.2","gene_symbol":"AC131097.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241808312,"end":241812016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226756.1","gene_symbol":"AC007365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64644612,"end":64646698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152086.8","gene_symbol":"TUBA3E","gene_name":"tubulin alpha 3e [Source:HGNC Symbol;Acc:HGNC:20765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"112714","summary":"Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulin. The genes encoding these microtubule constituents are part of the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. This gene encodes an alpha tubulin that highly conserved among species. A missense mutation in this gene has been potentially linked to microlissencephaly and global developmental delay. [provided by RefSeq, Jul 2016]","start":130191743,"end":130198461,"strand":-1,"description":"tubulin alpha 3e [Source:HGNC Symbol;Acc:HGNC:20765]"}, {"versioned_ensembl_gene_id":"ENSG00000161011.19","gene_symbol":"SQSTM1","gene_name":"sequestosome 1 [Source:HGNC Symbol;Acc:HGNC:11280]","synonyms":"PDB3,p62B,p62,p60,OSIL,A170","biotype":"protein_coding","ncbi_id":"8878","summary":"This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq, Mar 2009]","start":179806398,"end":179838078,"strand":1,"description":"sequestosome 1 [Source:HGNC Symbol;Acc:HGNC:11280]"}, {"versioned_ensembl_gene_id":"ENSG00000260870.1","gene_symbol":"NDUFB10P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52272]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128711","summary":null,"start":57325472,"end":57326447,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52272]"}, {"versioned_ensembl_gene_id":"ENSG00000262497.1","gene_symbol":"FAM187B2P","gene_name":"family with sequence similarity 187 member B2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49213]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421621","summary":null,"start":35232291,"end":35233003,"strand":-1,"description":"family with sequence similarity 187 member B2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49213]"}, {"versioned_ensembl_gene_id":"ENSG00000237089.2","gene_symbol":"PCNPP4","gene_name":"PEST containing nuclear protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874220","summary":null,"start":75537547,"end":75538702,"strand":-1,"description":"PEST containing nuclear protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41976]"}, {"versioned_ensembl_gene_id":"ENSG00000273113.1","gene_symbol":"AC133528.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":241581922,"end":241582726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215023.2","gene_symbol":"AC131097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241800916,"end":241801907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224775.2","gene_symbol":"BRAFP1","gene_name":"BRAF pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18615]","synonyms":"BRAFPS2,BRAF2","biotype":"unprocessed_pseudogene","ncbi_id":"286494","summary":null,"start":75582676,"end":75585506,"strand":1,"description":"BRAF pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18615]"}, {"versioned_ensembl_gene_id":"ENSG00000204099.11","gene_symbol":"NEU4","gene_name":"neuraminidase 4 [Source:HGNC Symbol;Acc:HGNC:21328]","synonyms":null,"biotype":"protein_coding","ncbi_id":"129807","summary":"The protein encoded by this gene belongs to a family of glycohydrolytic enzymes, which remove terminal sialic acid residues from various sialo derivatives, such as glycoproteins, glycolipids, oligosaccharides, and gangliosides. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2009]","start":241808825,"end":241817413,"strand":1,"description":"neuraminidase 4 [Source:HGNC Symbol;Acc:HGNC:21328]"}, {"versioned_ensembl_gene_id":"ENSG00000170324.20","gene_symbol":"FRMPD2","gene_name":"FERM and PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28572]","synonyms":"PDZK5C,PDZD5C,MGC35285","biotype":"protein_coding","ncbi_id":"143162","summary":"This gene encodes a peripheral membrane protein and is located in a region of chromosome 10q that contains a segmental duplication. This copy of the gene is full-length and is in the telomeric duplicated region. Two other more centromerically proximal copies of the gene are partial and may represent pseudogenes. This full-length gene appears to function in the establishment and maintenance of cell polarization. The protein is recruited to cell-cell junctions in an E-cadherin-dependent manner, and is selectively localized at the basolateral membrane in polarized epithelial cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2009]","start":48153088,"end":48274870,"strand":-1,"description":"FERM and PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28572]"}, {"versioned_ensembl_gene_id":"ENSG00000235645.2","gene_symbol":"AL450311.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69684899,"end":69692452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186082.9","gene_symbol":"KRT18P14","gene_name":"keratin 18 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:6433]","synonyms":"KRT18L4","biotype":"processed_pseudogene","ncbi_id":"119722","summary":null,"start":35860249,"end":35861498,"strand":-1,"description":"keratin 18 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:6433]"}, {"versioned_ensembl_gene_id":"ENSG00000254919.1","gene_symbol":"AC090692.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35915051,"end":35918739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250928.1","gene_symbol":"AC008629.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119011471,"end":119012056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261678.2","gene_symbol":"SCRT1","gene_name":"scratch family transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:15950]","synonyms":"ZNF898,DKFZp547F072","biotype":"protein_coding","ncbi_id":"83482","summary":"This gene encodes a C2H2-type zinc finger transcriptional repressor that binds to E-box motifs. The encoded protein may promote neural differention and may be involved in cancers with neuroendocrine features. [provided by RefSeq, Jul 2013]","start":144330565,"end":144336281,"strand":-1,"description":"scratch family transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:15950]"}, {"versioned_ensembl_gene_id":"ENSG00000135722.8","gene_symbol":"FBXL8","gene_name":"F-box and leucine rich repeat protein 8 [Source:HGNC Symbol;Acc:HGNC:17875]","synonyms":"Fbl8","biotype":"protein_coding","ncbi_id":"55336","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class. It shares 78% sequence identity with the mouse protein. [provided by RefSeq, Jul 2008]","start":67159931,"end":67164570,"strand":1,"description":"F-box and leucine rich repeat protein 8 [Source:HGNC Symbol;Acc:HGNC:17875]"}, {"versioned_ensembl_gene_id":"ENSG00000250678.1","gene_symbol":"AC008629.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119010060,"end":119010542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248979.2","gene_symbol":"LAMTOR3P2","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39727]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874516","summary":null,"start":119132651,"end":119132882,"strand":-1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39727]"}, {"versioned_ensembl_gene_id":"ENSG00000230469.1","gene_symbol":"RPL5P26","gene_name":"ribosomal protein L5 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36247]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271206","summary":null,"start":69778962,"end":69779838,"strand":1,"description":"ribosomal protein L5 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36247]"}, {"versioned_ensembl_gene_id":"ENSG00000226194.5","gene_symbol":"LINC02519","gene_name":"long intergenic non-protein coding RNA 2519 [Source:HGNC Symbol;Acc:HGNC:53510]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378147","summary":null,"start":169369998,"end":169388385,"strand":-1,"description":"long intergenic non-protein coding RNA 2519 [Source:HGNC Symbol;Acc:HGNC:53510]"}, {"versioned_ensembl_gene_id":"ENSG00000196275.13","gene_symbol":"GTF2IRD2","gene_name":"GTF2I repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30775]","synonyms":"GTF2IRD2A,FLJ37938","biotype":"protein_coding","ncbi_id":"84163","summary":"This gene is one of several closely related genes on chromosome 7 encoding proteins containing helix-loop-helix motifs. These proteins may function as regulators of transcription. The encoded protein is unique in that its C-terminus is derived from CHARLIE8 transposable element sequence. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, and loss of this locus may contribute to the cognitive phenotypes observed in this disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":74796144,"end":74851551,"strand":-1,"description":"GTF2I repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30775]"}, {"versioned_ensembl_gene_id":"ENSG00000230756.1","gene_symbol":"RHOQP3","gene_name":"ras homolog family member Q pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37837]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284988","summary":null,"start":130212870,"end":130213490,"strand":-1,"description":"ras homolog family member Q pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37837]"}, {"versioned_ensembl_gene_id":"ENSG00000274423.1","gene_symbol":"AC242843.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149345661,"end":149357612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213225.7","gene_symbol":"NOC2LP1","gene_name":"NOC2 like nucleolar associated transcriptional repressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52285]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"643276","summary":null,"start":130229379,"end":130232106,"strand":1,"description":"NOC2 like nucleolar associated transcriptional repressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52285]"}, {"versioned_ensembl_gene_id":"ENSG00000140396.12","gene_symbol":"NCOA2","gene_name":"nuclear receptor coactivator 2 [Source:HGNC Symbol;Acc:HGNC:7669]","synonyms":"TIF2,NCoA-2,KAT13C,GRIP1,bHLHe75","biotype":"protein_coding","ncbi_id":"10499","summary":"The protein encoded by this gene functions as a transcriptional coactivator for nuclear hormone receptors, including steroid, thyroid, retinoid, and vitamin D receptors. The encoded protein acts as an intermediary factor for the ligand-dependent activity of these nuclear receptors, which regulate their target genes upon binding of cognate response elements. This gene has been found to be involved in translocations that result in fusions with other genes in various cancers, including the lysine acetyltransferase 6A (KAT6A) gene in acute myeloid leukemia, the ETS variant 6 (ETV6) gene in acute lymphoblastic leukemia, and the hes related family bHLH transcription factor with YRPW motif 1 (HEY1) gene in mesenchymal chondrosarcoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":70109762,"end":70403805,"strand":-1,"description":"nuclear receptor coactivator 2 [Source:HGNC Symbol;Acc:HGNC:7669]"}, {"versioned_ensembl_gene_id":"ENSG00000225415.2","gene_symbol":"CCRL1P1","gene_name":"C-C motif chemokine receptor like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21142]","synonyms":"dJ509I19.4,CCRL1P","biotype":"processed_pseudogene","ncbi_id":"285737","summary":null,"start":138822747,"end":138823799,"strand":1,"description":"C-C motif chemokine receptor like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21142]"}, {"versioned_ensembl_gene_id":"ENSG00000253197.5","gene_symbol":"AC117834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92882984,"end":92965645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273819.1","gene_symbol":"ENPP7P7","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48690]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421859","summary":null,"start":67812557,"end":67873367,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48690]"}, {"versioned_ensembl_gene_id":"ENSG00000251347.2","gene_symbol":"IRF5P1","gene_name":"interferon regulatory factor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41981]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420406","summary":null,"start":92972575,"end":92974738,"strand":1,"description":"interferon regulatory factor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41981]"}, {"versioned_ensembl_gene_id":"ENSG00000254792.1","gene_symbol":"AP003716.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67840942,"end":67841049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276377.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22431917,"end":22432206,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199683.1","gene_symbol":"RN7SKP185","gene_name":"RNA, 7SK small nuclear pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:45909]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479178","summary":null,"start":37975156,"end":37975481,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:45909]"}, {"versioned_ensembl_gene_id":"ENSG00000239129.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29883006,"end":29883109,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000252594.1","gene_symbol":"RNU6-656P","gene_name":"RNA, U6 small nuclear 656, pseudogene [Source:HGNC Symbol;Acc:HGNC:47619]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479857","summary":null,"start":46831050,"end":46831156,"strand":1,"description":"RNA, U6 small nuclear 656, pseudogene [Source:HGNC Symbol;Acc:HGNC:47619]"}, {"versioned_ensembl_gene_id":"ENSG00000274359.1","gene_symbol":"AC012314.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221633.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":109018909,"end":109019116,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000276134.1","gene_symbol":"RN7SKP117","gene_name":"RNA, 7SK small nuclear pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:45841]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479147","summary":null,"start":125350868,"end":125351131,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:45841]"}, {"versioned_ensembl_gene_id":"ENSG00000202537.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":86347062,"end":86347195,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000207433.1","gene_symbol":"RNU6-246P","gene_name":"RNA, U6 small nuclear 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:47209]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481884","summary":null,"start":15544188,"end":15544294,"strand":1,"description":"RNA, U6 small nuclear 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:47209]"}, {"versioned_ensembl_gene_id":"ENSG00000199536.1","gene_symbol":"RNU6-315P","gene_name":"RNA, U6 small nuclear 315, pseudogene [Source:HGNC Symbol;Acc:HGNC:47278]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479707","summary":null,"start":170149845,"end":170149951,"strand":1,"description":"RNA, U6 small nuclear 315, pseudogene [Source:HGNC Symbol;Acc:HGNC:47278]"}, {"versioned_ensembl_gene_id":"ENSG00000202193.1","gene_symbol":"RNA5SP427","gene_name":"RNA, 5S ribosomal pseudogene 427 [Source:HGNC Symbol;Acc:HGNC:43327]","synonyms":"RN5S427","biotype":"rRNA","ncbi_id":"100873678","summary":null,"start":53337453,"end":53337571,"strand":1,"description":"RNA, 5S ribosomal pseudogene 427 [Source:HGNC Symbol;Acc:HGNC:43327]"}, {"versioned_ensembl_gene_id":"ENSG00000278773.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30061080,"end":30061183,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000202177.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101955077,"end":101955185,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207245.1","gene_symbol":"SNORD116-29","gene_name":"small nucleolar RNA, C/D box 116-29 [Source:HGNC Symbol;Acc:HGNC:33348]","synonyms":"HBII-85-29","biotype":"snoRNA","ncbi_id":"100033821","summary":null,"start":25106521,"end":25106603,"strand":1,"description":"small nucleolar RNA, C/D box 116-29 [Source:HGNC Symbol;Acc:HGNC:33348]"}, {"versioned_ensembl_gene_id":"ENSG00000280549.1","gene_symbol":"PADI3","gene_name":"peptidyl arginine deiminase 3 [Source:HGNC Symbol;Acc:HGNC:18337]","synonyms":"PDI3","biotype":"protein_coding","ncbi_id":"51702","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type III enzyme modulates hair structural proteins, such as filaggrin in the hair follicle and trichohyalin in the inner root sheath, during hair follicle formation. Together with the type I enzyme, this enzyme may also play a role in terminal differentiation of the epidermis. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]","start":17249098,"end":17284233,"strand":1,"description":"peptidyl arginine deiminase 3 [Source:HGNC Symbol;Acc:HGNC:18337]"}, {"versioned_ensembl_gene_id":"ENSG00000252714.1","gene_symbol":"RNA5SP392","gene_name":"RNA, 5S ribosomal pseudogene 392 [Source:HGNC Symbol;Acc:HGNC:43292]","synonyms":"RN5S392","biotype":"rRNA","ncbi_id":"100873645","summary":null,"start":40331537,"end":40331648,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 392 [Source:HGNC Symbol;Acc:HGNC:43292]"}, {"versioned_ensembl_gene_id":"ENSG00000263597.1","gene_symbol":"MIR3936","gene_name":"microRNA 3936 [Source:HGNC Symbol;Acc:HGNC:38947]","synonyms":"hsa-mir-3936","biotype":"miRNA","ncbi_id":"100500865","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132365490,"end":132365599,"strand":-1,"description":"microRNA 3936 [Source:HGNC Symbol;Acc:HGNC:38947]"}, {"versioned_ensembl_gene_id":"ENSG00000222094.1","gene_symbol":"RNU2-65P","gene_name":"RNA, U2 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:48558]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480226","summary":null,"start":72045183,"end":72045367,"strand":1,"description":"RNA, U2 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:48558]"}, {"versioned_ensembl_gene_id":"ENSG00000200626.1","gene_symbol":"RNA5SP325","gene_name":"RNA, 5S ribosomal pseudogene 325 [Source:HGNC Symbol;Acc:HGNC:43225]","synonyms":"RN5S325","biotype":"rRNA","ncbi_id":"100873591","summary":null,"start":106970021,"end":106970150,"strand":1,"description":"RNA, 5S ribosomal pseudogene 325 [Source:HGNC Symbol;Acc:HGNC:43225]"}, {"versioned_ensembl_gene_id":"ENSG00000202495.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50171197,"end":50171297,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212136.1","gene_symbol":"RNU6-696P","gene_name":"RNA, U6 small nuclear 696, pseudogene [Source:HGNC Symbol;Acc:HGNC:47659]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479873","summary":null,"start":37045530,"end":37045636,"strand":1,"description":"RNA, U6 small nuclear 696, pseudogene [Source:HGNC Symbol;Acc:HGNC:47659]"}, {"versioned_ensembl_gene_id":"ENSG00000222940.1","gene_symbol":"RNU6-370P","gene_name":"RNA, U6 small nuclear 370, pseudogene [Source:HGNC Symbol;Acc:HGNC:47333]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481295","summary":null,"start":24045835,"end":24045938,"strand":1,"description":"RNA, U6 small nuclear 370, pseudogene [Source:HGNC Symbol;Acc:HGNC:47333]"}, {"versioned_ensembl_gene_id":"ENSG00000264788.1","gene_symbol":"MIR3148","gene_name":"microRNA 3148 [Source:HGNC Symbol;Acc:HGNC:38215]","synonyms":"hsa-mir-3148","biotype":"miRNA","ncbi_id":"100422876","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29957272,"end":29957348,"strand":-1,"description":"microRNA 3148 [Source:HGNC Symbol;Acc:HGNC:38215]"}, {"versioned_ensembl_gene_id":"ENSG00000252637.1","gene_symbol":"RNA5SP268","gene_name":"RNA, 5S ribosomal pseudogene 268 [Source:HGNC Symbol;Acc:HGNC:43168]","synonyms":"RN5S268","biotype":"rRNA","ncbi_id":"100873521","summary":null,"start":67099302,"end":67099425,"strand":1,"description":"RNA, 5S ribosomal pseudogene 268 [Source:HGNC Symbol;Acc:HGNC:43168]"}, {"versioned_ensembl_gene_id":"ENSG00000283792.1","gene_symbol":"MIR4453","gene_name":"microRNA 4453 [Source:HGNC Symbol;Acc:HGNC:41892]","synonyms":"hsa-mir-4453","biotype":"miRNA","ncbi_id":"100616193","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":152536428,"end":152536516,"strand":1,"description":"microRNA 4453 [Source:HGNC Symbol;Acc:HGNC:41892]"}, {"versioned_ensembl_gene_id":"ENSG00000199673.1","gene_symbol":"SNORD16","gene_name":"small nucleolar RNA, C/D box 16 [Source:HGNC Symbol;Acc:HGNC:32712]","synonyms":"U16","biotype":"snoRNA","ncbi_id":"595097","summary":null,"start":66502812,"end":66502910,"strand":-1,"description":"small nucleolar RNA, C/D box 16 [Source:HGNC Symbol;Acc:HGNC:32712]"}, {"versioned_ensembl_gene_id":"ENSG00000207274.1","gene_symbol":"SNORA70I","gene_name":"small nucleolar RNA, H/ACA box 70I [Source:HGNC Symbol;Acc:HGNC:52215]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617008","summary":null,"start":214846947,"end":214847081,"strand":1,"description":"small nucleolar RNA, H/ACA box 70I [Source:HGNC Symbol;Acc:HGNC:52215]"}, {"versioned_ensembl_gene_id":"ENSG00000277999.1","gene_symbol":"AC009093.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29272220,"end":29272772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238242.1","gene_symbol":"AC097066.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60114875,"end":60149679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222854.1","gene_symbol":"RNA5SP59","gene_name":"RNA, 5S ribosomal pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:42836]","synonyms":"RN5S59","biotype":"rRNA","ncbi_id":"106480357","summary":null,"start":144701050,"end":144701159,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:42836]"}, {"versioned_ensembl_gene_id":"ENSG00000276031.1","gene_symbol":"RN7SL197P","gene_name":"RNA, 7SL, cytoplasmic 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:46213]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480975","summary":null,"start":49721949,"end":49722247,"strand":1,"description":"RNA, 7SL, cytoplasmic 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:46213]"}, {"versioned_ensembl_gene_id":"ENSG00000274062.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43284139,"end":43284329,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000238387.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":9578028,"end":9578131,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000266515.1","gene_symbol":"MIR4452","gene_name":"microRNA 4452 [Source:HGNC Symbol;Acc:HGNC:41539]","synonyms":"hsa-mir-4452","biotype":"miRNA","ncbi_id":"100616463","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86542482,"end":86542552,"strand":-1,"description":"microRNA 4452 [Source:HGNC Symbol;Acc:HGNC:41539]"}, {"versioned_ensembl_gene_id":"ENSG00000273882.1","gene_symbol":"MIR8066","gene_name":"microRNA 8066 [Source:HGNC Symbol;Acc:HGNC:50043]","synonyms":"hsa-mir-8066","biotype":"miRNA","ncbi_id":"102465868","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101240795,"end":101240872,"strand":-1,"description":"microRNA 8066 [Source:HGNC Symbol;Acc:HGNC:50043]"}, {"versioned_ensembl_gene_id":"ENSG00000276700.1","gene_symbol":"RNA5-8S5","gene_name":"RNA, 5.8S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:37660]","synonyms":"RN5-8S1","biotype":"rRNA","ncbi_id":"110255170","summary":null,"start":128877,"end":129029,"strand":1,"description":"RNA, 5.8S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:37660]"}, {"versioned_ensembl_gene_id":"ENSG00000239249.3","gene_symbol":"RN7SL757P","gene_name":"RNA, 7SL, cytoplasmic 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:46773]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480530","summary":null,"start":28056153,"end":28056453,"strand":-1,"description":"RNA, 7SL, cytoplasmic 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:46773]"}, {"versioned_ensembl_gene_id":"ENSG00000201363.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44344839,"end":44344933,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199732.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96309221,"end":96309322,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207281.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40339059,"end":40339164,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263367.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31127920,"end":31128019,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207552.1","gene_symbol":"MIR633","gene_name":"microRNA 633 [Source:HGNC Symbol;Acc:HGNC:32889]","synonyms":"MIRN633,hsa-mir-633","biotype":"miRNA","ncbi_id":"693218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62944215,"end":62944312,"strand":1,"description":"microRNA 633 [Source:HGNC Symbol;Acc:HGNC:32889]"}, {"versioned_ensembl_gene_id":"ENSG00000278055.1","gene_symbol":"MESTIT1_2","gene_name":"MEST intronic transcript 1, antisense RNA conserved region 2 [Source:RFAM;Acc:RF02149]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130488304,"end":130488538,"strand":1,"description":"MEST intronic transcript 1, antisense RNA conserved region 2 [Source:RFAM;Acc:RF02149]"}, {"versioned_ensembl_gene_id":"ENSG00000201176.1","gene_symbol":"RNU6-853P","gene_name":"RNA, U6 small nuclear 853, pseudogene [Source:HGNC Symbol;Acc:HGNC:47816]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479943","summary":null,"start":168885355,"end":168885461,"strand":1,"description":"RNA, U6 small nuclear 853, pseudogene [Source:HGNC Symbol;Acc:HGNC:47816]"}, {"versioned_ensembl_gene_id":"ENSG00000202092.1","gene_symbol":"RNA5SP190","gene_name":"RNA, 5S ribosomal pseudogene 190 [Source:HGNC Symbol;Acc:HGNC:43090]","synonyms":"RN5S190","biotype":"rRNA","ncbi_id":"100873452","summary":null,"start":119445716,"end":119445833,"strand":1,"description":"RNA, 5S ribosomal pseudogene 190 [Source:HGNC Symbol;Acc:HGNC:43090]"}, {"versioned_ensembl_gene_id":"ENSG00000281311.1","gene_symbol":"SNORA50","gene_name":"Small nucleolar RNA SNORA50 [Source:RFAM;Acc:RF00407]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":64146337,"end":64146471,"strand":1,"description":"Small nucleolar RNA SNORA50 [Source:RFAM;Acc:RF00407]"}, {"versioned_ensembl_gene_id":"ENSG00000200227.1","gene_symbol":"RNA5SP197","gene_name":"RNA, 5S ribosomal pseudogene 197 [Source:HGNC Symbol;Acc:HGNC:43097]","synonyms":"RN5S197","biotype":"rRNA","ncbi_id":"100873459","summary":null,"start":151477459,"end":151477577,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 197 [Source:HGNC Symbol;Acc:HGNC:43097]"}, {"versioned_ensembl_gene_id":"ENSG00000222659.1","gene_symbol":"RNU2-8P","gene_name":"RNA, U2 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48501]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480200","summary":null,"start":121580332,"end":121580521,"strand":-1,"description":"RNA, U2 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48501]"}, {"versioned_ensembl_gene_id":"ENSG00000238908.1","gene_symbol":"RNA5SP484","gene_name":"RNA, 5S ribosomal pseudogene 484 [Source:HGNC Symbol;Acc:HGNC:43384]","synonyms":"RN5S484","biotype":"rRNA","ncbi_id":"100873726","summary":null,"start":40854119,"end":40854229,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 484 [Source:HGNC Symbol;Acc:HGNC:43384]"}, {"versioned_ensembl_gene_id":"ENSG00000276132.1","gene_symbol":"snoZ278","gene_name":"Small nucleolar RNA Z278 [Source:RFAM;Acc:RF00201]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29375114,"end":29375225,"strand":1,"description":"Small nucleolar RNA Z278 [Source:RFAM;Acc:RF00201]"}, {"versioned_ensembl_gene_id":"ENSG00000212269.1","gene_symbol":"RNU6-788P","gene_name":"RNA, U6 small nuclear 788, pseudogene [Source:HGNC Symbol;Acc:HGNC:47751]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480609","summary":null,"start":23641489,"end":23641592,"strand":-1,"description":"RNA, U6 small nuclear 788, pseudogene [Source:HGNC Symbol;Acc:HGNC:47751]"}, {"versioned_ensembl_gene_id":"ENSG00000276055.1","gene_symbol":"CLRN1-AS1","gene_name":"CLRN1 antisense RNA 1 conserved region [Source:RFAM;Acc:RF02089]","synonyms":"UCRP,CLRN1OS","biotype":"misc_RNA","ncbi_id":"116933","summary":null,"start":151079506,"end":151079584,"strand":1,"description":"CLRN1 antisense RNA 1 conserved region [Source:RFAM;Acc:RF02089]"}, {"versioned_ensembl_gene_id":"ENSG00000201737.1","gene_symbol":"RNU1-133P","gene_name":"RNA, U1 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48475]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481631","summary":null,"start":200775584,"end":200775750,"strand":1,"description":"RNA, U1 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48475]"}, {"versioned_ensembl_gene_id":"ENSG00000263600.1","gene_symbol":"MIR3915","gene_name":"microRNA 3915 [Source:HGNC Symbol;Acc:HGNC:38955]","synonyms":"hsa-mir-3915","biotype":"miRNA","ncbi_id":"100500915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32583656,"end":32583752,"strand":-1,"description":"microRNA 3915 [Source:HGNC Symbol;Acc:HGNC:38955]"}, {"versioned_ensembl_gene_id":"ENSG00000263861.1","gene_symbol":"MIR3927","gene_name":"microRNA 3927 [Source:HGNC Symbol;Acc:HGNC:38901]","synonyms":"hsa-mir-3927","biotype":"miRNA","ncbi_id":"100500898","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109511475,"end":109511545,"strand":-1,"description":"microRNA 3927 [Source:HGNC Symbol;Acc:HGNC:38901]"}, {"versioned_ensembl_gene_id":"ENSG00000265942.2","gene_symbol":"RN7SL577P","gene_name":"RNA, 7SL, cytoplasmic 577, pseudogene [Source:HGNC Symbol;Acc:HGNC:46593]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481080","summary":null,"start":49042341,"end":49042643,"strand":-1,"description":"RNA, 7SL, cytoplasmic 577, pseudogene [Source:HGNC Symbol;Acc:HGNC:46593]"}, {"versioned_ensembl_gene_id":"ENSG00000265507.1","gene_symbol":"MIR4435-1","gene_name":"microRNA 4435-1 [Source:HGNC Symbol;Acc:HGNC:41713]","synonyms":"hsa-mir-4435-1","biotype":"miRNA","ncbi_id":"100616499","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87629755,"end":87629834,"strand":1,"description":"microRNA 4435-1 [Source:HGNC Symbol;Acc:HGNC:41713]"}, {"versioned_ensembl_gene_id":"ENSG00000199912.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7800361,"end":7800467,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211591.1","gene_symbol":"MIR762","gene_name":"microRNA 762 [Source:HGNC Symbol;Acc:HGNC:37303]","synonyms":"hsa-mir-762","biotype":"miRNA","ncbi_id":"100313837","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30893903,"end":30893985,"strand":1,"description":"microRNA 762 [Source:HGNC Symbol;Acc:HGNC:37303]"}, {"versioned_ensembl_gene_id":"ENSG00000263581.1","gene_symbol":"MIR548X2","gene_name":"microRNA 548x-2 [Source:HGNC Symbol;Acc:HGNC:41734]","synonyms":"hsa-mir-548x-2","biotype":"miRNA","ncbi_id":"100616302","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65966330,"end":65966429,"strand":-1,"description":"microRNA 548x-2 [Source:HGNC Symbol;Acc:HGNC:41734]"}, {"versioned_ensembl_gene_id":"ENSG00000281434.2","gene_symbol":"NDUFA10","gene_name":"NADH:ubiquinone oxidoreductase subunit A10 [Source:HGNC Symbol;Acc:HGNC:7684]","synonyms":"CI-42k","biotype":"protein_coding","ncbi_id":"4705","summary":"The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016]","start":239892456,"end":240025408,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A10 [Source:HGNC Symbol;Acc:HGNC:7684]"}, {"versioned_ensembl_gene_id":"ENSG00000200829.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20480844,"end":20480955,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222790.1","gene_symbol":"RNU4-14P","gene_name":"RNA, U4 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46950]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481176","summary":null,"start":140397323,"end":140397444,"strand":-1,"description":"RNA, U4 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46950]"}, {"versioned_ensembl_gene_id":"ENSG00000200975.1","gene_symbol":"RNU1-7P","gene_name":"RNA, U1 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:48306]","synonyms":"RNU1-7","biotype":"snRNA","ncbi_id":"106481952","summary":null,"start":8206434,"end":8206597,"strand":-1,"description":"RNA, U1 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:48306]"}, {"versioned_ensembl_gene_id":"ENSG00000212382.1","gene_symbol":"RNU6-159P","gene_name":"RNA, U6 small nuclear 159, pseudogene [Source:HGNC Symbol;Acc:HGNC:47122]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480557","summary":null,"start":27863251,"end":27863356,"strand":1,"description":"RNA, U6 small nuclear 159, pseudogene [Source:HGNC Symbol;Acc:HGNC:47122]"}, {"versioned_ensembl_gene_id":"ENSG00000251823.2","gene_symbol":"RNA5SP162","gene_name":"RNA, 5S ribosomal pseudogene 162 [Source:HGNC Symbol;Acc:HGNC:43062]","synonyms":"RN5S162","biotype":"rRNA","ncbi_id":"100873427","summary":null,"start":228558296,"end":228558339,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 162 [Source:HGNC Symbol;Acc:HGNC:43062]"}, {"versioned_ensembl_gene_id":"ENSG00000284035.1","gene_symbol":"MIR5187","gene_name":"microRNA 5187 [Source:HGNC Symbol;Acc:HGNC:43523]","synonyms":"hsa-mir-5187","biotype":"miRNA","ncbi_id":"100847090","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":161227186,"end":161227261,"strand":1,"description":"microRNA 5187 [Source:HGNC Symbol;Acc:HGNC:43523]"}, {"versioned_ensembl_gene_id":"ENSG00000212446.1","gene_symbol":"RNU6-131P","gene_name":"RNA, U6 small nuclear 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:47094]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479624","summary":null,"start":44135883,"end":44135989,"strand":-1,"description":"RNA, U6 small nuclear 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:47094]"}, {"versioned_ensembl_gene_id":"ENSG00000274589.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18538885,"end":18539189,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253602.2","gene_symbol":"RN7SL260P","gene_name":"RNA, 7SL, cytoplasmic 260, pseudogene [Source:HGNC Symbol;Acc:HGNC:46276]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480497","summary":null,"start":142247585,"end":142247866,"strand":-1,"description":"RNA, 7SL, cytoplasmic 260, pseudogene [Source:HGNC Symbol;Acc:HGNC:46276]"}, {"versioned_ensembl_gene_id":"ENSG00000200764.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":207687960,"end":207688059,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221300.1","gene_symbol":"SNORD75","gene_name":"Small nucleolar RNA SNORD75 [Source:RFAM;Acc:RF00612]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692195","summary":null,"start":42440377,"end":42440436,"strand":1,"description":"Small nucleolar RNA SNORD75 [Source:RFAM;Acc:RF00612]"}, {"versioned_ensembl_gene_id":"ENSG00000283499.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":48109353,"end":48109410,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000274500.1","gene_symbol":"MESTIT1_3","gene_name":"MEST intronic transcript 1, antisense RNA conserved region 3 [Source:RFAM;Acc:RF02150]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130489868,"end":130489966,"strand":1,"description":"MEST intronic transcript 1, antisense RNA conserved region 3 [Source:RFAM;Acc:RF02150]"}, {"versioned_ensembl_gene_id":"ENSG00000200756.1","gene_symbol":"RNU6-236P","gene_name":"RNA, U6 small nuclear 236, pseudogene [Source:HGNC Symbol;Acc:HGNC:47199]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481252","summary":null,"start":139717985,"end":139718090,"strand":-1,"description":"RNA, U6 small nuclear 236, pseudogene [Source:HGNC Symbol;Acc:HGNC:47199]"}, {"versioned_ensembl_gene_id":"ENSG00000202335.1","gene_symbol":"SNORD50","gene_name":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":110496352,"end":110496421,"strand":-1,"description":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]"}, {"versioned_ensembl_gene_id":"ENSG00000277660.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":90796,"end":90899,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000265558.1","gene_symbol":"MIR3918","gene_name":"microRNA 3918 [Source:HGNC Symbol;Acc:HGNC:38919]","synonyms":"hsa-mir-3918","biotype":"miRNA","ncbi_id":"100500851","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":158764661,"end":158764753,"strand":-1,"description":"microRNA 3918 [Source:HGNC Symbol;Acc:HGNC:38919]"}, {"versioned_ensembl_gene_id":"ENSG00000278049.1","gene_symbol":"ZNRD1-AS1_1","gene_name":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30031073,"end":30031140,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]"}, {"versioned_ensembl_gene_id":"ENSG00000251866.1","gene_symbol":"SCARNA21B","gene_name":"small Cajal body-specific RNA 21B [Source:HGNC Symbol;Acc:HGNC:52237]","synonyms":null,"biotype":"scaRNA","ncbi_id":"107397391","summary":null,"start":15542165,"end":15542304,"strand":1,"description":"small Cajal body-specific RNA 21B [Source:HGNC Symbol;Acc:HGNC:52237]"}, {"versioned_ensembl_gene_id":"ENSG00000266297.1","gene_symbol":"MIR744","gene_name":"microRNA 744 [Source:HGNC Symbol;Acc:HGNC:33658]","synonyms":"MIRN744,hsa-mir-744","biotype":"miRNA","ncbi_id":"100126313","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12081899,"end":12081996,"strand":1,"description":"microRNA 744 [Source:HGNC Symbol;Acc:HGNC:33658]"}, {"versioned_ensembl_gene_id":"ENSG00000207615.3","gene_symbol":"MIR515-2","gene_name":"microRNA 515-2 [Source:HGNC Symbol;Acc:HGNC:32097]","synonyms":"MIRN515-2,hsa-mir-515-2","biotype":"miRNA","ncbi_id":"574465","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53685009,"end":53685091,"strand":1,"description":"microRNA 515-2 [Source:HGNC Symbol;Acc:HGNC:32097]"}, {"versioned_ensembl_gene_id":"ENSG00000222419.1","gene_symbol":"RNA5SP511","gene_name":"RNA, 5S ribosomal pseudogene 511 [Source:HGNC Symbol;Acc:HGNC:43411]","synonyms":"RN5S511","biotype":"rRNA","ncbi_id":"100873562","summary":null,"start":103850797,"end":103850911,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 511 [Source:HGNC Symbol;Acc:HGNC:43411]"}, {"versioned_ensembl_gene_id":"ENSG00000244642.3","gene_symbol":"RN7SL396P","gene_name":"RNA, 7SL, cytoplasmic 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:46412]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479368","summary":null,"start":119862662,"end":119862956,"strand":1,"description":"RNA, 7SL, cytoplasmic 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:46412]"}, {"versioned_ensembl_gene_id":"ENSG00000207383.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":112579484,"end":112579584,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000231756.1","gene_symbol":"AL449983.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16473188,"end":16476237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283813.1","gene_symbol":"MIR4485","gene_name":"microRNA 4485 [Source:HGNC Symbol;Acc:HGNC:41628]","synonyms":"hsa-mir-4485","biotype":"miRNA","ncbi_id":"100616263","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10508270,"end":10508326,"strand":-1,"description":"microRNA 4485 [Source:HGNC Symbol;Acc:HGNC:41628]"}, {"versioned_ensembl_gene_id":"ENSG00000199701.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":94713715,"end":94713812,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222701.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30471587,"end":30471703,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251858.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":41594463,"end":41594591,"strand":1,"description":"Small nucleolar RNA 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Symbol;Acc:HGNC:23412]","synonyms":"LCN1L1,bA430N14.2","biotype":"unprocessed_pseudogene","ncbi_id":"286310","summary":null,"start":133224905,"end":133228591,"strand":-1,"description":"lipocalin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23412]"}, {"versioned_ensembl_gene_id":"ENSG00000241834.3","gene_symbol":"RN7SL149P","gene_name":"RNA, 7SL, cytoplasmic 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:46165]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480961","summary":null,"start":41840059,"end":41840339,"strand":-1,"description":"RNA, 7SL, cytoplasmic 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:46165]"}, {"versioned_ensembl_gene_id":"ENSG00000201984.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29139283,"end":29139384,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242985.3","gene_symbol":"RN7SL50P","gene_name":"RNA, 7SL, 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{"versioned_ensembl_gene_id":"ENSG00000284357.1","gene_symbol":"MIR34A","gene_name":"microRNA 34a [Source:HGNC Symbol;Acc:HGNC:31635]","synonyms":"MIRN34A,hsa-mir-34a","biotype":"miRNA","ncbi_id":"407040","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. This miRNA is a member of the highly conserved miR-34 family. This miRNA functions as a tumor suppressor and dysregulation or loss of the host gene from which this miRNA is processed is associated with cancer progression in numerous cell types. [provided by RefSeq, Sep 2015]","start":9151668,"end":9151777,"strand":-1,"description":"microRNA 34a [Source:HGNC Symbol;Acc:HGNC:31635]"}, {"versioned_ensembl_gene_id":"ENSG00000212529.1","gene_symbol":"SNORA57","gene_name":"Small nucleolar RNA SNORA57 [Source:RFAM;Acc:RF00191]","synonyms":"U99","biotype":"snoRNA","ncbi_id":"692158","summary":null,"start":172252334,"end":172252478,"strand":-1,"description":"Small nucleolar RNA SNORA57 [Source:RFAM;Acc:RF00191]"}, {"versioned_ensembl_gene_id":"ENSG00000253078.1","gene_symbol":"RNU6-1116P","gene_name":"RNA, U6 small nuclear 1116, pseudogene [Source:HGNC Symbol;Acc:HGNC:48079]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480057","summary":null,"start":37435510,"end":37435608,"strand":-1,"description":"RNA, U6 small nuclear 1116, pseudogene [Source:HGNC Symbol;Acc:HGNC:48079]"}, {"versioned_ensembl_gene_id":"ENSG00000222733.1","gene_symbol":"RNY4P29","gene_name":"RNA, Ro-associated Y4 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42497]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873823","summary":null,"start":58527655,"end":58527751,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42497]"}, {"versioned_ensembl_gene_id":"ENSG00000201361.1","gene_symbol":"RNA5SP433","gene_name":"RNA, 5S ribosomal pseudogene 433 [Source:HGNC Symbol;Acc:HGNC:43333]","synonyms":"RN5S433","biotype":"rRNA","ncbi_id":"100873683","summary":null,"start":84262815,"end":84262928,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 433 [Source:HGNC Symbol;Acc:HGNC:43333]"}, {"versioned_ensembl_gene_id":"ENSG00000242201.3","gene_symbol":"RN7SL215P","gene_name":"RNA, 7SL, cytoplasmic 215, pseudogene [Source:HGNC Symbol;Acc:HGNC:46231]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480980","summary":null,"start":194145674,"end":194145971,"strand":1,"description":"RNA, 7SL, cytoplasmic 215, pseudogene [Source:HGNC Symbol;Acc:HGNC:46231]"}, {"versioned_ensembl_gene_id":"ENSG00000201393.1","gene_symbol":"SNORA71","gene_name":"Small nucleolar RNA SNORA71 [Source:RFAM;Acc:RF00056]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":78367507,"end":78367623,"strand":1,"description":"Small nucleolar RNA SNORA71 [Source:RFAM;Acc:RF00056]"}, {"versioned_ensembl_gene_id":"ENSG00000251704.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"ACA40,SNORA40A","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":16199203,"end":16199295,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000222998.1","gene_symbol":"RN7SKP259","gene_name":"RNA, 7SK small nuclear pseudogene 259 [Source:HGNC Symbol;Acc:HGNC:45983]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481751","summary":null,"start":57451690,"end":57452022,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 259 [Source:HGNC Symbol;Acc:HGNC:45983]"}, {"versioned_ensembl_gene_id":"ENSG00000265125.5","gene_symbol":"AC011824.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33565764,"end":33624122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183154.1","gene_symbol":"AC138356.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37734761,"end":37737426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207076.1","gene_symbol":"RNU6-1113P","gene_name":"RNA, U6 small nuclear 1113, pseudogene [Source:HGNC Symbol;Acc:HGNC:48076]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480056","summary":null,"start":43474186,"end":43474292,"strand":1,"description":"RNA, U6 small nuclear 1113, pseudogene [Source:HGNC Symbol;Acc:HGNC:48076]"}, {"versioned_ensembl_gene_id":"ENSG00000274703.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000251843.1","gene_symbol":"RNU6-803P","gene_name":"RNA, U6 small nuclear 803, pseudogene [Source:HGNC Symbol;Acc:HGNC:47766]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481434","summary":null,"start":53719064,"end":53719165,"strand":-1,"description":"RNA, U6 small nuclear 803, pseudogene [Source:HGNC Symbol;Acc:HGNC:47766]"}, {"versioned_ensembl_gene_id":"ENSG00000198972.3","gene_symbol":"MIRLET7E","gene_name":"microRNA let-7e [Source:HGNC Symbol;Acc:HGNC:31482]","synonyms":"MIRNLET7E,hsa-let-7e","biotype":"miRNA","ncbi_id":"406887","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51692786,"end":51692864,"strand":1,"description":"microRNA let-7e [Source:HGNC Symbol;Acc:HGNC:31482]"}, {"versioned_ensembl_gene_id":"ENSG00000284094.1","gene_symbol":"MIR6073","gene_name":"microRNA 6073 [Source:HGNC Symbol;Acc:HGNC:50128]","synonyms":"hsa-mir-6073","biotype":"miRNA","ncbi_id":"102464826","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15969533,"end":15969621,"strand":-1,"description":"microRNA 6073 [Source:HGNC Symbol;Acc:HGNC:50128]"}, {"versioned_ensembl_gene_id":"ENSG00000202431.1","gene_symbol":"RNU6-438P","gene_name":"RNA, U6 small nuclear 438, pseudogene [Source:HGNC Symbol;Acc:HGNC:47401]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479760","summary":null,"start":34297496,"end":34297598,"strand":-1,"description":"RNA, U6 small nuclear 438, pseudogene [Source:HGNC Symbol;Acc:HGNC:47401]"}, {"versioned_ensembl_gene_id":"ENSG00000222511.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8796571,"end":8796673,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207271.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36626015,"end":36626138,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266760.1","gene_symbol":"MIR4464","gene_name":"microRNA 4464 [Source:HGNC Symbol;Acc:HGNC:41528]","synonyms":"hsa-mir-4464","biotype":"miRNA","ncbi_id":"100616109","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90312742,"end":90312833,"strand":1,"description":"microRNA 4464 [Source:HGNC Symbol;Acc:HGNC:41528]"}, {"versioned_ensembl_gene_id":"ENSG00000221332.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":75398860,"end":75399067,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000202191.1","gene_symbol":"SNORD113-1","gene_name":"small nucleolar RNA, C/D box 113-1 [Source:HGNC Symbol;Acc:HGNC:32980]","synonyms":"14q(I-1)","biotype":"snoRNA","ncbi_id":"767561","summary":"Small nucleolar RNAs (snoRNAs), like SNORD113-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD113-1 is 1 of 9 tandem SNORD113 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":100924824,"end":100924892,"strand":1,"description":"small nucleolar RNA, C/D box 113-1 [Source:HGNC Symbol;Acc:HGNC:32980]"}, {"versioned_ensembl_gene_id":"ENSG00000240203.3","gene_symbol":"RN7SL567P","gene_name":"RNA, 7SL, cytoplasmic 567, pseudogene [Source:HGNC Symbol;Acc:HGNC:46583]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481976","summary":null,"start":42676189,"end":42676491,"strand":-1,"description":"RNA, 7SL, cytoplasmic 567, pseudogene [Source:HGNC Symbol;Acc:HGNC:46583]"}, {"versioned_ensembl_gene_id":"ENSG00000266291.1","gene_symbol":"MIR3180-3","gene_name":"microRNA 3180-3 [Source:HGNC Symbol;Acc:HGNC:38239]","synonyms":"hsa-mir-3180-3","biotype":"miRNA","ncbi_id":"100422836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18402178,"end":18402271,"strand":-1,"description":"microRNA 3180-3 [Source:HGNC Symbol;Acc:HGNC:38239]"}, {"versioned_ensembl_gene_id":"ENSG00000225758.1","gene_symbol":"RPS17P17","gene_name":"ribosomal protein S17 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35647]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271230","summary":null,"start":140470866,"end":140471274,"strand":-1,"description":"ribosomal protein S17 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35647]"}, {"versioned_ensembl_gene_id":"ENSG00000272717.1","gene_symbol":"AC112236.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139556799,"end":139557643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235968.1","gene_symbol":"AC079112.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68023694,"end":68024766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216099.3","gene_symbol":"MIR889","gene_name":"microRNA 889 [Source:HGNC Symbol;Acc:HGNC:33651]","synonyms":"MIRN889,hsa-mir-889","biotype":"miRNA","ncbi_id":"100126345","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101047901,"end":101047979,"strand":1,"description":"microRNA 889 [Source:HGNC Symbol;Acc:HGNC:33651]"}, {"versioned_ensembl_gene_id":"ENSG00000222365.1","gene_symbol":"SNORD12B","gene_name":"small nucleolar RNA, C/D box 12B [Source:HGNC Symbol;Acc:HGNC:33573]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113393","summary":null,"start":49280319,"end":49280409,"strand":1,"description":"small nucleolar RNA, C/D box 12B [Source:HGNC Symbol;Acc:HGNC:33573]"}, {"versioned_ensembl_gene_id":"ENSG00000275669.1","gene_symbol":"MIR6744","gene_name":"microRNA 6744 [Source:HGNC Symbol;Acc:HGNC:50051]","synonyms":"hsa-mir-6744","biotype":"miRNA","ncbi_id":"102466725","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1256605,"end":1256670,"strand":1,"description":"microRNA 6744 [Source:HGNC Symbol;Acc:HGNC:50051]"}, {"versioned_ensembl_gene_id":"ENSG00000201527.1","gene_symbol":"RNA5SP478","gene_name":"RNA, 5S ribosomal pseudogene 478 [Source:HGNC Symbol;Acc:HGNC:43378]","synonyms":"RN5S478","biotype":"rRNA","ncbi_id":"100873720","summary":null,"start":23160857,"end":23160971,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 478 [Source:HGNC Symbol;Acc:HGNC:43378]"}, {"versioned_ensembl_gene_id":"ENSG00000195401.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68735720,"end":68735823,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212172.1","gene_symbol":"RNU1-149P","gene_name":"RNA, U1 small nuclear 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:48491]","synonyms":null,"biotype":"snRNA","ncbi_id":"107048983","summary":null,"start":22195469,"end":22195629,"strand":-1,"description":"RNA, U1 small nuclear 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:48491]"}, {"versioned_ensembl_gene_id":"ENSG00000201016.1","gene_symbol":"RNU6-374P","gene_name":"RNA, U6 small nuclear 374, pseudogene [Source:HGNC Symbol;Acc:HGNC:47337]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481296","summary":null,"start":25701217,"end":25701324,"strand":-1,"description":"RNA, U6 small nuclear 374, pseudogene [Source:HGNC Symbol;Acc:HGNC:47337]"}, {"versioned_ensembl_gene_id":"ENSG00000200941.1","gene_symbol":"RNU6-694P","gene_name":"RNA, U6 small nuclear 694, pseudogene [Source:HGNC Symbol;Acc:HGNC:47657]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479872","summary":null,"start":4386410,"end":4386556,"strand":-1,"description":"RNA, U6 small nuclear 694, pseudogene [Source:HGNC Symbol;Acc:HGNC:47657]"}, {"versioned_ensembl_gene_id":"ENSG00000202060.1","gene_symbol":"RNA5SP455","gene_name":"RNA, 5S ribosomal pseudogene 455 [Source:HGNC Symbol;Acc:HGNC:43355]","synonyms":"RN5S455","biotype":"rRNA","ncbi_id":"100873700","summary":null,"start":44071583,"end":44071701,"strand":1,"description":"RNA, 5S ribosomal pseudogene 455 [Source:HGNC Symbol;Acc:HGNC:43355]"}, {"versioned_ensembl_gene_id":"ENSG00000239555.3","gene_symbol":"RN7SL841P","gene_name":"RNA, 7SL, cytoplasmic 841, pseudogene [Source:HGNC Symbol;Acc:HGNC:46857]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481150","summary":null,"start":55291379,"end":55291675,"strand":-1,"description":"RNA, 7SL, cytoplasmic 841, pseudogene [Source:HGNC Symbol;Acc:HGNC:46857]"}, {"versioned_ensembl_gene_id":"ENSG00000207431.2","gene_symbol":"RNU6-906P","gene_name":"RNA, U6 small nuclear 906, pseudogene [Source:HGNC Symbol;Acc:HGNC:47869]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481465","summary":null,"start":146639700,"end":146639769,"strand":1,"description":"RNA, U6 small nuclear 906, pseudogene [Source:HGNC Symbol;Acc:HGNC:47869]"}, {"versioned_ensembl_gene_id":"ENSG00000201701.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":32037526,"end":32037653,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000239398.3","gene_symbol":"RN7SL342P","gene_name":"RNA, 7SL, cytoplasmic 342, pseudogene [Source:HGNC Symbol;Acc:HGNC:46358]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479349","summary":null,"start":59972914,"end":59973207,"strand":1,"description":"RNA, 7SL, cytoplasmic 342, pseudogene [Source:HGNC Symbol;Acc:HGNC:46358]"}, {"versioned_ensembl_gene_id":"ENSG00000200871.1","gene_symbol":"RNU6-810P","gene_name":"RNA, U6 small nuclear 810, pseudogene [Source:HGNC Symbol;Acc:HGNC:47773]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481437","summary":null,"start":29134014,"end":29134120,"strand":1,"description":"RNA, U6 small nuclear 810, pseudogene [Source:HGNC Symbol;Acc:HGNC:47773]"}, {"versioned_ensembl_gene_id":"ENSG00000266410.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33177507,"end":33177602,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275859.1","gene_symbol":"MIR6720","gene_name":"microRNA 6720 [Source:HGNC Symbol;Acc:HGNC:50032]","synonyms":"hsa-mir-6720","biotype":"miRNA","ncbi_id":"102466720","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1390314,"end":1390411,"strand":-1,"description":"microRNA 6720 [Source:HGNC Symbol;Acc:HGNC:50032]"}, {"versioned_ensembl_gene_id":"ENSG00000202350.1","gene_symbol":"RNU6-326P","gene_name":"RNA, U6 small nuclear 326, pseudogene [Source:HGNC Symbol;Acc:HGNC:47289]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481282","summary":null,"start":45843634,"end":45843740,"strand":1,"description":"RNA, U6 small nuclear 326, pseudogene [Source:HGNC Symbol;Acc:HGNC:47289]"}, {"versioned_ensembl_gene_id":"ENSG00000202225.1","gene_symbol":"RNA5SP240","gene_name":"RNA, 5S ribosomal pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:43140]","synonyms":"RN5S240","biotype":"rRNA","ncbi_id":"100873498","summary":null,"start":120981426,"end":120981553,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:43140]"}, {"versioned_ensembl_gene_id":"ENSG00000120265.16","gene_symbol":"PCMT1","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:8728]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5110","summary":"This gene encodes a member of the type II class of protein carboxyl methyltransferase enzymes. The encoded enzyme plays a role in protein repair by recognizing and converting D-aspartyl and L-isoaspartyl residues resulting from spontaneous deamidation back to the normal L-aspartyl form. The encoded protein may play a protective role in the pathogenesis of Alzheimer's disease, and single nucleotide polymorphisms in this gene have been associated with spina bifida and premature ovarian failure. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":149749443,"end":149811420,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:8728]"}, {"versioned_ensembl_gene_id":"ENSG00000234718.7","gene_symbol":"AC007161.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":7738524,"end":7742574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284332.1","gene_symbol":"MIR1302-2","gene_name":"microRNA 1302-2 [Source:HGNC Symbol;Acc:HGNC:35294]","synonyms":"MIRN1302-2,hsa-mir-1302-2","biotype":"miRNA","ncbi_id":"100302278","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30366,"end":30503,"strand":1,"description":"microRNA 1302-2 [Source:HGNC Symbol;Acc:HGNC:35294]"}, {"versioned_ensembl_gene_id":"ENSG00000212204.1","gene_symbol":"RNA5SP91","gene_name":"RNA, 5S ribosomal pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:42889]","synonyms":"RN5S91","biotype":"rRNA","ncbi_id":"100873324","summary":null,"start":33285769,"end":33285887,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:42889]"}, {"versioned_ensembl_gene_id":"ENSG00000202428.1","gene_symbol":"RNU6-108P","gene_name":"RNA, U6 small nuclear 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:47071]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481875","summary":null,"start":57536252,"end":57536358,"strand":-1,"description":"RNA, U6 small nuclear 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:47071]"}, {"versioned_ensembl_gene_id":"ENSG00000158615.8","gene_symbol":"PPP1R15B","gene_name":"protein phosphatase 1 regulatory subunit 15B [Source:HGNC Symbol;Acc:HGNC:14951]","synonyms":"FLJ14744","biotype":"protein_coding","ncbi_id":"84919","summary":"This gene encodes a protein phosphatase I-interacting protein that promotes the dephosphorylation of eukaryotic translation initiation factor 2A to regulate translation under conditions of cellular stress. The transcribed messenger RNA contains two upstream open reading frames (ORFs) that repress translation of the main protein coding ORF under normal conditions, while the protein coding ORF is expressed at high levels in response to stress. Continual translation of the mRNA under conditions of eukaryotic translation initiation factor 2A inactivation is thought to create a feedback loop for reactivation of the gene during recovery from stress. In addition, it has been shown that this protein plays a role in membrane traffic that is independent of translation and that it is required for exocytosis from erythroleukemia cells. Allelic variants of this gene are associated with microcephaly, short stature, and impaired glucose metabolism. [provided by RefSeq, Feb 2016]","start":204403387,"end":204411791,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 15B [Source:HGNC Symbol;Acc:HGNC:14951]"}, {"versioned_ensembl_gene_id":"ENSG00000213409.4","gene_symbol":"C1QBPP2","gene_name":"complement C1q binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422299","summary":null,"start":66761575,"end":66762399,"strand":-1,"description":"complement C1q binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51618]"}, {"versioned_ensembl_gene_id":"ENSG00000268677.1","gene_symbol":"AC011495.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49688853,"end":49690573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258504.2","gene_symbol":"AL157871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100291117,"end":100294656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258982.1","gene_symbol":"AL133523.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100207407,"end":100238555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107282.7","gene_symbol":"APBA1","gene_name":"amyloid beta precursor protein binding family A member 1 [Source:HGNC Symbol;Acc:HGNC:578]","synonyms":"D9S411E,X11,MINT1","biotype":"protein_coding","ncbi_id":"320","summary":"The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adapter protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It stabilizes APP and inhibits production of proteolytic APP fragments including the A beta peptide that is deposited in the brains of Alzheimer's disease patients. This gene product is believed to be involved in signal transduction processes. It is also regarded as a putative vesicular trafficking protein in the brain that can form a complex with the potential to couple synaptic vesicle exocytosis to neuronal cell adhesion. [provided by RefSeq, Jul 2008]","start":69427530,"end":69672306,"strand":-1,"description":"amyloid beta precursor protein binding family A member 1 [Source:HGNC Symbol;Acc:HGNC:578]"}, {"versioned_ensembl_gene_id":"ENSG00000240518.2","gene_symbol":"AC116353.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140609085,"end":140609400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108039.17","gene_symbol":"XPNPEP1","gene_name":"X-prolyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:12822]","synonyms":"XPNPEP,XPNPEPL1,XPNPEPL","biotype":"protein_coding","ncbi_id":"7511","summary":"This gene encodes the cytosolic form of a metalloaminopeptidase that catalyzes the cleavage of the N-terminal amino acid adjacent to a proline residue. The gene product may play a role in degradation and maturation of tachykinins, neuropeptides, and peptide hormones. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Nov 2009]","start":109864766,"end":109923553,"strand":-1,"description":"X-prolyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:12822]"}, {"versioned_ensembl_gene_id":"ENSG00000013306.15","gene_symbol":"SLC25A39","gene_name":"solute carrier family 25 member 39 [Source:HGNC Symbol;Acc:HGNC:24279]","synonyms":"FLJ22407,CGI-69","biotype":"protein_coding","ncbi_id":"51629","summary":"This gene encodes a member of the SLC25 transporter or mitochondrial carrier family of proteins. Members of this family are encoded by the nuclear genome while their protein products are usually embedded in the inner mitochondrial membrane and exhibit wide-ranging substrate specificity. Although the encoded protein is currently considered an orphan transporter, this protein is related to other carriers known to transport amino acids. This protein may play a role in iron homeostasis. [provided by RefSeq, Mar 2016]","start":44319625,"end":44324870,"strand":-1,"description":"solute carrier family 25 member 39 [Source:HGNC Symbol;Acc:HGNC:24279]"}, {"versioned_ensembl_gene_id":"ENSG00000283155.1","gene_symbol":"AC116353.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":140562443,"end":140592123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283602.1","gene_symbol":"AC116353.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":140569962,"end":140594570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251453.1","gene_symbol":"HAUS1P1","gene_name":"HAUS augmin like complex subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43760]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728921","summary":null,"start":140581504,"end":140582335,"strand":1,"description":"HAUS augmin like complex subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43760]"}, {"versioned_ensembl_gene_id":"ENSG00000197694.15","gene_symbol":"SPTAN1","gene_name":"spectrin alpha, non-erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11273]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6709","summary":"Spectrins are a family of filamentous cytoskeletal proteins that function as essential scaffold proteins that stabilize the plasma membrane and organize intracellular organelles. Spectrins are composed of alpha and beta dimers that associate to form tetramers linked in a head-to-head arrangement. This gene encodes an alpha spectrin that is specifically expressed in nonerythrocytic cells. The encoded protein has been implicated in other cellular functions including DNA repair and cell cycle regulation. Mutations in this gene are the cause of early infantile epileptic encephalopathy-5. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]","start":128552558,"end":128633662,"strand":1,"description":"spectrin alpha, non-erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11273]"}, {"versioned_ensembl_gene_id":"ENSG00000233436.7","gene_symbol":"BTBD18","gene_name":"BTB domain containing 18 [Source:HGNC Symbol;Acc:HGNC:37214]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643376","summary":null,"start":57743514,"end":57751781,"strand":-1,"description":"BTB domain containing 18 [Source:HGNC Symbol;Acc:HGNC:37214]"}, {"versioned_ensembl_gene_id":"ENSG00000143318.12","gene_symbol":"CASQ1","gene_name":"calsequestrin 1 [Source:HGNC Symbol;Acc:HGNC:1512]","synonyms":"PDIB1,CASQ","biotype":"protein_coding","ncbi_id":"844","summary":"This gene encodes the skeletal muscle specific member of the calsequestrin protein family. Calsequestrin functions as a luminal sarcoplasmic reticulum calcium sensor in both cardiac and skeletal muscle cells. This protein, also known as calmitine, functions as a calcium regulator in the mitochondria of skeletal muscle. This protein is absent in patients with Duchenne and Becker types of muscular dystrophy. [provided by RefSeq, Jun 2013]","start":160190556,"end":160201886,"strand":1,"description":"calsequestrin 1 [Source:HGNC Symbol;Acc:HGNC:1512]"}, {"versioned_ensembl_gene_id":"ENSG00000183979.7","gene_symbol":"NPB","gene_name":"neuropeptide B [Source:HGNC Symbol;Acc:HGNC:30099]","synonyms":"PPNPB,PPL7","biotype":"protein_coding","ncbi_id":"256933","summary":"This gene encodes a member of the neuropeptide B/W family of proteins and preproprotein that is proteolytically processed to generate multiple protein products. The encoded products include neuropeptide B-23 and a C-terminally extended form, neuropeptide B-29, which are characterized by an N-terminal brominated tryptophan amino acid. Both of the encoded peptides bind with higher affinity to neuropeptide B/W (NPB/W) receptor 1 compared to the related NPB/W receptor 2. These peptides may regulate feeding, pain perception, and stress in rodents. [provided by RefSeq, Jul 2015]","start":81900745,"end":81902905,"strand":1,"description":"neuropeptide B [Source:HGNC Symbol;Acc:HGNC:30099]"}, {"versioned_ensembl_gene_id":"ENSG00000164331.9","gene_symbol":"ANKRA2","gene_name":"ankyrin repeat family A member 2 [Source:HGNC Symbol;Acc:HGNC:13208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57763","summary":null,"start":73552335,"end":73565686,"strand":-1,"description":"ankyrin repeat family A member 2 [Source:HGNC Symbol;Acc:HGNC:13208]"}, {"versioned_ensembl_gene_id":"ENSG00000227417.3","gene_symbol":"AC114402.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203805621,"end":203806263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243250.1","gene_symbol":"AP002884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112235371,"end":112236025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234648.1","gene_symbol":"AL162151.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98973314,"end":98973471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259119.1","gene_symbol":"AL132796.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98925137,"end":98927805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188783.5","gene_symbol":"PRELP","gene_name":"proline and arginine rich end leucine rich repeat protein [Source:HGNC Symbol;Acc:HGNC:9357]","synonyms":"SLRR2A,prolargin","biotype":"protein_coding","ncbi_id":"5549","summary":"The protein encoded by this gene is a leucine-rich repeat protein present in connective tissue extracellular matrix. This protein functions as a molecule anchoring basement membranes to the underlying connective tissue. This protein has been shown to bind type I collagen to basement membranes and type II collagen to cartilage. It also binds the basement membrane heparan sulfate proteoglycan perlecan. This protein is suggested to be involved in the pathogenesis of Hutchinson-Gilford progeria (HGP), which is reported to lack the binding of collagen in basement membranes and cartilage. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":203475828,"end":203491352,"strand":1,"description":"proline and arginine rich end leucine rich repeat protein [Source:HGNC Symbol;Acc:HGNC:9357]"}, {"versioned_ensembl_gene_id":"ENSG00000224160.1","gene_symbol":"CICP10","gene_name":"capicua transcriptional repressor pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37901]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462787","summary":null,"start":242119856,"end":242120053,"strand":-1,"description":"capicua transcriptional repressor pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37901]"}, {"versioned_ensembl_gene_id":"ENSG00000255807.1","gene_symbol":"PTP4A1P2","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499563","summary":null,"start":133033503,"end":133033956,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41929]"}, {"versioned_ensembl_gene_id":"ENSG00000259535.1","gene_symbol":"RPL21P12","gene_name":"ribosomal protein L21 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:19810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122409","summary":null,"start":103148597,"end":103149408,"strand":1,"description":"ribosomal protein L21 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:19810]"}, {"versioned_ensembl_gene_id":"ENSG00000139915.19","gene_symbol":"MDGA2","gene_name":"MAM domain containing glycosylphosphatidylinositol anchor 2 [Source:HGNC Symbol;Acc:HGNC:19835]","synonyms":"MAMDC1","biotype":"protein_coding","ncbi_id":"161357","summary":null,"start":46840092,"end":47674954,"strand":-1,"description":"MAM domain containing glycosylphosphatidylinositol anchor 2 [Source:HGNC Symbol;Acc:HGNC:19835]"}, {"versioned_ensembl_gene_id":"ENSG00000280119.1","gene_symbol":"AC093642.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":242001209,"end":242006013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237940.3","gene_symbol":"LINC01238","gene_name":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]","synonyms":"FLJ40615,FLJ40615","biotype":"lincRNA","ncbi_id":"102723927","summary":null,"start":241970683,"end":241977276,"strand":1,"description":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]"}, {"versioned_ensembl_gene_id":"ENSG00000226423.1","gene_symbol":"AC093642.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242025183,"end":242026176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240083.2","gene_symbol":"RPS3AP22","gene_name":"ribosomal protein S3a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36573]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130786","summary":null,"start":88381957,"end":88382725,"strand":1,"description":"ribosomal protein S3a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36573]"}, {"versioned_ensembl_gene_id":"ENSG00000250156.3","gene_symbol":"LINC02060","gene_name":"long intergenic non-protein coding RNA 2060 [Source:HGNC Symbol;Acc:HGNC:52904]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546226","summary":null,"start":88408982,"end":88439090,"strand":-1,"description":"long intergenic non-protein coding RNA 2060 [Source:HGNC Symbol;Acc:HGNC:52904]"}, {"versioned_ensembl_gene_id":"ENSG00000279259.1","gene_symbol":"AC087741.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80147250,"end":80148596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230684.1","gene_symbol":"AL158207.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129933536,"end":129936541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185215.8","gene_symbol":"TNFAIP2","gene_name":"TNF alpha induced protein 2 [Source:HGNC Symbol;Acc:HGNC:11895]","synonyms":"EXOC3L3,B94","biotype":"protein_coding","ncbi_id":"7127","summary":"This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. The expression of this gene was shown to be induced by retinoic acid in a cell line expressing a oncogenic version of the retinoic acid receptor alpha fusion protein, which suggested that this gene may be a retinoic acid target gene in acute promyelocytic leukemia. [provided by RefSeq, Jul 2008]","start":103123442,"end":103137439,"strand":1,"description":"TNF alpha induced protein 2 [Source:HGNC Symbol;Acc:HGNC:11895]"}, {"versioned_ensembl_gene_id":"ENSG00000186625.13","gene_symbol":"KATNA1","gene_name":"katanin catalytic subunit A1 [Source:HGNC Symbol;Acc:HGNC:6216]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11104","summary":"Microtubules, polymers of alpha and beta tubulin subunits, form the mitotic spindle of a dividing cell and help to organize membranous organelles during interphase. Katanin is a heterodimer that consists of a 60 kDa ATPase (p60 subunit A 1) and an 80 kDa accessory protein (p80 subunit B 1). The p60 subunit acts to sever and disassemble microtubules, while the p80 subunit targets the enzyme to the centrosome. This gene encodes the p80 subunit. This protein is a member of the AAA family of ATPases. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Feb 2011]","start":149594873,"end":149648972,"strand":-1,"description":"katanin catalytic subunit A1 [Source:HGNC Symbol;Acc:HGNC:6216]"}, {"versioned_ensembl_gene_id":"ENSG00000258553.5","gene_symbol":"AL157911.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59969116,"end":60091783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258746.2","gene_symbol":"AL162632.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45502742,"end":45503140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225147.1","gene_symbol":"RPS12P10","gene_name":"ribosomal protein S12 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35824]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271056","summary":null,"start":142566700,"end":142567076,"strand":1,"description":"ribosomal protein S12 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35824]"}, {"versioned_ensembl_gene_id":"ENSG00000164151.11","gene_symbol":"ICE1","gene_name":"interactor of little elongation complex ELL subunit 1 [Source:HGNC Symbol;Acc:HGNC:29154]","synonyms":"KIAA0947","biotype":"protein_coding","ncbi_id":"23379","summary":null,"start":5420664,"end":5490234,"strand":1,"description":"interactor of little elongation complex ELL subunit 1 [Source:HGNC Symbol;Acc:HGNC:29154]"}, {"versioned_ensembl_gene_id":"ENSG00000173894.10","gene_symbol":"CBX2","gene_name":"chromobox 2 [Source:HGNC Symbol;Acc:HGNC:1552]","synonyms":"MGC10561,CDCA6","biotype":"protein_coding","ncbi_id":"84733","summary":"This gene encodes a component of the polycomb multiprotein complex, which is required to maintain the transcriptionally repressive state of many genes throughout development via chromatin remodeling and modification of histones. Disruption of this gene in mice results in male-to-female gonadal sex reversal. Mutations in this gene are also associated with gonadal dysgenesis in humans. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Mar 2010]","start":79778132,"end":79787983,"strand":1,"description":"chromobox 2 [Source:HGNC Symbol;Acc:HGNC:1552]"}, {"versioned_ensembl_gene_id":"ENSG00000241187.1","gene_symbol":"AC008379.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154729231,"end":154729694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055211.12","gene_symbol":"GINM1","gene_name":"glycoprotein integral membrane 1 [Source:HGNC Symbol;Acc:HGNC:21074]","synonyms":"dJ12G14.2,C6orf72","biotype":"protein_coding","ncbi_id":"116254","summary":null,"start":149566294,"end":149591748,"strand":1,"description":"glycoprotein integral membrane 1 [Source:HGNC Symbol;Acc:HGNC:21074]"}, {"versioned_ensembl_gene_id":"ENSG00000267890.1","gene_symbol":"AC010624.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50075123,"end":50075902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136816.15","gene_symbol":"TOR1B","gene_name":"torsin family 1 member B [Source:HGNC Symbol;Acc:HGNC:11995]","synonyms":"MGC4386,DQ1","biotype":"protein_coding","ncbi_id":"27348","summary":"The protein encoded by this gene is an ATPase found primarily in the endoplasmic reticulum and nuclear envelope. This gene has a highly-similar neighboring gene, TOR1A, that encodes a protein that is likely to interact in a complex with this protein. Finally, this protein may act as a chaperone and play a role in maintaining the integrity of the nuclear envelope and endoplasmic reticulum. Several transcript variants, some protein-coding and others non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]","start":129803153,"end":129811281,"strand":1,"description":"torsin family 1 member B [Source:HGNC Symbol;Acc:HGNC:11995]"}, {"versioned_ensembl_gene_id":"ENSG00000246640.1","gene_symbol":"PICART1","gene_name":"p53-inducible cancer-associated RNA transcript 1 [Source:NCBI gene;Acc:284080]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284080","summary":null,"start":50050349,"end":50055739,"strand":-1,"description":"p53-inducible cancer-associated RNA transcript 1 [Source:NCBI gene;Acc:284080]"}, {"versioned_ensembl_gene_id":"ENSG00000233909.1","gene_symbol":"UBE2V1P4","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44886]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724816","summary":null,"start":129791196,"end":129791837,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44886]"}, {"versioned_ensembl_gene_id":"ENSG00000228915.3","gene_symbol":"OR7E128P","gene_name":"olfactory receptor family 7 subfamily E member 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:15305]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81175","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71893410,"end":71894433,"strand":1,"description":"olfactory receptor family 7 subfamily E member 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:15305]"}, {"versioned_ensembl_gene_id":"ENSG00000275017.1","gene_symbol":"AL353748.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88391362,"end":88391832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250635.1","gene_symbol":"CXXC5-AS1","gene_name":"CXXC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53009]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139648999,"end":139649728,"strand":-1,"description":"CXXC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53009]"}, {"versioned_ensembl_gene_id":"ENSG00000069399.14","gene_symbol":"BCL3","gene_name":"B-cell CLL/lymphoma 3 [Source:HGNC Symbol;Acc:HGNC:998]","synonyms":"D19S37,BCL4","biotype":"protein_coding","ncbi_id":"602","summary":"This gene is a proto-oncogene candidate. It is identified by its translocation into the immunoglobulin alpha-locus in some cases of B-cell leukemia. The protein encoded by this gene contains seven ankyrin repeats, which are most closely related to those found in I kappa B proteins. This protein functions as a transcriptional co-activator that activates through its association with NF-kappa B homodimers. The expression of this gene can be induced by NF-kappa B, which forms a part of the autoregulatory loop that controls the nuclear residence of p50 NF-kappa B. [provided by RefSeq, Jul 2008]","start":44747705,"end":44760044,"strand":1,"description":"B-cell CLL/lymphoma 3 [Source:HGNC Symbol;Acc:HGNC:998]"}, {"versioned_ensembl_gene_id":"ENSG00000217716.3","gene_symbol":"RPS10P3","gene_name":"ribosomal protein S10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"158104","summary":null,"start":88016300,"end":88016793,"strand":1,"description":"ribosomal protein S10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23684]"}, {"versioned_ensembl_gene_id":"ENSG00000261578.1","gene_symbol":"AP003119.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":76800364,"end":76804555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229258.5","gene_symbol":"AL445488.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":211829846,"end":211853703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248671.7","gene_symbol":"ALG1L9P","gene_name":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:NCBI gene;Acc:285407]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285407","summary":null,"start":71794363,"end":71818238,"strand":-1,"description":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:NCBI gene;Acc:285407]"}, {"versioned_ensembl_gene_id":"ENSG00000213585.10","gene_symbol":"VDAC1","gene_name":"voltage dependent anion channel 1 [Source:HGNC Symbol;Acc:HGNC:12669]","synonyms":"PORIN,MGC111064","biotype":"protein_coding","ncbi_id":"7416","summary":"This gene encodes a voltage-dependent anion channel protein that is a major component of the outer mitochondrial membrane. The encoded protein facilitates the exchange of metabolites and ions across the outer mitochondrial membrane and may regulate mitochondrial functions. This protein also forms channels in the plasma membrane and may be involved in transmembrane electron transport. Alternate splicing results in multiple transcript variants. Multiple pseudogenes of this gene are found on chromosomes 1, 2 3, 6, 9, 12, X and Y.[provided by RefSeq, Sep 2010]","start":133971915,"end":134005133,"strand":-1,"description":"voltage dependent anion channel 1 [Source:HGNC Symbol;Acc:HGNC:12669]"}, {"versioned_ensembl_gene_id":"ENSG00000152254.10","gene_symbol":"G6PC2","gene_name":"glucose-6-phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:28906]","synonyms":"IGRP","biotype":"protein_coding","ncbi_id":"57818","summary":"This gene encodes an enzyme belonging to the glucose-6-phosphatase catalytic subunit family. These enzymes are part of a multicomponent integral membrane system that catalyzes the hydrolysis of glucose-6-phosphate, the terminal step in gluconeogenic and glycogenolytic pathways, allowing the release of glucose into the bloodstream. The family member encoded by this gene is found in pancreatic islets and does not exhibit phosphohydrolase activity, but it is a major target of cell-mediated autoimmunity in diabetes. Several alternatively spliced transcript variants of this gene have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":168901240,"end":168910000,"strand":1,"description":"glucose-6-phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:28906]"}, {"versioned_ensembl_gene_id":"ENSG00000223776.5","gene_symbol":"LGALS8-AS1","gene_name":"LGALS8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40340]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287902","summary":null,"start":236523052,"end":236524508,"strand":-1,"description":"LGALS8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40340]"}, {"versioned_ensembl_gene_id":"ENSG00000273058.2","gene_symbol":"AL359921.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":236536162,"end":236536704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269091.5","gene_symbol":"AC010624.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50043196,"end":50051062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183077.15","gene_symbol":"AFMID","gene_name":"arylformamidase [Source:HGNC Symbol;Acc:HGNC:20910]","synonyms":"DKFZp686F03259,KF","biotype":"protein_coding","ncbi_id":"125061","summary":null,"start":78187317,"end":78207701,"strand":1,"description":"arylformamidase [Source:HGNC Symbol;Acc:HGNC:20910]"}, {"versioned_ensembl_gene_id":"ENSG00000278311.4","gene_symbol":"GGNBP2","gene_name":"gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19357]","synonyms":"ZNF403,ZFP403,LZK1,FLJ22561,FLJ21230,DIF3,DIF-3","biotype":"protein_coding","ncbi_id":"79893","summary":null,"start":36544888,"end":36589848,"strand":1,"description":"gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19357]"}, {"versioned_ensembl_gene_id":"ENSG00000198873.11","gene_symbol":"GRK5","gene_name":"G protein-coupled receptor kinase 5 [Source:HGNC Symbol;Acc:HGNC:4544]","synonyms":"GPRK5","biotype":"protein_coding","ncbi_id":"2869","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating their deactivation. It has also been shown to play a role in regulating the motility of polymorphonuclear leukocytes (PMNs). [provided by RefSeq, Jul 2008]","start":119207589,"end":119459742,"strand":1,"description":"G protein-coupled receptor kinase 5 [Source:HGNC Symbol;Acc:HGNC:4544]"}, {"versioned_ensembl_gene_id":"ENSG00000268041.2","gene_symbol":"AC010616.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41907705,"end":41928516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271109.1","gene_symbol":"AC008555.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34849278,"end":34860576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269086.2","gene_symbol":"AC008555.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34837889,"end":34855304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229795.2","gene_symbol":"RPS21P1","gene_name":"ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36401]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271090","summary":null,"start":235432985,"end":235433231,"strand":1,"description":"ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36401]"}, {"versioned_ensembl_gene_id":"ENSG00000235495.1","gene_symbol":"AC007422.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67565604,"end":67684077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235718.8","gene_symbol":"MFRP","gene_name":"membrane frizzled-related protein [Source:HGNC Symbol;Acc:HGNC:18121]","synonyms":"C1QTNF5,rd6,NNO2,FLJ30570","biotype":"protein_coding","ncbi_id":"83552","summary":"This gene encodes a member of the frizzled-related protein family. The encoded protein plays an important role in eye development and mutations in this gene have been associated with nanophthalmos, posterior microphthalmia, retinitis pigmentosa, foveoschisis, and optic disc drusen. The protein is encoded by a bicistronic transcript which also encodes C1q and tumor necrosis factor related protein 5 (C1QTNF5). [provided by RefSeq, Jun 2013]","start":119338942,"end":119346673,"strand":-1,"description":"membrane frizzled-related protein [Source:HGNC Symbol;Acc:HGNC:18121]"}, {"versioned_ensembl_gene_id":"ENSG00000238259.1","gene_symbol":"AC067940.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":168231921,"end":168232220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248736.1","gene_symbol":"AC112192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2965006,"end":2967628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248137.1","gene_symbol":"AC094105.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2831021,"end":2835139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219702.1","gene_symbol":"AL078599.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81764211,"end":81764503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232939.1","gene_symbol":"AL158829.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109760360,"end":109772043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228053.1","gene_symbol":"AL158823.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110024881,"end":110025358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258678.1","gene_symbol":"LINC02317","gene_name":"long intergenic non-protein coding RNA 2317 [Source:HGNC Symbol;Acc:HGNC:53236]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101930294","summary":null,"start":90452063,"end":90455117,"strand":-1,"description":"long intergenic non-protein coding RNA 2317 [Source:HGNC Symbol;Acc:HGNC:53236]"}, {"versioned_ensembl_gene_id":"ENSG00000179820.15","gene_symbol":"MYADM","gene_name":"myeloid associated differentiation marker [Source:HGNC Symbol;Acc:HGNC:7544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91663","summary":null,"start":53866223,"end":53876437,"strand":1,"description":"myeloid associated differentiation marker [Source:HGNC Symbol;Acc:HGNC:7544]"}, {"versioned_ensembl_gene_id":"ENSG00000150316.11","gene_symbol":"CWC15","gene_name":"CWC15 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:26939]","synonyms":"HSPC148,Cwf15,C11orf5,AD002","biotype":"protein_coding","ncbi_id":"51503","summary":null,"start":94962622,"end":94973612,"strand":-1,"description":"CWC15 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:26939]"}, {"versioned_ensembl_gene_id":"ENSG00000255774.1","gene_symbol":"AP000439.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69477133,"end":69479940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255606.1","gene_symbol":"AP000439.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69438365,"end":69444743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259133.5","gene_symbol":"AL161757.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56648965,"end":56730535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253600.1","gene_symbol":"AC008446.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164601002,"end":164601452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273777.4","gene_symbol":"CEACAM20","gene_name":"carcinoembryonic antigen related cell adhesion molecule 20 [Source:HGNC Symbol;Acc:HGNC:24879]","synonyms":"UNQ9366","biotype":"protein_coding","ncbi_id":"125931","summary":null,"start":44501677,"end":44529788,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 20 [Source:HGNC Symbol;Acc:HGNC:24879]"}, {"versioned_ensembl_gene_id":"ENSG00000119720.17","gene_symbol":"NRDE2","gene_name":"NRDE-2, necessary for RNA interference, domain containing [Source:HGNC Symbol;Acc:HGNC:20186]","synonyms":"FLJ14051,C14orf102","biotype":"protein_coding","ncbi_id":"55051","summary":null,"start":90267856,"end":90332137,"strand":-1,"description":"NRDE-2, necessary for RNA interference, domain containing [Source:HGNC Symbol;Acc:HGNC:20186]"}, {"versioned_ensembl_gene_id":"ENSG00000056558.10","gene_symbol":"TRAF1","gene_name":"TNF receptor associated factor 1 [Source:HGNC Symbol;Acc:HGNC:12031]","synonyms":"EBI6","biotype":"protein_coding","ncbi_id":"7185","summary":"The protein encoded by this gene is a member of the TNF receptor (TNFR) associated factor (TRAF) protein family. TRAF proteins associate with, and mediate the signal transduction from various receptors of the TNFR superfamily. This protein and TRAF2 form a heterodimeric complex, which is required for TNF-alpha-mediated activation of MAPK8/JNK and NF-kappaB. The protein complex formed by this protein and TRAF2 also interacts with inhibitor-of-apoptosis proteins (IAPs), and thus mediates the anti-apoptotic signals from TNF receptors. The expression of this protein can be induced by Epstein-Barr virus (EBV). EBV infection membrane protein 1 (LMP1) is found to interact with this and other TRAF proteins; this interaction is thought to link LMP1-mediated B lymphocyte transformation to the signal transduction from TNFR family receptors. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":120902393,"end":120929173,"strand":-1,"description":"TNF receptor associated factor 1 [Source:HGNC Symbol;Acc:HGNC:12031]"}, {"versioned_ensembl_gene_id":"ENSG00000270506.1","gene_symbol":"AC021646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93035261,"end":93035744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257746.1","gene_symbol":"AC138123.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93090522,"end":93107600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258171.1","gene_symbol":"LINC02412","gene_name":"long intergenic non-protein coding RNA 2412 [Source:HGNC Symbol;Acc:HGNC:53341]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724933","summary":null,"start":93174366,"end":93181832,"strand":1,"description":"long intergenic non-protein coding RNA 2412 [Source:HGNC Symbol;Acc:HGNC:53341]"}, {"versioned_ensembl_gene_id":"ENSG00000172927.7","gene_symbol":"MYEOV","gene_name":"myeloma overexpressed [Source:HGNC Symbol;Acc:HGNC:7563]","synonyms":"OCIM","biotype":"protein_coding","ncbi_id":"26579","summary":null,"start":69294138,"end":69367726,"strand":1,"description":"myeloma overexpressed [Source:HGNC Symbol;Acc:HGNC:7563]"}, {"versioned_ensembl_gene_id":"ENSG00000249842.1","gene_symbol":"AC010486.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85446974,"end":85447758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213275.2","gene_symbol":"IFITM9P","gene_name":"interferon induced transmembrane protein 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33972]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390218","summary":null,"start":69303412,"end":69303807,"strand":-1,"description":"interferon induced transmembrane protein 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33972]"}, {"versioned_ensembl_gene_id":"ENSG00000249023.1","gene_symbol":"AC010486.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85429702,"end":85430184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236900.1","gene_symbol":"TIMM9P1","gene_name":"TIMM9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862726","summary":null,"start":74344550,"end":74344805,"strand":-1,"description":"TIMM9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39928]"}, {"versioned_ensembl_gene_id":"ENSG00000256469.1","gene_symbol":"AP002383.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94874052,"end":94925521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204427.11","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"BAT5,NG26,D6S82E","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31686949,"end":31703444,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000279222.1","gene_symbol":"AC025183.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1858409,"end":1859890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250417.1","gene_symbol":"LINC02116","gene_name":"long intergenic non-protein coding RNA 2116 [Source:HGNC Symbol;Acc:HGNC:52971]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929034","summary":null,"start":1855970,"end":1856568,"strand":-1,"description":"long intergenic non-protein coding RNA 2116 [Source:HGNC Symbol;Acc:HGNC:52971]"}, {"versioned_ensembl_gene_id":"ENSG00000156110.13","gene_symbol":"ADK","gene_name":"adenosine kinase [Source:HGNC Symbol;Acc:HGNC:257]","synonyms":"AK","biotype":"protein_coding","ncbi_id":"132","summary":"This gene an enzyme which catalyzes the transfer of the gamma-phosphate from ATP to adenosine, thereby serving as a regulator of concentrations of both extracellular adenosine and intracellular adenine nucleotides. Adenosine has widespread effects on the cardiovascular, nervous, respiratory, and immune systems and inhibitors of the enzyme could play an important pharmacological role in increasing intravascular adenosine concentrations and acting as anti-inflammatory agents. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":74151185,"end":74709303,"strand":1,"description":"adenosine kinase [Source:HGNC Symbol;Acc:HGNC:257]"}, {"versioned_ensembl_gene_id":"ENSG00000264940.4","gene_symbol":"SNORD3C","gene_name":"small nucleolar RNA, C/D box 3C [Source:HGNC Symbol;Acc:HGNC:33191]","synonyms":"U3-3,RNU3-3","biotype":"snoRNA","ncbi_id":"780853","summary":null,"start":19189665,"end":19190245,"strand":-1,"description":"small nucleolar RNA, C/D box 3C [Source:HGNC Symbol;Acc:HGNC:33191]"}, {"versioned_ensembl_gene_id":"ENSG00000273755.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713341,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000196371.3","gene_symbol":"FUT4","gene_name":"fucosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:4015]","synonyms":"FUC-TIV,FCT3A,ELFT,CD15","biotype":"protein_coding","ncbi_id":"2526","summary":"The product of this gene transfers fucose to N-acetyllactosamine polysaccharides to generate fucosylated carbohydrate structures. It catalyzes the synthesis of the non-sialylated antigen, Lewis x (CD15). [provided by RefSeq, Jan 2009]","start":94543840,"end":94549898,"strand":1,"description":"fucosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:4015]"}, {"versioned_ensembl_gene_id":"ENSG00000217231.2","gene_symbol":"AL109755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144036618,"end":144037704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254134.1","gene_symbol":"IGHVII-74-1","gene_name":"immunoglobulin heavy variable (II)-74-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5690]","synonyms":"IGHV(II)-74-1","biotype":"IG_V_pseudogene","ncbi_id":"28357","summary":null,"start":106821174,"end":106821414,"strand":-1,"description":"immunoglobulin heavy variable (II)-74-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5690]"}, {"versioned_ensembl_gene_id":"ENSG00000270419.1","gene_symbol":"CAHM","gene_name":"colon adenocarcinoma hypermethylated (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:42860]","synonyms":"LINC00468","biotype":"lincRNA","ncbi_id":"100526820","summary":null,"start":163413065,"end":163413960,"strand":-1,"description":"colon adenocarcinoma hypermethylated (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:42860]"}, {"versioned_ensembl_gene_id":"ENSG00000231635.1","gene_symbol":"ATP5BP1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:831]","synonyms":"ATPSBL1,ATPMBL1,ATP5BL1","biotype":"processed_pseudogene","ncbi_id":"507","summary":null,"start":98206151,"end":98207724,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:831]"}, {"versioned_ensembl_gene_id":"ENSG00000269877.3","gene_symbol":"AC008753.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53787597,"end":53788169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259868.2","gene_symbol":"AL163952.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55896547,"end":55962970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280411.1","gene_symbol":"AC245369.3","gene_name":"Immunoglobulin heavy variable 1-69D [Source:UniProtKB/Swiss-Prot;Acc:A0A0B4J2H0]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106762092,"end":106762588,"strand":-1,"description":"Immunoglobulin heavy variable 1-69D [Source:UniProtKB/Swiss-Prot;Acc:A0A0B4J2H0]"}, {"versioned_ensembl_gene_id":"ENSG00000272386.1","gene_symbol":"AC015802.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":76551352,"end":76551750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011347.9","gene_symbol":"SYT7","gene_name":"synaptotagmin 7 [Source:HGNC Symbol;Acc:HGNC:11514]","synonyms":"SYT-VII,PCANAP7,MGC150517,IPCA-7","biotype":"protein_coding","ncbi_id":"9066","summary":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. A similar protein in rodents mediates hormone secretion and lysosome exocytosis. In humans, expression of this gene has been associated with prostate cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":61515313,"end":61581148,"strand":-1,"description":"synaptotagmin 7 [Source:HGNC Symbol;Acc:HGNC:11514]"}, {"versioned_ensembl_gene_id":"ENSG00000230321.1","gene_symbol":"MTCO2P27","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52156]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075291","summary":null,"start":12504905,"end":12505976,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52156]"}, {"versioned_ensembl_gene_id":"ENSG00000137492.7","gene_symbol":"THAP12","gene_name":"THAP domain containing 12 [Source:HGNC Symbol;Acc:HGNC:9440]","synonyms":"THAP0,PRKRIR,P52rIPK,DAP4","biotype":"protein_coding","ncbi_id":"5612","summary":null,"start":76349956,"end":76380971,"strand":-1,"description":"THAP domain containing 12 [Source:HGNC Symbol;Acc:HGNC:9440]"}, {"versioned_ensembl_gene_id":"ENSG00000189152.10","gene_symbol":"GRAPL","gene_name":"GRB2 related adaptor protein like [Source:HGNC Symbol;Acc:HGNC:37240]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400581","summary":null,"start":19127469,"end":19159176,"strand":1,"description":"GRB2 related adaptor protein like [Source:HGNC Symbol;Acc:HGNC:37240]"}, {"versioned_ensembl_gene_id":"ENSG00000005102.12","gene_symbol":"MEOX1","gene_name":"mesenchyme homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7013]","synonyms":"MOX1","biotype":"protein_coding","ncbi_id":"4222","summary":"This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":43640388,"end":43661954,"strand":-1,"description":"mesenchyme homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7013]"}, {"versioned_ensembl_gene_id":"ENSG00000062370.16","gene_symbol":"ZNF112","gene_name":"zinc finger protein 112 [Source:HGNC Symbol;Acc:HGNC:12892]","synonyms":"ZNF228,ZFP112","biotype":"protein_coding","ncbi_id":"7771","summary":null,"start":44326555,"end":44367217,"strand":-1,"description":"zinc finger protein 112 [Source:HGNC Symbol;Acc:HGNC:12892]"}, {"versioned_ensembl_gene_id":"ENSG00000129673.9","gene_symbol":"AANAT","gene_name":"aralkylamine N-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:19]","synonyms":"SNAT","biotype":"protein_coding","ncbi_id":"15","summary":"The protein encoded by this gene belongs to the acetyltransferase superfamily. It is the penultimate enzyme in melatonin synthesis and controls the night/day rhythm in melatonin production in the vertebrate pineal gland. Melatonin is essential for the function of the circadian clock that influences activity and sleep. This enzyme is regulated by cAMP-dependent phosphorylation that promotes its interaction with 14-3-3 proteins and thus protects the enzyme against proteasomal degradation. This gene may contribute to numerous genetic diseases such as delayed sleep phase syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":76453351,"end":76470117,"strand":1,"description":"aralkylamine N-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:19]"}, {"versioned_ensembl_gene_id":"ENSG00000268994.3","gene_symbol":"FAM236B","gene_name":"family with sequence similarity 236 member B [Source:HGNC Symbol;Acc:HGNC:52640]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132304","summary":null,"start":72781865,"end":72782660,"strand":-1,"description":"family with sequence similarity 236 member B [Source:HGNC Symbol;Acc:HGNC:52640]"}, {"versioned_ensembl_gene_id":"ENSG00000241537.1","gene_symbol":"AC134050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72772539,"end":72773471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187621.14","gene_symbol":"TCL6","gene_name":"T-cell leukemia/lymphoma 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13463]","synonyms":"TNG2,TNG1,TCL6e1","biotype":"processed_transcript","ncbi_id":"27004","summary":null,"start":95650498,"end":95679833,"strand":1,"description":"T-cell leukemia/lymphoma 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13463]"}, {"versioned_ensembl_gene_id":"ENSG00000227217.1","gene_symbol":"AL356276.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157691762,"end":157696459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258661.1","gene_symbol":"AL079303.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36647083,"end":36658801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129250.11","gene_symbol":"KIF1C","gene_name":"kinesin family member 1C [Source:HGNC Symbol;Acc:HGNC:6317]","synonyms":"SPAX2,SAX2,SPG58","biotype":"protein_coding","ncbi_id":"10749","summary":"The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014]","start":4997948,"end":5028401,"strand":1,"description":"kinesin family member 1C [Source:HGNC Symbol;Acc:HGNC:6317]"}, {"versioned_ensembl_gene_id":"ENSG00000227495.1","gene_symbol":"AC004771.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5019214,"end":5020093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258708.1","gene_symbol":"SLC25A21-AS1","gene_name":"SLC25A21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44298]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129794","summary":null,"start":37171888,"end":37173811,"strand":1,"description":"SLC25A21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44298]"}, {"versioned_ensembl_gene_id":"ENSG00000230104.1","gene_symbol":"AC018712.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172674212,"end":172674898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248126.1","gene_symbol":"AC091849.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1598127,"end":1598247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230769.1","gene_symbol":"Z98048.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40788777,"end":40789267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085552.16","gene_symbol":"IGSF9","gene_name":"immunoglobulin superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:18132]","synonyms":"Nrt1,KIAA1355,IGSF9A","biotype":"protein_coding","ncbi_id":"57549","summary":null,"start":159927039,"end":159945604,"strand":-1,"description":"immunoglobulin superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:18132]"}, {"versioned_ensembl_gene_id":"ENSG00000253742.1","gene_symbol":"IGHV3-60","gene_name":"immunoglobulin heavy variable 3-60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5614]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28417","summary":null,"start":106631197,"end":106631653,"strand":-1,"description":"immunoglobulin heavy variable 3-60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5614]"}, {"versioned_ensembl_gene_id":"ENSG00000236783.1","gene_symbol":"RPS15AP27","gene_name":"ribosomal protein S15a pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271613","summary":null,"start":107963703,"end":107964045,"strand":-1,"description":"ribosomal protein S15a pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37011]"}, {"versioned_ensembl_gene_id":"ENSG00000260097.2","gene_symbol":"SPDYE6","gene_name":"speedy/RINGO cell cycle regulator family member E6 [Source:HGNC Symbol;Acc:HGNC:35465]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729597","summary":"This gene encodes a cell cycle regulatory protein which plays an important role in cell cycle progression by binding and activating cyclin-dependent kinases. The encoded protein belongs to a family of cyclin-dependent kinase regulators that contain a speedy box domain which is required for cyclin-dependent kinase activation. [provided by RefSeq, Jul 2017]","start":102347206,"end":102356444,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E6 [Source:HGNC Symbol;Acc:HGNC:35465]"}, {"versioned_ensembl_gene_id":"ENSG00000143951.15","gene_symbol":"WDPCP","gene_name":"WD repeat containing planar cell polarity effector [Source:HGNC Symbol;Acc:HGNC:28027]","synonyms":"hFrtz,fritz,C2orf86,BBS15","biotype":"protein_coding","ncbi_id":"51057","summary":"This gene encodes a cytoplasmic WD40 repeat protein. A similar gene in frogs encodes a planar cell polarity protein that plays a critical role in collective cell movement and ciliogenesis by mediating septin localization. Mutations in this gene are associated with Bardet-Biedl syndrome 15 and may also play a role in Meckel-Gruber syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":63121383,"end":63827843,"strand":-1,"description":"WD repeat containing planar cell polarity effector [Source:HGNC Symbol;Acc:HGNC:28027]"}, {"versioned_ensembl_gene_id":"ENSG00000249693.2","gene_symbol":"THEGL","gene_name":"theg spermatid protein like [Source:HGNC Symbol;Acc:HGNC:43771]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506564","summary":null,"start":56530609,"end":56603507,"strand":1,"description":"theg spermatid protein like [Source:HGNC Symbol;Acc:HGNC:43771]"}, {"versioned_ensembl_gene_id":"ENSG00000253808.1","gene_symbol":"IGHVII-46-1","gene_name":"immunoglobulin heavy variable (II)-46-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5682]","synonyms":"IGHV(II)-46-1","biotype":"IG_V_pseudogene","ncbi_id":"28365","summary":null,"start":106515818,"end":106515854,"strand":-1,"description":"immunoglobulin heavy variable (II)-46-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5682]"}, {"versioned_ensembl_gene_id":"ENSG00000177556.11","gene_symbol":"ATOX1","gene_name":"antioxidant 1 copper chaperone [Source:HGNC Symbol;Acc:HGNC:798]","synonyms":"HAH1","biotype":"protein_coding","ncbi_id":"475","summary":"This gene encodes a copper chaperone that plays a role in copper homeostasis by binding and transporting cytosolic copper to ATPase proteins in the trans-Golgi network for later incorporation to the ceruloplasmin. This protein also functions as an antioxidant against superoxide and hydrogen peroxide, and therefore, may play a significant role in cancer carcinogenesis. Because of its cytogenetic location, this gene represents a candidate gene for 5q-syndrome. [provided by RefSeq, Jul 2008]","start":151742316,"end":151772532,"strand":-1,"description":"antioxidant 1 copper chaperone [Source:HGNC Symbol;Acc:HGNC:798]"}, {"versioned_ensembl_gene_id":"ENSG00000279908.1","gene_symbol":"AC026748.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1383159,"end":1386409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150403.17","gene_symbol":"TMCO3","gene_name":"transmembrane and coiled-coil domains 3 [Source:HGNC Symbol;Acc:HGNC:20329]","synonyms":"FLJ20623,C13orf11","biotype":"protein_coding","ncbi_id":"55002","summary":"This gene encodes a member of the monovalent cation:proton antiporter 2 (CPA2) family of transporter proteins. Members of this family typically couple the export of monovalent cations, such as potassium or sodium, to the import of protons across cellular membranes. Mutations in this gene have been identified in patients with a rare inherited vision defect, cornea guttata with anterior polar cataract. [provided by RefSeq, Mar 2017]","start":113490995,"end":113554590,"strand":1,"description":"transmembrane and coiled-coil domains 3 [Source:HGNC Symbol;Acc:HGNC:20329]"}, {"versioned_ensembl_gene_id":"ENSG00000095321.16","gene_symbol":"CRAT","gene_name":"carnitine O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2342]","synonyms":"CAT1","biotype":"protein_coding","ncbi_id":"1384","summary":"This gene encodes carnitine O-acetyltransferase, a member of the carnitine acyltransferase family and a key metabolic pathway enzyme which plays an important role in energy homeostasis and fat metabolism. This enzyme catalyzes the reversible transfer of acyl groups from an acyl-CoA thioester to carnitine and regulates the ratio of acyl-CoA/CoA. It is found in both the mitochondria and the peroxisome. Alternative splicing results in transcript variants encoding different isoforms that may localize to different subcellular compartments. [provided by RefSeq, Oct 2016]","start":129094810,"end":129111189,"strand":-1,"description":"carnitine O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2342]"}, {"versioned_ensembl_gene_id":"ENSG00000234055.1","gene_symbol":"AL158151.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129097854,"end":129100266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143473.12","gene_symbol":"KCNH1","gene_name":"potassium voltage-gated channel subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:6250]","synonyms":"Kv10.1,h-eag,eag1,eag","biotype":"protein_coding","ncbi_id":"3756","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit of a voltage-gated non-inactivating delayed rectifier potassium channel. It is activated at the onset of myoblast differentiation. The gene is highly expressed in brain and in myoblasts. Overexpression of the gene may confer a growth advantage to cancer cells and favor tumor cell proliferation. Alternative splicing of this gene results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":210676823,"end":211134180,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:6250]"}, {"versioned_ensembl_gene_id":"ENSG00000249400.1","gene_symbol":"HMGB3P17","gene_name":"high mobility group box 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39309]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419948","summary":null,"start":123468781,"end":123469429,"strand":-1,"description":"high mobility group box 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39309]"}, {"versioned_ensembl_gene_id":"ENSG00000255083.2","gene_symbol":"OR5AK1P","gene_name":"olfactory receptor family 5 subfamily AK member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15250]","synonyms":"OR5AK5P","biotype":"unprocessed_pseudogene","ncbi_id":"81230","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57018100,"end":57019021,"strand":1,"description":"olfactory receptor family 5 subfamily AK member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15250]"}, {"versioned_ensembl_gene_id":"ENSG00000229737.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"BPG126D10.10,OTTHUMG00000086663","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577378,"end":29577667,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000255293.1","gene_symbol":"WIZP1","gene_name":"widely interspaced zinc finger motifs pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645598","summary":null,"start":23403805,"end":23406103,"strand":1,"description":"widely interspaced zinc finger motifs pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51696]"}, {"versioned_ensembl_gene_id":"ENSG00000271491.1","gene_symbol":"AC100767.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23370116,"end":23377644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231871.5","gene_symbol":"IPO9-AS1","gene_name":"IPO9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40892]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873949","summary":null,"start":201688259,"end":201829559,"strand":-1,"description":"IPO9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40892]"}, {"versioned_ensembl_gene_id":"ENSG00000241701.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30223924,"end":30315930,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000254768.5","gene_symbol":"AC104009.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22283730,"end":22338245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253915.1","gene_symbol":"AC104371.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135625185,"end":135625981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228547.5","gene_symbol":"OR7E26P","gene_name":"olfactory receptor family 7 subfamily E member 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:8398]","synonyms":"OR912-95,OR7E70P,OR7E69P,OR7E68P,OR7E67P,OR1-73,OR1-72,OR1-51","biotype":"unprocessed_pseudogene","ncbi_id":"401637","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14999050,"end":15000055,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:8398]"}, {"versioned_ensembl_gene_id":"ENSG00000278797.1","gene_symbol":"AC011551.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46533669,"end":46534351,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254203.1","gene_symbol":"IGHVII-33-1","gene_name":"immunoglobulin heavy variable (II)-33-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5678]","synonyms":"IGHV(II)-33-1","biotype":"IG_V_pseudogene","ncbi_id":"28369","summary":null,"start":106367385,"end":106367664,"strand":-1,"description":"immunoglobulin heavy variable (II)-33-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5678]"}, {"versioned_ensembl_gene_id":"ENSG00000211955.2","gene_symbol":"IGHV3-33","gene_name":"immunoglobulin heavy variable 3-33 [Source:HGNC Symbol;Acc:HGNC:5596]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28434","summary":null,"start":106359793,"end":106360324,"strand":-1,"description":"immunoglobulin heavy variable 3-33 [Source:HGNC Symbol;Acc:HGNC:5596]"}, {"versioned_ensembl_gene_id":"ENSG00000270474.2","gene_symbol":"IGHV3-29","gene_name":"immunoglobulin heavy variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5590]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28440","summary":null,"start":106356145,"end":106356591,"strand":-1,"description":"immunoglobulin heavy variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5590]"}, {"versioned_ensembl_gene_id":"ENSG00000233613.5","gene_symbol":"DCUN1D2-AS","gene_name":"DCUN1D2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:39889]","synonyms":"DCUN1D2-AS2","biotype":"antisense_RNA","ncbi_id":"100874229","summary":null,"start":113468901,"end":113476135,"strand":1,"description":"DCUN1D2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:39889]"}, {"versioned_ensembl_gene_id":"ENSG00000224566.2","gene_symbol":"FAM96AP2","gene_name":"family with sequence similarity 96 member A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391174","summary":null,"start":228114997,"end":228115473,"strand":-1,"description":"family with sequence similarity 96 member A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43862]"}, {"versioned_ensembl_gene_id":"ENSG00000249992.1","gene_symbol":"TMEM158","gene_name":"transmembrane protein 158 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:30293]","synonyms":"RIS1,p40BBp","biotype":"protein_coding","ncbi_id":"25907","summary":"Constitutive activation of the Ras pathway triggers an irreversible proliferation arrest reminiscent of replicative senescence. Transcription of this gene is upregulated in response to activation of the Ras pathway, but not under other conditions that induce senescence. The encoded protein is similar to a rat cell surface receptor proposed to function in a neuronal survival pathway. An allelic polymorphism in this gene results in both functional and non-functional (frameshifted) alleles; the reference genome represents the functional allele. [provided by RefSeq, Jul 2015]","start":45224466,"end":45226278,"strand":-1,"description":"transmembrane protein 158 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:30293]"}, {"versioned_ensembl_gene_id":"ENSG00000233314.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30059208,"end":30062832,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000224094.1","gene_symbol":"RPS24P8","gene_name":"ribosomal protein S24 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216336","summary":null,"start":45159774,"end":45160175,"strand":-1,"description":"ribosomal protein S24 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37016]"}, {"versioned_ensembl_gene_id":"ENSG00000257949.6","gene_symbol":"TEN1","gene_name":"TEN1, CST complex subunit [Source:HGNC Symbol;Acc:HGNC:37242]","synonyms":"FLJ39785,C17orf106","biotype":"protein_coding","ncbi_id":"100134934","summary":"C17ORF106, or TEN1, appears to function in a telomere-associated complex with STN1 (OBFC1; MIM 613128) and CTC1 (C17ORF68; MIM 613129) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009]","start":75979220,"end":76000586,"strand":1,"description":"TEN1, CST complex subunit [Source:HGNC Symbol;Acc:HGNC:37242]"}, {"versioned_ensembl_gene_id":"ENSG00000276210.2","gene_symbol":"LINC00226","gene_name":"long intergenic non-protein coding RNA 226 [Source:HGNC Symbol;Acc:HGNC:20168]","synonyms":"C14orf97,NCRNA00226","biotype":"lincRNA","ncbi_id":"338004","summary":null,"start":106287674,"end":106288828,"strand":1,"description":"long intergenic non-protein coding RNA 226 [Source:HGNC Symbol;Acc:HGNC:20168]"}, {"versioned_ensembl_gene_id":"ENSG00000204950.3","gene_symbol":"LRRC10B","gene_name":"leucine rich repeat containing 10B [Source:HGNC Symbol;Acc:HGNC:37215]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390205","summary":null,"start":61508800,"end":61511018,"strand":1,"description":"leucine rich repeat containing 10B [Source:HGNC Symbol;Acc:HGNC:37215]"}, {"versioned_ensembl_gene_id":"ENSG00000204338.8","gene_symbol":"CYP21A1P","gene_name":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]","synonyms":"CYP21A,P450c21A,CYP21P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1590","summary":null,"start":32005636,"end":32008451,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]"}, {"versioned_ensembl_gene_id":"ENSG00000215424.9","gene_symbol":"MCM3AP-AS1","gene_name":"MCM3AP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16417]","synonyms":"NCRNA00031,MCM3APAS,MCM3AP-AS,FLJ10508,C21orf85","biotype":"antisense_RNA","ncbi_id":"114044","summary":null,"start":46229217,"end":46259390,"strand":1,"description":"MCM3AP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16417]"}, {"versioned_ensembl_gene_id":"ENSG00000228137.1","gene_symbol":"AP001469.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46246890,"end":46247682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226984.1","gene_symbol":"AL035410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114459934,"end":114460360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154025.15","gene_symbol":"SLC5A10","gene_name":"solute carrier family 5 member 10 [Source:HGNC Symbol;Acc:HGNC:23155]","synonyms":"SGLT5","biotype":"protein_coding","ncbi_id":"125206","summary":"This gene is a member of the sodium/glucose transporter family. Members of this family are sodium-dependent transporters and can be divided into two subfamilies based on sequence homology, one that co-transports sugars and the second that transports molecules such as ascorbate, choline, iodide, lipoate, monocaroboxylates, and pantothenate. The protein encoded by this gene has the highest affinity for mannose and has been reported to be most highly expressed in the kidney. This protein may function as a kidney-specific, sodium-dependent mannose and fructose co-transporter. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":18950345,"end":19022595,"strand":1,"description":"solute carrier family 5 member 10 [Source:HGNC Symbol;Acc:HGNC:23155]"}, {"versioned_ensembl_gene_id":"ENSG00000230603.1","gene_symbol":"AC011753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109665209,"end":109665742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225975.6","gene_symbol":"LINC01534","gene_name":"long intergenic non-protein coding RNA 1534 [Source:HGNC Symbol;Acc:HGNC:51281]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927621","summary":null,"start":36685440,"end":36687449,"strand":-1,"description":"long intergenic non-protein coding RNA 1534 [Source:HGNC Symbol;Acc:HGNC:51281]"}, {"versioned_ensembl_gene_id":"ENSG00000086758.15","gene_symbol":"HUWE1","gene_name":"HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:30892]","synonyms":"UREB1,KIAA0312,Ib772","biotype":"protein_coding","ncbi_id":"10075","summary":"This gene encodes a protein containing a C-terminal HECT (E6AP type E3 ubiquitin protein ligase) domain that functions as an E3 ubiquitin ligase. The encoded protein is required for the ubiquitination and subsequent degradation of the anti-apoptotic protein Mcl1 (myeloid cell leukemia sequence 1 (BCL2-related)). This protein also ubiquitinates the p53 tumor suppressor, core histones, and DNA polymerase beta. Mutations in this gene are associated with Turner type X-linked syndromic cognitive disability. [provided by RefSeq, Aug 2013]","start":53532096,"end":53686729,"strand":-1,"description":"HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:30892]"}, {"versioned_ensembl_gene_id":"ENSG00000101986.11","gene_symbol":"ABCD1","gene_name":"ATP binding cassette subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:61]","synonyms":"AMN,ALDP,ALD,adrenoleukodystrophy","biotype":"protein_coding","ncbi_id":"215","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system. [provided by RefSeq, Jul 2008]","start":153724868,"end":153744762,"strand":1,"description":"ATP binding cassette subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:61]"}, {"versioned_ensembl_gene_id":"ENSG00000276070.4","gene_symbol":"CCL4L2","gene_name":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9560","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this family member is similar to the chemokine (C-C motif) ligand 4 product, which inhibits HIV entry by binding to the cellular receptor CCR5. The copy number of this gene varies among individuals, where most individuals have one to five copies. This gene copy contains a non-consensus splice acceptor site at the 3' terminal exon found in other highly similar gene copies, and it thus uses other alternative splice sites for the 3' terminal exon, resulting in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":36210924,"end":36212878,"strand":1,"description":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]"}, {"versioned_ensembl_gene_id":"ENSG00000119328.11","gene_symbol":"FAM206A","gene_name":"family with sequence similarity 206 member A [Source:HGNC Symbol;Acc:HGNC:1364]","synonyms":"C9orf6,Simiate,FLJ20457,CG-8","biotype":"protein_coding","ncbi_id":"54942","summary":null,"start":108934181,"end":108950744,"strand":1,"description":"family with sequence similarity 206 member A [Source:HGNC Symbol;Acc:HGNC:1364]"}, {"versioned_ensembl_gene_id":"ENSG00000122861.15","gene_symbol":"PLAU","gene_name":"plasminogen activator, urokinase [Source:HGNC Symbol;Acc:HGNC:9052]","synonyms":"UPA,URK","biotype":"protein_coding","ncbi_id":"5328","summary":"This gene encodes a secreted serine protease that converts plasminogen to plasmin. The encoded preproprotein is proteolytically processed to generate A and B polypeptide chains. These chains associate via a single disulfide bond to form the catalytically inactive high molecular weight urokinase-type plasminogen activator (HMW-uPA). HMW-uPA can be further processed into the catalytically active low molecular weight urokinase-type plasminogen activator (LMW-uPA). This low molecular weight form does not bind to the urokinase-type plasminogen activator receptor. Mutations in this gene may be associated with Quebec platelet disorder and late-onset Alzheimer's disease. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":73909177,"end":73917497,"strand":1,"description":"plasminogen activator, urokinase [Source:HGNC Symbol;Acc:HGNC:9052]"}, {"versioned_ensembl_gene_id":"ENSG00000255428.1","gene_symbol":"AP002008.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":111414242,"end":111418186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250706.1","gene_symbol":"AC079340.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152146385,"end":152178573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274572.1","gene_symbol":"ZYXP1","gene_name":"zyxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51695]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480342","summary":null,"start":137424904,"end":137425021,"strand":-1,"description":"zyxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51695]"}, {"versioned_ensembl_gene_id":"ENSG00000253879.1","gene_symbol":"AC087664.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59601378,"end":59613775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204152.10","gene_symbol":"TIMM23B","gene_name":"translocase of inner mitochondrial membrane 23 homolog B [Source:HGNC Symbol;Acc:HGNC:23581]","synonyms":"bA592B15.7","biotype":"protein_coding","ncbi_id":"100652748","summary":null,"start":49942033,"end":49974850,"strand":1,"description":"translocase of inner mitochondrial membrane 23 homolog B [Source:HGNC Symbol;Acc:HGNC:23581]"}, {"versioned_ensembl_gene_id":"ENSG00000253883.1","gene_symbol":"IGHV3-19","gene_name":"immunoglobulin heavy variable 3-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5584]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28446","summary":null,"start":106196700,"end":106196990,"strand":-1,"description":"immunoglobulin heavy variable 3-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5584]"}, {"versioned_ensembl_gene_id":"ENSG00000211945.2","gene_symbol":"IGHV1-18","gene_name":"immunoglobulin heavy variable 1-18 [Source:HGNC Symbol;Acc:HGNC:5549]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28468","summary":null,"start":106184901,"end":106185394,"strand":-1,"description":"immunoglobulin heavy variable 1-18 [Source:HGNC Symbol;Acc:HGNC:5549]"}, {"versioned_ensembl_gene_id":"ENSG00000148343.18","gene_symbol":"MIGA2","gene_name":"mitoguardin 2 [Source:HGNC Symbol;Acc:HGNC:23621]","synonyms":"FLJ14596,FLJ00199,FAM73B,C9orf54","biotype":"protein_coding","ncbi_id":"84895","summary":null,"start":129036621,"end":129072082,"strand":1,"description":"mitoguardin 2 [Source:HGNC Symbol;Acc:HGNC:23621]"}, {"versioned_ensembl_gene_id":"ENSG00000235594.1","gene_symbol":"AL139824.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56267872,"end":56269231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242706.2","gene_symbol":"RPS27AP9","gene_name":"ribosomal protein S27a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271376","summary":null,"start":80498534,"end":80498971,"strand":-1,"description":"ribosomal protein S27a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35630]"}, {"versioned_ensembl_gene_id":"ENSG00000226389.3","gene_symbol":"MAPK6PS6","gene_name":"mitogen-activated protein kinase 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18978]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"282967","summary":null,"start":49771841,"end":49773299,"strand":1,"description":"mitogen-activated protein kinase 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18978]"}, {"versioned_ensembl_gene_id":"ENSG00000204856.11","gene_symbol":"FAM216A","gene_name":"family with sequence similarity 216 member A [Source:HGNC Symbol;Acc:HGNC:30180]","synonyms":"HSU79274,C12orf24","biotype":"protein_coding","ncbi_id":"29902","summary":null,"start":110468364,"end":110490385,"strand":1,"description":"family with sequence similarity 216 member A [Source:HGNC Symbol;Acc:HGNC:30180]"}, {"versioned_ensembl_gene_id":"ENSG00000103365.15","gene_symbol":"GGA2","gene_name":"golgi associated, gamma adaptin ear containing, ARF binding protein 2 [Source:HGNC Symbol;Acc:HGNC:16064]","synonyms":"VEAR,KIAA1080","biotype":"protein_coding","ncbi_id":"23062","summary":"This gene encodes a member of the Golgi-localized, gamma adaptin ear-containing, ARF-binding (GGA) family. This family includes ubiquitous coat proteins that regulate the trafficking of proteins between the trans-Golgi network and the lysosome. These proteins share an amino-terminal VHS domain which mediates sorting of the mannose 6-phosphate receptors at the trans-Golgi network. They also contain a carboxy-terminal region with homology to the ear domain of gamma-adaptins. This family member may play a significant role in cargo molecules regulation and clathrin-coated vesicle assembly. [provided by RefSeq, Jul 2008]","start":23463542,"end":23521995,"strand":-1,"description":"golgi associated, gamma adaptin ear containing, ARF binding protein 2 [Source:HGNC Symbol;Acc:HGNC:16064]"}, {"versioned_ensembl_gene_id":"ENSG00000197444.9","gene_symbol":"OGDHL","gene_name":"oxoglutarate dehydrogenase like [Source:HGNC Symbol;Acc:HGNC:25590]","synonyms":"FLJ10851","biotype":"protein_coding","ncbi_id":"55753","summary":"The protein encoded by this gene is similar to oxoglutarate dehydrogenase (OGDH) of the OGDH complex, which degrades glucose and glutamate. This gene encodes several isoforms, including some that appear to localize to mitochondria. The encoded protein down-regulates the AKT signaling cascade and can suppress the growth of cervical cancer cells. [provided by RefSeq, Dec 2016]","start":49734643,"end":49762379,"strand":-1,"description":"oxoglutarate dehydrogenase like [Source:HGNC Symbol;Acc:HGNC:25590]"}, {"versioned_ensembl_gene_id":"ENSG00000270890.1","gene_symbol":"AL049844.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143858062,"end":143858689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229529.7","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"HLA-75,dJ377H14.4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29788968,"end":29795307,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000274259.2","gene_symbol":"AL662799.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33437363,"end":33454453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099869.7","gene_symbol":"IGF2-AS","gene_name":"IGF2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:14062]","synonyms":"PEG8,IGF2AS,IGF2-AS1","biotype":"antisense_RNA","ncbi_id":"51214","summary":"This gene is expressed in antisense to the insulin-like growth factor 2 (IGF2) gene and is imprinted and paternally expressed. It is thought to be non-coding because the putative protein is not conserved and translation is predicted to trigger nonsense mediated decay (NMD). Transcripts from this gene are produced in tumors and may function to suppress cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":2140501,"end":2148666,"strand":1,"description":"IGF2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:14062]"}, {"versioned_ensembl_gene_id":"ENSG00000251627.1","gene_symbol":"AC010395.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110983563,"end":110984466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110245.11","gene_symbol":"APOC3","gene_name":"apolipoprotein C3 [Source:HGNC Symbol;Acc:HGNC:610]","synonyms":null,"biotype":"protein_coding","ncbi_id":"345","summary":"This gene encodes a protein component of triglyceride (TG)-rich lipoproteins (TRLs) including very low density lipoproteins (VLDL), high density lipoproteins (HDL) and chylomicrons. The encoded protein plays a role in role in the metabolism of these TRLs through multiple modes. This protein has been shown to promote the secretion of VLDL1, inhibit lipoprotein lipase enzyme activity, and delay catabolism of TRL remnants. Mutations in this gene are associated with low plasma triglyceride levels and reduced risk of ischemic cardiovascular disease, and hyperalphalipoproteinemia, which is characterized by elevated levels of high density lipoprotein (HDL) and HDL cholesterol in human patients. This gene and other related genes comprise an apolipoprotein gene cluster on chromosome 11. [provided by RefSeq, Sep 2017]","start":116829706,"end":116833072,"strand":1,"description":"apolipoprotein C3 [Source:HGNC Symbol;Acc:HGNC:610]"}, {"versioned_ensembl_gene_id":"ENSG00000256725.1","gene_symbol":"AC095350.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130628316,"end":130716281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226605.1","gene_symbol":"AC092567.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62826064,"end":62858438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224583.1","gene_symbol":"AL356277.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74642384,"end":74652002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248449.2","gene_symbol":"PCDHGB8P","gene_name":"protocadherin gamma subfamily B, 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8715]","synonyms":"PCDH-PSI3","biotype":"transcribed_unitary_pseudogene","ncbi_id":"56120","summary":null,"start":141426286,"end":141429158,"strand":1,"description":"protocadherin gamma subfamily B, 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8715]"}, {"versioned_ensembl_gene_id":"ENSG00000259964.6","gene_symbol":"THSD4-AS1","gene_name":"THSD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51420]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929196","summary":null,"start":71147650,"end":71189042,"strand":-1,"description":"THSD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51420]"}, {"versioned_ensembl_gene_id":"ENSG00000177369.8","gene_symbol":"FLJ40194","gene_name":"uncharacterized FLJ40194 [Source:NCBI gene;Acc:124871]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"124871","summary":null,"start":49248239,"end":49258662,"strand":1,"description":"uncharacterized FLJ40194 [Source:NCBI gene;Acc:124871]"}, {"versioned_ensembl_gene_id":"ENSG00000132591.11","gene_symbol":"ERAL1","gene_name":"Era like 12S mitochondrial rRNA chaperone 1 [Source:HGNC Symbol;Acc:HGNC:3424]","synonyms":"HERA-B","biotype":"protein_coding","ncbi_id":"26284","summary":"The protein encoded by this gene is a GTPase that localizes to the mitochondrion. The encoded protein binds to the 3' terminal stem loop of 12S mitochondrial rRNA and is required for proper assembly of the 28S small mitochondrial ribosomal subunit. Deletion of this gene has been shown to cause mitochondrial dysfunction, growth retardation, and apoptosis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":28854938,"end":28861067,"strand":1,"description":"Era like 12S mitochondrial rRNA chaperone 1 [Source:HGNC Symbol;Acc:HGNC:3424]"}, {"versioned_ensembl_gene_id":"ENSG00000243063.1","gene_symbol":"IGKV3-7","gene_name":"immunoglobulin kappa variable 3-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5821]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28915","summary":null,"start":88978468,"end":88979081,"strand":-1,"description":"immunoglobulin kappa variable 3-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5821]"}, {"versioned_ensembl_gene_id":"ENSG00000240350.2","gene_symbol":"AC017002.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111491273,"end":111570974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269288.1","gene_symbol":"AC092070.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53240675,"end":53241913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229118.1","gene_symbol":"AC068491.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111265283,"end":111279880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181616.9","gene_symbol":"OR52H1","gene_name":"olfactory receptor family 52 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15218]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390067","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5544489,"end":5548533,"strand":-1,"description":"olfactory receptor family 52 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15218]"}, {"versioned_ensembl_gene_id":"ENSG00000177283.7","gene_symbol":"FZD8","gene_name":"frizzled class receptor 8 [Source:HGNC Symbol;Acc:HGNC:4046]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8325","summary":"This intronless gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. This gene is highly expressed in two human cancer cell lines, indicating that it may play a role in several types of cancer. The crystal structure of the extracellular cysteine-rich domain of a similar mouse protein has been determined. [provided by RefSeq, Jul 2008]","start":35638249,"end":35642278,"strand":-1,"description":"frizzled class receptor 8 [Source:HGNC Symbol;Acc:HGNC:4046]"}, {"versioned_ensembl_gene_id":"ENSG00000183723.12","gene_symbol":"CMTM4","gene_name":"CKLF like MARVEL transmembrane domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19175]","synonyms":"CKLFSF4","biotype":"protein_coding","ncbi_id":"146223","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 16. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":66614750,"end":66696707,"strand":-1,"description":"CKLF like MARVEL transmembrane domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19175]"}, {"versioned_ensembl_gene_id":"ENSG00000198398.2","gene_symbol":"TMEM207","gene_name":"transmembrane protein 207 [Source:HGNC Symbol;Acc:HGNC:33705]","synonyms":null,"biotype":"protein_coding","ncbi_id":"131920","summary":null,"start":190428655,"end":190449876,"strand":-1,"description":"transmembrane protein 207 [Source:HGNC Symbol;Acc:HGNC:33705]"}, {"versioned_ensembl_gene_id":"ENSG00000248553.1","gene_symbol":"OR52H2P","gene_name":"olfactory receptor family 52 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15219]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"81261","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5551662,"end":5552563,"strand":-1,"description":"olfactory receptor family 52 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15219]"}, {"versioned_ensembl_gene_id":"ENSG00000269001.2","gene_symbol":"AC092070.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53197111,"end":53214522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161558.10","gene_symbol":"TMEM143","gene_name":"transmembrane protein 143 [Source:HGNC Symbol;Acc:HGNC:25603]","synonyms":"FLJ10922","biotype":"protein_coding","ncbi_id":"55260","summary":null,"start":48332356,"end":48364237,"strand":-1,"description":"transmembrane protein 143 [Source:HGNC Symbol;Acc:HGNC:25603]"}, {"versioned_ensembl_gene_id":"ENSG00000160182.2","gene_symbol":"TFF1","gene_name":"trefoil factor 1 [Source:HGNC Symbol;Acc:HGNC:11755]","synonyms":"pS2,pNR-2,HPS2,HP1.A,D21S21,BCEI","biotype":"protein_coding","ncbi_id":"7031","summary":"Members of the trefoil family are characterized by having at least one copy of the trefoil motif, a 40-amino acid domain that contains three conserved disulfides. They are stable secretory proteins expressed in gastrointestinal mucosa. Their functions are not defined, but they may protect the mucosa from insults, stabilize the mucus layer, and affect healing of the epithelium. This gene, which is expressed in the gastric mucosa, has also been studied because of its expression in human tumors. This gene and two other related trefoil family member genes are found in a cluster on chromosome 21. [provided by RefSeq, Jul 2008]","start":42362282,"end":42366594,"strand":-1,"description":"trefoil factor 1 [Source:HGNC Symbol;Acc:HGNC:11755]"}, {"versioned_ensembl_gene_id":"ENSG00000205038.11","gene_symbol":"PKHD1L1","gene_name":"PKHD1 like 1 [Source:HGNC Symbol;Acc:HGNC:20313]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93035","summary":null,"start":109362477,"end":109530330,"strand":1,"description":"PKHD1 like 1 [Source:HGNC Symbol;Acc:HGNC:20313]"}, {"versioned_ensembl_gene_id":"ENSG00000187483.9","gene_symbol":"SERPINA13P","gene_name":"serpin family A member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:30909]","synonyms":"UNQ6121,SERPINA13","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388007","summary":null,"start":94640725,"end":94646994,"strand":1,"description":"serpin family A member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:30909]"}, {"versioned_ensembl_gene_id":"ENSG00000258805.1","gene_symbol":"ADIPOR1P2","gene_name":"adiponectin receptor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44911]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390503","summary":null,"start":94633705,"end":94634524,"strand":1,"description":"adiponectin receptor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44911]"}, {"versioned_ensembl_gene_id":"ENSG00000248569.1","gene_symbol":"AC026410.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80351021,"end":80351956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227087.4","gene_symbol":"RBMX2P5","gene_name":"RNA binding motif protein, X-linked 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39927]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391804","summary":null,"start":80331573,"end":80332541,"strand":-1,"description":"RNA binding motif protein, X-linked 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39927]"}, {"versioned_ensembl_gene_id":"ENSG00000283251.1","gene_symbol":"AC008687.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49056088,"end":49058761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268108.1","gene_symbol":"AC008687.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49060613,"end":49061132,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247373.3","gene_symbol":"AC055713.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123575891,"end":123585115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267091.1","gene_symbol":"CTBP2P7","gene_name":"C-terminal binding protein 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45199]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401914","summary":null,"start":36496916,"end":36498159,"strand":-1,"description":"C-terminal binding protein 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45199]"}, {"versioned_ensembl_gene_id":"ENSG00000265474.1","gene_symbol":"AC010761.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28745569,"end":28747652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265840.1","gene_symbol":"AC010761.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28749731,"end":28750079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275688.4","gene_symbol":"CCL15-CCL14","gene_name":"CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]","synonyms":null,"biotype":"protein_coding","ncbi_id":"348249","summary":"A cluster of CC chemokine genes exists on chromosome 17q11.2. The CC chemokines are secreted proteins characterized by two adjacent cysteines. The genes chemokine (C-C motif) ligand 14 and chemokine (C-C motif) ligand 15 are adjacent loci and express read-through transcripts spanning both loci. The read-through transcripts were originally interpreted as bicistronic transcripts, but they are represented as non-coding because they are candidates for nonsense-mediated mRNA decay (NMD). [provided by RefSeq, Dec 2009]","start":35983656,"end":36001621,"strand":-1,"description":"CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]"}, {"versioned_ensembl_gene_id":"ENSG00000278079.6","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816470,"end":54830813,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000230484.2","gene_symbol":"OR51A10P","gene_name":"olfactory receptor family 51 subfamily A member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:15185]","synonyms":"OR51A13,OR51A11P","biotype":"unitary_pseudogene","ncbi_id":"81295","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5468486,"end":5469422,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:15185]"}, {"versioned_ensembl_gene_id":"ENSG00000113790.10","gene_symbol":"EHHADH","gene_name":"enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3247]","synonyms":"ECHD","biotype":"protein_coding","ncbi_id":"1962","summary":"The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":185190624,"end":185281990,"strand":-1,"description":"enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3247]"}, {"versioned_ensembl_gene_id":"ENSG00000076604.14","gene_symbol":"TRAF4","gene_name":"TNF receptor associated factor 4 [Source:HGNC Symbol;Acc:HGNC:12034]","synonyms":"CART1,RNF83,MLN62","biotype":"protein_coding","ncbi_id":"9618","summary":"This gene encodes a member of the TNF receptor associated factor (TRAF) family. TRAF proteins are associated with, and mediate signal transduction from members of the TNF receptor superfamily. The encoded protein has been shown to interact with neurotrophin receptor, p75 (NTR/NTSR1), and negatively regulate NTR induced cell death and NF-kappa B activation. This protein has been found to bind to p47phox, a cytosolic regulatory factor included in a multi-protein complex known as NAD(P)H oxidase. This protein thus, is thought to be involved in the oxidative activation of MAPK8/JNK. Alternatively spliced transcript variants have been observed but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]","start":28743984,"end":28750958,"strand":1,"description":"TNF receptor associated factor 4 [Source:HGNC Symbol;Acc:HGNC:12034]"}, {"versioned_ensembl_gene_id":"ENSG00000109787.12","gene_symbol":"KLF3","gene_name":"Kruppel like factor 3 [Source:HGNC Symbol;Acc:HGNC:16516]","synonyms":"BKLF","biotype":"protein_coding","ncbi_id":"51274","summary":null,"start":38664196,"end":38701042,"strand":1,"description":"Kruppel like factor 3 [Source:HGNC Symbol;Acc:HGNC:16516]"}, {"versioned_ensembl_gene_id":"ENSG00000144451.18","gene_symbol":"SPAG16","gene_name":"sperm associated antigen 16 [Source:HGNC Symbol;Acc:HGNC:23225]","synonyms":"WDR29,PF20,FLJ22724,DKFZp666P1710","biotype":"protein_coding","ncbi_id":"79582","summary":"Cilia and flagella are comprised of a microtubular backbone, the axoneme, which is organized by the basal body and surrounded by plasma membrane. SPAG16 encodes 2 major proteins that associate with the axoneme of sperm tail and the nucleus of postmeiotic germ cells, respectively (Zhang et al., 2007 [PubMed 17699735]).[supplied by OMIM, Jul 2008]","start":213284379,"end":214410501,"strand":1,"description":"sperm associated antigen 16 [Source:HGNC Symbol;Acc:HGNC:23225]"}, {"versioned_ensembl_gene_id":"ENSG00000213917.2","gene_symbol":"RPL5P8","gene_name":"ribosomal protein L5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36290]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130523","summary":null,"start":214280638,"end":214281452,"strand":-1,"description":"ribosomal protein L5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36290]"}, {"versioned_ensembl_gene_id":"ENSG00000187068.2","gene_symbol":"C3orf70","gene_name":"chromosome 3 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:33731]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285382","summary":null,"start":185078050,"end":185153014,"strand":-1,"description":"chromosome 3 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:33731]"}, {"versioned_ensembl_gene_id":"ENSG00000232849.1","gene_symbol":"LINC00363","gene_name":"long intergenic non-protein coding RNA 363 [Source:HGNC Symbol;Acc:HGNC:42684]","synonyms":"TCONS_00021586","biotype":"lincRNA","ncbi_id":"104326053","summary":null,"start":93056657,"end":93057926,"strand":1,"description":"long intergenic non-protein coding RNA 363 [Source:HGNC Symbol;Acc:HGNC:42684]"}, {"versioned_ensembl_gene_id":"ENSG00000267099.1","gene_symbol":"NTF6G","gene_name":"neurotrophin 6 gamma (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8027]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"4912","summary":null,"start":49029726,"end":49030341,"strand":1,"description":"neurotrophin 6 gamma (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8027]"}, {"versioned_ensembl_gene_id":"ENSG00000168214.20","gene_symbol":"RBPJ","gene_name":"recombination signal binding protein for immunoglobulin kappa J region [Source:HGNC Symbol;Acc:HGNC:5724]","synonyms":"SUH,RBPSUH,RBPJK,RBP-J,KBF2,IGKJRB1,IGKJRB,CBF1","biotype":"protein_coding","ncbi_id":"3516","summary":"The protein encoded by this gene is a transcriptional regulator important in the Notch signaling pathway. The encoded protein acts as a repressor when not bound to Notch proteins and an activator when bound to Notch proteins. It is thought to function by recruiting chromatin remodeling complexes containing histone deacetylase or histone acetylase proteins to Notch signaling pathway genes. Several transcript variants encoding different isoforms have been found for this gene, and several pseudogenes of this gene exist on chromosome 9. [provided by RefSeq, Oct 2013]","start":26163455,"end":26435131,"strand":1,"description":"recombination signal binding protein for immunoglobulin kappa J region [Source:HGNC Symbol;Acc:HGNC:5724]"}, {"versioned_ensembl_gene_id":"ENSG00000186017.14","gene_symbol":"ZNF566","gene_name":"zinc finger protein 566 [Source:HGNC Symbol;Acc:HGNC:25919]","synonyms":"MGC12515,FLJ14779","biotype":"protein_coding","ncbi_id":"84924","summary":null,"start":36445119,"end":36489902,"strand":-1,"description":"zinc finger protein 566 [Source:HGNC Symbol;Acc:HGNC:25919]"}, {"versioned_ensembl_gene_id":"ENSG00000233607.1","gene_symbol":"LINC01392","gene_name":"long intergenic non-protein coding RNA 1392 [Source:HGNC Symbol;Acc:HGNC:50668]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355291","summary":null,"start":115061537,"end":115231355,"strand":-1,"description":"long intergenic non-protein coding RNA 1392 [Source:HGNC Symbol;Acc:HGNC:50668]"}, {"versioned_ensembl_gene_id":"ENSG00000277748.1","gene_symbol":"AC006262.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46249394,"end":46250163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184293.7","gene_symbol":"CLECL1","gene_name":"C-type lectin like 1 [Source:HGNC Symbol;Acc:HGNC:24462]","synonyms":"DCAL1","biotype":"protein_coding","ncbi_id":"160365","summary":"This gene encodes a type II transmembrane, C-type lectin-like protein that is highly expressed on dendritic and B cells. This protein may act as a T-cell costimulatory molecule that enhances interleukin-4 production, and maybe involved in the regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":9715860,"end":9733299,"strand":-1,"description":"C-type lectin like 1 [Source:HGNC Symbol;Acc:HGNC:24462]"}, {"versioned_ensembl_gene_id":"ENSG00000232174.3","gene_symbol":"AC113340.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138620329,"end":138620964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105393.15","gene_symbol":"BABAM1","gene_name":"BRISC and BRCA1 A complex member 1 [Source:HGNC Symbol;Acc:HGNC:25008]","synonyms":"NBA1,MERIT40,HSPC142,FLJ20571,C19orf62","biotype":"protein_coding","ncbi_id":"29086","summary":null,"start":17267350,"end":17281249,"strand":1,"description":"BRISC and BRCA1 A complex member 1 [Source:HGNC Symbol;Acc:HGNC:25008]"}, {"versioned_ensembl_gene_id":"ENSG00000124172.9","gene_symbol":"ATP5E","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit [Source:HGNC Symbol;Acc:HGNC:838]","synonyms":null,"biotype":"protein_coding","ncbi_id":"514","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the epsilon subunit of the catalytic core. Two pseudogenes of this gene are located on chromosomes 4 and 13. Read-through transcripts that include exons from this gene are expressed from the upstream gene SLMO2.[provided by RefSeq, Mar 2011]","start":59025467,"end":59032382,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit [Source:HGNC Symbol;Acc:HGNC:838]"}, {"versioned_ensembl_gene_id":"ENSG00000005812.10","gene_symbol":"FBXL3","gene_name":"F-box and leucine rich repeat protein 3 [Source:HGNC Symbol;Acc:HGNC:13599]","synonyms":"FBXL3A,FBL3A,FBL3","biotype":"protein_coding","ncbi_id":"26224","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains several tandem leucine-rich repeats and is localized in the nucleus. [provided by RefSeq, Jul 2008]","start":76992598,"end":77027195,"strand":-1,"description":"F-box and leucine rich repeat protein 3 [Source:HGNC Symbol;Acc:HGNC:13599]"}, {"versioned_ensembl_gene_id":"ENSG00000095906.16","gene_symbol":"NUBP2","gene_name":"nucleotide binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8042]","synonyms":"CFD1","biotype":"protein_coding","ncbi_id":"10101","summary":"This gene encodes an adenosine triphosphate (ATP) and metal-binding protein that is required for the assembly of cyotosolic iron-sulfur proteins. The encoded protein functions in a heterotetramer with nucleotide-binding protein 1 (NUBP1). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2013]","start":1782901,"end":1789191,"strand":1,"description":"nucleotide binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8042]"}, {"versioned_ensembl_gene_id":"ENSG00000165650.11","gene_symbol":"PDZD8","gene_name":"PDZ domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26974]","synonyms":"PDZK8,FLJ34427,bA129M16.2","biotype":"protein_coding","ncbi_id":"118987","summary":null,"start":117277274,"end":117375467,"strand":-1,"description":"PDZ domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26974]"}, {"versioned_ensembl_gene_id":"ENSG00000065371.17","gene_symbol":"ROPN1","gene_name":"rhophilin associated tail protein 1 [Source:HGNC Symbol;Acc:HGNC:17692]","synonyms":"ropporin,ROPN1A,ODF6,CT91","biotype":"protein_coding","ncbi_id":"54763","summary":"The protein encoded by this gene is found in the fibrous sheath of spermatazoa, where it interacts with rhophilin, a Rho GTPase binding protein. The encoded protein also can bind an A-kinase anchoring protein (AKAP110) and a calcium-binding tyrosine phosphorylation-regulated protein (CABYR). This protein may be involved in sperm motility and has been shown to be a cancer-testis antigen in hematologic malignancies. Several transcript variants, some protein-coding and some non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]","start":123968521,"end":123992178,"strand":-1,"description":"rhophilin associated tail protein 1 [Source:HGNC Symbol;Acc:HGNC:17692]"}, {"versioned_ensembl_gene_id":"ENSG00000264595.1","gene_symbol":"AC103808.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76227990,"end":76233387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229988.1","gene_symbol":"HBBP1","gene_name":"hemoglobin subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4828]","synonyms":"HBHP,HBH1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3044","summary":null,"start":5241954,"end":5243537,"strand":-1,"description":"hemoglobin subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4828]"}, {"versioned_ensembl_gene_id":"ENSG00000268964.1","gene_symbol":"ERVV-2","gene_name":"endogenous retrovirus group V member 2, envelope [Source:HGNC Symbol;Acc:HGNC:39051]","synonyms":"ENVV2","biotype":"protein_coding","ncbi_id":"100271846","summary":"Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of an HERV provirus on human chromosome 19 that has inactivating mutations in the gag and pol genes. This envelope glycoprotein gene appears to have been selectively preserved. The gene's protein product is expressed in the placenta and acts as a syncytin in Old World monkeys, but has lost the fusogenic activity in humans and other primate lineages. [provided by RefSeq, Jun 2015]","start":53044738,"end":53051076,"strand":1,"description":"endogenous retrovirus group V member 2, envelope [Source:HGNC Symbol;Acc:HGNC:39051]"}, {"versioned_ensembl_gene_id":"ENSG00000264444.1","gene_symbol":"AC096708.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68866517,"end":68867028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267757.4","gene_symbol":"EML2-AS1","gene_name":"EML2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48331]","synonyms":"C19orf83","biotype":"processed_transcript","ncbi_id":"100287177","summary":null,"start":45641494,"end":45642840,"strand":1,"description":"EML2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48331]"}, {"versioned_ensembl_gene_id":"ENSG00000273485.1","gene_symbol":"AL139339.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103450196,"end":103450852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269480.1","gene_symbol":"AC020913.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17207138,"end":17208010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226115.1","gene_symbol":"AP001476.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46056516,"end":46057567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242866.9","gene_symbol":"STRC","gene_name":"stereocilin [Source:HGNC Symbol;Acc:HGNC:16035]","synonyms":"DFNB16","biotype":"protein_coding","ncbi_id":"161497","summary":"This gene encodes a protein that is associated with the hair bundle of the sensory hair cells in the inner ear. The hair bundle is composed of stiff microvilli called stereocilia and is involved with mechanoreception of sound waves. This gene is part of a tandem duplication on chromosome 15; the second copy is a pseudogene. Mutations in this gene cause autosomal recessive non-syndromic deafness. [provided by RefSeq, Jul 2008]","start":43599398,"end":43618800,"strand":-1,"description":"stereocilin [Source:HGNC Symbol;Acc:HGNC:16035]"}, {"versioned_ensembl_gene_id":"ENSG00000125788.5","gene_symbol":"DEFB126","gene_name":"defensin beta 126 [Source:HGNC Symbol;Acc:HGNC:15900]","synonyms":"DEFB-26,C20orf8,bA530N10.1","biotype":"protein_coding","ncbi_id":"81623","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. The encoded protein is highly similar to an epididymal-specific secretory protein (ESP13.2) from cynomolgus monkey. Mutation of this gene is associated with impaired sperm function. [provided by RefSeq, Nov 2014]","start":142369,"end":145751,"strand":1,"description":"defensin beta 126 [Source:HGNC Symbol;Acc:HGNC:15900]"}, {"versioned_ensembl_gene_id":"ENSG00000253326.2","gene_symbol":"AL606534.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":243054861,"end":243056394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215800.2","gene_symbol":"RSL24D1P4","gene_name":"ribosomal L24 domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37884]","synonyms":"RSL24D1P19","biotype":"processed_pseudogene","ncbi_id":"391183","summary":null,"start":242772620,"end":242773103,"strand":1,"description":"ribosomal L24 domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37884]"}, {"versioned_ensembl_gene_id":"ENSG00000234484.1","gene_symbol":"AL032821.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132752675,"end":132753951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227000.2","gene_symbol":"HSPD1P14","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35143]","synonyms":"HSPD1-17P","biotype":"processed_pseudogene","ncbi_id":"100287140","summary":null,"start":33838523,"end":33840140,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35143]"}, {"versioned_ensembl_gene_id":"ENSG00000258584.1","gene_symbol":"FAM181A-AS1","gene_name":"FAM181A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20133]","synonyms":"C14orf86","biotype":"antisense_RNA","ncbi_id":"283592","summary":null,"start":93904730,"end":93927066,"strand":-1,"description":"FAM181A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20133]"}, {"versioned_ensembl_gene_id":"ENSG00000259792.1","gene_symbol":"AC104758.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77993405,"end":77995289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231859.1","gene_symbol":"AC079781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97906429,"end":97906822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258872.2","gene_symbol":"FDPSP3","gene_name":"farnesyl diphosphate synthase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3634]","synonyms":"FPSL3,FDPSL3","biotype":"transcribed_processed_pseudogene","ncbi_id":"2227","summary":null,"start":54884849,"end":54886213,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3634]"}, {"versioned_ensembl_gene_id":"ENSG00000231543.9","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31879966,"end":31927861,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000267405.1","gene_symbol":"AC005180.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44794747,"end":44797783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177234.7","gene_symbol":"LINC01561","gene_name":"long intergenic non-protein coding RNA 1561 [Source:HGNC Symbol;Acc:HGNC:31365]","synonyms":"FLJ37402,Em:AC023282.2,C10orf85","biotype":"lincRNA","ncbi_id":"404216","summary":null,"start":120597949,"end":120600124,"strand":1,"description":"long intergenic non-protein coding RNA 1561 [Source:HGNC Symbol;Acc:HGNC:31365]"}, {"versioned_ensembl_gene_id":"ENSG00000267505.1","gene_symbol":"AC005180.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44793199,"end":44794474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100351.16","gene_symbol":"GRAP2","gene_name":"GRB2-related adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:4563]","synonyms":"Mona,Grf40,GrbX,GRBLG,GADS","biotype":"protein_coding","ncbi_id":"9402","summary":"This gene encodes a member of the GRB2/Sem5/Drk family. This member is an adaptor-like protein involved in leukocyte-specific protein-tyrosine kinase signaling. Like its related family member, GRB2-related adaptor protein (GRAP), this protein contains an SH2 domain flanked by two SH3 domains. This protein interacts with other proteins, such as GRB2-associated binding protein 1 (GAB1) and the SLP-76 leukocyte protein (LCP2), through its SH3 domains. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":39901082,"end":39973721,"strand":1,"description":"GRB2-related adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:4563]"}, {"versioned_ensembl_gene_id":"ENSG00000049883.14","gene_symbol":"PTCD2","gene_name":"pentatricopeptide repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:25734]","synonyms":"FLJ12598","biotype":"protein_coding","ncbi_id":"79810","summary":null,"start":72320367,"end":72368395,"strand":1,"description":"pentatricopeptide repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:25734]"}, {"versioned_ensembl_gene_id":"ENSG00000268734.1","gene_symbol":"AC245128.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54890673,"end":54891420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226533.1","gene_symbol":"BTBD9-AS1","gene_name":"BTBD9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40959]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929425","summary":null,"start":38481692,"end":38482531,"strand":1,"description":"BTBD9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40959]"}, {"versioned_ensembl_gene_id":"ENSG00000171451.13","gene_symbol":"DSEL","gene_name":"dermatan sulfate epimerase-like [Source:HGNC Symbol;Acc:HGNC:18144]","synonyms":"FLJ11477,DE-epi2,C18orf4,NCAG1","biotype":"protein_coding","ncbi_id":"92126","summary":null,"start":67506582,"end":67516980,"strand":-1,"description":"dermatan sulfate epimerase-like [Source:HGNC Symbol;Acc:HGNC:18144]"}, {"versioned_ensembl_gene_id":"ENSG00000265533.1","gene_symbol":"AC114689.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67516546,"end":67899619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224446.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529354,"end":29533502,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000230791.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31576870,"end":31579655,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000173966.7","gene_symbol":"AC095040.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53575713,"end":53576387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177051.5","gene_symbol":"FBXO46","gene_name":"F-box protein 46 [Source:HGNC Symbol;Acc:HGNC:25069]","synonyms":"FBXO34L,Fbx46,20D7-FC4","biotype":"protein_coding","ncbi_id":"23403","summary":"Members of the F-box protein family, such as FBXO46, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":45710629,"end":45730904,"strand":-1,"description":"F-box protein 46 [Source:HGNC Symbol;Acc:HGNC:25069]"}, {"versioned_ensembl_gene_id":"ENSG00000266707.1","gene_symbol":"AC006120.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66197693,"end":66198238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164400.5","gene_symbol":"CSF2","gene_name":"colony stimulating factor 2 [Source:HGNC Symbol;Acc:HGNC:2434]","synonyms":"GMCSF,GM-CSF","biotype":"protein_coding","ncbi_id":"1437","summary":"The protein encoded by this gene is a cytokine that controls the production, differentiation, and function of granulocytes and macrophages. The active form of the protein is found extracellularly as a homodimer. This gene has been localized to a cluster of related genes at chromosome region 5q31, which is known to be associated with interstitial deletions in the 5q- syndrome and acute myelogenous leukemia. Other genes in the cluster include those encoding interleukins 4, 5, and 13. This gene plays a role in promoting tissue inflammation. Elevated levels of cytokines, including the one produced by this gene, have been detected in SARS-CoV-2 infected patients that develop acute respiratory distress syndrome. Mice deficient in this gene or its receptor develop pulmonary alveolar proteinosis. [provided by RefSeq, Aug 2020]","start":132073790,"end":132076170,"strand":1,"description":"colony stimulating factor 2 [Source:HGNC Symbol;Acc:HGNC:2434]"}, {"versioned_ensembl_gene_id":"ENSG00000224475.1","gene_symbol":"AC073900.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97200708,"end":97201483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135144.7","gene_symbol":"DTX1","gene_name":"deltex E3 ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:3060]","synonyms":"hDx-1","biotype":"protein_coding","ncbi_id":"1840","summary":"Studies in Drosophila have identified this gene as encoding a positive regulator of the Notch-signaling pathway. The human gene encodes a protein of unknown function; however, it may play a role in basic helix-loop-helix transcription factor activity. [provided by RefSeq, Jul 2008]","start":113056709,"end":113098028,"strand":1,"description":"deltex E3 ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:3060]"}, {"versioned_ensembl_gene_id":"ENSG00000265142.8","gene_symbol":"MIR133A1HG","gene_name":"MIR133A1 host gene [Source:HGNC Symbol;Acc:HGNC:49594]","synonyms":"MIR1-2HG","biotype":"antisense_RNA","ncbi_id":"102723167","summary":null,"start":21825487,"end":21831410,"strand":-1,"description":"MIR133A1 host gene [Source:HGNC Symbol;Acc:HGNC:49594]"}, {"versioned_ensembl_gene_id":"ENSG00000129244.8","gene_symbol":"ATP1B2","gene_name":"ATPase Na+/K+ transporting subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:805]","synonyms":"AMOG","biotype":"protein_coding","ncbi_id":"482","summary":"The protein encoded by this gene belongs to the family of Na+/K+ and H+/K+ ATPases beta chain proteins, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The beta subunit regulates, through assembly of alpha/beta heterodimers, the number of sodium pumps transported to the plasma membrane. The glycoprotein subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes a beta 2 subunit. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":7646627,"end":7657768,"strand":1,"description":"ATPase Na+/K+ transporting subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:805]"}, {"versioned_ensembl_gene_id":"ENSG00000280019.1","gene_symbol":"CU633906.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6272135,"end":6276532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275552.1","gene_symbol":"AC243965.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22595808,"end":22598946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159658.10","gene_symbol":"EFCAB14","gene_name":"EF-hand calcium binding domain 14 [Source:HGNC Symbol;Acc:HGNC:29051]","synonyms":"KIAA0494","biotype":"protein_coding","ncbi_id":"9813","summary":null,"start":46675159,"end":46719064,"strand":-1,"description":"EF-hand calcium binding domain 14 [Source:HGNC Symbol;Acc:HGNC:29051]"}, {"versioned_ensembl_gene_id":"ENSG00000277171.1","gene_symbol":"AC010975.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":79547151,"end":79548128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162951.10","gene_symbol":"LRRTM1","gene_name":"leucine rich repeat transmembrane neuronal 1 [Source:HGNC Symbol;Acc:HGNC:19408]","synonyms":"FLJ32082","biotype":"protein_coding","ncbi_id":"347730","summary":null,"start":80288351,"end":80304749,"strand":-1,"description":"leucine rich repeat transmembrane neuronal 1 [Source:HGNC Symbol;Acc:HGNC:19408]"}, {"versioned_ensembl_gene_id":"ENSG00000242473.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755023,"end":54767371,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000221957.8","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832676,"end":54848569,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000281354.1","gene_symbol":"AP000350.13","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23856427,"end":23857039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166049.10","gene_symbol":"PASD1","gene_name":"PAS domain containing repressor 1 [Source:HGNC Symbol;Acc:HGNC:20686]","synonyms":"CT63","biotype":"protein_coding","ncbi_id":"139135","summary":"This gene encodes a protein that is thought to function as a transcription factor. The protein is a cancer-associated antigen that can stimulate autologous T-cell responses, and it is therefore considered to be a potential immunotherapeutic target for the treatment of various hematopoietic malignancies, including diffuse large B-cell lymphoma. [provided by RefSeq, May 2010]","start":151563622,"end":151676739,"strand":1,"description":"PAS domain containing repressor 1 [Source:HGNC Symbol;Acc:HGNC:20686]"}, {"versioned_ensembl_gene_id":"ENSG00000284658.1","gene_symbol":"AL513478.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66204896,"end":66208833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092841.18","gene_symbol":"MYL6","gene_name":"myosin light chain 6 [Source:HGNC Symbol;Acc:HGNC:7587]","synonyms":"MLC3NM,MLC1SM,ESMLC","biotype":"protein_coding","ncbi_id":"4637","summary":"Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain that is expressed in smooth muscle and non-muscle tissues. Genomic sequences representing several pseudogenes have been described and two transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":56158161,"end":56163496,"strand":1,"description":"myosin light chain 6 [Source:HGNC Symbol;Acc:HGNC:7587]"}, {"versioned_ensembl_gene_id":"ENSG00000284611.1","gene_symbol":"AL513478.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66182326,"end":66188451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259828.1","gene_symbol":"AL355596.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141447011,"end":141451006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179476.7","gene_symbol":"C14orf28","gene_name":"chromosome 14 open reading frame 28 [Source:HGNC Symbol;Acc:HGNC:19834]","synonyms":"DRIP-1","biotype":"protein_coding","ncbi_id":"122525","summary":null,"start":44897295,"end":44907257,"strand":1,"description":"chromosome 14 open reading frame 28 [Source:HGNC Symbol;Acc:HGNC:19834]"}, {"versioned_ensembl_gene_id":"ENSG00000234147.1","gene_symbol":"AL035446.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140845958,"end":140852924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148204.11","gene_symbol":"CRB2","gene_name":"crumbs 2, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:18688]","synonyms":"FLJ38464,FLJ16786","biotype":"protein_coding","ncbi_id":"286204","summary":"This gene encodes a member of a family of proteins that are components of the Crumbs cell polarity complex. In mammals, members of this family are thought to play a role in many cellular processes in early embryonic development. A similar protein in Drosophila determines apicobasal polarity in embryonic epithelial cells. Mutations in this gene are associated with focal segmental glomerulosclerosis 9, and with ventriculomegaly with cystic kidney disease. [provided by RefSeq, Aug 2016]","start":123356170,"end":123380324,"strand":1,"description":"crumbs 2, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:18688]"}, {"versioned_ensembl_gene_id":"ENSG00000214176.9","gene_symbol":"PLEKHM1P1","gene_name":"pleckstrin homology and RUN domain containing M1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35411]","synonyms":"PLEKHM1P,LOC440456","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440456","summary":null,"start":64779259,"end":64837154,"strand":-1,"description":"pleckstrin homology and RUN domain containing M1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35411]"}, {"versioned_ensembl_gene_id":"ENSG00000170786.12","gene_symbol":"SDR16C5","gene_name":"short chain dehydrogenase/reductase family 16C member 5 [Source:HGNC Symbol;Acc:HGNC:30311]","synonyms":"RDHE2,RDH-E2,EPHD-2","biotype":"protein_coding","ncbi_id":"195814","summary":"This gene encodes a member of the short-chain alcohol dehydrogenase/reductase superfamily of proteins and is involved in the oxidation of retinol to retinaldehyde. The encoded protein is associated with the endoplasmic reticulum and is predicted to contain three transmembrane helices, suggesting that it is an integral membrane protein. It recognizes all-trans-retinol and all-trans-retinaldehyde as substrates and exhibits a strong preference for NAD(+)/NADH as cofactors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":56300010,"end":56320776,"strand":-1,"description":"short chain dehydrogenase/reductase family 16C member 5 [Source:HGNC Symbol;Acc:HGNC:30311]"}, {"versioned_ensembl_gene_id":"ENSG00000119522.16","gene_symbol":"DENND1A","gene_name":"DENN domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29324]","synonyms":"KIAA1608,FLJ21129,FAM31A","biotype":"protein_coding","ncbi_id":"57706","summary":"Clathrin (see MIM 118955)-mediated endocytosis is a major mechanism for internalization of proteins and lipids. Members of the connecdenn family, such as DENND1A, function as guanine nucleotide exchange factors (GEFs) for the early endosomal small GTPase RAB35 (MIM 604199) and bind to clathrin and clathrin adaptor protein-2 (AP2; see MIM 601024). Thus, connecdenns link RAB35 activation with the clathrin machinery (Marat and McPherson, 2010 [PubMed 20154091]).[supplied by OMIM, Nov 2010]","start":123379654,"end":123930152,"strand":-1,"description":"DENN domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29324]"}, {"versioned_ensembl_gene_id":"ENSG00000171159.4","gene_symbol":"C9orf16","gene_name":"chromosome 9 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:17823]","synonyms":"MGC4639,FLJ12823,EST00098","biotype":"protein_coding","ncbi_id":"79095","summary":null,"start":128160260,"end":128163928,"strand":1,"description":"chromosome 9 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:17823]"}, {"versioned_ensembl_gene_id":"ENSG00000211875.1","gene_symbol":"TRAJ14","gene_name":"T-cell receptor alpha joining 14 [Source:HGNC Symbol;Acc:HGNC:12042]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28741","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22530327,"end":22530378,"strand":1,"description":"T-cell receptor alpha joining 14 [Source:HGNC Symbol;Acc:HGNC:12042]"}, {"versioned_ensembl_gene_id":"ENSG00000174684.6","gene_symbol":"B4GAT1","gene_name":"beta-1,4-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15685]","synonyms":"iGNT,iGAT,BETA3GNTI,B3GNT6,B3GNT1,B3GN-T1","biotype":"protein_coding","ncbi_id":"11041","summary":"This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase family. This enzyme is a type II transmembrane protein. It is essential for the synthesis of poly-N-acetyllactosamine, a determinant for the blood group i antigen. [provided by RefSeq, Jul 2008]","start":66345372,"end":66347692,"strand":-1,"description":"beta-1,4-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15685]"}, {"versioned_ensembl_gene_id":"ENSG00000258633.1","gene_symbol":"AL049870.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44876874,"end":44897077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198719.8","gene_symbol":"DLL1","gene_name":"delta like canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2908]","synonyms":null,"biotype":"protein_coding","ncbi_id":"28514","summary":" DLL1 is a human homolog of the Notch Delta ligand and is a member of the delta/serrate/jagged family. It plays a role in mediating cell fate decisions during hematopoiesis. It may play a role in cell-to-cell communication. [provided by RefSeq, Jul 2008]","start":170282206,"end":170306565,"strand":-1,"description":"delta like canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2908]"}, {"versioned_ensembl_gene_id":"ENSG00000196696.12","gene_symbol":"PDXDC2P-NPIPB14P","gene_name":"nuclear pore complex-interacting protein [Source:NCBI gene;Acc:283970]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"283970","summary":"This locus represents naturally-occurring readthrough transcription between two pseudogenes, PDXDC2P (pyridoxal dependent decarboxylase domain containing 2, pseudogene) and NPIPB14P (nuclear pore complex interacting protein family, member B14, pseudogene). The individual pseudogene loci are not curated as transcribed regions. Readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Feb 2017]","start":69976297,"end":70065948,"strand":-1,"description":"nuclear pore complex-interacting protein [Source:NCBI gene;Acc:283970]"}, {"versioned_ensembl_gene_id":"ENSG00000226232.8","gene_symbol":"NPIPB14P","gene_name":"nuclear pore complex interacting protein family member B14, pseudogene [Source:HGNC Symbol;Acc:HGNC:41990]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"109729168","summary":null,"start":69976388,"end":69996188,"strand":-1,"description":"nuclear pore complex interacting protein family member B14, pseudogene [Source:HGNC Symbol;Acc:HGNC:41990]"}, {"versioned_ensembl_gene_id":"ENSG00000228208.6","gene_symbol":"C1orf143","gene_name":"chromosome 1 open reading frame 143 [Source:HGNC Symbol;Acc:HGNC:32045]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440714","summary":null,"start":218510096,"end":218525978,"strand":1,"description":"chromosome 1 open reading frame 143 [Source:HGNC Symbol;Acc:HGNC:32045]"}, {"versioned_ensembl_gene_id":"ENSG00000167397.14","gene_symbol":"VKORC1","gene_name":"vitamin K epoxide reductase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:23663]","synonyms":"VKCFD2","biotype":"protein_coding","ncbi_id":"79001","summary":"This gene encodes the catalytic subunit of the vitamin K epoxide reductase complex, which is responsible for the reduction of inactive vitamin K 2,3-epoxide to active vitamin K in the endoplasmic reticulum membrane. Vitamin K is a required co-factor for carboxylation of glutamic acid residues by vitamin K-dependent gamma-carboxylase in blood-clotting enzymes. Allelic variation in this gene is associated with vitamin k-dependent clotting factors combined deficiency of 2, and increased resistance or sensitivity to warfarin, an inhibitor of vitamin K epoxide reductase. Pseudogenes of this gene are located on chromosomes 1 and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":31090842,"end":31095980,"strand":-1,"description":"vitamin K epoxide reductase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:23663]"}, {"versioned_ensembl_gene_id":"ENSG00000082153.17","gene_symbol":"BZW1","gene_name":"basic leucine zipper and W2 domains 1 [Source:HGNC Symbol;Acc:HGNC:18380]","synonyms":"KIAA0005,BZAP45","biotype":"protein_coding","ncbi_id":"9689","summary":null,"start":200810594,"end":200827338,"strand":1,"description":"basic leucine zipper and W2 domains 1 [Source:HGNC Symbol;Acc:HGNC:18380]"}, {"versioned_ensembl_gene_id":"ENSG00000176473.13","gene_symbol":"WDR25","gene_name":"WD repeat domain 25 [Source:HGNC Symbol;Acc:HGNC:21064]","synonyms":"MGC4645,C14orf67","biotype":"protein_coding","ncbi_id":"79446","summary":"This gene encodes a protein containing 7 WD repeats. WD repeats are approximately 30 to 40-amino acid domains containing several conserved residues, typically having a Tryptophan-Aspartic acid dipeptide (WD) at the C-terminal end. WD domains are involved in protein-protein interactions in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":100376418,"end":100530303,"strand":1,"description":"WD repeat domain 25 [Source:HGNC Symbol;Acc:HGNC:21064]"}, {"versioned_ensembl_gene_id":"ENSG00000264131.1","gene_symbol":"AC007631.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65186159,"end":65187018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145216.15","gene_symbol":"FIP1L1","gene_name":"factor interacting with PAPOLA and CPSF1 [Source:HGNC Symbol;Acc:HGNC:19124]","synonyms":"FIP1,DKFZp586K0717","biotype":"protein_coding","ncbi_id":"81608","summary":"This gene encodes a subunit of the CPSF (cleavage and polyadenylation specificity factor) complex that polyadenylates the 3' end of mRNA precursors. This gene, the homolog of yeast Fip1 (factor interacting with PAP), binds to U-rich sequences of pre-mRNA and stimulates poly(A) polymerase activity. Its N-terminus contains a PAP-binding site and its C-terminus an RNA-binding domain. An interstitial chromosomal deletion on 4q12 creates an in-frame fusion of human genes FIP1L1 and PDGFRA (platelet-derived growth factor receptor, alpha). The FIP1L1-PDGFRA fusion gene encodes a constitutively activated tyrosine kinase that joins the first 233 amino acids of FIP1L1 to the last 523 amino acids of PDGFRA. This gene fusion and chromosomal deletion is the cause of some forms of idiopathic hypereosinophilic syndrome (HES). This syndrome, recently reclassified as chronic eosinophilic leukemia (CEL), is responsive to treatment with tyrosine kinase inhibitors. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":53377643,"end":53460861,"strand":1,"description":"factor interacting with PAPOLA and CPSF1 [Source:HGNC Symbol;Acc:HGNC:19124]"}, {"versioned_ensembl_gene_id":"ENSG00000274364.1","gene_symbol":"AL110115.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31535263,"end":31535626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230613.1","gene_symbol":"HM13-AS1","gene_name":"HM13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41940]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874042","summary":null,"start":31567707,"end":31573263,"strand":-1,"description":"HM13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41940]"}, {"versioned_ensembl_gene_id":"ENSG00000280179.1","gene_symbol":"CU639417.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6084364,"end":6091407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095794.19","gene_symbol":"CREM","gene_name":"cAMP responsive element modulator [Source:HGNC Symbol;Acc:HGNC:2352]","synonyms":"hCREM-2","biotype":"protein_coding","ncbi_id":"1390","summary":"This gene encodes a bZIP transcription factor that binds to the cAMP responsive element found in many viral and cellular promoters. It is an important component of cAMP-mediated signal transduction during the spermatogenetic cycle, as well as other complex processes. Alternative promoter and translation initiation site usage allows this gene to exert spatial and temporal specificity to cAMP responsiveness. Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene, with some of them functioning as activators and some as repressors of transcription. [provided by RefSeq, Jul 2008]","start":35126791,"end":35212958,"strand":1,"description":"cAMP responsive element modulator [Source:HGNC Symbol;Acc:HGNC:2352]"}, {"versioned_ensembl_gene_id":"ENSG00000280095.1","gene_symbol":"CU639417.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6081193,"end":6082585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259503.1","gene_symbol":"AC048383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70321576,"end":70326742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233343.1","gene_symbol":"ATP6V1G1P4","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37671]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462843","summary":null,"start":35158306,"end":35158640,"strand":1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37671]"}, {"versioned_ensembl_gene_id":"ENSG00000104907.12","gene_symbol":"TRMT1","gene_name":"tRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25980]","synonyms":"TRM1,FLJ20244","biotype":"protein_coding","ncbi_id":"55621","summary":"This gene encodes a tRNA-modifying enzyme that acts as a dimethyltransferase, modifying a single guanine residue at position 26 of the tRNA. The encoded enzyme has both mono- and dimethylase activity when exogenously expressed, and uses S-adenosyl methionine as a methyl donor. The C-terminal region of the encoded protein has both a zinc finger motif, and an arginine/proline-rich region. Mutations in this gene have been implicated in autosomal recessive intellectual disorder (ARID). Alternative splicing results in multiple transcript variants encoding different isoforms. There is a pseudogene of this gene on the X chromosome. [provided by RefSeq, May 2017]","start":13104902,"end":13117567,"strand":-1,"description":"tRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25980]"}, {"versioned_ensembl_gene_id":"ENSG00000267180.1","gene_symbol":"AC007136.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":2030853,"end":2031051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267283.1","gene_symbol":"AC005306.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1989401,"end":1990370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279248.1","gene_symbol":"AP003400.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89533645,"end":89534043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269980.1","gene_symbol":"AC068768.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123262060,"end":123262402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237187.8","gene_symbol":"NR2F1-AS1","gene_name":"NR2F1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48622]","synonyms":"FLJ42709","biotype":"antisense_RNA","ncbi_id":"441094","summary":null,"start":93409359,"end":93585648,"strand":-1,"description":"NR2F1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48622]"}, {"versioned_ensembl_gene_id":"ENSG00000232667.10","gene_symbol":"AC004862.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80312574,"end":80391474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148297.15","gene_symbol":"MED22","gene_name":"mediator complex subunit 22 [Source:HGNC Symbol;Acc:HGNC:11477]","synonyms":"SRB6,Med24,SURF5","biotype":"protein_coding","ncbi_id":"6837","summary":"This gene encodes a protein component of the mediator complex, which functions in the regulation of transcription by bridging interactions between gene-specific regulatory factors, RNA polymerase II, and general transcription factors. Alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2013]","start":133338323,"end":133348131,"strand":-1,"description":"mediator complex subunit 22 [Source:HGNC Symbol;Acc:HGNC:11477]"}, {"versioned_ensembl_gene_id":"ENSG00000235976.2","gene_symbol":"Z80107.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101989481,"end":101989872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267374.1","gene_symbol":"AC016205.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39206924,"end":39800318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157796.17","gene_symbol":"WDR19","gene_name":"WD repeat domain 19 [Source:HGNC Symbol;Acc:HGNC:18340]","synonyms":"Pwdmp,Oseg6,ORF26,NPHP13,KIAA1638,IFT144,FLJ23127,DYF-2","biotype":"protein_coding","ncbi_id":"57728","summary":"The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":39182404,"end":39285810,"strand":1,"description":"WD repeat domain 19 [Source:HGNC Symbol;Acc:HGNC:18340]"}, {"versioned_ensembl_gene_id":"ENSG00000280024.1","gene_symbol":"AC048347.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127372243,"end":127372669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279952.1","gene_symbol":"AC068787.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127462507,"end":127463197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214415.3","gene_symbol":"GNAT3","gene_name":"G protein subunit alpha transducin 3 [Source:HGNC Symbol;Acc:HGNC:22800]","synonyms":"gustducin,GDCA","biotype":"protein_coding","ncbi_id":"346562","summary":"Sweet, bitter, and umami tastes are transmitted from taste receptors by a specific guanine nucleotide binding protein. The protein encoded by this gene is the alpha subunit of this heterotrimeric G protein, which is found not only in the oral epithelium but also in gut tissues. Variations in this gene have been linked to metabolic syndrome. [provided by RefSeq, Dec 2015]","start":80458671,"end":80512020,"strand":-1,"description":"G protein subunit alpha transducin 3 [Source:HGNC Symbol;Acc:HGNC:22800]"}, {"versioned_ensembl_gene_id":"ENSG00000258283.1","gene_symbol":"AC011603.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48995150,"end":48996334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175745.11","gene_symbol":"NR2F1","gene_name":"nuclear receptor subfamily 2 group F member 1 [Source:HGNC Symbol;Acc:HGNC:7975]","synonyms":"COUP-TFI,TFCOUP1,TCFCOUP1,SVP44,ERBAL3,EAR-3","biotype":"protein_coding","ncbi_id":"7025","summary":"The protein encoded by this gene is a nuclear hormone receptor and transcriptional regulator. The encoded protein acts as a homodimer and binds to 5'-AGGTCA-3' repeats. Defects in this gene are a cause of Bosch-Boonstra optic atrophy syndrome (BBOAS). [provided by RefSeq, Apr 2014]","start":93583337,"end":93594615,"strand":1,"description":"nuclear receptor subfamily 2 group F member 1 [Source:HGNC Symbol;Acc:HGNC:7975]"}, {"versioned_ensembl_gene_id":"ENSG00000257913.2","gene_symbol":"DDN-AS1","gene_name":"DDN and PRKAG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53464]","synonyms":"CAT1507","biotype":"antisense_RNA","ncbi_id":"105369758","summary":null,"start":48998367,"end":49019235,"strand":1,"description":"DDN and PRKAG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53464]"}, {"versioned_ensembl_gene_id":"ENSG00000226625.1","gene_symbol":"RBM17P1","gene_name":"RNA binding motif protein 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133330","summary":null,"start":39154075,"end":39155479,"strand":1,"description":"RNA binding motif protein 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50366]"}, {"versioned_ensembl_gene_id":"ENSG00000232629.8","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32756098,"end":32763534,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000214298.3","gene_symbol":"MRPS21P6","gene_name":"mitochondrial ribosomal protein S21 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29753]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359770","summary":null,"start":125166677,"end":125166937,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29753]"}, {"versioned_ensembl_gene_id":"ENSG00000241907.1","gene_symbol":"RPS20P4","gene_name":"ribosomal protein S20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10407]","synonyms":"RPS20B","biotype":"processed_pseudogene","ncbi_id":"6226","summary":null,"start":150021567,"end":150021921,"strand":-1,"description":"ribosomal protein S20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10407]"}, {"versioned_ensembl_gene_id":"ENSG00000135956.8","gene_symbol":"TMEM127","gene_name":"transmembrane protein 127 [Source:HGNC Symbol;Acc:HGNC:26038]","synonyms":"FLJ22257,FLJ20507","biotype":"protein_coding","ncbi_id":"55654","summary":"This gene encodes a transmembrane protein with 3 predicted transmembrane domains. The protein is associated with a subpopulation of vesicular organelles corresponding to early endosomal structures, with the Golgi, and with lysosomes, and may participate in protein trafficking between these structures. Mutations in this gene and several other genes cause pheochromocytomas. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Aug 2010]","start":96248516,"end":96265994,"strand":-1,"description":"transmembrane protein 127 [Source:HGNC Symbol;Acc:HGNC:26038]"}, {"versioned_ensembl_gene_id":"ENSG00000211858.1","gene_symbol":"TRAJ31","gene_name":"T-cell receptor alpha joining 31 [Source:HGNC Symbol;Acc:HGNC:12061]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28724","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22510968,"end":22511024,"strand":1,"description":"T-cell receptor alpha joining 31 [Source:HGNC Symbol;Acc:HGNC:12061]"}, {"versioned_ensembl_gene_id":"ENSG00000177202.2","gene_symbol":"SPACA4","gene_name":"sperm acrosome associated 4 [Source:HGNC Symbol;Acc:HGNC:16441]","synonyms":"SAMP14","biotype":"protein_coding","ncbi_id":"171169","summary":null,"start":48606743,"end":48607714,"strand":1,"description":"sperm acrosome associated 4 [Source:HGNC Symbol;Acc:HGNC:16441]"}, {"versioned_ensembl_gene_id":"ENSG00000256358.1","gene_symbol":"AC016489.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64308316,"end":64308690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227297.1","gene_symbol":"AL035541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57599695,"end":57601200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211857.1","gene_symbol":"TRAJ32","gene_name":"T-cell receptor alpha joining 32 [Source:HGNC Symbol;Acc:HGNC:12062]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28723","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22509341,"end":22509406,"strand":1,"description":"T-cell receptor alpha joining 32 [Source:HGNC Symbol;Acc:HGNC:12062]"}, {"versioned_ensembl_gene_id":"ENSG00000226167.1","gene_symbol":"AP4B1-AS1","gene_name":"AP4B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44114]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287722","summary":null,"start":113856635,"end":113901237,"strand":1,"description":"AP4B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44114]"}, {"versioned_ensembl_gene_id":"ENSG00000106078.17","gene_symbol":"COBL","gene_name":"cordon-bleu WH2 repeat protein [Source:HGNC Symbol;Acc:HGNC:22199]","synonyms":"KIAA0633","biotype":"protein_coding","ncbi_id":"23242","summary":"This gene encodes a protein that contains WH2 domains (WASP, Wiskott-Aldrich syndrome protein, homology domain-2) that interact with actin. The encoded actin regulator protein is required for growth and assembly of brush border microvilli that play a role in maintaining intestinal homeostasis. A similar protein in mouse functions in midbrain neural tube closure. A pseudogene of this gene is located on chromosome X. [provided by RefSeq, Oct 2016]","start":51016212,"end":51316818,"strand":-1,"description":"cordon-bleu WH2 repeat protein [Source:HGNC Symbol;Acc:HGNC:22199]"}, {"versioned_ensembl_gene_id":"ENSG00000258807.5","gene_symbol":"AL359237.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87710419,"end":87872291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228204.2","gene_symbol":"AC004830.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50866747,"end":51022990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135778.11","gene_symbol":"NTPCR","gene_name":"nucleoside-triphosphatase, cancer-related [Source:HGNC Symbol;Acc:HGNC:28204]","synonyms":"C1orf57,MGC13186,HCR-NTPase","biotype":"protein_coding","ncbi_id":"84284","summary":"The protein encoded by this gene is a non-specific nucleoside triphosphatase that is slow-acting in vitro. This gene is overexpressed in many tumor tissues, and while it is not essential for the cell, overexpression is cytotoxic. However, the cytotoxicity is not related to its triphosphatase activity. [provided by RefSeq, Jul 2016]","start":232950605,"end":232983882,"strand":1,"description":"nucleoside-triphosphatase, cancer-related [Source:HGNC Symbol;Acc:HGNC:28204]"}, {"versioned_ensembl_gene_id":"ENSG00000231940.1","gene_symbol":"RPS7P3","gene_name":"ribosomal protein S7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440732","summary":null,"start":233288868,"end":233289447,"strand":-1,"description":"ribosomal protein S7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36518]"}, {"versioned_ensembl_gene_id":"ENSG00000008196.12","gene_symbol":"TFAP2B","gene_name":"transcription factor AP-2 beta [Source:HGNC Symbol;Acc:HGNC:11743]","synonyms":"AP2-B","biotype":"protein_coding","ncbi_id":"7021","summary":"This gene encodes a member of the AP-2 family of transcription factors. AP-2 proteins form homo- or hetero-dimers with other AP-2 family members and bind specific DNA sequences. They are thought to stimulate cell proliferation and suppress terminal differentiation of specific cell types during embryonic development. Specific AP-2 family members differ in their expression patterns and binding affinity for different promoters. This protein functions as both a transcriptional activator and repressor. Mutations in this gene result in autosomal dominant Char syndrome, suggesting that this gene functions in the differentiation of neural crest cell derivatives. [provided by RefSeq, Jul 2008]","start":50818723,"end":50847613,"strand":1,"description":"transcription factor AP-2 beta [Source:HGNC Symbol;Acc:HGNC:11743]"}, {"versioned_ensembl_gene_id":"ENSG00000165915.13","gene_symbol":"SLC39A13","gene_name":"solute carrier family 39 member 13 [Source:HGNC Symbol;Acc:HGNC:20859]","synonyms":"FLJ25785","biotype":"protein_coding","ncbi_id":"91252","summary":"This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome. Alternate transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]","start":47407132,"end":47416501,"strand":1,"description":"solute carrier family 39 member 13 [Source:HGNC Symbol;Acc:HGNC:20859]"}, {"versioned_ensembl_gene_id":"ENSG00000270361.1","gene_symbol":"AL451085.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154937370,"end":154938059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279610.1","gene_symbol":"C20orf181","gene_name":"chromosome 20 open reading frame 181 [Source:HGNC Symbol;Acc:HGNC:16174]","synonyms":"dJ824A14.1","biotype":"TEC","ncbi_id":"100128998","summary":null,"start":63843436,"end":63843915,"strand":-1,"description":"chromosome 20 open reading frame 181 [Source:HGNC Symbol;Acc:HGNC:16174]"}, {"versioned_ensembl_gene_id":"ENSG00000263412.1","gene_symbol":"AC004477.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":48045141,"end":48048073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270554.1","gene_symbol":"AC069431.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182843521,"end":182844619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213448.3","gene_symbol":"RPS23P2","gene_name":"ribosomal protein S23 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36568]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391701","summary":null,"start":137448087,"end":137448501,"strand":1,"description":"ribosomal protein S23 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36568]"}, {"versioned_ensembl_gene_id":"ENSG00000255121.2","gene_symbol":"AP003392.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118994824,"end":118998004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153714.5","gene_symbol":"LURAP1L","gene_name":"leucine rich adaptor protein 1 like [Source:HGNC Symbol;Acc:HGNC:31452]","synonyms":"MGC46502,FLJ38505,C9orf150,bA3L8.2","biotype":"protein_coding","ncbi_id":"286343","summary":null,"start":12775021,"end":12822131,"strand":1,"description":"leucine rich adaptor protein 1 like [Source:HGNC Symbol;Acc:HGNC:31452]"}, {"versioned_ensembl_gene_id":"ENSG00000256525.6","gene_symbol":"POLG2","gene_name":"DNA polymerase gamma 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9180]","synonyms":"MTPOLB,HP55","biotype":"protein_coding","ncbi_id":"11232","summary":"This gene encodes the processivity subunit of the mitochondrial DNA polymerase gamma. The encoded protein forms a heterotrimer containing one catalytic subunit and two processivity subunits. This protein enhances DNA binding and promotes processive DNA synthesis. Mutations in this gene result in autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions.[provided by RefSeq, Sep 2009]","start":64477785,"end":64497036,"strand":-1,"description":"DNA polymerase gamma 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9180]"}, {"versioned_ensembl_gene_id":"ENSG00000228085.1","gene_symbol":"AC009296.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50843578,"end":50843732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272969.1","gene_symbol":"AC024243.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55547112,"end":55547889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242280.1","gene_symbol":"SLC16A1P1","gene_name":"SLC16A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422547","summary":null,"start":143985142,"end":143986651,"strand":1,"description":"SLC16A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48931]"}, {"versioned_ensembl_gene_id":"ENSG00000251567.5","gene_symbol":"AC018680.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136118675,"end":136395471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082213.17","gene_symbol":"C5orf22","gene_name":"chromosome 5 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:25639]","synonyms":"FLJ11193","biotype":"protein_coding","ncbi_id":"55322","summary":null,"start":31532266,"end":31555058,"strand":1,"description":"chromosome 5 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:25639]"}, {"versioned_ensembl_gene_id":"ENSG00000276699.1","gene_symbol":"TRAJ36","gene_name":"T-cell receptor alpha joining 36 [Source:HGNC Symbol;Acc:HGNC:12066]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28719","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22505110,"end":22505167,"strand":1,"description":"T-cell receptor alpha joining 36 [Source:HGNC Symbol;Acc:HGNC:12066]"}, {"versioned_ensembl_gene_id":"ENSG00000272801.1","gene_symbol":"AC004080.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":27147366,"end":27152598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146147.14","gene_symbol":"MLIP","gene_name":"muscular LMNA interacting protein [Source:HGNC Symbol;Acc:HGNC:21355]","synonyms":"MGC18257,CIP,C6orf142","biotype":"protein_coding","ncbi_id":"90523","summary":null,"start":53929982,"end":54266280,"strand":1,"description":"muscular LMNA interacting protein [Source:HGNC Symbol;Acc:HGNC:21355]"}, {"versioned_ensembl_gene_id":"ENSG00000224221.1","gene_symbol":"AC019205.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73391038,"end":73391767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232175.1","gene_symbol":"AL122003.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":232917235,"end":232918018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164796.17","gene_symbol":"CSMD3","gene_name":"CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:HGNC:19291]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114788","summary":null,"start":112222928,"end":113437099,"strand":-1,"description":"CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:HGNC:19291]"}, {"versioned_ensembl_gene_id":"ENSG00000229214.1","gene_symbol":"LINC00242","gene_name":"long intergenic non-protein coding RNA 242 [Source:HGNC Symbol;Acc:HGNC:21249]","synonyms":"dJ266L20.5,C6orf122,NCRNA00242,FLJ31451","biotype":"lincRNA","ncbi_id":"401288","summary":null,"start":169788790,"end":169798825,"strand":-1,"description":"long intergenic non-protein coding RNA 242 [Source:HGNC Symbol;Acc:HGNC:21249]"}, {"versioned_ensembl_gene_id":"ENSG00000236996.1","gene_symbol":"MLIP-IT1","gene_name":"MLIP intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41461]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874282","summary":null,"start":53998890,"end":54007152,"strand":1,"description":"MLIP intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41461]"}, {"versioned_ensembl_gene_id":"ENSG00000106006.6","gene_symbol":"HOXA6","gene_name":"homeobox A6 [Source:HGNC Symbol;Acc:HGNC:5107]","synonyms":"HOX1B,HOX1","biotype":"protein_coding","ncbi_id":"3203","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. [provided by RefSeq, Jul 2008]","start":27145396,"end":27150603,"strand":-1,"description":"homeobox A6 [Source:HGNC Symbol;Acc:HGNC:5107]"}, {"versioned_ensembl_gene_id":"ENSG00000258730.1","gene_symbol":"ITPK1-AS1","gene_name":"ITPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20132]","synonyms":"C14orf85,NCRNA00203,ITPK1AS,ITPK1-AS","biotype":"antisense_RNA","ncbi_id":"319085","summary":null,"start":93067452,"end":93072152,"strand":1,"description":"ITPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20132]"}, {"versioned_ensembl_gene_id":"ENSG00000271605.5","gene_symbol":"MILR1","gene_name":"mast cell immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:27570]","synonyms":"MCA-32,C17orf60,Allergin-1","biotype":"protein_coding","ncbi_id":"284021","summary":null,"start":64449037,"end":64468643,"strand":1,"description":"mast cell immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:27570]"}, {"versioned_ensembl_gene_id":"ENSG00000197818.11","gene_symbol":"SLC9A8","gene_name":"solute carrier family 9 member A8 [Source:HGNC Symbol;Acc:HGNC:20728]","synonyms":"NHE8,KIAA0939","biotype":"protein_coding","ncbi_id":"23315","summary":"Sodium-hydrogen exchangers (NHEs), such as SLC9A8, are integral transmembrane proteins that exchange extracellular Na+ for intracellular H+. NHEs have multiple functions, including intracellular pH homeostasis, cell volume regulation, and electroneutral NaCl absorption in epithelia (Xu et al., 2008 [PubMed 18209477]).[supplied by OMIM, Apr 2009]","start":49812713,"end":49892242,"strand":1,"description":"solute carrier family 9 member A8 [Source:HGNC Symbol;Acc:HGNC:20728]"}, {"versioned_ensembl_gene_id":"ENSG00000273433.1","gene_symbol":"AC004080.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":27128969,"end":27152561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269486.2","gene_symbol":"AC011455.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38935297,"end":38938632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122592.7","gene_symbol":"HOXA7","gene_name":"homeobox A7 [Source:HGNC Symbol;Acc:HGNC:5108]","synonyms":"HOX1A,HOX1","biotype":"protein_coding","ncbi_id":"3204","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. For example, the encoded protein represses the transcription of differentiation-specific genes during keratinocyte proliferation, but this repression is then overcome by differentiation signals. This gene is highly similar to the antennapedia (Antp) gene of Drosophila. [provided by RefSeq, Jul 2008]","start":27153716,"end":27157936,"strand":-1,"description":"homeobox A7 [Source:HGNC Symbol;Acc:HGNC:5108]"}, {"versioned_ensembl_gene_id":"ENSG00000213424.8","gene_symbol":"KRT222","gene_name":"keratin 222 [Source:HGNC Symbol;Acc:HGNC:28695]","synonyms":"MGC45562,KRT222P,KA21","biotype":"protein_coding","ncbi_id":"125113","summary":null,"start":40654665,"end":40665181,"strand":-1,"description":"keratin 222 [Source:HGNC Symbol;Acc:HGNC:28695]"}, {"versioned_ensembl_gene_id":"ENSG00000164334.15","gene_symbol":"FAM170A","gene_name":"family with sequence similarity 170 member A [Source:HGNC Symbol;Acc:HGNC:27963]","synonyms":"ZNFD","biotype":"protein_coding","ncbi_id":"340069","summary":null,"start":119629559,"end":119635822,"strand":1,"description":"family with sequence similarity 170 member A [Source:HGNC Symbol;Acc:HGNC:27963]"}, {"versioned_ensembl_gene_id":"ENSG00000213663.4","gene_symbol":"AC010409.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119547131,"end":119547606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105523.3","gene_symbol":"FAM83E","gene_name":"family with sequence similarity 83 member E [Source:HGNC Symbol;Acc:HGNC:25972]","synonyms":"FLJ20200","biotype":"protein_coding","ncbi_id":"54854","summary":null,"start":48600810,"end":48614854,"strand":-1,"description":"family with sequence similarity 83 member E [Source:HGNC Symbol;Acc:HGNC:25972]"}, {"versioned_ensembl_gene_id":"ENSG00000105538.9","gene_symbol":"RASIP1","gene_name":"Ras interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24716]","synonyms":"FLJ20401,RAIN","biotype":"protein_coding","ncbi_id":"54922","summary":null,"start":48720587,"end":48740721,"strand":-1,"description":"Ras interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24716]"}, {"versioned_ensembl_gene_id":"ENSG00000080007.7","gene_symbol":"DDX43","gene_name":"DEAD-box helicase 43 [Source:HGNC Symbol;Acc:HGNC:18677]","synonyms":"CT13,HAGE,DKFZp434H2114","biotype":"protein_coding","ncbi_id":"55510","summary":" The protein encoded by this gene is an ATP-dependent RNA helicase in the DEAD-box family and displays tumor-specific expression. [provided by RefSeq, Jul 2008]","start":73394748,"end":73417569,"strand":1,"description":"DEAD-box helicase 43 [Source:HGNC Symbol;Acc:HGNC:18677]"}, {"versioned_ensembl_gene_id":"ENSG00000232022.7","gene_symbol":"FAAHP1","gene_name":"fatty acid amide hydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50679]","synonyms":"LINC00505","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729041","summary":null,"start":46432129,"end":46482493,"strand":1,"description":"fatty acid amide hydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50679]"}, {"versioned_ensembl_gene_id":"ENSG00000232855.6","gene_symbol":"AF165147.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28439346,"end":28674848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100225.17","gene_symbol":"FBXO7","gene_name":"F-box protein 7 [Source:HGNC Symbol;Acc:HGNC:13586]","synonyms":"PARK15,FBX7,Fbx","biotype":"protein_coding","ncbi_id":"25793","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it may play a role in regulation of hematopoiesis. Alternatively spliced transcript variants of this gene have been identified with the full-length natures of only some variants being determined. [provided by RefSeq, Jul 2008]","start":32474676,"end":32498829,"strand":1,"description":"F-box protein 7 [Source:HGNC Symbol;Acc:HGNC:13586]"}, {"versioned_ensembl_gene_id":"ENSG00000160695.14","gene_symbol":"VPS11","gene_name":"VPS11, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14583]","synonyms":"RNF108,PEP5","biotype":"protein_coding","ncbi_id":"55823","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps11 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":119067692,"end":119081978,"strand":1,"description":"VPS11, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14583]"}, {"versioned_ensembl_gene_id":"ENSG00000166167.17","gene_symbol":"BTRC","gene_name":"beta-transducin repeat containing E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:1144]","synonyms":"Fwd1,FBXW1A,bTrCP1,bTrCP,betaTrCP,beta-TrCP1","biotype":"protein_coding","ncbi_id":"8945","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbws class; in addition to an F-box, this protein contains multiple WD-40 repeats. The encoded protein mediates degradation of CD4 via its interaction with HIV-1 Vpu. It has also been shown to ubiquitinate phosphorylated NFKBIA (nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha), targeting it for degradation and thus activating nuclear factor kappa-B. Alternatively spliced transcript variants have been described. A related pseudogene exists in chromosome 6. [provided by RefSeq, Mar 2012]","start":101354033,"end":101557321,"strand":1,"description":"beta-transducin repeat containing E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:1144]"}, {"versioned_ensembl_gene_id":"ENSG00000058063.15","gene_symbol":"ATP11B","gene_name":"ATPase phospholipid transporting 11B (putative) [Source:HGNC Symbol;Acc:HGNC:13553]","synonyms":"KIAA0956,ATPIR,ATPIF","biotype":"protein_coding","ncbi_id":"23200","summary":"P-type ATPases, such as ATP11B, are phosphorylated in their intermediate state and drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily transports heavy metal ions, such as Cu(2+) or Cd(2+). Another subfamily transports non-heavy metal ions, such as H(+), Na(+), K(+), or Ca(+). A third subfamily transports amphipaths, such as phosphatidylserine.[supplied by OMIM, Feb 2005]","start":182793500,"end":182921635,"strand":1,"description":"ATPase phospholipid transporting 11B (putative) [Source:HGNC Symbol;Acc:HGNC:13553]"}, {"versioned_ensembl_gene_id":"ENSG00000243468.5","gene_symbol":"INGX","gene_name":"inhibitor of growth family, X-linked (pseudogene) [Source:HGNC Symbol;Acc:HGNC:6064]","synonyms":"ING2,ING1-like","biotype":"transcribed_processed_pseudogene","ncbi_id":"27160","summary":null,"start":71491682,"end":71492928,"strand":-1,"description":"inhibitor of growth family, X-linked (pseudogene) [Source:HGNC Symbol;Acc:HGNC:6064]"}, {"versioned_ensembl_gene_id":"ENSG00000213018.2","gene_symbol":"AL590762.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71420083,"end":71420514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248884.1","gene_symbol":"AC010280.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68430427,"end":68434481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271751.1","gene_symbol":"AP003392.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119065263,"end":119065677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181418.7","gene_symbol":"DDN","gene_name":"dendrin [Source:HGNC Symbol;Acc:HGNC:24458]","synonyms":"KIAA0749","biotype":"protein_coding","ncbi_id":"23109","summary":null,"start":48995149,"end":48999309,"strand":-1,"description":"dendrin [Source:HGNC Symbol;Acc:HGNC:24458]"}, {"versioned_ensembl_gene_id":"ENSG00000160131.13","gene_symbol":"VMA21","gene_name":"VMA21, vacuolar ATPase assembly factor [Source:HGNC Symbol;Acc:HGNC:22082]","synonyms":"XMEA,MEAX","biotype":"protein_coding","ncbi_id":"203547","summary":"This gene encodes a chaperone for assembly of lysosomal vacuolar ATPase.[provided by RefSeq, Jul 2012]","start":151396515,"end":151409364,"strand":1,"description":"VMA21, vacuolar ATPase assembly factor [Source:HGNC Symbol;Acc:HGNC:22082]"}, {"versioned_ensembl_gene_id":"ENSG00000226766.1","gene_symbol":"FABP7P1","gene_name":"fatty acid binding protein 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506953","summary":null,"start":243624666,"end":243625056,"strand":-1,"description":"fatty acid binding protein 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41951]"}, {"versioned_ensembl_gene_id":"ENSG00000101294.16","gene_symbol":"HM13","gene_name":"histocompatibility minor 13 [Source:HGNC Symbol;Acc:HGNC:16435]","synonyms":"IMP1,H13,dJ324O17.1,SPPL1,SPP,PSL3,PSENL3,IMPAS","biotype":"protein_coding","ncbi_id":"81502","summary":"The protein encoded by this gene, which localizes to the endoplasmic reticulum, catalyzes intramembrane proteolysis of some signal peptides after they have been cleaved from a preprotein. This activity is required to generate signal sequence-derived human lymphocyte antigen-E epitopes that are recognized by the immune system, and to process hepatitis C virus core protein. The encoded protein is an integral membrane protein with sequence motifs characteristic of the presenilin-type aspartic proteases. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31514428,"end":31577923,"strand":1,"description":"histocompatibility minor 13 [Source:HGNC Symbol;Acc:HGNC:16435]"}, {"versioned_ensembl_gene_id":"ENSG00000235262.1","gene_symbol":"KDM5C-IT1","gene_name":"KDM5C intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41384]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874299","summary":null,"start":53212408,"end":53214679,"strand":-1,"description":"KDM5C intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41384]"}, {"versioned_ensembl_gene_id":"ENSG00000152402.10","gene_symbol":"GUCY1A2","gene_name":"guanylate cyclase 1 soluble subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:4684]","synonyms":"GUC1A2,GC-SA2","biotype":"protein_coding","ncbi_id":"2977","summary":"Soluble guanylate cyclases are heterodimeric proteins that catalyze the conversion of GTP to 3',5'-cyclic GMP and pyrophosphate. The protein encoded by this gene is an alpha subunit of this complex and it interacts with a beta subunit to form the guanylate cyclase enzyme, which is activated by nitric oxide. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":106674012,"end":107018524,"strand":-1,"description":"guanylate cyclase 1 soluble subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:4684]"}, {"versioned_ensembl_gene_id":"ENSG00000102195.9","gene_symbol":"GPR50","gene_name":"G protein-coupled receptor 50 [Source:HGNC Symbol;Acc:HGNC:4506]","synonyms":"Mel1c,H9","biotype":"protein_coding","ncbi_id":"9248","summary":"This gene product belongs to the G-protein coupled receptor 1 family. Even though this protein shares similarity with the melatonin receptors, it does not bind melatonin, however, it inhibits melatonin receptor 1A function through heterodimerization. Polymorphic variants of this gene have been associated with bipolar affective disorder in women. [provided by RefSeq, Jan 2010]","start":151176653,"end":151181465,"strand":1,"description":"G protein-coupled receptor 50 [Source:HGNC Symbol;Acc:HGNC:4506]"}, {"versioned_ensembl_gene_id":"ENSG00000202259.1","gene_symbol":"RNU6-1318P","gene_name":"RNA, U6 small nuclear 1318, pseudogene [Source:HGNC Symbol;Acc:HGNC:48281]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480141","summary":null,"start":100000637,"end":100000739,"strand":-1,"description":"RNA, U6 small nuclear 1318, pseudogene [Source:HGNC Symbol;Acc:HGNC:48281]"}, {"versioned_ensembl_gene_id":"ENSG00000211850.1","gene_symbol":"TRAJ39","gene_name":"T-cell receptor alpha joining 39 [Source:HGNC Symbol;Acc:HGNC:12069]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28716","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22501601,"end":22501663,"strand":1,"description":"T-cell receptor alpha joining 39 [Source:HGNC Symbol;Acc:HGNC:12069]"}, {"versioned_ensembl_gene_id":"ENSG00000211849.1","gene_symbol":"TRAJ40","gene_name":"T-cell receptor alpha joining 40 [Source:HGNC Symbol;Acc:HGNC:12071]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28715","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22499689,"end":22499749,"strand":1,"description":"T-cell receptor alpha joining 40 [Source:HGNC Symbol;Acc:HGNC:12071]"}, {"versioned_ensembl_gene_id":"ENSG00000250813.1","gene_symbol":"SERF1AP1","gene_name":"small EDRK-rich factor 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44061]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131921","summary":null,"start":137301001,"end":137301187,"strand":-1,"description":"small EDRK-rich factor 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44061]"}, {"versioned_ensembl_gene_id":"ENSG00000152034.10","gene_symbol":"MCHR2","gene_name":"melanin concentrating hormone receptor 2 [Source:HGNC Symbol;Acc:HGNC:20867]","synonyms":"SLT,MCH2R,MCH2,GPR145","biotype":"protein_coding","ncbi_id":"84539","summary":null,"start":99919910,"end":99994247,"strand":-1,"description":"melanin concentrating hormone receptor 2 [Source:HGNC Symbol;Acc:HGNC:20867]"}, {"versioned_ensembl_gene_id":"ENSG00000172985.10","gene_symbol":"SH3RF3","gene_name":"SH3 domain containing ring finger 3 [Source:HGNC Symbol;Acc:HGNC:24699]","synonyms":"SH3MD4,POSH2,FLJ00204","biotype":"protein_coding","ncbi_id":"344558","summary":null,"start":109129348,"end":109504632,"strand":1,"description":"SH3 domain containing ring finger 3 [Source:HGNC Symbol;Acc:HGNC:24699]"}, {"versioned_ensembl_gene_id":"ENSG00000254463.1","gene_symbol":"AC087276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43466392,"end":43466871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254907.1","gene_symbol":"AC087276.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43328748,"end":43359296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000097021.19","gene_symbol":"ACOT7","gene_name":"acyl-CoA thioesterase 7 [Source:HGNC Symbol;Acc:HGNC:24157]","synonyms":"MGC1126,LACH1,hBACH,CTE-II,BACH,ACT,ACH1","biotype":"protein_coding","ncbi_id":"11332","summary":"This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized. [provided by RefSeq, Jul 2008]","start":6264269,"end":6394391,"strand":-1,"description":"acyl-CoA thioesterase 7 [Source:HGNC Symbol;Acc:HGNC:24157]"}, {"versioned_ensembl_gene_id":"ENSG00000254661.2","gene_symbol":"AC009869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15910957,"end":15927443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219257.2","gene_symbol":"NPM1P38","gene_name":"nucleophosmin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45217]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128985","summary":null,"start":100050372,"end":100051236,"strand":-1,"description":"nucleophosmin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45217]"}, {"versioned_ensembl_gene_id":"ENSG00000276701.2","gene_symbol":"MIF","gene_name":"macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Source:HGNC Symbol;Acc:HGNC:7097]","synonyms":"GLIF,GIF","biotype":"protein_coding","ncbi_id":"4282","summary":"This gene encodes a lymphokine involved in cell-mediated immunity, immunoregulation, and inflammation. It plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. This lymphokine and the JAB1 protein form a complex in the cytosol near the peripheral plasma membrane, which may indicate an additional role in integrin signaling pathways. [provided by RefSeq, Jul 2008]","start":23894004,"end":23895227,"strand":1,"description":"macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Source:HGNC Symbol;Acc:HGNC:7097]"}, {"versioned_ensembl_gene_id":"ENSG00000273377.1","gene_symbol":"AC004853.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143980905,"end":143981820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254695.1","gene_symbol":"AC087379.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15643885,"end":15705368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106829.18","gene_symbol":"TLE4","gene_name":"transducin like enhancer of split 4 [Source:HGNC Symbol;Acc:HGNC:11840]","synonyms":"GRG4,ESG,E(spI)","biotype":"protein_coding","ncbi_id":"7091","summary":null,"start":79571773,"end":79726882,"strand":1,"description":"transducin like enhancer of split 4 [Source:HGNC Symbol;Acc:HGNC:11840]"}, {"versioned_ensembl_gene_id":"ENSG00000203908.3","gene_symbol":"KHDC3L","gene_name":"KH domain containing 3 like, subcortical maternal complex member [Source:HGNC Symbol;Acc:HGNC:33699]","synonyms":"ECAT1,C6orf221","biotype":"protein_coding","ncbi_id":"154288","summary":"The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole. [provided by RefSeq, Dec 2011]","start":73362677,"end":73364171,"strand":1,"description":"KH domain containing 3 like, subcortical maternal complex member [Source:HGNC Symbol;Acc:HGNC:33699]"}, {"versioned_ensembl_gene_id":"ENSG00000269667.1","gene_symbol":"AC092723.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85981750,"end":85984723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158201.9","gene_symbol":"ABHD3","gene_name":"abhydrolase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18718]","synonyms":"LABH3","biotype":"protein_coding","ncbi_id":"171586","summary":"This gene encodes a protein containing an alpha/beta hydrolase fold, which is a catalytic domain found in a very wide range of enzymes. The function of this protein has not been determined. [provided by RefSeq, Jul 2008]","start":21650897,"end":21704805,"strand":-1,"description":"abhydrolase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18718]"}, {"versioned_ensembl_gene_id":"ENSG00000132915.10","gene_symbol":"PDE6A","gene_name":"phosphodiesterase 6A [Source:HGNC Symbol;Acc:HGNC:8785]","synonyms":"RP43,PDEA","biotype":"protein_coding","ncbi_id":"5145","summary":"This gene encodes the cyclic-GMP (cGMP)-specific phosphodiesterase 6A alpha subunit, expressed in cells of the retinal rod outer segment. The phosphodiesterase 6 holoenzyme is a heterotrimer composed of an alpha, beta, and two gamma subunits. cGMP is an important regulator of rod cell membrane current, and its dynamic concentration is established by phosphodiesterase 6A cGMP hydrolysis and guanylate cyclase cGMP synthesis. The protein is a subunit of a key phototransduction enzyme and participates in processes of transmission and amplification of the visual signal. Mutations in this gene have been identified as one cause of autosomal recessive retinitis pigmentosa. [provided by RefSeq, Jul 2008]","start":149857955,"end":149944793,"strand":-1,"description":"phosphodiesterase 6A [Source:HGNC Symbol;Acc:HGNC:8785]"}, {"versioned_ensembl_gene_id":"ENSG00000270916.1","gene_symbol":"RPL12P50","gene_name":"ribosomal protein L12 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:51942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075212","summary":null,"start":151023607,"end":151023722,"strand":-1,"description":"ribosomal protein L12 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:51942]"}, {"versioned_ensembl_gene_id":"ENSG00000254146.1","gene_symbol":"HMGB1P46","gene_name":"high mobility group box 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:39279]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419978","summary":null,"start":107173200,"end":107173809,"strand":-1,"description":"high mobility group box 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:39279]"}, {"versioned_ensembl_gene_id":"ENSG00000218521.1","gene_symbol":"AL589655.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38002832,"end":38003313,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143321.18","gene_symbol":"HDGF","gene_name":"heparin binding growth factor [Source:HGNC Symbol;Acc:HGNC:4856]","synonyms":"HMG1L2","biotype":"protein_coding","ncbi_id":"3068","summary":"This gene encodes a member of the hepatoma-derived growth factor family. The encoded protein has mitogenic and DNA-binding activity and may play a role in cellular proliferation and differentiation. High levels of expression of this gene enhance the growth of many tumors. This gene was thought initially to be located on chromosome X; however, that location has been determined to correspond to a related pseudogene. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jan 2016]","start":156742107,"end":156766925,"strand":-1,"description":"heparin binding growth factor [Source:HGNC Symbol;Acc:HGNC:4856]"}, {"versioned_ensembl_gene_id":"ENSG00000214252.4","gene_symbol":"AZGP1P2","gene_name":"alpha-2-glycoprotein 1, zinc-binding pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:912]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"401393","summary":null,"start":101287482,"end":101289771,"strand":-1,"description":"alpha-2-glycoprotein 1, zinc-binding pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:912]"}, {"versioned_ensembl_gene_id":"ENSG00000278683.1","gene_symbol":"AC006329.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101273322,"end":101273715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140287.10","gene_symbol":"HDC","gene_name":"histidine decarboxylase [Source:HGNC Symbol;Acc:HGNC:4855]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3067","summary":"This gene encodes a member of the group II decarboxylase family and forms a homodimer that converts L-histidine to histamine in a pyridoxal phosphate dependent manner. Histamine regulates several physiologic processes, including neurotransmission, gastric acid secretion,inflamation, and smooth muscle tone.[provided by RefSeq, Aug 2010]","start":50241947,"end":50266026,"strand":-1,"description":"histidine decarboxylase [Source:HGNC Symbol;Acc:HGNC:4855]"}, {"versioned_ensembl_gene_id":"ENSG00000183311.16","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30709720,"end":30714946,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000132465.10","gene_symbol":"JCHAIN","gene_name":"joining chain of multimeric IgA and IgM [Source:HGNC Symbol;Acc:HGNC:5713]","synonyms":"JCH,IGJ,IGCJ","biotype":"protein_coding","ncbi_id":"3512","summary":null,"start":70655541,"end":70681817,"strand":-1,"description":"joining chain of multimeric IgA and IgM [Source:HGNC Symbol;Acc:HGNC:5713]"}, {"versioned_ensembl_gene_id":"ENSG00000259019.1","gene_symbol":"EIF4BP1","gene_name":"eukaryotic translation initiation factor 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19929]","synonyms":"EIF4BP","biotype":"transcribed_processed_pseudogene","ncbi_id":"319118","summary":null,"start":44077534,"end":44077884,"strand":-1,"description":"eukaryotic translation initiation factor 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19929]"}, {"versioned_ensembl_gene_id":"ENSG00000259137.1","gene_symbol":"AL109766.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44120210,"end":44120761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259148.1","gene_symbol":"YWHAZP1","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19938]","synonyms":"YWHAZP","biotype":"processed_pseudogene","ncbi_id":"319120","summary":null,"start":44290997,"end":44291718,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19938]"}, {"versioned_ensembl_gene_id":"ENSG00000276257.1","gene_symbol":"AL513478.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66084804,"end":66085031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259028.1","gene_symbol":"AL135746.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87568181,"end":87569399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258958.1","gene_symbol":"AL157688.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87323753,"end":87332390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100532.11","gene_symbol":"CGRRF1","gene_name":"cell growth regulator with ring finger domain 1 [Source:HGNC Symbol;Acc:HGNC:15528]","synonyms":"RNF197,CGR19","biotype":"protein_coding","ncbi_id":"10668","summary":null,"start":54509812,"end":54539309,"strand":1,"description":"cell growth regulator with ring finger domain 1 [Source:HGNC Symbol;Acc:HGNC:15528]"}, {"versioned_ensembl_gene_id":"ENSG00000258804.1","gene_symbol":"LINC01148","gene_name":"long intergenic non-protein coding RNA 1148 [Source:HGNC Symbol;Acc:HGNC:27507]","synonyms":"LOC283585","biotype":"lincRNA","ncbi_id":"283585","summary":null,"start":86905778,"end":86922755,"strand":1,"description":"long intergenic non-protein coding RNA 1148 [Source:HGNC Symbol;Acc:HGNC:27507]"}, {"versioned_ensembl_gene_id":"ENSG00000258994.1","gene_symbol":"LINC02309","gene_name":"long intergenic non-protein coding RNA 2309 [Source:HGNC Symbol;Acc:HGNC:53228]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370607","summary":null,"start":86332376,"end":86401285,"strand":1,"description":"long intergenic non-protein coding RNA 2309 [Source:HGNC Symbol;Acc:HGNC:53228]"}, {"versioned_ensembl_gene_id":"ENSG00000136908.17","gene_symbol":"DPM2","gene_name":"dolichyl-phosphate mannosyltransferase subunit 2, regulatory [Source:HGNC Symbol;Acc:HGNC:3006]","synonyms":"MGC111193,MGC21559","biotype":"protein_coding","ncbi_id":"8818","summary":"Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. The protein encoded by this gene is a hydrophobic protein that contains 2 predicted transmembrane domains and a putative ER localization signal near the C terminus. This protein associates with DPM1 in vivo and is required for the ER localization and stable expression of DPM1 and also enhances the binding of dolichol-phosphate to DPM1. [provided by RefSeq, Jul 2008]","start":127935099,"end":127938484,"strand":-1,"description":"dolichyl-phosphate mannosyltransferase subunit 2, regulatory [Source:HGNC Symbol;Acc:HGNC:3006]"}, {"versioned_ensembl_gene_id":"ENSG00000225125.2","gene_symbol":"RANP4","gene_name":"RAN, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39859]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130621","summary":null,"start":136807223,"end":136807877,"strand":-1,"description":"RAN, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39859]"}, {"versioned_ensembl_gene_id":"ENSG00000253877.5","gene_symbol":"LINC01608","gene_name":"long intergenic non-protein coding RNA 1608 [Source:HGNC Symbol;Acc:HGNC:51662]","synonyms":"TCONS_00015136","biotype":"lincRNA","ncbi_id":"101927459","summary":null,"start":110937690,"end":111027433,"strand":-1,"description":"long intergenic non-protein coding RNA 1608 [Source:HGNC Symbol;Acc:HGNC:51662]"}, {"versioned_ensembl_gene_id":"ENSG00000270105.1","gene_symbol":"AC136475.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":322186,"end":322727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124193.14","gene_symbol":"SRSF6","gene_name":"serine and arginine rich splicing factor 6 [Source:HGNC Symbol;Acc:HGNC:10788]","synonyms":"SRP55,SFRS6,B52","biotype":"protein_coding","ncbi_id":"6431","summary":"The protein encoded by this gene is involved in mRNA splicing and may play a role in the determination of alternative splicing. The encoded nuclear protein belongs to the splicing factor SR family and has been shown to bind with and modulate another member of the family, SFRS12. Alternative splicing results in multiple transcript variants. In addition, two pseudogenes, one on chromosome 17 and the other on the X chromosome, have been found for this gene.[provided by RefSeq, Sep 2010]","start":43457928,"end":43464247,"strand":1,"description":"serine and arginine rich splicing factor 6 [Source:HGNC Symbol;Acc:HGNC:10788]"}, {"versioned_ensembl_gene_id":"ENSG00000236799.1","gene_symbol":"AL355340.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114994657,"end":114996593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117020.16","gene_symbol":"AKT3","gene_name":"AKT serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:393]","synonyms":"RAC-gamma,PRKBG,PKBG","biotype":"protein_coding","ncbi_id":"10000","summary":"The protein encoded by this gene is a member of the AKT, also called PKB, serine/threonine protein kinase family. AKT kinases are known to be regulators of cell signaling in response to insulin and growth factors. They are involved in a wide variety of biological processes including cell proliferation, differentiation, apoptosis, tumorigenesis, as well as glycogen synthesis and glucose uptake. This kinase has been shown to be stimulated by platelet-derived growth factor (PDGF), insulin, and insulin-like growth factor 1 (IGF1). Alternatively splice transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":243488233,"end":243851079,"strand":-1,"description":"AKT serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:393]"}, {"versioned_ensembl_gene_id":"ENSG00000268614.1","gene_symbol":"AC008878.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7533595,"end":7540059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143294.14","gene_symbol":"PRCC","gene_name":"papillary renal cell carcinoma (translocation-associated) [Source:HGNC Symbol;Acc:HGNC:9343]","synonyms":"RCCP1","biotype":"protein_coding","ncbi_id":"5546","summary":"This gene encodes a protein that may play a role in pre-mRNA splicing. Chromosomal translocations (X;1)(p11;q21) that result in fusion of this gene to TFE3 (GeneID 7030) have been associated with papillary renal cell carcinoma. A PRCC-TFE3 fusion protein is expressed in affected carcinomas and is likely associated with altered gene transactivation. This fusion protein has also been associated with disruption of the cell cycle.[provided by RefSeq, Aug 2010]","start":156750610,"end":156800817,"strand":1,"description":"papillary renal cell carcinoma (translocation-associated) [Source:HGNC Symbol;Acc:HGNC:9343]"}, {"versioned_ensembl_gene_id":"ENSG00000092969.11","gene_symbol":"TGFB2","gene_name":"transforming growth factor beta 2 [Source:HGNC Symbol;Acc:HGNC:11768]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7042","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGF-beta family members. Disruption of the TGF-beta/SMAD pathway has been implicated in a variety of human cancers. A chromosomal translocation that includes this gene is associated with Peters' anomaly, a congenital defect of the anterior chamber of the eye. Mutations in this gene may be associated with Loeys-Dietz syndrome. This gene encodes multiple isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]","start":218346235,"end":218444619,"strand":1,"description":"transforming growth factor beta 2 [Source:HGNC Symbol;Acc:HGNC:11768]"}, {"versioned_ensembl_gene_id":"ENSG00000223389.1","gene_symbol":"SDCBP2P1","gene_name":"syndecan binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44685]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480801","summary":null,"start":73322837,"end":73323450,"strand":1,"description":"syndecan binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44685]"}, {"versioned_ensembl_gene_id":"ENSG00000228890.1","gene_symbol":"TTTY21","gene_name":"testis-specific transcript, Y-linked 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18845]","synonyms":"NCRNA00146","biotype":"lincRNA","ncbi_id":"252953","summary":null,"start":9717653,"end":9721296,"strand":-1,"description":"testis-specific transcript, Y-linked 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18845]"}, {"versioned_ensembl_gene_id":"ENSG00000259986.1","gene_symbol":"AC103876.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83179182,"end":83439445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235531.9","gene_symbol":"MSC-AS1","gene_name":"MSC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48724]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132891","summary":null,"start":71828167,"end":72118393,"strand":1,"description":"MSC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48724]"}, {"versioned_ensembl_gene_id":"ENSG00000241607.1","gene_symbol":"AC245096.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37441523,"end":37442068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102921.7","gene_symbol":"N4BP1","gene_name":"NEDD4 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29850]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9683","summary":null,"start":48538726,"end":48620148,"strand":-1,"description":"NEDD4 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29850]"}, {"versioned_ensembl_gene_id":"ENSG00000105697.7","gene_symbol":"HAMP","gene_name":"hepcidin antimicrobial peptide [Source:HGNC Symbol;Acc:HGNC:15598]","synonyms":"LEAP1,LEAP-1,HFE2B,HEPC","biotype":"protein_coding","ncbi_id":"57817","summary":"The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity against bacteria and fungi. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Oct 2014]","start":35280716,"end":35285143,"strand":1,"description":"hepcidin antimicrobial peptide [Source:HGNC Symbol;Acc:HGNC:15598]"}, {"versioned_ensembl_gene_id":"ENSG00000259044.1","gene_symbol":"AL357172.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85202849,"end":85239474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243696.4","gene_symbol":"AC006254.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52813282,"end":52835729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160633.12","gene_symbol":"SAFB","gene_name":"scaffold attachment factor B [Source:HGNC Symbol;Acc:HGNC:10520]","synonyms":"SAFB1,HET","biotype":"protein_coding","ncbi_id":"6294","summary":"This gene encodes a DNA-binding protein which has high specificity for scaffold or matrix attachment region DNA elements (S/MAR DNA). This protein is thought to be involved in attaching the base of chromatin loops to the nuclear matrix but there is conflicting evidence as to whether this protein is a component of chromatin or a nuclear matrix protein. Scaffold attachment factors are a specific subset of nuclear matrix proteins (NMP) that specifically bind to S/MAR. The encoded protein is thought to serve as a molecular base to assemble a 'transcriptosome complex' in the vicinity of actively transcribed genes. It is involved in the regulation of heat shock protein 27 transcription, can act as an estrogen receptor co-repressor and is a candidate for breast tumorigenesis. This gene is arranged head-to-head with a similar gene whose product has the same functions. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2011]","start":5623035,"end":5668478,"strand":1,"description":"scaffold attachment factor B [Source:HGNC Symbol;Acc:HGNC:10520]"}, {"versioned_ensembl_gene_id":"ENSG00000227988.1","gene_symbol":"TDGF1P1","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421177","summary":null,"start":38395369,"end":38395895,"strand":-1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42350]"}, {"versioned_ensembl_gene_id":"ENSG00000254241.1","gene_symbol":"MTCO1P47","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:52112]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075284","summary":null,"start":110933263,"end":110934533,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:52112]"}, {"versioned_ensembl_gene_id":"ENSG00000036565.14","gene_symbol":"SLC18A1","gene_name":"solute carrier family 18 member A1 [Source:HGNC Symbol;Acc:HGNC:10934]","synonyms":"CGAT,VMAT1,VAT1","biotype":"protein_coding","ncbi_id":"6570","summary":"The vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993 [PubMed 7905859]). See also SLC18A2 (MIM 193001).[supplied by OMIM, Mar 2008]","start":20144855,"end":20183206,"strand":-1,"description":"solute carrier family 18 member A1 [Source:HGNC Symbol;Acc:HGNC:10934]"}, {"versioned_ensembl_gene_id":"ENSG00000008197.4","gene_symbol":"TFAP2D","gene_name":"transcription factor AP-2 delta [Source:HGNC Symbol;Acc:HGNC:15581]","synonyms":"TFAP2BL1","biotype":"protein_coding","ncbi_id":"83741","summary":null,"start":50713828,"end":50772988,"strand":1,"description":"transcription factor AP-2 delta [Source:HGNC Symbol;Acc:HGNC:15581]"}, {"versioned_ensembl_gene_id":"ENSG00000255923.1","gene_symbol":"AC078878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126864465,"end":126865422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229321.1","gene_symbol":"AC008269.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206866795,"end":206868289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227899.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30692588,"end":30702703,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000212930.3","gene_symbol":"AC093281.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91223419,"end":91223967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174744.13","gene_symbol":"BRMS1","gene_name":"breast cancer metastasis suppressor 1 [Source:HGNC Symbol;Acc:HGNC:17262]","synonyms":"DKFZP564A063","biotype":"protein_coding","ncbi_id":"25855","summary":"This gene reduces the metastatic potential, but not the tumorogenicity, of human breast cancer and melanoma cell lines. The protein encoded by this gene localizes primarily to the nucleus and is a component of the mSin3a family of histone deacetylase complexes (HDAC). The protein contains two coiled-coil motifs and several imperfect leucine zipper motifs. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":66337333,"end":66345125,"strand":-1,"description":"breast cancer metastasis suppressor 1 [Source:HGNC Symbol;Acc:HGNC:17262]"}, {"versioned_ensembl_gene_id":"ENSG00000261244.1","gene_symbol":"AC104758.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77916522,"end":77922019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110375.2","gene_symbol":"UPK2","gene_name":"uroplakin 2 [Source:HGNC Symbol;Acc:HGNC:12579]","synonyms":"UPII,UP2,MGC138598","biotype":"protein_coding","ncbi_id":"7379","summary":"This gene encodes one of the proteins of the highly conserved urothelium-specific integral membrane proteins of the asymmetric unit membrane which forms urothelium apical plaques in mammals. The asymmetric unit membrane is believed to strengthen the urothelium by preventing cell rupture during bladder distention. The encoded protein is expressed in the peripheral blood of bladder cancer patients with transitional cell carcinomas.[provided by RefSeq, Sep 2009]","start":118925164,"end":118958559,"strand":1,"description":"uroplakin 2 [Source:HGNC Symbol;Acc:HGNC:12579]"}, {"versioned_ensembl_gene_id":"ENSG00000254756.1","gene_symbol":"AP001107.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66334494,"end":66339875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279108.1","gene_symbol":"AC008537.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40840159,"end":40842039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275489.1","gene_symbol":"C17orf98","gene_name":"chromosome 17 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:34492]","synonyms":"LOC388381","biotype":"protein_coding","ncbi_id":"388381","summary":null,"start":38835088,"end":38841455,"strand":-1,"description":"chromosome 17 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:34492]"}, {"versioned_ensembl_gene_id":"ENSG00000188886.3","gene_symbol":"ASTL","gene_name":"astacin like metalloendopeptidase [Source:HGNC Symbol;Acc:HGNC:31704]","synonyms":"SAS1B,ovastacin","biotype":"protein_coding","ncbi_id":"431705","summary":null,"start":96123850,"end":96138436,"strand":-1,"description":"astacin like metalloendopeptidase [Source:HGNC Symbol;Acc:HGNC:31704]"}, {"versioned_ensembl_gene_id":"ENSG00000198420.9","gene_symbol":"TCAF1","gene_name":"TRPM8 channel associated factor 1 [Source:HGNC Symbol;Acc:HGNC:22201]","synonyms":"FAM115A,KIAA0738","biotype":"protein_coding","ncbi_id":"9747","summary":null,"start":143851375,"end":143902198,"strand":-1,"description":"TRPM8 channel associated factor 1 [Source:HGNC Symbol;Acc:HGNC:22201]"}, {"versioned_ensembl_gene_id":"ENSG00000235801.1","gene_symbol":"BX927220.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30560894,"end":30563845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254914.1","gene_symbol":"AC109810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42939775,"end":42939998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267751.5","gene_symbol":"AC009005.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":567210,"end":572228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198816.6","gene_symbol":"ZNF358","gene_name":"zinc finger protein 358 [Source:HGNC Symbol;Acc:HGNC:16838]","synonyms":"ZFEND,FLJ10390","biotype":"protein_coding","ncbi_id":"140467","summary":null,"start":7515292,"end":7521026,"strand":1,"description":"zinc finger protein 358 [Source:HGNC Symbol;Acc:HGNC:16838]"}, {"versioned_ensembl_gene_id":"ENSG00000226819.1","gene_symbol":"MEIS1-AS3","gene_name":"MEIS1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40369]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"730198","summary":null,"start":66426735,"end":66433470,"strand":-1,"description":"MEIS1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40369]"}, {"versioned_ensembl_gene_id":"ENSG00000230379.5","gene_symbol":"AP000146.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24938431,"end":24992817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211835.1","gene_symbol":"TRAJ56","gene_name":"T-cell receptor alpha joining 56 [Source:HGNC Symbol;Acc:HGNC:12088]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28699","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22479521,"end":22479582,"strand":1,"description":"T-cell receptor alpha joining 56 [Source:HGNC Symbol;Acc:HGNC:12088]"}, {"versioned_ensembl_gene_id":"ENSG00000130772.13","gene_symbol":"MED18","gene_name":"mediator complex subunit 18 [Source:HGNC Symbol;Acc:HGNC:25944]","synonyms":"p28b,FLJ20045,SRB5","biotype":"protein_coding","ncbi_id":"54797","summary":"MED18 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008]","start":28329002,"end":28335967,"strand":1,"description":"mediator complex subunit 18 [Source:HGNC Symbol;Acc:HGNC:25944]"}, {"versioned_ensembl_gene_id":"ENSG00000235619.1","gene_symbol":"RPL36AP33","gene_name":"ribosomal protein L36a pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36475]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100191039","summary":null,"start":35507564,"end":35507873,"strand":1,"description":"ribosomal protein L36a pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36475]"}, {"versioned_ensembl_gene_id":"ENSG00000271182.1","gene_symbol":"AC123912.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21634833,"end":21635175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266184.1","gene_symbol":"AC018371.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26831520,"end":26832432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263846.1","gene_symbol":"CIAPIN1P","gene_name":"cytokine induced apoptosis inhibitor 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31087]","synonyms":"HsT2384","biotype":"processed_pseudogene","ncbi_id":"728599","summary":null,"start":26599408,"end":26600338,"strand":1,"description":"cytokine induced apoptosis inhibitor 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31087]"}, {"versioned_ensembl_gene_id":"ENSG00000228370.1","gene_symbol":"BX927133.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497042,"end":29510088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184903.9","gene_symbol":"IMMP2L","gene_name":"inner mitochondrial membrane peptidase subunit 2 [Source:HGNC Symbol;Acc:HGNC:14598]","synonyms":"IMMP2L-IT1,IMP2","biotype":"protein_coding","ncbi_id":"83943","summary":"This gene encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for this gene. [provided by RefSeq, Sep 2011]","start":110663051,"end":111562517,"strand":-1,"description":"inner mitochondrial membrane peptidase subunit 2 [Source:HGNC Symbol;Acc:HGNC:14598]"}, {"versioned_ensembl_gene_id":"ENSG00000124772.11","gene_symbol":"CPNE5","gene_name":"copine 5 [Source:HGNC Symbol;Acc:HGNC:2318]","synonyms":"KIAA1599,CPN5,COPN5","biotype":"protein_coding","ncbi_id":"57699","summary":"Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene is one of several genes that encode a calcium-dependent protein containing two N-terminal type II C2 domains and an integrin A domain-like sequence in the C-terminus. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. More variants may exist, but their full-length natures could not be determined. [provided by RefSeq, Sep 2015]","start":36740775,"end":36840002,"strand":-1,"description":"copine 5 [Source:HGNC Symbol;Acc:HGNC:2318]"}, {"versioned_ensembl_gene_id":"ENSG00000259035.1","gene_symbol":"AL355838.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81741002,"end":82030349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173114.12","gene_symbol":"LRRN3","gene_name":"leucine rich repeat neuronal 3 [Source:HGNC Symbol;Acc:HGNC:17200]","synonyms":"NLRR3,FLJ11129,FIGLER5","biotype":"protein_coding","ncbi_id":"54674","summary":null,"start":111091006,"end":111125454,"strand":1,"description":"leucine rich repeat neuronal 3 [Source:HGNC Symbol;Acc:HGNC:17200]"}, {"versioned_ensembl_gene_id":"ENSG00000230178.1","gene_symbol":"OR4F3","gene_name":"olfactory receptor family 4 subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:8300]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26683","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":181367268,"end":181368262,"strand":1,"description":"olfactory receptor family 4 subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:8300]"}, {"versioned_ensembl_gene_id":"ENSG00000241723.1","gene_symbol":"AC074276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158275809,"end":158276421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197771.12","gene_symbol":"MCMBP","gene_name":"minichromosome maintenance complex binding protein [Source:HGNC Symbol;Acc:HGNC:25782]","synonyms":"C10orf119,MCM-BP,FLJ13081","biotype":"protein_coding","ncbi_id":"79892","summary":"This gene encodes a protein which is a component of the hexameric minichromosome maintenance (MCM) complex which regulates initiation and elongation of DNA. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":119829404,"end":119892556,"strand":-1,"description":"minichromosome maintenance complex binding protein [Source:HGNC Symbol;Acc:HGNC:25782]"}, {"versioned_ensembl_gene_id":"ENSG00000093134.14","gene_symbol":"VNN3","gene_name":"vanin 3 [Source:HGNC Symbol;Acc:HGNC:16431]","synonyms":"HSA238982","biotype":"protein_coding","ncbi_id":"55350","summary":"This gene is the central gene in a cluster of three vanin genes on chromosome 6q23-q24. Extensive alternative splicing has been described; the two most common variants are represented as RefSeqs. [provided by RefSeq, Apr 2014]","start":132722787,"end":132734765,"strand":-1,"description":"vanin 3 [Source:HGNC Symbol;Acc:HGNC:16431]"}, {"versioned_ensembl_gene_id":"ENSG00000251291.1","gene_symbol":"LINC02462","gene_name":"long intergenic non-protein coding RNA 2462 [Source:HGNC Symbol;Acc:HGNC:53399]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377434","summary":null,"start":134423867,"end":134457852,"strand":1,"description":"long intergenic non-protein coding RNA 2462 [Source:HGNC Symbol;Acc:HGNC:53399]"}, {"versioned_ensembl_gene_id":"ENSG00000226571.1","gene_symbol":"AL158850.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139271362,"end":139287307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228614.1","gene_symbol":"AL513211.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53790875,"end":53794274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211819.3","gene_symbol":"TRAV40","gene_name":"T-cell receptor alpha variable 40 [Source:HGNC Symbol;Acc:HGNC:12141]","synonyms":"TCRAV40S1,TCRAV31S1","biotype":"TR_V_gene","ncbi_id":"28641","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22314490,"end":22314919,"strand":1,"description":"T-cell receptor alpha variable 40 [Source:HGNC Symbol;Acc:HGNC:12141]"}, {"versioned_ensembl_gene_id":"ENSG00000180872.4","gene_symbol":"DEFB112","gene_name":"defensin beta 112 [Source:HGNC Symbol;Acc:HGNC:18093]","synonyms":"DEFB-12","biotype":"protein_coding","ncbi_id":"245915","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. [provided by RefSeq, Oct 2014]","start":50043575,"end":50048651,"strand":-1,"description":"defensin beta 112 [Source:HGNC Symbol;Acc:HGNC:18093]"}, {"versioned_ensembl_gene_id":"ENSG00000163376.11","gene_symbol":"KBTBD8","gene_name":"kelch repeat and BTB domain containing 8 [Source:HGNC Symbol;Acc:HGNC:30691]","synonyms":"TA-KRP,KIAA1842","biotype":"protein_coding","ncbi_id":"84541","summary":null,"start":66998307,"end":67011210,"strand":1,"description":"kelch repeat and BTB domain containing 8 [Source:HGNC Symbol;Acc:HGNC:30691]"}, {"versioned_ensembl_gene_id":"ENSG00000270300.2","gene_symbol":"PHACTR2P1","gene_name":"phosphatase and actin regulator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49488]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100533676","summary":null,"start":119793589,"end":119816642,"strand":-1,"description":"phosphatase and actin regulator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49488]"}, {"versioned_ensembl_gene_id":"ENSG00000280381.1","gene_symbol":"AC026362.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123087256,"end":123092821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248401.2","gene_symbol":"AC114781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83247179,"end":83248206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238273.3","gene_symbol":"AC108058.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105363038,"end":105378839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235491.1","gene_symbol":"LINC01889","gene_name":"long intergenic non-protein coding RNA 1889 [Source:HGNC Symbol;Acc:HGNC:52708]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373597","summary":null,"start":125710969,"end":125765842,"strand":1,"description":"long intergenic non-protein coding RNA 1889 [Source:HGNC Symbol;Acc:HGNC:52708]"}, {"versioned_ensembl_gene_id":"ENSG00000280402.1","gene_symbol":"AC093525.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2578395,"end":2579963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226965.1","gene_symbol":"AC092167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110432239,"end":110534754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278330.1","gene_symbol":"AC018529.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77112602,"end":77115726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278424.1","gene_symbol":"AC073114.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110215891,"end":110216380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232199.1","gene_symbol":"RPL3P8","gene_name":"ribosomal protein L3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646620","summary":null,"start":109998434,"end":109999624,"strand":-1,"description":"ribosomal protein L3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35498]"}, {"versioned_ensembl_gene_id":"ENSG00000251661.3","gene_symbol":"AC136475.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":318640,"end":325631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281787.1","gene_symbol":"AF250324.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189790922,"end":189906229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204356.13","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"RDP,NELF-E,RDBP,D6S45,RD","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":31952087,"end":31959110,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000109111.14","gene_symbol":"SUPT6H","gene_name":"SPT6 homolog, histone chaperone [Source:HGNC Symbol;Acc:HGNC:11470]","synonyms":"SPT6H,KIAA0162","biotype":"protein_coding","ncbi_id":"6830","summary":null,"start":28662091,"end":28702684,"strand":1,"description":"SPT6 homolog, histone chaperone [Source:HGNC Symbol;Acc:HGNC:11470]"}, {"versioned_ensembl_gene_id":"ENSG00000282675.1","gene_symbol":"AC245078.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11155045,"end":11155955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240827.1","gene_symbol":"AC021660.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98620065,"end":98620618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203685.9","gene_symbol":"STUM","gene_name":"stum, mechanosensory transduction mediator homolog [Source:HGNC Symbol;Acc:HGNC:30491]","synonyms":"DKFZp761P211,C1orf95","biotype":"protein_coding","ncbi_id":"375057","summary":null,"start":226548800,"end":226609214,"strand":1,"description":"stum, mechanosensory transduction mediator homolog [Source:HGNC Symbol;Acc:HGNC:30491]"}, {"versioned_ensembl_gene_id":"ENSG00000106927.11","gene_symbol":"AMBP","gene_name":"alpha-1-microglobulin/bikunin precursor [Source:HGNC Symbol;Acc:HGNC:453]","synonyms":"UTI,ITILC,ITIL,ITI,IATIL,HI30,HCP,EDC1","biotype":"protein_coding","ncbi_id":"259","summary":"This gene encodes a complex glycoprotein secreted in plasma. The precursor is proteolytically processed into distinct functioning proteins: alpha-1-microglobulin, which belongs to the superfamily of lipocalin transport proteins and may play a role in the regulation of inflammatory processes, and bikunin, which is a urinary trypsin inhibitor belonging to the superfamily of Kunitz-type protease inhibitors and plays an important role in many physiological and pathological processes. This gene is located on chromosome 9 in a cluster of lipocalin genes. [provided by RefSeq, Jul 2008]","start":114060127,"end":114078472,"strand":-1,"description":"alpha-1-microglobulin/bikunin precursor [Source:HGNC Symbol;Acc:HGNC:453]"}, {"versioned_ensembl_gene_id":"ENSG00000138336.8","gene_symbol":"TET1","gene_name":"tet methylcytosine dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:29484]","synonyms":"LCX,KIAA1676,CXXC6,bA119F7.1","biotype":"protein_coding","ncbi_id":"80312","summary":"DNA methylation is an epigenetic mechanism that is important for controlling gene expression. The protein encoded by this gene is a demethylase that belongs to the TET (ten-eleven translocation) family. Members of the TET protein family play a role in the DNA methylation process and gene activation. [provided by RefSeq, Sep 2015]","start":68560656,"end":68694482,"strand":1,"description":"tet methylcytosine dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:29484]"}, {"versioned_ensembl_gene_id":"ENSG00000105698.15","gene_symbol":"USF2","gene_name":"upstream transcription factor 2, c-fos interacting [Source:HGNC Symbol;Acc:HGNC:12594]","synonyms":"FIP,bHLHb12","biotype":"protein_coding","ncbi_id":"7392","summary":"This gene encodes a member of the basic helix-loop-helix leucine zipper family of transcription factors. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs and is involved in regulating multiple cellular processes. [provided by RefSeq, Mar 2016]","start":35268978,"end":35279821,"strand":1,"description":"upstream transcription factor 2, c-fos interacting [Source:HGNC Symbol;Acc:HGNC:12594]"}, {"versioned_ensembl_gene_id":"ENSG00000105492.15","gene_symbol":"SIGLEC6","gene_name":"sialic acid binding Ig like lectin 6 [Source:HGNC Symbol;Acc:HGNC:10875]","synonyms":"SIGLEC-6,OB-BP1,CD33L1,CD33L,CD327","biotype":"protein_coding","ncbi_id":"946","summary":"This gene encodes a member of the SIGLEC (sialic acid binding immunoglobulin-like lectin) family of proteins. The encoded transmembrane receptor binds sialyl-TN glycans and leptin. Placental expression of the encoded protein is upregulated in preeclampsia. [provided by RefSeq, Jul 2016]","start":51519525,"end":51531856,"strand":-1,"description":"sialic acid binding Ig like lectin 6 [Source:HGNC Symbol;Acc:HGNC:10875]"}, {"versioned_ensembl_gene_id":"ENSG00000244470.2","gene_symbol":"AC105918.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104886118,"end":104886955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185614.4","gene_symbol":"FAM212A","gene_name":"family with sequence similarity 212 member A [Source:HGNC Symbol;Acc:HGNC:32480]","synonyms":"INKA1,C3orf54","biotype":"protein_coding","ncbi_id":"389119","summary":null,"start":49803254,"end":49805030,"strand":1,"description":"family with sequence similarity 212 member A [Source:HGNC Symbol;Acc:HGNC:32480]"}, {"versioned_ensembl_gene_id":"ENSG00000269405.6","gene_symbol":"NXF2","gene_name":"nuclear RNA export factor 2 [Source:HGNC Symbol;Acc:HGNC:8072]","synonyms":"TAPL-2,CT39","biotype":"protein_coding","ncbi_id":"56001","summary":"This gene encodes a member of a family of nuclear RNA export proteins. The encoded protein is associated with the nuclear envelope and aids in the export of mRNAs. There is a closely related paralog of this gene located adjacent on chromosome X and on the opposite strand. [provided by RefSeq, Aug 2013]","start":102247161,"end":102326719,"strand":1,"description":"nuclear RNA export factor 2 [Source:HGNC Symbol;Acc:HGNC:8072]"}, {"versioned_ensembl_gene_id":"ENSG00000273746.1","gene_symbol":"AC234791.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102259043,"end":102261692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136160.14","gene_symbol":"EDNRB","gene_name":"endothelin receptor type B [Source:HGNC Symbol;Acc:HGNC:3180]","synonyms":"HSCR2,HSCR,ETB","biotype":"protein_coding","ncbi_id":"1910","summary":"The protein encoded by this gene is a G protein-coupled receptor which activates a phosphatidylinositol-calcium second messenger system. Its ligand, endothelin, consists of a family of three potent vasoactive peptides: ET1, ET2, and ET3. Studies suggest that the multigenic disorder, Hirschsprung disease type 2, is due to mutations in the endothelin receptor type B gene. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":77895481,"end":77919768,"strand":-1,"description":"endothelin receptor type B [Source:HGNC Symbol;Acc:HGNC:3180]"}, {"versioned_ensembl_gene_id":"ENSG00000226148.1","gene_symbol":"SLC25A39P1","gene_name":"solute carrier family 25 member 39 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43859]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420877","summary":null,"start":202796030,"end":202797094,"strand":1,"description":"solute carrier family 25 member 39 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43859]"}, {"versioned_ensembl_gene_id":"ENSG00000249614.1","gene_symbol":"LINC02503","gene_name":"long intergenic non-protein coding RNA 2503 [Source:HGNC Symbol;Acc:HGNC:53492]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377349","summary":null,"start":103961616,"end":104036923,"strand":1,"description":"long intergenic non-protein coding RNA 2503 [Source:HGNC Symbol;Acc:HGNC:53492]"}, {"versioned_ensembl_gene_id":"ENSG00000271723.5","gene_symbol":"MROH7-TTC4","gene_name":"MROH7-TTC4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527960","summary":"This locus represents naturally occurring read-through transcription between the neighboring MROH7 (maestro heat-like repeat family member 7) and TTC4 (tetratricopeptide repeat domain 4) genes. Alternative splicing results in multiple transcript variants, which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to produce protein products. [provided by RefSeq, Aug 2013]","start":54641786,"end":54742308,"strand":1,"description":"MROH7-TTC4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49180]"}, {"versioned_ensembl_gene_id":"ENSG00000147274.14","gene_symbol":"RBMX","gene_name":"RNA binding motif protein, X-linked [Source:HGNC Symbol;Acc:HGNC:9910]","synonyms":"RNMX,HNRNPG,hnRNP-G","biotype":"protein_coding","ncbi_id":"27316","summary":"This gene belongs to the RBMY gene family which includes candidate Y chromosome spermatogenesis genes. This gene, an active X chromosome homolog of the Y chromosome RBMY gene, is widely expressed whereas the RBMY gene evolved a male-specific function in spermatogenesis. Pseudogenes of this gene, found on chromosomes 1, 4, 9, 11, and 6, were likely derived by retrotransposition from the original gene. Alternatively spliced transcript variants encoding different isoforms have been identified. A snoRNA gene (SNORD61) is found in one of its introns. [provided by RefSeq, Sep 2009]","start":136848004,"end":136880764,"strand":-1,"description":"RNA binding motif protein, X-linked [Source:HGNC Symbol;Acc:HGNC:9910]"}, {"versioned_ensembl_gene_id":"ENSG00000221093.1","gene_symbol":"SNORA3","gene_name":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56121242,"end":56121352,"strand":-1,"description":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]"}, {"versioned_ensembl_gene_id":"ENSG00000104522.15","gene_symbol":"TSTA3","gene_name":"tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:HGNC:12390]","synonyms":"SDR4E1,P35B,FX","biotype":"protein_coding","ncbi_id":"7264","summary":"Tissue specific transplantation antigen P35B is a NADP(H)-binding protein. It catalyze the two-step epimerase and the reductase reactions in GDP-D-mannose metabolism, converting GDP-4-keto-6-D-deoxymannose to GDP-L-fucose. GDP-L-fucose is the substrate of several fucosyltransferases involved in the expression of many glycoconjugates, including blood group ABH antigens and developmental adhesion antigens. Mutations in this gene may cause leukocyte adhesion deficiency, type II. [provided by RefSeq, Jul 2008]","start":143612618,"end":143618048,"strand":-1,"description":"tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:HGNC:12390]"}, {"versioned_ensembl_gene_id":"ENSG00000139668.8","gene_symbol":"WDFY2","gene_name":"WD repeat and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20482]","synonyms":"ZFYVE22","biotype":"protein_coding","ncbi_id":"115825","summary":"This gene encodes a protein that contains two WD domains and an FYVE zinc finger region. The function of this gene is unknown. An alternatively spliced transcript variant of this gene may exist. [provided by RefSeq, Jul 2008]","start":51584455,"end":51767707,"strand":1,"description":"WD repeat and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20482]"}, {"versioned_ensembl_gene_id":"ENSG00000228577.1","gene_symbol":"AC010731.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206606497,"end":206609812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196388.8","gene_symbol":"INCA1","gene_name":"inhibitor of CDK, cyclin A1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:32224]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388324","summary":null,"start":4988130,"end":4997610,"strand":-1,"description":"inhibitor of CDK, cyclin A1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:32224]"}, {"versioned_ensembl_gene_id":"ENSG00000181392.14","gene_symbol":"SYNE4","gene_name":"spectrin repeat containing nuclear envelope family member 4 [Source:HGNC Symbol;Acc:HGNC:26703]","synonyms":"Nesprin-4,Nesp4,FLJ36445,DFNB76,C19orf46","biotype":"protein_coding","ncbi_id":"163183","summary":"This gene is a member of the nesprin family of genes, that encode KASH (Klarsicht, Anc-1, Syne Homology) domain-containing proteins. In addition to the KASH domain, this protein also contains a coiled-coil and leucine zipper region, a spectrin repeat, and a kinesin-1 binding region. This protein localizes to the outer nuclear membrane, and is part of the linker of nucleoskeleton and cytoskeleton (LINC) complex in the nuclear envelope. LINC complexes are formed by SUN (Sad1, UNC-84)-KASH pairs, and are thought to mechanically couple nuclear components to the cytoskeleton. Mutations in this gene have been associated with progressive high-frequency hearing loss. The absence of this protein in mice also caused hearing loss, and changes in hair cell morphology in the ears. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":36003307,"end":36008793,"strand":-1,"description":"spectrin repeat containing nuclear envelope family member 4 [Source:HGNC Symbol;Acc:HGNC:26703]"}, {"versioned_ensembl_gene_id":"ENSG00000168062.9","gene_symbol":"BATF2","gene_name":"basic leucine zipper ATF-like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:25163]","synonyms":"MGC20410","biotype":"protein_coding","ncbi_id":"116071","summary":null,"start":64987943,"end":64997045,"strand":-1,"description":"basic leucine zipper ATF-like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:25163]"}, {"versioned_ensembl_gene_id":"ENSG00000270647.5","gene_symbol":"TAF15","gene_name":"TATA-box binding protein associated factor 15 [Source:HGNC Symbol;Acc:HGNC:11547]","synonyms":"TAF2N,RBP56,Npl3,hTAFII68","biotype":"protein_coding","ncbi_id":"8148","summary":"This gene encodes a member of the TET family of RNA-binding proteins. The encoded protein plays a role in RNA polymerase II gene transcription as a component of a distinct subset of multi-subunit transcription initiation factor TFIID complexes. Translocations involving this gene play a role in acute leukemia and extraskeletal myxoid chondrosarcoma, and mutations in this gene may play a role in amyotrophic lateral sclerosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":35713791,"end":35864615,"strand":1,"description":"TATA-box binding protein associated factor 15 [Source:HGNC Symbol;Acc:HGNC:11547]"}, {"versioned_ensembl_gene_id":"ENSG00000276294.1","gene_symbol":"AC078899.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20330121,"end":20331517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271638.1","gene_symbol":"BNIP3P19","gene_name":"BCL2 interacting protein 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480281","summary":null,"start":20323992,"end":20324568,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49699]"}, {"versioned_ensembl_gene_id":"ENSG00000271583.1","gene_symbol":"AC103881.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146833501,"end":146834038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233246.1","gene_symbol":"AL513327.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33350352,"end":33363245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198526.7","gene_symbol":"PABPC1P2","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8559]","synonyms":"PABP4,PABP2,PABPCP4,PABPCP2","biotype":"processed_pseudogene","ncbi_id":"728773","summary":null,"start":146587506,"end":146589310,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8559]"}, {"versioned_ensembl_gene_id":"ENSG00000223459.5","gene_symbol":"TCAF1P1","gene_name":"TRPM8 channel associated factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33604]","synonyms":"FAM115B","biotype":"unprocessed_pseudogene","ncbi_id":"653199","summary":null,"start":143598040,"end":143604839,"strand":1,"description":"TRPM8 channel associated factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33604]"}, {"versioned_ensembl_gene_id":"ENSG00000264019.1","gene_symbol":"AC018521.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47946802,"end":47948275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230162.1","gene_symbol":"CT45A11P","gene_name":"cancer/testis antigen family 45 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:51336]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129813","summary":null,"start":135942478,"end":135947139,"strand":-1,"description":"cancer/testis antigen family 45 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:51336]"}, {"versioned_ensembl_gene_id":"ENSG00000167183.2","gene_symbol":"PRR15L","gene_name":"proline rich 15 like [Source:HGNC Symbol;Acc:HGNC:28149]","synonyms":"ATAD4,MGC11242","biotype":"protein_coding","ncbi_id":"79170","summary":null,"start":47951967,"end":47957878,"strand":-1,"description":"proline rich 15 like [Source:HGNC Symbol;Acc:HGNC:28149]"}, {"versioned_ensembl_gene_id":"ENSG00000136897.7","gene_symbol":"MRPL50","gene_name":"mitochondrial ribosomal protein L50 [Source:HGNC Symbol;Acc:HGNC:16654]","synonyms":"MRP-L50,FLJ20493","biotype":"protein_coding","ncbi_id":"54534","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a putative 39S subunit protein and belongs to the L47P ribosomal protein family. Pseudogenes corresponding to this gene are found on chromosomes 2p, 2q, 5p, and 10q. [provided by RefSeq, Jul 2008]","start":101387633,"end":101398614,"strand":-1,"description":"mitochondrial ribosomal protein L50 [Source:HGNC Symbol;Acc:HGNC:16654]"}, {"versioned_ensembl_gene_id":"ENSG00000185701.7","gene_symbol":"OR5M5P","gene_name":"olfactory receptor family 5 subfamily M member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14810]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390166","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56526568,"end":56527503,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14810]"}, {"versioned_ensembl_gene_id":"ENSG00000271366.1","gene_symbol":"AC002128.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35251440,"end":35253639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272915.1","gene_symbol":"AC018635.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128264526,"end":128264889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255790.5","gene_symbol":"AC078950.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11399381,"end":11486678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181371.4","gene_symbol":"OR5M8","gene_name":"olfactory receptor family 5 subfamily M member 8 [Source:HGNC Symbol;Acc:HGNC:14846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219484","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56490349,"end":56491395,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 8 [Source:HGNC Symbol;Acc:HGNC:14846]"}, {"versioned_ensembl_gene_id":"ENSG00000235357.1","gene_symbol":"LINC01621","gene_name":"long intergenic non-protein coding RNA 1621 [Source:HGNC Symbol;Acc:HGNC:14109]","synonyms":"C6orf7","biotype":"lincRNA","ncbi_id":"89758","summary":null,"start":79803583,"end":79807225,"strand":-1,"description":"long intergenic non-protein coding RNA 1621 [Source:HGNC Symbol;Acc:HGNC:14109]"}, {"versioned_ensembl_gene_id":"ENSG00000091483.6","gene_symbol":"FH","gene_name":"fumarate hydratase [Source:HGNC Symbol;Acc:HGNC:3700]","synonyms":"fumarase","biotype":"protein_coding","ncbi_id":"2271","summary":"The protein encoded by this gene is an enzymatic component of the tricarboxylic acid (TCA) cycle, or Krebs cycle, and catalyzes the formation of L-malate from fumarate. It exists in both a cytosolic form and an N-terminal extended form, differing only in the translation start site used. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension generates the same form as in the cytoplasm. It is similar to some thermostable class II fumarases and functions as a homotetramer. Mutations in this gene can cause fumarase deficiency and lead to progressive encephalopathy. [provided by RefSeq, Jul 2008]","start":241497603,"end":241519761,"strand":-1,"description":"fumarate hydratase [Source:HGNC Symbol;Acc:HGNC:3700]"}, {"versioned_ensembl_gene_id":"ENSG00000258625.2","gene_symbol":"OR11H5P","gene_name":"olfactory receptor family 11 subfamily H member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15348]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390440","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20204606,"end":20210498,"strand":1,"description":"olfactory receptor family 11 subfamily H member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15348]"}, {"versioned_ensembl_gene_id":"ENSG00000180828.2","gene_symbol":"BHLHE22","gene_name":"basic helix-loop-helix family member e22 [Source:HGNC Symbol;Acc:HGNC:11963]","synonyms":"BHLHB5,Beta3,TNRC20,CAGL85,bHLHe22","biotype":"protein_coding","ncbi_id":"27319","summary":"This gene encodes a protein that belongs to the basic helix-loop-helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis. [provided by RefSeq, Oct 2016]","start":64580367,"end":64583628,"strand":1,"description":"basic helix-loop-helix family member e22 [Source:HGNC Symbol;Acc:HGNC:11963]"}, {"versioned_ensembl_gene_id":"ENSG00000243729.4","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"protein_coding","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29353749,"end":29431967,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000234347.8","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425439,"end":29457001,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000255441.1","gene_symbol":"AC008750.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51415724,"end":51417425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233206.1","gene_symbol":"RPS3AP1","gene_name":"ribosomal protein S3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10422]","synonyms":"RPS3AP","biotype":"processed_pseudogene","ncbi_id":"101241875","summary":null,"start":20430443,"end":20430762,"strand":-1,"description":"ribosomal protein S3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10422]"}, {"versioned_ensembl_gene_id":"ENSG00000206280.7","gene_symbol":"ZBTB22","gene_name":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]","synonyms":"fru,ZNF297,BING1,ZBTB22A,fruitless,ZNF297A","biotype":"protein_coding","ncbi_id":"9278","summary":null,"start":33243252,"end":33246776,"strand":-1,"description":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]"}, {"versioned_ensembl_gene_id":"ENSG00000262366.1","gene_symbol":"NDUFA3P6","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479052","summary":null,"start":31174573,"end":31174822,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45055]"}, {"versioned_ensembl_gene_id":"ENSG00000234439.1","gene_symbol":"KRT18P2","gene_name":"keratin 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6435]","synonyms":"OTTHUMG00000078062","biotype":"processed_pseudogene","ncbi_id":"54044","summary":null,"start":20424949,"end":20426206,"strand":-1,"description":"keratin 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6435]"}, {"versioned_ensembl_gene_id":"ENSG00000233676.2","gene_symbol":"FDPSP6","gene_name":"farnesyl diphosphate synthase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:3637]","synonyms":"FDPSP","biotype":"processed_pseudogene","ncbi_id":"54051","summary":null,"start":20388334,"end":20388845,"strand":1,"description":"farnesyl diphosphate synthase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:3637]"}, {"versioned_ensembl_gene_id":"ENSG00000229953.1","gene_symbol":"AL590666.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156646507,"end":156661424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235482.1","gene_symbol":"RPL21P135","gene_name":"ribosomal protein L21 pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:44539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419391","summary":null,"start":37748110,"end":37748900,"strand":1,"description":"ribosomal protein L21 pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:44539]"}, {"versioned_ensembl_gene_id":"ENSG00000253737.1","gene_symbol":"AP003469.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101139665,"end":101140929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226856.5","gene_symbol":"AC093901.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118132128,"end":118186386,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207112.1","gene_symbol":"SNORA25","gene_name":"small nucleolar RNA, H/ACA box 25 [Source:HGNC Symbol;Acc:HGNC:32615]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":93730513,"end":93730646,"strand":-1,"description":"small nucleolar RNA, H/ACA box 25 [Source:HGNC Symbol;Acc:HGNC:32615]"}, {"versioned_ensembl_gene_id":"ENSG00000223448.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31620003,"end":31621970,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000231584.8","gene_symbol":"FAHD2CP","gene_name":"fumarylacetoacetate hydrolase domain containing 2C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44135]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729234","summary":null,"start":96010551,"end":96023380,"strand":1,"description":"fumarylacetoacetate hydrolase domain containing 2C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44135]"}, {"versioned_ensembl_gene_id":"ENSG00000224233.1","gene_symbol":"AL645937.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181510,"end":29182445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065183.15","gene_symbol":"WDR3","gene_name":"WD repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:12755]","synonyms":"UTP12,FLJ12796,DIP2","biotype":"protein_coding","ncbi_id":"10885","summary":"This gene encodes a nuclear protein containing 10 WD repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, which usually include a trp-asp at the C-terminal end. Proteins belonging to the WD repeat family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]","start":117929720,"end":117966542,"strand":1,"description":"WD repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:12755]"}, {"versioned_ensembl_gene_id":"ENSG00000185873.7","gene_symbol":"TMPRSS11B","gene_name":"transmembrane protease, serine 11B [Source:HGNC Symbol;Acc:HGNC:25398]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132724","summary":null,"start":68226653,"end":68245720,"strand":-1,"description":"transmembrane protease, serine 11B [Source:HGNC Symbol;Acc:HGNC:25398]"}, {"versioned_ensembl_gene_id":"ENSG00000205718.9","gene_symbol":"MBD3L4","gene_name":"methyl-CpG binding domain protein 3 like 4 [Source:HGNC Symbol;Acc:HGNC:37206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653656","summary":"This gene encodes a member of a family of proteins that are related to methyl-CpG-binding proteins but lack the methyl-CpG binding domain. There is no definitive support for transcription of this locus, and the transcript structure is inferred from other family members. [provided by RefSeq, Aug 2009]","start":7037748,"end":7040179,"strand":-1,"description":"methyl-CpG binding domain protein 3 like 4 [Source:HGNC Symbol;Acc:HGNC:37206]"}, {"versioned_ensembl_gene_id":"ENSG00000260395.1","gene_symbol":"AC092119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21998310,"end":21999656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273040.1","gene_symbol":"BX908720.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837838,"end":28838975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241880.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29720644,"end":29721114,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000270610.1","gene_symbol":"AL160191.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70234495,"end":70235095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182365.4","gene_symbol":"OR5F2P","gene_name":"olfactory receptor family 5 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15286]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56015017,"end":56015957,"strand":-1,"description":"olfactory receptor family 5 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15286]"}, {"versioned_ensembl_gene_id":"ENSG00000251686.1","gene_symbol":"OR10J8P","gene_name":"olfactory receptor family 10 subfamily J member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:19638]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"343409","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159366161,"end":159367089,"strand":1,"description":"olfactory receptor family 10 subfamily J member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:19638]"}, {"versioned_ensembl_gene_id":"ENSG00000167965.17","gene_symbol":"MLST8","gene_name":"MTOR associated protein, LST8 homolog [Source:HGNC Symbol;Acc:HGNC:24825]","synonyms":"Pop3,Lst8,GBL,GbetaL","biotype":"protein_coding","ncbi_id":"64223","summary":null,"start":2204248,"end":2209416,"strand":1,"description":"MTOR associated protein, LST8 homolog [Source:HGNC Symbol;Acc:HGNC:24825]"}, {"versioned_ensembl_gene_id":"ENSG00000258816.1","gene_symbol":"AC121758.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56855694,"end":56855886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231934.1","gene_symbol":"LINC01598","gene_name":"long intergenic non-protein coding RNA 1598 [Source:HGNC Symbol;Acc:HGNC:51597]","synonyms":"TCONS_00028363","biotype":"antisense_RNA","ncbi_id":"105379478","summary":null,"start":30323812,"end":30361730,"strand":-1,"description":"long intergenic non-protein coding RNA 1598 [Source:HGNC Symbol;Acc:HGNC:51597]"}, {"versioned_ensembl_gene_id":"ENSG00000255273.1","gene_symbol":"AF238378.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7082971,"end":7083328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253321.1","gene_symbol":"AC099554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90353037,"end":90356609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204555.3","gene_symbol":"CFTRP3","gene_name":"cystic fibrosis transmembrane conductance regulator pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481718","summary":null,"start":30214765,"end":30214976,"strand":-1,"description":"cystic fibrosis transmembrane conductance regulator pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51352]"}, {"versioned_ensembl_gene_id":"ENSG00000227206.1","gene_symbol":"AL645937.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29124210,"end":29128908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197587.10","gene_symbol":"DMBX1","gene_name":"diencephalon/mesencephalon homeobox 1 [Source:HGNC Symbol;Acc:HGNC:19026]","synonyms":"PAXB,OTX3","biotype":"protein_coding","ncbi_id":"127343","summary":"This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":46506996,"end":46514226,"strand":1,"description":"diencephalon/mesencephalon homeobox 1 [Source:HGNC Symbol;Acc:HGNC:19026]"}, {"versioned_ensembl_gene_id":"ENSG00000100678.18","gene_symbol":"SLC8A3","gene_name":"solute carrier family 8 member A3 [Source:HGNC Symbol;Acc:HGNC:11070]","synonyms":"NCX3","biotype":"protein_coding","ncbi_id":"6547","summary":"This gene encodes a member of the sodium/calcium exchanger integral membrane protein family. Na+/Ca2+ exchange proteins are involved in maintaining Ca2+ homeostasis in a wide variety of cell types. The protein is regulated by intracellular calcium ions and is found in both the plasma membrane and intracellular organellar membranes, where exchange of Na+ for Ca2+ occurs in an electrogenic manner. Alternative splicing has been observed for this gene and multiple variants have been described. [provided by RefSeq, Aug 2013]","start":70044217,"end":70189070,"strand":-1,"description":"solute carrier family 8 member A3 [Source:HGNC Symbol;Acc:HGNC:11070]"}, {"versioned_ensembl_gene_id":"ENSG00000250756.1","gene_symbol":"AC018645.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32788334,"end":32788442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142910.15","gene_symbol":"TINAGL1","gene_name":"tubulointerstitial nephritis antigen like 1 [Source:HGNC Symbol;Acc:HGNC:19168]","synonyms":"TINAGRP,P3ECSL,LIECG3,LCN7,ARG1","biotype":"protein_coding","ncbi_id":"64129","summary":"The protein encoded by this gene is similar in sequence to tubulointerstitial nephritis antigen, a secreted glycoprotein that is recognized by antibodies in some types of immune-related tubulointerstitial nephritis. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":31576485,"end":31587686,"strand":1,"description":"tubulointerstitial nephritis antigen like 1 [Source:HGNC Symbol;Acc:HGNC:19168]"}, {"versioned_ensembl_gene_id":"ENSG00000274110.4","gene_symbol":"LAIR1","gene_name":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]","synonyms":"CD305","biotype":"protein_coding","ncbi_id":"3903","summary":"The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":54283996,"end":54300924,"strand":-1,"description":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]"}, {"versioned_ensembl_gene_id":"ENSG00000136144.11","gene_symbol":"RCBTB1","gene_name":"RCC1 and BTB domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:18243]","synonyms":"FLJ10716,CLLL7,CLLD7","biotype":"protein_coding","ncbi_id":"55213","summary":"This gene encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCBTB1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies. [provided by RefSeq, Jul 2008]","start":49531946,"end":49585583,"strand":-1,"description":"RCC1 and BTB domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:18243]"}, {"versioned_ensembl_gene_id":"ENSG00000198225.5","gene_symbol":"FKBP1C","gene_name":"FK506 binding protein 1C [Source:HGNC Symbol;Acc:HGNC:21376]","synonyms":"bA184C23.2","biotype":"protein_coding","ncbi_id":"642489","summary":null,"start":63211446,"end":63213024,"strand":1,"description":"FK506 binding protein 1C [Source:HGNC Symbol;Acc:HGNC:21376]"}, {"versioned_ensembl_gene_id":"ENSG00000269069.1","gene_symbol":"AC007842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40023384,"end":40025502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204702.5","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"dJ80I19.2,OR2J1P,hs6M1-4,OR6-5","biotype":"polymorphic_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29099657,"end":29102701,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000136531.15","gene_symbol":"SCN2A","gene_name":"sodium voltage-gated channel alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:10588]","synonyms":"SCN2A2,SCN2A1,Nav1.2,HBSCII,HBSCI","biotype":"protein_coding","ncbi_id":"6326","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with four repeat domains, each of which is composed of six membrane-spanning segments, and one or more regulatory beta subunits. Voltage-gated sodium channels function in the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. Allelic variants of this gene are associated with seizure disorders and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":165194993,"end":165392310,"strand":1,"description":"sodium voltage-gated channel alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:10588]"}, {"versioned_ensembl_gene_id":"ENSG00000282911.1","gene_symbol":"ABBA01031663.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29448517,"end":29449306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171853.15","gene_symbol":"TRAPPC12","gene_name":"trafficking protein particle complex 12 [Source:HGNC Symbol;Acc:HGNC:24284]","synonyms":"TTC15,TTC-15,CGI-87","biotype":"protein_coding","ncbi_id":"51112","summary":null,"start":3379675,"end":3485094,"strand":1,"description":"trafficking protein particle complex 12 [Source:HGNC Symbol;Acc:HGNC:24284]"}, {"versioned_ensembl_gene_id":"ENSG00000032742.17","gene_symbol":"IFT88","gene_name":"intraflagellar transport 88 [Source:HGNC Symbol;Acc:HGNC:20606]","synonyms":"TTC10,Tg737,MGC26259,hTg737,D13S1056E","biotype":"protein_coding","ncbi_id":"8100","summary":"This gene encodes a member of the tetratrico peptide repeat (TPR) family. The encoded protein is involved in cilium biogenesis. Mutations of a similar gene in mouse can cause polycystic kidney disease. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2017]","start":20567069,"end":20691437,"strand":1,"description":"intraflagellar transport 88 [Source:HGNC Symbol;Acc:HGNC:20606]"}, {"versioned_ensembl_gene_id":"ENSG00000183648.9","gene_symbol":"NDUFB1","gene_name":"NADH:ubiquinone oxidoreductase subunit B1 [Source:HGNC Symbol;Acc:HGNC:7695]","synonyms":"MNLL,CI-MNLL","biotype":"protein_coding","ncbi_id":"4707","summary":null,"start":92116122,"end":92121917,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B1 [Source:HGNC Symbol;Acc:HGNC:7695]"}, {"versioned_ensembl_gene_id":"ENSG00000171100.14","gene_symbol":"MTM1","gene_name":"myotubularin 1 [Source:HGNC Symbol;Acc:HGNC:7448]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4534","summary":"This gene encodes a dual-specificity phosphatase that acts on both phosphotyrosine and phosphoserine. It is required for muscle cell differentiation and mutations in this gene have been identified as being responsible for X-linked myotubular myopathy. [provided by RefSeq, Jul 2008]","start":150568619,"end":150673322,"strand":1,"description":"myotubularin 1 [Source:HGNC Symbol;Acc:HGNC:7448]"}, {"versioned_ensembl_gene_id":"ENSG00000256625.1","gene_symbol":"AC092747.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27121910,"end":27147664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256226.1","gene_symbol":"AC092747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27105151,"end":27161393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223963.2","gene_symbol":"THAP12P8","gene_name":"THAP domain containing 12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39572]","synonyms":"PRKRIRP8","biotype":"processed_pseudogene","ncbi_id":"645939","summary":null,"start":240769420,"end":240771534,"strand":-1,"description":"THAP domain containing 12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39572]"}, {"versioned_ensembl_gene_id":"ENSG00000255183.1","gene_symbol":"AP000756.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87718354,"end":87719411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258719.1","gene_symbol":"AC009396.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78695321,"end":78698122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258662.1","gene_symbol":"AC022469.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79246668,"end":79249023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228927.10","gene_symbol":"TSPY3","gene_name":"testis specific protein, Y-linked 3 [Source:HGNC Symbol;Acc:HGNC:33876]","synonyms":"CT78","biotype":"protein_coding","ncbi_id":"728137","summary":null,"start":9398421,"end":9401223,"strand":1,"description":"testis specific protein, Y-linked 3 [Source:HGNC Symbol;Acc:HGNC:33876]"}, {"versioned_ensembl_gene_id":"ENSG00000223694.1","gene_symbol":"ADH5P3","gene_name":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22991]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131810","summary":null,"start":240170155,"end":240171291,"strand":1,"description":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22991]"}, {"versioned_ensembl_gene_id":"ENSG00000267412.1","gene_symbol":"AC092068.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2610155,"end":2611862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147912.12","gene_symbol":"FBXO10","gene_name":"F-box protein 10 [Source:HGNC Symbol;Acc:HGNC:13589]","synonyms":"FBX10","biotype":"protein_coding","ncbi_id":"26267","summary":"Members of the F-box protein family, such as FBXO10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":37510892,"end":37576349,"strand":-1,"description":"F-box protein 10 [Source:HGNC Symbol;Acc:HGNC:13589]"}, {"versioned_ensembl_gene_id":"ENSG00000269021.1","gene_symbol":"AC063977.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51280862,"end":51283022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242071.3","gene_symbol":"RPL7AP6","gene_name":"ribosomal protein L7a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326310","summary":null,"start":69885340,"end":69886140,"strand":-1,"description":"ribosomal protein L7a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19785]"}, {"versioned_ensembl_gene_id":"ENSG00000272411.1","gene_symbol":"AC116312.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148970340,"end":148970653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215127.6","gene_symbol":"SYT14P1","gene_name":"synaptotagmin 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33429]","synonyms":"SYTDEP,SYT14L,CHR415SYT","biotype":"transcribed_processed_pseudogene","ncbi_id":"401135","summary":null,"start":68061822,"end":68063269,"strand":-1,"description":"synaptotagmin 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33429]"}, {"versioned_ensembl_gene_id":"ENSG00000227730.2","gene_symbol":"MTND6P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39468]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480427","summary":null,"start":5091093,"end":5091604,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39468]"}, {"versioned_ensembl_gene_id":"ENSG00000213088.9","gene_symbol":"ACKR1","gene_name":"atypical chemokine receptor 1 (Duffy blood group) [Source:HGNC Symbol;Acc:HGNC:4035]","synonyms":"GPD,FY,Dfy,DARC,CD234,CCBP1","biotype":"protein_coding","ncbi_id":"2532","summary":"The protein encoded by this gene is a glycosylated membrane protein and a non-specific receptor for several chemokines. The encoded protein is the receptor for the human malarial parasites Plasmodium vivax and Plasmodium knowlesi. Polymorphisms in this gene are the basis of the Duffy blood group system. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":159203307,"end":159206500,"strand":1,"description":"atypical chemokine receptor 1 (Duffy blood group) [Source:HGNC Symbol;Acc:HGNC:4035]"}, {"versioned_ensembl_gene_id":"ENSG00000206487.11","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30636534,"end":30642598,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000254566.1","gene_symbol":"AC087277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36321158,"end":36323440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226841.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31519466,"end":31520981,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000264301.1","gene_symbol":"LINC01444","gene_name":"long intergenic non-protein coding RNA 1444 [Source:HGNC Symbol;Acc:HGNC:50769]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927642","summary":null,"start":14969001,"end":14970468,"strand":-1,"description":"long intergenic non-protein coding RNA 1444 [Source:HGNC Symbol;Acc:HGNC:50769]"}, {"versioned_ensembl_gene_id":"ENSG00000264061.1","gene_symbol":"FGF7P1","gene_name":"fibroblast growth factor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21455]","synonyms":"HsT283","biotype":"unprocessed_pseudogene","ncbi_id":"387559","summary":null,"start":14888709,"end":14890086,"strand":-1,"description":"fibroblast growth factor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21455]"}, {"versioned_ensembl_gene_id":"ENSG00000226538.1","gene_symbol":"RPL35AP4","gene_name":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]","synonyms":"BPG294E21.7,OTTHUMG00000140156","biotype":"processed_pseudogene","ncbi_id":"100048922","summary":null,"start":33529535,"end":33529636,"strand":-1,"description":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]"}, {"versioned_ensembl_gene_id":"ENSG00000229396.1","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"processed_transcript","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33469139,"end":33469421,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000079313.13","gene_symbol":"REXO1","gene_name":"RNA exonuclease 1 homolog [Source:HGNC Symbol;Acc:HGNC:24616]","synonyms":"TCEB3BP1,KIAA1138,EloA-BP1","biotype":"protein_coding","ncbi_id":"57455","summary":null,"start":1815246,"end":1848463,"strand":-1,"description":"RNA exonuclease 1 homolog [Source:HGNC Symbol;Acc:HGNC:24616]"}, {"versioned_ensembl_gene_id":"ENSG00000230580.1","gene_symbol":"AC021016.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":218354075,"end":218354572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136147.17","gene_symbol":"PHF11","gene_name":"PHD finger protein 11 [Source:HGNC Symbol;Acc:HGNC:17024]","synonyms":"NY-REN-34,IGER,BCAP","biotype":"protein_coding","ncbi_id":"51131","summary":"This gene encodes a protein containing a PHD (plant homeodomain) type zinc finger. This gene has been identified in some studies as a candidate gene for asthma. Naturally-occurring readthrough transcription may occur from the upstream SETDB2 (SET domain bifurcated 2) gene to this locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":49495610,"end":49528987,"strand":1,"description":"PHD finger protein 11 [Source:HGNC Symbol;Acc:HGNC:17024]"}, {"versioned_ensembl_gene_id":"ENSG00000225007.1","gene_symbol":"AC000067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19667023,"end":19667555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279919.1","gene_symbol":"AC068880.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19277284,"end":19277573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250571.6","gene_symbol":"GLI4","gene_name":"GLI family zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:4320]","synonyms":"HKR4,ZNF928","biotype":"protein_coding","ncbi_id":"2738","summary":null,"start":143267433,"end":143276931,"strand":1,"description":"GLI family zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:4320]"}, {"versioned_ensembl_gene_id":"ENSG00000225094.3","gene_symbol":"SETP20","gene_name":"SET pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42939]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389217","summary":null,"start":109553243,"end":109554094,"strand":-1,"description":"SET pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42939]"}, {"versioned_ensembl_gene_id":"ENSG00000077254.14","gene_symbol":"USP33","gene_name":"ubiquitin specific peptidase 33 [Source:HGNC Symbol;Acc:HGNC:20059]","synonyms":"VDU1,KIAA1097","biotype":"protein_coding","ncbi_id":"23032","summary":"This gene encodes a deubiquinating enzyme important in a variety of processes, including Slit-dependent cell migration and beta-2 adrenergic receptor signaling. The protein is negatively regulated through ubiquitination by von Hippel-Lindau tumor protein (VHL). Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012]","start":77695987,"end":77759852,"strand":-1,"description":"ubiquitin specific peptidase 33 [Source:HGNC Symbol;Acc:HGNC:20059]"}, {"versioned_ensembl_gene_id":"ENSG00000261505.1","gene_symbol":"AL031714.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1317891,"end":1322845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250754.5","gene_symbol":"LINC02436","gene_name":"long intergenic non-protein coding RNA 2436 [Source:HGNC Symbol;Acc:HGNC:53368]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928877","summary":null,"start":185051896,"end":185107248,"strand":1,"description":"long intergenic non-protein coding RNA 2436 [Source:HGNC Symbol;Acc:HGNC:53368]"}, {"versioned_ensembl_gene_id":"ENSG00000244692.3","gene_symbol":"RN7SL724P","gene_name":"RNA, 7SL, cytoplasmic 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:46740]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479487","summary":null,"start":139609669,"end":139609939,"strand":-1,"description":"RNA, 7SL, cytoplasmic 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:46740]"}, {"versioned_ensembl_gene_id":"ENSG00000241604.3","gene_symbol":"RN7SL340P","gene_name":"RNA, 7SL, cytoplasmic 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:46356]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481016","summary":null,"start":29233090,"end":29233385,"strand":-1,"description":"RNA, 7SL, cytoplasmic 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:46356]"}, {"versioned_ensembl_gene_id":"ENSG00000170421.12","gene_symbol":"KRT8","gene_name":"keratin 8 [Source:HGNC Symbol;Acc:HGNC:6446]","synonyms":"KO,K8,K2C8,CYK8,CK8,CARD2","biotype":"protein_coding","ncbi_id":"3856","summary":"This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":52897187,"end":52949954,"strand":-1,"description":"keratin 8 [Source:HGNC Symbol;Acc:HGNC:6446]"}, {"versioned_ensembl_gene_id":"ENSG00000171307.18","gene_symbol":"ZDHHC16","gene_name":"zinc finger DHHC-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20714]","synonyms":"APH2","biotype":"protein_coding","ncbi_id":"84287","summary":null,"start":97446131,"end":97457370,"strand":1,"description":"zinc finger DHHC-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20714]"}, {"versioned_ensembl_gene_id":"ENSG00000254544.1","gene_symbol":"PCNAP4","gene_name":"proliferating cell nuclear antigen pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390102","summary":null,"start":19274540,"end":19275269,"strand":-1,"description":"proliferating cell nuclear antigen pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43737]"}, {"versioned_ensembl_gene_id":"ENSG00000268336.1","gene_symbol":"SIGLEC20P","gene_name":"sialic acid binding Ig like lectin 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:15609]","synonyms":"SIGLECP4","biotype":"unprocessed_pseudogene","ncbi_id":"114192","summary":null,"start":51184905,"end":51190809,"strand":1,"description":"sialic acid binding Ig like lectin 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:15609]"}, {"versioned_ensembl_gene_id":"ENSG00000132763.14","gene_symbol":"MMACHC","gene_name":"methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria [Source:HGNC Symbol;Acc:HGNC:24525]","synonyms":"DKFZP564I122,cblC","biotype":"protein_coding","ncbi_id":"25974","summary":"The exact function of the protein encoded by this gene is not known, however, its C-terminal region shows similarity to TonB, a bacterial protein involved in energy transduction for cobalamin (vitamin B12) uptake. Hence, it is postulated that this protein may have a role in the binding and intracellular trafficking of cobalamin. Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC. [provided by RefSeq, Oct 2009]","start":45500053,"end":45513382,"strand":1,"description":"methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria [Source:HGNC Symbol;Acc:HGNC:24525]"}, {"versioned_ensembl_gene_id":"ENSG00000149256.15","gene_symbol":"TENM4","gene_name":"teneurin transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:29945]","synonyms":"Ten-M4,ODZ4,KIAA1302","biotype":"protein_coding","ncbi_id":"26011","summary":"The protein encoded by this gene plays a role in establishing proper neuronal connectivity during development. Defects in this gene have been associated with hereditary essential tremor-5. [provided by RefSeq, Oct 2016]","start":78652831,"end":79440948,"strand":-1,"description":"teneurin transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:29945]"}, {"versioned_ensembl_gene_id":"ENSG00000254672.1","gene_symbol":"AL136146.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35967010,"end":35968676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171608.15","gene_symbol":"PIK3CD","gene_name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta [Source:HGNC Symbol;Acc:HGNC:8977]","synonyms":"p110D","biotype":"protein_coding","ncbi_id":"5293","summary":"Phosphoinositide 3-kinases (PI3Ks) phosphorylate inositol lipids and are involved in the immune response. The protein encoded by this gene is a class I PI3K found primarily in leukocytes. Like other class I PI3Ks (p110-alpha p110-beta, and p110-gamma), the encoded protein binds p85 adapter proteins and GTP-bound RAS. However, unlike the other class I PI3Ks, this protein phosphorylates itself, not p85 protein.[provided by RefSeq, Jul 2010]","start":9651732,"end":9729114,"strand":1,"description":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta [Source:HGNC Symbol;Acc:HGNC:8977]"}, {"versioned_ensembl_gene_id":"ENSG00000227509.1","gene_symbol":"LINC01839","gene_name":"long intergenic non-protein coding RNA 1839 [Source:HGNC Symbol;Acc:HGNC:41330]","synonyms":"EIF2B5-IT1","biotype":"lincRNA","ncbi_id":"105374251","summary":null,"start":184505113,"end":184508399,"strand":1,"description":"long intergenic non-protein coding RNA 1839 [Source:HGNC Symbol;Acc:HGNC:41330]"}, {"versioned_ensembl_gene_id":"ENSG00000239650.4","gene_symbol":"GUSBP4","gene_name":"glucuronidase, beta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:18220]","synonyms":"SMA3-L,GUSBL2,FLJ13549,C6orf216,SMAC3L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"375513","summary":null,"start":57919784,"end":57930291,"strand":-1,"description":"glucuronidase, beta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:18220]"}, {"versioned_ensembl_gene_id":"ENSG00000135766.8","gene_symbol":"EGLN1","gene_name":"egl-9 family hypoxia inducible factor 1 [Source:HGNC Symbol;Acc:HGNC:1232]","synonyms":"ZMYND6,SM-20,PHD2,HIFPH2,C1orf12","biotype":"protein_coding","ncbi_id":"54583","summary":"The protein encoded by this gene catalyzes the post-translational formation of 4-hydroxyproline in hypoxia-inducible factor (HIF) alpha proteins. HIF is a transcriptional complex that plays a central role in mammalian oxygen homeostasis. This protein functions as a cellular oxygen sensor, and under normal oxygen concentration, modification by prolyl hydroxylation is a key regulatory event that targets HIF subunits for proteasomal destruction via the von Hippel-Lindau ubiquitylation complex. Mutations in this gene are associated with erythrocytosis familial type 3 (ECYT3). [provided by RefSeq, Nov 2009]","start":231363751,"end":231425044,"strand":-1,"description":"egl-9 family hypoxia inducible factor 1 [Source:HGNC Symbol;Acc:HGNC:1232]"}, {"versioned_ensembl_gene_id":"ENSG00000213032.3","gene_symbol":"NDUFA3P3","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45052]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644482","summary":null,"start":225964179,"end":225964428,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45052]"}, {"versioned_ensembl_gene_id":"ENSG00000282620.1","gene_symbol":"MAPT-IT1","gene_name":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100130148","summary":null,"start":45907408,"end":45910423,"strand":1,"description":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]"}, {"versioned_ensembl_gene_id":"ENSG00000143416.20","gene_symbol":"SELENBP1","gene_name":"selenium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10719]","synonyms":"LPSB,hSP56,hSBP","biotype":"protein_coding","ncbi_id":"8991","summary":"This gene encodes a member of the selenium-binding protein family. Selenium is an essential nutrient that exhibits potent anticarcinogenic properties, and deficiency of selenium may cause certain neurologic diseases. The effects of selenium in preventing cancer and neurologic diseases may be mediated by selenium-binding proteins, and decreased expression of this gene may be associated with several types of cancer. The encoded protein may play a selenium-dependent role in ubiquitination/deubiquitination-mediated protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]","start":151364302,"end":151372733,"strand":-1,"description":"selenium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10719]"}, {"versioned_ensembl_gene_id":"ENSG00000185942.11","gene_symbol":"NKAIN3","gene_name":"sodium/potassium transporting ATPase interacting 3 [Source:HGNC Symbol;Acc:HGNC:26829]","synonyms":"FLJ39630,FAM77D","biotype":"protein_coding","ncbi_id":"286183","summary":"NKAIN3 is a member of a family of mammalian proteins (see NKAIN1; MIM 612871) with similarity to Drosophila Nkain (Gorokhova et al., 2007 [PubMed 17606467]).[supplied by OMIM, Jun 2009]","start":62248591,"end":62999652,"strand":1,"description":"sodium/potassium transporting ATPase interacting 3 [Source:HGNC Symbol;Acc:HGNC:26829]"}, {"versioned_ensembl_gene_id":"ENSG00000233122.2","gene_symbol":"CTAGE7P","gene_name":"CTAGE family member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:25111]","synonyms":"MGC33437,CTAGEP,CTAGE7,bA500G10.2,rcCTAGE5","biotype":"processed_pseudogene","ncbi_id":"119437","summary":null,"start":130106046,"end":130108481,"strand":1,"description":"CTAGE family member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:25111]"}, {"versioned_ensembl_gene_id":"ENSG00000137266.14","gene_symbol":"SLC22A23","gene_name":"solute carrier family 22 member 23 [Source:HGNC Symbol;Acc:HGNC:21106]","synonyms":"FLJ22174,C6orf85","biotype":"protein_coding","ncbi_id":"63027","summary":"SLC22A23 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]","start":3268962,"end":3457022,"strand":-1,"description":"solute carrier family 22 member 23 [Source:HGNC Symbol;Acc:HGNC:21106]"}, {"versioned_ensembl_gene_id":"ENSG00000263501.1","gene_symbol":"AC005828.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63305262,"end":63313521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240015.2","gene_symbol":"AC084024.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38123274,"end":38124651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131470.14","gene_symbol":"PSMC3IP","gene_name":"PSMC3 interacting protein [Source:HGNC Symbol;Acc:HGNC:17928]","synonyms":"TBPIP,HUMGT198A,Hop2,GT198","biotype":"protein_coding","ncbi_id":"29893","summary":"This gene encodes a protein that functions in meiotic recombination. It is a subunit of the PSMC3IP/MND1 complex, which interacts with PSMC3/TBP1 to stimulate DMC1- and RAD51-mediated strand exchange during meiosis. The protein encoded by this gene can also co-activate ligand-driven transcription mediated by estrogen, androgen, glucocorticoid, progesterone, and thyroid nuclear receptors. Mutations in this gene cause XX female gonadal dysgenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":42572315,"end":42577831,"strand":-1,"description":"PSMC3 interacting protein [Source:HGNC Symbol;Acc:HGNC:17928]"}, {"versioned_ensembl_gene_id":"ENSG00000141622.13","gene_symbol":"RNF165","gene_name":"ring finger protein 165 [Source:HGNC Symbol;Acc:HGNC:31696]","synonyms":"RNF111L2,ARKL2","biotype":"protein_coding","ncbi_id":"494470","summary":"Encoded in regions involved in pericentric inversions in patients with bipolar affective disorder. [provided by RefSeq, Jul 2008]","start":46326809,"end":46463140,"strand":1,"description":"ring finger protein 165 [Source:HGNC Symbol;Acc:HGNC:31696]"}, {"versioned_ensembl_gene_id":"ENSG00000264907.1","gene_symbol":"PRELID3BP3","gene_name":"PRELI domain containing 3B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49065]","synonyms":"SLMO2P3","biotype":"processed_pseudogene","ncbi_id":"100128712","summary":null,"start":62841101,"end":62841645,"strand":1,"description":"PRELI domain containing 3B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49065]"}, {"versioned_ensembl_gene_id":"ENSG00000188807.12","gene_symbol":"TMEM201","gene_name":"transmembrane protein 201 [Source:HGNC Symbol;Acc:HGNC:33719]","synonyms":"SAMP1,RP13-15M17.2,NET5,Ima1","biotype":"protein_coding","ncbi_id":"199953","summary":null,"start":9588922,"end":9614873,"strand":1,"description":"transmembrane protein 201 [Source:HGNC Symbol;Acc:HGNC:33719]"}, {"versioned_ensembl_gene_id":"ENSG00000216412.4","gene_symbol":"RPL12P2","gene_name":"ribosomal protein L12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16070]","synonyms":"dJ441G21.1","biotype":"processed_pseudogene","ncbi_id":"646875","summary":null,"start":37091314,"end":37091806,"strand":1,"description":"ribosomal protein L12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16070]"}, {"versioned_ensembl_gene_id":"ENSG00000149091.15","gene_symbol":"DGKZ","gene_name":"diacylglycerol kinase zeta [Source:HGNC Symbol;Acc:HGNC:2857]","synonyms":"DGK-ZETA,DAGK6,DAGK5,hDGKzeta","biotype":"protein_coding","ncbi_id":"8525","summary":"The protein encoded by this gene belongs to the eukaryotic diacylglycerol kinase family. It may attenuate protein kinase C activity by regulating diacylglycerol levels in intracellular signaling cascade and signal transduction. Alternative splicing occurs at this locus and multiple transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Nov 2010]","start":46332905,"end":46380554,"strand":1,"description":"diacylglycerol kinase zeta [Source:HGNC Symbol;Acc:HGNC:2857]"}, {"versioned_ensembl_gene_id":"ENSG00000188818.12","gene_symbol":"ZDHHC11","gene_name":"zinc finger DHHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:19158]","synonyms":"ZNF399,FLJ13153","biotype":"protein_coding","ncbi_id":"79844","summary":null,"start":795606,"end":850986,"strand":-1,"description":"zinc finger DHHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:19158]"}, {"versioned_ensembl_gene_id":"ENSG00000237320.2","gene_symbol":"AC019064.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34998273,"end":35000160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005238.19","gene_symbol":"FAM214B","gene_name":"family with sequence similarity 214 member B [Source:HGNC Symbol;Acc:HGNC:25666]","synonyms":"KIAA1539,FLJ11560,bA182N22.6","biotype":"protein_coding","ncbi_id":"80256","summary":null,"start":35104112,"end":35116341,"strand":-1,"description":"family with sequence similarity 214 member B [Source:HGNC Symbol;Acc:HGNC:25666]"}, {"versioned_ensembl_gene_id":"ENSG00000258913.1","gene_symbol":"C14orf144","gene_name":"chromosome 14 open reading frame 144 [Source:NCBI gene;Acc:145195]","synonyms":null,"biotype":"lincRNA","ncbi_id":"145195","summary":null,"start":104223584,"end":104288069,"strand":1,"description":"chromosome 14 open reading frame 144 [Source:NCBI gene;Acc:145195]"}, {"versioned_ensembl_gene_id":"ENSG00000106993.11","gene_symbol":"CDC37L1","gene_name":"cell division cycle 37 like 1 [Source:HGNC Symbol;Acc:HGNC:17179]","synonyms":"HARC,FLJ20639,CDC37B","biotype":"protein_coding","ncbi_id":"55664","summary":"CDC37L1 is a cytoplasmic phosphoprotein that exists in complex with HSP90 (HSPCA; MIM 140571) as well as several other proteins involved in HSP90-mediated protein folding (Scholz et al., 2001 [PubMed 11413142]).[supplied by OMIM, Mar 2008]","start":4679559,"end":4708398,"strand":1,"description":"cell division cycle 37 like 1 [Source:HGNC Symbol;Acc:HGNC:17179]"}, {"versioned_ensembl_gene_id":"ENSG00000107438.8","gene_symbol":"PDLIM1","gene_name":"PDZ and LIM domain 1 [Source:HGNC Symbol;Acc:HGNC:2067]","synonyms":"hCLIM1,CLP36,CLP-36,CLIM1","biotype":"protein_coding","ncbi_id":"9124","summary":"This gene encodes a member of the enigma protein family. The protein contains two protein interacting domains, a PDZ domain at the amino terminal end and one to three LIM domains at the carboxyl terminal. It is a cytoplasmic protein associated with the cytoskeleton. The protein may function as an adapter to bring other LIM-interacting proteins to the cytoskeleton. Pseudogenes associated with this gene are located on chromosomes 3, 14 and 17. [provided by RefSeq, Oct 2012]","start":95237572,"end":95291024,"strand":-1,"description":"PDZ and LIM domain 1 [Source:HGNC Symbol;Acc:HGNC:2067]"}, {"versioned_ensembl_gene_id":"ENSG00000229110.1","gene_symbol":"AC006355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79124739,"end":79125750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226230.1","gene_symbol":"AC007237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78486530,"end":78487028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257675.1","gene_symbol":"BTBD10P1","gene_name":"BTB domain containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128678","summary":null,"start":52748776,"end":52750127,"strand":1,"description":"BTB domain containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51540]"}, {"versioned_ensembl_gene_id":"ENSG00000146618.3","gene_symbol":"FERD3L","gene_name":"Fer3 like bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:16660]","synonyms":"NATO3,N-TWIST,bHLHa31","biotype":"protein_coding","ncbi_id":"222894","summary":null,"start":19144782,"end":19145421,"strand":-1,"description":"Fer3 like bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:16660]"}, {"versioned_ensembl_gene_id":"ENSG00000108599.14","gene_symbol":"AKAP10","gene_name":"A-kinase anchoring protein 10 [Source:HGNC Symbol;Acc:HGNC:368]","synonyms":"PRKA10,MGC9414,D-AKAP2","biotype":"protein_coding","ncbi_id":"11216","summary":"This gene encodes a member of the A-kinase anchor protein family. A-kinase anchor proteins bind to the regulatory subunits of protein kinase A (PKA) and confine the holoenzyme to discrete locations within the cell. The encoded protein is localized to mitochondria and interacts with both the type I and type II regulatory subunits of PKA. Polymorphisms in this gene may be associated with increased risk of arrhythmias and sudden cardiac death. [provided by RefSeq, May 2012]","start":19904302,"end":19978343,"strand":-1,"description":"A-kinase anchoring protein 10 [Source:HGNC Symbol;Acc:HGNC:368]"}, {"versioned_ensembl_gene_id":"ENSG00000236536.1","gene_symbol":"AC003986.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19119933,"end":19121916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255078.1","gene_symbol":"OR4A6P","gene_name":"olfactory receptor family 4 subfamily A member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15163]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390131","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54724847,"end":54725816,"strand":1,"description":"olfactory receptor family 4 subfamily A member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15163]"}, {"versioned_ensembl_gene_id":"ENSG00000125484.11","gene_symbol":"GTF3C4","gene_name":"general transcription factor IIIC subunit 4 [Source:HGNC Symbol;Acc:HGNC:4667]","synonyms":"TFIIIC90,KAT12","biotype":"protein_coding","ncbi_id":"9329","summary":null,"start":132670035,"end":132694955,"strand":1,"description":"general transcription factor IIIC subunit 4 [Source:HGNC Symbol;Acc:HGNC:4667]"}, {"versioned_ensembl_gene_id":"ENSG00000274100.1","gene_symbol":"AL627230.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67721884,"end":67722094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280693.2","gene_symbol":"SH3PXD2A-AS1","gene_name":"SH3PXD2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45242]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505839","summary":null,"start":103745966,"end":103755423,"strand":1,"description":"SH3PXD2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45242]"}, {"versioned_ensembl_gene_id":"ENSG00000243548.3","gene_symbol":"RN7SL101P","gene_name":"RNA, 7SL, cytoplasmic 101, pseudogene [Source:HGNC Symbol;Acc:HGNC:46117]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479260","summary":null,"start":28711198,"end":28711476,"strand":1,"description":"RNA, 7SL, cytoplasmic 101, pseudogene [Source:HGNC Symbol;Acc:HGNC:46117]"}, {"versioned_ensembl_gene_id":"ENSG00000227025.1","gene_symbol":"CR388205.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29996063,"end":29997058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008324.11","gene_symbol":"SS18L2","gene_name":"SS18 like 2 [Source:HGNC Symbol;Acc:HGNC:15593]","synonyms":"KIAA-iso","biotype":"protein_coding","ncbi_id":"51188","summary":"Synovial sarcomas occur most frequently in the extremities around large joints. More than 90% of cases have a recurrent and specific chromosomal translocation, t(X;18)(p11.2;q11.2), in which the 5-prime end of the SS18 gene (MIM 600192) is fused in-frame to the 3-prime end of the SSX1 (MIM 312820), SSX2 (MIM 300192), or SSX4 (MIM 300326) gene. The SS18L2 gene is homologous to SS18.[supplied by OMIM, Jul 2002]","start":42581840,"end":42595114,"strand":1,"description":"SS18 like 2 [Source:HGNC Symbol;Acc:HGNC:15593]"}, {"versioned_ensembl_gene_id":"ENSG00000081377.16","gene_symbol":"CDC14B","gene_name":"cell division cycle 14B [Source:HGNC Symbol;Acc:HGNC:1719]","synonyms":"hCDC14B,CDC14B3,Cdc14B2,Cdc14B1","biotype":"protein_coding","ncbi_id":"8555","summary":"The protein encoded by this gene is a member of the dual specificity protein tyrosine phosphatase family. This protein is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit of cell mitosis and initiation of DNA replication, which suggests the role in cell cycle control. This protein has been shown to interact with and dephosphorylates tumor suppressor protein p53, and is thought to regulate the function of p53. Alternative splice of this gene results in 3 transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":96490241,"end":96619830,"strand":-1,"description":"cell division cycle 14B [Source:HGNC Symbol;Acc:HGNC:1719]"}, {"versioned_ensembl_gene_id":"ENSG00000262721.1","gene_symbol":"AC135048.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":30875766,"end":30895216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232407.3","gene_symbol":"AC104164.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60690225,"end":60690719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205784.2","gene_symbol":"ARRDC5","gene_name":"arrestin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:31407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645432","summary":null,"start":4890437,"end":4902867,"strand":-1,"description":"arrestin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:31407]"}, {"versioned_ensembl_gene_id":"ENSG00000229661.1","gene_symbol":"BUD31P2","gene_name":"BUD31 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480332","summary":null,"start":75201491,"end":75201790,"strand":1,"description":"BUD31 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51562]"}, {"versioned_ensembl_gene_id":"ENSG00000203760.8","gene_symbol":"CENPW","gene_name":"centromere protein W [Source:HGNC Symbol;Acc:HGNC:21488]","synonyms":"CUG2,C6orf173","biotype":"protein_coding","ncbi_id":"387103","summary":null,"start":126340174,"end":126348875,"strand":1,"description":"centromere protein W [Source:HGNC Symbol;Acc:HGNC:21488]"}, {"versioned_ensembl_gene_id":"ENSG00000224584.2","gene_symbol":"UBE2V1P13","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52411]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505982","summary":null,"start":214612960,"end":214613398,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52411]"}, {"versioned_ensembl_gene_id":"ENSG00000077157.21","gene_symbol":"PPP1R12B","gene_name":"protein phosphatase 1 regulatory subunit 12B [Source:HGNC Symbol;Acc:HGNC:7619]","synonyms":"PP1bp55,MYPT2,MGC87886,MGC131980","biotype":"protein_coding","ncbi_id":"4660","summary":"Myosin phosphatase is a protein complex comprised of three subunits: a catalytic subunit (PP1c-delta, protein phosphatase 1, catalytic subunit delta), a large regulatory subunit (MYPT, myosin phosphatase target) and small regulatory subunit (sm-M20). Two isoforms of MYPT have been isolated--MYPT1 and MYPT2, the first of which is widely expressed, and the second of which may be specific to heart, skeletal muscle, and brain. Each of the MYPT isoforms functions to bind PP1c-delta and increase phosphatase activity. This locus encodes both MYTP2 and M20. Alternatively spliced transcript variants encoding different isoforms have been identified. Related pseudogenes have been defined on the Y chromosome. [provided by RefSeq, Oct 2011]","start":202348699,"end":202592706,"strand":1,"description":"protein phosphatase 1 regulatory subunit 12B [Source:HGNC Symbol;Acc:HGNC:7619]"}, {"versioned_ensembl_gene_id":"ENSG00000278735.1","gene_symbol":"AL627230.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67718821,"end":67719022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224263.1","gene_symbol":"CYCSP12","gene_name":"cytochrome c, somatic pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:24386]","synonyms":"HCP13,HCP12,CYCSP13","biotype":"processed_pseudogene","ncbi_id":"360168","summary":null,"start":11878830,"end":11879129,"strand":-1,"description":"cytochrome c, somatic pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:24386]"}, {"versioned_ensembl_gene_id":"ENSG00000254565.1","gene_symbol":"MTND2P26","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42127]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873349","summary":null,"start":103406213,"end":103407241,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42127]"}, {"versioned_ensembl_gene_id":"ENSG00000243167.1","gene_symbol":"RPS10P28","gene_name":"ribosomal protein S10 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35511]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132372","summary":null,"start":42670005,"end":42670816,"strand":1,"description":"ribosomal protein S10 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35511]"}, {"versioned_ensembl_gene_id":"ENSG00000224546.2","gene_symbol":"EIF4BP3","gene_name":"eukaryotic translation initiation factor 4B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128771","summary":null,"start":96146007,"end":96147856,"strand":1,"description":"eukaryotic translation initiation factor 4B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37936]"}, {"versioned_ensembl_gene_id":"ENSG00000236525.1","gene_symbol":"AC007278.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":102433957,"end":102435340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176695.7","gene_symbol":"OR4F17","gene_name":"olfactory receptor family 4 subfamily F member 17 [Source:HGNC Symbol;Acc:HGNC:15381]","synonyms":"OR4F19,OR4F18,OR4F11P","biotype":"protein_coding","ncbi_id":"81099","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":107104,"end":117102,"strand":1,"description":"olfactory receptor family 4 subfamily F member 17 [Source:HGNC Symbol;Acc:HGNC:15381]"}, {"versioned_ensembl_gene_id":"ENSG00000223932.6","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31700683,"end":31705737,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000115607.9","gene_symbol":"IL18RAP","gene_name":"interleukin 18 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5989]","synonyms":"CD218b,AcPL","biotype":"protein_coding","ncbi_id":"8807","summary":"The protein encoded by this gene is an accessory subunit of the heterodimeric receptor for interleukin 18 (IL18), a proinflammatory cytokine involved in inducing cell-mediated immunity. This protein enhances the IL18-binding activity of the IL18 receptor and plays a role in signaling by IL18. Mutations in this gene are associated with Crohn's disease and inflammatory bowel disease, and susceptibility to celiac disease and leprosy. Alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2014]","start":102418689,"end":102452565,"strand":1,"description":"interleukin 18 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5989]"}, {"versioned_ensembl_gene_id":"ENSG00000243295.1","gene_symbol":"AC114400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59065150,"end":59119509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243903.1","gene_symbol":"AC138057.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59380024,"end":59388704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242545.1","gene_symbol":"AC126121.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59464330,"end":59510678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201354.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140609847,"end":140609955,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238594.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":150164584,"end":150164686,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000152104.11","gene_symbol":"PTPN14","gene_name":"protein tyrosine phosphatase, non-receptor type 14 [Source:HGNC Symbol;Acc:HGNC:9647]","synonyms":"PEZ","biotype":"protein_coding","ncbi_id":"5784","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N-terminal noncatalytic domain similar to that of band 4.1 superfamily cytoskeleton-associated proteins, which suggested the membrane or cytoskeleton localization of this protein. It appears to regulate lymphatic development in mammals, and a loss of function mutation has been found in a kindred with a lymphedema-choanal atresia. [provided by RefSeq, Sep 2010]","start":214348696,"end":214552449,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 14 [Source:HGNC Symbol;Acc:HGNC:9647]"}, {"versioned_ensembl_gene_id":"ENSG00000163660.11","gene_symbol":"CCNL1","gene_name":"cyclin L1 [Source:HGNC Symbol;Acc:HGNC:20569]","synonyms":"ania-6a","biotype":"protein_coding","ncbi_id":"57018","summary":null,"start":157146508,"end":157160760,"strand":-1,"description":"cyclin L1 [Source:HGNC Symbol;Acc:HGNC:20569]"}, {"versioned_ensembl_gene_id":"ENSG00000241804.1","gene_symbol":"AC126121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59535863,"end":59536415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255042.3","gene_symbol":"AC109635.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50279828,"end":50298452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278643.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11033727,"end":11033912,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000202137.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":201808681,"end":201808782,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206973.1","gene_symbol":"RNU6-1145P","gene_name":"RNA, U6 small nuclear 1145, pseudogene [Source:HGNC Symbol;Acc:HGNC:48108]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481541","summary":null,"start":61605616,"end":61605722,"strand":1,"description":"RNA, U6 small nuclear 1145, pseudogene [Source:HGNC Symbol;Acc:HGNC:48108]"}, {"versioned_ensembl_gene_id":"ENSG00000275868.1","gene_symbol":"MIR8054","gene_name":"microRNA 8054 [Source:HGNC Symbol;Acc:HGNC:50177]","synonyms":"hsa-mir-8054","biotype":"miRNA","ncbi_id":"102465860","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23419105,"end":23419190,"strand":-1,"description":"microRNA 8054 [Source:HGNC Symbol;Acc:HGNC:50177]"}, {"versioned_ensembl_gene_id":"ENSG00000200419.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45591984,"end":45592085,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207624.1","gene_symbol":"MIR194-1","gene_name":"microRNA 194-1 [Source:HGNC Symbol;Acc:HGNC:31564]","synonyms":"MIRN194-1,hsa-mir-194-1","biotype":"miRNA","ncbi_id":"406969","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":220118157,"end":220118241,"strand":-1,"description":"microRNA 194-1 [Source:HGNC Symbol;Acc:HGNC:31564]"}, {"versioned_ensembl_gene_id":"ENSG00000265291.1","gene_symbol":"MIR4710","gene_name":"microRNA 4710 [Source:HGNC Symbol;Acc:HGNC:41727]","synonyms":"hsa-mir-4710","biotype":"miRNA","ncbi_id":"100616300","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104677694,"end":104677749,"strand":-1,"description":"microRNA 4710 [Source:HGNC Symbol;Acc:HGNC:41727]"}, {"versioned_ensembl_gene_id":"ENSG00000222472.1","gene_symbol":"RN7SKP7","gene_name":"RNA, 7SK small nuclear pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42625]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873851","summary":null,"start":96949249,"end":96949533,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42625]"}, {"versioned_ensembl_gene_id":"ENSG00000202199.1","gene_symbol":"RNU1-115P","gene_name":"RNA, U1 small nuclear 115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48457]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480188","summary":null,"start":133238657,"end":133238816,"strand":-1,"description":"RNA, U1 small nuclear 115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48457]"}, {"versioned_ensembl_gene_id":"ENSG00000207622.1","gene_symbol":"MIR619","gene_name":"microRNA 619 [Source:HGNC Symbol;Acc:HGNC:32875]","synonyms":"MIRN619,hsa-mir-619","biotype":"miRNA","ncbi_id":"693204","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":108836908,"end":108837006,"strand":-1,"description":"microRNA 619 [Source:HGNC Symbol;Acc:HGNC:32875]"}, {"versioned_ensembl_gene_id":"ENSG00000276398.1","gene_symbol":"RMST_9","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 9 [Source:RFAM;Acc:RF01970]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97560856,"end":97561048,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 9 [Source:RFAM;Acc:RF01970]"}, {"versioned_ensembl_gene_id":"ENSG00000212425.1","gene_symbol":"RNA5SP105","gene_name":"RNA, 5S ribosomal pseudogene 105 [Source:HGNC Symbol;Acc:HGNC:42903]","synonyms":"RN5S105","biotype":"rRNA","ncbi_id":"100873376","summary":null,"start":137512098,"end":137512210,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 105 [Source:HGNC Symbol;Acc:HGNC:42903]"}, {"versioned_ensembl_gene_id":"ENSG00000238924.2","gene_symbol":"RNU7-82P","gene_name":"RNA, U7 small nuclear 82 pseudogene [Source:HGNC Symbol;Acc:HGNC:34178]","synonyms":"U7.82,RNU7-163P","biotype":"snRNA","ncbi_id":"100151679","summary":null,"start":163470205,"end":163470266,"strand":-1,"description":"RNA, U7 small nuclear 82 pseudogene [Source:HGNC Symbol;Acc:HGNC:34178]"}, {"versioned_ensembl_gene_id":"ENSG00000258101.2","gene_symbol":"AC010173.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49232790,"end":49264756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283818.1","gene_symbol":"MIR7844","gene_name":"microRNA 7844 [Source:HGNC Symbol;Acc:HGNC:50044]","synonyms":"hsa-mir-7844","biotype":"miRNA","ncbi_id":"102465834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94571231,"end":94571352,"strand":-1,"description":"microRNA 7844 [Source:HGNC Symbol;Acc:HGNC:50044]"}, {"versioned_ensembl_gene_id":"ENSG00000201270.1","gene_symbol":"RNU6-755P","gene_name":"RNA, U6 small nuclear 755, pseudogene [Source:HGNC Symbol;Acc:HGNC:47718]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481915","summary":null,"start":164980035,"end":164980137,"strand":-1,"description":"RNA, U6 small nuclear 755, pseudogene [Source:HGNC Symbol;Acc:HGNC:47718]"}, {"versioned_ensembl_gene_id":"ENSG00000201595.1","gene_symbol":"RNA5SP132","gene_name":"RNA, 5S ribosomal pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:43032]","synonyms":"RN5S132","biotype":"rRNA","ncbi_id":"100873401","summary":null,"start":51694465,"end":51694582,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:43032]"}, {"versioned_ensembl_gene_id":"ENSG00000221638.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":75627950,"end":75628168,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000284416.1","gene_symbol":"MIR1908","gene_name":"microRNA 1908 [Source:HGNC Symbol;Acc:HGNC:35392]","synonyms":"MIRN1908,hsa-mir-1908","biotype":"miRNA","ncbi_id":"100302263","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61815161,"end":61815240,"strand":-1,"description":"microRNA 1908 [Source:HGNC Symbol;Acc:HGNC:35392]"}, {"versioned_ensembl_gene_id":"ENSG00000265407.1","gene_symbol":"MIR4324","gene_name":"microRNA 4324 [Source:HGNC Symbol;Acc:HGNC:38392]","synonyms":"hsa-mir-4324","biotype":"miRNA","ncbi_id":"100422979","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49308797,"end":49308868,"strand":-1,"description":"microRNA 4324 [Source:HGNC Symbol;Acc:HGNC:38392]"}, {"versioned_ensembl_gene_id":"ENSG00000201309.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":134283092,"end":134283193,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281859.1","gene_symbol":"SNORD38B","gene_name":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]","synonyms":"U38B,RNU38B,U38B,RNU38B","biotype":"snoRNA","ncbi_id":"94163","summary":null,"start":44778390,"end":44778458,"strand":1,"description":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]"}, {"versioned_ensembl_gene_id":"ENSG00000200256.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75835215,"end":75835323,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251750.1","gene_symbol":"RNU5F-8P","gene_name":"RNA, U5F small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42531]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873839","summary":null,"start":240653367,"end":240653477,"strand":1,"description":"RNA, U5F small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42531]"}, {"versioned_ensembl_gene_id":"ENSG00000273829.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50054143,"end":50054430,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000239039.1","gene_symbol":"SNORD13","gene_name":"small nucleolar RNA, C/D box 13 [Source:HGNC Symbol;Acc:HGNC:32711]","synonyms":"U13,SNORD13A,RNU13","biotype":"snoRNA","ncbi_id":"692084","summary":null,"start":33513475,"end":33513578,"strand":1,"description":"small nucleolar RNA, C/D box 13 [Source:HGNC Symbol;Acc:HGNC:32711]"}, {"versioned_ensembl_gene_id":"ENSG00000202360.1","gene_symbol":"RN7SKP249","gene_name":"RNA, 7SK small nuclear pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:45973]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480910","summary":null,"start":101137959,"end":101138313,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:45973]"}, {"versioned_ensembl_gene_id":"ENSG00000200719.1","gene_symbol":"RNA5SP260","gene_name":"RNA, 5S ribosomal pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:43160]","synonyms":"RN5S260","biotype":"rRNA","ncbi_id":"100873514","summary":null,"start":29048494,"end":29048604,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:43160]"}, {"versioned_ensembl_gene_id":"ENSG00000251998.1","gene_symbol":"RNU6-168P","gene_name":"RNA, U6 small nuclear 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:47131]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479640","summary":null,"start":163796065,"end":163796165,"strand":-1,"description":"RNA, U6 small nuclear 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:47131]"}, {"versioned_ensembl_gene_id":"ENSG00000278257.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000199362.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75837544,"end":75837645,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252914.1","gene_symbol":"RNU6-789P","gene_name":"RNA, U6 small nuclear 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:47752]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479915","summary":null,"start":136721394,"end":136721495,"strand":-1,"description":"RNA, U6 small nuclear 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:47752]"}, {"versioned_ensembl_gene_id":"ENSG00000199567.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86019608,"end":86019715,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273866.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37578669,"end":37578922,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199631.1","gene_symbol":"SNORD33","gene_name":"small nucleolar RNA, C/D box 33 [Source:HGNC Symbol;Acc:HGNC:10160]","synonyms":"U33,RNU33","biotype":"snoRNA","ncbi_id":"26818","summary":null,"start":49490615,"end":49490699,"strand":1,"description":"small nucleolar RNA, C/D box 33 [Source:HGNC Symbol;Acc:HGNC:10160]"}, {"versioned_ensembl_gene_id":"ENSG00000212516.1","gene_symbol":"RNU6-1268P","gene_name":"RNA, U6 small nuclear 1268, pseudogene [Source:HGNC Symbol;Acc:HGNC:48231]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480654","summary":null,"start":19422815,"end":19422921,"strand":-1,"description":"RNA, U6 small nuclear 1268, pseudogene [Source:HGNC Symbol;Acc:HGNC:48231]"}, {"versioned_ensembl_gene_id":"ENSG00000253063.1","gene_symbol":"RNU6-494P","gene_name":"RNA, U6 small nuclear 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:47457]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479785","summary":null,"start":32477382,"end":32477471,"strand":-1,"description":"RNA, U6 small nuclear 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:47457]"}, {"versioned_ensembl_gene_id":"ENSG00000273715.4","gene_symbol":"AC138827.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70150924,"end":70167868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238705.1","gene_symbol":"MIR1976","gene_name":"microRNA 1976 [Source:HGNC Symbol;Acc:HGNC:37064]","synonyms":"hsa-mir-1976","biotype":"miRNA","ncbi_id":"100302190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26554542,"end":26554593,"strand":1,"description":"microRNA 1976 [Source:HGNC Symbol;Acc:HGNC:37064]"}, {"versioned_ensembl_gene_id":"ENSG00000200526.1","gene_symbol":"RNY4P14","gene_name":"RNA, Ro-associated Y4 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:34064]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379584","summary":null,"start":39785415,"end":39785510,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:34064]"}, {"versioned_ensembl_gene_id":"ENSG00000200986.1","gene_symbol":"RNU6-819P","gene_name":"RNA, U6 small nuclear 819, pseudogene [Source:HGNC Symbol;Acc:HGNC:47782]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479928","summary":null,"start":47131781,"end":47131887,"strand":-1,"description":"RNA, U6 small nuclear 819, pseudogene [Source:HGNC Symbol;Acc:HGNC:47782]"}, {"versioned_ensembl_gene_id":"ENSG00000212221.1","gene_symbol":"RNU6-220P","gene_name":"RNA, U6 small nuclear 220, pseudogene [Source:HGNC Symbol;Acc:HGNC:47183]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481247","summary":null,"start":143350172,"end":143350278,"strand":1,"description":"RNA, U6 small nuclear 220, pseudogene [Source:HGNC Symbol;Acc:HGNC:47183]"}, {"versioned_ensembl_gene_id":"ENSG00000201331.1","gene_symbol":"SNORD115-23","gene_name":"small nucleolar RNA, C/D box 115-23 [Source:HGNC Symbol;Acc:HGNC:33042]","synonyms":"HBII-52-23","biotype":"snoRNA","ncbi_id":"100033800","summary":null,"start":25211796,"end":25211877,"strand":1,"description":"small nucleolar RNA, C/D box 115-23 [Source:HGNC Symbol;Acc:HGNC:33042]"}, {"versioned_ensembl_gene_id":"ENSG00000239189.1","gene_symbol":"RNU6-634P","gene_name":"RNA, U6 small nuclear 634, pseudogene [Source:HGNC Symbol;Acc:HGNC:47597]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479847","summary":null,"start":55499950,"end":55500055,"strand":1,"description":"RNA, U6 small nuclear 634, pseudogene [Source:HGNC Symbol;Acc:HGNC:47597]"}, {"versioned_ensembl_gene_id":"ENSG00000272230.1","gene_symbol":"MIR3666","gene_name":"microRNA 3666 [Source:HGNC Symbol;Acc:HGNC:38940]","synonyms":"hsa-mir-3666","biotype":"miRNA","ncbi_id":"100500896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114653345,"end":114653455,"strand":1,"description":"microRNA 3666 [Source:HGNC Symbol;Acc:HGNC:38940]"}, {"versioned_ensembl_gene_id":"ENSG00000274848.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30816030,"end":30816302,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275455.1","gene_symbol":"MIR7852","gene_name":"microRNA 7852 [Source:HGNC Symbol;Acc:HGNC:50201]","synonyms":"hsa-mir-7852","biotype":"miRNA","ncbi_id":"102465839","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":107897223,"end":107897304,"strand":1,"description":"microRNA 7852 [Source:HGNC Symbol;Acc:HGNC:50201]"}, {"versioned_ensembl_gene_id":"ENSG00000275502.1","gene_symbol":"DAOA-AS1_2","gene_name":"DAOA antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02091]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105462302,"end":105462505,"strand":1,"description":"DAOA antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02091]"}, {"versioned_ensembl_gene_id":"ENSG00000207941.1","gene_symbol":"MIR552","gene_name":"microRNA 552 [Source:HGNC Symbol;Acc:HGNC:32808]","synonyms":"MIRN552,hsa-mir-552","biotype":"miRNA","ncbi_id":"693137","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34669599,"end":34669694,"strand":-1,"description":"microRNA 552 [Source:HGNC Symbol;Acc:HGNC:32808]"}, {"versioned_ensembl_gene_id":"ENSG00000238584.1","gene_symbol":"RNU7-167P","gene_name":"RNA, U7 small nuclear 167 pseudogene [Source:HGNC Symbol;Acc:HGNC:45701]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479088","summary":null,"start":35249772,"end":35249833,"strand":1,"description":"RNA, U7 small nuclear 167 pseudogene [Source:HGNC Symbol;Acc:HGNC:45701]"}, {"versioned_ensembl_gene_id":"ENSG00000207938.1","gene_symbol":"MIR511","gene_name":"microRNA 511 [Source:HGNC Symbol;Acc:HGNC:32077]","synonyms":"hsa-mir-511-2,hsa-mir-511-1,MIRN511-2,MIRN511-1,MIR511-2,MIR511-1","biotype":"miRNA","ncbi_id":"574445","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17845107,"end":17845193,"strand":1,"description":"microRNA 511 [Source:HGNC Symbol;Acc:HGNC:32077]"}, {"versioned_ensembl_gene_id":"ENSG00000269167.1","gene_symbol":"CR753845.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31988350,"end":31989286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269651.1","gene_symbol":"AC022146.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8173272,"end":8175567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284029.1","gene_symbol":"MIR6805","gene_name":"microRNA 6805 [Source:HGNC Symbol;Acc:HGNC:50215]","synonyms":"hsa-mir-6805","biotype":"miRNA","ncbi_id":"102465483","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55388181,"end":55388242,"strand":1,"description":"microRNA 6805 [Source:HGNC Symbol;Acc:HGNC:50215]"}, {"versioned_ensembl_gene_id":"ENSG00000276532.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18605054,"end":18605356,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000221065.1","gene_symbol":"MIR1233-2","gene_name":"microRNA 1233-2 [Source:HGNC Symbol;Acc:HGNC:38277]","synonyms":"hsa-mir-1233-2","biotype":"miRNA","ncbi_id":"100422845","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34528290,"end":34528371,"strand":-1,"description":"microRNA 1233-2 [Source:HGNC Symbol;Acc:HGNC:38277]"}, {"versioned_ensembl_gene_id":"ENSG00000274621.1","gene_symbol":"MIR6867","gene_name":"microRNA 6867 [Source:HGNC Symbol;Acc:HGNC:50134]","synonyms":"hsa-mir-6867","biotype":"miRNA","ncbi_id":"102465523","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40193597,"end":40193663,"strand":1,"description":"microRNA 6867 [Source:HGNC Symbol;Acc:HGNC:50134]"}, {"versioned_ensembl_gene_id":"ENSG00000275399.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"CLR19.9,NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54972989,"end":55008845,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000266072.1","gene_symbol":"MIR5693","gene_name":"microRNA 5693 [Source:HGNC Symbol;Acc:HGNC:43499]","synonyms":"hsa-mir-5693","biotype":"miRNA","ncbi_id":"100847003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51348567,"end":51348639,"strand":-1,"description":"microRNA 5693 [Source:HGNC Symbol;Acc:HGNC:43499]"}, {"versioned_ensembl_gene_id":"ENSG00000264501.2","gene_symbol":"RN7SL731P","gene_name":"RNA, 7SL, cytoplasmic 731, pseudogene [Source:HGNC Symbol;Acc:HGNC:46747]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107048981","summary":null,"start":10306465,"end":10306757,"strand":1,"description":"RNA, 7SL, cytoplasmic 731, pseudogene [Source:HGNC Symbol;Acc:HGNC:46747]"}, {"versioned_ensembl_gene_id":"ENSG00000278365.1","gene_symbol":"AC012314.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238789.1","gene_symbol":"RNU7-152P","gene_name":"RNA, U7 small nuclear 152 pseudogene [Source:HGNC Symbol;Acc:HGNC:45686]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479081","summary":null,"start":155654963,"end":155655026,"strand":-1,"description":"RNA, U7 small nuclear 152 pseudogene [Source:HGNC Symbol;Acc:HGNC:45686]"}, {"versioned_ensembl_gene_id":"ENSG00000207205.1","gene_symbol":"RNVU1-15","gene_name":"RNA, variant U1 small nuclear 15 [Source:HGNC Symbol;Acc:HGNC:48320]","synonyms":"RNU1-121,vU1.16,vU1.15,RNVU1-16,RNU1-66","biotype":"snRNA","ncbi_id":"101954267","summary":null,"start":144412576,"end":144412740,"strand":1,"description":"RNA, variant U1 small nuclear 15 [Source:HGNC Symbol;Acc:HGNC:48320]"}, {"versioned_ensembl_gene_id":"ENSG00000277578.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":84642487,"end":84642763,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202035.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73403788,"end":73403889,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199803.1","gene_symbol":"RNU6-1159P","gene_name":"RNA, U6 small nuclear 1159, pseudogene [Source:HGNC Symbol;Acc:HGNC:48122]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481939","summary":null,"start":15021553,"end":15021659,"strand":-1,"description":"RNA, U6 small nuclear 1159, pseudogene [Source:HGNC Symbol;Acc:HGNC:48122]"}, {"versioned_ensembl_gene_id":"ENSG00000222796.1","gene_symbol":"RNU6-383P","gene_name":"RNA, U6 small nuclear 383, pseudogene [Source:HGNC Symbol;Acc:HGNC:47346]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479736","summary":null,"start":150955494,"end":150955587,"strand":-1,"description":"RNA, U6 small nuclear 383, pseudogene [Source:HGNC Symbol;Acc:HGNC:47346]"}, {"versioned_ensembl_gene_id":"ENSG00000159335.15","gene_symbol":"PTMS","gene_name":"parathymosin [Source:HGNC Symbol;Acc:HGNC:9629]","synonyms":"ParaT","biotype":"protein_coding","ncbi_id":"5763","summary":null,"start":6765516,"end":6770952,"strand":1,"description":"parathymosin [Source:HGNC Symbol;Acc:HGNC:9629]"}, {"versioned_ensembl_gene_id":"ENSG00000198976.1","gene_symbol":"MIR429","gene_name":"microRNA 429 [Source:HGNC Symbol;Acc:HGNC:13784]","synonyms":"MIRN429,hsa-mir-429","biotype":"miRNA","ncbi_id":"554210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1169005,"end":1169087,"strand":1,"description":"microRNA 429 [Source:HGNC Symbol;Acc:HGNC:13784]"}, {"versioned_ensembl_gene_id":"ENSG00000274293.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38150050,"end":38150138,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000200587.1","gene_symbol":"RNA5SP514","gene_name":"RNA, 5S ribosomal pseudogene 514 [Source:HGNC Symbol;Acc:HGNC:43414]","synonyms":"RN5S514","biotype":"rRNA","ncbi_id":"100873565","summary":null,"start":131938846,"end":131938956,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 514 [Source:HGNC Symbol;Acc:HGNC:43414]"}, {"versioned_ensembl_gene_id":"ENSG00000212545.1","gene_symbol":"RNU6-337P","gene_name":"RNA, U6 small nuclear 337, pseudogene [Source:HGNC Symbol;Acc:HGNC:47300]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479716","summary":null,"start":79030240,"end":79030345,"strand":1,"description":"RNA, U6 small nuclear 337, pseudogene [Source:HGNC Symbol;Acc:HGNC:47300]"}, {"versioned_ensembl_gene_id":"ENSG00000199712.1","gene_symbol":"SNORD115-2","gene_name":"small nucleolar RNA, C/D box 115-2 [Source:HGNC Symbol;Acc:HGNC:33021]","synonyms":"HBII-52-2","biotype":"snoRNA","ncbi_id":"100033437","summary":null,"start":25172635,"end":25172716,"strand":1,"description":"small nucleolar RNA, C/D box 115-2 [Source:HGNC Symbol;Acc:HGNC:33021]"}, {"versioned_ensembl_gene_id":"ENSG00000222202.1","gene_symbol":"RNU4-26P","gene_name":"RNA, U4 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:46962]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479569","summary":null,"start":20418321,"end":20418427,"strand":1,"description":"RNA, U4 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:46962]"}, {"versioned_ensembl_gene_id":"ENSG00000221533.1","gene_symbol":"MIR1184-1","gene_name":"microRNA 1184-1 [Source:HGNC Symbol;Acc:HGNC:35265]","synonyms":"MIRN1184,MIR1184,hsa-mir-1184","biotype":"miRNA","ncbi_id":"100302111","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154887360,"end":154887458,"strand":-1,"description":"microRNA 1184-1 [Source:HGNC Symbol;Acc:HGNC:35265]"}, {"versioned_ensembl_gene_id":"ENSG00000265347.1","gene_symbol":"MIR4291","gene_name":"microRNA 4291 [Source:HGNC Symbol;Acc:HGNC:38267]","synonyms":"hsa-mir-4291","biotype":"miRNA","ncbi_id":"100422927","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93819357,"end":93819421,"strand":1,"description":"microRNA 4291 [Source:HGNC Symbol;Acc:HGNC:38267]"}, {"versioned_ensembl_gene_id":"ENSG00000263790.1","gene_symbol":"MIR4473","gene_name":"microRNA 4473 [Source:HGNC Symbol;Acc:HGNC:41540]","synonyms":"hsa-mir-4473","biotype":"miRNA","ncbi_id":"100616229","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20411148,"end":20411238,"strand":-1,"description":"microRNA 4473 [Source:HGNC Symbol;Acc:HGNC:41540]"}, {"versioned_ensembl_gene_id":"ENSG00000223259.1","gene_symbol":"RNA5SP508","gene_name":"RNA, 5S ribosomal pseudogene 508 [Source:HGNC Symbol;Acc:HGNC:43408]","synonyms":"RN5S508","biotype":"rRNA","ncbi_id":"100873559","summary":null,"start":76655009,"end":76655127,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 508 [Source:HGNC Symbol;Acc:HGNC:43408]"}, {"versioned_ensembl_gene_id":"ENSG00000202308.1","gene_symbol":"RNU6-996P","gene_name":"RNA, U6 small nuclear 996, pseudogene [Source:HGNC Symbol;Acc:HGNC:47959]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481928","summary":null,"start":107663140,"end":107663246,"strand":-1,"description":"RNA, U6 small nuclear 996, pseudogene [Source:HGNC Symbol;Acc:HGNC:47959]"}, {"versioned_ensembl_gene_id":"ENSG00000274740.1","gene_symbol":"AC013791.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2871437,"end":2871498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221063.3","gene_symbol":"MIR1296","gene_name":"microRNA 1296 [Source:HGNC Symbol;Acc:HGNC:35249]","synonyms":"MIRN1296,hsa-mir-1296","biotype":"miRNA","ncbi_id":"100302150","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63372957,"end":63373048,"strand":-1,"description":"microRNA 1296 [Source:HGNC Symbol;Acc:HGNC:35249]"}, {"versioned_ensembl_gene_id":"ENSG00000199936.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85460144,"end":85460252,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200279.1","gene_symbol":"SNORD114-10","gene_name":"small nucleolar RNA, C/D box 114-10 [Source:HGNC Symbol;Acc:HGNC:32998]","synonyms":"14q(II-10)","biotype":"snoRNA","ncbi_id":"767588","summary":null,"start":100967052,"end":100967123,"strand":1,"description":"small nucleolar RNA, C/D box 114-10 [Source:HGNC Symbol;Acc:HGNC:32998]"}, {"versioned_ensembl_gene_id":"ENSG00000265919.1","gene_symbol":"MIR4280","gene_name":"microRNA 4280 [Source:HGNC Symbol;Acc:HGNC:38334]","synonyms":"hsa-mir-4280","biotype":"miRNA","ncbi_id":"100422887","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87114879,"end":87114954,"strand":-1,"description":"microRNA 4280 [Source:HGNC Symbol;Acc:HGNC:38334]"}, {"versioned_ensembl_gene_id":"ENSG00000207784.3","gene_symbol":"MIR542","gene_name":"microRNA 542 [Source:HGNC Symbol;Acc:HGNC:32534]","synonyms":"MIRN542,hsa-mir-542","biotype":"miRNA","ncbi_id":"664617","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134541341,"end":134541437,"strand":-1,"description":"microRNA 542 [Source:HGNC Symbol;Acc:HGNC:32534]"}, {"versioned_ensembl_gene_id":"ENSG00000252658.1","gene_symbol":"RNU6-786P","gene_name":"RNA, U6 small nuclear 786, pseudogene [Source:HGNC Symbol;Acc:HGNC:47749]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481429","summary":null,"start":157934168,"end":157934257,"strand":1,"description":"RNA, U6 small nuclear 786, pseudogene [Source:HGNC Symbol;Acc:HGNC:47749]"}, {"versioned_ensembl_gene_id":"ENSG00000274306.1","gene_symbol":"MIR5088","gene_name":"microRNA 5088 [Source:HGNC Symbol;Acc:HGNC:43489]","synonyms":"hsa-mir-5088","biotype":"miRNA","ncbi_id":"100847074","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49682117,"end":49682195,"strand":1,"description":"microRNA 5088 [Source:HGNC Symbol;Acc:HGNC:43489]"}, {"versioned_ensembl_gene_id":"ENSG00000252970.1","gene_symbol":"RNA5SP159","gene_name":"RNA, 5S ribosomal pseudogene 159 [Source:HGNC Symbol;Acc:HGNC:43059]","synonyms":"RN5S159","biotype":"rRNA","ncbi_id":"100873425","summary":null,"start":39936753,"end":39936855,"strand":1,"description":"RNA, 5S ribosomal pseudogene 159 [Source:HGNC Symbol;Acc:HGNC:43059]"}, {"versioned_ensembl_gene_id":"ENSG00000283152.1","gene_symbol":"MIR3120","gene_name":"microRNA 3120 [Source:HGNC Symbol;Acc:HGNC:38295]","synonyms":"hsa-mir-3120","biotype":"miRNA","ncbi_id":"100422882","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":172138808,"end":172138888,"strand":1,"description":"microRNA 3120 [Source:HGNC Symbol;Acc:HGNC:38295]"}, {"versioned_ensembl_gene_id":"ENSG00000264803.1","gene_symbol":"MIR378C","gene_name":"microRNA 378c [Source:HGNC Symbol;Acc:HGNC:38374]","synonyms":"hsa-mir-378c","biotype":"miRNA","ncbi_id":"100422867","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":130962588,"end":130962668,"strand":-1,"description":"microRNA 378c [Source:HGNC Symbol;Acc:HGNC:38374]"}, {"versioned_ensembl_gene_id":"ENSG00000201517.1","gene_symbol":"RNU6-707P","gene_name":"RNA, U6 small nuclear 707, pseudogene [Source:HGNC Symbol;Acc:HGNC:47670]","synonyms":null,"biotype":"snRNA","ncbi_id":"107075318","summary":null,"start":48153980,"end":48154074,"strand":-1,"description":"RNA, U6 small nuclear 707, pseudogene [Source:HGNC Symbol;Acc:HGNC:47670]"}, {"versioned_ensembl_gene_id":"ENSG00000221662.1","gene_symbol":"MIR1290","gene_name":"microRNA 1290 [Source:HGNC Symbol;Acc:HGNC:35283]","synonyms":"MIRN1290,hsa-mir-1290","biotype":"miRNA","ncbi_id":"100302276","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18897071,"end":18897148,"strand":-1,"description":"microRNA 1290 [Source:HGNC Symbol;Acc:HGNC:35283]"}, {"versioned_ensembl_gene_id":"ENSG00000109762.15","gene_symbol":"SNX25","gene_name":"sorting nexin 25 [Source:HGNC Symbol;Acc:HGNC:21883]","synonyms":"SBBI31","biotype":"protein_coding","ncbi_id":"83891","summary":null,"start":185204237,"end":185370185,"strand":1,"description":"sorting nexin 25 [Source:HGNC Symbol;Acc:HGNC:21883]"}, {"versioned_ensembl_gene_id":"ENSG00000278378.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000252721.1","gene_symbol":"RNU6-798P","gene_name":"RNA, U6 small nuclear 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:47761]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479919","summary":null,"start":97192923,"end":97193025,"strand":-1,"description":"RNA, U6 small nuclear 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:47761]"}, {"versioned_ensembl_gene_id":"ENSG00000265281.1","gene_symbol":"MIR3935","gene_name":"microRNA 3935 [Source:HGNC Symbol;Acc:HGNC:38918]","synonyms":"hsa-mir-3935","biotype":"miRNA","ncbi_id":"100500891","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56245520,"end":56245623,"strand":1,"description":"microRNA 3935 [Source:HGNC Symbol;Acc:HGNC:38918]"}, {"versioned_ensembl_gene_id":"ENSG00000273657.1","gene_symbol":"MIR6792","gene_name":"microRNA 6792 [Source:HGNC Symbol;Acc:HGNC:50054]","synonyms":"hsa-mir-6792","biotype":"miRNA","ncbi_id":"102465475","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7617439,"end":7617505,"strand":1,"description":"microRNA 6792 [Source:HGNC Symbol;Acc:HGNC:50054]"}, {"versioned_ensembl_gene_id":"ENSG00000284246.1","gene_symbol":"MIR6716","gene_name":"microRNA 6716 [Source:HGNC Symbol;Acc:HGNC:50048]","synonyms":"hsa-mir-6716","biotype":"miRNA","ncbi_id":"102466719","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":118644000,"end":118644079,"strand":1,"description":"microRNA 6716 [Source:HGNC Symbol;Acc:HGNC:50048]"}, {"versioned_ensembl_gene_id":"ENSG00000277580.1","gene_symbol":"RNU6-747P","gene_name":"RNA, U6 small nuclear 747, pseudogene [Source:HGNC Symbol;Acc:HGNC:47710]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480399","summary":null,"start":243081156,"end":243081259,"strand":-1,"description":"RNA, U6 small nuclear 747, pseudogene [Source:HGNC Symbol;Acc:HGNC:47710]"}, {"versioned_ensembl_gene_id":"ENSG00000276839.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":182576772,"end":182577040,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222389.1","gene_symbol":"RNU2-28P","gene_name":"RNA, U2 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:48521]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480670","summary":null,"start":81509476,"end":81509664,"strand":1,"description":"RNA, U2 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:48521]"}, {"versioned_ensembl_gene_id":"ENSG00000275134.1","gene_symbol":"MEG8_2","gene_name":"Maternally expressed 8 exon 2 [Source:RFAM;Acc:RF02146]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100898958,"end":100899079,"strand":1,"description":"Maternally expressed 8 exon 2 [Source:RFAM;Acc:RF02146]"}, {"versioned_ensembl_gene_id":"ENSG00000252143.1","gene_symbol":"SCARNA17","gene_name":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]","synonyms":"U91,mgU12-22/U4-8","biotype":"scaRNA","ncbi_id":"677769","summary":null,"start":21544897,"end":21545039,"strand":1,"description":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]"}, {"versioned_ensembl_gene_id":"ENSG00000206620.1","gene_symbol":"SNORD45C","gene_name":"small nucleolar RNA, C/D box 45C [Source:HGNC Symbol;Acc:HGNC:32720]","synonyms":"U45C","biotype":"snoRNA","ncbi_id":"692085","summary":null,"start":75787072,"end":75787150,"strand":1,"description":"small nucleolar RNA, C/D box 45C [Source:HGNC Symbol;Acc:HGNC:32720]"}, {"versioned_ensembl_gene_id":"ENSG00000200113.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":37419628,"end":37419767,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000277467.1","gene_symbol":"RN7SL628P","gene_name":"RNA, 7SL, cytoplasmic 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:46644]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479451","summary":null,"start":30612724,"end":30612960,"strand":1,"description":"RNA, 7SL, cytoplasmic 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:46644]"}, {"versioned_ensembl_gene_id":"ENSG00000221025.1","gene_symbol":"MIR1250","gene_name":"microRNA 1250 [Source:HGNC Symbol;Acc:HGNC:35316]","synonyms":"MIRN1250,hsa-mir-1250","biotype":"miRNA","ncbi_id":"100302229","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81133196,"end":81133308,"strand":-1,"description":"microRNA 1250 [Source:HGNC Symbol;Acc:HGNC:35316]"}, {"versioned_ensembl_gene_id":"ENSG00000207442.1","gene_symbol":"SNORD116-6","gene_name":"small nucleolar RNA, C/D box 116-6 [Source:HGNC Symbol;Acc:HGNC:33072]","synonyms":"HBII-85-6","biotype":"snoRNA","ncbi_id":"100033418","summary":null,"start":25065026,"end":25065121,"strand":1,"description":"small nucleolar RNA, C/D box 116-6 [Source:HGNC Symbol;Acc:HGNC:33072]"}, {"versioned_ensembl_gene_id":"ENSG00000241739.1","gene_symbol":"AC010469.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31840492,"end":31840971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274340.1","gene_symbol":"AC032011.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62387327,"end":62388875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266655.1","gene_symbol":"MIR3908","gene_name":"microRNA 3908 [Source:HGNC Symbol;Acc:HGNC:38991]","synonyms":"hsa-mir-3908","biotype":"miRNA","ncbi_id":"100500909","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123536409,"end":123536534,"strand":1,"description":"microRNA 3908 [Source:HGNC Symbol;Acc:HGNC:38991]"}, {"versioned_ensembl_gene_id":"ENSG00000273500.1","gene_symbol":"MIR6129","gene_name":"microRNA 6129 [Source:HGNC Symbol;Acc:HGNC:50220]","synonyms":"hsa-mir-6129","biotype":"miRNA","ncbi_id":"102465137","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49288346,"end":49288454,"strand":-1,"description":"microRNA 6129 [Source:HGNC Symbol;Acc:HGNC:50220]"}, {"versioned_ensembl_gene_id":"ENSG00000274988.1","gene_symbol":"MIR6876","gene_name":"microRNA 6876 [Source:HGNC Symbol;Acc:HGNC:50181]","synonyms":"hsa-mir-6876","biotype":"miRNA","ncbi_id":"102465527","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25345402,"end":25345474,"strand":1,"description":"microRNA 6876 [Source:HGNC Symbol;Acc:HGNC:50181]"}, {"versioned_ensembl_gene_id":"ENSG00000199085.3","gene_symbol":"MIR148A","gene_name":"microRNA 148a [Source:HGNC Symbol;Acc:HGNC:31535]","synonyms":"MIRN148A,MIRN148,hsa-mir-148a,hsa-mir-148","biotype":"miRNA","ncbi_id":"406940","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25949919,"end":25949986,"strand":-1,"description":"microRNA 148a [Source:HGNC Symbol;Acc:HGNC:31535]"}, {"versioned_ensembl_gene_id":"ENSG00000240183.3","gene_symbol":"RN7SL297P","gene_name":"RNA, 7SL, cytoplasmic 297, pseudogene [Source:HGNC Symbol;Acc:HGNC:46313]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479330","summary":null,"start":111930175,"end":111930467,"strand":1,"description":"RNA, 7SL, cytoplasmic 297, pseudogene [Source:HGNC Symbol;Acc:HGNC:46313]"}, {"versioned_ensembl_gene_id":"ENSG00000265527.1","gene_symbol":"MIR5690","gene_name":"microRNA 5690 [Source:HGNC Symbol;Acc:HGNC:43490]","synonyms":"hsa-mir-5690","biotype":"miRNA","ncbi_id":"100847048","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35664717,"end":35664789,"strand":-1,"description":"microRNA 5690 [Source:HGNC Symbol;Acc:HGNC:43490]"}, {"versioned_ensembl_gene_id":"ENSG00000221737.1","gene_symbol":"MIR548I1","gene_name":"microRNA 548i-1 [Source:HGNC Symbol;Acc:HGNC:35352]","synonyms":"MIRN548I1,hsa-mir-548i-1","biotype":"miRNA","ncbi_id":"100302204","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":125790404,"end":125790552,"strand":-1,"description":"microRNA 548i-1 [Source:HGNC Symbol;Acc:HGNC:35352]"}, {"versioned_ensembl_gene_id":"ENSG00000278525.1","gene_symbol":"RN7SL607P","gene_name":"RNA, 7SL, cytoplasmic 607, pseudogene [Source:HGNC Symbol;Acc:HGNC:46623]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481088","summary":null,"start":20738433,"end":20738731,"strand":-1,"description":"RNA, 7SL, cytoplasmic 607, pseudogene [Source:HGNC Symbol;Acc:HGNC:46623]"}, {"versioned_ensembl_gene_id":"ENSG00000252620.1","gene_symbol":"RNU6ATAC24P","gene_name":"RNA, U6atac small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:46923]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479554","summary":null,"start":195523087,"end":195523221,"strand":-1,"description":"RNA, U6atac small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:46923]"}, {"versioned_ensembl_gene_id":"ENSG00000267379.1","gene_symbol":"AC008569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14402717,"end":14408723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270830.1","gene_symbol":"AC022441.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50903608,"end":50903743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283513.1","gene_symbol":"MIR941-3","gene_name":"microRNA 941-3 [Source:HGNC Symbol;Acc:HGNC:33686]","synonyms":"MIRN941-3,hsa-mir-941-3","biotype":"miRNA","ncbi_id":"100126352","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63919561,"end":63919632,"strand":1,"description":"microRNA 941-3 [Source:HGNC Symbol;Acc:HGNC:33686]"}, {"versioned_ensembl_gene_id":"ENSG00000199017.2","gene_symbol":"MIR1-1","gene_name":"microRNA 1-1 [Source:HGNC Symbol;Acc:HGNC:31499]","synonyms":"MIRN1-1,hsa-mir-1-1","biotype":"miRNA","ncbi_id":"406904","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62554306,"end":62554376,"strand":1,"description":"microRNA 1-1 [Source:HGNC Symbol;Acc:HGNC:31499]"}, {"versioned_ensembl_gene_id":"ENSG00000284331.1","gene_symbol":"MIR4741","gene_name":"microRNA 4741 [Source:HGNC Symbol;Acc:HGNC:41661]","synonyms":"hsa-mir-4741","biotype":"miRNA","ncbi_id":"100616139","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22933349,"end":22933438,"strand":1,"description":"microRNA 4741 [Source:HGNC Symbol;Acc:HGNC:41661]"}, {"versioned_ensembl_gene_id":"ENSG00000264722.1","gene_symbol":"MIR3670-2","gene_name":"microRNA 3670-2 [Source:HGNC Symbol;Acc:HGNC:43460]","synonyms":"hsa-mir-3670-2","biotype":"miRNA","ncbi_id":"100846994","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16306370,"end":16306434,"strand":1,"description":"microRNA 3670-2 [Source:HGNC Symbol;Acc:HGNC:43460]"}, {"versioned_ensembl_gene_id":"ENSG00000200060.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108738484,"end":108738604,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207742.3","gene_symbol":"MIR487A","gene_name":"microRNA 487a [Source:HGNC Symbol;Acc:HGNC:32343]","synonyms":"MIRN487A,MIRN487,hsa-mir-487a,hsa-mir-487","biotype":"miRNA","ncbi_id":"619555","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101052446,"end":101052525,"strand":1,"description":"microRNA 487a [Source:HGNC Symbol;Acc:HGNC:32343]"}, {"versioned_ensembl_gene_id":"ENSG00000207244.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":8961575,"end":8961708,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000252734.1","gene_symbol":"RNU6-980P","gene_name":"RNA, U6 small nuclear 980, pseudogene [Source:HGNC Symbol;Acc:HGNC:47943]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481489","summary":null,"start":53732981,"end":53733083,"strand":-1,"description":"RNA, U6 small nuclear 980, pseudogene [Source:HGNC Symbol;Acc:HGNC:47943]"}, {"versioned_ensembl_gene_id":"ENSG00000200028.1","gene_symbol":"RNA5SP98","gene_name":"RNA, 5S ribosomal pseudogene 98 [Source:HGNC Symbol;Acc:HGNC:42896]","synonyms":"RN5S98","biotype":"rRNA","ncbi_id":"100873331","summary":null,"start":76772909,"end":76773045,"strand":1,"description":"RNA, 5S ribosomal pseudogene 98 [Source:HGNC Symbol;Acc:HGNC:42896]"}, {"versioned_ensembl_gene_id":"ENSG00000252597.1","gene_symbol":"RNU7-137P","gene_name":"RNA, U7 small nuclear 137 pseudogene [Source:HGNC Symbol;Acc:HGNC:45671]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480821","summary":null,"start":18095571,"end":18095632,"strand":-1,"description":"RNA, U7 small nuclear 137 pseudogene [Source:HGNC Symbol;Acc:HGNC:45671]"}, {"versioned_ensembl_gene_id":"ENSG00000240302.3","gene_symbol":"RN7SL717P","gene_name":"RNA, 7SL, cytoplasmic 717, pseudogene [Source:HGNC Symbol;Acc:HGNC:46733]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481118","summary":null,"start":199901081,"end":199901377,"strand":-1,"description":"RNA, 7SL, cytoplasmic 717, pseudogene [Source:HGNC Symbol;Acc:HGNC:46733]"}, {"versioned_ensembl_gene_id":"ENSG00000202283.1","gene_symbol":"SNORA33","gene_name":"Small nucleolar RNA SNORA33 [Source:RFAM;Acc:RF00438]","synonyms":"ACA33","biotype":"snoRNA","ncbi_id":"594839","summary":null,"start":103583135,"end":103583268,"strand":1,"description":"Small nucleolar RNA SNORA33 [Source:RFAM;Acc:RF00438]"}, {"versioned_ensembl_gene_id":"ENSG00000199570.1","gene_symbol":"RNU6-228P","gene_name":"RNA, U6 small nuclear 228, pseudogene [Source:HGNC Symbol;Acc:HGNC:47191]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479668","summary":null,"start":14352320,"end":14352425,"strand":1,"description":"RNA, U6 small nuclear 228, pseudogene [Source:HGNC Symbol;Acc:HGNC:47191]"}, {"versioned_ensembl_gene_id":"ENSG00000207174.1","gene_symbol":"SNORD116-15","gene_name":"small nucleolar RNA, C/D box 116-15 [Source:HGNC Symbol;Acc:HGNC:33081]","synonyms":"HBII-85-15","biotype":"snoRNA","ncbi_id":"100033427","summary":null,"start":25081287,"end":25081378,"strand":1,"description":"small nucleolar RNA, C/D box 116-15 [Source:HGNC Symbol;Acc:HGNC:33081]"}, {"versioned_ensembl_gene_id":"ENSG00000200168.1","gene_symbol":"RNA5SP350","gene_name":"RNA, 5S ribosomal pseudogene 350 [Source:HGNC Symbol;Acc:HGNC:43250]","synonyms":"RN5S350","biotype":"rRNA","ncbi_id":"106481794","summary":null,"start":111040098,"end":111040208,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 350 [Source:HGNC Symbol;Acc:HGNC:43250]"}, {"versioned_ensembl_gene_id":"ENSG00000277613.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":90796,"end":90899,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201931.1","gene_symbol":"RNA5SP172","gene_name":"RNA, 5S ribosomal pseudogene 172 [Source:HGNC Symbol;Acc:HGNC:43072]","synonyms":"RN5S172","biotype":"rRNA","ncbi_id":"106478997","summary":null,"start":177457111,"end":177457228,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 172 [Source:HGNC Symbol;Acc:HGNC:43072]"}, {"versioned_ensembl_gene_id":"ENSG00000283238.1","gene_symbol":"MIR1245B","gene_name":"microRNA 1245b [Source:HGNC Symbol;Acc:HGNC:41794]","synonyms":"hsa-mir-1245b","biotype":"miRNA","ncbi_id":"100616324","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188978093,"end":188978161,"strand":-1,"description":"microRNA 1245b [Source:HGNC Symbol;Acc:HGNC:41794]"}, {"versioned_ensembl_gene_id":"ENSG00000207713.3","gene_symbol":"MIR200C","gene_name":"microRNA 200c [Source:HGNC Symbol;Acc:HGNC:31580]","synonyms":"MIRN200C,hsa-mir-200c","biotype":"miRNA","ncbi_id":"406985","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6963699,"end":6963766,"strand":1,"description":"microRNA 200c [Source:HGNC Symbol;Acc:HGNC:31580]"}, {"versioned_ensembl_gene_id":"ENSG00000278573.1","gene_symbol":"AC007325.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":59711,"end":60316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222338.1","gene_symbol":"RNU6-174P","gene_name":"RNA, U6 small nuclear 174, pseudogene [Source:HGNC Symbol;Acc:HGNC:47137]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481231","summary":null,"start":3726222,"end":3726327,"strand":-1,"description":"RNA, U6 small nuclear 174, pseudogene [Source:HGNC Symbol;Acc:HGNC:47137]"}, {"versioned_ensembl_gene_id":"ENSG00000200388.1","gene_symbol":"RNU6-618P","gene_name":"RNA, U6 small nuclear 618, pseudogene [Source:HGNC Symbol;Acc:HGNC:47581]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481376","summary":null,"start":31396390,"end":31396501,"strand":1,"description":"RNA, U6 small nuclear 618, pseudogene [Source:HGNC Symbol;Acc:HGNC:47581]"}, {"versioned_ensembl_gene_id":"ENSG00000212265.1","gene_symbol":"RNA5SP185","gene_name":"RNA, 5S ribosomal pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:43085]","synonyms":"RN5S185","biotype":"rRNA","ncbi_id":"100873447","summary":null,"start":56260333,"end":56260446,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:43085]"}, {"versioned_ensembl_gene_id":"ENSG00000252086.1","gene_symbol":"RNA5SP76","gene_name":"RNA, 5S ribosomal pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:42853]","synonyms":"RN5S76","biotype":"rRNA","ncbi_id":"100873310","summary":null,"start":219761789,"end":219761875,"strand":1,"description":"RNA, 5S ribosomal pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:42853]"}, {"versioned_ensembl_gene_id":"ENSG00000207131.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87826173,"end":87826285,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223208.1","gene_symbol":"RNU6-1217P","gene_name":"RNA, U6 small nuclear 1217, pseudogene [Source:HGNC Symbol;Acc:HGNC:48180]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481564","summary":null,"start":119434005,"end":119434108,"strand":-1,"description":"RNA, U6 small nuclear 1217, pseudogene [Source:HGNC Symbol;Acc:HGNC:48180]"}, {"versioned_ensembl_gene_id":"ENSG00000207206.1","gene_symbol":"RNU6-1035P","gene_name":"RNA, U6 small nuclear 1035, pseudogene [Source:HGNC Symbol;Acc:HGNC:47998]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481507","summary":null,"start":81725243,"end":81725349,"strand":-1,"description":"RNA, U6 small nuclear 1035, pseudogene [Source:HGNC Symbol;Acc:HGNC:47998]"}, {"versioned_ensembl_gene_id":"ENSG00000240584.3","gene_symbol":"RN7SL547P","gene_name":"RNA, 7SL, cytoplasmic 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:46563]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479421","summary":null,"start":7633562,"end":7633851,"strand":-1,"description":"RNA, 7SL, cytoplasmic 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:46563]"}, {"versioned_ensembl_gene_id":"ENSG00000265820.1","gene_symbol":"MIR3177","gene_name":"microRNA 3177 [Source:HGNC Symbol;Acc:HGNC:38364]","synonyms":"hsa-mir-3177","biotype":"miRNA","ncbi_id":"100423012","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1734985,"end":1735066,"strand":1,"description":"microRNA 3177 [Source:HGNC Symbol;Acc:HGNC:38364]"}, {"versioned_ensembl_gene_id":"ENSG00000221801.1","gene_symbol":"MIR548H2","gene_name":"microRNA 548h-2 [Source:HGNC Symbol;Acc:HGNC:35343]","synonyms":"MIRN548H2,hsa-mir-548h-2","biotype":"miRNA","ncbi_id":"100313773","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11306440,"end":11306527,"strand":-1,"description":"microRNA 548h-2 [Source:HGNC Symbol;Acc:HGNC:35343]"}, {"versioned_ensembl_gene_id":"ENSG00000252167.1","gene_symbol":"RNA5SP287","gene_name":"RNA, 5S ribosomal pseudogene 287 [Source:HGNC Symbol;Acc:HGNC:43187]","synonyms":"RN5S287","biotype":"rRNA","ncbi_id":"100873540","summary":null,"start":81885496,"end":81885598,"strand":1,"description":"RNA, 5S ribosomal pseudogene 287 [Source:HGNC Symbol;Acc:HGNC:43187]"}, {"versioned_ensembl_gene_id":"ENSG00000252277.1","gene_symbol":"SNORD116-30","gene_name":"small nucleolar RNA, C/D box 116-30 [Source:HGNC Symbol;Acc:HGNC:42797]","synonyms":"HBII-85-30","biotype":"snoRNA","ncbi_id":"100873856","summary":null,"start":25108268,"end":25108352,"strand":1,"description":"small nucleolar RNA, C/D box 116-30 [Source:HGNC Symbol;Acc:HGNC:42797]"}, {"versioned_ensembl_gene_id":"ENSG00000263941.2","gene_symbol":"RN7SL32P","gene_name":"RNA, 7SL, cytoplasmic 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46048]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480930","summary":null,"start":233205199,"end":233205479,"strand":1,"description":"RNA, 7SL, cytoplasmic 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46048]"}, {"versioned_ensembl_gene_id":"ENSG00000266423.1","gene_symbol":"MIR3163","gene_name":"microRNA 3163 [Source:HGNC Symbol;Acc:HGNC:38209]","synonyms":"hsa-mir-3163","biotype":"miRNA","ncbi_id":"100423029","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66934434,"end":66934506,"strand":-1,"description":"microRNA 3163 [Source:HGNC Symbol;Acc:HGNC:38209]"}, {"versioned_ensembl_gene_id":"ENSG00000222248.1","gene_symbol":"RNA5SP201","gene_name":"RNA, 5S ribosomal pseudogene 201 [Source:HGNC Symbol;Acc:HGNC:43101]","synonyms":"RN5S201","biotype":"rRNA","ncbi_id":"100873462","summary":null,"start":3088686,"end":3088809,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 201 [Source:HGNC Symbol;Acc:HGNC:43101]"}, {"versioned_ensembl_gene_id":"ENSG00000276323.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"amida,amida,FB1,FB1,INO80F,INO80F","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000251958.1","gene_symbol":"RNU6-1102P","gene_name":"RNA, U6 small nuclear 1102, pseudogene 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[Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202014.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48153434,"end":48153535,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207003.1","gene_symbol":"RNU6-611P","gene_name":"RNA, U6 small nuclear 611, pseudogene [Source:HGNC Symbol;Acc:HGNC:47574]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479836","summary":null,"start":45047458,"end":45047561,"strand":1,"description":"RNA, U6 small nuclear 611, pseudogene [Source:HGNC Symbol;Acc:HGNC:47574]"}, {"versioned_ensembl_gene_id":"ENSG00000266569.2","gene_symbol":"RN7SL377P","gene_name":"RNA, 7SL, cytoplasmic 377, pseudogene [Source:HGNC Symbol;Acc:HGNC:46393]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479360","summary":null,"start":72822894,"end":72823171,"strand":-1,"description":"RNA, 7SL, cytoplasmic 377, 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{"versioned_ensembl_gene_id":"ENSG00000200759.1","gene_symbol":"RNU6-884P","gene_name":"RNA, U6 small nuclear 884, pseudogene [Source:HGNC Symbol;Acc:HGNC:47847]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479957","summary":null,"start":151022746,"end":151022852,"strand":-1,"description":"RNA, U6 small nuclear 884, pseudogene [Source:HGNC Symbol;Acc:HGNC:47847]"}, {"versioned_ensembl_gene_id":"ENSG00000277551.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54913656,"end":54913762,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000243352.3","gene_symbol":"RN7SL8P","gene_name":"RNA, 7SL, cytoplasmic 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:10043]","synonyms":"RN7SLP5,RN7SL433P,7L63","biotype":"misc_RNA","ncbi_id":"6034","summary":null,"start":104911928,"end":104912193,"strand":1,"description":"RNA, 7SL, 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147272335,"end":147272408,"strand":-1,"description":"microRNA 510 [Source:HGNC Symbol;Acc:HGNC:32147]"}, {"versioned_ensembl_gene_id":"ENSG00000206693.1","gene_symbol":"SNORA56","gene_name":"small nucleolar RNA, H/ACA box 56 [Source:HGNC Symbol;Acc:HGNC:32650]","synonyms":"ACA56","biotype":"snoRNA","ncbi_id":"677835","summary":"Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residue U1664 of 28S rRNA. [provided by RefSeq, Feb 2009]","start":154774998,"end":154775126,"strand":1,"description":"small nucleolar RNA, H/ACA box 56 [Source:HGNC Symbol;Acc:HGNC:32650]"}, {"versioned_ensembl_gene_id":"ENSG00000234353.2","gene_symbol":"AP000346.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23638492,"end":23640762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267195.1","gene_symbol":"MIR212","gene_name":"microRNA 212 [Source:HGNC Symbol;Acc:HGNC:31589]","synonyms":"MIRN212,hsa-mir-212","biotype":"miRNA","ncbi_id":"406994","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2050271,"end":2050380,"strand":-1,"description":"microRNA 212 [Source:HGNC Symbol;Acc:HGNC:31589]"}, {"versioned_ensembl_gene_id":"ENSG00000207996.1","gene_symbol":"MIR301A","gene_name":"microRNA 301a [Source:HGNC Symbol;Acc:HGNC:31622]","synonyms":"MIRN301A,MIRN301,hsa-mir-301a,hsa-mir-301","biotype":"miRNA","ncbi_id":"407027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59151136,"end":59151221,"strand":-1,"description":"microRNA 301a [Source:HGNC Symbol;Acc:HGNC:31622]"}, {"versioned_ensembl_gene_id":"ENSG00000252397.1","gene_symbol":"RNU5A-4P","gene_name":"RNA, U5A small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42521]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873870","summary":null,"start":33829539,"end":33829649,"strand":-1,"description":"RNA, U5A small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42521]"}, {"versioned_ensembl_gene_id":"ENSG00000207468.1","gene_symbol":"SNORA19","gene_name":"small nucleolar RNA, H/ACA box 19 [Source:HGNC Symbol;Acc:HGNC:32609]","synonyms":"ACA19","biotype":"snoRNA","ncbi_id":"641451","summary":null,"start":119060011,"end":119060138,"strand":-1,"description":"small nucleolar RNA, H/ACA box 19 [Source:HGNC Symbol;Acc:HGNC:32609]"}, {"versioned_ensembl_gene_id":"ENSG00000244532.1","gene_symbol":"RN7SL380P","gene_name":"RNA, 7SL, cytoplasmic 380, pseudogene [Source:HGNC Symbol;Acc:HGNC:46396]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479361","summary":null,"start":6783854,"end":6784161,"strand":-1,"description":"RNA, 7SL, cytoplasmic 380, pseudogene [Source:HGNC Symbol;Acc:HGNC:46396]"}, {"versioned_ensembl_gene_id":"ENSG00000252983.1","gene_symbol":"RNU7-35P","gene_name":"RNA, U7 small nuclear 35 pseudogene [Source:HGNC Symbol;Acc:HGNC:34131]","synonyms":"U7.35","biotype":"snRNA","ncbi_id":"100147822","summary":null,"start":43194421,"end":43194482,"strand":1,"description":"RNA, U7 small nuclear 35 pseudogene [Source:HGNC Symbol;Acc:HGNC:34131]"}, {"versioned_ensembl_gene_id":"ENSG00000220986.1","gene_symbol":"SNORA50D","gene_name":"small nucleolar RNA, H/ACA box 50D [Source:HGNC Symbol;Acc:HGNC:50433]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616958","summary":null,"start":69160806,"end":69160939,"strand":1,"description":"small nucleolar RNA, H/ACA box 50D [Source:HGNC Symbol;Acc:HGNC:50433]"}, {"versioned_ensembl_gene_id":"ENSG00000253059.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":35756327,"end":35756463,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000284197.1","gene_symbol":"MIR658","gene_name":"microRNA 658 [Source:HGNC Symbol;Acc:HGNC:32914]","synonyms":"hsa-mir-658,MIRN658","biotype":"miRNA","ncbi_id":"724028","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37844272,"end":37844371,"strand":-1,"description":"microRNA 658 [Source:HGNC Symbol;Acc:HGNC:32914]"}, {"versioned_ensembl_gene_id":"ENSG00000207654.4","gene_symbol":"MIR128-1","gene_name":"microRNA 128-1 [Source:HGNC Symbol;Acc:HGNC:31510]","synonyms":"MIRN128A,MIRN128-1,hsa-mir-128a,hsa-mir-128-1","biotype":"miRNA","ncbi_id":"406915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":135665397,"end":135665478,"strand":1,"description":"microRNA 128-1 [Source:HGNC Symbol;Acc:HGNC:31510]"}, {"versioned_ensembl_gene_id":"ENSG00000278818.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55285227,"end":55285558,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212229.1","gene_symbol":"SNORD65","gene_name":"Small nucleolar RNA SNORD65 [Source:RFAM;Acc:RF00571]","synonyms":"SNORD65A,HBII-135","biotype":"snoRNA","ncbi_id":"692106","summary":null,"start":67210408,"end":67210480,"strand":-1,"description":"Small nucleolar RNA SNORD65 [Source:RFAM;Acc:RF00571]"}, {"versioned_ensembl_gene_id":"ENSG00000277698.1","gene_symbol":"MIR6770-2","gene_name":"microRNA 6770-2 [Source:HGNC Symbol;Acc:HGNC:50115]","synonyms":"hsa-mir-6770-2","biotype":"miRNA","ncbi_id":"102465908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16329305,"end":16329364,"strand":1,"description":"microRNA 6770-2 [Source:HGNC Symbol;Acc:HGNC:50115]"}, {"versioned_ensembl_gene_id":"ENSG00000202275.1","gene_symbol":"SNORD51","gene_name":"Small nucleolar RNA SNORD51 [Source:RFAM;Acc:RF00280]","synonyms":"U51,RNU51","biotype":"snoRNA","ncbi_id":"26798","summary":null,"start":103797272,"end":103797348,"strand":-1,"description":"Small nucleolar RNA SNORD51 [Source:RFAM;Acc:RF00280]"}, {"versioned_ensembl_gene_id":"ENSG00000274953.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000283705.1","gene_symbol":"MIR92A1","gene_name":"microRNA 92a-1 [Source:HGNC Symbol;Acc:HGNC:31643]","synonyms":"MIRN92A1,MIRN92-1,hsa-mir-92a-1,hsa-mir-92-1","biotype":"miRNA","ncbi_id":"407048","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91351314,"end":91351391,"strand":1,"description":"microRNA 92a-1 [Source:HGNC Symbol;Acc:HGNC:31643]"}, {"versioned_ensembl_gene_id":"ENSG00000206697.1","gene_symbol":"RNY1P8","gene_name":"RNA, Ro-associated Y1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42485]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873807","summary":null,"start":73227147,"end":73227260,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42485]"}, {"versioned_ensembl_gene_id":"ENSG00000200530.1","gene_symbol":"SNORD35B","gene_name":"small nucleolar RNA, C/D box 35B [Source:HGNC Symbol;Acc:HGNC:17365]","synonyms":"U35B,RNU35B","biotype":"snoRNA","ncbi_id":"84546","summary":null,"start":49497720,"end":49497806,"strand":1,"description":"small nucleolar RNA, C/D box 35B [Source:HGNC Symbol;Acc:HGNC:17365]"}, {"versioned_ensembl_gene_id":"ENSG00000212100.2","gene_symbol":"MIR764","gene_name":"microRNA 764 [Source:HGNC Symbol;Acc:HGNC:37306]","synonyms":"hsa-mir-764","biotype":"miRNA","ncbi_id":"100313838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114639435,"end":114639519,"strand":1,"description":"microRNA 764 [Source:HGNC Symbol;Acc:HGNC:37306]"}, {"versioned_ensembl_gene_id":"ENSG00000206609.1","gene_symbol":"SNORD116-11","gene_name":"small nucleolar RNA, C/D box 116-11 [Source:HGNC Symbol;Acc:HGNC:33077]","synonyms":"HBII-85-11","biotype":"snoRNA","ncbi_id":"100033423","summary":null,"start":25075929,"end":25076020,"strand":1,"description":"small nucleolar RNA, C/D box 116-11 [Source:HGNC Symbol;Acc:HGNC:33077]"}, {"versioned_ensembl_gene_id":"ENSG00000199664.1","gene_symbol":"RNU6-1266P","gene_name":"RNA, U6 small nuclear 1266, pseudogene [Source:HGNC Symbol;Acc:HGNC:48229]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480118","summary":null,"start":77776951,"end":77777055,"strand":-1,"description":"RNA, U6 small nuclear 1266, pseudogene [Source:HGNC Symbol;Acc:HGNC:48229]"}, {"versioned_ensembl_gene_id":"ENSG00000201744.1","gene_symbol":"RNU6-34P","gene_name":"RNA, U6 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:34278]","synonyms":"RNU6-34","biotype":"snRNA","ncbi_id":"100873749","summary":null,"start":96152297,"end":96152403,"strand":-1,"description":"RNA, U6 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:34278]"}, {"versioned_ensembl_gene_id":"ENSG00000212329.1","gene_symbol":"RNU6-316P","gene_name":"RNA, U6 small nuclear 316, pseudogene [Source:HGNC Symbol;Acc:HGNC:47279]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481279","summary":null,"start":14190700,"end":14190806,"strand":1,"description":"RNA, U6 small nuclear 316, pseudogene [Source:HGNC Symbol;Acc:HGNC:47279]"}, {"versioned_ensembl_gene_id":"ENSG00000201644.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75662120,"end":75662213,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278261.1","gene_symbol":"SNORD1A","gene_name":"small nucleolar RNA, C/D box 1A [Source:HGNC Symbol;Acc:HGNC:32556]","synonyms":"snR38A,R38A","biotype":"snoRNA","ncbi_id":"677848","summary":null,"start":76561634,"end":76561705,"strand":1,"description":"small nucleolar RNA, C/D box 1A [Source:HGNC Symbol;Acc:HGNC:32556]"}, {"versioned_ensembl_gene_id":"ENSG00000212580.1","gene_symbol":"SNORA75","gene_name":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":49888868,"end":49888986,"strand":-1,"description":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]"}, {"versioned_ensembl_gene_id":"ENSG00000241175.3","gene_symbol":"RN7SL494P","gene_name":"RNA, 7SL, cytoplasmic 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:46510]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481057","summary":null,"start":50244628,"end":50244931,"strand":-1,"description":"RNA, 7SL, cytoplasmic 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:46510]"}, {"versioned_ensembl_gene_id":"ENSG00000273932.1","gene_symbol":"MIR6877","gene_name":"microRNA 6877 [Source:HGNC Symbol;Acc:HGNC:50205]","synonyms":"hsa-mir-6877","biotype":"miRNA","ncbi_id":"102465528","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133051996,"end":133052059,"strand":1,"description":"microRNA 6877 [Source:HGNC Symbol;Acc:HGNC:50205]"}, {"versioned_ensembl_gene_id":"ENSG00000266035.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32036120,"end":32036240,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000222874.1","gene_symbol":"RN7SKP33","gene_name":"RNA, 7SK small nuclear pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:45757]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480843","summary":null,"start":46859333,"end":46859672,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:45757]"}, {"versioned_ensembl_gene_id":"ENSG00000251752.1","gene_symbol":"RNU4-29P","gene_name":"RNA, U4 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:46965]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481181","summary":null,"start":83275941,"end":83276114,"strand":1,"description":"RNA, U4 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:46965]"}, {"versioned_ensembl_gene_id":"ENSG00000252953.1","gene_symbol":"RNU6-232P","gene_name":"RNA, U6 small nuclear 232, pseudogene [Source:HGNC Symbol;Acc:HGNC:47195]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480388","summary":null,"start":125388934,"end":125388997,"strand":1,"description":"RNA, U6 small nuclear 232, pseudogene [Source:HGNC Symbol;Acc:HGNC:47195]"}, {"versioned_ensembl_gene_id":"ENSG00000200393.1","gene_symbol":"RNU6-698P","gene_name":"RNA, U6 small nuclear 698, pseudogene [Source:HGNC Symbol;Acc:HGNC:47661]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481401","summary":null,"start":53653685,"end":53653791,"strand":1,"description":"RNA, U6 small nuclear 698, pseudogene [Source:HGNC Symbol;Acc:HGNC:47661]"}, {"versioned_ensembl_gene_id":"ENSG00000275222.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8998849,"end":8999100,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222971.1","gene_symbol":"RNA5SP222","gene_name":"RNA, 5S ribosomal pseudogene 222 [Source:HGNC Symbol;Acc:HGNC:43122]","synonyms":"RN5S222","biotype":"rRNA","ncbi_id":"100873481","summary":null,"start":146340420,"end":146340524,"strand":1,"description":"RNA, 5S ribosomal pseudogene 222 [Source:HGNC Symbol;Acc:HGNC:43122]"}, {"versioned_ensembl_gene_id":"ENSG00000277295.1","gene_symbol":"RN7SL489P","gene_name":"RNA, 7SL, cytoplasmic 489, pseudogene [Source:HGNC Symbol;Acc:HGNC:46505]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481056","summary":null,"start":75268430,"end":75268652,"strand":1,"description":"RNA, 7SL, cytoplasmic 489, pseudogene [Source:HGNC Symbol;Acc:HGNC:46505]"}, {"versioned_ensembl_gene_id":"ENSG00000251841.1","gene_symbol":"RNU6-1334P","gene_name":"RNA, U6 small nuclear 1334, pseudogene [Source:HGNC Symbol;Acc:HGNC:48297]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480148","summary":null,"start":2784749,"end":2784853,"strand":1,"description":"RNA, U6 small nuclear 1334, pseudogene [Source:HGNC Symbol;Acc:HGNC:48297]"}, {"versioned_ensembl_gene_id":"ENSG00000207227.1","gene_symbol":"RNU6-900P","gene_name":"RNA, U6 small nuclear 900, pseudogene [Source:HGNC Symbol;Acc:HGNC:47863]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481463","summary":null,"start":37891347,"end":37891448,"strand":1,"description":"RNA, U6 small nuclear 900, pseudogene [Source:HGNC Symbol;Acc:HGNC:47863]"}, {"versioned_ensembl_gene_id":"ENSG00000207222.1","gene_symbol":"RNU6-456P","gene_name":"RNA, U6 small nuclear 456, pseudogene [Source:HGNC Symbol;Acc:HGNC:47419]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481323","summary":null,"start":134500178,"end":134500284,"strand":-1,"description":"RNA, U6 small nuclear 456, pseudogene [Source:HGNC Symbol;Acc:HGNC:47419]"}, {"versioned_ensembl_gene_id":"ENSG00000263755.2","gene_symbol":"RN7SL498P","gene_name":"RNA, 7SL, cytoplasmic 498, pseudogene [Source:HGNC Symbol;Acc:HGNC:46514]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479405","summary":null,"start":6001733,"end":6002030,"strand":1,"description":"RNA, 7SL, cytoplasmic 498, pseudogene [Source:HGNC Symbol;Acc:HGNC:46514]"}, {"versioned_ensembl_gene_id":"ENSG00000264349.1","gene_symbol":"MIR4258","gene_name":"microRNA 4258 [Source:HGNC Symbol;Acc:HGNC:38281]","synonyms":"hsa-mir-4258","biotype":"miRNA","ncbi_id":"100423020","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154975693,"end":154975783,"strand":1,"description":"microRNA 4258 [Source:HGNC Symbol;Acc:HGNC:38281]"}, {"versioned_ensembl_gene_id":"ENSG00000221059.1","gene_symbol":"RNU6ATAC6P","gene_name":"RNA, U6atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46905]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479545","summary":null,"start":87910220,"end":87910345,"strand":1,"description":"RNA, U6atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46905]"}, {"versioned_ensembl_gene_id":"ENSG00000252243.1","gene_symbol":"RNU6-412P","gene_name":"RNA, U6 small nuclear 412, pseudogene [Source:HGNC Symbol;Acc:HGNC:47375]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481308","summary":null,"start":46531237,"end":46531342,"strand":-1,"description":"RNA, U6 small nuclear 412, pseudogene [Source:HGNC Symbol;Acc:HGNC:47375]"}, {"versioned_ensembl_gene_id":"ENSG00000251997.1","gene_symbol":"RNA5SP458","gene_name":"RNA, 5S ribosomal pseudogene 458 [Source:HGNC Symbol;Acc:HGNC:43358]","synonyms":"RN5S458","biotype":"rRNA","ncbi_id":"106479016","summary":null,"start":50319002,"end":50319120,"strand":1,"description":"RNA, 5S ribosomal pseudogene 458 [Source:HGNC Symbol;Acc:HGNC:43358]"}, {"versioned_ensembl_gene_id":"ENSG00000200648.1","gene_symbol":"RNU6-226P","gene_name":"RNA, U6 small nuclear 226, pseudogene [Source:HGNC Symbol;Acc:HGNC:47189]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481249","summary":null,"start":175703898,"end":175704004,"strand":1,"description":"RNA, U6 small nuclear 226, pseudogene [Source:HGNC Symbol;Acc:HGNC:47189]"}, {"versioned_ensembl_gene_id":"ENSG00000263881.1","gene_symbol":"MIR4436B2","gene_name":"microRNA 4436b-2 [Source:HGNC Symbol;Acc:HGNC:43451]","synonyms":"hsa-mir-4436b-2","biotype":"miRNA","ncbi_id":"100847033","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110284853,"end":110284943,"strand":1,"description":"microRNA 4436b-2 [Source:HGNC Symbol;Acc:HGNC:43451]"}, {"versioned_ensembl_gene_id":"ENSG00000252334.1","gene_symbol":"RNU6-1337P","gene_name":"RNA, U6 small nuclear 1337, pseudogene [Source:HGNC Symbol;Acc:HGNC:48300]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481602","summary":null,"start":58483749,"end":58483843,"strand":-1,"description":"RNA, U6 small nuclear 1337, pseudogene [Source:HGNC Symbol;Acc:HGNC:48300]"}, {"versioned_ensembl_gene_id":"ENSG00000263527.1","gene_symbol":"MIR4526","gene_name":"microRNA 4526 [Source:HGNC Symbol;Acc:HGNC:41618]","synonyms":"hsa-mir-4526","biotype":"miRNA","ncbi_id":"100616130","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13611114,"end":13611200,"strand":1,"description":"microRNA 4526 [Source:HGNC Symbol;Acc:HGNC:41618]"}, {"versioned_ensembl_gene_id":"ENSG00000207599.1","gene_symbol":"MIR520E","gene_name":"microRNA 520e [Source:HGNC Symbol;Acc:HGNC:32093]","synonyms":"MIRN520E,hsa-mir-520e","biotype":"miRNA","ncbi_id":"574461","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53675711,"end":53675797,"strand":1,"description":"microRNA 520e [Source:HGNC Symbol;Acc:HGNC:32093]"}, {"versioned_ensembl_gene_id":"ENSG00000119950.20","gene_symbol":"MXI1","gene_name":"MAX interactor 1, dimerization protein [Source:HGNC Symbol;Acc:HGNC:7534]","synonyms":"MXI,MXD2,MAD2,bHLHc11","biotype":"protein_coding","ncbi_id":"4601","summary":"Expression of the c-myc gene, which produces an oncogenic transcription factor, is tightly regulated in normal cells but is frequently deregulated in human cancers. The protein encoded by this gene is a transcriptional repressor thought to negatively regulate MYC function, and is therefore a potential tumor suppressor. This protein inhibits the transcriptional activity of MYC by competing for MAX, another basic helix-loop-helix protein that binds to MYC and is required for its function. Defects in this gene are frequently found in patients with prostate tumors. Three alternatively spliced transcripts encoding different isoforms have been described. Additional alternatively spliced transcripts may exist but the products of these transcripts have not been verified experimentally. [provided by RefSeq, Jul 2008]","start":110207605,"end":110287365,"strand":1,"description":"MAX interactor 1, dimerization protein [Source:HGNC Symbol;Acc:HGNC:7534]"}, {"versioned_ensembl_gene_id":"ENSG00000275101.1","gene_symbol":"MIR6766","gene_name":"microRNA 6766 [Source:HGNC Symbol;Acc:HGNC:49941]","synonyms":"hsa-mir-6766","biotype":"miRNA","ncbi_id":"102466983","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89326739,"end":89326810,"strand":-1,"description":"microRNA 6766 [Source:HGNC Symbol;Acc:HGNC:49941]"}, {"versioned_ensembl_gene_id":"ENSG00000199781.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":232828653,"end":232828751,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284204.1","gene_symbol":"MIR19A","gene_name":"microRNA 19a [Source:HGNC Symbol;Acc:HGNC:31574]","synonyms":"hsa-mir-19a,MIRN19A","biotype":"miRNA","ncbi_id":"406979","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91350891,"end":91350972,"strand":1,"description":"microRNA 19a [Source:HGNC Symbol;Acc:HGNC:31574]"}, {"versioned_ensembl_gene_id":"ENSG00000211581.1","gene_symbol":"MIR765","gene_name":"microRNA 765 [Source:HGNC Symbol;Acc:HGNC:33141]","synonyms":"MIRN765,hsa-mir-765","biotype":"miRNA","ncbi_id":"768220","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":156936131,"end":156936244,"strand":-1,"description":"microRNA 765 [Source:HGNC Symbol;Acc:HGNC:33141]"}, {"versioned_ensembl_gene_id":"ENSG00000207306.1","gene_symbol":"RNU6-1152P","gene_name":"RNA, U6 small nuclear 1152, pseudogene [Source:HGNC Symbol;Acc:HGNC:48115]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480073","summary":null,"start":48196680,"end":48196786,"strand":-1,"description":"RNA, U6 small nuclear 1152, pseudogene [Source:HGNC Symbol;Acc:HGNC:48115]"}, {"versioned_ensembl_gene_id":"ENSG00000200261.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":112169286,"end":112169397,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274170.1","gene_symbol":"RFPL3-AS1_2","gene_name":"RFPL3 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02172]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32368497,"end":32368567,"strand":1,"description":"RFPL3 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02172]"}, {"versioned_ensembl_gene_id":"ENSG00000263968.2","gene_symbol":"RN7SL381P","gene_name":"RNA, 7SL, cytoplasmic 381, pseudogene [Source:HGNC Symbol;Acc:HGNC:46397]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479362","summary":null,"start":85659378,"end":85659675,"strand":1,"description":"RNA, 7SL, cytoplasmic 381, pseudogene [Source:HGNC Symbol;Acc:HGNC:46397]"}, {"versioned_ensembl_gene_id":"ENSG00000252255.1","gene_symbol":"RNU2-35P","gene_name":"RNA, U2 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48528]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480212","summary":null,"start":125649746,"end":125649887,"strand":1,"description":"RNA, U2 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48528]"}, {"versioned_ensembl_gene_id":"ENSG00000281707.1","gene_symbol":"AC099669.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44528955,"end":44529391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244218.3","gene_symbol":"RN7SL81P","gene_name":"RNA, 7SL, cytoplasmic 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:46097]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479253","summary":null,"start":128761338,"end":128761598,"strand":1,"description":"RNA, 7SL, cytoplasmic 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:46097]"}, {"versioned_ensembl_gene_id":"ENSG00000278519.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000260682.3","gene_symbol":"RN7SKP176","gene_name":"RNA, 7SK small nuclear pseudogene 176 [Source:HGNC Symbol;Acc:HGNC:45900]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106635536","summary":null,"start":81961926,"end":81962243,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 176 [Source:HGNC Symbol;Acc:HGNC:45900]"}, {"versioned_ensembl_gene_id":"ENSG00000201816.1","gene_symbol":"SNORA73","gene_name":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56079394,"end":56079594,"strand":-1,"description":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]"}, {"versioned_ensembl_gene_id":"ENSG00000199378.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100021804,"end":100021906,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207317.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140019492,"end":140019592,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222544.1","gene_symbol":"RNU6-735P","gene_name":"RNA, U6 small nuclear 735, pseudogene [Source:HGNC Symbol;Acc:HGNC:47698]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481412","summary":null,"start":95438737,"end":95438843,"strand":-1,"description":"RNA, U6 small nuclear 735, pseudogene [Source:HGNC Symbol;Acc:HGNC:47698]"}, {"versioned_ensembl_gene_id":"ENSG00000207121.1","gene_symbol":"RNU6-1230P","gene_name":"RNA, U6 small nuclear 1230, pseudogene [Source:HGNC Symbol;Acc:HGNC:48193]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481944","summary":null,"start":149934376,"end":149934483,"strand":1,"description":"RNA, U6 small nuclear 1230, pseudogene [Source:HGNC Symbol;Acc:HGNC:48193]"}, {"versioned_ensembl_gene_id":"ENSG00000238561.1","gene_symbol":"RNU6ATAC28P","gene_name":"RNA, U6atac small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46927]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479555","summary":null,"start":83750384,"end":83750501,"strand":1,"description":"RNA, U6atac small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46927]"}, {"versioned_ensembl_gene_id":"ENSG00000265633.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30942815,"end":30943117,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000267169.1","gene_symbol":"AC022098.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14137179,"end":14171267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215217.6","gene_symbol":"C5orf49","gene_name":"chromosome 5 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:27028]","synonyms":"LOC134121","biotype":"protein_coding","ncbi_id":"134121","summary":null,"start":7830378,"end":7851490,"strand":-1,"description":"chromosome 5 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:27028]"}, {"versioned_ensembl_gene_id":"ENSG00000262815.1","gene_symbol":"AC087501.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9464742,"end":9467422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264974.1","gene_symbol":"MIR4789","gene_name":"microRNA 4789 [Source:HGNC Symbol;Acc:HGNC:41719]","synonyms":"hsa-mir-4789","biotype":"miRNA","ncbi_id":"100616395","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":175369540,"end":175369621,"strand":1,"description":"microRNA 4789 [Source:HGNC Symbol;Acc:HGNC:41719]"}, {"versioned_ensembl_gene_id":"ENSG00000200486.1","gene_symbol":"SNORD115-11","gene_name":"small nucleolar RNA, C/D box 115-11 [Source:HGNC Symbol;Acc:HGNC:33030]","synonyms":"HBII-52-11","biotype":"snoRNA","ncbi_id":"100033448","summary":null,"start":25189414,"end":25189495,"strand":1,"description":"small nucleolar RNA, C/D box 115-11 [Source:HGNC Symbol;Acc:HGNC:33030]"}, {"versioned_ensembl_gene_id":"ENSG00000252556.1","gene_symbol":"RNU6-256P","gene_name":"RNA, U6 small nuclear 256, pseudogene [Source:HGNC Symbol;Acc:HGNC:47219]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479680","summary":null,"start":122004355,"end":122004451,"strand":1,"description":"RNA, U6 small nuclear 256, pseudogene [Source:HGNC Symbol;Acc:HGNC:47219]"}, {"versioned_ensembl_gene_id":"ENSG00000200706.1","gene_symbol":"SNORD45","gene_name":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":38207274,"end":38207345,"strand":1,"description":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]"}, {"versioned_ensembl_gene_id":"ENSG00000252856.1","gene_symbol":"RNA5SP503","gene_name":"RNA, 5S ribosomal pseudogene 503 [Source:HGNC Symbol;Acc:HGNC:43403]","synonyms":"RN5S503","biotype":"rRNA","ncbi_id":"100873554","summary":null,"start":48206258,"end":48206374,"strand":1,"description":"RNA, 5S ribosomal pseudogene 503 [Source:HGNC Symbol;Acc:HGNC:43403]"}, {"versioned_ensembl_gene_id":"ENSG00000207930.1","gene_symbol":"MIR603","gene_name":"microRNA 603 [Source:HGNC Symbol;Acc:HGNC:32859]","synonyms":"MIRN603,hsa-mir-603","biotype":"miRNA","ncbi_id":"693188","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24275685,"end":24275781,"strand":1,"description":"microRNA 603 [Source:HGNC Symbol;Acc:HGNC:32859]"}, {"versioned_ensembl_gene_id":"ENSG00000252082.1","gene_symbol":"RNU6-547P","gene_name":"RNA, U6 small nuclear 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:47510]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481902","summary":null,"start":172703124,"end":172703225,"strand":1,"description":"RNA, U6 small nuclear 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:47510]"}, {"versioned_ensembl_gene_id":"ENSG00000221125.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":49949316,"end":49949527,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000278764.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46266690,"end":46266971,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277668.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130603461,"end":130603724,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200407.1","gene_symbol":"RNU6-1169P","gene_name":"RNA, U6 small nuclear 1169, pseudogene [Source:HGNC Symbol;Acc:HGNC:48132]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480080","summary":null,"start":41448742,"end":41448844,"strand":-1,"description":"RNA, U6 small nuclear 1169, pseudogene [Source:HGNC Symbol;Acc:HGNC:48132]"}, {"versioned_ensembl_gene_id":"ENSG00000201135.1","gene_symbol":"RNU6-777P","gene_name":"RNA, U6 small nuclear 777, pseudogene [Source:HGNC Symbol;Acc:HGNC:47740]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481426","summary":null,"start":12077881,"end":12077984,"strand":-1,"description":"RNA, U6 small nuclear 777, pseudogene [Source:HGNC Symbol;Acc:HGNC:47740]"}, {"versioned_ensembl_gene_id":"ENSG00000201291.1","gene_symbol":"RNU1-34P","gene_name":"RNA, U1 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:48376]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481607","summary":null,"start":75473738,"end":75473894,"strand":-1,"description":"RNA, U1 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:48376]"}, {"versioned_ensembl_gene_id":"ENSG00000251917.1","gene_symbol":"RNU1-86P","gene_name":"RNA, U1 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:48428]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480666","summary":null,"start":23946618,"end":23946771,"strand":-1,"description":"RNA, U1 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:48428]"}, {"versioned_ensembl_gene_id":"ENSG00000281808.1","gene_symbol":"SNORA17","gene_name":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":136726748,"end":136726879,"strand":-1,"description":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]"}, {"versioned_ensembl_gene_id":"ENSG00000252361.1","gene_symbol":"RNU6-118P","gene_name":"RNA, U6 small nuclear 118, pseudogene [Source:HGNC Symbol;Acc:HGNC:47081]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479618","summary":null,"start":62815966,"end":62816067,"strand":-1,"description":"RNA, U6 small nuclear 118, pseudogene [Source:HGNC Symbol;Acc:HGNC:47081]"}, {"versioned_ensembl_gene_id":"ENSG00000267723.1","gene_symbol":"AC011509.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14254189,"end":14293205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266913.1","gene_symbol":"LINC01841","gene_name":"long intergenic non-protein coding RNA 1841 [Source:HGNC Symbol;Acc:HGNC:52655]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372288","summary":null,"start":14305458,"end":14370196,"strand":-1,"description":"long intergenic non-protein coding RNA 1841 [Source:HGNC Symbol;Acc:HGNC:52655]"}, {"versioned_ensembl_gene_id":"ENSG00000267406.1","gene_symbol":"AC011509.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14267807,"end":14269377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262961.1","gene_symbol":"AC006236.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5730289,"end":5731085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255919.1","gene_symbol":"AC226150.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133217210,"end":133217675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072071.16","gene_symbol":"ADGRL1","gene_name":"adhesion G protein-coupled receptor L1 [Source:HGNC Symbol;Acc:HGNC:20973]","synonyms":"LPHN1,LEC2,KIAA0821,CIRL1","biotype":"protein_coding","ncbi_id":"22859","summary":"This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cysteine-rich GPS (G-protein-coupled-receptor proteolysis site) domain resulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with substantial similarity to the secretin/calcitonin family of GPCRs) being non-covalently bound at the cell membrane. Latrophilin-1 has been shown to recruit the neurotoxin from black widow spider venom, alpha-latrotoxin, to the synapse plasma membrane. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Oct 2008]","start":14147743,"end":14206187,"strand":-1,"description":"adhesion G protein-coupled receptor L1 [Source:HGNC Symbol;Acc:HGNC:20973]"}, {"versioned_ensembl_gene_id":"ENSG00000165799.4","gene_symbol":"RNASE7","gene_name":"ribonuclease A family member 7 [Source:HGNC Symbol;Acc:HGNC:19278]","synonyms":"RAE1","biotype":"protein_coding","ncbi_id":"84659","summary":"The protein encoded by this gene belongs to the pancreatic ribonuclease family, a subset of the ribonuclease A superfamily. The protein has broad-spectrum antimicrobial activity against bacteria and fungi. [provided by RefSeq, Oct 2014]","start":21042226,"end":21044234,"strand":1,"description":"ribonuclease A family member 7 [Source:HGNC Symbol;Acc:HGNC:19278]"}, {"versioned_ensembl_gene_id":"ENSG00000258604.1","gene_symbol":"AL161668.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21024172,"end":21029271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255472.1","gene_symbol":"AL161668.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21032818,"end":21033895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232086.1","gene_symbol":"AL159990.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70708047,"end":70712863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265453.1","gene_symbol":"AC026254.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27281094,"end":27281415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049860.13","gene_symbol":"HEXB","gene_name":"hexosaminidase subunit beta [Source:HGNC Symbol;Acc:HGNC:4879]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3074","summary":"Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":74640023,"end":74722647,"strand":1,"description":"hexosaminidase subunit beta [Source:HGNC Symbol;Acc:HGNC:4879]"}, {"versioned_ensembl_gene_id":"ENSG00000257070.1","gene_symbol":"AP003170.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113769660,"end":113769994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256603.1","gene_symbol":"AP003170.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113770393,"end":113771691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243353.1","gene_symbol":"RPS29P19","gene_name":"ribosomal protein S29 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36118]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271383","summary":null,"start":113751116,"end":113751286,"strand":-1,"description":"ribosomal protein S29 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36118]"}, {"versioned_ensembl_gene_id":"ENSG00000133056.13","gene_symbol":"PIK3C2B","gene_name":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta [Source:HGNC Symbol;Acc:HGNC:8972]","synonyms":"PI3K-C2beta,C2-PI3K","biotype":"protein_coding","ncbi_id":"5287","summary":"The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. The PI3-kinase activity of this protein is sensitive to low nanomolar levels of the inhibitor wortmanin. The C2 domain of this protein was shown to bind phospholipids but not Ca2+, which suggests that this enzyme may function in a calcium-independent manner. [provided by RefSeq, Jul 2008]","start":204422628,"end":204494724,"strand":-1,"description":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta [Source:HGNC Symbol;Acc:HGNC:8972]"}, {"versioned_ensembl_gene_id":"ENSG00000251041.1","gene_symbol":"AC106732.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74321631,"end":74340152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250446.1","gene_symbol":"LINC01332","gene_name":"long intergenic non-protein coding RNA 1332 [Source:HGNC Symbol;Acc:HGNC:50540]","synonyms":"TCONS_00009701","biotype":"lincRNA","ncbi_id":"106144530","summary":null,"start":74327995,"end":74334766,"strand":-1,"description":"long intergenic non-protein coding RNA 1332 [Source:HGNC Symbol;Acc:HGNC:50540]"}, {"versioned_ensembl_gene_id":"ENSG00000248942.1","gene_symbol":"LINC01335","gene_name":"long intergenic non-protein coding RNA 1335 [Source:HGNC Symbol;Acc:HGNC:50542]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102503429","summary":null,"start":74306410,"end":74308325,"strand":-1,"description":"long intergenic non-protein coding RNA 1335 [Source:HGNC Symbol;Acc:HGNC:50542]"}, {"versioned_ensembl_gene_id":"ENSG00000265265.1","gene_symbol":"AC233702.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21519514,"end":21521269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254984.1","gene_symbol":"FTLP6","gene_name":"ferritin light chain pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37954]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462788","summary":null,"start":66771246,"end":66771667,"strand":-1,"description":"ferritin light chain pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37954]"}, {"versioned_ensembl_gene_id":"ENSG00000219133.2","gene_symbol":"AL592114.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204346776,"end":204347258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204706.14","gene_symbol":"MAMDC2-AS1","gene_name":"MAMDC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48719]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507244","summary":null,"start":70033921,"end":70175888,"strand":-1,"description":"MAMDC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48719]"}, {"versioned_ensembl_gene_id":"ENSG00000170498.8","gene_symbol":"KISS1","gene_name":"KiSS-1 metastasis-suppressor [Source:HGNC Symbol;Acc:HGNC:6341]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3814","summary":"This gene is a metastasis suppressor gene that suppresses metastases of melanomas and breast carcinomas without affecting tumorigenicity. The encoded protein may inhibit chemotaxis and invasion and thereby attenuate metastasis in malignant melanomas. Studies suggest a putative role in the regulation of events downstream of cell-matrix adhesion, perhaps involving cytoskeletal reorganization. A protein product of this gene, kisspeptin, stimulates gonadotropin-releasing hormone (GnRH)-induced gonadotropin secretion and regulates the pubertal activation of GnRH nuerons. A polymorphism in the terminal exon of this mRNA results in two protein isoforms. An adenosine present at the polymorphic site represents the third position in a stop codon. When the adenosine is absent, a downstream stop codon is utilized and the encoded protein extends for an additional seven amino acid residues. [provided by RefSeq, Mar 2012]","start":204190341,"end":204196486,"strand":-1,"description":"KiSS-1 metastasis-suppressor [Source:HGNC Symbol;Acc:HGNC:6341]"}, {"versioned_ensembl_gene_id":"ENSG00000166682.10","gene_symbol":"TMPRSS5","gene_name":"transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:HGNC:14908]","synonyms":"MGC148044,MGC141886","biotype":"protein_coding","ncbi_id":"80975","summary":"This gene encodes a protein that belongs to the serine protease family. Serine proteases are known to be involved in many physiological and pathological processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":113687550,"end":113706373,"strand":-1,"description":"transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:HGNC:14908]"}, {"versioned_ensembl_gene_id":"ENSG00000131495.8","gene_symbol":"NDUFA2","gene_name":"NADH:ubiquinone oxidoreductase subunit A2 [Source:HGNC Symbol;Acc:HGNC:7685]","synonyms":"B8","biotype":"protein_coding","ncbi_id":"4695","summary":"The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":140638740,"end":140647785,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A2 [Source:HGNC Symbol;Acc:HGNC:7685]"}, {"versioned_ensembl_gene_id":"ENSG00000214944.9","gene_symbol":"ARHGEF28","gene_name":"Rho guanine nucleotide exchange factor 28 [Source:HGNC Symbol;Acc:HGNC:30322]","synonyms":"RIP2,RGNEF,p190RhoGEF","biotype":"protein_coding","ncbi_id":"64283","summary":"This gene encodes a member of the Rho guanine nucleotide exchange factor family. The encoded protein interacts with low molecular weight neurofilament mRNA and may be involved in the formation of amyotrophic lateral sclerosis neurofilament aggregates. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]","start":73626158,"end":73941993,"strand":1,"description":"Rho guanine nucleotide exchange factor 28 [Source:HGNC Symbol;Acc:HGNC:30322]"}, {"versioned_ensembl_gene_id":"ENSG00000126461.14","gene_symbol":"SCAF1","gene_name":"SR-related CTD associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30403]","synonyms":"SR-A1,FLJ00034","biotype":"protein_coding","ncbi_id":"58506","summary":null,"start":49642125,"end":49658642,"strand":1,"description":"SR-related CTD associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30403]"}, {"versioned_ensembl_gene_id":"ENSG00000251365.1","gene_symbol":"AC122710.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6765891,"end":6771953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188032.9","gene_symbol":"C19orf67","gene_name":"chromosome 19 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:34354]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646457","summary":null,"start":14081619,"end":14085875,"strand":-1,"description":"chromosome 19 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:34354]"}, {"versioned_ensembl_gene_id":"ENSG00000243388.1","gene_symbol":"RPL3P3","gene_name":"ribosomal protein L3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23550]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645798","summary":null,"start":56978409,"end":56979621,"strand":1,"description":"ribosomal protein L3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23550]"}, {"versioned_ensembl_gene_id":"ENSG00000269846.1","gene_symbol":"AL136172.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37095785,"end":37097178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260912.1","gene_symbol":"AL158206.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":19453209,"end":19455173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188710.2","gene_symbol":"QRFP","gene_name":"pyroglutamylated RFamide peptide [Source:HGNC Symbol;Acc:HGNC:29982]","synonyms":"P518,26RFa","biotype":"protein_coding","ncbi_id":"347148","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products. The encoded products are members of the RFamide family of neuropeptides, characterized by their common protein C-terminus consisting of an arginine (R) and an amidated phenylalanine (F). These products include the neuropeptides 26RFa and the N-terminally extended form, 43RFa. Both of these neuropeptides bind to the pyroglutamylated RFamide peptide receptor (QRFPR) and may regulate blood pressure, reproduction and food intake in rodents. [provided by RefSeq, Jul 2015]","start":130892702,"end":130896812,"strand":-1,"description":"pyroglutamylated RFamide peptide [Source:HGNC Symbol;Acc:HGNC:29982]"}, {"versioned_ensembl_gene_id":"ENSG00000234915.1","gene_symbol":"AL360091.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":212299495,"end":212331713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230063.1","gene_symbol":"AL360091.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":212297448,"end":212299579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126460.10","gene_symbol":"PRRG2","gene_name":"proline rich and Gla domain 2 [Source:HGNC Symbol;Acc:HGNC:9470]","synonyms":"PRGP2","biotype":"protein_coding","ncbi_id":"5639","summary":"The protein encoded by this gene is a single-pass transmembrane protein containing an N-terminal gamma-carboxyglutamic acid (Gla) domain and tandem Pro/Leu-Pro-Xaa-Tyr (PY) motifs at its C-terminal end. The Gla domain is exposed on the cell surface while the PY motifs are cytoplasmic. The PY motifs of the encoded protein have been shown to interact with YAP1, a WW domain-containing protein. Therefore, it is thought that the encoded protein may be part of a signal transduction pathway. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":49580646,"end":49591015,"strand":1,"description":"proline rich and Gla domain 2 [Source:HGNC Symbol;Acc:HGNC:9470]"}, {"versioned_ensembl_gene_id":"ENSG00000205476.8","gene_symbol":"CCDC85C","gene_name":"coiled-coil domain containing 85C [Source:HGNC Symbol;Acc:HGNC:35459]","synonyms":null,"biotype":"protein_coding","ncbi_id":"317762","summary":null,"start":99500180,"end":99604026,"strand":-1,"description":"coiled-coil domain containing 85C [Source:HGNC Symbol;Acc:HGNC:35459]"}, {"versioned_ensembl_gene_id":"ENSG00000137496.17","gene_symbol":"IL18BP","gene_name":"interleukin 18 binding protein [Source:HGNC Symbol;Acc:HGNC:5987]","synonyms":"IL18BPa","biotype":"protein_coding","ncbi_id":"10068","summary":"The protein encoded by this gene functions as an inhibitor of the proinflammatory cytokine, IL18. It binds IL18, prevents the binding of IL18 to its receptor, and thus inhibits IL18-induced IFN-gamma production, resulting in reduced T-helper type 1 immune responses. This protein is constitutively expressed and secreted in mononuclear cells. Elevated level of this protein is detected in the intestinal tissues of patients with Crohn's disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":71998541,"end":72005715,"strand":1,"description":"interleukin 18 binding protein [Source:HGNC Symbol;Acc:HGNC:5987]"}, {"versioned_ensembl_gene_id":"ENSG00000108018.15","gene_symbol":"SORCS1","gene_name":"sortilin related VPS10 domain containing receptor 1 [Source:HGNC Symbol;Acc:HGNC:16697]","synonyms":"sorCS1","biotype":"protein_coding","ncbi_id":"114815","summary":"This gene encodes one family member of vacuolar protein sorting 10 (VPS10) domain-containing receptor proteins. The VPS10 domain name comes from the yeast carboxypeptidase Y sorting receptor Vps10 protein. Members of this gene family are large with many exons but the CDS lengths are usually less than 3700 nt. Very large introns typically separate the exons encoding the VPS10 domain; the remaining exons are separated by much smaller-sized introns. These genes are strongly expressed in the central nervous system. Two of the five family members (sortilin and sortilin-related receptor) are synthesized as preproproteins; it is not yet known if this encoded protein is also a preproprotein. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":106573663,"end":107164534,"strand":-1,"description":"sortilin related VPS10 domain containing receptor 1 [Source:HGNC Symbol;Acc:HGNC:16697]"}, {"versioned_ensembl_gene_id":"ENSG00000186765.11","gene_symbol":"FSCN2","gene_name":"fascin actin-bundling protein 2, retinal [Source:HGNC Symbol;Acc:HGNC:3960]","synonyms":"RP30,RFSN","biotype":"protein_coding","ncbi_id":"25794","summary":"This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":81528396,"end":81537130,"strand":1,"description":"fascin actin-bundling protein 2, retinal [Source:HGNC Symbol;Acc:HGNC:3960]"}, {"versioned_ensembl_gene_id":"ENSG00000247993.2","gene_symbol":"FOXD1-AS1","gene_name":"FOXD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50658]","synonyms":"TCONS_00009423","biotype":"lincRNA","ncbi_id":"106144539","summary":null,"start":73446357,"end":73446984,"strand":1,"description":"FOXD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50658]"}, {"versioned_ensembl_gene_id":"ENSG00000267394.1","gene_symbol":"AC004596.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44198882,"end":44216565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260793.2","gene_symbol":"AC003102.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44221401,"end":44223710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267080.5","gene_symbol":"ASB16-AS1","gene_name":"ASB16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25442]","synonyms":"DKFZp762C2414,C17orf65","biotype":"antisense_RNA","ncbi_id":"339201","summary":null,"start":44175973,"end":44186717,"strand":-1,"description":"ASB16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25442]"}, {"versioned_ensembl_gene_id":"ENSG00000120306.9","gene_symbol":"CYSTM1","gene_name":"cysteine rich transmembrane module containing 1 [Source:HGNC Symbol;Acc:HGNC:30239]","synonyms":"ORF1-FL49,C5orf32","biotype":"protein_coding","ncbi_id":"84418","summary":null,"start":140174642,"end":140282052,"strand":1,"description":"cysteine rich transmembrane module containing 1 [Source:HGNC Symbol;Acc:HGNC:30239]"}, {"versioned_ensembl_gene_id":"ENSG00000137731.13","gene_symbol":"FXYD2","gene_name":"FXYD domain containing ion transport regulator 2 [Source:HGNC Symbol;Acc:HGNC:4026]","synonyms":"MGC12372,HOMG2,ATP1G1","biotype":"protein_coding","ncbi_id":"486","summary":"This gene encodes a member of the FXYD family of transmembrane proteins. This particular protein encodes the sodium/potassium-transporting ATPase subunit gamma. Mutations in this gene have been associated with Renal Hypomagnesemia-2. Alternatively spliced transcript variants have been described. Read-through transcripts have been observed between this locus and the upstream FXYD domain-containing ion transport regulator 6 (FXYD6, GeneID 53826) locus.[provided by RefSeq, Feb 2011]","start":117800844,"end":117828698,"strand":-1,"description":"FXYD domain containing ion transport regulator 2 [Source:HGNC Symbol;Acc:HGNC:4026]"}, {"versioned_ensembl_gene_id":"ENSG00000262833.1","gene_symbol":"AC016245.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80801640,"end":80805632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236733.1","gene_symbol":"AL354794.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68822403,"end":68843275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090554.12","gene_symbol":"FLT3LG","gene_name":"fms related tyrosine kinase 3 ligand [Source:HGNC Symbol;Acc:HGNC:3766]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2323","summary":"Dendritic cells (DCs) provide the key link between innate and adaptive immunity by recognizing pathogens and priming pathogen-specific immune responses. FLT3LG controls the development of DCs and is particularly important for plasmacytoid DCs and CD8 (see MIM 186910)-positive classical DCs and their CD103 (ITGAE; MIM 604682)-positive tissue counterparts (summary by Sathaliyawala et al., 2010 [PubMed 20933441]).[supplied by OMIM, Jan 2011]","start":49474207,"end":49486231,"strand":1,"description":"fms related tyrosine kinase 3 ligand [Source:HGNC Symbol;Acc:HGNC:3766]"}, {"versioned_ensembl_gene_id":"ENSG00000177103.13","gene_symbol":"DSCAML1","gene_name":"DS cell adhesion molecule like 1 [Source:HGNC Symbol;Acc:HGNC:14656]","synonyms":"KIAA1132","biotype":"protein_coding","ncbi_id":"57453","summary":"The protein encoded by this gene is a member of the Ig superfamily of cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes of the same cell type. [provided by RefSeq, Sep 2016]","start":117427773,"end":117817525,"strand":-1,"description":"DS cell adhesion molecule like 1 [Source:HGNC Symbol;Acc:HGNC:14656]"}, {"versioned_ensembl_gene_id":"ENSG00000165914.14","gene_symbol":"TTC7B","gene_name":"tetratricopeptide repeat domain 7B [Source:HGNC Symbol;Acc:HGNC:19858]","synonyms":"TTC7L1","biotype":"protein_coding","ncbi_id":"145567","summary":null,"start":90524564,"end":90816479,"strand":-1,"description":"tetratricopeptide repeat domain 7B [Source:HGNC Symbol;Acc:HGNC:19858]"}, {"versioned_ensembl_gene_id":"ENSG00000141564.13","gene_symbol":"RPTOR","gene_name":"regulatory associated protein of MTOR complex 1 [Source:HGNC Symbol;Acc:HGNC:30287]","synonyms":"KIAA1303,raptor,Mip1,KOG1","biotype":"protein_coding","ncbi_id":"57521","summary":"This gene encodes a component of a signaling pathway that regulates cell growth in response to nutrient and insulin levels. The encoded protein forms a stoichiometric complex with the mTOR kinase, and also associates with eukaryotic initiation factor 4E-binding protein-1 and ribosomal protein S6 kinase. The protein positively regulates the downstream effector ribosomal protein S6 kinase, and negatively regulates the mTOR kinase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":80544819,"end":80966371,"strand":1,"description":"regulatory associated protein of MTOR complex 1 [Source:HGNC Symbol;Acc:HGNC:30287]"}, {"versioned_ensembl_gene_id":"ENSG00000266925.1","gene_symbol":"AC015818.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20507413,"end":20508931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279588.2","gene_symbol":"AC087762.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":100782417,"end":100786189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198040.10","gene_symbol":"ZNF84","gene_name":"zinc finger protein 84 [Source:HGNC Symbol;Acc:HGNC:13159]","synonyms":"HPF2","biotype":"protein_coding","ncbi_id":"7637","summary":null,"start":133037292,"end":133063304,"strand":1,"description":"zinc finger protein 84 [Source:HGNC Symbol;Acc:HGNC:13159]"}, {"versioned_ensembl_gene_id":"ENSG00000242837.1","gene_symbol":"RPL21P13","gene_name":"ribosomal protein L21 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:19812]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319144","summary":null,"start":103241492,"end":103241972,"strand":1,"description":"ribosomal protein L21 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:19812]"}, {"versioned_ensembl_gene_id":"ENSG00000187742.14","gene_symbol":"SECISBP2","gene_name":"SECIS binding protein 2 [Source:HGNC Symbol;Acc:HGNC:30972]","synonyms":"SBP2","biotype":"protein_coding","ncbi_id":"79048","summary":"The protein encoded by this gene is one of the essential components of the machinery involved in co-translational insertion of selenocysteine (Sec) into selenoproteins. Sec is encoded by the UGA codon, which normally signals translation termination. The recoding of UGA as Sec codon requires a Sec insertion sequence (SECIS) element; present in the 3' untranslated regions of eukaryotic selenoprotein mRNAs. This protein specifically binds to the SECIS element, which is stimulated by a Sec-specific translation elongation factor. Mutations in this gene have been associated with reduction in enzymatic activity of type II iodothyronine deiodinase (a selenoprotein) and abnormal thyroid hormone metabolism. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]","start":89318506,"end":89359662,"strand":1,"description":"SECIS binding protein 2 [Source:HGNC Symbol;Acc:HGNC:30972]"}, {"versioned_ensembl_gene_id":"ENSG00000146242.8","gene_symbol":"TPBG","gene_name":"trophoblast glycoprotein [Source:HGNC Symbol;Acc:HGNC:12004]","synonyms":"5T4-AG,5T4","biotype":"protein_coding","ncbi_id":"7162","summary":"This gene encodes a leucine-rich transmembrane glycoprotein that may be involved in cell adhesion. The encoded protein is an oncofetal antigen that is specific to trophoblast cells. In adults this protein is highly expressed in many tumor cells and is associated with poor clinical outcome in numerous cancers. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]","start":82363206,"end":82370828,"strand":1,"description":"trophoblast glycoprotein [Source:HGNC Symbol;Acc:HGNC:12004]"}, {"versioned_ensembl_gene_id":"ENSG00000250490.1","gene_symbol":"LINC02145","gene_name":"long intergenic non-protein coding RNA 2145 [Source:HGNC Symbol;Acc:HGNC:53005]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401172","summary":null,"start":6310441,"end":6339884,"strand":-1,"description":"long intergenic non-protein coding RNA 2145 [Source:HGNC Symbol;Acc:HGNC:53005]"}, {"versioned_ensembl_gene_id":"ENSG00000101336.13","gene_symbol":"HCK","gene_name":"HCK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:4840]","synonyms":"JTK9","biotype":"protein_coding","ncbi_id":"3055","summary":"The protein encoded by this gene is a member of the Src family of tyrosine kinases. This protein is primarily hemopoietic, particularly in cells of the myeloid and B-lymphoid lineages. It may help couple the Fc receptor to the activation of the respiratory burst. In addition, it may play a role in neutrophil migration and in the degranulation of neutrophils. Multiple isoforms with different subcellular distributions are produced due to both alternative splicing and the use of alternative translation initiation codons, including a non-AUG (CUG) codon. [provided by RefSeq, Feb 2010]","start":32052188,"end":32101856,"strand":1,"description":"HCK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:4840]"}, {"versioned_ensembl_gene_id":"ENSG00000271904.1","gene_symbol":"AC091826.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88433892,"end":88498697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248172.1","gene_symbol":"AC009720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49996889,"end":50016844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143476.17","gene_symbol":"DTL","gene_name":"denticleless E3 ubiquitin protein ligase homolog [Source:HGNC Symbol;Acc:HGNC:30288]","synonyms":"RAMP,L2DTL,DCAF2,CDT2","biotype":"protein_coding","ncbi_id":"51514","summary":null,"start":212035553,"end":212107400,"strand":1,"description":"denticleless E3 ubiquitin protein ligase homolog [Source:HGNC Symbol;Acc:HGNC:30288]"}, {"versioned_ensembl_gene_id":"ENSG00000148344.10","gene_symbol":"PTGES","gene_name":"prostaglandin E synthase [Source:HGNC Symbol;Acc:HGNC:9599]","synonyms":"MGST1L1,MGST1-L1,MGST-IV,TP53I12,PIG12","biotype":"protein_coding","ncbi_id":"9536","summary":"The protein encoded by this gene is a glutathione-dependent prostaglandin E synthase. The expression of this gene has been shown to be induced by proinflammatory cytokine interleukin 1 beta (IL1B). Its expression can also be induced by tumor suppressor protein TP53, and may be involved in TP53 induced apoptosis. Knockout studies in mice suggest that this gene may contribute to the pathogenesis of collagen-induced arthritis and mediate acute pain during inflammatory responses. [provided by RefSeq, Jul 2008]","start":129738331,"end":129753047,"strand":-1,"description":"prostaglandin E synthase [Source:HGNC Symbol;Acc:HGNC:9599]"}, {"versioned_ensembl_gene_id":"ENSG00000260220.6","gene_symbol":"CCDC187","gene_name":"coiled-coil domain containing 187 [Source:HGNC Symbol;Acc:HGNC:30942]","synonyms":"MGC50722","biotype":"protein_coding","ncbi_id":"399693","summary":null,"start":136249971,"end":136306901,"strand":-1,"description":"coiled-coil domain containing 187 [Source:HGNC Symbol;Acc:HGNC:30942]"}, {"versioned_ensembl_gene_id":"ENSG00000279813.1","gene_symbol":"CR392000.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":136249978,"end":136251205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254593.1","gene_symbol":"OR7E126P","gene_name":"olfactory receptor family 7 subfamily E member 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:15304]","synonyms":"OR11-1,hg500","biotype":"unprocessed_pseudogene","ncbi_id":"81176","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71903194,"end":71904081,"strand":1,"description":"olfactory receptor family 7 subfamily E member 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:15304]"}, {"versioned_ensembl_gene_id":"ENSG00000167157.10","gene_symbol":"PRRX2","gene_name":"paired related homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21338]","synonyms":"PRX2,PMX2","biotype":"protein_coding","ncbi_id":"51450","summary":"The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins. Expression is localized to proliferating fetal fibroblasts and the developing dermal layer, with downregulated expression in adult skin. Increases in expression of this gene during fetal but not adult wound healing suggest a possible role in mechanisms that control mammalian dermal regeneration and prevent formation of scar response to wounding. The expression patterns provide evidence consistent with a role in fetal skin development and a possible role in cellular proliferation. [provided by RefSeq, Jul 2008]","start":129665641,"end":129722674,"strand":1,"description":"paired related homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21338]"}, {"versioned_ensembl_gene_id":"ENSG00000213315.5","gene_symbol":"AL122020.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90766531,"end":90766989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227987.1","gene_symbol":"AC092675.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":98346995,"end":98351140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251066.1","gene_symbol":"AC026700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85549409,"end":85549952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272696.1","gene_symbol":"AL359091.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128316337,"end":128316909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153832.11","gene_symbol":"FBXO36","gene_name":"F-box protein 36 [Source:HGNC Symbol;Acc:HGNC:27020]","synonyms":"FLJ37592,Fbx36","biotype":"protein_coding","ncbi_id":"130888","summary":"Members of the F-box protein family, such as FBXO36, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":229922302,"end":230013109,"strand":1,"description":"F-box protein 36 [Source:HGNC Symbol;Acc:HGNC:27020]"}, {"versioned_ensembl_gene_id":"ENSG00000236024.1","gene_symbol":"PRRX2-AS1","gene_name":"PRRX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50684]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929437","summary":null,"start":129712896,"end":129718635,"strand":-1,"description":"PRRX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50684]"}, {"versioned_ensembl_gene_id":"ENSG00000165661.16","gene_symbol":"QSOX2","gene_name":"quiescin sulfhydryl oxidase 2 [Source:HGNC Symbol;Acc:HGNC:30249]","synonyms":"SOXN,QSCN6L1,DKFZp762A2013","biotype":"protein_coding","ncbi_id":"169714","summary":"QSOX2 is a member of the sulfhydryl oxidase/quiescin-6 (Q6) family (QSOX1; MIM 603120) that regulates the sensitization of neuroblastoma cells for IFN-gamma (IFNG; MIM 147570)-induced cell death (Wittke et al., 2003 [PubMed 14633699]).[supplied by OMIM, Jun 2009]","start":136206333,"end":136245841,"strand":-1,"description":"quiescin sulfhydryl oxidase 2 [Source:HGNC Symbol;Acc:HGNC:30249]"}, {"versioned_ensembl_gene_id":"ENSG00000107187.15","gene_symbol":"LHX3","gene_name":"LIM homeobox 3 [Source:HGNC Symbol;Acc:HGNC:6595]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8022","summary":"This gene encodes a member of a large family of proteins which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene cause combined pituitary hormone deficiency 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":136196250,"end":136205109,"strand":-1,"description":"LIM homeobox 3 [Source:HGNC Symbol;Acc:HGNC:6595]"}, {"versioned_ensembl_gene_id":"ENSG00000249689.1","gene_symbol":"AC138517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139492538,"end":139493105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232347.1","gene_symbol":"AL390728.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":247210691,"end":247241823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233901.5","gene_symbol":"LINC01503","gene_name":"long intergenic non-protein coding RNA 1503 [Source:HGNC Symbol;Acc:HGNC:51184]","synonyms":"lnc-PPP2R4-5","biotype":"lincRNA","ncbi_id":"100506119","summary":null,"start":129332300,"end":129359538,"strand":1,"description":"long intergenic non-protein coding RNA 1503 [Source:HGNC Symbol;Acc:HGNC:51184]"}, {"versioned_ensembl_gene_id":"ENSG00000241084.1","gene_symbol":"AL161785.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129259062,"end":129261581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235007.2","gene_symbol":"AL161785.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129258354,"end":129259846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263873.1","gene_symbol":"AP003396.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":119417951,"end":119419114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244062.1","gene_symbol":"AC080128.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133760300,"end":133762363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130348.11","gene_symbol":"QRSL1","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 [Source:HGNC Symbol;Acc:HGNC:21020]","synonyms":"GatA,FLJ13447,FLJ12189,FLJ10989,DKFZP564C1278","biotype":"protein_coding","ncbi_id":"55278","summary":null,"start":106629578,"end":106668417,"strand":1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 [Source:HGNC Symbol;Acc:HGNC:21020]"}, {"versioned_ensembl_gene_id":"ENSG00000181619.11","gene_symbol":"GPR135","gene_name":"G protein-coupled receptor 135 [Source:HGNC Symbol;Acc:HGNC:19991]","synonyms":"PAFR,HUMNPIIY20","biotype":"protein_coding","ncbi_id":"64582","summary":null,"start":59429022,"end":59465342,"strand":-1,"description":"G protein-coupled receptor 135 [Source:HGNC Symbol;Acc:HGNC:19991]"}, {"versioned_ensembl_gene_id":"ENSG00000258782.3","gene_symbol":"AL121694.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":59479274,"end":59525437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151838.11","gene_symbol":"CCDC175","gene_name":"coiled-coil domain containing 175 [Source:HGNC Symbol;Acc:HGNC:19847]","synonyms":"C14orf38","biotype":"protein_coding","ncbi_id":"729665","summary":null,"start":59504539,"end":59576831,"strand":-1,"description":"coiled-coil domain containing 175 [Source:HGNC Symbol;Acc:HGNC:19847]"}, {"versioned_ensembl_gene_id":"ENSG00000273891.1","gene_symbol":"AL731566.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121965764,"end":121967700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204571.6","gene_symbol":"KRTAP5-11","gene_name":"keratin associated protein 5-11 [Source:HGNC Symbol;Acc:HGNC:23606]","synonyms":"KRTAP5.11,KRTAP5-6","biotype":"protein_coding","ncbi_id":"440051","summary":null,"start":71579714,"end":71603353,"strand":-1,"description":"keratin associated protein 5-11 [Source:HGNC Symbol;Acc:HGNC:23606]"}, {"versioned_ensembl_gene_id":"ENSG00000073008.14","gene_symbol":"PVR","gene_name":"poliovirus receptor [Source:HGNC Symbol;Acc:HGNC:9705]","synonyms":"Tage4,PVS,NECL5,Necl-5,HVED,CD155","biotype":"protein_coding","ncbi_id":"5817","summary":"The protein encoded by this gene is a transmembrane glycoprotein belonging to the immunoglobulin superfamily. The external domain mediates cell attachment to the extracellular matrix molecule vitronectin, while its intracellular domain interacts with the dynein light chain Tctex-1/DYNLT1. The gene is specific to the primate lineage, and serves as a cellular receptor for poliovirus in the first step of poliovirus replication. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":44643798,"end":44663583,"strand":1,"description":"poliovirus receptor [Source:HGNC Symbol;Acc:HGNC:9705]"}, {"versioned_ensembl_gene_id":"ENSG00000276206.1","gene_symbol":"AC012314.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54031412,"end":54031504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163781.12","gene_symbol":"TOPBP1","gene_name":"topoisomerase (DNA) II binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17008]","synonyms":"TOP2BP1,KIAA0259","biotype":"protein_coding","ncbi_id":"11073","summary":"This gene encodes a binding protein which interacts with the C-terminal region of topoisomerase II beta. This interaction suggests a supportive role for this protein in the catalytic reactions of topoisomerase II beta through transient breakages of DNA strands. [provided by RefSeq, Jul 2008]","start":133598175,"end":133661893,"strand":-1,"description":"topoisomerase (DNA) II binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17008]"}, {"versioned_ensembl_gene_id":"ENSG00000249994.1","gene_symbol":"AC025187.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4033713,"end":4041764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255191.1","gene_symbol":"AP003555.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69985876,"end":70015815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186895.2","gene_symbol":"FGF3","gene_name":"fibroblast growth factor 3 [Source:HGNC Symbol;Acc:HGNC:3681]","synonyms":"INT2,HBGF-3","biotype":"protein_coding","ncbi_id":"2248","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its similarity with mouse fgf3/int-2, a proto-oncogene activated in virally induced mammary tumors in the mouse. Frequent amplification of this gene has been found in human tumors, which may be important for neoplastic transformation and tumor progression. Studies of the similar genes in mouse and chicken suggested the role in inner ear formation. [provided by RefSeq, Jul 2008]","start":69810224,"end":69819024,"strand":-1,"description":"fibroblast growth factor 3 [Source:HGNC Symbol;Acc:HGNC:3681]"}, {"versioned_ensembl_gene_id":"ENSG00000260348.1","gene_symbol":"AP007216.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69909184,"end":69910994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245552.6","gene_symbol":"AP000787.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95150539,"end":95234104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186451.1","gene_symbol":"SPATA12","gene_name":"spermatogenesis associated 12 [Source:HGNC Symbol;Acc:HGNC:23221]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353324","summary":"This gene is expressed primarily in testis and may play a role in testicular development and spermatogenesis. The encoded protein may be upregulated in response to ultraviolet-C radiation. [provided by RefSeq, Dec 2015]","start":57060441,"end":57075432,"strand":1,"description":"spermatogenesis associated 12 [Source:HGNC Symbol;Acc:HGNC:23221]"}, {"versioned_ensembl_gene_id":"ENSG00000248477.6","gene_symbol":"AC139495.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69607099,"end":69624049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111962.7","gene_symbol":"UST","gene_name":"uronyl 2-sulfotransferase [Source:HGNC Symbol;Acc:HGNC:17223]","synonyms":"2OST","biotype":"protein_coding","ncbi_id":"10090","summary":"Uronyl 2-sulfotransferase transfers sulfate to the 2-position of uronyl residues, such as iduronyl residues in dermatan sulfate and glucuronyl residues in chondroitin sulfate (Kobayashi et al., 1999 [PubMed 10187838]).[supplied by OMIM, Mar 2008]","start":148747328,"end":149076990,"strand":1,"description":"uronyl 2-sulfotransferase [Source:HGNC Symbol;Acc:HGNC:17223]"}, {"versioned_ensembl_gene_id":"ENSG00000259136.1","gene_symbol":"AL137100.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57044646,"end":57044960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182544.8","gene_symbol":"MFSD5","gene_name":"major facilitator superfamily domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28156]","synonyms":"MGC11308","biotype":"protein_coding","ncbi_id":"84975","summary":null,"start":53251251,"end":53254405,"strand":1,"description":"major facilitator superfamily domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28156]"}, {"versioned_ensembl_gene_id":"ENSG00000248107.1","gene_symbol":"LINC02039","gene_name":"long intergenic non-protein coding RNA 2039 [Source:HGNC Symbol;Acc:HGNC:52879]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546228","summary":null,"start":126179577,"end":126193850,"strand":1,"description":"long intergenic non-protein coding RNA 2039 [Source:HGNC Symbol;Acc:HGNC:52879]"}, {"versioned_ensembl_gene_id":"ENSG00000269037.1","gene_symbol":"LINC01838","gene_name":"long intergenic non-protein coding RNA 1838 [Source:HGNC Symbol;Acc:HGNC:52654]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652911","summary":null,"start":34905315,"end":34908188,"strand":1,"description":"long intergenic non-protein coding RNA 1838 [Source:HGNC Symbol;Acc:HGNC:52654]"}, {"versioned_ensembl_gene_id":"ENSG00000262495.1","gene_symbol":"AC012146.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5060356,"end":5062123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152315.4","gene_symbol":"KCNK13","gene_name":"potassium two pore domain channel subfamily K member 13 [Source:HGNC Symbol;Acc:HGNC:6275]","synonyms":"K2p13.1,THIK1,THIK-1","biotype":"protein_coding","ncbi_id":"56659","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a potassium channel containing two pore-forming domains. This protein is an open channel that can be stimulated by arachidonic acid and inhibited by the anesthetic halothane. [provided by RefSeq, Jul 2013]","start":90061765,"end":90185857,"strand":1,"description":"potassium two pore domain channel subfamily K member 13 [Source:HGNC Symbol;Acc:HGNC:6275]"}, {"versioned_ensembl_gene_id":"ENSG00000197822.10","gene_symbol":"OCLN","gene_name":"occludin [Source:HGNC Symbol;Acc:HGNC:8104]","synonyms":"PPP1R115","biotype":"protein_coding","ncbi_id":"100506658","summary":"This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]","start":69492292,"end":69558104,"strand":1,"description":"occludin [Source:HGNC Symbol;Acc:HGNC:8104]"}, {"versioned_ensembl_gene_id":"ENSG00000255947.1","gene_symbol":"AP002754.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61654665,"end":61655702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197380.10","gene_symbol":"DACT3","gene_name":"dishevelled binding antagonist of beta catenin 3 [Source:HGNC Symbol;Acc:HGNC:30745]","synonyms":"RRR1,MGC15476,DAPPER3","biotype":"protein_coding","ncbi_id":"147906","summary":null,"start":46647612,"end":46661138,"strand":-1,"description":"dishevelled binding antagonist of beta catenin 3 [Source:HGNC Symbol;Acc:HGNC:30745]"}, {"versioned_ensembl_gene_id":"ENSG00000122378.13","gene_symbol":"FAM213A","gene_name":"family with sequence similarity 213 member A [Source:HGNC Symbol;Acc:HGNC:28651]","synonyms":"PAMM,MGC4248,C10orf58,Adrx","biotype":"protein_coding","ncbi_id":"84293","summary":null,"start":80407829,"end":80437115,"strand":1,"description":"family with sequence similarity 213 member A [Source:HGNC Symbol;Acc:HGNC:28651]"}, {"versioned_ensembl_gene_id":"ENSG00000277382.1","gene_symbol":"AC005837.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76709760,"end":76710045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095203.14","gene_symbol":"EPB41L4B","gene_name":"erythrocyte membrane protein band 4.1 like 4B [Source:HGNC Symbol;Acc:HGNC:19818]","synonyms":"EHM2","biotype":"protein_coding","ncbi_id":"54566","summary":null,"start":109171975,"end":109320964,"strand":-1,"description":"erythrocyte membrane protein band 4.1 like 4B [Source:HGNC Symbol;Acc:HGNC:19818]"}, {"versioned_ensembl_gene_id":"ENSG00000277176.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54831023,"end":54842954,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000213954.3","gene_symbol":"ATP5HP3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"138864","summary":null,"start":14068932,"end":14069417,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49625]"}, {"versioned_ensembl_gene_id":"ENSG00000270175.1","gene_symbol":"AC023509.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53500162,"end":53500936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284725.1","gene_symbol":"AC093762.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227724440,"end":227724757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163092.19","gene_symbol":"XIRP2","gene_name":"xin actin binding repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:14303]","synonyms":"CMYA3","biotype":"protein_coding","ncbi_id":"129446","summary":null,"start":166888487,"end":167259753,"strand":1,"description":"xin actin binding repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:14303]"}, {"versioned_ensembl_gene_id":"ENSG00000269119.1","gene_symbol":"HNRNPA1P52","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:48782]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645001","summary":null,"start":41829692,"end":41830938,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:48782]"}, {"versioned_ensembl_gene_id":"ENSG00000267173.1","gene_symbol":"AC245748.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":44329695,"end":44401608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254933.1","gene_symbol":"AP000785.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76190725,"end":76195071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057657.15","gene_symbol":"PRDM1","gene_name":"PR/SET domain 1 [Source:HGNC Symbol;Acc:HGNC:9346]","synonyms":"PRDI-BF1,BLIMP1","biotype":"protein_coding","ncbi_id":"639","summary":"This gene encodes a protein that acts as a repressor of beta-interferon gene expression. The protein binds specifically to the PRDI (positive regulatory domain I element) of the beta-IFN gene promoter. Transcription of this gene increases upon virus induction. Two alternatively spliced transcript variants that encode different isoforms have been reported. [provided by RefSeq, Jul 2008]","start":106086320,"end":106109939,"strand":1,"description":"PR/SET domain 1 [Source:HGNC Symbol;Acc:HGNC:9346]"}, {"versioned_ensembl_gene_id":"ENSG00000248600.1","gene_symbol":"AC025465.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124455373,"end":124460098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198342.9","gene_symbol":"ZNF442","gene_name":"zinc finger protein 442 [Source:HGNC Symbol;Acc:HGNC:20877]","synonyms":"FLJ14356","biotype":"protein_coding","ncbi_id":"79973","summary":null,"start":12345949,"end":12365905,"strand":-1,"description":"zinc finger protein 442 [Source:HGNC Symbol;Acc:HGNC:20877]"}, {"versioned_ensembl_gene_id":"ENSG00000267518.1","gene_symbol":"AC090699.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76345761,"end":76346081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228157.4","gene_symbol":"AC007952.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19092974,"end":19096837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237523.1","gene_symbol":"LINC00857","gene_name":"long intergenic non-protein coding RNA 857 [Source:HGNC Symbol;Acc:HGNC:45114]","synonyms":null,"biotype":"lincRNA","ncbi_id":"439990","summary":null,"start":80207710,"end":80219657,"strand":1,"description":"long intergenic non-protein coding RNA 857 [Source:HGNC Symbol;Acc:HGNC:45114]"}, {"versioned_ensembl_gene_id":"ENSG00000161594.6","gene_symbol":"KLHL10","gene_name":"kelch like family member 10 [Source:HGNC Symbol;Acc:HGNC:18829]","synonyms":"FLJ32662","biotype":"protein_coding","ncbi_id":"317719","summary":"The protein encoded by this gene belongs to the kelch repeat-containing family, and contains an N-terminal BTB/POZ domain a BACK domain and six C-terminal kelch repeats. Kelch domains are thought to form a four stranded beta-sheet blade structure that can fold into a beta-propeller domain when multiple kelch repeats are found together. Mutations in this gene have been associated with oligozoospermia in some infertile males. [provided by RefSeq, Jul 2016]","start":41835685,"end":41848384,"strand":1,"description":"kelch like family member 10 [Source:HGNC Symbol;Acc:HGNC:18829]"}, {"versioned_ensembl_gene_id":"ENSG00000250862.1","gene_symbol":"HMGB1P29","gene_name":"high mobility group box 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:39120]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873892","summary":null,"start":124220579,"end":124221077,"strand":-1,"description":"high mobility group box 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:39120]"}, {"versioned_ensembl_gene_id":"ENSG00000251421.2","gene_symbol":"AC016556.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124395603,"end":124400655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175093.4","gene_symbol":"SPSB4","gene_name":"splA/ryanodine receptor domain and SOCS box containing 4 [Source:HGNC Symbol;Acc:HGNC:30630]","synonyms":"SSB-4","biotype":"protein_coding","ncbi_id":"92369","summary":null,"start":141051402,"end":141148611,"strand":1,"description":"splA/ryanodine receptor domain and SOCS box containing 4 [Source:HGNC Symbol;Acc:HGNC:30630]"}, {"versioned_ensembl_gene_id":"ENSG00000266258.1","gene_symbol":"LINC01909","gene_name":"long intergenic non-protein coding RNA 1909 [Source:HGNC Symbol;Acc:HGNC:52728]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927481","summary":null,"start":70335439,"end":70352459,"strand":1,"description":"long intergenic non-protein coding RNA 1909 [Source:HGNC Symbol;Acc:HGNC:52728]"}, {"versioned_ensembl_gene_id":"ENSG00000231944.1","gene_symbol":"PHKA1-AS1","gene_name":"PHKA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40446]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928259","summary":null,"start":72688950,"end":72712348,"strand":1,"description":"PHKA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40446]"}, {"versioned_ensembl_gene_id":"ENSG00000268683.1","gene_symbol":"AC020910.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":34638122,"end":34640689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152749.7","gene_symbol":"GPR180","gene_name":"G protein-coupled receptor 180 [Source:HGNC Symbol;Acc:HGNC:28899]","synonyms":"ITR","biotype":"protein_coding","ncbi_id":"160897","summary":"This gene encodes a protein that is a member of the G protein-coupled receptor superfamily. This protein is produced predominantly in vascular smooth muscle cells and may play an important role in the regulation of vascular remodeling. [provided by RefSeq, Jul 2008]","start":94601903,"end":94634645,"strand":1,"description":"G protein-coupled receptor 180 [Source:HGNC Symbol;Acc:HGNC:28899]"}, {"versioned_ensembl_gene_id":"ENSG00000241356.1","gene_symbol":"OR5G3","gene_name":"olfactory receptor family 5 subfamily G member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15287]","synonyms":"OR5G6P,OR5G3P","biotype":"polymorphic_pseudogene","ncbi_id":"81193","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":56819576,"end":56820504,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15287]"}, {"versioned_ensembl_gene_id":"ENSG00000253149.3","gene_symbol":"AC245166.1","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106329432,"end":106329684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147654.14","gene_symbol":"EBAG9","gene_name":"estrogen receptor binding site associated, antigen, 9 [Source:HGNC Symbol;Acc:HGNC:3123]","synonyms":"RCAS1,EB9","biotype":"protein_coding","ncbi_id":"9166","summary":"This gene was identified as an estrogen-responsive gene. Regulation of transcription by estrogen is mediated by estrogen receptor, which binds to the estrogen-responsive element found in the 5'-flanking region of this gene. The encoded protein is a tumor-associated antigen that is expressed at high frequency in a variety of cancers. Alternate splicing results in multiple transcript variants. A pseudogene of this gene has been defined on chromosome 10. [provided by RefSeq, Jul 2013]","start":109539711,"end":109565996,"strand":1,"description":"estrogen receptor binding site associated, antigen, 9 [Source:HGNC Symbol;Acc:HGNC:3123]"}, {"versioned_ensembl_gene_id":"ENSG00000233707.3","gene_symbol":"RPL22P11","gene_name":"ribosomal protein L22 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35603]","synonyms":"RPL22P15","biotype":"processed_pseudogene","ncbi_id":"402100","summary":null,"start":109737139,"end":109737523,"strand":-1,"description":"ribosomal protein L22 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35603]"}, {"versioned_ensembl_gene_id":"ENSG00000250539.1","gene_symbol":"KRT8P33","gene_name":"keratin 8 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418737","summary":null,"start":123400922,"end":123402344,"strand":-1,"description":"keratin 8 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39867]"}, {"versioned_ensembl_gene_id":"ENSG00000151224.12","gene_symbol":"MAT1A","gene_name":"methionine adenosyltransferase 1A [Source:HGNC Symbol;Acc:HGNC:6903]","synonyms":"SAMS1,SAMS,MATA1,MAT","biotype":"protein_coding","ncbi_id":"4143","summary":"This gene catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. The encoded protein is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in this gene are associated with methionine adenosyltransferase deficiency. [provided by RefSeq, Jul 2008]","start":80271820,"end":80289684,"strand":-1,"description":"methionine adenosyltransferase 1A [Source:HGNC Symbol;Acc:HGNC:6903]"}, {"versioned_ensembl_gene_id":"ENSG00000255255.1","gene_symbol":"PPP1R1AP1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16316]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"94304","summary":null,"start":75911204,"end":75911628,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16316]"}, {"versioned_ensembl_gene_id":"ENSG00000255081.1","gene_symbol":"AP003168.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75914201,"end":75915213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235096.2","gene_symbol":"AC118555.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":246025897,"end":246035603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225222.2","gene_symbol":"CHCHD4P5","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479039","summary":null,"start":246178778,"end":246179204,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44493]"}, {"versioned_ensembl_gene_id":"ENSG00000284631.1","gene_symbol":"AC064853.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227616998,"end":227618655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175906.4","gene_symbol":"ARL4D","gene_name":"ADP ribosylation factor like GTPase 4D [Source:HGNC Symbol;Acc:HGNC:656]","synonyms":"ARF4L","biotype":"protein_coding","ncbi_id":"379","summary":"ADP-ribosylation factor 4D is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4D is closely similar to ARL4A and ARL4C and each has a nuclear localization signal and an unusually high guanine nucleotide exchange rate. This protein may play a role in membrane-associated intracellular trafficking. [provided by RefSeq, Jul 2021]","start":43398959,"end":43401137,"strand":1,"description":"ADP ribosylation factor like GTPase 4D [Source:HGNC Symbol;Acc:HGNC:656]"}, {"versioned_ensembl_gene_id":"ENSG00000244630.2","gene_symbol":"AC022493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80855507,"end":80855843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240973.1","gene_symbol":"AC093714.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115679345,"end":115682618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188825.13","gene_symbol":"LINC00910","gene_name":"long intergenic non-protein coding RNA 910 [Source:HGNC Symbol;Acc:HGNC:44361]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100130581","summary":null,"start":43369845,"end":43389199,"strand":-1,"description":"long intergenic non-protein coding RNA 910 [Source:HGNC Symbol;Acc:HGNC:44361]"}, {"versioned_ensembl_gene_id":"ENSG00000188878.19","gene_symbol":"FBF1","gene_name":"Fas binding factor 1 [Source:HGNC Symbol;Acc:HGNC:24674]","synonyms":"KIAA1863,FLJ00103,FBF-1,ALB","biotype":"protein_coding","ncbi_id":"85302","summary":null,"start":75909574,"end":75941140,"strand":-1,"description":"Fas binding factor 1 [Source:HGNC Symbol;Acc:HGNC:24674]"}, {"versioned_ensembl_gene_id":"ENSG00000242072.1","gene_symbol":"AC092590.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115647461,"end":115676329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132481.6","gene_symbol":"TRIM47","gene_name":"tripartite motif containing 47 [Source:HGNC Symbol;Acc:HGNC:19020]","synonyms":"RNF100,GOA","biotype":"protein_coding","ncbi_id":"91107","summary":null,"start":75874161,"end":75878575,"strand":-1,"description":"tripartite motif containing 47 [Source:HGNC Symbol;Acc:HGNC:19020]"}, {"versioned_ensembl_gene_id":"ENSG00000248969.1","gene_symbol":"AC137810.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35678484,"end":35827018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138376.10","gene_symbol":"BARD1","gene_name":"BRCA1 associated RING domain 1 [Source:HGNC Symbol;Acc:HGNC:952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"580","summary":"This gene encodes a protein which interacts with the N-terminal region of BRCA1. In addition to its ability to bind BRCA1 in vivo and in vitro, it shares homology with the 2 most conserved regions of BRCA1: the N-terminal RING motif and the C-terminal BRCT domain. The RING motif is a cysteine-rich sequence found in a variety of proteins that regulate cell growth, including the products of tumor suppressor genes and dominant protooncogenes. This protein also contains 3 tandem ankyrin repeats. The BARD1/BRCA1 interaction is disrupted by tumorigenic amino acid substitutions in BRCA1, implying that the formation of a stable complex between these proteins may be an essential aspect of BRCA1 tumor suppression. This protein may be the target of oncogenic mutations in breast or ovarian cancer. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":214725646,"end":214809711,"strand":-1,"description":"BRCA1 associated RING domain 1 [Source:HGNC Symbol;Acc:HGNC:952]"}, {"versioned_ensembl_gene_id":"ENSG00000080166.15","gene_symbol":"DCT","gene_name":"dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2709]","synonyms":"TYRP2","biotype":"protein_coding","ncbi_id":"1638","summary":null,"start":94436808,"end":94479682,"strand":-1,"description":"dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2709]"}, {"versioned_ensembl_gene_id":"ENSG00000143669.13","gene_symbol":"LYST","gene_name":"lysosomal trafficking regulator [Source:HGNC Symbol;Acc:HGNC:1968]","synonyms":"CHS,CHS1","biotype":"protein_coding","ncbi_id":"1130","summary":"This gene encodes a protein that regulates intracellular protein trafficking in endosomes, and may be involved in pigmentation. Mutations in this gene are associated with Chediak-Higashi syndrome, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants, though the full-length nature of some of these variants has not been determined. [provided by RefSeq, Apr 2013]","start":235661041,"end":235883640,"strand":-1,"description":"lysosomal trafficking regulator [Source:HGNC Symbol;Acc:HGNC:1968]"}, {"versioned_ensembl_gene_id":"ENSG00000268810.1","gene_symbol":"AC007193.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46382492,"end":46383169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235674.2","gene_symbol":"LDHAP2","gene_name":"lactate dehydrogenase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6537]","synonyms":"LDHAL2","biotype":"processed_pseudogene","ncbi_id":"100190799","summary":null,"start":235738005,"end":235738989,"strand":1,"description":"lactate dehydrogenase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6537]"}, {"versioned_ensembl_gene_id":"ENSG00000277596.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54727609,"end":54736462,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000238194.1","gene_symbol":"AL121908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59626464,"end":59628289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245954.6","gene_symbol":"LINC02273","gene_name":"long intergenic non-protein coding RNA 2273 [Source:HGNC Symbol;Acc:HGNC:53188]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996286","summary":null,"start":152100754,"end":152104720,"strand":1,"description":"long intergenic non-protein coding RNA 2273 [Source:HGNC Symbol;Acc:HGNC:53188]"}, {"versioned_ensembl_gene_id":"ENSG00000254101.5","gene_symbol":"LINC02055","gene_name":"long intergenic non-protein coding RNA 2055 [Source:HGNC Symbol;Acc:HGNC:52895]","synonyms":"RP1130-1","biotype":"lincRNA","ncbi_id":"107986980","summary":null,"start":136530798,"end":136984935,"strand":1,"description":"long intergenic non-protein coding RNA 2055 [Source:HGNC Symbol;Acc:HGNC:52895]"}, {"versioned_ensembl_gene_id":"ENSG00000230166.1","gene_symbol":"RPL35AP24","gene_name":"ribosomal protein L35a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35544]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271631","summary":null,"start":49909613,"end":49909942,"strand":1,"description":"ribosomal protein L35a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35544]"}, {"versioned_ensembl_gene_id":"ENSG00000144583.4","gene_symbol":"MARCH4","gene_name":"membrane associated ring-CH-type finger 4 [Source:HGNC Symbol;Acc:HGNC:29269]","synonyms":"RNF174,MARCH-IV,KIAA1399","biotype":"protein_coding","ncbi_id":"57574","summary":"MARCH4 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH4 reduces surface accumulation of several membrane glycoproteins by directing them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010]","start":216257865,"end":216372027,"strand":-1,"description":"membrane associated ring-CH-type finger 4 [Source:HGNC Symbol;Acc:HGNC:29269]"}, {"versioned_ensembl_gene_id":"ENSG00000238224.1","gene_symbol":"AC104462.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":245614773,"end":245615145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231612.1","gene_symbol":"AC104462.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":245673732,"end":245676478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230504.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824881,"end":29825861,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000181090.20","gene_symbol":"EHMT1","gene_name":"euchromatic histone lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24650]","synonyms":"KMT1D,KIAA1876,FLJ12879,Eu-HMTase1,bA188C12.1","biotype":"protein_coding","ncbi_id":"79813","summary":"The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]","start":137618963,"end":137870016,"strand":1,"description":"euchromatic histone lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24650]"}, {"versioned_ensembl_gene_id":"ENSG00000232139.5","gene_symbol":"LINC00867","gene_name":"long intergenic non-protein coding RNA 867 [Source:HGNC Symbol;Acc:HGNC:45265]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506126","summary":null,"start":118357108,"end":118365103,"strand":1,"description":"long intergenic non-protein coding RNA 867 [Source:HGNC Symbol;Acc:HGNC:45265]"}, {"versioned_ensembl_gene_id":"ENSG00000234773.7","gene_symbol":"AC012618.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12195015,"end":12237767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279790.1","gene_symbol":"AL590552.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73971346,"end":73973115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253497.1","gene_symbol":"IGKV1-13","gene_name":"immunoglobulin kappa variable 1-13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5731]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28939","summary":null,"start":89045995,"end":89046466,"strand":-1,"description":"immunoglobulin kappa variable 1-13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5731]"}, {"versioned_ensembl_gene_id":"ENSG00000242953.1","gene_symbol":"AC139453.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75395404,"end":75395536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160349.9","gene_symbol":"LCN1","gene_name":"lipocalin 1 [Source:HGNC Symbol;Acc:HGNC:6525]","synonyms":"VEGP,TP,TLC,PMFA,MGC71975","biotype":"protein_coding","ncbi_id":"3933","summary":"This gene encodes a member of the lipocalin family of small secretory proteins. Lipocalins are extracellular transport proteins that bind to a variety of hydrophobic ligands. The encoded protein is the primary lipid binding protein in tears and is overproduced in response to multiple stimuli including infection and stress. The encoded protein may be a marker for chromosome aneuploidy as well as an autoantigen in Sjogren's syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and two pseudogenes of this gene are also located on the long arm of chromosome 9. [provided by RefSeq, Nov 2011]","start":135521438,"end":135526532,"strand":1,"description":"lipocalin 1 [Source:HGNC Symbol;Acc:HGNC:6525]"}, {"versioned_ensembl_gene_id":"ENSG00000274379.1","gene_symbol":"AL121612.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94918253,"end":94918734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240914.1","gene_symbol":"AL121612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94800849,"end":94801463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223572.9","gene_symbol":"CKMT1A","gene_name":"creatine kinase, mitochondrial 1A [Source:HGNC Symbol;Acc:HGNC:31736]","synonyms":"CKMT1","biotype":"protein_coding","ncbi_id":"548596","summary":"Mitochondrial creatine (MtCK) kinase is responsible for the transfer of high energy phosphate from mitochondria to the cytosolic carrier, creatine. It belongs to the creatine kinase isoenzyme family. It exists as two isoenzymes, sarcomeric MtCK and ubiquitous MtCK, encoded by separate genes. Mitochondrial creatine kinase occurs in two different oligomeric forms: dimers and octamers, in contrast to the exclusively dimeric cytosolic creatine kinase isoenzymes. Many malignant cancers with poor prognosis have shown overexpression of ubiquitous mitochondrial creatine kinase; this may be related to high energy turnover and failure to eliminate cancer cells via apoptosis. Ubiquitous mitochondrial creatine kinase has 80% homology with the coding exons of sarcomeric mitochondrial creatine kinase. Two genes located near each other on chromosome 15 have been identified which encode identical mitochondrial creatine kinase proteins. [provided by RefSeq, Jul 2008]","start":43692886,"end":43699222,"strand":1,"description":"creatine kinase, mitochondrial 1A [Source:HGNC Symbol;Acc:HGNC:31736]"}, {"versioned_ensembl_gene_id":"ENSG00000235354.1","gene_symbol":"RPS29P16","gene_name":"ribosomal protein S29 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132499","summary":null,"start":103348601,"end":103348771,"strand":1,"description":"ribosomal protein S29 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35560]"}, {"versioned_ensembl_gene_id":"ENSG00000243466.1","gene_symbol":"IGKV1-5","gene_name":"immunoglobulin kappa variable 1-5 [Source:HGNC Symbol;Acc:HGNC:5741]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28299","summary":null,"start":88947301,"end":88947957,"strand":-1,"description":"immunoglobulin kappa variable 1-5 [Source:HGNC Symbol;Acc:HGNC:5741]"}, {"versioned_ensembl_gene_id":"ENSG00000137727.12","gene_symbol":"ARHGAP20","gene_name":"Rho GTPase activating protein 20 [Source:HGNC Symbol;Acc:HGNC:18357]","synonyms":"KIAA1391","biotype":"protein_coding","ncbi_id":"57569","summary":"The protein encoded by this gene is an activator of RHO-type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth. [provided by RefSeq, Sep 2016]","start":110577042,"end":110713189,"strand":-1,"description":"Rho GTPase activating protein 20 [Source:HGNC Symbol;Acc:HGNC:18357]"}, {"versioned_ensembl_gene_id":"ENSG00000154227.13","gene_symbol":"CERS3","gene_name":"ceramide synthase 3 [Source:HGNC Symbol;Acc:HGNC:23752]","synonyms":"MGC27091,LASS3","biotype":"protein_coding","ncbi_id":"204219","summary":"This gene is a member of the ceramide synthase family of genes. The ceramide synthase enzymes regulate sphingolipid synthesis by catalyzing the formation of ceramides from sphingoid base and acyl-coA substrates. This family member is involved in the synthesis of ceramides with ultra-long-chain acyl moieties (ULC-Cers), important to the epidermis in its role in creating a protective barrier from the environment. The protein encoded by this gene has also been implicated in modification of the lipid structures required for spermatogenesis. Mutations in this gene have been associated with male fertility defects, and epidermal defects, including ichthyosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":100400395,"end":100544995,"strand":-1,"description":"ceramide synthase 3 [Source:HGNC Symbol;Acc:HGNC:23752]"}, {"versioned_ensembl_gene_id":"ENSG00000225136.1","gene_symbol":"PGBD4P5","gene_name":"piggyBac transposable element derived 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421123","summary":null,"start":88922328,"end":88922753,"strand":-1,"description":"piggyBac transposable element derived 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44070]"}, {"versioned_ensembl_gene_id":"ENSG00000197794.2","gene_symbol":"IGKV7-3","gene_name":"immunoglobulin kappa variable 7-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5839]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28905","summary":null,"start":88915081,"end":88915378,"strand":-1,"description":"immunoglobulin kappa variable 7-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5839]"}, {"versioned_ensembl_gene_id":"ENSG00000259887.1","gene_symbol":"AC068987.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51848223,"end":51852729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113520.10","gene_symbol":"IL4","gene_name":"interleukin 4 [Source:HGNC Symbol;Acc:HGNC:6014]","synonyms":"BSF1,BCGF1,BCGF-1,MGC79402,IL-4","biotype":"protein_coding","ncbi_id":"3565","summary":"The protein encoded by this gene is a pleiotropic cytokine produced by activated T cells. This cytokine is a ligand for interleukin 4 receptor. The interleukin 4 receptor also binds to IL13, which may contribute to many overlapping functions of this cytokine and IL13. STAT6, a signal transducer and activator of transcription, has been shown to play a central role in mediating the immune regulatory signal of this cytokine. This gene, IL3, IL5, IL13, and CSF2 form a cytokine gene cluster on chromosome 5q, with this gene particularly close to IL13. This gene, IL13 and IL5 are found to be regulated coordinately by several long-range regulatory elements in an over 120 kilobase range on the chromosome. IL4 is considered an important cytokine for tissue repair, counterbalancing the effects of proinflammatory type 1 cytokines, however, it also promotes allergic airway inflammation. Moreover, IL-4, a type 2 cytokine, mediates and regulates a variety of human host responses such as allergic, anti-parasitic, wound healing, and acute inflammation. This cytokine has been reported to promote resolution of neutrophil-mediated acute lung injury. In an allergic response, IL-4 has an essential role in the production of allergen-specific immunoglobin (Ig) E. This pro-inflammatory cytokine has been observed to be increased in COVID-19 (Coronavirus disease 2019) patients, but is not necessarily associated with severe COVID-19 pathology. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Aug 2020]","start":132673986,"end":132682676,"strand":1,"description":"interleukin 4 [Source:HGNC Symbol;Acc:HGNC:6014]"}, {"versioned_ensembl_gene_id":"ENSG00000250886.1","gene_symbol":"AC010368.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35081223,"end":35081992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163347.5","gene_symbol":"CLDN1","gene_name":"claudin 1 [Source:HGNC Symbol;Acc:HGNC:2032]","synonyms":"SEMP1,ILVASC","biotype":"protein_coding","ncbi_id":"9076","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. Loss of function mutations result in neonatal ichthyosis-sclerosing cholangitis syndrome. [provided by RefSeq, Jul 2008]","start":190305701,"end":190322475,"strand":-1,"description":"claudin 1 [Source:HGNC Symbol;Acc:HGNC:2032]"}, {"versioned_ensembl_gene_id":"ENSG00000070081.15","gene_symbol":"NUCB2","gene_name":"nucleobindin 2 [Source:HGNC Symbol;Acc:HGNC:8044]","synonyms":"NEFA","biotype":"protein_coding","ncbi_id":"4925","summary":"This gene encodes a protein with a suggested role in calcium level maintenance, eating regulation in the hypothalamus, and release of tumor necrosis factor from vascular endothelial cells. This protein binds calcium and has EF-folding domains. [provided by RefSeq, Oct 2011]","start":17208153,"end":17349974,"strand":1,"description":"nucleobindin 2 [Source:HGNC Symbol;Acc:HGNC:8044]"}, {"versioned_ensembl_gene_id":"ENSG00000187747.2","gene_symbol":"OR52B6","gene_name":"olfactory receptor family 52 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:15211]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340980","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5580877,"end":5581884,"strand":1,"description":"olfactory receptor family 52 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:15211]"}, {"versioned_ensembl_gene_id":"ENSG00000225531.1","gene_symbol":"AL807761.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107116829,"end":107117557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226047.1","gene_symbol":"AL807761.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107117459,"end":107121705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234604.2","gene_symbol":"AL021068.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169474060,"end":169474159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269307.1","gene_symbol":"AC010463.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17267418,"end":17282966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118242.15","gene_symbol":"MREG","gene_name":"melanoregulin [Source:HGNC Symbol;Acc:HGNC:25478]","synonyms":"WDT2,FLJ10116,DSU","biotype":"protein_coding","ncbi_id":"55686","summary":null,"start":215942805,"end":216034096,"strand":-1,"description":"melanoregulin [Source:HGNC Symbol;Acc:HGNC:25478]"}, {"versioned_ensembl_gene_id":"ENSG00000237937.5","gene_symbol":"AP000770.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116639422,"end":116658252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281183.1","gene_symbol":"NPTN-IT1","gene_name":"NPTN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:45091]","synonyms":"lncRNA-LET","biotype":"sense_intronic","ncbi_id":"101241892","summary":null,"start":73567012,"end":73569294,"strand":-1,"description":"NPTN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:45091]"}, {"versioned_ensembl_gene_id":"ENSG00000115425.13","gene_symbol":"PECR","gene_name":"peroxisomal trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:18281]","synonyms":"TERP,SDR29C1,HSA250303","biotype":"protein_coding","ncbi_id":"55825","summary":null,"start":215996329,"end":216082955,"strand":-1,"description":"peroxisomal trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:18281]"}, {"versioned_ensembl_gene_id":"ENSG00000260254.1","gene_symbol":"AP000997.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115638563,"end":115646962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060971.17","gene_symbol":"ACAA1","gene_name":"acetyl-CoA acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:82]","synonyms":null,"biotype":"protein_coding","ncbi_id":"30","summary":"This gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of this enzyme leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":38103129,"end":38137242,"strand":-1,"description":"acetyl-CoA acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:82]"}, {"versioned_ensembl_gene_id":"ENSG00000085511.19","gene_symbol":"MAP3K4","gene_name":"mitogen-activated protein kinase kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6856]","synonyms":"MTK1,MEKK4,MAPKKK4,KIAA0213","biotype":"protein_coding","ncbi_id":"4216","summary":"The central core of each mitogen-activated protein kinase (MAPK) pathway is a conserved cascade of 3 protein kinases: an activated MAPK kinase kinase (MAPKKK) phosphorylates and activates a specific MAPK kinase (MAPKK), which then activates a specific MAPK. While the ERK MAPKs are activated by mitogenic stimulation, the CSBP2 and JNK MAPKs are activated by environmental stresses such as osmotic shock, UV irradiation, wound stress, and inflammatory factors. This gene encodes a MAPKKK, the MEKK4 protein, also called MTK1. This protein contains a protein kinase catalytic domain at the C terminus. The N-terminal nonkinase domain may contain a regulatory domain. Expression of MEKK4 in mammalian cells activated the CSBP2 and JNK MAPK pathways, but not the ERK pathway. In vitro kinase studies indicated that recombinant MEKK4 can specifically phosphorylate and activate PRKMK6 and SERK1, MAPKKs that activate CSBP2 and JNK, respectively but cannot phosphorylate PRKMK1, an MAPKK that activates ERKs. MEKK4 is a major mediator of environmental stresses that activate the CSBP2 MAPK pathway, and a minor mediator of the JNK pathway. Several alternatively spliced transcripts encoding distinct isoforms have been described. [provided by RefSeq, May 2014]","start":160991727,"end":161117385,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6856]"}, {"versioned_ensembl_gene_id":"ENSG00000124459.11","gene_symbol":"ZNF45","gene_name":"zinc finger protein 45 [Source:HGNC Symbol;Acc:HGNC:13111]","synonyms":"ZNF13","biotype":"protein_coding","ncbi_id":"7596","summary":null,"start":43912629,"end":43935278,"strand":-1,"description":"zinc finger protein 45 [Source:HGNC Symbol;Acc:HGNC:13111]"}, {"versioned_ensembl_gene_id":"ENSG00000164300.16","gene_symbol":"SERINC5","gene_name":"serine incorporator 5 [Source:HGNC Symbol;Acc:HGNC:18825]","synonyms":"TPO1,C5orf12","biotype":"protein_coding","ncbi_id":"256987","summary":null,"start":80111651,"end":80256079,"strand":-1,"description":"serine incorporator 5 [Source:HGNC Symbol;Acc:HGNC:18825]"}, {"versioned_ensembl_gene_id":"ENSG00000120327.6","gene_symbol":"PCDHB14","gene_name":"protocadherin beta 14 [Source:HGNC Symbol;Acc:HGNC:8685]","synonyms":"PCDH-BETA14","biotype":"protein_coding","ncbi_id":"56122","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141222932,"end":141227759,"strand":1,"description":"protocadherin beta 14 [Source:HGNC Symbol;Acc:HGNC:8685]"}, {"versioned_ensembl_gene_id":"ENSG00000230026.2","gene_symbol":"AL357556.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235361153,"end":235362540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255555.1","gene_symbol":"AP000857.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84936689,"end":84955705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254787.1","gene_symbol":"AP001825.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84720826,"end":84800701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255689.1","gene_symbol":"AP003174.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115582297,"end":115600339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125454.11","gene_symbol":"SLC25A19","gene_name":"solute carrier family 25 member 19 [Source:HGNC Symbol;Acc:HGNC:14409]","synonyms":"TPC,MUP1,MCPHA,DNC","biotype":"protein_coding","ncbi_id":"60386","summary":"This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":75272981,"end":75289510,"strand":-1,"description":"solute carrier family 25 member 19 [Source:HGNC Symbol;Acc:HGNC:14409]"}, {"versioned_ensembl_gene_id":"ENSG00000269729.1","gene_symbol":"AC006262.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46163893,"end":46180647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268621.5","gene_symbol":"IGFL2-AS1","gene_name":"IGFL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52559]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645553","summary":null,"start":46189166,"end":46203083,"strand":-1,"description":"IGFL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52559]"}, {"versioned_ensembl_gene_id":"ENSG00000242970.2","gene_symbol":"AC068522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58588420,"end":58588764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235541.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28969118,"end":28970448,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000279935.1","gene_symbol":"AL353611.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134992958,"end":134995854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258203.5","gene_symbol":"AC004801.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48005277,"end":48011227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146006.7","gene_symbol":"LRRTM2","gene_name":"leucine rich repeat transmembrane neuronal 2 [Source:HGNC Symbol;Acc:HGNC:19409]","synonyms":"KIAA0416","biotype":"protein_coding","ncbi_id":"26045","summary":null,"start":138868923,"end":138875368,"strand":-1,"description":"leucine rich repeat transmembrane neuronal 2 [Source:HGNC Symbol;Acc:HGNC:19409]"}, {"versioned_ensembl_gene_id":"ENSG00000188425.3","gene_symbol":"NANOS2","gene_name":"nanos C2HC-type zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:23292]","synonyms":"ZC2HC12B,NOS2","biotype":"protein_coding","ncbi_id":"339345","summary":null,"start":45913214,"end":45914870,"strand":-1,"description":"nanos C2HC-type zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:23292]"}, {"versioned_ensembl_gene_id":"ENSG00000170604.4","gene_symbol":"IRF2BP1","gene_name":"interferon regulatory factor 2 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21728]","synonyms":"DKFZP434M154,IRF-2BP1","biotype":"protein_coding","ncbi_id":"26145","summary":null,"start":45883607,"end":45886170,"strand":-1,"description":"interferon regulatory factor 2 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21728]"}, {"versioned_ensembl_gene_id":"ENSG00000268204.1","gene_symbol":"AC008763.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7633766,"end":7636990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141756.18","gene_symbol":"FKBP10","gene_name":"FK506 binding protein 10 [Source:HGNC Symbol;Acc:HGNC:18169]","synonyms":"hFKBP65,FLJ23833,FLJ22041,FLJ20683,FKBP6","biotype":"protein_coding","ncbi_id":"60681","summary":"The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. This protein localizes to the endoplasmic reticulum and acts as a molecular chaperone. Alternatively spliced variants encoding different isoforms have been reported, but their biological validity has not been determined.[provided by RefSeq, Nov 2009]","start":41812680,"end":41823217,"strand":1,"description":"FK506 binding protein 10 [Source:HGNC Symbol;Acc:HGNC:18169]"}, {"versioned_ensembl_gene_id":"ENSG00000042304.11","gene_symbol":"C2orf83","gene_name":"chromosome 2 open reading frame 83 [Source:HGNC Symbol;Acc:HGNC:25344]","synonyms":"DKFZp547H025","biotype":"protein_coding","ncbi_id":"56918","summary":null,"start":227610090,"end":227648606,"strand":-1,"description":"chromosome 2 open reading frame 83 [Source:HGNC Symbol;Acc:HGNC:25344]"}, {"versioned_ensembl_gene_id":"ENSG00000279825.1","gene_symbol":"AC003957.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19030857,"end":19033529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269800.1","gene_symbol":"PLEKHA3P1","gene_name":"pleckstrin homology domain containing A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19648]","synonyms":"PLEKHA3P","biotype":"processed_pseudogene","ncbi_id":"91405","summary":null,"start":41521043,"end":41521989,"strand":-1,"description":"pleckstrin homology domain containing A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19648]"}, {"versioned_ensembl_gene_id":"ENSG00000188522.14","gene_symbol":"FAM83G","gene_name":"family with sequence similarity 83 member G [Source:HGNC Symbol;Acc:HGNC:32554]","synonyms":"PAWS1,FLJ41564","biotype":"protein_coding","ncbi_id":"644815","summary":null,"start":18968789,"end":19004804,"strand":-1,"description":"family with sequence similarity 83 member G [Source:HGNC Symbol;Acc:HGNC:32554]"}, {"versioned_ensembl_gene_id":"ENSG00000274933.5","gene_symbol":"TBC1D3I","gene_name":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724862","summary":null,"start":36253456,"end":36264553,"strand":-1,"description":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]"}, {"versioned_ensembl_gene_id":"ENSG00000196666.4","gene_symbol":"FAM180B","gene_name":"family with sequence similarity 180 member B [Source:HGNC Symbol;Acc:HGNC:34451]","synonyms":"LOC399888","biotype":"protein_coding","ncbi_id":"399888","summary":null,"start":47586693,"end":47589194,"strand":1,"description":"family with sequence similarity 180 member B [Source:HGNC Symbol;Acc:HGNC:34451]"}, {"versioned_ensembl_gene_id":"ENSG00000249715.11","gene_symbol":"FER1L5","gene_name":"fer-1 like family member 5 [Source:HGNC Symbol;Acc:HGNC:19044]","synonyms":"DKFZp434I0121","biotype":"protein_coding","ncbi_id":"90342","summary":null,"start":96642737,"end":96704887,"strand":1,"description":"fer-1 like family member 5 [Source:HGNC Symbol;Acc:HGNC:19044]"}, {"versioned_ensembl_gene_id":"ENSG00000251366.1","gene_symbol":"DBIP2","gene_name":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2691]","synonyms":"DBIL1","biotype":"processed_pseudogene","ncbi_id":"1623","summary":null,"start":80603383,"end":80603644,"strand":-1,"description":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2691]"}, {"versioned_ensembl_gene_id":"ENSG00000278395.1","gene_symbol":"AC243829.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36241701,"end":36241806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278097.1","gene_symbol":"AC243829.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36225246,"end":36226807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253665.1","gene_symbol":"AC022733.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40114651,"end":40127468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103356.15","gene_symbol":"EARS2","gene_name":"glutamyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29419]","synonyms":"MSE1,KIAA1970","biotype":"protein_coding","ncbi_id":"124454","summary":"This gene encodes a member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of glutamate to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 12 (COXPD12). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":23522014,"end":23557731,"strand":-1,"description":"glutamyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29419]"}, {"versioned_ensembl_gene_id":"ENSG00000124098.9","gene_symbol":"FAM210B","gene_name":"family with sequence similarity 210 member B [Source:HGNC Symbol;Acc:HGNC:16102]","synonyms":"DKFZP434A1114,dJ1167H4.1,C20orf108","biotype":"protein_coding","ncbi_id":"116151","summary":null,"start":56358915,"end":56368663,"strand":1,"description":"family with sequence similarity 210 member B [Source:HGNC Symbol;Acc:HGNC:16102]"}, {"versioned_ensembl_gene_id":"ENSG00000114982.17","gene_symbol":"KANSL3","gene_name":"KAT8 regulatory NSL complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25473]","synonyms":"Rcd1,NSL3,KIAA1310,FLJ10081","biotype":"protein_coding","ncbi_id":"55683","summary":null,"start":96593170,"end":96642787,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25473]"}, {"versioned_ensembl_gene_id":"ENSG00000253839.1","gene_symbol":"AC013546.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136489448,"end":136529876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000061455.10","gene_symbol":"PRDM6","gene_name":"PR/SET domain 6 [Source:HGNC Symbol;Acc:HGNC:9350]","synonyms":"PRISM,KMT8C","biotype":"protein_coding","ncbi_id":"93166","summary":"The protein encoded by this gene is a transcriptional repressor and a member of the PRDM family. Family members contain a PR domain and multiple zinc-finger domains. The encoded protein is involved in regulation of vascular smooth muscle cells (VSMC) contractile proteins. Mutations in this gene result in patent ductus arteriosus 3 (PDA3). [provided by RefSeq, Apr 2017]","start":123089121,"end":123194266,"strand":1,"description":"PR/SET domain 6 [Source:HGNC Symbol;Acc:HGNC:9350]"}, {"versioned_ensembl_gene_id":"ENSG00000276434.1","gene_symbol":"AL136221.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113339450,"end":113339958,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233581.1","gene_symbol":"AC069155.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216303325,"end":216321737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230843.1","gene_symbol":"AL139824.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56295967,"end":56299160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234750.1","gene_symbol":"AC012618.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12284337,"end":12285185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260804.3","gene_symbol":"LINC01963","gene_name":"long intergenic non-protein coding RNA 1963 [Source:HGNC Symbol;Acc:HGNC:25283]","synonyms":"DKFZp434H1419","biotype":"lincRNA","ncbi_id":"150967","summary":null,"start":216217045,"end":216220192,"strand":1,"description":"long intergenic non-protein coding RNA 1963 [Source:HGNC Symbol;Acc:HGNC:25283]"}, {"versioned_ensembl_gene_id":"ENSG00000274563.1","gene_symbol":"GU182343.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54766539,"end":54781397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186834.3","gene_symbol":"HEXIM1","gene_name":"hexamethylene bisacetamide inducible 1 [Source:HGNC Symbol;Acc:HGNC:24953]","synonyms":"MAQ1,HIS1,EDG1,CLP-1","biotype":"protein_coding","ncbi_id":"10614","summary":"Expression of this gene is induced by hexamethylene-bis-acetamide in vascular smooth muscle cells. This gene has no introns. [provided by RefSeq, Jul 2008]","start":45148502,"end":45152101,"strand":1,"description":"hexamethylene bisacetamide inducible 1 [Source:HGNC Symbol;Acc:HGNC:24953]"}, {"versioned_ensembl_gene_id":"ENSG00000272102.1","gene_symbol":"AL133406.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105273220,"end":105273760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249290.5","gene_symbol":"AC010181.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140449435,"end":140460351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248991.1","gene_symbol":"AC097375.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151919468,"end":151943933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232895.2","gene_symbol":"AL121999.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114206427,"end":114262278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253957.1","gene_symbol":"IGHV3-22","gene_name":"immunoglobulin heavy variable 3-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5587]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28443","summary":null,"start":106257762,"end":106258223,"strand":-1,"description":"immunoglobulin heavy variable 3-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5587]"}, {"versioned_ensembl_gene_id":"ENSG00000211923.1","gene_symbol":"IGHD3-10","gene_name":"immunoglobulin heavy diversity 3-10 [Source:HGNC Symbol;Acc:HGNC:5495]","synonyms":"DXP'1,IGHD310","biotype":"IG_D_gene","ncbi_id":"28499","summary":null,"start":105904497,"end":105904527,"strand":-1,"description":"immunoglobulin heavy diversity 3-10 [Source:HGNC Symbol;Acc:HGNC:5495]"}, {"versioned_ensembl_gene_id":"ENSG00000160336.14","gene_symbol":"ZNF761","gene_name":"zinc finger protein 761 [Source:HGNC Symbol;Acc:HGNC:23179]","synonyms":"KIAA2033,FLJ35333,FLJ16231","biotype":"protein_coding","ncbi_id":"388561","summary":null,"start":53431993,"end":53458261,"strand":1,"description":"zinc finger protein 761 [Source:HGNC Symbol;Acc:HGNC:23179]"}, {"versioned_ensembl_gene_id":"ENSG00000167004.12","gene_symbol":"PDIA3","gene_name":"protein disulfide isomerase family A member 3 [Source:HGNC Symbol;Acc:HGNC:4606]","synonyms":"PI-PLC,P58,HsT17083,GRP58,GRP57,ERp61,ERp60,ERp57","biotype":"protein_coding","ncbi_id":"2923","summary":"This gene encodes a protein of the endoplasmic reticulum that interacts with lectin chaperones calreticulin and calnexin to modulate folding of newly synthesized glycoproteins. The protein was once thought to be a phospholipase; however, it has been demonstrated that the protein actually has protein disulfide isomerase activity. It is thought that complexes of lectins and this protein mediate protein folding by promoting formation of disulfide bonds in their glycoprotein substrates. This protein also functions as a molecular chaperone that prevents the formation of protein aggregates. [provided by RefSeq, Dec 2016]","start":43746392,"end":43773279,"strand":1,"description":"protein disulfide isomerase family A member 3 [Source:HGNC Symbol;Acc:HGNC:4606]"}, {"versioned_ensembl_gene_id":"ENSG00000211947.2","gene_symbol":"IGHV3-21","gene_name":"immunoglobulin heavy variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5586]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28444","summary":null,"start":106235064,"end":106235594,"strand":-1,"description":"immunoglobulin heavy variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5586]"}, {"versioned_ensembl_gene_id":"ENSG00000249906.1","gene_symbol":"AC006487.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49505657,"end":49574064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180219.1","gene_symbol":"FAM71C","gene_name":"family with sequence similarity 71 member C [Source:HGNC Symbol;Acc:HGNC:28594]","synonyms":"MGC39520","biotype":"protein_coding","ncbi_id":"196472","summary":null,"start":99647753,"end":99650046,"strand":1,"description":"family with sequence similarity 71 member C [Source:HGNC Symbol;Acc:HGNC:28594]"}, {"versioned_ensembl_gene_id":"ENSG00000205771.6","gene_symbol":"CATSPER2P1","gene_name":"cation channel sperm associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31054]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440278","summary":"Catsper genes belong to a family of putative cation channels that are specific to spermatozoa and localize to the flagellum. This gene is part of a tandem repeat on chromosome 15q15; this copy of the gene is thought to be a pseudogene. [provided by RefSeq, Oct 2008]","start":43726918,"end":43747094,"strand":-1,"description":"cation channel sperm associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31054]"}, {"versioned_ensembl_gene_id":"ENSG00000230048.8","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"NG37,G7c,C6orf27","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31747771,"end":31759475,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000064300.8","gene_symbol":"NGFR","gene_name":"nerve growth factor receptor [Source:HGNC Symbol;Acc:HGNC:7809]","synonyms":"TNFRSF16,p75NTR,CD271","biotype":"protein_coding","ncbi_id":"4804","summary":"Nerve growth factor receptor contains an extracellular domain containing four 40-amino acid repeats with 6 cysteine residues at conserved positions followed by a serine/threonine-rich region, a single transmembrane domain, and a 155-amino acid cytoplasmic domain. The cysteine-rich region contains the nerve growth factor binding domain. [provided by RefSeq, Jul 2008]","start":49495293,"end":49515017,"strand":1,"description":"nerve growth factor receptor [Source:HGNC Symbol;Acc:HGNC:7809]"}, {"versioned_ensembl_gene_id":"ENSG00000163518.10","gene_symbol":"FCRL4","gene_name":"Fc receptor like 4 [Source:HGNC Symbol;Acc:HGNC:18507]","synonyms":"IRTA1,IGFP2,FCRH4,CD307d","biotype":"protein_coding","ncbi_id":"83417","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein has four extracellular C2-type immunoglobulin domains, a transmembrane domain and a cytoplasmic domain that contains three immune-receptor tyrosine-based inhibitory motifs. This protein may play a role in the function of memory B-cells in the epithelia. Aberrations in the chromosomal region encoding this gene are associated with non-Hodgkin lymphoma and multiple myeloma. [provided by RefSeq, Apr 2009]","start":157573749,"end":157598080,"strand":-1,"description":"Fc receptor like 4 [Source:HGNC Symbol;Acc:HGNC:18507]"}, {"versioned_ensembl_gene_id":"ENSG00000171357.5","gene_symbol":"LURAP1","gene_name":"leucine rich adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:32327]","synonyms":"LRAP35a,FLJ25163,C1orf190","biotype":"protein_coding","ncbi_id":"541468","summary":null,"start":46203334,"end":46221261,"strand":1,"description":"leucine rich adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:32327]"}, {"versioned_ensembl_gene_id":"ENSG00000245261.1","gene_symbol":"AL133375.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43213801,"end":43223860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132740.8","gene_symbol":"IGHMBP2","gene_name":"immunoglobulin mu binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5542]","synonyms":"HMN6,HCSA,CMT2S,CATF1,ZFAND7,SMUBP2,SMARD1","biotype":"protein_coding","ncbi_id":"3508","summary":"This gene encodes a helicase superfamily member that binds a specific DNA sequence from the immunoglobulin mu chain switch region. Mutations in this gene lead to spinal muscle atrophy with respiratory distress type 1. [provided by RefSeq, Jul 2008]","start":68903842,"end":68940602,"strand":1,"description":"immunoglobulin mu binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5542]"}, {"versioned_ensembl_gene_id":"ENSG00000225129.1","gene_symbol":"AL035250.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59352195,"end":59357774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147099.19","gene_symbol":"HDAC8","gene_name":"histone deacetylase 8 [Source:HGNC Symbol;Acc:HGNC:13315]","synonyms":"WTS,RPD3,MRXS6,HDACL1","biotype":"protein_coding","ncbi_id":"55869","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class I of the histone deacetylase family. It catalyzes the deacetylation of lysine residues in the histone N-terminal tails and represses transcription in large multiprotein complexes with transcriptional co-repressors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":72329516,"end":72573103,"strand":-1,"description":"histone deacetylase 8 [Source:HGNC Symbol;Acc:HGNC:13315]"}, {"versioned_ensembl_gene_id":"ENSG00000172350.9","gene_symbol":"ABCG4","gene_name":"ATP binding cassette subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:13884]","synonyms":"WHITE2","biotype":"protein_coding","ncbi_id":"64137","summary":"The protein encoded by this gene is a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). The encoded protein is a member of the White subfamily and plays an important role in cellular cholesterol homeostasis. This protein functions as either a homodimer or as a heterodimer with another ABC subfamily protein such as ABCG1. [provided by RefSeq, Jan 2017]","start":119149012,"end":119162653,"strand":1,"description":"ATP binding cassette subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:13884]"}, {"versioned_ensembl_gene_id":"ENSG00000164402.13","gene_symbol":"SEPT8","gene_name":"septin 8 [Source:HGNC Symbol;Acc:HGNC:16511]","synonyms":"SEP2,KIAA0202","biotype":"protein_coding","ncbi_id":"23176","summary":"This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":132750817,"end":132807241,"strand":-1,"description":"septin 8 [Source:HGNC Symbol;Acc:HGNC:16511]"}, {"versioned_ensembl_gene_id":"ENSG00000085871.8","gene_symbol":"MGST2","gene_name":"microsomal glutathione S-transferase 2 [Source:HGNC Symbol;Acc:HGNC:7063]","synonyms":"MGST-II","biotype":"protein_coding","ncbi_id":"4258","summary":"The MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family consists of six human proteins, several of which are involved in the production of leukotrienes and prostaglandin E, important mediators of inflammation. This gene encodes a protein which catalyzes the conjugation of leukotriene A4 and reduced glutathione to produce leukotriene C4. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2011]","start":139665768,"end":139740745,"strand":1,"description":"microsomal glutathione S-transferase 2 [Source:HGNC Symbol;Acc:HGNC:7063]"}, {"versioned_ensembl_gene_id":"ENSG00000211918.1","gene_symbol":"IGHD2-15","gene_name":"immunoglobulin heavy diversity 2-15 [Source:HGNC Symbol;Acc:HGNC:5489]","synonyms":"IGHD215,D2","biotype":"IG_D_gene","ncbi_id":"28503","summary":null,"start":105897957,"end":105897987,"strand":-1,"description":"immunoglobulin heavy diversity 2-15 [Source:HGNC Symbol;Acc:HGNC:5489]"}, {"versioned_ensembl_gene_id":"ENSG00000276044.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54833799,"end":54844782,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000254048.1","gene_symbol":"AC105150.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58991720,"end":58992938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227326.2","gene_symbol":"BX005428.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29800695,"end":29801491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085998.13","gene_symbol":"POMGNT1","gene_name":"protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) [Source:HGNC Symbol;Acc:HGNC:19139]","synonyms":"MGAT1.2,MEB,LGMD2O,FLJ20277","biotype":"protein_coding","ncbi_id":"55624","summary":"This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":46188682,"end":46220305,"strand":-1,"description":"protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) [Source:HGNC Symbol;Acc:HGNC:19139]"}, {"versioned_ensembl_gene_id":"ENSG00000124780.13","gene_symbol":"KCNK17","gene_name":"potassium two pore domain channel subfamily K member 17 [Source:HGNC Symbol;Acc:HGNC:14465]","synonyms":"TALK-2,K2p17.1,TASK4,TASK-4,TALK2","biotype":"protein_coding","ncbi_id":"89822","summary":"The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations. This gene is activated at alkaline pH. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":39299001,"end":39314553,"strand":-1,"description":"potassium two pore domain channel subfamily K member 17 [Source:HGNC Symbol;Acc:HGNC:14465]"}, {"versioned_ensembl_gene_id":"ENSG00000100697.14","gene_symbol":"DICER1","gene_name":"dicer 1, ribonuclease III [Source:HGNC Symbol;Acc:HGNC:17098]","synonyms":"MNG1,KIAA0928,K12H4.8-LIKE,HERNA,Dicer","biotype":"protein_coding","ncbi_id":"23405","summary":"This gene encodes a protein possessing an RNA helicase motif containing a DEXH box in its amino terminus and an RNA motif in the carboxy terminus. The encoded protein functions as a ribonuclease and is required by the RNA interference and small temporal RNA (stRNA) pathways to produce the active small RNA component that represses gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":95086228,"end":95158010,"strand":-1,"description":"dicer 1, ribonuclease III [Source:HGNC Symbol;Acc:HGNC:17098]"}, {"versioned_ensembl_gene_id":"ENSG00000260221.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"dJ377H14.3,C6orf101,HLA-90","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29797915,"end":29799945,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000149179.13","gene_symbol":"C11orf49","gene_name":"chromosome 11 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28720]","synonyms":"MGC4707,FLJ22210","biotype":"protein_coding","ncbi_id":"79096","summary":null,"start":46936689,"end":47164385,"strand":1,"description":"chromosome 11 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28720]"}, {"versioned_ensembl_gene_id":"ENSG00000139890.9","gene_symbol":"REM2","gene_name":"RRAD and GEM like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:20248]","synonyms":"FLJ38964","biotype":"protein_coding","ncbi_id":"161253","summary":null,"start":22883165,"end":22887686,"strand":1,"description":"RRAD and GEM like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:20248]"}, {"versioned_ensembl_gene_id":"ENSG00000100292.16","gene_symbol":"HMOX1","gene_name":"heme oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:5013]","synonyms":"HO-1,bK286B10","biotype":"protein_coding","ncbi_id":"3162","summary":"Heme oxygenase, an essential enzyme in heme catabolism, cleaves heme to form biliverdin, which is subsequently converted to bilirubin by biliverdin reductase, and carbon monoxide, a putative neurotransmitter. Heme oxygenase activity is induced by its substrate heme and by various nonheme substances. Heme oxygenase occurs as 2 isozymes, an inducible heme oxygenase-1 and a constitutive heme oxygenase-2. HMOX1 and HMOX2 belong to the heme oxygenase family. [provided by RefSeq, Jul 2008]","start":35380361,"end":35394214,"strand":1,"description":"heme oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:5013]"}, {"versioned_ensembl_gene_id":"ENSG00000282041.1","gene_symbol":"Z82244.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35376422,"end":35377261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116350.16","gene_symbol":"SRSF4","gene_name":"serine and arginine rich splicing factor 4 [Source:HGNC Symbol;Acc:HGNC:10786]","synonyms":"SRP75,SFRS4","biotype":"protein_coding","ncbi_id":"6429","summary":"This gene encodes a member of the arginine/serine-rich splicing factor family. The encoded protein likely functions in mRNA processing. [provided by RefSeq, Feb 2009]","start":29147743,"end":29181987,"strand":-1,"description":"serine and arginine rich splicing factor 4 [Source:HGNC Symbol;Acc:HGNC:10786]"}, {"versioned_ensembl_gene_id":"ENSG00000111450.13","gene_symbol":"STX2","gene_name":"syntaxin 2 [Source:HGNC Symbol;Acc:HGNC:3403]","synonyms":"STX2C,STX2B,STX2A,EPM,EPIM","biotype":"protein_coding","ncbi_id":"2054","summary":"The product of this gene belongs to the syntaxin/epimorphin family of proteins. The syntaxins are a large protein family implicated in the targeting and fusion of intracellular transport vesicles. The product of this gene regulates epithelial-mesenchymal interactions and epithelial cell morphogenesis and activation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":130789600,"end":130839266,"strand":-1,"description":"syntaxin 2 [Source:HGNC Symbol;Acc:HGNC:3403]"}, {"versioned_ensembl_gene_id":"ENSG00000157426.13","gene_symbol":"AASDH","gene_name":"aminoadipate-semialdehyde dehydrogenase [Source:HGNC Symbol;Acc:HGNC:23993]","synonyms":"NRPS998,LYS2,ACSF4","biotype":"protein_coding","ncbi_id":"132949","summary":"This gene encodes a member of the non-ribosome peptide syntesase (NRPS) enzyme family. The encoded protein contains an AMP-binding domain, PP-binding (phosphopantetheine, or pantetheine 4'phosphate-binding) domain and the Pyrrolo-quinoline quinon (PQQ) binding domain. The protein is expressed in several adult tissues. [provided by RefSeq, Apr 2016]","start":56338287,"end":56387508,"strand":-1,"description":"aminoadipate-semialdehyde dehydrogenase [Source:HGNC Symbol;Acc:HGNC:23993]"}, {"versioned_ensembl_gene_id":"ENSG00000147400.8","gene_symbol":"CETN2","gene_name":"centrin 2 [Source:HGNC Symbol;Acc:HGNC:1867]","synonyms":"CEN2,CALT","biotype":"protein_coding","ncbi_id":"1069","summary":" Caltractin belongs to a family of calcium-binding proteins and is a structural component of the centrosome. The high level of conservation from algae to humans and its association with the centrosome suggested that caltractin plays a fundamental role in the structure and function of the microtubule-organizing center, possibly required for the proper duplication and segregation of the centrosome. [provided by RefSeq, Jul 2008]","start":152826973,"end":152830777,"strand":-1,"description":"centrin 2 [Source:HGNC Symbol;Acc:HGNC:1867]"}, {"versioned_ensembl_gene_id":"ENSG00000148935.10","gene_symbol":"GAS2","gene_name":"growth arrest specific 2 [Source:HGNC Symbol;Acc:HGNC:4167]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2620","summary":"The protein encoded by this gene is a caspase-3 substrate that plays a role in regulating microfilament and cell shape changes during apoptosis. It can also modulate cell susceptibility to p53-dependent apoptosis by inhibiting calpain activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2017]","start":22625642,"end":22813055,"strand":1,"description":"growth arrest specific 2 [Source:HGNC Symbol;Acc:HGNC:4167]"}, {"versioned_ensembl_gene_id":"ENSG00000112419.14","gene_symbol":"PHACTR2","gene_name":"phosphatase and actin regulator 2 [Source:HGNC Symbol;Acc:HGNC:20956]","synonyms":"KIAA0680,C6orf56","biotype":"protein_coding","ncbi_id":"9749","summary":null,"start":143536845,"end":143831185,"strand":1,"description":"phosphatase and actin regulator 2 [Source:HGNC Symbol;Acc:HGNC:20956]"}, {"versioned_ensembl_gene_id":"ENSG00000126261.12","gene_symbol":"UBA2","gene_name":"ubiquitin like modifier activating enzyme 2 [Source:HGNC Symbol;Acc:HGNC:30661]","synonyms":"SAE2,HRIHFB2115,FLJ13058,ARX","biotype":"protein_coding","ncbi_id":"10054","summary":"Posttranslational modification of proteins by the addition of the small protein SUMO (see SUMO1; MIM 601912), or sumoylation, regulates protein structure and intracellular localization. SAE1 (MIM 613294) and UBA2 form a heterodimer that functions as a SUMO-activating enzyme for the sumoylation of proteins (Okuma et al., 1999 [PubMed 9920803]).[supplied by OMIM, Mar 2010]","start":34428352,"end":34471251,"strand":1,"description":"ubiquitin like modifier activating enzyme 2 [Source:HGNC Symbol;Acc:HGNC:30661]"}, {"versioned_ensembl_gene_id":"ENSG00000135521.8","gene_symbol":"LTV1","gene_name":"LTV1 ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:21173]","synonyms":"FLJ14909,dJ468K18.4,C6orf93","biotype":"protein_coding","ncbi_id":"84946","summary":null,"start":143843344,"end":143863812,"strand":1,"description":"LTV1 ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:21173]"}, {"versioned_ensembl_gene_id":"ENSG00000235166.7","gene_symbol":"LINC01440","gene_name":"long intergenic non-protein coding RNA 1440 [Source:HGNC Symbol;Acc:HGNC:50762]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723578","summary":null,"start":55408898,"end":55482777,"strand":1,"description":"long intergenic non-protein coding RNA 1440 [Source:HGNC Symbol;Acc:HGNC:50762]"}, {"versioned_ensembl_gene_id":"ENSG00000185896.10","gene_symbol":"LAMP1","gene_name":"lysosomal associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:6499]","synonyms":"CD107a","biotype":"protein_coding","ncbi_id":"3916","summary":"The protein encoded by this gene is a member of a family of membrane glycoproteins. This glycoprotein provides selectins with carbohydrate ligands. It may also play a role in tumor cell metastasis. [provided by RefSeq, Jul 2008]","start":113297241,"end":113323672,"strand":1,"description":"lysosomal associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:6499]"}, {"versioned_ensembl_gene_id":"ENSG00000140025.15","gene_symbol":"EFCAB11","gene_name":"EF-hand calcium binding domain 11 [Source:HGNC Symbol;Acc:HGNC:20357]","synonyms":"C14orf143","biotype":"protein_coding","ncbi_id":"90141","summary":null,"start":89794669,"end":89954777,"strand":-1,"description":"EF-hand calcium binding domain 11 [Source:HGNC Symbol;Acc:HGNC:20357]"}, {"versioned_ensembl_gene_id":"ENSG00000124205.15","gene_symbol":"EDN3","gene_name":"endothelin 3 [Source:HGNC Symbol;Acc:HGNC:3178]","synonyms":"ET3","biotype":"protein_coding","ncbi_id":"1908","summary":"The protein encoded by this gene is a member of the endothelin family. Endothelins are endothelium-derived vasoactive peptides involved in a variety of biological functions. The active form of this protein is a 21 amino acid peptide processed from the precursor protein. The active peptide is a ligand for endothelin receptor type B (EDNRB). The interaction of this endothelin with EDNRB is essential for development of neural crest-derived cell lineages, such as melanocytes and enteric neurons. Mutations in this gene and EDNRB have been associated with Hirschsprung disease (HSCR) and Waardenburg syndrome (WS), which are congenital disorders involving neural crest-derived cells. Altered expression of this gene is implicated in tumorigenesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":59300427,"end":59325992,"strand":1,"description":"endothelin 3 [Source:HGNC Symbol;Acc:HGNC:3178]"}, {"versioned_ensembl_gene_id":"ENSG00000277801.1","gene_symbol":"AL138478.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89156743,"end":89157574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133265.10","gene_symbol":"HSPBP1","gene_name":"HSPA (Hsp70) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24989]","synonyms":"FES1,HspBP1","biotype":"protein_coding","ncbi_id":"23640","summary":null,"start":55262231,"end":55280381,"strand":-1,"description":"HSPA (Hsp70) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24989]"}, {"versioned_ensembl_gene_id":"ENSG00000256660.5","gene_symbol":"CLEC12B","gene_name":"C-type lectin domain family 12 member B [Source:HGNC Symbol;Acc:HGNC:31966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387837","summary":null,"start":10010627,"end":10018619,"strand":1,"description":"C-type lectin domain family 12 member B [Source:HGNC Symbol;Acc:HGNC:31966]"}, {"versioned_ensembl_gene_id":"ENSG00000259053.1","gene_symbol":"AL137230.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":89412312,"end":89954659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259151.2","gene_symbol":"CAP2P1","gene_name":"cyclase associated actin cytoskeleton regulatory protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20142]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"353163","summary":null,"start":89290205,"end":89291594,"strand":-1,"description":"cyclase associated actin cytoskeleton regulatory protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20142]"}, {"versioned_ensembl_gene_id":"ENSG00000255434.1","gene_symbol":"AP001922.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75596144,"end":75597270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271494.1","gene_symbol":"AC034205.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151380341,"end":151382381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258792.4","gene_symbol":"AL137230.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89628921,"end":89642671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246090.6","gene_symbol":"AP002026.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99088857,"end":99301356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249065.2","gene_symbol":"PCNAP1","gene_name":"proliferating cell nuclear antigen pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8732]","synonyms":"p1PCNA","biotype":"transcribed_processed_pseudogene","ncbi_id":"359806","summary":null,"start":99160514,"end":99161645,"strand":-1,"description":"proliferating cell nuclear antigen pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8732]"}, {"versioned_ensembl_gene_id":"ENSG00000144747.15","gene_symbol":"TMF1","gene_name":"TATA element modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:11870]","synonyms":"TMF,ARA160","biotype":"protein_coding","ncbi_id":"7110","summary":null,"start":69019827,"end":69052303,"strand":-1,"description":"TATA element modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:11870]"}, {"versioned_ensembl_gene_id":"ENSG00000213777.5","gene_symbol":"AC011487.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53503392,"end":53512687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274892.1","gene_symbol":"AC011487.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53512092,"end":53512616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144339.11","gene_symbol":"TMEFF2","gene_name":"transmembrane protein with EGF like and two follistatin like domains 2 [Source:HGNC Symbol;Acc:HGNC:11867]","synonyms":"TR,TPEF,TENB2,HPP1,CT120.2","biotype":"protein_coding","ncbi_id":"23671","summary":"This gene encodes a member of the tomoregulin family of transmembrane proteins. This protein has been shown to function as both an oncogene and a tumor suppressor depending on the cellular context and may regulate prostate cancer cell invasion. Multiple soluble forms of this protein have been identified that arise from both an alternative splice variant and ectodomain shedding. Additionally, this gene has been found to be hypermethylated in multiple cancer types. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":191949043,"end":192195709,"strand":-1,"description":"transmembrane protein with EGF like and two follistatin like domains 2 [Source:HGNC Symbol;Acc:HGNC:11867]"}, {"versioned_ensembl_gene_id":"ENSG00000148156.7","gene_symbol":"ACTL7B","gene_name":"actin like 7B [Source:HGNC Symbol;Acc:HGNC:162]","synonyms":"Tact1","biotype":"protein_coding","ncbi_id":"10880","summary":"The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":108854589,"end":108856967,"strand":-1,"description":"actin like 7B [Source:HGNC Symbol;Acc:HGNC:162]"}, {"versioned_ensembl_gene_id":"ENSG00000259216.2","gene_symbol":"AC084757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48725338,"end":48725827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259700.3","gene_symbol":"AC012379.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":48810701,"end":48811909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204007.6","gene_symbol":"GLT6D1","gene_name":"glycosyltransferase 6 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23671]","synonyms":"GLTDC1","biotype":"protein_coding","ncbi_id":"360203","summary":"The GT6 glycosyltransferases gene family, which includes the ABO blood group (ABO; MIM 110300) and GLT6D1, shows a complex evolution pattern, with multiple events of gain and loss in different mammal species. In humans, the ABO gene is considered the sole functional member, although the O allele is null and is fixed in certain populations (summary by Casals et al. (2009) [PubMed 19218399]).[supplied by OMIM, Jan 2011]","start":135623656,"end":135639540,"strand":-1,"description":"glycosyltransferase 6 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23671]"}, {"versioned_ensembl_gene_id":"ENSG00000168497.4","gene_symbol":"CAVIN2","gene_name":"caveolae associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10690]","synonyms":"SDR,SDPR,PS-p68,cavin-2","biotype":"protein_coding","ncbi_id":"8436","summary":"This gene encodes a calcium-independent phospholipid-binding protein whose expression increases in serum-starved cells. This protein is a substrate for protein kinase C (PKC) phosphorylation and recruits polymerase I and transcript release factor (PTRF) to caveolae. Removal of this protein causes caveolae loss and its over-expression results in caveolae deformation and membrane tubulation.[provided by RefSeq, Sep 2009]","start":191834302,"end":191847255,"strand":-1,"description":"caveolae associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10690]"}, {"versioned_ensembl_gene_id":"ENSG00000231678.2","gene_symbol":"AL358779.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108701370,"end":108703092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169253.3","gene_symbol":"AL669983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108626833,"end":108627150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233655.1","gene_symbol":"IGHD4-4","gene_name":"immunoglobulin heavy diversity 4-4 [Source:HGNC Symbol;Acc:HGNC:5505]","synonyms":"IGHD44,DA4","biotype":"IG_D_gene","ncbi_id":"28496","summary":null,"start":105913222,"end":105913237,"strand":-1,"description":"immunoglobulin heavy diversity 4-4 [Source:HGNC Symbol;Acc:HGNC:5505]"}, {"versioned_ensembl_gene_id":"ENSG00000236543.2","gene_symbol":"AL354761.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":135604345,"end":135618952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228131.1","gene_symbol":"IGHD6-6","gene_name":"immunoglobulin heavy diversity 6-6 [Source:HGNC Symbol;Acc:HGNC:5517]","synonyms":"IGHD66,D(N4)","biotype":"IG_D_gene","ncbi_id":"28488","summary":null,"start":105910410,"end":105910427,"strand":-1,"description":"immunoglobulin heavy diversity 6-6 [Source:HGNC Symbol;Acc:HGNC:5517]"}, {"versioned_ensembl_gene_id":"ENSG00000233766.7","gene_symbol":"AC098617.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":191846539,"end":192044525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132429.9","gene_symbol":"POPDC3","gene_name":"popeye domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17649]","synonyms":"MGC22671,bA355M14.1,POP3","biotype":"protein_coding","ncbi_id":"64208","summary":"This gene encodes a member of the POP family of proteins containing three putative transmembrane domains. This gene is expressed in cardiac and skeletal muscle and may play an important role in these tissues during development. Alternatively spliced transcript variants have been found. [provided by RefSeq, Nov 2008]","start":105158280,"end":105179995,"strand":-1,"description":"popeye domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17649]"}, {"versioned_ensembl_gene_id":"ENSG00000277632.1","gene_symbol":"CCL3","gene_name":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]","synonyms":"SCYA3,MIP-1-alpha,LD78ALPHA,G0S19-1","biotype":"protein_coding","ncbi_id":"6348","summary":"This locus represents a small inducible cytokine. The encoded protein, also known as macrophage inflammatory protein 1 alpha, plays a role in inflammatory responses through binding to the receptors CCR1, CCR4 and CCR5. Polymorphisms at this locus may be associated with both resistance and susceptibility to infection by human immunodeficiency virus type 1.[provided by RefSeq, Sep 2010]","start":36088256,"end":36090169,"strand":-1,"description":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]"}, {"versioned_ensembl_gene_id":"ENSG00000132470.13","gene_symbol":"ITGB4","gene_name":"integrin subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:6158]","synonyms":"CD104","biotype":"protein_coding","ncbi_id":"3691","summary":"Integrins are heterodimers comprised of alpha and beta subunits, that are noncovalently associated transmembrane glycoprotein receptors. Different combinations of alpha and beta polypeptides form complexes that vary in their ligand-binding specificities. Integrins mediate cell-matrix or cell-cell adhesion, and transduced signals that regulate gene expression and cell growth. This gene encodes the integrin beta 4 subunit, a receptor for the laminins. This subunit tends to associate with alpha 6 subunit and is likely to play a pivotal role in the biology of invasive carcinoma. Mutations in this gene are associated with epidermolysis bullosa with pyloric atresia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75721328,"end":75757818,"strand":1,"description":"integrin subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:6158]"}, {"versioned_ensembl_gene_id":"ENSG00000166763.7","gene_symbol":"STRCP1","gene_name":"stereocilin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33915]","synonyms":"STRCP","biotype":"unprocessed_pseudogene","ncbi_id":"554225","summary":null,"start":43699488,"end":43718184,"strand":-1,"description":"stereocilin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33915]"}, {"versioned_ensembl_gene_id":"ENSG00000237339.5","gene_symbol":"LINC01502","gene_name":"long intergenic non-protein coding RNA 1502 [Source:HGNC Symbol;Acc:HGNC:51183]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100130954","summary":null,"start":135574935,"end":135587112,"strand":1,"description":"long intergenic non-protein coding RNA 1502 [Source:HGNC Symbol;Acc:HGNC:51183]"}, {"versioned_ensembl_gene_id":"ENSG00000229887.4","gene_symbol":"HNRNPA1P6","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:5032]","synonyms":"HNRPA1L,HNRNPA1L1,HNRNPA1L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729423","summary":null,"start":58047889,"end":58049335,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:5032]"}, {"versioned_ensembl_gene_id":"ENSG00000277089.4","gene_symbol":"AC243829.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36072866,"end":36090134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261118.1","gene_symbol":"AC092123.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89492017,"end":89504460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225231.1","gene_symbol":"LINC02470","gene_name":"long intergenic non-protein coding RNA 2470 [Source:HGNC Symbol;Acc:HGNC:53409]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506159","summary":null,"start":9936579,"end":9943495,"strand":-1,"description":"long intergenic non-protein coding RNA 2470 [Source:HGNC Symbol;Acc:HGNC:53409]"}, {"versioned_ensembl_gene_id":"ENSG00000261517.1","gene_symbol":"LINC00558","gene_name":"long intergenic non-protein coding RNA 558 [Source:HGNC Symbol;Acc:HGNC:43702]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861552","summary":null,"start":53815419,"end":53876119,"strand":1,"description":"long intergenic non-protein coding RNA 558 [Source:HGNC Symbol;Acc:HGNC:43702]"}, {"versioned_ensembl_gene_id":"ENSG00000198346.10","gene_symbol":"ZNF813","gene_name":"zinc finger protein 813 [Source:HGNC Symbol;Acc:HGNC:33257]","synonyms":"FLJ16542","biotype":"protein_coding","ncbi_id":"126017","summary":null,"start":53467735,"end":53496255,"strand":1,"description":"zinc finger protein 813 [Source:HGNC Symbol;Acc:HGNC:33257]"}, {"versioned_ensembl_gene_id":"ENSG00000255357.1","gene_symbol":"AC055878.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22492112,"end":22502846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230936.1","gene_symbol":"AC073347.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55342316,"end":55344958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242076.2","gene_symbol":"IGKV1-33","gene_name":"immunoglobulin kappa variable 1-33 [Source:HGNC Symbol;Acc:HGNC:5737]","synonyms":"IGKV133,O18","biotype":"IG_V_gene","ncbi_id":"28933","summary":null,"start":89266494,"end":89268506,"strand":-1,"description":"immunoglobulin kappa variable 1-33 [Source:HGNC Symbol;Acc:HGNC:5737]"}, {"versioned_ensembl_gene_id":"ENSG00000241434.1","gene_symbol":"AC022137.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53495887,"end":53496037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255323.5","gene_symbol":"LINC01495","gene_name":"long intergenic non-protein coding RNA 1495 [Source:HGNC Symbol;Acc:HGNC:51161]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723378","summary":null,"start":22445688,"end":22492019,"strand":-1,"description":"long intergenic non-protein coding RNA 1495 [Source:HGNC Symbol;Acc:HGNC:51161]"}, {"versioned_ensembl_gene_id":"ENSG00000198099.8","gene_symbol":"ADH4","gene_name":"alcohol dehydrogenase 4 (class II), pi polypeptide [Source:HGNC Symbol;Acc:HGNC:252]","synonyms":"ADH-2","biotype":"protein_coding","ncbi_id":"127","summary":"This gene encodes class II alcohol dehydrogenase 4 pi subunit, which is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. Class II alcohol dehydrogenase is a homodimer composed of 2 pi subunits. It exhibits a high activity for oxidation of long-chain aliphatic alcohols and aromatic alcohols and is less sensitive to pyrazole. This gene is localized to chromosome 4 in the cluster of alcohol dehydrogenase genes. [provided by RefSeq, Jul 2008]","start":99123657,"end":99157792,"strand":-1,"description":"alcohol dehydrogenase 4 (class II), pi polypeptide [Source:HGNC Symbol;Acc:HGNC:252]"}, {"versioned_ensembl_gene_id":"ENSG00000252128.1","gene_symbol":"SNORD27","gene_name":"Small nucleolar RNA SNORD27 [Source:RFAM;Acc:RF00086]","synonyms":"U27,RNU27","biotype":"snoRNA","ncbi_id":"9301","summary":null,"start":21139886,"end":21139957,"strand":-1,"description":"Small nucleolar RNA SNORD27 [Source:RFAM;Acc:RF00086]"}, {"versioned_ensembl_gene_id":"ENSG00000227234.1","gene_symbol":"SPANXB1","gene_name":"SPANX family member B1 [Source:HGNC Symbol;Acc:HGNC:14329]","synonyms":"SPANXF2,SPANXF1,SPANXB2,CT11.2","biotype":"protein_coding","ncbi_id":"728695","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular family member contains an additional 18 nucleotides in its coding region compared to the other family members in the same gene cluster. This family member is also subject to gene copy number variation. Although the protein encoded by this gene contains consensus nuclear localization signals, the major site for subcellular localization of expressed protein is in the cytoplasmic droplets of ejaculated spermatozoa. This protein provides a biochemical marker for studying the unique structures in spermatazoa, while attempting to further define its role in spermatogenesis. [provided by RefSeq, Apr 2014]","start":141002591,"end":141003706,"strand":1,"description":"SPANX family member B1 [Source:HGNC Symbol;Acc:HGNC:14329]"}, {"versioned_ensembl_gene_id":"ENSG00000134955.11","gene_symbol":"SLC37A2","gene_name":"solute carrier family 37 member 2 [Source:HGNC Symbol;Acc:HGNC:20644]","synonyms":"FLJ00171","biotype":"protein_coding","ncbi_id":"219855","summary":null,"start":125063067,"end":125090312,"strand":1,"description":"solute carrier family 37 member 2 [Source:HGNC Symbol;Acc:HGNC:20644]"}, {"versioned_ensembl_gene_id":"ENSG00000122406.12","gene_symbol":"RPL5","gene_name":"ribosomal protein L5 [Source:HGNC Symbol;Acc:HGNC:10360]","synonyms":"PPP1R135,L5","biotype":"protein_coding","ncbi_id":"6125","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L18P family of ribosomal proteins and component of the 60S subunit. The encoded protein binds 5S rRNA to form a stable complex called the 5S ribonucleoprotein particle (RNP), which is necessary for the transport of nonribosome-associated cytoplasmic 5S rRNA to the nucleolus for assembly into ribosomes. The encoded protein may also function to inhibit tumorigenesis through the activation of downstream tumor suppressors and the downregulation of oncoprotein expression. Mutations in this gene have been identified in patients with Diamond-Blackfan Anemia (DBA). This gene is co-transcribed with the small nucleolar RNA gene U21, which is located in its fifth intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. [provided by RefSeq, Mar 2017]","start":92832025,"end":92841924,"strand":1,"description":"ribosomal protein L5 [Source:HGNC Symbol;Acc:HGNC:10360]"}, {"versioned_ensembl_gene_id":"ENSG00000273919.1","gene_symbol":"AL450423.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53345211,"end":53410880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229269.1","gene_symbol":"AL451048.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140931738,"end":140997448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213557.4","gene_symbol":"AC068050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108040213,"end":108040592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163394.5","gene_symbol":"CCKAR","gene_name":"cholecystokinin A receptor [Source:HGNC Symbol;Acc:HGNC:1570]","synonyms":null,"biotype":"protein_coding","ncbi_id":"886","summary":"This gene encodes a G-protein coupled receptor that binds non-sulfated members of the cholecystokinin (CCK) family of peptide hormones. This receptor is a major physiologic mediator of pancreatic enzyme secretion and smooth muscle contraction of the gallbladder and stomach. In the central and peripheral nervous system this receptor regulates satiety and the release of beta-endorphin and dopamine. [provided by RefSeq, Jul 2008]","start":26481400,"end":26490462,"strand":-1,"description":"cholecystokinin A receptor [Source:HGNC Symbol;Acc:HGNC:1570]"}, {"versioned_ensembl_gene_id":"ENSG00000231616.8","gene_symbol":"AL354733.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83831586,"end":83868532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231293.1","gene_symbol":"RPL36AP6","gene_name":"ribosomal protein L36a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23365]","synonyms":"bA380I20.1","biotype":"processed_pseudogene","ncbi_id":"641556","summary":null,"start":107834509,"end":107834829,"strand":-1,"description":"ribosomal protein L36a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23365]"}, {"versioned_ensembl_gene_id":"ENSG00000177380.13","gene_symbol":"PPFIA3","gene_name":"PTPRF interacting protein alpha 3 [Source:HGNC Symbol;Acc:HGNC:9247]","synonyms":"MGC126569,MGC126567,LPNA3,KIAA0654","biotype":"protein_coding","ncbi_id":"8541","summary":"The protein encoded by this gene is a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. Liprins interact with members of LAR family of transmembrane protein tyrosine phosphatases, which are known to be important for axon guidance and mammary gland development. Liprin family protein has been shown to localize phosphatase LAR to cell focal adhesions and may be involved in the molecular organization of presynaptic active zones. [provided by RefSeq, Jul 2008]","start":49119389,"end":49151026,"strand":1,"description":"PTPRF interacting protein alpha 3 [Source:HGNC Symbol;Acc:HGNC:9247]"}, {"versioned_ensembl_gene_id":"ENSG00000225510.2","gene_symbol":"PCDH8P1","gene_name":"protocadherin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39937]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100133285","summary":null,"start":53199981,"end":53202753,"strand":1,"description":"protocadherin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39937]"}, {"versioned_ensembl_gene_id":"ENSG00000243238.1","gene_symbol":"IGKV2-30","gene_name":"immunoglobulin kappa variable 2-30 [Source:HGNC Symbol;Acc:HGNC:5785]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28919","summary":null,"start":89244781,"end":89245596,"strand":-1,"description":"immunoglobulin kappa variable 2-30 [Source:HGNC Symbol;Acc:HGNC:5785]"}, {"versioned_ensembl_gene_id":"ENSG00000248725.3","gene_symbol":"AC097488.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85246157,"end":85246912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226499.1","gene_symbol":"AL136380.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44843921,"end":44844082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162600.11","gene_symbol":"OMA1","gene_name":"OMA1 zinc metallopeptidase [Source:HGNC Symbol;Acc:HGNC:29661]","synonyms":"ZMPOMA1,YKR087C,MPRP-1,FLJ33782","biotype":"protein_coding","ncbi_id":"115209","summary":null,"start":58415384,"end":58546802,"strand":-1,"description":"OMA1 zinc metallopeptidase [Source:HGNC Symbol;Acc:HGNC:29661]"}, {"versioned_ensembl_gene_id":"ENSG00000130427.2","gene_symbol":"EPO","gene_name":"erythropoietin [Source:HGNC Symbol;Acc:HGNC:3415]","synonyms":"EP","biotype":"protein_coding","ncbi_id":"2056","summary":"This gene encodes a secreted, glycosylated cytokine composed of four alpha helical bundles. The encoded protein is mainly synthesized in the kidney, secreted into the blood plasma, and binds to the erythropoietin receptor to promote red blood cell production, or erythropoiesis, in the bone marrow. Expression of this gene is upregulated under hypoxic conditions, in turn leading to increased erythropoiesis and enhanced oxygen-carrying capacity of the blood. Expression of this gene has also been observed in brain and in the eye, and elevated expression levels have been observed in diabetic retinopathy and ocular hypertension. Recombinant forms of the encoded protein exhibit neuroprotective activity against a variety of potential brain injuries, as well as antiapoptotic functions in several tissue types, and have been used in the treatment of anemia and to enhance the efficacy of cancer therapies. [provided by RefSeq, Aug 2017]","start":100720800,"end":100723700,"strand":1,"description":"erythropoietin [Source:HGNC Symbol;Acc:HGNC:3415]"}, {"versioned_ensembl_gene_id":"ENSG00000172273.12","gene_symbol":"HINFP","gene_name":"histone H4 transcription factor [Source:HGNC Symbol;Acc:HGNC:17850]","synonyms":"MIZF,HiNF-P,DKFZP434F162,ZNF743","biotype":"protein_coding","ncbi_id":"25988","summary":"This gene encodes a transcription factor that interacts with methyl-CpG-binding protein-2 (MBD2), a component of the MeCP1 histone deacetylase (HDAC) complex, and plays a role in DNA methylation and transcription repression. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Aug 2011]","start":119121587,"end":119136044,"strand":1,"description":"histone H4 transcription factor [Source:HGNC Symbol;Acc:HGNC:17850]"}, {"versioned_ensembl_gene_id":"ENSG00000270202.1","gene_symbol":"AP003973.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111107060,"end":111107750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188599.17","gene_symbol":"NPIPP1","gene_name":"nuclear pore complex interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35407]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100874381","summary":null,"start":15104312,"end":15123498,"strand":-1,"description":"nuclear pore complex interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35407]"}, {"versioned_ensembl_gene_id":"ENSG00000259670.1","gene_symbol":"AC012379.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48783190,"end":48784121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281508.1","gene_symbol":"CDR1","gene_name":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]","synonyms":"CDR,CDR62A,CDR34,CDR,CDR62A,CDR34","biotype":"antisense_RNA","ncbi_id":"1038","summary":"Autoantibodies directed against the protein encoded by this intronless gene have been found in some patients with paraneoplastic cerebellar degeneration. The encoded protein contains several hexapeptide repeats. [provided by RefSeq, Jan 2010]","start":140783176,"end":140784660,"strand":1,"description":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]"}, {"versioned_ensembl_gene_id":"ENSG00000184258.6","gene_symbol":"CDR1","gene_name":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]","synonyms":"CDR,CDR62A,CDR34,CDR,CDR62A,CDR34","biotype":"protein_coding","ncbi_id":"1038","summary":"Autoantibodies directed against the protein encoded by this intronless gene have been found in some patients with paraneoplastic cerebellar degeneration. The encoded protein contains several hexapeptide repeats. [provided by RefSeq, Jan 2010]","start":140782405,"end":140784871,"strand":-1,"description":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]"}, {"versioned_ensembl_gene_id":"ENSG00000279325.1","gene_symbol":"AL136359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53193667,"end":53198540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255149.1","gene_symbol":"AP002963.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110876994,"end":110877177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237092.1","gene_symbol":"LINC01065","gene_name":"long intergenic non-protein coding RNA 1065 [Source:HGNC Symbol;Acc:HGNC:49103]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723875","summary":null,"start":53146539,"end":53151808,"strand":-1,"description":"long intergenic non-protein coding RNA 1065 [Source:HGNC Symbol;Acc:HGNC:49103]"}, {"versioned_ensembl_gene_id":"ENSG00000233497.4","gene_symbol":"HNRNPA1P60","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:48790]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"120364","summary":null,"start":110788026,"end":110788976,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:48790]"}, {"versioned_ensembl_gene_id":"ENSG00000254098.1","gene_symbol":"IGKV2-26","gene_name":"immunoglobulin kappa variable 2-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5782]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28922","summary":null,"start":89196096,"end":89196829,"strand":-1,"description":"immunoglobulin kappa variable 2-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5782]"}, {"versioned_ensembl_gene_id":"ENSG00000253202.1","gene_symbol":"IGKV3-25","gene_name":"immunoglobulin kappa variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5818]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28911","summary":null,"start":89192500,"end":89192752,"strand":-1,"description":"immunoglobulin kappa variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5818]"}, {"versioned_ensembl_gene_id":"ENSG00000172336.4","gene_symbol":"POP7","gene_name":"POP7 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:19949]","synonyms":"RPP20,RPP2","biotype":"protein_coding","ncbi_id":"10248","summary":null,"start":100706053,"end":100707495,"strand":1,"description":"POP7 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:19949]"}, {"versioned_ensembl_gene_id":"ENSG00000189042.13","gene_symbol":"ZNF567","gene_name":"zinc finger protein 567 [Source:HGNC Symbol;Acc:HGNC:28696]","synonyms":"MGC45586","biotype":"protein_coding","ncbi_id":"163081","summary":null,"start":36687612,"end":36727701,"strand":1,"description":"zinc finger protein 567 [Source:HGNC Symbol;Acc:HGNC:28696]"}, {"versioned_ensembl_gene_id":"ENSG00000206517.12","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425381,"end":29456943,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000241294.1","gene_symbol":"IGKV2-24","gene_name":"immunoglobulin kappa variable 2-24 [Source:HGNC Symbol;Acc:HGNC:5781]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28923","summary":null,"start":89176328,"end":89177160,"strand":-1,"description":"immunoglobulin kappa variable 2-24 [Source:HGNC Symbol;Acc:HGNC:5781]"}, {"versioned_ensembl_gene_id":"ENSG00000230668.1","gene_symbol":"AL844175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140681106,"end":140687705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197912.14","gene_symbol":"SPG7","gene_name":"SPG7, paraplegin matrix AAA peptidase subunit [Source:HGNC Symbol;Acc:HGNC:11237]","synonyms":"SPG5C,CMAR,CAR","biotype":"protein_coding","ncbi_id":"6687","summary":"This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014]","start":89490917,"end":89557768,"strand":1,"description":"SPG7, paraplegin matrix AAA peptidase subunit [Source:HGNC Symbol;Acc:HGNC:11237]"}, {"versioned_ensembl_gene_id":"ENSG00000274627.1","gene_symbol":"AC092123.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89516797,"end":89522217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196083.9","gene_symbol":"IL1RAP","gene_name":"interleukin 1 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5995]","synonyms":"IL1R3,IL-1RAcP,C3orf13","biotype":"protein_coding","ncbi_id":"3556","summary":"This gene encodes a component of the interleukin 1 receptor complex, which initiates signalling events that result in the activation of interleukin 1-responsive genes. Alternative splicing of this gene results in membrane-bound and soluble isoforms differing in their C-terminus. The ratio of soluble to membrane-bound forms increases during acute-phase induction or stress. [provided by RefSeq, Jul 2018]","start":190514051,"end":190659750,"strand":1,"description":"interleukin 1 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5995]"}, {"versioned_ensembl_gene_id":"ENSG00000273370.1","gene_symbol":"AC108747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":190659216,"end":190659750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186335.8","gene_symbol":"SLC36A2","gene_name":"solute carrier family 36 member 2 [Source:HGNC Symbol;Acc:HGNC:18762]","synonyms":"tramdorin,TRAMD1,PAT2","biotype":"protein_coding","ncbi_id":"153201","summary":"This gene encodes a pH-dependent proton-coupled amino acid transporter that belongs to the amino acid auxin permease 1 protein family. The encoded protein primarily transports small amino acids such as glycine, alanine and proline. Mutations in this gene are associated with iminoglycinuria and hyperglycinuria. [provided by RefSeq, Sep 2010]","start":151314978,"end":151347590,"strand":-1,"description":"solute carrier family 36 member 2 [Source:HGNC Symbol;Acc:HGNC:18762]"}, {"versioned_ensembl_gene_id":"ENSG00000114854.7","gene_symbol":"TNNC1","gene_name":"troponin C1, slow skeletal and cardiac type [Source:HGNC Symbol;Acc:HGNC:11943]","synonyms":"TNNC","biotype":"protein_coding","ncbi_id":"7134","summary":"Troponin is a central regulatory protein of striated muscle contraction, and together with tropomyosin, is located on the actin filament. Troponin consists of 3 subunits: TnI, which is the inhibitor of actomyosin ATPase; TnT, which contains the binding site for tropomyosin; and TnC, the protein encoded by this gene. The binding of calcium to TnC abolishes the inhibitory action of TnI, thus allowing the interaction of actin with myosin, the hydrolysis of ATP, and the generation of tension. Mutations in this gene are associated with cardiomyopathy dilated type 1Z. [provided by RefSeq, Oct 2008]","start":52451102,"end":52454070,"strand":-1,"description":"troponin C1, slow skeletal and cardiac type [Source:HGNC Symbol;Acc:HGNC:11943]"}, {"versioned_ensembl_gene_id":"ENSG00000228615.1","gene_symbol":"AC093166.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111742586,"end":111744662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227842.1","gene_symbol":"AC093166.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111717508,"end":111717837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211920.1","gene_symbol":"IGHD6-13","gene_name":"immunoglobulin heavy diversity 6-13 [Source:HGNC Symbol;Acc:HGNC:5514]","synonyms":"IGHD613,DN1","biotype":"IG_D_gene","ncbi_id":"28487","summary":null,"start":105901142,"end":105901162,"strand":-1,"description":"immunoglobulin heavy diversity 6-13 [Source:HGNC Symbol;Acc:HGNC:5514]"}, {"versioned_ensembl_gene_id":"ENSG00000227108.1","gene_symbol":"IGHD1-14","gene_name":"immunoglobulin heavy diversity 1-14 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5483]","synonyms":"IGHD114,DM2","biotype":"IG_D_gene","ncbi_id":"28508","summary":null,"start":105900638,"end":105900654,"strand":-1,"description":"immunoglobulin heavy diversity 1-14 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5483]"}, {"versioned_ensembl_gene_id":"ENSG00000278234.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":150241777,"end":150241860,"strand":1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000241015.2","gene_symbol":"TPM3P9","gene_name":"tropomyosin 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44142]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"147804","summary":null,"start":53431984,"end":53444670,"strand":1,"description":"tropomyosin 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44142]"}, {"versioned_ensembl_gene_id":"ENSG00000182154.7","gene_symbol":"MRPL41","gene_name":"mitochondrial ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:14492]","synonyms":"RPML27,PIG3,MRPL27,MRP-L27,BMRP","biotype":"protein_coding","ncbi_id":"64975","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the YmL27 ribosomal protein family. [provided by RefSeq, Jul 2008]","start":137551199,"end":137552555,"strand":1,"description":"mitochondrial ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:14492]"}, {"versioned_ensembl_gene_id":"ENSG00000172460.16","gene_symbol":"PRSS30P","gene_name":"protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]","synonyms":"TMPRSS8P,TMPRSS8,MGC5228,Disp","biotype":"transcribed_unitary_pseudogene","ncbi_id":"124221","summary":null,"start":2839568,"end":2842744,"strand":-1,"description":"protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]"}, {"versioned_ensembl_gene_id":"ENSG00000211915.1","gene_symbol":"IGHD5-18","gene_name":"immunoglobulin heavy diversity 5-18 [Source:HGNC Symbol;Acc:HGNC:5509]","synonyms":"IGHD518","biotype":"IG_D_gene","ncbi_id":"28490","summary":null,"start":105893542,"end":105893561,"strand":-1,"description":"immunoglobulin heavy diversity 5-18 [Source:HGNC Symbol;Acc:HGNC:5509]"}, {"versioned_ensembl_gene_id":"ENSG00000237020.1","gene_symbol":"IGHD1-20","gene_name":"immunoglobulin heavy diversity 1-20 [Source:HGNC Symbol;Acc:HGNC:5484]","synonyms":"IGHD120","biotype":"IG_D_gene","ncbi_id":"28507","summary":null,"start":105891191,"end":105891207,"strand":-1,"description":"immunoglobulin heavy diversity 1-20 [Source:HGNC Symbol;Acc:HGNC:5484]"}, {"versioned_ensembl_gene_id":"ENSG00000211914.1","gene_symbol":"IGHD6-19","gene_name":"immunoglobulin heavy diversity 6-19 [Source:HGNC Symbol;Acc:HGNC:5515]","synonyms":"IGHD619","biotype":"IG_D_gene","ncbi_id":"28486","summary":null,"start":105891699,"end":105891719,"strand":-1,"description":"immunoglobulin heavy diversity 6-19 [Source:HGNC Symbol;Acc:HGNC:5515]"}, {"versioned_ensembl_gene_id":"ENSG00000227800.1","gene_symbol":"IGHD4-17","gene_name":"immunoglobulin heavy diversity 4-17 [Source:HGNC Symbol;Acc:HGNC:5503]","synonyms":"IGHD417","biotype":"IG_D_gene","ncbi_id":"28494","summary":null,"start":105894508,"end":105894523,"strand":-1,"description":"immunoglobulin heavy diversity 4-17 [Source:HGNC Symbol;Acc:HGNC:5503]"}, {"versioned_ensembl_gene_id":"ENSG00000107833.10","gene_symbol":"NPM3","gene_name":"nucleophosmin/nucleoplasmin 3 [Source:HGNC Symbol;Acc:HGNC:7931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10360","summary":"The protein encoded by this gene is related to the nuclear chaperone phosphoproteins, nucleoplasmin and nucleophosmin. This protein is strongly expressed in diverse cell types where it localizes primarily to the nucleus. Based on its similarity to nucleoplasmin and nucleophosmin, this protein likely functions as a molecular chaperone in the cell nucleus. [provided by RefSeq, Oct 2008]","start":101781325,"end":101783413,"strand":-1,"description":"nucleophosmin/nucleoplasmin 3 [Source:HGNC Symbol;Acc:HGNC:7931]"}, {"versioned_ensembl_gene_id":"ENSG00000244620.1","gene_symbol":"AC246787.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105890084,"end":105896577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279953.1","gene_symbol":"AC117503.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123649068,"end":123650485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224818.1","gene_symbol":"AC096677.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":201464383,"end":201465146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260558.1","gene_symbol":"AC018557.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66738263,"end":66739326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246777.1","gene_symbol":"AC044802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66751752,"end":66754740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162078.11","gene_symbol":"ZG16B","gene_name":"zymogen granule protein 16B [Source:HGNC Symbol;Acc:HGNC:30456]","synonyms":"PRO1567,JCLN2,HRPE773","biotype":"protein_coding","ncbi_id":"124220","summary":null,"start":2830169,"end":2839585,"strand":1,"description":"zymogen granule protein 16B [Source:HGNC Symbol;Acc:HGNC:30456]"}, {"versioned_ensembl_gene_id":"ENSG00000260465.1","gene_symbol":"AC018557.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66720897,"end":66731785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168955.3","gene_symbol":"TM4SF20","gene_name":"transmembrane 4 L six family member 20 [Source:HGNC Symbol;Acc:HGNC:26230]","synonyms":"TCCE518,FLJ22800","biotype":"protein_coding","ncbi_id":"79853","summary":"The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5. [provided by RefSeq, Jul 2016]","start":227362156,"end":227381995,"strand":-1,"description":"transmembrane 4 L six family member 20 [Source:HGNC Symbol;Acc:HGNC:26230]"}, {"versioned_ensembl_gene_id":"ENSG00000243492.6","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLA-92,HLAL,HLA92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30249483,"end":30256765,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000112167.9","gene_symbol":"SAYSD1","gene_name":"SAYSVFN motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21025]","synonyms":"FLJ11101,C6orf64","biotype":"protein_coding","ncbi_id":"55776","summary":null,"start":39104064,"end":39115189,"strand":-1,"description":"SAYSVFN motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21025]"}, {"versioned_ensembl_gene_id":"ENSG00000203809.6","gene_symbol":"LIN28B-AS1","gene_name":"LIN28B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:21553]","synonyms":"LINC00577,dJ439I14.1,C6orf220","biotype":"lincRNA","ncbi_id":"100113403","summary":null,"start":104864464,"end":104941447,"strand":-1,"description":"LIN28B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:21553]"}, {"versioned_ensembl_gene_id":"ENSG00000111364.15","gene_symbol":"DDX55","gene_name":"DEAD-box helicase 55 [Source:HGNC Symbol;Acc:HGNC:20085]","synonyms":"KIAA1595","biotype":"protein_coding","ncbi_id":"57696","summary":"This gene encodes a member of protein family containing a characteristic Asp-Glu-Ala-Asp (DEAD) motif. These proteins are putative RNA helicases, and may be involved in a range of nuclear processes including translational initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Multiple alternatively spliced transcript variants have been found for this gene. Pseudogenes have been identified on chromosomes 1 and 12. [provided by RefSeq, Feb 2016]","start":123602077,"end":123620941,"strand":1,"description":"DEAD-box helicase 55 [Source:HGNC Symbol;Acc:HGNC:20085]"}, {"versioned_ensembl_gene_id":"ENSG00000276570.1","gene_symbol":"AC010327.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55227219,"end":55230279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241863.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30319108,"end":30336684,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000211911.1","gene_symbol":"IGHD3-22","gene_name":"immunoglobulin heavy diversity 3-22 [Source:HGNC Symbol;Acc:HGNC:5497]","synonyms":"IGHD322","biotype":"IG_D_gene","ncbi_id":"28497","summary":null,"start":105886031,"end":105886061,"strand":-1,"description":"immunoglobulin heavy diversity 3-22 [Source:HGNC Symbol;Acc:HGNC:5497]"}, {"versioned_ensembl_gene_id":"ENSG00000148513.17","gene_symbol":"ANKRD30A","gene_name":"ankyrin repeat domain 30A [Source:HGNC Symbol;Acc:HGNC:17234]","synonyms":"NY-BR-1","biotype":"protein_coding","ncbi_id":"91074","summary":"This gene encodes a DNA-binding transcription factor that is uniquely expressed in mammary epithelium and the testis. Altered expression levels have been associated with breast cancer progression. [provided by RefSeq, Nov 2016]","start":37125788,"end":37384111,"strand":1,"description":"ankyrin repeat domain 30A [Source:HGNC Symbol;Acc:HGNC:17234]"}, {"versioned_ensembl_gene_id":"ENSG00000276071.1","gene_symbol":"AC074138.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36668102,"end":36669404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186334.9","gene_symbol":"SLC36A3","gene_name":"solute carrier family 36 member 3 [Source:HGNC Symbol;Acc:HGNC:19659]","synonyms":"tramdorin2,TRAMD2,PAT3","biotype":"protein_coding","ncbi_id":"285641","summary":null,"start":151276762,"end":151303766,"strand":-1,"description":"solute carrier family 36 member 3 [Source:HGNC Symbol;Acc:HGNC:19659]"}, {"versioned_ensembl_gene_id":"ENSG00000259469.1","gene_symbol":"AC084757.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48729080,"end":48729844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228894.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ31598,FLJ25550,Em:AB014087.1","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30280607,"end":30316946,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000225825.1","gene_symbol":"IGHD6-25","gene_name":"immunoglobulin heavy diversity 6-25 [Source:HGNC Symbol;Acc:HGNC:5516]","synonyms":"IGHD625","biotype":"IG_D_gene","ncbi_id":"28485","summary":null,"start":105881539,"end":105881556,"strand":-1,"description":"immunoglobulin heavy diversity 6-25 [Source:HGNC Symbol;Acc:HGNC:5516]"}, {"versioned_ensembl_gene_id":"ENSG00000134595.8","gene_symbol":"SOX3","gene_name":"SRY-box 3 [Source:HGNC Symbol;Acc:HGNC:11199]","synonyms":"PHP","biotype":"protein_coding","ncbi_id":"6658","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene have been associated with X-linked cognitive disability with growth hormone deficiency. [provided by RefSeq, Jul 2008]","start":140502985,"end":140505116,"strand":-1,"description":"SRY-box 3 [Source:HGNC Symbol;Acc:HGNC:11199]"}, {"versioned_ensembl_gene_id":"ENSG00000227335.1","gene_symbol":"IGHJ1P","gene_name":"immunoglobulin heavy joining 1P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5533]","synonyms":"Jpsi1","biotype":"IG_J_pseudogene","ncbi_id":"28482","summary":null,"start":105865624,"end":105865678,"strand":-1,"description":"immunoglobulin heavy joining 1P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5533]"}, {"versioned_ensembl_gene_id":"ENSG00000236597.1","gene_symbol":"IGHD7-27","gene_name":"immunoglobulin heavy diversity 7-27 [Source:HGNC Symbol;Acc:HGNC:5518]","synonyms":"IGHD727,DHQ52","biotype":"IG_D_gene","ncbi_id":"28484","summary":null,"start":105865551,"end":105865561,"strand":-1,"description":"immunoglobulin heavy diversity 7-27 [Source:HGNC Symbol;Acc:HGNC:5518]"}, {"versioned_ensembl_gene_id":"ENSG00000240041.1","gene_symbol":"IGHJ4","gene_name":"immunoglobulin heavy joining 4 [Source:HGNC Symbol;Acc:HGNC:5538]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28477","summary":null,"start":105864215,"end":105864260,"strand":-1,"description":"immunoglobulin heavy joining 4 [Source:HGNC Symbol;Acc:HGNC:5538]"}, {"versioned_ensembl_gene_id":"ENSG00000161526.14","gene_symbol":"SAP30BP","gene_name":"SAP30 binding protein [Source:HGNC Symbol;Acc:HGNC:30785]","synonyms":"HTRP,HTRG,HCNGP","biotype":"protein_coding","ncbi_id":"29115","summary":null,"start":75667116,"end":75708062,"strand":1,"description":"SAP30 binding protein [Source:HGNC Symbol;Acc:HGNC:30785]"}, {"versioned_ensembl_gene_id":"ENSG00000101079.20","gene_symbol":"NDRG3","gene_name":"NDRG family member 3 [Source:HGNC Symbol;Acc:HGNC:14462]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57446","summary":null,"start":36651766,"end":36746078,"strand":-1,"description":"NDRG family member 3 [Source:HGNC Symbol;Acc:HGNC:14462]"}, {"versioned_ensembl_gene_id":"ENSG00000229944.3","gene_symbol":"EIF4EP2","gene_name":"eukaryotic translation initiation factor 4E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131693","summary":null,"start":49424269,"end":49424922,"strand":-1,"description":"eukaryotic translation initiation factor 4E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32428]"}, {"versioned_ensembl_gene_id":"ENSG00000186244.7","gene_symbol":"AC091180.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49400429,"end":49400800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262039.1","gene_symbol":"AC091180.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49370740,"end":49476988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249302.2","gene_symbol":"FTH1P24","gene_name":"ferritin heavy chain 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37642]","synonyms":"FTHL24","biotype":"processed_pseudogene","ncbi_id":"100462797","summary":null,"start":139546266,"end":139546727,"strand":1,"description":"ferritin heavy chain 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37642]"}, {"versioned_ensembl_gene_id":"ENSG00000174175.16","gene_symbol":"SELP","gene_name":"selectin P [Source:HGNC Symbol;Acc:HGNC:10721]","synonyms":"PSEL,PADGEM,GRMP,GMP140,CD62P,CD62","biotype":"protein_coding","ncbi_id":"6403","summary":"This gene encodes a 140 kDa protein that is stored in the alpha-granules of platelets and Weibel-Palade bodies of endothelial cells. This protein redistributes to the plasma membrane during platelet activation and degranulation and mediates the interaction of activated endothelial cells or platelets with leukocytes. The membrane protein is a calcium-dependent receptor that binds to sialylated forms of Lewis blood group carbohydrate antigens on neutrophils and monocytes. Alternative splice variants may occur but are not well documented. [provided by RefSeq, Jul 2008]","start":169588849,"end":169630193,"strand":-1,"description":"selectin P [Source:HGNC Symbol;Acc:HGNC:10721]"}, {"versioned_ensembl_gene_id":"ENSG00000134987.11","gene_symbol":"WDR36","gene_name":"WD repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:30696]","synonyms":"UTP21,TA-WDRP,GLC1G","biotype":"protein_coding","ncbi_id":"134430","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Mutations in this gene have been associated with adult-onset primary open-angle glaucoma (POAG). [provided by RefSeq, Jul 2008]","start":111091716,"end":111130502,"strand":1,"description":"WD repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:30696]"}, {"versioned_ensembl_gene_id":"ENSG00000244703.3","gene_symbol":"CD46P1","gene_name":"CD46 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6959]","synonyms":"MCPL,CD46P","biotype":"unprocessed_pseudogene","ncbi_id":"4182","summary":null,"start":207645234,"end":207657410,"strand":1,"description":"CD46 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6959]"}, {"versioned_ensembl_gene_id":"ENSG00000259161.2","gene_symbol":"AL137779.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101843394,"end":101844122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259088.1","gene_symbol":"AL137779.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101796555,"end":101810321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120725.12","gene_symbol":"SIL1","gene_name":"SIL1 nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:24624]","synonyms":"ULG5,MSS,BAP","biotype":"protein_coding","ncbi_id":"64374","summary":"This gene encodes a resident endoplasmic reticulum (ER), N-linked glycoprotein with an N-terminal ER targeting sequence, 2 putative N-glycosylation sites, and a C-terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco-Sjogren syndrome. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":138946720,"end":139293557,"strand":-1,"description":"SIL1 nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:24624]"}, {"versioned_ensembl_gene_id":"ENSG00000236478.2","gene_symbol":"AC012513.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":216174896,"end":216176032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188393.8","gene_symbol":"CLEC2A","gene_name":"C-type lectin domain family 2 member A [Source:HGNC Symbol;Acc:HGNC:24191]","synonyms":"INPE5792,UNQ5792,PILAR,KACL","biotype":"protein_coding","ncbi_id":"387836","summary":"CLEC2A belongs to the CLEC2 family of activation-induced, natural killer gene complex-encoded C-type lectin-like receptors (Spreu et al., 2007 [PubMed 18046548]).[supplied by OMIM, May 2008]","start":9898673,"end":9932381,"strand":-1,"description":"C-type lectin domain family 2 member A [Source:HGNC Symbol;Acc:HGNC:24191]"}, {"versioned_ensembl_gene_id":"ENSG00000239951.1","gene_symbol":"IGKV3-20","gene_name":"immunoglobulin kappa variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5817]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28912","summary":null,"start":89142574,"end":89143160,"strand":-1,"description":"immunoglobulin kappa variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5817]"}, {"versioned_ensembl_gene_id":"ENSG00000157227.12","gene_symbol":"MMP14","gene_name":"matrix metallopeptidase 14 [Source:HGNC Symbol;Acc:HGNC:7160]","synonyms":"MT1-MMP","biotype":"protein_coding","ncbi_id":"4323","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the protein encoded by this gene is a member of the membrane-type MMP (MT-MMP) subfamily; each member of this subfamily contains a potential transmembrane domain suggesting that these proteins are expressed at the cell surface rather than secreted. This protein activates MMP2 protein, and this activity may be involved in tumor invasion. [provided by RefSeq, Jul 2008]","start":22836557,"end":22849027,"strand":1,"description":"matrix metallopeptidase 14 [Source:HGNC Symbol;Acc:HGNC:7160]"}, {"versioned_ensembl_gene_id":"ENSG00000197808.11","gene_symbol":"ZNF461","gene_name":"zinc finger protein 461 [Source:HGNC Symbol;Acc:HGNC:21629]","synonyms":"MGC33911,GIOT-1","biotype":"protein_coding","ncbi_id":"92283","summary":null,"start":36637192,"end":36666853,"strand":-1,"description":"zinc finger protein 461 [Source:HGNC Symbol;Acc:HGNC:21629]"}, {"versioned_ensembl_gene_id":"ENSG00000239912.1","gene_symbol":"RPL39P36","gene_name":"ribosomal protein L39 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271526","summary":null,"start":53413190,"end":53413345,"strand":1,"description":"ribosomal protein L39 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36076]"}, {"versioned_ensembl_gene_id":"ENSG00000224994.10","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30316275,"end":30333529,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000136861.17","gene_symbol":"CDK5RAP2","gene_name":"CDK5 regulatory subunit associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18672]","synonyms":"CEP215,C48,MCPH3,FLJ10867","biotype":"protein_coding","ncbi_id":"55755","summary":"This gene encodes a regulator of CDK5 (cyclin-dependent kinase 5) activity. The protein encoded by this gene is localized to the centrosome and Golgi complex, interacts with CDK5R1 and pericentrin (PCNT), plays a role in centriole engagement and microtubule nucleation, and has been linked to primary microcephaly and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":120388869,"end":120580170,"strand":-1,"description":"CDK5 regulatory subunit associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18672]"}, {"versioned_ensembl_gene_id":"ENSG00000248428.1","gene_symbol":"AC010395.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110970951,"end":111008899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274736.4","gene_symbol":"CCL23","gene_name":"C-C motif chemokine ligand 23 [Source:HGNC Symbol;Acc:HGNC:10622]","synonyms":"SCYA23,MPIF-1,MIP-3,CKb8,Ckb-8","biotype":"protein_coding","ncbi_id":"6368","summary":"This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, displays chemotactic activity on resting T lymphocytes and monocytes, lower activity on neutrophils and no activity on activated T lymphocytes. The protein is also a strong suppressor of colony formation by a multipotential hematopoietic progenitor cell line. In addition, the product of this gene is a potent agonist of the chemokine (C-C motif) receptor 1. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":36013056,"end":36017968,"strand":-1,"description":"C-C motif chemokine ligand 23 [Source:HGNC Symbol;Acc:HGNC:10622]"}, {"versioned_ensembl_gene_id":"ENSG00000278690.1","gene_symbol":"AC244100.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36012504,"end":36012891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079246.15","gene_symbol":"XRCC5","gene_name":"X-ray repair cross complementing 5 [Source:HGNC Symbol;Acc:HGNC:12833]","synonyms":"KUB2,Ku86,KU80,KARP-1","biotype":"protein_coding","ncbi_id":"7520","summary":"The protein encoded by this gene is the 80-kilodalton subunit of the Ku heterodimer protein which is also known as ATP-dependant DNA helicase II or DNA repair protein XRCC5. Ku is the DNA-binding component of the DNA-dependent protein kinase, and it functions together with the DNA ligase IV-XRCC4 complex in the repair of DNA double-strand break by non-homologous end joining and the completion of V(D)J recombination events. This gene functionally complements Chinese hamster xrs-6, a mutant defective in DNA double-strand break repair and in ability to undergo V(D)J recombination. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. [provided by RefSeq, Jul 2008]","start":216107464,"end":216206303,"strand":1,"description":"X-ray repair cross complementing 5 [Source:HGNC Symbol;Acc:HGNC:12833]"}, {"versioned_ensembl_gene_id":"ENSG00000117425.13","gene_symbol":"PTCH2","gene_name":"patched 2 [Source:HGNC Symbol;Acc:HGNC:9586]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8643","summary":"This gene encodes a transmembrane receptor of the patched gene family. The encoded protein may function as a tumor suppressor in the hedgehog signaling pathway. Alterations in this gene have been associated with nevoid basal cell carcinoma syndrome, basal cell carcinoma, medulloblastoma, and susceptibility to congenital macrostomia. Alternatively spliced transcript variants have been described.[provided by RefSeq, Oct 2009]","start":44819844,"end":44843063,"strand":-1,"description":"patched 2 [Source:HGNC Symbol;Acc:HGNC:9586]"}, {"versioned_ensembl_gene_id":"ENSG00000170615.14","gene_symbol":"SLC26A5","gene_name":"solute carrier family 26 member 5 [Source:HGNC Symbol;Acc:HGNC:9359]","synonyms":"PRES,DFNB61","biotype":"protein_coding","ncbi_id":"375611","summary":"This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]","start":103352730,"end":103446177,"strand":-1,"description":"solute carrier family 26 member 5 [Source:HGNC Symbol;Acc:HGNC:9359]"}, {"versioned_ensembl_gene_id":"ENSG00000166164.15","gene_symbol":"BRD7","gene_name":"bromodomain containing 7 [Source:HGNC Symbol;Acc:HGNC:14310]","synonyms":"CELTIX1,BP75","biotype":"protein_coding","ncbi_id":"29117","summary":"This gene encodes a protein which is a member of the bromodomain-containing protein family. The product of this gene has been identified as a component of one form of the SWI/SNF chromatin remodeling complex, and as a protein which interacts with p53 and is required for p53-dependent oncogene-induced senescence which prevents tumor growth. Pseudogenes have been described on chromosomes 2, 3, 6, 13 and 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":50313487,"end":50368934,"strand":-1,"description":"bromodomain containing 7 [Source:HGNC Symbol;Acc:HGNC:14310]"}, {"versioned_ensembl_gene_id":"ENSG00000136826.14","gene_symbol":"KLF4","gene_name":"Kruppel like factor 4 [Source:HGNC Symbol;Acc:HGNC:6348]","synonyms":"GKLF,EZF","biotype":"protein_coding","ncbi_id":"9314","summary":"This gene encodes a protein that belongs to the Kruppel family of transcription factors. The encoded zinc finger protein is required for normal development of the barrier function of skin. The encoded protein is thought to control the G1-to-S transition of the cell cycle following DNA damage by mediating the tumor suppressor gene p53. Mice lacking this gene have a normal appearance but lose weight rapidly, and die shortly after birth due to fluid evaporation resulting from compromised epidermal barrier function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":107484852,"end":107490482,"strand":-1,"description":"Kruppel like factor 4 [Source:HGNC Symbol;Acc:HGNC:6348]"}, {"versioned_ensembl_gene_id":"ENSG00000256343.7","gene_symbol":"AC095350.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130651371,"end":130669233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236267.1","gene_symbol":"AP006216.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116813204,"end":116814003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224942.1","gene_symbol":"AL137014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140397062,"end":140398311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203666.12","gene_symbol":"EFCAB2","gene_name":"EF-hand calcium binding domain 2 [Source:HGNC Symbol;Acc:HGNC:28166]","synonyms":"MGC12458,DRC8,CFAP200","biotype":"protein_coding","ncbi_id":"84288","summary":"The gene encodes a protein that contains two EF-hand calcium-binding domains although its function has yet to be determined. Alternatively spliced transcripts have been observed. [provided by RefSeq, Mar 2014]","start":244969705,"end":245127164,"strand":1,"description":"EF-hand calcium binding domain 2 [Source:HGNC Symbol;Acc:HGNC:28166]"}, {"versioned_ensembl_gene_id":"ENSG00000237162.1","gene_symbol":"AC007098.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62939916,"end":62940282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271736.1","gene_symbol":"AL138900.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157280716,"end":157283068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228239.1","gene_symbol":"AL138900.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157232231,"end":157237136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284592.1","gene_symbol":"AL357143.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157203604,"end":157205062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108469.14","gene_symbol":"RECQL5","gene_name":"RecQ like helicase 5 [Source:HGNC Symbol;Acc:HGNC:9950]","synonyms":"RecQ5,FLJ90603","biotype":"protein_coding","ncbi_id":"9400","summary":"The protein encoded by this gene is a helicase that is important for genome stability. The encoded protein also prevents aberrant homologous recombination by displacing RAD51 from ssDNA. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":75626845,"end":75667189,"strand":-1,"description":"RecQ like helicase 5 [Source:HGNC Symbol;Acc:HGNC:9950]"}, {"versioned_ensembl_gene_id":"ENSG00000217178.1","gene_symbol":"AL357563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74282266,"end":74282660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229582.3","gene_symbol":"AL358074.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":125743754,"end":125746552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143382.14","gene_symbol":"ADAMTSL4","gene_name":"ADAMTS like 4 [Source:HGNC Symbol;Acc:HGNC:19706]","synonyms":"TSRC1,DKFZP434K1772","biotype":"protein_coding","ncbi_id":"54507","summary":"This gene is a member of ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs)-like gene family and encodes a protein with seven thrombospondin type 1 repeats. The thrombospondin type 1 repeat domain is found in many proteins with diverse biological functions including cellular adhesion, angiogenesis, and patterning of the developing nervous system. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Sep 2014]","start":150549369,"end":150560937,"strand":1,"description":"ADAMTS like 4 [Source:HGNC Symbol;Acc:HGNC:19706]"}, {"versioned_ensembl_gene_id":"ENSG00000253159.2","gene_symbol":"PCDHGA12","gene_name":"protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:HGNC:8699]","synonyms":"PCDH-GAMMA-A12,KIAA0588,FIB3,CDH21","biotype":"protein_coding","ncbi_id":"26025","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141430589,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:HGNC:8699]"}, {"versioned_ensembl_gene_id":"ENSG00000218483.1","gene_symbol":"AL356277.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74610449,"end":74610715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227236.2","gene_symbol":"AL583844.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235614674,"end":235616397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264270.1","gene_symbol":"AC087749.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75683543,"end":75684799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223786.1","gene_symbol":"AL357507.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74069451,"end":74690727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253305.2","gene_symbol":"PCDHGB6","gene_name":"protocadherin gamma subfamily B, 6 [Source:HGNC Symbol;Acc:HGNC:8713]","synonyms":"PCDH-GAMMA-B6","biotype":"protein_coding","ncbi_id":"56100","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141408021,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 6 [Source:HGNC Symbol;Acc:HGNC:8713]"}, {"versioned_ensembl_gene_id":"ENSG00000264829.1","gene_symbol":"AC087749.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75679474,"end":75679967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262209.2","gene_symbol":"PCDHGB3","gene_name":"protocadherin gamma subfamily B, 3 [Source:HGNC Symbol;Acc:HGNC:8710]","synonyms":"PCDH-GAMMA-B3","biotype":"protein_coding","ncbi_id":"56102","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141370264,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 3 [Source:HGNC Symbol;Acc:HGNC:8710]"}, {"versioned_ensembl_gene_id":"ENSG00000143384.12","gene_symbol":"MCL1","gene_name":"MCL1, BCL2 family apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:6943]","synonyms":"Mcl-1,BCL2L3","biotype":"protein_coding","ncbi_id":"4170","summary":"This gene encodes an anti-apoptotic protein, which is a member of the Bcl-2 family. Alternative splicing results in multiple transcript variants. The longest gene product (isoform 1) enhances cell survival by inhibiting apoptosis while the alternatively spliced shorter gene products (isoform 2 and isoform 3) promote apoptosis and are death-inducing. [provided by RefSeq, Oct 2010]","start":150574551,"end":150579738,"strand":-1,"description":"MCL1, BCL2 family apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:6943]"}, {"versioned_ensembl_gene_id":"ENSG00000235761.2","gene_symbol":"MTCO3P46","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075293","summary":null,"start":235542159,"end":235542390,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52165]"}, {"versioned_ensembl_gene_id":"ENSG00000203804.4","gene_symbol":"ADAMTSL4-AS1","gene_name":"ADAMTSL4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32041]","synonyms":"FLJ45786,C1orf138","biotype":"processed_transcript","ncbi_id":"574406","summary":null,"start":150560202,"end":150574552,"strand":-1,"description":"ADAMTSL4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32041]"}, {"versioned_ensembl_gene_id":"ENSG00000234836.7","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"IRT-1,AIF-1,IBA1,Em:AF129756.17","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31597358,"end":31599195,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000224392.1","gene_symbol":"AL935156.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29229258,"end":29230188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276399.1","gene_symbol":"FLJ36000","gene_name":"uncharacterized FLJ36000 [Source:NCBI gene;Acc:284124]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284124","summary":null,"start":22406019,"end":22413744,"strand":1,"description":"uncharacterized FLJ36000 [Source:NCBI gene;Acc:284124]"}, {"versioned_ensembl_gene_id":"ENSG00000261934.2","gene_symbol":"PCDHGA9","gene_name":"protocadherin gamma subfamily A, 9 [Source:HGNC Symbol;Acc:HGNC:8707]","synonyms":"PCDH-GAMMA-A9","biotype":"protein_coding","ncbi_id":"56107","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141402932,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 9 [Source:HGNC Symbol;Acc:HGNC:8707]"}, {"versioned_ensembl_gene_id":"ENSG00000122136.13","gene_symbol":"OBP2A","gene_name":"odorant binding protein 2A [Source:HGNC Symbol;Acc:HGNC:23380]","synonyms":"OBP,LCN13,hOBPIIa","biotype":"protein_coding","ncbi_id":"29991","summary":"This gene encodes a small extracellular protein belonging to the lipocalin superfamily. The protein is thought to transport small, hydrophobic, volatile molecules or odorants through the nasal mucus to olfactory receptors, and may also function as a scavenger of highly concentrated or toxic odors. The protein is expressed as a monomer in the nasal mucus, and can bind diverse types of odorants with a higher affinity for aldehydes and fatty acids. This gene and a highly similar family member are located in a cluster of lipocalin genes on chromosome 9. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":135546139,"end":135549969,"strand":1,"description":"odorant binding protein 2A [Source:HGNC Symbol;Acc:HGNC:23380]"}, {"versioned_ensembl_gene_id":"ENSG00000152942.18","gene_symbol":"RAD17","gene_name":"RAD17 checkpoint clamp loader component [Source:HGNC Symbol;Acc:HGNC:9807]","synonyms":"RAD17Sp,CCYC,Rad24","biotype":"protein_coding","ncbi_id":"5884","summary":"The protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad17, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This protein shares strong similarity with DNA replication factor C (RFC), and can form a complex with RFCs. This protein binds to chromatin prior to DNA damage and is phosphorylated by the checkpoint kinase ATR following damage. This protein recruits the RAD1-RAD9-HUS1 checkpoint protein complex onto chromatin after DNA damage, which may be required for its phosphorylation. The phosphorylation of this protein is required for the DNA-damage-induced cell cycle G2 arrest, and is thought to be a critical early event during checkpoint signaling in DNA-damaged cells. Multiple alternatively spliced transcript variants of this gene, which encode four distinct protein isoforms, have been reported. Two pseudogenes, located on chromosomes 7 and 13, have been identified. [provided by RefSeq, Jul 2013]","start":69369293,"end":69414801,"strand":1,"description":"RAD17 checkpoint clamp loader component [Source:HGNC Symbol;Acc:HGNC:9807]"}, {"versioned_ensembl_gene_id":"ENSG00000101266.17","gene_symbol":"CSNK2A1","gene_name":"casein kinase 2 alpha 1 [Source:HGNC Symbol;Acc:HGNC:2457]","synonyms":"Cka2,Cka1","biotype":"protein_coding","ncbi_id":"1457","summary":"Casein kinase II is a serine/threonine protein kinase that phosphorylates acidic proteins such as casein. It is involved in various cellular processes, including cell cycle control, apoptosis, and circadian rhythm. The kinase exists as a tetramer and is composed of an alpha, an alpha-prime, and two beta subunits. The alpha subunits contain the catalytic activity while the beta subunits undergo autophosphorylation. The protein encoded by this gene represents the alpha subunit. Multiple transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Apr 2018]","start":473591,"end":543821,"strand":-1,"description":"casein kinase 2 alpha 1 [Source:HGNC Symbol;Acc:HGNC:2457]"}, {"versioned_ensembl_gene_id":"ENSG00000254122.2","gene_symbol":"PCDHGB7","gene_name":"protocadherin gamma subfamily B, 7 [Source:HGNC Symbol;Acc:HGNC:8714]","synonyms":"PCDH-GAMMA-B7,ME6","biotype":"protein_coding","ncbi_id":"56099","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141417645,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 7 [Source:HGNC Symbol;Acc:HGNC:8714]"}, {"versioned_ensembl_gene_id":"ENSG00000280026.1","gene_symbol":"AC005618.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141350109,"end":141350662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253485.2","gene_symbol":"PCDHGA5","gene_name":"protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:HGNC:8703]","synonyms":"PCDH-GAMMA-A5,ME3,CDH-GAMMA-A5","biotype":"protein_coding","ncbi_id":"56110","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141364232,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:HGNC:8703]"}, {"versioned_ensembl_gene_id":"ENSG00000203326.11","gene_symbol":"ZNF525","gene_name":"zinc finger protein 525 [Source:HGNC Symbol;Acc:HGNC:29423]","synonyms":"KIAA1979","biotype":"protein_coding","ncbi_id":"170958","summary":null,"start":53365693,"end":53392217,"strand":1,"description":"zinc finger protein 525 [Source:HGNC Symbol;Acc:HGNC:29423]"}, {"versioned_ensembl_gene_id":"ENSG00000146830.9","gene_symbol":"GIGYF1","gene_name":"GRB10 interacting GYF protein 1 [Source:HGNC Symbol;Acc:HGNC:9126]","synonyms":"GYF1,PERQ1","biotype":"protein_coding","ncbi_id":"64599","summary":"This gene encodes a member of the gyf family of adaptor proteins. The encoded protein contains a gyf protein interaction domain. It binds growth factor receptor bound 10, another adaptor protein that binds activated insulin-like growth factor 1 and insulin receptors and regulates receptor signaling. [provided by RefSeq, Apr 2017]","start":100679507,"end":100689448,"strand":-1,"description":"GRB10 interacting GYF protein 1 [Source:HGNC Symbol;Acc:HGNC:9126]"}, {"versioned_ensembl_gene_id":"ENSG00000271401.1","gene_symbol":"AC010680.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178644717,"end":178645179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283127.1","gene_symbol":"AF146191.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189979902,"end":189982379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000039319.16","gene_symbol":"ZFYVE16","gene_name":"zinc finger FYVE-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20756]","synonyms":"PPP1R69,KIAA0305","biotype":"protein_coding","ncbi_id":"9765","summary":"This gene encodes an endosomal protein that belongs to the FYVE zinc finger family of proteins. The encoded protein is thought to regulate membrane trafficking in the endosome. This protein functions as a scaffold protein in the transforming growth factor-beta signaling pathway and is involved in positive and negative feedback regulation of the bone morphogenetic protein signaling pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":80408013,"end":80479350,"strand":1,"description":"zinc finger FYVE-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20756]"}, {"versioned_ensembl_gene_id":"ENSG00000258515.1","gene_symbol":"AL355075.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20451305,"end":20451918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231110.1","gene_symbol":"FO393408.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140216035,"end":140216804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081853.14","gene_symbol":"PCDHGA2","gene_name":"protocadherin gamma subfamily A, 2 [Source:HGNC Symbol;Acc:HGNC:8700]","synonyms":"PCDH-GAMMA-A2","biotype":"protein_coding","ncbi_id":"56113","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141338760,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 2 [Source:HGNC Symbol;Acc:HGNC:8700]"}, {"versioned_ensembl_gene_id":"ENSG00000232714.1","gene_symbol":"MTND3P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42153]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873185","summary":null,"start":235541759,"end":235542097,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42153]"}, {"versioned_ensembl_gene_id":"ENSG00000161057.11","gene_symbol":"PSMC2","gene_name":"proteasome 26S subunit, ATPase 2 [Source:HGNC Symbol;Acc:HGNC:9548]","synonyms":"S7,Nbla10058,MSS1","biotype":"protein_coding","ncbi_id":"5701","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. This subunit has been shown to interact with several of the basal transcription factors so, in addition to participation in proteasome functions, this subunit may participate in the regulation of transcription. This subunit may also compete with PSMC3 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2011]","start":103344254,"end":103369395,"strand":1,"description":"proteasome 26S subunit, ATPase 2 [Source:HGNC Symbol;Acc:HGNC:9548]"}, {"versioned_ensembl_gene_id":"ENSG00000233506.2","gene_symbol":"AL929561.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29137868,"end":29138804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256064.1","gene_symbol":"AC063926.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130419535,"end":130421019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196417.12","gene_symbol":"ZNF765","gene_name":"zinc finger protein 765 [Source:HGNC Symbol;Acc:HGNC:25092]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91661","summary":null,"start":53389793,"end":53430413,"strand":1,"description":"zinc finger protein 765 [Source:HGNC Symbol;Acc:HGNC:25092]"}, {"versioned_ensembl_gene_id":"ENSG00000240382.3","gene_symbol":"IGKV1-17","gene_name":"immunoglobulin kappa variable 1-17 [Source:HGNC Symbol;Acc:HGNC:5733]","synonyms":"IGKV117,A30","biotype":"IG_V_gene","ncbi_id":"28937","summary":null,"start":89117342,"end":89117844,"strand":-1,"description":"immunoglobulin kappa variable 1-17 [Source:HGNC Symbol;Acc:HGNC:5733]"}, {"versioned_ensembl_gene_id":"ENSG00000237643.1","gene_symbol":"AL365226.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70394887,"end":70399417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254473.1","gene_symbol":"AL354920.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83707594,"end":83713378,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230707.1","gene_symbol":"AL589987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140091743,"end":140092561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187889.12","gene_symbol":"FYB2","gene_name":"FYN binding protein 2 [Source:HGNC Symbol;Acc:HGNC:27295]","synonyms":"RP4-758N20.2,FLJ43208,C1orf168,ARAP","biotype":"protein_coding","ncbi_id":"199920","summary":null,"start":56718804,"end":56819696,"strand":-1,"description":"FYN binding protein 2 [Source:HGNC Symbol;Acc:HGNC:27295]"}, {"versioned_ensembl_gene_id":"ENSG00000240864.3","gene_symbol":"IGKV1-16","gene_name":"immunoglobulin kappa variable 1-16 [Source:HGNC Symbol;Acc:HGNC:5732]","synonyms":"L1,IGKV116","biotype":"IG_V_gene","ncbi_id":"28938","summary":null,"start":89099859,"end":89100361,"strand":-1,"description":"immunoglobulin kappa variable 1-16 [Source:HGNC Symbol;Acc:HGNC:5732]"}, {"versioned_ensembl_gene_id":"ENSG00000254372.1","gene_symbol":"AC040914.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135455865,"end":135456952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240764.3","gene_symbol":"PCDHGC5","gene_name":"protocadherin gamma subfamily C, 5 [Source:HGNC Symbol;Acc:HGNC:8718]","synonyms":"PCDH-GAMMA-C5","biotype":"protein_coding","ncbi_id":"56097","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141489121,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily C, 5 [Source:HGNC Symbol;Acc:HGNC:8718]"}, {"versioned_ensembl_gene_id":"ENSG00000250684.4","gene_symbol":"ADI1P2","gene_name":"acireductone dioxygenase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288971","summary":null,"start":102688317,"end":102688906,"strand":-1,"description":"acireductone dioxygenase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52340]"}, {"versioned_ensembl_gene_id":"ENSG00000233145.1","gene_symbol":"AL589987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140017268,"end":140018037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163900.10","gene_symbol":"TMEM41A","gene_name":"transmembrane protein 41A [Source:HGNC Symbol;Acc:HGNC:30544]","synonyms":"MGC15397","biotype":"protein_coding","ncbi_id":"90407","summary":null,"start":185476496,"end":185499057,"strand":-1,"description":"transmembrane protein 41A [Source:HGNC Symbol;Acc:HGNC:30544]"}, {"versioned_ensembl_gene_id":"ENSG00000212215.1","gene_symbol":"RNU6-913P","gene_name":"RNA, U6 small nuclear 913, pseudogene [Source:HGNC Symbol;Acc:HGNC:47876]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481467","summary":null,"start":61664145,"end":61664239,"strand":-1,"description":"RNA, U6 small nuclear 913, pseudogene [Source:HGNC Symbol;Acc:HGNC:47876]"}, {"versioned_ensembl_gene_id":"ENSG00000265735.2","gene_symbol":"RN7SL5P","gene_name":"RNA, 7SL, cytoplasmic 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10040]","synonyms":"RN7SLP2,RN7SL249P,7LEM1","biotype":"misc_RNA","ncbi_id":"6031","summary":null,"start":9442060,"end":9442380,"strand":1,"description":"RNA, 7SL, cytoplasmic 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10040]"}, {"versioned_ensembl_gene_id":"ENSG00000112164.5","gene_symbol":"GLP1R","gene_name":"glucagon like peptide 1 receptor [Source:HGNC Symbol;Acc:HGNC:4324]","synonyms":"GLP-1R","biotype":"protein_coding","ncbi_id":"2740","summary":"This gene encodes a 7-transmembrane protein that functions as a receptor for glucagon-like peptide 1 (GLP-1) hormone, which stimulates glucose-induced insulin secretion. This receptor, which functions at the cell surface, becomes internalized in response to GLP-1 and GLP-1 analogs, and it plays an important role in the signaling cascades leading to insulin secretion. It also displays neuroprotective effects in animal models. Polymorphisms in this gene are associated with diabetes. The protein is an important drug target for the treatment of type 2 diabetes and stroke. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":39048798,"end":39087743,"strand":1,"description":"glucagon like peptide 1 receptor [Source:HGNC Symbol;Acc:HGNC:4324]"}, {"versioned_ensembl_gene_id":"ENSG00000260586.1","gene_symbol":"AC064799.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71342324,"end":71348471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278408.1","gene_symbol":"AC108861.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71547280,"end":71549832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120868.13","gene_symbol":"APAF1","gene_name":"apoptotic peptidase activating factor 1 [Source:HGNC Symbol;Acc:HGNC:576]","synonyms":"CED4,APAF-1","biotype":"protein_coding","ncbi_id":"317","summary":"This gene encodes a cytoplasmic protein that initiates apoptosis. This protein contains several copies of the WD-40 domain, a caspase recruitment domain (CARD), and an ATPase domain (NB-ARC). Upon binding cytochrome c and dATP, this protein forms an oligomeric apoptosome. The apoptosome binds and cleaves caspase 9 preproprotein, releasing its mature, activated form. Activated caspase 9 stimulates the subsequent caspase cascade that commits the cell to apoptosis. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":98645141,"end":98735433,"strand":1,"description":"apoptotic peptidase activating factor 1 [Source:HGNC Symbol;Acc:HGNC:576]"}, {"versioned_ensembl_gene_id":"ENSG00000233533.1","gene_symbol":"MKNK2P1","gene_name":"MAP kinase interacting serine/threonine kinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44970]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389948","summary":null,"start":36944111,"end":36944738,"strand":-1,"description":"MAP kinase interacting serine/threonine kinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44970]"}, {"versioned_ensembl_gene_id":"ENSG00000225362.8","gene_symbol":"CT62","gene_name":"cancer/testis antigen 62 [Source:HGNC Symbol;Acc:HGNC:27286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"196993","summary":null,"start":71110244,"end":71115494,"strand":-1,"description":"cancer/testis antigen 62 [Source:HGNC Symbol;Acc:HGNC:27286]"}, {"versioned_ensembl_gene_id":"ENSG00000260625.2","gene_symbol":"AC026471.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31508471,"end":31509256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259781.1","gene_symbol":"HMGB1P6","gene_name":"high mobility group box 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:4998]","synonyms":"HMGB1L6,HMG1L6","biotype":"processed_pseudogene","ncbi_id":"645292","summary":null,"start":71164770,"end":71165415,"strand":-1,"description":"high mobility group box 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:4998]"}, {"versioned_ensembl_gene_id":"ENSG00000212664.5","gene_symbol":"AC064799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71341158,"end":71341712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135018.13","gene_symbol":"UBQLN1","gene_name":"ubiquilin 1 [Source:HGNC Symbol;Acc:HGNC:12508]","synonyms":"DA41,XDRP1,PLIC-1,DSK2","biotype":"protein_coding","ncbi_id":"29979","summary":"This gene encodes an ubiquitin-like protein (ubiquilin) that shares a high degree of similarity with related products in yeast, rat and frog. Ubiquilins contain an N-terminal ubiquitin-like domain and a C-terminal ubiquitin-associated domain. They physically associate with both proteasomes and ubiquitin ligases, and thus are thought to functionally link the ubiquitination machinery to the proteasome to affect in vivo protein degradation. This ubiquilin has also been shown to modulate accumulation of presenilin proteins, and it is found in lesions associated with Alzheimer's and Parkinson's disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":83659963,"end":83708203,"strand":-1,"description":"ubiquilin 1 [Source:HGNC Symbol;Acc:HGNC:12508]"}, {"versioned_ensembl_gene_id":"ENSG00000105819.13","gene_symbol":"PMPCB","gene_name":"peptidase, mitochondrial processing beta subunit [Source:HGNC Symbol;Acc:HGNC:9119]","synonyms":"MPPP52,MPPB","biotype":"protein_coding","ncbi_id":"9512","summary":"This gene is a member of the peptidase M16 family and encodes a protein with a zinc-binding motif. This protein is located in the mitochondrial matrix and catalyzes the cleavage of the leader peptides of precursor proteins newly imported into the mitochondria, though it only functions as part of a heterodimeric complex. [provided by RefSeq, Jul 2008]","start":103297422,"end":103329511,"strand":1,"description":"peptidase, mitochondrial processing beta subunit [Source:HGNC Symbol;Acc:HGNC:9119]"}, {"versioned_ensembl_gene_id":"ENSG00000117036.11","gene_symbol":"ETV3","gene_name":"ETS variant 3 [Source:HGNC Symbol;Acc:HGNC:3492]","synonyms":"PE-1","biotype":"protein_coding","ncbi_id":"2117","summary":null,"start":157121191,"end":157138474,"strand":-1,"description":"ETS variant 3 [Source:HGNC Symbol;Acc:HGNC:3492]"}, {"versioned_ensembl_gene_id":"ENSG00000243053.2","gene_symbol":"RPL31P58","gene_name":"ribosomal protein L31 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:35862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271485","summary":null,"start":28802444,"end":28802822,"strand":1,"description":"ribosomal protein L31 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:35862]"}, {"versioned_ensembl_gene_id":"ENSG00000115504.14","gene_symbol":"EHBP1","gene_name":"EH domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29144]","synonyms":"NACSIN,KIAA0903","biotype":"protein_coding","ncbi_id":"23301","summary":"This gene encodes an Eps15 homology domain binding protein. The encoded protein may play a role in endocytic trafficking. A single nucleotide polymorphism in this gene is associated with an aggressive form of prostate cancer. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":62673851,"end":63046487,"strand":1,"description":"EH domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29144]"}, {"versioned_ensembl_gene_id":"ENSG00000250324.2","gene_symbol":"MRPL22P1","gene_name":"mitochondrial ribosomal protein L22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29700]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359738","summary":null,"start":56320719,"end":56321334,"strand":-1,"description":"mitochondrial ribosomal protein L22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29700]"}, {"versioned_ensembl_gene_id":"ENSG00000253953.2","gene_symbol":"PCDHGB4","gene_name":"protocadherin gamma subfamily B, 4 [Source:HGNC Symbol;Acc:HGNC:8711]","synonyms":"PCDH-GAMMA-B4,FIB2,CDH20","biotype":"protein_coding","ncbi_id":"8641","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. This particular family member is expressed in fibroblasts and is thought to play a role in wound healing in response to injury. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141387698,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 4 [Source:HGNC Symbol;Acc:HGNC:8711]"}, {"versioned_ensembl_gene_id":"ENSG00000231609.5","gene_symbol":"AC009501.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63043922,"end":63048640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233118.2","gene_symbol":"UBE2V1P8","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44893]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724706","summary":null,"start":40942251,"end":40942515,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44893]"}, {"versioned_ensembl_gene_id":"ENSG00000238959.1","gene_symbol":"RNU7-19P","gene_name":"RNA, U7 small nuclear 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:34115]","synonyms":"U7.19","biotype":"snRNA","ncbi_id":"100147767","summary":null,"start":73027808,"end":73027873,"strand":1,"description":"RNA, U7 small nuclear 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:34115]"}, {"versioned_ensembl_gene_id":"ENSG00000265706.1","gene_symbol":"SNORD53B","gene_name":"small nucleolar RNA, C/D box 53B [Source:HGNC Symbol;Acc:HGNC:52229]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617012","summary":null,"start":28927983,"end":28928060,"strand":1,"description":"small nucleolar RNA, C/D box 53B [Source:HGNC Symbol;Acc:HGNC:52229]"}, {"versioned_ensembl_gene_id":"ENSG00000206523.3","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"dJ80I19.2,OR2J1P,hs6M1-4,OR6-5","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100937,"end":29101875,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000206524.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR6-4,OR2B3P","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086195,"end":29087300,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000254083.5","gene_symbol":"LINC01591","gene_name":"long intergenic non-protein coding RNA 1591 [Source:HGNC Symbol;Acc:HGNC:27819]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286094","summary":null,"start":135234131,"end":135299719,"strand":1,"description":"long intergenic non-protein coding RNA 1591 [Source:HGNC Symbol;Acc:HGNC:27819]"}, {"versioned_ensembl_gene_id":"ENSG00000251218.1","gene_symbol":"AC103764.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134849935,"end":134881899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124440.15","gene_symbol":"HIF3A","gene_name":"hypoxia inducible factor 3 alpha subunit [Source:HGNC Symbol;Acc:HGNC:15825]","synonyms":"PASD7,MOP7,IPAS,bHLHe17","biotype":"protein_coding","ncbi_id":"64344","summary":"The protein encoded by this gene is the alpha-3 subunit of one of several alpha/beta-subunit heterodimeric transcription factors that regulate many adaptive responses to low oxygen tension (hypoxia). The alpha-3 subunit lacks the transactivation domain found in factors containing either the alpha-1 or alpha-2 subunits. It is thought that factors containing the alpha-3 subunit are negative regulators of hypoxia-inducible gene expression. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2011]","start":46297046,"end":46343433,"strand":1,"description":"hypoxia inducible factor 3 alpha subunit [Source:HGNC Symbol;Acc:HGNC:15825]"}, {"versioned_ensembl_gene_id":"ENSG00000253433.1","gene_symbol":"NCRNA00250","gene_name":"non-protein coding RNA 250 [Source:NCBI gene;Acc:552853]","synonyms":"C8orf24","biotype":"lincRNA","ncbi_id":"552853","summary":null,"start":134838069,"end":134842637,"strand":1,"description":"non-protein coding RNA 250 [Source:NCBI gene;Acc:552853]"}, {"versioned_ensembl_gene_id":"ENSG00000269124.1","gene_symbol":"AC007193.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46320197,"end":46340004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140688.16","gene_symbol":"C16orf58","gene_name":"chromosome 16 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:25848]","synonyms":"FLJ13868","biotype":"protein_coding","ncbi_id":"64755","summary":"This gene encodes a putative transmembrane protein containing a conserved DUF647 domain that may be involved in protein-protein interaction. The encoded protein is related to a plant protein that participates in ultraviolet B light-sensing during root morphogenesis. [provided by RefSeq, Feb 2013]","start":31489471,"end":31509309,"strand":-1,"description":"chromosome 16 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:25848]"}, {"versioned_ensembl_gene_id":"ENSG00000240053.8","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"G5b,C6orf19","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31670167,"end":31673776,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000229638.1","gene_symbol":"RPL4P4","gene_name":"ribosomal protein L4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36179]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647276","summary":null,"start":185417495,"end":185418778,"strand":-1,"description":"ribosomal protein L4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36179]"}, {"versioned_ensembl_gene_id":"ENSG00000271045.1","gene_symbol":"NDUFB9P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52269]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075233","summary":null,"start":69349936,"end":69350445,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52269]"}, {"versioned_ensembl_gene_id":"ENSG00000253265.1","gene_symbol":"IGKV2-14","gene_name":"immunoglobulin kappa variable 2-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5777]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28927","summary":null,"start":89078010,"end":89078784,"strand":-1,"description":"immunoglobulin kappa variable 2-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5777]"}, {"versioned_ensembl_gene_id":"ENSG00000173065.13","gene_symbol":"FAM222B","gene_name":"family with sequence similarity 222 member B [Source:HGNC Symbol;Acc:HGNC:25563]","synonyms":"FLJ10700,C17orf63","biotype":"protein_coding","ncbi_id":"55731","summary":null,"start":28755978,"end":28855232,"strand":-1,"description":"family with sequence similarity 222 member B [Source:HGNC Symbol;Acc:HGNC:25563]"}, {"versioned_ensembl_gene_id":"ENSG00000203933.2","gene_symbol":"CXorf66","gene_name":"chromosome X open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33743]","synonyms":"SGPX,RP11-35F15.2","biotype":"protein_coding","ncbi_id":"347487","summary":"The protein encoded by this gene is predicted to be a type I membrane protein, however, its exact function is not known. [provided by RefSeq, Sep 2009]","start":139955725,"end":139965520,"strand":-1,"description":"chromosome X open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33743]"}, {"versioned_ensembl_gene_id":"ENSG00000253939.1","gene_symbol":"AC007991.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39903775,"end":39995248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258021.1","gene_symbol":"AC025259.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51900565,"end":51901336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240184.6","gene_symbol":"PCDHGC3","gene_name":"protocadherin gamma subfamily C, 3 [Source:HGNC Symbol;Acc:HGNC:8716]","synonyms":"PCDH2,PCDH-GAMMA-C3,PC43,PC-43","biotype":"protein_coding","ncbi_id":"5098","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141475947,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily C, 3 [Source:HGNC Symbol;Acc:HGNC:8716]"}, {"versioned_ensembl_gene_id":"ENSG00000265402.1","gene_symbol":"AC011260.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51612639,"end":51613110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113327.16","gene_symbol":"GABRG2","gene_name":"gamma-aminobutyric acid type A receptor gamma2 subunit [Source:HGNC Symbol;Acc:HGNC:4087]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2566","summary":"This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammlian brain, where it acts at GABA-A receptors, which are ligand-gated chloride channels. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene have been associated with epilepsy and febrile seizures. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":162000057,"end":162162977,"strand":1,"description":"gamma-aminobutyric acid type A receptor gamma2 subunit [Source:HGNC Symbol;Acc:HGNC:4087]"}, {"versioned_ensembl_gene_id":"ENSG00000228404.1","gene_symbol":"AP001468.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46185079,"end":46188941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232683.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31593261,"end":31593534,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000136110.12","gene_symbol":"CNMD","gene_name":"chondromodulin [Source:HGNC Symbol;Acc:HGNC:17005]","synonyms":"MYETS1,LECT1,CHM1,CHM-I,BRICD3","biotype":"protein_coding","ncbi_id":"11061","summary":"This gene encodes a glycosylated transmembrane protein that is cleaved to form a mature, secreted protein. The N-terminus of the precursor protein shares characteristics with other surfactant proteins and is sometimes called chondrosurfactant protein although no biological activity has yet been defined for it. The C-terminus of the precursor protein contains a 25 kDa mature protein called leukocyte cell-derived chemotaxin-1 or chondromodulin-1. The mature protein promotes chondrocyte growth and inhibits angiogenesis. This gene is expressed in the avascular zone of prehypertrophic cartilage and its expression decreases during chondrocyte hypertrophy and vascular invasion. The mature protein likely plays a role in endochondral bone development by permitting cartilaginous anlagen to be vascularized and replaced by bone. It may be involved also in the broad control of tissue vascularization during development. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":52703264,"end":52739812,"strand":-1,"description":"chondromodulin [Source:HGNC Symbol;Acc:HGNC:17005]"}, {"versioned_ensembl_gene_id":"ENSG00000242276.2","gene_symbol":"RPL5P3","gene_name":"ribosomal protein L5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31034]","synonyms":"HsT18216","biotype":"processed_pseudogene","ncbi_id":"400385","summary":null,"start":71063101,"end":71063989,"strand":-1,"description":"ribosomal protein L5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31034]"}, {"versioned_ensembl_gene_id":"ENSG00000276634.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54762712,"end":54778593,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000162409.10","gene_symbol":"PRKAA2","gene_name":"protein kinase AMP-activated catalytic subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:9377]","synonyms":"PRKAA,AMPKa2,AMPK","biotype":"protein_coding","ncbi_id":"5563","summary":"The protein encoded by this gene is a catalytic subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. Studies of the mouse counterpart suggest that this catalytic subunit may control whole-body insulin sensitivity and is necessary for maintaining myocardial energy homeostasis during ischemia. [provided by RefSeq, Jul 2008]","start":56645322,"end":56715335,"strand":1,"description":"protein kinase AMP-activated catalytic subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:9377]"}, {"versioned_ensembl_gene_id":"ENSG00000107831.12","gene_symbol":"FGF8","gene_name":"fibroblast growth factor 8 [Source:HGNC Symbol;Acc:HGNC:3686]","synonyms":"AIGF","biotype":"protein_coding","ncbi_id":"2253","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008]","start":101770130,"end":101780369,"strand":-1,"description":"fibroblast growth factor 8 [Source:HGNC Symbol;Acc:HGNC:3686]"}, {"versioned_ensembl_gene_id":"ENSG00000274926.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54699775,"end":54714233,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000162910.18","gene_symbol":"MRPL55","gene_name":"mitochondrial ribosomal protein L55 [Source:HGNC Symbol;Acc:HGNC:16686]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128308","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Multiple transcript variants encoding two different isoforms were identified through sequence analysis. [provided by RefSeq, Jul 2008]","start":228106679,"end":228109312,"strand":-1,"description":"mitochondrial ribosomal protein L55 [Source:HGNC Symbol;Acc:HGNC:16686]"}, {"versioned_ensembl_gene_id":"ENSG00000238077.1","gene_symbol":"NMNAT1P3","gene_name":"NMNAT1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391603","summary":null,"start":190166764,"end":190167651,"strand":1,"description":"NMNAT1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49165]"}, {"versioned_ensembl_gene_id":"ENSG00000277924.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"cl-6,nkat2,nkat2a,nkat2b,p58,CD158B2","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54668491,"end":54683019,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000104852.14","gene_symbol":"SNRNP70","gene_name":"small nuclear ribonucleoprotein U1 subunit 70 [Source:HGNC Symbol;Acc:HGNC:11150]","synonyms":"RPU1,RNPU1Z,U1-70K,SNRP70,Snp1","biotype":"protein_coding","ncbi_id":"6625","summary":null,"start":49085419,"end":49108605,"strand":1,"description":"small nuclear ribonucleoprotein U1 subunit 70 [Source:HGNC Symbol;Acc:HGNC:11150]"}, {"versioned_ensembl_gene_id":"ENSG00000230157.1","gene_symbol":"ATP5G1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19815]","synonyms":"ATP5GP3","biotype":"processed_pseudogene","ncbi_id":"319136","summary":null,"start":105536861,"end":105537239,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19815]"}, {"versioned_ensembl_gene_id":"ENSG00000277795.1","gene_symbol":"AC244517.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141259235,"end":141261364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258114.1","gene_symbol":"AC005871.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117425194,"end":117490419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250299.5","gene_symbol":"MRPS31P4","gene_name":"mitochondrial ribosomal protein S31 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42649]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100885866","summary":null,"start":52600119,"end":52637446,"strand":1,"description":"mitochondrial ribosomal protein S31 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42649]"}, {"versioned_ensembl_gene_id":"ENSG00000163931.15","gene_symbol":"TKT","gene_name":"transketolase [Source:HGNC Symbol;Acc:HGNC:11834]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7086","summary":"This gene encodes a thiamine-dependent enzyme which plays a role in the channeling of excess sugar phosphates to glycolysis in the pentose phosphate pathway. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]","start":53224707,"end":53256052,"strand":-1,"description":"transketolase [Source:HGNC Symbol;Acc:HGNC:11834]"}, {"versioned_ensembl_gene_id":"ENSG00000224257.1","gene_symbol":"VWC2L-IT1","gene_name":"VWC2L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41508]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100885780","summary":null,"start":214510196,"end":214536890,"strand":1,"description":"VWC2L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41508]"}, {"versioned_ensembl_gene_id":"ENSG00000177728.16","gene_symbol":"TMEM94","gene_name":"transmembrane protein 94 [Source:HGNC Symbol;Acc:HGNC:28983]","synonyms":"KIAA0195","biotype":"protein_coding","ncbi_id":"9772","summary":null,"start":75441159,"end":75500090,"strand":1,"description":"transmembrane protein 94 [Source:HGNC Symbol;Acc:HGNC:28983]"}, {"versioned_ensembl_gene_id":"ENSG00000132749.10","gene_symbol":"TESMIN","gene_name":"testis expressed metallothionein like protein [Source:HGNC Symbol;Acc:HGNC:7446]","synonyms":"MTL5,CXCDC2","biotype":"protein_coding","ncbi_id":"9633","summary":"Metallothionein proteins are highly conserved low-molecular-weight cysteine-rich proteins that are induced by and bind to heavy metal ions and have no enzymatic activity. They may play a central role in the regulation of cell growth and differentiation and are involved in spermatogenesis. This gene encodes a metallothionein-like protein which has been shown to be expressed differentially in mouse testis and ovary. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":68707440,"end":68751564,"strand":-1,"description":"testis expressed metallothionein like protein [Source:HGNC Symbol;Acc:HGNC:7446]"}, {"versioned_ensembl_gene_id":"ENSG00000011304.19","gene_symbol":"PTBP1","gene_name":"polypyrimidine tract binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9583]","synonyms":"PTB4,PTB3,PTB2,PTB-1,PTB,pPTB,HNRPI,HNRNP-I","biotype":"protein_coding","ncbi_id":"5725","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA-binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has four repeats of quasi-RNA recognition motif (RRM) domains that bind RNAs. This protein binds to the intronic polypyrimidine tracts that requires pre-mRNA splicing and acts via the protein degradation ubiquitin-proteasome pathway. It may also promote the binding of U2 snRNP to pre-mRNAs. This protein is localized in the nucleoplasm and it is also detected in the perinucleolar structure. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":797075,"end":812327,"strand":1,"description":"polypyrimidine tract binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9583]"}, {"versioned_ensembl_gene_id":"ENSG00000183305.13","gene_symbol":"MAGEA2B","gene_name":"MAGE family member A2B [Source:HGNC Symbol;Acc:HGNC:19340]","synonyms":"MGC16973,MAGEA2b,MAGEA2,MAGE2","biotype":"protein_coding","ncbi_id":"266740","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci. [provided by RefSeq, Jul 2008]","start":152714586,"end":152718607,"strand":1,"description":"MAGE family member A2B [Source:HGNC Symbol;Acc:HGNC:19340]"}, {"versioned_ensembl_gene_id":"ENSG00000201031.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":149094353,"end":149094462,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000172590.18","gene_symbol":"MRPL52","gene_name":"mitochondrial ribosomal protein L52 [Source:HGNC Symbol;Acc:HGNC:16655]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122704","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein which has no bacterial homolog. Multiple transcript variants encoding different protein isoforms were identified through sequence analysis. [provided by RefSeq, Jul 2008]","start":22829879,"end":22835037,"strand":1,"description":"mitochondrial ribosomal protein L52 [Source:HGNC Symbol;Acc:HGNC:16655]"}, {"versioned_ensembl_gene_id":"ENSG00000213062.4","gene_symbol":"AL021068.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169486076,"end":169486986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183324.10","gene_symbol":"REC114","gene_name":"REC114 meiotic recombination protein [Source:HGNC Symbol;Acc:HGNC:25065]","synonyms":"LOC283677,FLJ44083,FLJ36860,FLJ27520,CT147,C15orf60","biotype":"protein_coding","ncbi_id":"283677","summary":"The protein encoded by this gene is orthologous to the mouse meiotic recombination protein REC114, which is involved in DNA double-strand break formation during meiosis. The encoded protein is conserved in most eukaryotes and was first discovered and characterized in yeast. [provided by RefSeq, Feb 2017]","start":73443158,"end":73560014,"strand":1,"description":"REC114 meiotic recombination protein [Source:HGNC Symbol;Acc:HGNC:25065]"}, {"versioned_ensembl_gene_id":"ENSG00000113212.6","gene_symbol":"PCDHB7","gene_name":"protocadherin beta 7 [Source:HGNC Symbol;Acc:HGNC:8692]","synonyms":"PCDH-BETA7","biotype":"protein_coding","ncbi_id":"56129","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. The transcript for this particular family member uses more than one polyadenylation site. [provided by RefSeq, Jul 2008]","start":141172619,"end":141176383,"strand":1,"description":"protocadherin beta 7 [Source:HGNC Symbol;Acc:HGNC:8692]"}, {"versioned_ensembl_gene_id":"ENSG00000113211.5","gene_symbol":"PCDHB6","gene_name":"protocadherin beta 6 [Source:HGNC Symbol;Acc:HGNC:8691]","synonyms":"PCDH-BETA6","biotype":"protein_coding","ncbi_id":"56130","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. Unlike the alpha and gamma clusters, the transcripts from these genes do not share common 3' exons. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell neural connections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":141150022,"end":141153287,"strand":1,"description":"protocadherin beta 6 [Source:HGNC Symbol;Acc:HGNC:8691]"}, {"versioned_ensembl_gene_id":"ENSG00000125445.10","gene_symbol":"MRPS7","gene_name":"mitochondrial ribosomal protein S7 [Source:HGNC Symbol;Acc:HGNC:14499]","synonyms":"RPMS7,RP-S7,MRP-S","biotype":"protein_coding","ncbi_id":"51081","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. In the prokaryotic ribosome, the comparable protein is thought to play an essential role in organizing the 3' domain of the 16 S rRNA in the vicinity of the P- and A-sites. Pseudogenes corresponding to this gene are found on chromosomes 8p and 12p. [provided by RefSeq, Jul 2008]","start":75261674,"end":75266373,"strand":1,"description":"mitochondrial ribosomal protein S7 [Source:HGNC Symbol;Acc:HGNC:14499]"}, {"versioned_ensembl_gene_id":"ENSG00000206526.2","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"dJ25J6.5,C6orf100","biotype":"protein_coding","ncbi_id":"729583","summary":null,"start":28943865,"end":28944525,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000270562.1","gene_symbol":"AC097634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71584943,"end":71587409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268053.1","gene_symbol":"AC007785.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46111079,"end":46113863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220913.1","gene_symbol":"AL391361.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160905770,"end":160913638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277855.1","gene_symbol":"AC097634.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71581721,"end":71628558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186952.14","gene_symbol":"TMEM232","gene_name":"transmembrane protein 232 [Source:HGNC Symbol;Acc:HGNC:37270]","synonyms":"FLJ43080","biotype":"protein_coding","ncbi_id":"642987","summary":null,"start":110289233,"end":110738956,"strand":-1,"description":"transmembrane protein 232 [Source:HGNC Symbol;Acc:HGNC:37270]"}, {"versioned_ensembl_gene_id":"ENSG00000242094.1","gene_symbol":"FOXP1-IT1","gene_name":"FOXP1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41335]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100506815","summary":null,"start":71570255,"end":71574457,"strand":-1,"description":"FOXP1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41335]"}, {"versioned_ensembl_gene_id":"ENSG00000175283.7","gene_symbol":"DOLK","gene_name":"dolichol kinase [Source:HGNC Symbol;Acc:HGNC:23406]","synonyms":"TMEM15,KIAA1094,DK1","biotype":"protein_coding","ncbi_id":"22845","summary":"The protein encoded by this gene catalyzes the CTP-mediated phosphorylation of dolichol, and is involved in the synthesis of Dol-P-Man, which is an essential glycosyl carrier lipid for C- and O-mannosylation, N- and O-linked glycosylation of proteins, and for the biosynthesis of glycosyl phosphatidylinositol anchors in endoplasmic reticulum. Mutations in this gene are associated with dolichol kinase deficiency.[provided by RefSeq, Apr 2010]","start":128945530,"end":128947619,"strand":-1,"description":"dolichol kinase [Source:HGNC Symbol;Acc:HGNC:23406]"}, {"versioned_ensembl_gene_id":"ENSG00000164024.11","gene_symbol":"METAP1","gene_name":"methionyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:15789]","synonyms":"MetAP1A,MAP1A,KIAA0094","biotype":"protein_coding","ncbi_id":"23173","summary":null,"start":98995620,"end":99062813,"strand":1,"description":"methionyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:15789]"}, {"versioned_ensembl_gene_id":"ENSG00000213305.3","gene_symbol":"HNRNPCP6","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421794","summary":null,"start":85020785,"end":85021655,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48817]"}, {"versioned_ensembl_gene_id":"ENSG00000114115.9","gene_symbol":"RBP1","gene_name":"retinol binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9919]","synonyms":"CRBP1,CRBP,CRABP-I,RBPC,CRBPI","biotype":"protein_coding","ncbi_id":"5947","summary":"This gene encodes the carrier protein involved in the transport of retinol (vitamin A alcohol) from the liver storage site to peripheral tissue. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":139517434,"end":139539829,"strand":-1,"description":"retinol binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9919]"}, {"versioned_ensembl_gene_id":"ENSG00000139329.4","gene_symbol":"LUM","gene_name":"lumican [Source:HGNC Symbol;Acc:HGNC:6724]","synonyms":"SLRR2D,LDC","biotype":"protein_coding","ncbi_id":"4060","summary":"This gene encodes a member of the small leucine-rich proteoglycan (SLRP) family that includes decorin, biglycan, fibromodulin, keratocan, epiphycan, and osteoglycin. In these bifunctional molecules, the protein moiety binds collagen fibrils and the highly charged hydrophilic glycosaminoglycans regulate interfibrillar spacings. Lumican is the major keratan sulfate proteoglycan of the cornea but is also distributed in interstitial collagenous matrices throughout the body. Lumican may regulate collagen fibril organization and circumferential growth, corneal transparency, and epithelial cell migration and tissue repair. [provided by RefSeq, Jul 2008]","start":91102629,"end":91111831,"strand":-1,"description":"lumican [Source:HGNC Symbol;Acc:HGNC:6724]"}, {"versioned_ensembl_gene_id":"ENSG00000218213.1","gene_symbol":"FTH1P26","gene_name":"ferritin heavy chain 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37644]","synonyms":"FTHL26","biotype":"processed_pseudogene","ncbi_id":"100420303","summary":null,"start":133676729,"end":133677429,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37644]"}, {"versioned_ensembl_gene_id":"ENSG00000088356.5","gene_symbol":"PDRG1","gene_name":"p53 and DNA damage regulated 1 [Source:HGNC Symbol;Acc:HGNC:16119]","synonyms":"dJ310O13.3,C20orf126","biotype":"protein_coding","ncbi_id":"81572","summary":null,"start":31944342,"end":31952092,"strand":-1,"description":"p53 and DNA damage regulated 1 [Source:HGNC Symbol;Acc:HGNC:16119]"}, {"versioned_ensembl_gene_id":"ENSG00000254106.1","gene_symbol":"LINC01848","gene_name":"long intergenic non-protein coding RNA 1848 [Source:HGNC Symbol;Acc:HGNC:52663]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100289673","summary":null,"start":109883182,"end":109884751,"strand":1,"description":"long intergenic non-protein coding RNA 1848 [Source:HGNC Symbol;Acc:HGNC:52663]"}, {"versioned_ensembl_gene_id":"ENSG00000114113.6","gene_symbol":"RBP2","gene_name":"retinol binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9920]","synonyms":"RBPC2,CRBPII,CRBP2,CRABP-II","biotype":"protein_coding","ncbi_id":"5948","summary":"This gene encodes an abundant protein present in the small intestinal epithelium. It is thought to participate in the uptake and/or intracellular metabolism of vitamin A. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. This protein may also modulate the supply of retinoic acid to the nuclei of endometrial cells during the menstrual cycle. [provided by RefSeq, Aug 2015]","start":139452884,"end":139480747,"strand":-1,"description":"retinol binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9920]"}, {"versioned_ensembl_gene_id":"ENSG00000118526.6","gene_symbol":"TCF21","gene_name":"transcription factor 21 [Source:HGNC Symbol;Acc:HGNC:11632]","synonyms":"POD1,bHLHa23","biotype":"protein_coding","ncbi_id":"6943","summary":"TCF21 encodes a transcription factor of the basic helix-loop-helix family. The TCF21 product is mesoderm specific, and expressed in embryonic epicardium, mesenchyme-derived tissues of lung, gut, gonad, and both mesenchymal and glomerular epithelial cells in the kidney. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":133889138,"end":133895553,"strand":1,"description":"transcription factor 21 [Source:HGNC Symbol;Acc:HGNC:11632]"}, {"versioned_ensembl_gene_id":"ENSG00000125207.7","gene_symbol":"PIWIL1","gene_name":"piwi like RNA-mediated gene silencing 1 [Source:HGNC Symbol;Acc:HGNC:9007]","synonyms":"PIWI,HIWI,CT80.1","biotype":"protein_coding","ncbi_id":"9271","summary":"This gene encodes a member of the PIWI subfamily of Argonaute proteins, evolutionarily conserved proteins containing both PAZ and Piwi motifs that play important roles in stem cell self-renewal, RNA silencing, and translational regulation in diverse organisms. The encoded protein may play a role as an intrinsic regulator of the self-renewal capacity of germline and hematopoietic stem cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":130337887,"end":130372637,"strand":1,"description":"piwi like RNA-mediated gene silencing 1 [Source:HGNC Symbol;Acc:HGNC:9007]"}, {"versioned_ensembl_gene_id":"ENSG00000130635.15","gene_symbol":"COL5A1","gene_name":"collagen type V alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2209]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1289","summary":"This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. The encoded procollagen protein occurs commonly as the heterotrimer pro-alpha1(V)-pro-alpha1(V)-pro-alpha2(V). Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":134641774,"end":134844843,"strand":1,"description":"collagen type V alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2209]"}, {"versioned_ensembl_gene_id":"ENSG00000239991.1","gene_symbol":"AC092059.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55166910,"end":55175732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140931.19","gene_symbol":"CMTM3","gene_name":"CKLF like MARVEL transmembrane domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19174]","synonyms":"FLJ31762,CKLFSF3,BNAS2","biotype":"protein_coding","ncbi_id":"123920","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 16. Alternatively spliced transcript variants containing different 5' UTRs, but encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":66603874,"end":66613892,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19174]"}, {"versioned_ensembl_gene_id":"ENSG00000269352.1","gene_symbol":"PTOV1-AS2","gene_name":"PTOV1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51284]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928378","summary":null,"start":49856970,"end":49859289,"strand":-1,"description":"PTOV1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51284]"}, {"versioned_ensembl_gene_id":"ENSG00000267053.6","gene_symbol":"AC012617.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36304580,"end":36312668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259219.1","gene_symbol":"AC084855.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99976481,"end":99980774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272907.1","gene_symbol":"AL844539.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837857,"end":28838994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042429.11","gene_symbol":"MED17","gene_name":"mediator complex subunit 17 [Source:HGNC Symbol;Acc:HGNC:2375]","synonyms":"TRAP80,SRB4,DRIP80,CRSP77,CRSP6","biotype":"protein_coding","ncbi_id":"9440","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008]","start":93784227,"end":93814963,"strand":1,"description":"mediator complex subunit 17 [Source:HGNC Symbol;Acc:HGNC:2375]"}, {"versioned_ensembl_gene_id":"ENSG00000162775.14","gene_symbol":"RBM15","gene_name":"RNA binding motif protein 15 [Source:HGNC Symbol;Acc:HGNC:14959]","synonyms":"OTT1,OTT","biotype":"protein_coding","ncbi_id":"64783","summary":"Members of the SPEN (Split-end) family of proteins, including RBM15, have repressor function in several signaling pathways and may bind to RNA through interaction with spliceosome components (Hiriart et al., 2005 [PubMed 16129689]).[supplied by OMIM, Feb 2009]","start":110338506,"end":110346681,"strand":1,"description":"RNA binding motif protein 15 [Source:HGNC Symbol;Acc:HGNC:14959]"}, {"versioned_ensembl_gene_id":"ENSG00000235458.1","gene_symbol":"CR753818.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29745766,"end":29745990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258469.1","gene_symbol":"CHMP4BP1","gene_name":"charged multivesicular body protein 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100307126","summary":null,"start":55298644,"end":55299231,"strand":1,"description":"charged multivesicular body protein 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43616]"}, {"versioned_ensembl_gene_id":"ENSG00000283412.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":87648489,"end":87648549,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000254715.3","gene_symbol":"OR7E154P","gene_name":"olfactory receptor family 7 subfamily E member 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:31309]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403296","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7705182,"end":7706113,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:31309]"}, {"versioned_ensembl_gene_id":"ENSG00000196357.11","gene_symbol":"ZNF565","gene_name":"zinc finger protein 565 [Source:HGNC Symbol;Acc:HGNC:26726]","synonyms":"FLJ36991","biotype":"protein_coding","ncbi_id":"147929","summary":null,"start":36182060,"end":36246257,"strand":-1,"description":"zinc finger protein 565 [Source:HGNC Symbol;Acc:HGNC:26726]"}, {"versioned_ensembl_gene_id":"ENSG00000179862.6","gene_symbol":"CITED4","gene_name":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4 [Source:HGNC Symbol;Acc:HGNC:18696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163732","summary":"The protein encoded by this intronless gene belongs to the CITED family of transcriptional coactivators that bind to several proteins, including CREB-binding protein (CBP) and p300, via a conserved 32 aa C-terminal motif, and regulate gene transcription. This protein also interacts with transcription factor AP2 (TFAP2), and thus may function as a co-activator for TFAP2. Hypermethylation and transcriptional downregulation of this gene has been observed in oligodendroglial tumors with deletions of chromosomal arms 1p and 19q, and associated with longer recurrence-free and overall survival of patients with oligodendroglial tumors. [provided by RefSeq, Aug 2011]","start":40861051,"end":40862366,"strand":-1,"description":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4 [Source:HGNC Symbol;Acc:HGNC:18696]"}, {"versioned_ensembl_gene_id":"ENSG00000218586.3","gene_symbol":"AC006971.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54933699,"end":54938184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187800.13","gene_symbol":"PEAR1","gene_name":"platelet endothelial aggregation receptor 1 [Source:HGNC Symbol;Acc:HGNC:33631]","synonyms":"MEGF12,JEDI,FLJ00193","biotype":"protein_coding","ncbi_id":"375033","summary":"PEAR1 is a platelet receptor that signals upon the formation of platelet-platelet contacts independent of platelet activation and secondary to platelet aggregation (Nanda et al., 2005 [PubMed 15851471]).[supplied by OMIM, Mar 2008]","start":156893698,"end":156916434,"strand":1,"description":"platelet endothelial aggregation receptor 1 [Source:HGNC Symbol;Acc:HGNC:33631]"}, {"versioned_ensembl_gene_id":"ENSG00000249995.1","gene_symbol":"ECM1P2","gene_name":"extracellular matrix protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481698","summary":null,"start":12639086,"end":12641009,"strand":1,"description":"extracellular matrix protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49737]"}, {"versioned_ensembl_gene_id":"ENSG00000223852.7","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672345,"end":29681055,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000229254.1","gene_symbol":"OR8C1P","gene_name":"olfactory receptor family 8 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8478]","synonyms":"OR912-45,OR912-106,OR8C4P,OR8C3P,OR11-175","biotype":"unprocessed_pseudogene","ncbi_id":"8580","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124376877,"end":124377801,"strand":-1,"description":"olfactory receptor family 8 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8478]"}, {"versioned_ensembl_gene_id":"ENSG00000144115.16","gene_symbol":"THNSL2","gene_name":"threonine synthase like 2 [Source:HGNC Symbol;Acc:HGNC:25602]","synonyms":"TSH2,SOFAT,FLJ10916","biotype":"protein_coding","ncbi_id":"55258","summary":"This gene encodes a threonine synthase-like protein. A similar enzyme in mouse can catalyze the degradation of O-phospho-homoserine to a-ketobutyrate, phosphate, and ammonia. This protein also has phospho-lyase activity on both gamma and beta phosphorylated substrates. In mouse an alternatively spliced form of this protein has been shown to act as a cytokine and can induce the production of the inflammatory cytokine IL6 in osteoblasts. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":88170295,"end":88186636,"strand":1,"description":"threonine synthase like 2 [Source:HGNC Symbol;Acc:HGNC:25602]"}, {"versioned_ensembl_gene_id":"ENSG00000198633.10","gene_symbol":"ZNF534","gene_name":"zinc finger protein 534 [Source:HGNC Symbol;Acc:HGNC:26337]","synonyms":"KRBO3,FLJ25344","biotype":"protein_coding","ncbi_id":"147658","summary":null,"start":52429187,"end":52452315,"strand":1,"description":"zinc finger protein 534 [Source:HGNC Symbol;Acc:HGNC:26337]"}, {"versioned_ensembl_gene_id":"ENSG00000205495.1","gene_symbol":"OR52J3","gene_name":"olfactory receptor family 52 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:14799]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119679","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5046526,"end":5047461,"strand":1,"description":"olfactory receptor family 52 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:14799]"}, {"versioned_ensembl_gene_id":"ENSG00000254364.1","gene_symbol":"AP000424.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100492528,"end":100493713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235485.1","gene_symbol":"AL021877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34589085,"end":34591278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237770.2","gene_symbol":"SPATA31D2P","gene_name":"SPATA31 subfamily D member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38607]","synonyms":"FAM75D2P","biotype":"unprocessed_pseudogene","ncbi_id":"100130636","summary":null,"start":81966564,"end":81972130,"strand":1,"description":"SPATA31 subfamily D member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38607]"}, {"versioned_ensembl_gene_id":"ENSG00000126787.12","gene_symbol":"DLGAP5","gene_name":"DLG associated protein 5 [Source:HGNC Symbol;Acc:HGNC:16864]","synonyms":"KIAA0008,HURP,DLG7,DLG1","biotype":"protein_coding","ncbi_id":"9787","summary":null,"start":55148112,"end":55191678,"strand":-1,"description":"DLG associated protein 5 [Source:HGNC Symbol;Acc:HGNC:16864]"}, {"versioned_ensembl_gene_id":"ENSG00000265289.1","gene_symbol":"AC104996.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30059339,"end":30065677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223458.2","gene_symbol":"LMO7DN-IT1","gene_name":"LMO7DN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49790]","synonyms":"TCONS_00021569,C13orf45-IT1","biotype":"sense_intronic","ncbi_id":"104326189","summary":null,"start":75876886,"end":75881127,"strand":1,"description":"LMO7DN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49790]"}, {"versioned_ensembl_gene_id":"ENSG00000261535.1","gene_symbol":"AC005086.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102153355,"end":102154463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177338.13","gene_symbol":"LINC00469","gene_name":"long intergenic non-protein coding RNA 469 [Source:HGNC Symbol;Acc:HGNC:26863]","synonyms":"C17orf54,FLJ40319","biotype":"lincRNA","ncbi_id":"283982","summary":null,"start":73750330,"end":73828520,"strand":-1,"description":"long intergenic non-protein coding RNA 469 [Source:HGNC Symbol;Acc:HGNC:26863]"}, {"versioned_ensembl_gene_id":"ENSG00000176884.14","gene_symbol":"GRIN1","gene_name":"glutamate ionotropic receptor NMDA type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4584]","synonyms":"NMDAR1,GluN1","biotype":"protein_coding","ncbi_id":"2902","summary":"The protein encoded by this gene is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligand-gated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. Cell-specific factors are thought to control expression of different isoforms, possibly contributing to the functional diversity of the subunits. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]","start":137138390,"end":137168762,"strand":1,"description":"glutamate ionotropic receptor NMDA type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4584]"}, {"versioned_ensembl_gene_id":"ENSG00000186150.4","gene_symbol":"UBL4B","gene_name":"ubiquitin like 4B [Source:HGNC Symbol;Acc:HGNC:32309]","synonyms":"FLJ25690","biotype":"protein_coding","ncbi_id":"164153","summary":null,"start":110112468,"end":110113945,"strand":1,"description":"ubiquitin like 4B [Source:HGNC Symbol;Acc:HGNC:32309]"}, {"versioned_ensembl_gene_id":"ENSG00000259744.1","gene_symbol":"AC009269.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70848883,"end":70849770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143816.7","gene_symbol":"WNT9A","gene_name":"Wnt family member 9A [Source:HGNC Symbol;Acc:HGNC:12778]","synonyms":"WNT14","biotype":"protein_coding","ncbi_id":"7483","summary":"The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is expressed in gastric cancer cell lines. The protein encoded by this gene shows 75% amino acid identity to chicken Wnt14, which has been shown to play a central role in initiating synovial joint formation in the chick limb. This gene is clustered with another family member, WNT3A, in the chromosome 1q42 region. [provided by RefSeq, Jul 2008]","start":227918656,"end":227947898,"strand":-1,"description":"Wnt family member 9A [Source:HGNC Symbol;Acc:HGNC:12778]"}, {"versioned_ensembl_gene_id":"ENSG00000224346.1","gene_symbol":"BICD1P1","gene_name":"BICD cargo adaptor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391472","summary":null,"start":200844240,"end":200845461,"strand":1,"description":"BICD cargo adaptor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51374]"}, {"versioned_ensembl_gene_id":"ENSG00000260031.1","gene_symbol":"RPL10P14","gene_name":"ribosomal protein L10 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:43897]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390729","summary":null,"start":50151280,"end":50151577,"strand":-1,"description":"ribosomal protein L10 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:43897]"}, {"versioned_ensembl_gene_id":"ENSG00000226416.1","gene_symbol":"MRPL23-AS1","gene_name":"MRPL23 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42812]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100133545","summary":null,"start":1983237,"end":1989920,"strand":-1,"description":"MRPL23 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42812]"}, {"versioned_ensembl_gene_id":"ENSG00000239886.5","gene_symbol":"KRTAP9-2","gene_name":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]","synonyms":"KAP9.2","biotype":"protein_coding","ncbi_id":"83899","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41226648,"end":41227652,"strand":1,"description":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]"}, {"versioned_ensembl_gene_id":"ENSG00000237950.1","gene_symbol":"AL357079.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43944370,"end":43946551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183148.6","gene_symbol":"ANKRD20A2","gene_name":"ankyrin repeat domain 20 family member A2 [Source:HGNC Symbol;Acc:HGNC:31979]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441430","summary":null,"start":40223285,"end":40266392,"strand":1,"description":"ankyrin repeat domain 20 family member A2 [Source:HGNC Symbol;Acc:HGNC:31979]"}, {"versioned_ensembl_gene_id":"ENSG00000223839.7","gene_symbol":"FAM95B1","gene_name":"family with sequence similarity 95 member B1 [Source:HGNC Symbol;Acc:HGNC:32318]","synonyms":"DKFZp686P0734","biotype":"lincRNA","ncbi_id":"100133036","summary":null,"start":40321299,"end":40329221,"strand":1,"description":"family with sequence similarity 95 member B1 [Source:HGNC Symbol;Acc:HGNC:32318]"}, {"versioned_ensembl_gene_id":"ENSG00000162402.13","gene_symbol":"USP24","gene_name":"ubiquitin specific peptidase 24 [Source:HGNC Symbol;Acc:HGNC:12623]","synonyms":"KIAA1057","biotype":"protein_coding","ncbi_id":"23358","summary":"Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP24 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Mar 2008]","start":55066359,"end":55215113,"strand":-1,"description":"ubiquitin specific peptidase 24 [Source:HGNC Symbol;Acc:HGNC:12623]"}, {"versioned_ensembl_gene_id":"ENSG00000254313.1","gene_symbol":"AC090821.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133786093,"end":133786268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172086.7","gene_symbol":"KRCC1","gene_name":"lysine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:28039]","synonyms":"FLJ22333","biotype":"protein_coding","ncbi_id":"51315","summary":null,"start":88027205,"end":88055729,"strand":-1,"description":"lysine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:28039]"}, {"versioned_ensembl_gene_id":"ENSG00000260973.1","gene_symbol":"AC009021.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22610531,"end":22612196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165606.8","gene_symbol":"DRGX","gene_name":"dorsal root ganglia homeobox [Source:HGNC Symbol;Acc:HGNC:21536]","synonyms":"PRRXL1,DRG11","biotype":"protein_coding","ncbi_id":"644168","summary":null,"start":49364181,"end":49396016,"strand":-1,"description":"dorsal root ganglia homeobox [Source:HGNC Symbol;Acc:HGNC:21536]"}, {"versioned_ensembl_gene_id":"ENSG00000232447.1","gene_symbol":"MTND5P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42034]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873210","summary":null,"start":84521725,"end":84523915,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42034]"}, {"versioned_ensembl_gene_id":"ENSG00000233349.1","gene_symbol":"LINC00333","gene_name":"long intergenic non-protein coding RNA 333 [Source:HGNC Symbol;Acc:HGNC:42050]","synonyms":"NCRNA00333","biotype":"lincRNA","ncbi_id":"100874128","summary":null,"start":84562364,"end":84563236,"strand":1,"description":"long intergenic non-protein coding RNA 333 [Source:HGNC Symbol;Acc:HGNC:42050]"}, {"versioned_ensembl_gene_id":"ENSG00000228597.1","gene_symbol":"MTND4P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873211","summary":null,"start":84520103,"end":84521568,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42035]"}, {"versioned_ensembl_gene_id":"ENSG00000164951.15","gene_symbol":"PDP1","gene_name":"pyruvate dehyrogenase phosphatase catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:9279]","synonyms":"PPM2C,PPM2A,PDP,PDH","biotype":"protein_coding","ncbi_id":"54704","summary":"Pyruvate dehydrogenase (E1) is one of the three components (E1, E2, and E3) of the large pyruvate dehydrogenase complex. Pyruvate dehydrogenase kinases catalyze phosphorylation of serine residues of E1 to inactivate the E1 component and inhibit the complex. Pyruvate dehydrogenase phosphatases catalyze the dephosphorylation and activation of the E1 component to reverse the effects of pyruvate dehydrogenase kinases. Pyruvate dehydrogenase phosphatase is a heterodimer consisting of catalytic and regulatory subunits. Two catalytic subunits have been reported; one is predominantly expressed in skeletal muscle and another one is is much more abundant in the liver. The catalytic subunit, encoded by this gene, is the former, and belongs to the protein phosphatase 2C (PP2C) superfamily. Along with the pyruvate dehydrogenase complex and pyruvate dehydrogenase kinases, this enzyme is located in the mitochondrial matrix. Mutation in this gene causes pyruvate dehydrogenase phosphatase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Jun 2009]","start":93857807,"end":93926066,"strand":1,"description":"pyruvate dehyrogenase phosphatase catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:9279]"}, {"versioned_ensembl_gene_id":"ENSG00000215244.2","gene_symbol":"AL137145.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6277687,"end":6335982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271196.1","gene_symbol":"AC113403.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138454540,"end":138454732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234485.5","gene_symbol":"OR7E46P","gene_name":"olfactory receptor family 7 subfamily E member 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:8420]","synonyms":"OST379,MCEEP","biotype":"unprocessed_pseudogene","ncbi_id":"402077","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71037685,"end":71038703,"strand":1,"description":"olfactory receptor family 7 subfamily E member 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:8420]"}, {"versioned_ensembl_gene_id":"ENSG00000273473.1","gene_symbol":"BX649601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134168769,"end":134169340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187048.12","gene_symbol":"CYP4A11","gene_name":"cytochrome P450 family 4 subfamily A member 11 [Source:HGNC Symbol;Acc:HGNC:2642]","synonyms":"CYP4AII,CYP4A2","biotype":"protein_coding","ncbi_id":"1579","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates medium-chain fatty acids such as laurate and myristate. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]","start":46929177,"end":46941484,"strand":-1,"description":"cytochrome P450 family 4 subfamily A member 11 [Source:HGNC Symbol;Acc:HGNC:2642]"}, {"versioned_ensembl_gene_id":"ENSG00000197984.4","gene_symbol":"OR51A8P","gene_name":"olfactory receptor family 51 subfamily A member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15189]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401662","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4830175,"end":4833072,"strand":1,"description":"olfactory receptor family 51 subfamily A member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15189]"}, {"versioned_ensembl_gene_id":"ENSG00000227023.1","gene_symbol":"OR51A3P","gene_name":"olfactory receptor family 51 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14794]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79532","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4937371,"end":4938294,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14794]"}, {"versioned_ensembl_gene_id":"ENSG00000133193.12","gene_symbol":"FAM104A","gene_name":"family with sequence similarity 104 member A [Source:HGNC Symbol;Acc:HGNC:25918]","synonyms":"FLJ14775","biotype":"protein_coding","ncbi_id":"84923","summary":null,"start":73207353,"end":73236753,"strand":-1,"description":"family with sequence similarity 104 member A [Source:HGNC Symbol;Acc:HGNC:25918]"}, {"versioned_ensembl_gene_id":"ENSG00000187021.14","gene_symbol":"PNLIPRP1","gene_name":"pancreatic lipase related protein 1 [Source:HGNC Symbol;Acc:HGNC:9156]","synonyms":"PLRP1","biotype":"protein_coding","ncbi_id":"5407","summary":null,"start":116590385,"end":116609175,"strand":1,"description":"pancreatic lipase related protein 1 [Source:HGNC Symbol;Acc:HGNC:9156]"}, {"versioned_ensembl_gene_id":"ENSG00000243232.4","gene_symbol":"PCDHAC2","gene_name":"protocadherin alpha subfamily C, 2 [Source:HGNC Symbol;Acc:HGNC:8677]","synonyms":"PCDH-ALPHA-C2","biotype":"protein_coding","ncbi_id":"56134","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140966235,"end":141012344,"strand":1,"description":"protocadherin alpha subfamily C, 2 [Source:HGNC Symbol;Acc:HGNC:8677]"}, {"versioned_ensembl_gene_id":"ENSG00000168710.17","gene_symbol":"AHCYL1","gene_name":"adenosylhomocysteinase like 1 [Source:HGNC Symbol;Acc:HGNC:344]","synonyms":"XPVKONA,PPP1R78,IRBIT","biotype":"protein_coding","ncbi_id":"10768","summary":"The protein encoded by this gene interacts with inositol 1,4,5-trisphosphate receptor, type 1 and may be involved in the conversion of S-adenosyl-L-homocysteine to L-homocysteine and adenosine. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":109984686,"end":110023741,"strand":1,"description":"adenosylhomocysteinase like 1 [Source:HGNC Symbol;Acc:HGNC:344]"}, {"versioned_ensembl_gene_id":"ENSG00000104517.12","gene_symbol":"UBR5","gene_name":"ubiquitin protein ligase E3 component n-recognin 5 [Source:HGNC Symbol;Acc:HGNC:16806]","synonyms":"KIAA0896,HYD,EDD1,EDD,DD5","biotype":"protein_coding","ncbi_id":"51366","summary":"This gene encodes a progestin-induced protein, which belongs to the HECT (homology to E6-AP carboxyl terminus) family. The HECT family proteins function as E3 ubiquitin-protein ligases, targeting specific proteins for ubiquitin-mediated proteolysis. This gene is localized to chromosome 8q22 which is disrupted in a variety of cancers. This gene potentially has a role in regulation of cell proliferation or differentiation. [provided by RefSeq, Jul 2008]","start":102253012,"end":102412841,"strand":-1,"description":"ubiquitin protein ligase E3 component n-recognin 5 [Source:HGNC Symbol;Acc:HGNC:16806]"}, {"versioned_ensembl_gene_id":"ENSG00000274294.1","gene_symbol":"AC015660.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99416584,"end":99417204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235831.6","gene_symbol":"BHLHE40-AS1","gene_name":"BHLHE40 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44471]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507582","summary":null,"start":4896809,"end":4979961,"strand":-1,"description":"BHLHE40 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44471]"}, {"versioned_ensembl_gene_id":"ENSG00000227171.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"HZFw1,LIRF","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30060156,"end":30065777,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000275154.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":91714915,"end":91715130,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000147206.16","gene_symbol":"NXF3","gene_name":"nuclear RNA export factor 3 [Source:HGNC Symbol;Acc:HGNC:8073]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56000","summary":"This gene is one member of a family of nuclear RNA export factor genes. Common domain features of this family are a noncanonical RNP-type RNA-binding domain (RBD), 4 leucine-rich repeats (LRRs), a nuclear transport factor 2 (NTF2)-like domain that allows heterodimerization with NTF2-related export protein-1 (NXT1), and a ubiquitin-associated domain that mediates interactions with nucleoporins. The LRRs and NTF2-like domains are required for export activity. Alternative splicing seems to be a common mechanism in this gene family. The encoded protein of this gene has shortened LRR and ubiquitin-associated domains and its RDB is unable to bind RNA. It is located in the nucleoplasm but is not associated with either the nuclear envelope or the nucleolus. [provided by RefSeq, Jul 2008]","start":103075810,"end":103093125,"strand":-1,"description":"nuclear RNA export factor 3 [Source:HGNC Symbol;Acc:HGNC:8073]"}, {"versioned_ensembl_gene_id":"ENSG00000232159.3","gene_symbol":"RAB9BP1","gene_name":"RAB9B, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9793]","synonyms":"RAB9P1","biotype":"processed_pseudogene","ncbi_id":"9366","summary":null,"start":105099473,"end":105100098,"strand":1,"description":"RAB9B, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9793]"}, {"versioned_ensembl_gene_id":"ENSG00000227971.1","gene_symbol":"AC078809.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189645327,"end":189645466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215788.9","gene_symbol":"TNFRSF25","gene_name":"TNF receptor superfamily member 25 [Source:HGNC Symbol;Acc:HGNC:11910]","synonyms":"TNFRSF12,LARD,DR3,DDR3,APO-3,WSL-LR,WSL-1,TRAMP,TR3","biotype":"protein_coding","ncbi_id":"8718","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is expressed preferentially in the tissues enriched in lymphocytes, and it may play a role in regulating lymphocyte homeostasis. This receptor has been shown to stimulate NF-kappa B activity and regulate cell apoptosis. The signal transduction of this receptor is mediated by various death domain containing adaptor proteins. Knockout studies in mice suggested the role of this gene in the removal of self-reactive T cells in the thymus. Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported, most of which are potentially secreted molecules. The alternative splicing of this gene in B and T cells encounters a programmed change upon T-cell activation, which predominantly produces full-length, membrane bound isoforms, and is thought to be involved in controlling lymphocyte proliferation induced by T-cell activation. [provided by RefSeq, Jul 2008]","start":6461151,"end":6466195,"strand":-1,"description":"TNF receptor superfamily member 25 [Source:HGNC Symbol;Acc:HGNC:11910]"}, {"versioned_ensembl_gene_id":"ENSG00000231222.1","gene_symbol":"ARF4P4","gene_name":"ADP ribosylation factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37628]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129023","summary":null,"start":80888348,"end":80888867,"strand":1,"description":"ADP ribosylation factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37628]"}, {"versioned_ensembl_gene_id":"ENSG00000185559.13","gene_symbol":"DLK1","gene_name":"delta like non-canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2907]","synonyms":"ZOG,Pref-1,pG2,FA1,Delta1","biotype":"protein_coding","ncbi_id":"8788","summary":"This gene encodes a transmembrane protein that contains multiple epidermal growth factor repeats that functions as a regulator of cell growth. The encoded protein is involved in the differentiation of several cell types including adipocytes. This gene is located in a region of chromosome 14 frequently showing unparental disomy, and is imprinted and expressed from the paternal allele. A single nucleotide variant in this gene is associated with child and adolescent obesity and shows polar overdominance, where heterozygotes carrying an active paternal allele express the phenotype, while mutant homozygotes are normal. [provided by RefSeq, Nov 2015]","start":100725705,"end":100738224,"strand":1,"description":"delta like non-canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2907]"}, {"versioned_ensembl_gene_id":"ENSG00000253564.1","gene_symbol":"AC100823.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73215929,"end":73216627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237898.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.7,dJ25J6.6,HCG16","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28987124,"end":28988405,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000197674.6","gene_symbol":"OR51C1P","gene_name":"olfactory receptor family 51 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15191]","synonyms":"OST734,OR51C3P,OR51C2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401661","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4690423,"end":4697831,"strand":-1,"description":"olfactory receptor family 51 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15191]"}, {"versioned_ensembl_gene_id":"ENSG00000221900.5","gene_symbol":"POM121L12","gene_name":"POM121 transmembrane nucleoporin like 12 [Source:HGNC Symbol;Acc:HGNC:25369]","synonyms":"DKFZp564N2472","biotype":"protein_coding","ncbi_id":"285877","summary":null,"start":53035642,"end":53036924,"strand":1,"description":"POM121 transmembrane nucleoporin like 12 [Source:HGNC Symbol;Acc:HGNC:25369]"}, {"versioned_ensembl_gene_id":"ENSG00000230257.2","gene_symbol":"NFE4","gene_name":"nuclear factor, erythroid 4 [Source:HGNC Symbol;Acc:HGNC:29902]","synonyms":"NF-E4","biotype":"protein_coding","ncbi_id":"58160","summary":"The erythroid-specific protein encoded by this gene, and the ubiquitous transcription factor CP2, form the stage selector protein (SSP) complex, which is involved in preferential expression of the gamma-globin genes in fetal erythroid cells. Alternate use of an in-frame upstream non-AUG (CUG) translation initiation codon, and a downstream AUG codon, results in two isoforms. While the long isoform (22 kDa) acts as an activator, the short isoform (14 kDa) has been shown to repress gamma-globin gene expression. This gene is located in an intron of the FBXL13 gene on the opposite strand. [provided by RefSeq, Jul 2008]","start":102973437,"end":102988856,"strand":1,"description":"nuclear factor, erythroid 4 [Source:HGNC Symbol;Acc:HGNC:29902]"}, {"versioned_ensembl_gene_id":"ENSG00000267361.1","gene_symbol":"AC005495.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69094289,"end":69095499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115484.14","gene_symbol":"CCT4","gene_name":"chaperonin containing TCP1 subunit 4 [Source:HGNC Symbol;Acc:HGNC:1617]","synonyms":"Cctd","biotype":"protein_coding","ncbi_id":"10575","summary":"The chaperonin containing TCP1 (MIM 186980) complex (CCT), also called the TCP1 ring complex, consists of 2 back-to-back rings, each containing 8 unique but homologous subunits, such as CCT4. CCT assists the folding of newly translated polypeptide substrates through multiple rounds of ATP-driven release and rebinding of partially folded intermediate forms. Substrates of CCT include the cytoskeletal proteins actin (see MIM 102560) and tubulin (see MIM 191130), as well as alpha-transducin (MIM 139330) (Won et al., 1998 [PubMed 9819444]).[supplied by OMIM, Mar 2008]","start":61868089,"end":61888804,"strand":-1,"description":"chaperonin containing TCP1 subunit 4 [Source:HGNC Symbol;Acc:HGNC:1617]"}, {"versioned_ensembl_gene_id":"ENSG00000241172.3","gene_symbol":"RN7SL70P","gene_name":"RNA, 7SL, cytoplasmic 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:46086]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479249","summary":null,"start":18957957,"end":18958258,"strand":-1,"description":"RNA, 7SL, cytoplasmic 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:46086]"}, {"versioned_ensembl_gene_id":"ENSG00000207014.1","gene_symbol":"SNORD116-3","gene_name":"small nucleolar RNA, C/D box 116-3 [Source:HGNC Symbol;Acc:HGNC:33069]","synonyms":"HBII-85-3","biotype":"snoRNA","ncbi_id":"100033415","summary":null,"start":25056860,"end":25056954,"strand":1,"description":"small nucleolar RNA, C/D box 116-3 [Source:HGNC Symbol;Acc:HGNC:33069]"}, {"versioned_ensembl_gene_id":"ENSG00000277464.1","gene_symbol":"RN7SL286P","gene_name":"RNA, 7SL, cytoplasmic 286, pseudogene [Source:HGNC Symbol;Acc:HGNC:46302]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479327","summary":null,"start":32602121,"end":32602411,"strand":1,"description":"RNA, 7SL, cytoplasmic 286, pseudogene [Source:HGNC Symbol;Acc:HGNC:46302]"}, {"versioned_ensembl_gene_id":"ENSG00000139549.2","gene_symbol":"DHH","gene_name":"desert hedgehog [Source:HGNC Symbol;Acc:HGNC:2865]","synonyms":"HHG-3,MGC35145","biotype":"protein_coding","ncbi_id":"50846","summary":"This gene encodes a member of the hedgehog family. The hedgehog gene family encodes signaling molecules that play an important role in regulating morphogenesis. This protein is predicted to be made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the organism. Defects in this protein have been associated with partial gonadal dysgenesis (PGD) accompanied by minifascicular polyneuropathy. This protein may be involved in both male gonadal differentiation and perineurial development. [provided by RefSeq, May 2010]","start":49089421,"end":49094819,"strand":-1,"description":"desert hedgehog [Source:HGNC Symbol;Acc:HGNC:2865]"}, {"versioned_ensembl_gene_id":"ENSG00000284438.1","gene_symbol":"AC018793.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4338660,"end":4339244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284546.1","gene_symbol":"AC018793.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4329865,"end":4330449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257292.2","gene_symbol":"AC117372.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38205098,"end":38206009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272688.1","gene_symbol":"AP005329.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3246401,"end":3247086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227189.2","gene_symbol":"AC092535.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1151372,"end":1153701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257173.1","gene_symbol":"AK6P2","gene_name":"adenylate kinase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51679]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128817","summary":null,"start":38078529,"end":38078999,"strand":-1,"description":"adenylate kinase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51679]"}, {"versioned_ensembl_gene_id":"ENSG00000182986.12","gene_symbol":"ZNF320","gene_name":"zinc finger protein 320 [Source:HGNC Symbol;Acc:HGNC:13842]","synonyms":"ZFPL,DKFZp686G16228","biotype":"protein_coding","ncbi_id":"162967","summary":"ZNF320 encodes a Kruppel-like zinc finger protein. Members of this protein family are involved in activation or repression of transcription.[supplied by OMIM, Jul 2002]","start":52863790,"end":52897693,"strand":-1,"description":"zinc finger protein 320 [Source:HGNC Symbol;Acc:HGNC:13842]"}, {"versioned_ensembl_gene_id":"ENSG00000255875.2","gene_symbol":"AC008813.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52809824,"end":52810708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256338.2","gene_symbol":"RPL41P2","gene_name":"ribosomal protein L41 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"22970","summary":null,"start":28315651,"end":28316059,"strand":1,"description":"ribosomal protein L41 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10357]"}, {"versioned_ensembl_gene_id":"ENSG00000068885.14","gene_symbol":"IFT80","gene_name":"intraflagellar transport 80 [Source:HGNC Symbol;Acc:HGNC:29262]","synonyms":"WDR56,KIAA1374","biotype":"protein_coding","ncbi_id":"57560","summary":"The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]","start":160256986,"end":160399880,"strand":-1,"description":"intraflagellar transport 80 [Source:HGNC Symbol;Acc:HGNC:29262]"}, {"versioned_ensembl_gene_id":"ENSG00000273348.1","gene_symbol":"AC027449.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22347846,"end":22348252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050438.16","gene_symbol":"SLC4A8","gene_name":"solute carrier family 4 member 8 [Source:HGNC Symbol;Acc:HGNC:11034]","synonyms":"NBC3","biotype":"protein_coding","ncbi_id":"9498","summary":"The protein encoded by this gene is a membrane protein that functions to transport sodium and bicarbonate ions across the cell membrane. The encoded protein is important for pH regulation in neurons. The activity of this protein can be inhibited by 4,4'-Di-isothiocyanatostilbene-2,2'-disulfonic acid (DIDS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":51391317,"end":51515763,"strand":1,"description":"solute carrier family 4 member 8 [Source:HGNC Symbol;Acc:HGNC:11034]"}, {"versioned_ensembl_gene_id":"ENSG00000147601.13","gene_symbol":"TERF1","gene_name":"telomeric repeat binding factor 1 [Source:HGNC Symbol;Acc:HGNC:11728]","synonyms":"TRF1,TRF,TRBF1,PIN2","biotype":"protein_coding","ncbi_id":"7013","summary":"This gene encodes a telomere specific protein which is a component of the telomere nucleoprotein complex. This protein is present at telomeres throughout the cell cycle and functions as an inhibitor of telomerase, acting in cis to limit the elongation of individual chromosome ends. The protein structure contains a C-terminal Myb motif, a dimerization domain near its N-terminus and an acidic N-terminus. Two transcripts of this gene are alternatively spliced products. [provided by RefSeq, Jul 2008]","start":73008864,"end":73048122,"strand":1,"description":"telomeric repeat binding factor 1 [Source:HGNC Symbol;Acc:HGNC:11728]"}, {"versioned_ensembl_gene_id":"ENSG00000278193.1","gene_symbol":"AC013562.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72660584,"end":72661470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229612.1","gene_symbol":"SUMO1P2","gene_name":"SUMO1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"474337","summary":null,"start":168898136,"end":168898439,"strand":1,"description":"SUMO1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33149]"}, {"versioned_ensembl_gene_id":"ENSG00000274235.1","gene_symbol":"AC022106.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":150950109,"end":150952460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174547.13","gene_symbol":"MRPL11","gene_name":"mitochondrial ribosomal protein L11 [Source:HGNC Symbol;Acc:HGNC:14042]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65003","summary":"This nuclear gene encodes a 39S subunit component of the mitochondial ribosome. Alternative splicing results in multiple transcript variants. Pseudogenes for this gene are found on chromosomes 5 and 12. [provided by RefSeq, May 2014]","start":66435075,"end":66466738,"strand":-1,"description":"mitochondrial ribosomal protein L11 [Source:HGNC Symbol;Acc:HGNC:14042]"}, {"versioned_ensembl_gene_id":"ENSG00000068079.7","gene_symbol":"IFI35","gene_name":"interferon induced protein 35 [Source:HGNC Symbol;Acc:HGNC:5399]","synonyms":"IFP35","biotype":"protein_coding","ncbi_id":"3430","summary":null,"start":43006725,"end":43014456,"strand":1,"description":"interferon induced protein 35 [Source:HGNC Symbol;Acc:HGNC:5399]"}, {"versioned_ensembl_gene_id":"ENSG00000070886.11","gene_symbol":"EPHA8","gene_name":"EPH receptor A8 [Source:HGNC Symbol;Acc:HGNC:3391]","synonyms":"Hek3,EEK","biotype":"protein_coding","ncbi_id":"2046","summary":"This gene encodes a member of the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. The protein encoded by this gene functions as a receptor for ephrin A2, A3 and A5 and plays a role in short-range contact-mediated axonal guidance during development of the mammalian nervous system. [provided by RefSeq, Jul 2008]","start":22563564,"end":22603594,"strand":1,"description":"EPH receptor A8 [Source:HGNC Symbol;Acc:HGNC:3391]"}, {"versioned_ensembl_gene_id":"ENSG00000176472.10","gene_symbol":"ZNF575","gene_name":"zinc finger protein 575 [Source:HGNC Symbol;Acc:HGNC:27606]","synonyms":"FLJ32567","biotype":"protein_coding","ncbi_id":"284346","summary":null,"start":43525497,"end":43536130,"strand":1,"description":"zinc finger protein 575 [Source:HGNC Symbol;Acc:HGNC:27606]"}, {"versioned_ensembl_gene_id":"ENSG00000197619.13","gene_symbol":"ZNF615","gene_name":"zinc finger protein 615 [Source:HGNC Symbol;Acc:HGNC:24740]","synonyms":"FLJ33710","biotype":"protein_coding","ncbi_id":"284370","summary":null,"start":51991332,"end":52008230,"strand":-1,"description":"zinc finger protein 615 [Source:HGNC Symbol;Acc:HGNC:24740]"}, {"versioned_ensembl_gene_id":"ENSG00000255234.5","gene_symbol":"AP000446.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83286128,"end":83423516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267472.1","gene_symbol":"AC005332.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68198921,"end":68199596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257316.1","gene_symbol":"AC087311.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32985838,"end":32987070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253116.1","gene_symbol":"AC027698.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58091442,"end":58106294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204450.7","gene_symbol":"TRIM64","gene_name":"tripartite motif containing 64 [Source:HGNC Symbol;Acc:HGNC:14663]","synonyms":"TRIM64A,C11orf28","biotype":"protein_coding","ncbi_id":"120146","summary":null,"start":89968502,"end":89975228,"strand":1,"description":"tripartite motif containing 64 [Source:HGNC Symbol;Acc:HGNC:14663]"}, {"versioned_ensembl_gene_id":"ENSG00000235455.1","gene_symbol":"IQCF5-AS1","gene_name":"IQCF5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41297]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928999","summary":null,"start":51873596,"end":51875767,"strand":1,"description":"IQCF5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41297]"}, {"versioned_ensembl_gene_id":"ENSG00000053900.10","gene_symbol":"ANAPC4","gene_name":"anaphase promoting complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:19990]","synonyms":"APC4","biotype":"protein_coding","ncbi_id":"29945","summary":"A large protein complex, termed the anaphase-promoting complex (APC), or the cyclosome, promotes metaphase-anaphase transition by ubiquitinating its specific substrates such as mitotic cyclins and anaphase inhibitor, which are subsequently degraded by the 26S proteasome. Biochemical studies have shown that the vertebrate APC contains eight subunits. The composition of the APC is highly conserved in organisms from yeast to humans. The exact function of this gene product is not known. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":25377213,"end":25418498,"strand":1,"description":"anaphase promoting complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:19990]"}, {"versioned_ensembl_gene_id":"ENSG00000219085.1","gene_symbol":"NPM1P37","gene_name":"nucleophosmin 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:45216]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422261","summary":null,"start":69705287,"end":69706160,"strand":-1,"description":"nucleophosmin 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:45216]"}, {"versioned_ensembl_gene_id":"ENSG00000269825.1","gene_symbol":"AC022150.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52650437,"end":52653284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093010.13","gene_symbol":"COMT","gene_name":"catechol-O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:2228]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1312","summary":"Catechol-O-methyltransferase catalyzes the transfer of a methyl group from S-adenosylmethionine to catecholamines, including the neurotransmitters dopamine, epinephrine, and norepinephrine. This O-methylation results in one of the major degradative pathways of the catecholamine transmitters. In addition to its role in the metabolism of endogenous substances, COMT is important in the metabolism of catechol drugs used in the treatment of hypertension, asthma, and Parkinson disease. COMT is found in two forms in tissues, a soluble form (S-COMT) and a membrane-bound form (MB-COMT). The differences between S-COMT and MB-COMT reside within the N-termini. Several transcript variants are formed through the use of alternative translation initiation sites and promoters. [provided by RefSeq, Sep 2008]","start":19941607,"end":19969975,"strand":1,"description":"catechol-O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:2228]"}, {"versioned_ensembl_gene_id":"ENSG00000136931.9","gene_symbol":"NR5A1","gene_name":"nuclear receptor subfamily 5 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7983]","synonyms":"SF-1,hSF-1,FTZF1,FTZ1,ELP,AD4BP","biotype":"protein_coding","ncbi_id":"2516","summary":"The protein encoded by this gene is a transcriptional activator involved in sex determination. The encoded protein binds DNA as a monomer. Defects in this gene are a cause of XY sex reversal with or without adrenal failure as well as adrenocortical insufficiency without ovarian defect. [provided by RefSeq, Jul 2008]","start":124481236,"end":124507430,"strand":-1,"description":"nuclear receptor subfamily 5 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7983]"}, {"versioned_ensembl_gene_id":"ENSG00000223833.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31579641,"end":31583730,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000063180.8","gene_symbol":"CA11","gene_name":"carbonic anhydrase 11 [Source:HGNC Symbol;Acc:HGNC:1370]","synonyms":"CARPX1,CARP2","biotype":"protein_coding","ncbi_id":"770","summary":" Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA XI is likely a secreted protein, however, radical changes at active site residues completely conserved in CA isozymes with catalytic activity, make it unlikely that it has carbonic anhydrase activity. It shares properties in common with two other acatalytic CA isoforms, CA VIII and CA X. CA XI is most abundantly expressed in brain, and may play a general role in the central nervous system. [provided by RefSeq, Jul 2008]","start":48637942,"end":48646312,"strand":-1,"description":"carbonic anhydrase 11 [Source:HGNC Symbol;Acc:HGNC:1370]"}, {"versioned_ensembl_gene_id":"ENSG00000188383.8","gene_symbol":"GPAT2P2","gene_name":"glycerol-3-phosphate acyltransferase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52331]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653924","summary":null,"start":97081098,"end":97083249,"strand":1,"description":"glycerol-3-phosphate acyltransferase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52331]"}, {"versioned_ensembl_gene_id":"ENSG00000270983.1","gene_symbol":"AL589674.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142062717,"end":142063053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262445.3","gene_symbol":"AC099684.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1995614,"end":2003671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204670.7","gene_symbol":"IGKV1OR2-3","gene_name":"immunoglobulin kappa variable 1/OR2-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5769]","synonyms":"IGKV1/OR2-3","biotype":"IG_V_pseudogene","ncbi_id":"28866","summary":null,"start":97060128,"end":97060415,"strand":1,"description":"immunoglobulin kappa variable 1/OR2-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5769]"}, {"versioned_ensembl_gene_id":"ENSG00000236476.2","gene_symbol":"AL593856.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46742329,"end":46743133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065809.13","gene_symbol":"FAM107B","gene_name":"family with sequence similarity 107 member B [Source:HGNC Symbol;Acc:HGNC:23726]","synonyms":"FLJ45505,C10orf45,MGC11034,HITS","biotype":"protein_coding","ncbi_id":"83641","summary":null,"start":14518557,"end":14774897,"strand":-1,"description":"family with sequence similarity 107 member B [Source:HGNC Symbol;Acc:HGNC:23726]"}, {"versioned_ensembl_gene_id":"ENSG00000131471.6","gene_symbol":"AOC3","gene_name":"amine oxidase, copper containing 3 [Source:HGNC Symbol;Acc:HGNC:550]","synonyms":"VAP1,VAP-1,HPAO","biotype":"protein_coding","ncbi_id":"8639","summary":"This gene encodes a member of the semicarbazide-sensitive amine oxidase family. Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of copper and quinone cofactor. The encoded protein is localized to the cell surface, has adhesive properties as well as monoamine oxidase activity, and may be involved in leukocyte trafficking. Alterations in levels of the encoded protein may be associated with many diseases, including diabetes mellitus. A pseudogene of this gene has been described and is located approximately 9-kb downstream on the same chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":42851184,"end":42858130,"strand":1,"description":"amine oxidase, copper containing 3 [Source:HGNC Symbol;Acc:HGNC:550]"}, {"versioned_ensembl_gene_id":"ENSG00000278903.3","gene_symbol":"CU633906.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6318434,"end":6360415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250111.3","gene_symbol":"AC107982.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18835707,"end":18842364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273634.1","gene_symbol":"AC079395.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97008368,"end":97009104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254310.1","gene_symbol":"AC025755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78753596,"end":78753873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248134.1","gene_symbol":"AC079395.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97018343,"end":97018604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254170.1","gene_symbol":"AC008802.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78708734,"end":78716082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264273.1","gene_symbol":"AC107982.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18859354,"end":18861466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206948.1","gene_symbol":"SNORA36A","gene_name":"small nucleolar RNA, H/ACA box 36A [Source:HGNC Symbol;Acc:HGNC:32628]","synonyms":"ACA36","biotype":"snoRNA","ncbi_id":"677817","summary":"Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residues U105 and U1244 of 18S rRNA. [provided by RefSeq, Feb 2009]","start":154768528,"end":154768659,"strand":1,"description":"small nucleolar RNA, H/ACA box 36A [Source:HGNC Symbol;Acc:HGNC:32628]"}, {"versioned_ensembl_gene_id":"ENSG00000239967.1","gene_symbol":"OR2A41P","gene_name":"olfactory receptor family 2 subfamily A member 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:31246]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403234","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144077721,"end":144077825,"strand":1,"description":"olfactory receptor family 2 subfamily A member 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:31246]"}, {"versioned_ensembl_gene_id":"ENSG00000135905.18","gene_symbol":"DOCK10","gene_name":"dedicator of cytokinesis 10 [Source:HGNC Symbol;Acc:HGNC:23479]","synonyms":"ZIZ3,KIAA0694","biotype":"protein_coding","ncbi_id":"55619","summary":"This gene encodes a member of the dedicator of cytokinesis protein family. Members of this family are guanosine nucleotide exchange factors for Rho GTPases and defined by the presence of conserved DOCK-homology regions. The encoded protein belongs to the D (or Zizimin) subfamily of DOCK proteins, which also contain an N-terminal pleckstrin homology domain. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2014]","start":224765090,"end":225042445,"strand":-1,"description":"dedicator of cytokinesis 10 [Source:HGNC Symbol;Acc:HGNC:23479]"}, {"versioned_ensembl_gene_id":"ENSG00000186431.18","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54874248,"end":54890472,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000144188.9","gene_symbol":"TRIM43CP","gene_name":"tripartite motif containing 43C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43981]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643445","summary":null,"start":97025981,"end":97031636,"strand":-1,"description":"tripartite motif containing 43C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43981]"}, {"versioned_ensembl_gene_id":"ENSG00000215154.6","gene_symbol":"AC141586.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":2603350,"end":2630494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248909.1","gene_symbol":"HMGB1P21","gene_name":"high mobility group box 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39106]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419947","summary":null,"start":78644265,"end":78644845,"strand":-1,"description":"high mobility group box 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39106]"}, {"versioned_ensembl_gene_id":"ENSG00000006128.11","gene_symbol":"TAC1","gene_name":"tachykinin precursor 1 [Source:HGNC Symbol;Acc:HGNC:11517]","synonyms":"TAC2,NPK,NKNA","biotype":"protein_coding","ncbi_id":"6863","summary":"This gene encodes four products of the tachykinin peptide hormone family, substance P and neurokinin A, as well as the related peptides, neuropeptide K and neuropeptide gamma. These hormones are thought to function as neurotransmitters which interact with nerve receptors and smooth muscle cells. They are known to induce behavioral responses and function as vasodilators and secretagogues. Substance P is an antimicrobial peptide with antibacterial and antifungal properties. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":97731908,"end":97740472,"strand":1,"description":"tachykinin precursor 1 [Source:HGNC Symbol;Acc:HGNC:11517]"}, {"versioned_ensembl_gene_id":"ENSG00000230343.1","gene_symbol":"AC018892.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97034442,"end":97034706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224552.9","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"NG26,D6S82E,BAT5","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31726403,"end":31742871,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000236847.1","gene_symbol":"AC018892.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97035461,"end":97037549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270748.1","gene_symbol":"IGKV2OR2-1","gene_name":"immunoglobulin kappa variable 2/OR2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5805]","synonyms":"IGKV2OR2-1A,IGKV2/OR2-1A,IGKV2/OR2-1","biotype":"IG_V_pseudogene","ncbi_id":"28861","summary":null,"start":97046588,"end":97046891,"strand":1,"description":"immunoglobulin kappa variable 2/OR2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5805]"}, {"versioned_ensembl_gene_id":"ENSG00000215444.2","gene_symbol":"AL138807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51734533,"end":51735067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205918.9","gene_symbol":"PDPK2P","gene_name":"3-phosphoinositide dependent protein kinase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49897]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653650","summary":null,"start":2616121,"end":2643296,"strand":-1,"description":"3-phosphoinositide dependent protein kinase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49897]"}, {"versioned_ensembl_gene_id":"ENSG00000168646.12","gene_symbol":"AXIN2","gene_name":"axin 2 [Source:HGNC Symbol;Acc:HGNC:904]","synonyms":"MGC126582,DKFZp781B0869","biotype":"protein_coding","ncbi_id":"8313","summary":"The Axin-related protein, Axin2, presumably plays an important role in the regulation of the stability of beta-catenin in the Wnt signaling pathway, like its rodent homologs, mouse conductin/rat axil. In mouse, conductin organizes a multiprotein complex of APC (adenomatous polyposis of the colon), beta-catenin, glycogen synthase kinase 3-beta, and conductin, which leads to the degradation of beta-catenin. Apparently, the deregulation of beta-catenin is an important event in the genesis of a number of malignancies. The AXIN2 gene has been mapped to 17q23-q24, a region that shows frequent loss of heterozygosity in breast cancer, neuroblastoma, and other tumors. Mutations in this gene have been associated with colorectal cancer with defective mismatch repair. [provided by RefSeq, Jul 2008]","start":65528563,"end":65561647,"strand":-1,"description":"axin 2 [Source:HGNC Symbol;Acc:HGNC:904]"}, {"versioned_ensembl_gene_id":"ENSG00000114268.11","gene_symbol":"PFKFB4","gene_name":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 [Source:HGNC Symbol;Acc:HGNC:8875]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5210","summary":"The protein encoded by this gene is one of four bifunctional kinase/phosphatases that regulate the concentration of the glycolytic byproduct fructose-2,6-bisphosphate (F2,6BP). The encoded protein is highly expressed in cancer cells and is induced by hypoxia. This protein is essential to the survival of cancer cells under conditions of hypoxia, because it increases the amount of F2,6BP and ATP at a time when the cell cannot produce much of them. This finding suggests that this protein may be a good target for disruption in cancer cells, hopefully imperiling their survival. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":48517684,"end":48562015,"strand":-1,"description":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 [Source:HGNC Symbol;Acc:HGNC:8875]"}, {"versioned_ensembl_gene_id":"ENSG00000248563.1","gene_symbol":"RPSAP2","gene_name":"ribosomal protein SA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18771]","synonyms":"LAMR1P2,bA60E24.1","biotype":"processed_pseudogene","ncbi_id":"442181","summary":null,"start":28732818,"end":28733705,"strand":1,"description":"ribosomal protein SA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18771]"}, {"versioned_ensembl_gene_id":"ENSG00000200040.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75928513,"end":75928625,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000198400.11","gene_symbol":"NTRK1","gene_name":"neurotrophic receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:8031]","synonyms":"MTC,TRKA,TRK","biotype":"protein_coding","ncbi_id":"4914","summary":"This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self-mutilating behavior, cognitive disability and cancer. Alternate transcriptional splice variants of this gene have been found, but only three have been characterized to date. [provided by RefSeq, Jul 2008]","start":156815640,"end":156881850,"strand":1,"description":"neurotrophic receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:8031]"}, {"versioned_ensembl_gene_id":"ENSG00000272678.1","gene_symbol":"AC112503.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123283593,"end":123283983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011478.11","gene_symbol":"QPCTL","gene_name":"glutaminyl-peptide cyclotransferase like [Source:HGNC Symbol;Acc:HGNC:25952]","synonyms":"FLJ20084","biotype":"protein_coding","ncbi_id":"54814","summary":null,"start":45692483,"end":45703989,"strand":1,"description":"glutaminyl-peptide cyclotransferase like [Source:HGNC Symbol;Acc:HGNC:25952]"}, {"versioned_ensembl_gene_id":"ENSG00000135298.13","gene_symbol":"ADGRB3","gene_name":"adhesion G protein-coupled receptor B3 [Source:HGNC Symbol;Acc:HGNC:945]","synonyms":"KIAA0550,BAI3","biotype":"protein_coding","ncbi_id":"577","summary":"This p53-target gene encodes a brain-specific angiogenesis inhibitor, a seven-span transmembrane protein, and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities, and may also play a role in angiogenesis. [provided by RefSeq, Jul 2008]","start":68635367,"end":69389511,"strand":1,"description":"adhesion G protein-coupled receptor B3 [Source:HGNC Symbol;Acc:HGNC:945]"}, {"versioned_ensembl_gene_id":"ENSG00000173175.14","gene_symbol":"ADCY5","gene_name":"adenylate cyclase 5 [Source:HGNC Symbol;Acc:HGNC:236]","synonyms":"AC5","biotype":"protein_coding","ncbi_id":"111","summary":"This gene encodes a member of the membrane-bound adenylyl cyclase enzymes. Adenylyl cyclases mediate G protein-coupled receptor signaling through the synthesis of the second messenger cAMP. Activity of the encoded protein is stimulated by the Gs alpha subunit of G protein-coupled receptors and is inhibited by protein kinase A, calcium and Gi alpha subunits. Single nucleotide polymorphisms in this gene may be associated with low birth weight and type 2 diabetes. Alternatively spliced transcript variants that encode different isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":123282296,"end":123449758,"strand":-1,"description":"adenylate cyclase 5 [Source:HGNC Symbol;Acc:HGNC:236]"}, {"versioned_ensembl_gene_id":"ENSG00000279057.1","gene_symbol":"AC141586.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2620222,"end":2621794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137486.16","gene_symbol":"ARRB1","gene_name":"arrestin beta 1 [Source:HGNC Symbol;Acc:HGNC:711]","synonyms":"ARR1","biotype":"protein_coding","ncbi_id":"408","summary":"Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. Arrestin beta 1 is a cytosolic protein and acts as a cofactor in the beta-adrenergic receptor kinase (BARK) mediated desensitization of beta-adrenergic receptors. Besides the central nervous system, it is expressed at high levels in peripheral blood leukocytes, and thus the BARK/beta-arrestin system is believed to play a major role in regulating receptor-mediated immune functions. Alternatively spliced transcripts encoding different isoforms of arrestin beta 1 have been described. [provided by RefSeq, Jan 2011]","start":75264182,"end":75351705,"strand":-1,"description":"arrestin beta 1 [Source:HGNC Symbol;Acc:HGNC:711]"}, {"versioned_ensembl_gene_id":"ENSG00000107518.16","gene_symbol":"ATRNL1","gene_name":"attractin like 1 [Source:HGNC Symbol;Acc:HGNC:29063]","synonyms":"KIAA0534,FLJ45344,ALP","biotype":"protein_coding","ncbi_id":"26033","summary":null,"start":115093365,"end":115948992,"strand":1,"description":"attractin like 1 [Source:HGNC Symbol;Acc:HGNC:29063]"}, {"versioned_ensembl_gene_id":"ENSG00000226065.1","gene_symbol":"ZBTB45P2","gene_name":"zinc finger and BTB domain containing 45 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49228]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729248","summary":null,"start":110383112,"end":110384642,"strand":1,"description":"zinc finger and BTB domain containing 45 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49228]"}, {"versioned_ensembl_gene_id":"ENSG00000119335.16","gene_symbol":"SET","gene_name":"SET nuclear proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10760]","synonyms":"PHAPII,IPP2A2,2PP2A","biotype":"protein_coding","ncbi_id":"6418","summary":"The protein encoded by this gene inhibits acetylation of nucleosomes, especially histone H4, by histone acetylases (HAT). This inhibition is most likely accomplished by masking histone lysines from being acetylated, and the consequence is to silence HAT-dependent transcription. The encoded protein is part of a complex localized to the endoplasmic reticulum but is found in the nucleus and inhibits apoptosis following attack by cytotoxic T lymphocytes. This protein can also enhance DNA replication of the adenovirus genome. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":128683424,"end":128696400,"strand":1,"description":"SET nuclear proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10760]"}, {"versioned_ensembl_gene_id":"ENSG00000143375.14","gene_symbol":"CGN","gene_name":"cingulin [Source:HGNC Symbol;Acc:HGNC:17429]","synonyms":"KIAA1319","biotype":"protein_coding","ncbi_id":"57530","summary":null,"start":151510510,"end":151538692,"strand":1,"description":"cingulin [Source:HGNC Symbol;Acc:HGNC:17429]"}, {"versioned_ensembl_gene_id":"ENSG00000175772.10","gene_symbol":"LINC01106","gene_name":"long intergenic non-protein coding RNA 1106 [Source:HGNC Symbol;Acc:HGNC:26769]","synonyms":"FLJ38359","biotype":"lincRNA","ncbi_id":"151009","summary":null,"start":110375138,"end":110384442,"strand":-1,"description":"long intergenic non-protein coding RNA 1106 [Source:HGNC Symbol;Acc:HGNC:26769]"}, {"versioned_ensembl_gene_id":"ENSG00000182578.13","gene_symbol":"CSF1R","gene_name":"colony stimulating factor 1 receptor [Source:HGNC Symbol;Acc:HGNC:2433]","synonyms":"FMS,CSFR,CD115,C-FMS","biotype":"protein_coding","ncbi_id":"1436","summary":"The protein encoded by this gene is the receptor for colony stimulating factor 1, a cytokine which controls the production, differentiation, and function of macrophages. This receptor mediates most if not all of the biological effects of this cytokine. Ligand binding activates the receptor kinase through a process of oligomerization and transphosphorylation. The encoded protein is a tyrosine kinase transmembrane receptor and member of the CSF1/PDGF receptor family of tyrosine-protein kinases. Mutations in this gene have been associated with a predisposition to myeloid malignancy. The first intron of this gene contains a transcriptionally inactive ribosomal protein L7 processed pseudogene oriented in the opposite direction. Alternative splicing results in multiple transcript variants. Expression of a splice variant from an LTR promoter has been found in Hodgkin lymphoma (HL), HL cell lines and anaplastic large cell lymphoma. [provided by RefSeq, Mar 2017]","start":150053291,"end":150113372,"strand":-1,"description":"colony stimulating factor 1 receptor [Source:HGNC Symbol;Acc:HGNC:2433]"}, {"versioned_ensembl_gene_id":"ENSG00000214646.8","gene_symbol":"AC104758.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":77941442,"end":77944582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241499.1","gene_symbol":"AL132838.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93244010,"end":93244323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011114.14","gene_symbol":"BTBD7","gene_name":"BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18269]","synonyms":"FUP1,FLJ10648","biotype":"protein_coding","ncbi_id":"55727","summary":null,"start":93237550,"end":93333092,"strand":-1,"description":"BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18269]"}, {"versioned_ensembl_gene_id":"ENSG00000139746.15","gene_symbol":"RBM26","gene_name":"RNA binding motif protein 26 [Source:HGNC Symbol;Acc:HGNC:20327]","synonyms":"ZC3H17,SE70-2,PRO1777,PPP1R132,FLJ20957,C13orf10,ARRS2","biotype":"protein_coding","ncbi_id":"64062","summary":null,"start":79311824,"end":79406477,"strand":-1,"description":"RNA binding motif protein 26 [Source:HGNC Symbol;Acc:HGNC:20327]"}, {"versioned_ensembl_gene_id":"ENSG00000204745.3","gene_symbol":"AC083899.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87125390,"end":87196647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261403.1","gene_symbol":"AC104758.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77954075,"end":77963654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223306.2","gene_symbol":"RNU6-1304P","gene_name":"RNA, U6 small nuclear 1304, pseudogene [Source:HGNC Symbol;Acc:HGNC:48267]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480135","summary":null,"start":225741275,"end":225741380,"strand":1,"description":"RNA, U6 small nuclear 1304, pseudogene [Source:HGNC Symbol;Acc:HGNC:48267]"}, {"versioned_ensembl_gene_id":"ENSG00000274967.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53290640,"end":53290751,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000169896.16","gene_symbol":"ITGAM","gene_name":"integrin subunit alpha M [Source:HGNC Symbol;Acc:HGNC:6149]","synonyms":"MAC-1,CR3A,CD11B","biotype":"protein_coding","ncbi_id":"3684","summary":"This gene encodes the integrin alpha M chain. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This I-domain containing alpha integrin combines with the beta 2 chain (ITGB2) to form a leukocyte-specific integrin referred to as macrophage receptor 1 ('Mac-1'), or inactivated-C3b (iC3b) receptor 3 ('CR3'). The alpha M beta 2 integrin is important in the adherence of neutrophils and monocytes to stimulated endothelium, and also in the phagocytosis of complement coated particles. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":31259990,"end":31332892,"strand":1,"description":"integrin subunit alpha M [Source:HGNC Symbol;Acc:HGNC:6149]"}, {"versioned_ensembl_gene_id":"ENSG00000169733.11","gene_symbol":"RFNG","gene_name":"RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:9974]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5986","summary":null,"start":82047902,"end":82051831,"strand":-1,"description":"RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:9974]"}, {"versioned_ensembl_gene_id":"ENSG00000226143.1","gene_symbol":"Z98752.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43549389,"end":43550949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234271.1","gene_symbol":"Z98752.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43523261,"end":43523572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125743.10","gene_symbol":"SNRPD2","gene_name":"small nuclear ribonucleoprotein D2 polypeptide [Source:HGNC Symbol;Acc:HGNC:11159]","synonyms":"SNRPD1,Sm-D2","biotype":"protein_coding","ncbi_id":"6633","summary":"The protein encoded by this gene belongs to the small nuclear ribonucleoprotein core protein family. It is required for pre-mRNA splicing and small nuclear ribonucleoprotein biogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":45687454,"end":45692569,"strand":-1,"description":"small nuclear ribonucleoprotein D2 polypeptide [Source:HGNC Symbol;Acc:HGNC:11159]"}, {"versioned_ensembl_gene_id":"ENSG00000277611.1","gene_symbol":"Z98752.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":43540171,"end":43569498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258131.1","gene_symbol":"AC007656.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96985656,"end":97185609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279190.1","gene_symbol":"AC007656.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":97150081,"end":97154627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184414.2","gene_symbol":"IRS3P","gene_name":"insulin receptor substrate 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:6127]","synonyms":"IRS3L","biotype":"processed_pseudogene","ncbi_id":"442338","summary":null,"start":100570131,"end":100571136,"strand":1,"description":"insulin receptor substrate 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:6127]"}, {"versioned_ensembl_gene_id":"ENSG00000257470.1","gene_symbol":"AC013417.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97024021,"end":97051129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172977.12","gene_symbol":"KAT5","gene_name":"lysine acetyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:5275]","synonyms":"ZC2HC5,TIP60,PLIP,HTATIP1,HTATIP,ESA1,cPLA2","biotype":"protein_coding","ncbi_id":"10524","summary":"The protein encoded by this gene belongs to the MYST family of histone acetyl transferases (HATs) and was originally isolated as an HIV-1 TAT-interactive protein. HATs play important roles in regulating chromatin remodeling, transcription and other nuclear processes by acetylating histone and nonhistone proteins. This protein is a histone acetylase that has a role in DNA repair and apoptosis and is thought to play an important role in signal transduction. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":65711996,"end":65719604,"strand":1,"description":"lysine acetyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:5275]"}, {"versioned_ensembl_gene_id":"ENSG00000266076.1","gene_symbol":"AC004805.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":65538102,"end":65641033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271587.1","gene_symbol":"AC004805.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65644308,"end":65644617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270870.1","gene_symbol":"AC004805.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65654914,"end":65655395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154240.16","gene_symbol":"CEP112","gene_name":"centrosomal protein 112 [Source:HGNC Symbol;Acc:HGNC:28514]","synonyms":"MGC33887,CCDC46","biotype":"protein_coding","ncbi_id":"201134","summary":"This gene encodes a coiled-coil domain containing protein that belongs to the cell division control protein 42 effector protein family. In neurons, it localizes to the cytoplasm of dendrites and is also enriched in the nucleus where it interacts with the RNA polymerase III transcriptional repressor Maf1 to regulate gamma-aminobutyric acid A receptor surface expression. In addition, the protein has been identified as a component of the human centrosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":65635538,"end":66192084,"strand":-1,"description":"centrosomal protein 112 [Source:HGNC Symbol;Acc:HGNC:28514]"}, {"versioned_ensembl_gene_id":"ENSG00000271074.1","gene_symbol":"AC012491.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211104934,"end":211105732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231017.1","gene_symbol":"AC013404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211298941,"end":211299189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187098.14","gene_symbol":"MITF","gene_name":"melanogenesis associated transcription factor [Source:HGNC Symbol;Acc:HGNC:7105]","synonyms":"WS2A,WS2,MI,bHLHe32","biotype":"protein_coding","ncbi_id":"4286","summary":"The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. [provided by RefSeq, Aug 2017]","start":69739435,"end":69968337,"strand":1,"description":"melanogenesis associated transcription factor [Source:HGNC Symbol;Acc:HGNC:7105]"}, {"versioned_ensembl_gene_id":"ENSG00000233623.2","gene_symbol":"PGAM1P11","gene_name":"phosphoglycerate mutase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42464]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420660","summary":null,"start":10058671,"end":10059648,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42464]"}, {"versioned_ensembl_gene_id":"ENSG00000130939.18","gene_symbol":"UBE4B","gene_name":"ubiquitination factor E4B [Source:HGNC Symbol;Acc:HGNC:12500]","synonyms":"UFD2,UBOX3,KIAA0684,E4","biotype":"protein_coding","ncbi_id":"10277","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes an additional conjugation factor, E4, which is involved in multiubiquitin chain assembly. This gene is also the strongest candidate in the neuroblastoma tumor suppressor genes. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":10032832,"end":10181239,"strand":1,"description":"ubiquitination factor E4B [Source:HGNC Symbol;Acc:HGNC:12500]"}, {"versioned_ensembl_gene_id":"ENSG00000262950.1","gene_symbol":"AC007861.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49442910,"end":49454078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180264.11","gene_symbol":"ADGRD2","gene_name":"adhesion G protein-coupled receptor D2 [Source:HGNC Symbol;Acc:HGNC:18651]","synonyms":"PGR24,GPR144","biotype":"protein_coding","ncbi_id":"347088","summary":null,"start":124451425,"end":124478589,"strand":1,"description":"adhesion G protein-coupled receptor D2 [Source:HGNC Symbol;Acc:HGNC:18651]"}, {"versioned_ensembl_gene_id":"ENSG00000237032.1","gene_symbol":"RPSAP7","gene_name":"ribosomal protein SA pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31461]","synonyms":"LAMR1P7","biotype":"processed_pseudogene","ncbi_id":"654506","summary":null,"start":14723171,"end":14724055,"strand":-1,"description":"ribosomal protein SA pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31461]"}, {"versioned_ensembl_gene_id":"ENSG00000253848.1","gene_symbol":"AC010834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93741193,"end":93744534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207234.1","gene_symbol":"RNU6-125P","gene_name":"RNA, U6 small nuclear 125, pseudogene [Source:HGNC Symbol;Acc:HGNC:47088]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479621","summary":null,"start":88816779,"end":88816885,"strand":1,"description":"RNA, U6 small nuclear 125, pseudogene [Source:HGNC Symbol;Acc:HGNC:47088]"}, {"versioned_ensembl_gene_id":"ENSG00000277615.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000265602.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30122351,"end":30122511,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000202071.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66003839,"end":66003940,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264370.1","gene_symbol":"MIR3125","gene_name":"microRNA 3125 [Source:HGNC Symbol;Acc:HGNC:38219]","synonyms":"hsa-mir-3125","biotype":"miRNA","ncbi_id":"100422986","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12737367,"end":12737444,"strand":1,"description":"microRNA 3125 [Source:HGNC Symbol;Acc:HGNC:38219]"}, {"versioned_ensembl_gene_id":"ENSG00000252795.1","gene_symbol":"RNU6-56P","gene_name":"RNA, U6 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:42546]","synonyms":"RNU6-56","biotype":"snRNA","ncbi_id":"100873764","summary":null,"start":38779424,"end":38779516,"strand":1,"description":"RNA, U6 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:42546]"}, {"versioned_ensembl_gene_id":"ENSG00000201725.1","gene_symbol":"RNU6-304P","gene_name":"RNA, U6 small nuclear 304, pseudogene [Source:HGNC Symbol;Acc:HGNC:47267]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481275","summary":null,"start":8883427,"end":8883533,"strand":-1,"description":"RNA, U6 small nuclear 304, pseudogene [Source:HGNC Symbol;Acc:HGNC:47267]"}, {"versioned_ensembl_gene_id":"ENSG00000222069.1","gene_symbol":"RN7SKP285","gene_name":"RNA, 7SK small nuclear pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:46009]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480920","summary":null,"start":103523562,"end":103523879,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:46009]"}, {"versioned_ensembl_gene_id":"ENSG00000252017.1","gene_symbol":"RNU6-1194P","gene_name":"RNA, U6 small nuclear 1194, pseudogene [Source:HGNC Symbol;Acc:HGNC:48157]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481557","summary":null,"start":282689,"end":282792,"strand":-1,"description":"RNA, U6 small nuclear 1194, pseudogene [Source:HGNC Symbol;Acc:HGNC:48157]"}, {"versioned_ensembl_gene_id":"ENSG00000275229.1","gene_symbol":"RNU1-68P","gene_name":"RNA, U1 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48410]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481615","summary":null,"start":149700151,"end":149700296,"strand":-1,"description":"RNA, U1 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48410]"}, {"versioned_ensembl_gene_id":"ENSG00000212485.1","gene_symbol":"RNU6-1197P","gene_name":"RNA, U6 small nuclear 1197, pseudogene [Source:HGNC Symbol;Acc:HGNC:48160]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481558","summary":null,"start":74079537,"end":74079643,"strand":1,"description":"RNA, U6 small nuclear 1197, pseudogene [Source:HGNC Symbol;Acc:HGNC:48160]"}, {"versioned_ensembl_gene_id":"ENSG00000251889.1","gene_symbol":"RNU4-49P","gene_name":"RNA, U4 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:46985]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481187","summary":null,"start":48340687,"end":48340826,"strand":-1,"description":"RNA, U4 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:46985]"}, {"versioned_ensembl_gene_id":"ENSG00000284216.1","gene_symbol":"MIR1909","gene_name":"microRNA 1909 [Source:HGNC Symbol;Acc:HGNC:35393]","synonyms":"MIRN1909,hsa-mir-1909","biotype":"miRNA","ncbi_id":"100302210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1816159,"end":1816238,"strand":-1,"description":"microRNA 1909 [Source:HGNC Symbol;Acc:HGNC:35393]"}, {"versioned_ensembl_gene_id":"ENSG00000266178.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30922332,"end":30922420,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284595.1","gene_symbol":"MIR6785","gene_name":"microRNA 6785 [Source:HGNC Symbol;Acc:HGNC:50206]","synonyms":"hsa-mir-6785","biotype":"miRNA","ncbi_id":"102466911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75498548,"end":75498628,"strand":1,"description":"microRNA 6785 [Source:HGNC Symbol;Acc:HGNC:50206]"}, {"versioned_ensembl_gene_id":"ENSG00000201241.1","gene_symbol":"RNU6-978P","gene_name":"RNA, U6 small nuclear 978, pseudogene [Source:HGNC Symbol;Acc:HGNC:47941]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479998","summary":null,"start":19883614,"end":19883716,"strand":1,"description":"RNA, U6 small nuclear 978, pseudogene [Source:HGNC Symbol;Acc:HGNC:47941]"}, {"versioned_ensembl_gene_id":"ENSG00000207839.1","gene_symbol":"MIR33B","gene_name":"microRNA 33b [Source:HGNC Symbol;Acc:HGNC:32791]","synonyms":"MIRN33B,hsa-mir-33b","biotype":"miRNA","ncbi_id":"693120","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17813836,"end":17813931,"strand":-1,"description":"microRNA 33b [Source:HGNC Symbol;Acc:HGNC:32791]"}, {"versioned_ensembl_gene_id":"ENSG00000206776.1","gene_symbol":"SNORA32","gene_name":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]","synonyms":"ACA32","biotype":"snoRNA","ncbi_id":"692063","summary":null,"start":119388348,"end":119388469,"strand":1,"description":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]"}, {"versioned_ensembl_gene_id":"ENSG00000212618.1","gene_symbol":"snoMBII-202","gene_name":"Small nucleolar RNA MBII-202 [Source:RFAM;Acc:RF00324]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":18943999,"end":18944073,"strand":1,"description":"Small nucleolar RNA MBII-202 [Source:RFAM;Acc:RF00324]"}, {"versioned_ensembl_gene_id":"ENSG00000276664.1","gene_symbol":"TUG1_1","gene_name":"Taurine upregulated gene 1 conserved region 1 [Source:RFAM;Acc:RF01882]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30971005,"end":30971149,"strand":1,"description":"Taurine upregulated gene 1 conserved region 1 [Source:RFAM;Acc:RF01882]"}, {"versioned_ensembl_gene_id":"ENSG00000199454.1","gene_symbol":"RNA5SP388","gene_name":"RNA, 5S ribosomal pseudogene 388 [Source:HGNC Symbol;Acc:HGNC:43288]","synonyms":"RN5S388","biotype":"rRNA","ncbi_id":"100873642","summary":null,"start":78177803,"end":78177921,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 388 [Source:HGNC Symbol;Acc:HGNC:43288]"}, {"versioned_ensembl_gene_id":"ENSG00000251767.1","gene_symbol":"RNU7-8P","gene_name":"RNA, U7 small nuclear 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:34104]","synonyms":"U7.8,RNU7-139P","biotype":"snRNA","ncbi_id":"100147756","summary":null,"start":77420325,"end":77420386,"strand":1,"description":"RNA, U7 small nuclear 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:34104]"}, {"versioned_ensembl_gene_id":"ENSG00000284494.1","gene_symbol":"AC270306.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179455294,"end":179455974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277014.1","gene_symbol":"MIR3179-4","gene_name":"microRNA 3179-4 [Source:HGNC Symbol;Acc:HGNC:50838]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504729","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18494493,"end":18494576,"strand":-1,"description":"microRNA 3179-4 [Source:HGNC Symbol;Acc:HGNC:50838]"}, {"versioned_ensembl_gene_id":"ENSG00000284532.1","gene_symbol":"MIR4723","gene_name":"microRNA 4723 [Source:HGNC Symbol;Acc:HGNC:41660]","synonyms":"hsa-mir-4723","biotype":"miRNA","ncbi_id":"100616388","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28360654,"end":28360734,"strand":1,"description":"microRNA 4723 [Source:HGNC Symbol;Acc:HGNC:41660]"}, {"versioned_ensembl_gene_id":"ENSG00000284344.1","gene_symbol":"MIR2117","gene_name":"microRNA 2117 [Source:HGNC Symbol;Acc:HGNC:37311]","synonyms":"hsa-mir-2117","biotype":"miRNA","ncbi_id":"100313779","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43444806,"end":43444885,"strand":1,"description":"microRNA 2117 [Source:HGNC Symbol;Acc:HGNC:37311]"}, {"versioned_ensembl_gene_id":"ENSG00000275451.1","gene_symbol":"MIR6085","gene_name":"microRNA 6085 [Source:HGNC Symbol;Acc:HGNC:50002]","synonyms":"hsa-mir-6085","biotype":"miRNA","ncbi_id":"102464834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62343029,"end":62343138,"strand":1,"description":"microRNA 6085 [Source:HGNC Symbol;Acc:HGNC:50002]"}, {"versioned_ensembl_gene_id":"ENSG00000199652.2","gene_symbol":"RNU1-35P","gene_name":"RNA, U1 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48377]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480157","summary":null,"start":135742343,"end":135742495,"strand":-1,"description":"RNA, U1 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48377]"}, {"versioned_ensembl_gene_id":"ENSG00000275633.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":54684540,"end":54709099,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000211579.2","gene_symbol":"MIR759","gene_name":"microRNA 759 [Source:HGNC Symbol;Acc:HGNC:37307]","synonyms":"hsa-mir-759","biotype":"miRNA","ncbi_id":"100313778","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52810050,"end":52810140,"strand":1,"description":"microRNA 759 [Source:HGNC Symbol;Acc:HGNC:37307]"}, {"versioned_ensembl_gene_id":"ENSG00000201221.1","gene_symbol":"RNU4-40P","gene_name":"RNA, U4 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:46976]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479576","summary":null,"start":35887659,"end":35887801,"strand":1,"description":"RNA, U4 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:46976]"}, {"versioned_ensembl_gene_id":"ENSG00000252428.1","gene_symbol":"RNA5SP285","gene_name":"RNA, 5S ribosomal pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:43185]","synonyms":"RN5S285","biotype":"rRNA","ncbi_id":"100873538","summary":null,"start":72299720,"end":72299838,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:43185]"}, {"versioned_ensembl_gene_id":"ENSG00000275524.1","gene_symbol":"SNORD115-26","gene_name":"small nucleolar RNA, C/D box 115-26 [Source:HGNC Symbol;Acc:HGNC:33045]","synonyms":"HBII-52-26","biotype":"snoRNA","ncbi_id":"100033802","summary":null,"start":25218617,"end":25218698,"strand":1,"description":"small nucleolar RNA, C/D box 115-26 [Source:HGNC Symbol;Acc:HGNC:33045]"}, {"versioned_ensembl_gene_id":"ENSG00000252739.1","gene_symbol":"RNU7-151P","gene_name":"RNA, U7 small nuclear 151 pseudogene [Source:HGNC Symbol;Acc:HGNC:45685]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480824","summary":null,"start":102837047,"end":102837099,"strand":-1,"description":"RNA, U7 small nuclear 151 pseudogene [Source:HGNC Symbol;Acc:HGNC:45685]"}, {"versioned_ensembl_gene_id":"ENSG00000284222.1","gene_symbol":"AC113189.11","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7439159,"end":7443327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283591.1","gene_symbol":"MIR4430","gene_name":"microRNA 4430 [Source:HGNC Symbol;Acc:HGNC:41646]","synonyms":"hsa-mir-4430","biotype":"miRNA","ncbi_id":"100616136","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33418516,"end":33418564,"strand":1,"description":"microRNA 4430 [Source:HGNC Symbol;Acc:HGNC:41646]"}, {"versioned_ensembl_gene_id":"ENSG00000206659.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":175022479,"end":175022580,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200237.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":9819954,"end":9820094,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000278036.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":27315120,"end":27315226,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200693.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":63651296,"end":63651499,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000212505.1","gene_symbol":"RNA5SP299","gene_name":"RNA, 5S ribosomal pseudogene 299 [Source:HGNC Symbol;Acc:HGNC:43199]","synonyms":"RN5S299","biotype":"rRNA","ncbi_id":"100873574","summary":null,"start":8656716,"end":8656831,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 299 [Source:HGNC Symbol;Acc:HGNC:43199]"}, {"versioned_ensembl_gene_id":"ENSG00000276753.1","gene_symbol":"MIR6821","gene_name":"microRNA 6821 [Source:HGNC Symbol;Acc:HGNC:49980]","synonyms":"hsa-mir-6821","biotype":"miRNA","ncbi_id":"102465493","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49962866,"end":49962939,"strand":1,"description":"microRNA 6821 [Source:HGNC Symbol;Acc:HGNC:49980]"}, {"versioned_ensembl_gene_id":"ENSG00000239964.3","gene_symbol":"RN7SL748P","gene_name":"RNA, 7SL, cytoplasmic 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:46764]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481125","summary":null,"start":36522191,"end":36522501,"strand":1,"description":"RNA, 7SL, cytoplasmic 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:46764]"}, {"versioned_ensembl_gene_id":"ENSG00000223224.1","gene_symbol":"SNORD71","gene_name":"small nucleolar RNA, C/D box 71 [Source:HGNC Symbol;Acc:HGNC:32732]","synonyms":"MIRN768,hsa-mir-768,HBII-239","biotype":"snoRNA","ncbi_id":"692111","summary":null,"start":71758402,"end":71758487,"strand":-1,"description":"small nucleolar RNA, C/D box 71 [Source:HGNC Symbol;Acc:HGNC:32732]"}, {"versioned_ensembl_gene_id":"ENSG00000284140.1","gene_symbol":"MIR3618","gene_name":"microRNA 3618 [Source:HGNC Symbol;Acc:HGNC:38937]","synonyms":"hsa-mir-3618","biotype":"miRNA","ncbi_id":"100500860","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20085746,"end":20085833,"strand":1,"description":"microRNA 3618 [Source:HGNC Symbol;Acc:HGNC:38937]"}, {"versioned_ensembl_gene_id":"ENSG00000284261.1","gene_symbol":"MIR4657","gene_name":"microRNA 4657 [Source:HGNC Symbol;Acc:HGNC:41706]","synonyms":"hsa-mir-4657","biotype":"miRNA","ncbi_id":"100616393","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44881748,"end":44881800,"strand":-1,"description":"microRNA 4657 [Source:HGNC Symbol;Acc:HGNC:41706]"}, {"versioned_ensembl_gene_id":"ENSG00000207771.1","gene_symbol":"MIR550A1","gene_name":"microRNA 550a-1 [Source:HGNC Symbol;Acc:HGNC:32804]","synonyms":"MIRN550-1,MIR550-1,hsa-mir-550-1","biotype":"miRNA","ncbi_id":"693133","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30289794,"end":30289890,"strand":1,"description":"microRNA 550a-1 [Source:HGNC Symbol;Acc:HGNC:32804]"}, {"versioned_ensembl_gene_id":"ENSG00000254172.1","gene_symbol":"RNU5A-3P","gene_name":"RNA, U5A small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42519]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873831","summary":null,"start":30643689,"end":30643802,"strand":1,"description":"RNA, U5A small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42519]"}, {"versioned_ensembl_gene_id":"ENSG00000199924.1","gene_symbol":"RNU6-1252P","gene_name":"RNA, U6 small nuclear 1252, pseudogene [Source:HGNC Symbol;Acc:HGNC:48215]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480113","summary":null,"start":52494849,"end":52494952,"strand":1,"description":"RNA, U6 small nuclear 1252, pseudogene [Source:HGNC Symbol;Acc:HGNC:48215]"}, {"versioned_ensembl_gene_id":"ENSG00000207142.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":42454720,"end":42454821,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222376.1","gene_symbol":"RN7SKP152","gene_name":"RNA, 7SK small nuclear pseudogene 152 [Source:HGNC Symbol;Acc:HGNC:45876]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479163","summary":null,"start":166180652,"end":166180966,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 152 [Source:HGNC Symbol;Acc:HGNC:45876]"}, {"versioned_ensembl_gene_id":"ENSG00000222997.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130505106,"end":130505201,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252484.1","gene_symbol":"RN7SKP49","gene_name":"RNA, 7SK small nuclear pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:45773]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480848","summary":null,"start":224107282,"end":224107541,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:45773]"}, {"versioned_ensembl_gene_id":"ENSG00000242251.3","gene_symbol":"RN7SL20P","gene_name":"RNA, 7SL, cytoplasmic 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46036]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479232","summary":null,"start":31757202,"end":31757498,"strand":1,"description":"RNA, 7SL, cytoplasmic 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46036]"}, {"versioned_ensembl_gene_id":"ENSG00000211574.1","gene_symbol":"MIR770","gene_name":"microRNA 770 [Source:HGNC Symbol;Acc:HGNC:33143]","synonyms":"MIRN770,hsa-mir-770","biotype":"miRNA","ncbi_id":"768222","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100852390,"end":100852487,"strand":1,"description":"microRNA 770 [Source:HGNC Symbol;Acc:HGNC:33143]"}, {"versioned_ensembl_gene_id":"ENSG00000283561.1","gene_symbol":"MIR376A2","gene_name":"microRNA 376a-2 [Source:HGNC Symbol;Acc:HGNC:32532]","synonyms":"MIRN376A2,hsa-mir-376a-2","biotype":"miRNA","ncbi_id":"664615","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101040069,"end":101040148,"strand":1,"description":"microRNA 376a-2 [Source:HGNC Symbol;Acc:HGNC:32532]"}, {"versioned_ensembl_gene_id":"ENSG00000221461.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":123180310,"end":123180525,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000242381.3","gene_symbol":"RN7SL741P","gene_name":"RNA, 7SL, cytoplasmic 741, pseudogene [Source:HGNC Symbol;Acc:HGNC:46757]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481124","summary":null,"start":25944478,"end":25944766,"strand":1,"description":"RNA, 7SL, cytoplasmic 741, pseudogene [Source:HGNC Symbol;Acc:HGNC:46757]"}, {"versioned_ensembl_gene_id":"ENSG00000276295.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153721328,"end":153721625,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000243847.3","gene_symbol":"RN7SL610P","gene_name":"RNA, 7SL, cytoplasmic 610, pseudogene [Source:HGNC Symbol;Acc:HGNC:46626]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479444","summary":null,"start":23996795,"end":23997085,"strand":-1,"description":"RNA, 7SL, cytoplasmic 610, pseudogene [Source:HGNC Symbol;Acc:HGNC:46626]"}, {"versioned_ensembl_gene_id":"ENSG00000252373.1","gene_symbol":"RNU6-358P","gene_name":"RNA, U6 small nuclear 358, pseudogene [Source:HGNC Symbol;Acc:HGNC:47321]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481291","summary":null,"start":31820564,"end":31820638,"strand":-1,"description":"RNA, U6 small nuclear 358, pseudogene [Source:HGNC Symbol;Acc:HGNC:47321]"}, {"versioned_ensembl_gene_id":"ENSG00000223258.1","gene_symbol":"RNU6-575P","gene_name":"RNA, U6 small nuclear 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:47538]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481363","summary":null,"start":43207762,"end":43207866,"strand":-1,"description":"RNA, U6 small nuclear 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:47538]"}, {"versioned_ensembl_gene_id":"ENSG00000274006.1","gene_symbol":"DLG2-AS1_1","gene_name":"DLG2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02112]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":84887207,"end":84887419,"strand":1,"description":"DLG2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02112]"}, {"versioned_ensembl_gene_id":"ENSG00000252685.1","gene_symbol":"RNU6-928P","gene_name":"RNA, U6 small nuclear 928, pseudogene [Source:HGNC Symbol;Acc:HGNC:47891]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479977","summary":null,"start":66638271,"end":66638374,"strand":1,"description":"RNA, U6 small nuclear 928, pseudogene [Source:HGNC Symbol;Acc:HGNC:47891]"}, {"versioned_ensembl_gene_id":"ENSG00000252003.1","gene_symbol":"RNU7-154P","gene_name":"RNA, U7 small nuclear 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:45688]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481802","summary":null,"start":122081720,"end":122081781,"strand":1,"description":"RNA, U7 small nuclear 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:45688]"}, {"versioned_ensembl_gene_id":"ENSG00000223109.1","gene_symbol":"MIR1538","gene_name":"microRNA 1538 [Source:HGNC Symbol;Acc:HGNC:35382]","synonyms":"MIRN1538,hsa-mir-1538","biotype":"miRNA","ncbi_id":"100302119","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69565808,"end":69565868,"strand":-1,"description":"microRNA 1538 [Source:HGNC Symbol;Acc:HGNC:35382]"}, {"versioned_ensembl_gene_id":"ENSG00000266417.1","gene_symbol":"MIR4424","gene_name":"microRNA 4424 [Source:HGNC Symbol;Acc:HGNC:41805]","synonyms":"hsa-mir-4424","biotype":"miRNA","ncbi_id":"100616328","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":178677749,"end":178677834,"strand":1,"description":"microRNA 4424 [Source:HGNC Symbol;Acc:HGNC:41805]"}, {"versioned_ensembl_gene_id":"ENSG00000265881.1","gene_symbol":"PDLIM1P2","gene_name":"PDZ and LIM domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48945]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419426","summary":null,"start":21444833,"end":21445439,"strand":-1,"description":"PDZ and LIM domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48945]"}, {"versioned_ensembl_gene_id":"ENSG00000243888.1","gene_symbol":"AL355140.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":69428248,"end":69428721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274314.1","gene_symbol":"MIR6749","gene_name":"microRNA 6749 [Source:HGNC Symbol;Acc:HGNC:50087]","synonyms":"hsa-mir-6749","biotype":"miRNA","ncbi_id":"102466727","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64902387,"end":64902455,"strand":-1,"description":"microRNA 6749 [Source:HGNC Symbol;Acc:HGNC:50087]"}, {"versioned_ensembl_gene_id":"ENSG00000265172.1","gene_symbol":"MIR4262","gene_name":"microRNA 4262 [Source:HGNC Symbol;Acc:HGNC:38308]","synonyms":"hsa-mir-4262","biotype":"miRNA","ncbi_id":"100422996","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11836933,"end":11836986,"strand":-1,"description":"microRNA 4262 [Source:HGNC Symbol;Acc:HGNC:38308]"}, {"versioned_ensembl_gene_id":"ENSG00000211513.5","gene_symbol":"MIR320E","gene_name":"microRNA 320e [Source:HGNC Symbol;Acc:HGNC:38230]","synonyms":"hsa-mir-320e","biotype":"miRNA","ncbi_id":"100422913","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46709293,"end":46709345,"strand":-1,"description":"microRNA 320e [Source:HGNC Symbol;Acc:HGNC:38230]"}, {"versioned_ensembl_gene_id":"ENSG00000266081.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32572064,"end":32572207,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000278701.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20340743,"end":20341045,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000251757.1","gene_symbol":"RNU6-848P","gene_name":"RNA, U6 small nuclear 848, pseudogene [Source:HGNC Symbol;Acc:HGNC:47811]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479941","summary":null,"start":130622838,"end":130622944,"strand":1,"description":"RNA, U6 small nuclear 848, pseudogene [Source:HGNC Symbol;Acc:HGNC:47811]"}, {"versioned_ensembl_gene_id":"ENSG00000243059.3","gene_symbol":"RN7SL400P","gene_name":"RNA, 7SL, cytoplasmic 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:46416]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481033","summary":null,"start":21102843,"end":21103138,"strand":-1,"description":"RNA, 7SL, cytoplasmic 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:46416]"}, {"versioned_ensembl_gene_id":"ENSG00000208005.1","gene_symbol":"MIR503","gene_name":"microRNA 503 [Source:HGNC Symbol;Acc:HGNC:32138]","synonyms":"MIRN503,hsa-mir-503","biotype":"miRNA","ncbi_id":"574506","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134546328,"end":134546398,"strand":-1,"description":"microRNA 503 [Source:HGNC Symbol;Acc:HGNC:32138]"}, {"versioned_ensembl_gene_id":"ENSG00000252931.1","gene_symbol":"RNU6-231P","gene_name":"RNA, U6 small nuclear 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:47194]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481251","summary":null,"start":85821855,"end":85821957,"strand":1,"description":"RNA, U6 small nuclear 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:47194]"}, {"versioned_ensembl_gene_id":"ENSG00000238311.1","gene_symbol":"SNORD13E","gene_name":"small nucleolar RNA, C/D box 13E [Source:HGNC Symbol;Acc:HGNC:52254]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617020","summary":null,"start":65696833,"end":65696936,"strand":-1,"description":"small nucleolar RNA, C/D box 13E [Source:HGNC Symbol;Acc:HGNC:52254]"}, {"versioned_ensembl_gene_id":"ENSG00000201610.1","gene_symbol":"RNA5SP84","gene_name":"RNA, 5S ribosomal pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:42882]","synonyms":"RN5S84","biotype":"rRNA","ncbi_id":"100873317","summary":null,"start":11517397,"end":11517503,"strand":1,"description":"RNA, 5S ribosomal pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:42882]"}, {"versioned_ensembl_gene_id":"ENSG00000274072.1","gene_symbol":"mascRNA-menRNA","gene_name":"MALAT1-associated small cytoplasmic RNA/MEN beta RNA [Source:RFAM;Acc:RF01684]","synonyms":null,"biotype":"sRNA","ncbi_id":null,"summary":null,"start":65506117,"end":65506173,"strand":1,"description":"MALAT1-associated small cytoplasmic RNA/MEN beta RNA [Source:RFAM;Acc:RF01684]"}, {"versioned_ensembl_gene_id":"ENSG00000201679.1","gene_symbol":"SNORD115-15","gene_name":"small nucleolar RNA, C/D box 115-15 [Source:HGNC Symbol;Acc:HGNC:33034]","synonyms":"HBII-52-15","biotype":"snoRNA","ncbi_id":"100033453","summary":null,"start":25197576,"end":25197656,"strand":1,"description":"small nucleolar RNA, C/D box 115-15 [Source:HGNC Symbol;Acc:HGNC:33034]"}, {"versioned_ensembl_gene_id":"ENSG00000252192.1","gene_symbol":"SNORA9","gene_name":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]","synonyms":"ACA9,SNORA9A","biotype":"snoRNA","ncbi_id":"677798","summary":null,"start":122492113,"end":122492241,"strand":-1,"description":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]"}, {"versioned_ensembl_gene_id":"ENSG00000184084.7","gene_symbol":"AC091868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73803296,"end":73803599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256757.1","gene_symbol":"AP002840.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113405321,"end":113412117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149295.13","gene_symbol":"DRD2","gene_name":"dopamine receptor D2 [Source:HGNC Symbol;Acc:HGNC:3023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1813","summary":"This gene encodes the D2 subtype of the dopamine receptor. This G-protein coupled receptor inhibits adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants encoding different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. [provided by RefSeq, Jul 2008]","start":113409615,"end":113475691,"strand":-1,"description":"dopamine receptor D2 [Source:HGNC Symbol;Acc:HGNC:3023]"}, {"versioned_ensembl_gene_id":"ENSG00000242888.1","gene_symbol":"AL133368.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99974336,"end":99975149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264060.1","gene_symbol":"MIR4316","gene_name":"microRNA 4316 [Source:HGNC Symbol;Acc:HGNC:38306]","synonyms":"hsa-mir-4316","biotype":"miRNA","ncbi_id":"100422851","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77396984,"end":77397054,"strand":-1,"description":"microRNA 4316 [Source:HGNC Symbol;Acc:HGNC:38306]"}, {"versioned_ensembl_gene_id":"ENSG00000264566.3","gene_symbol":"MIR23C","gene_name":"microRNA 23c [Source:HGNC Symbol;Acc:HGNC:38913]","synonyms":"hsa-mir-23c","biotype":"miRNA","ncbi_id":"100500809","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20017088,"end":20017187,"strand":-1,"description":"microRNA 23c [Source:HGNC Symbol;Acc:HGNC:38913]"}, {"versioned_ensembl_gene_id":"ENSG00000199133.3","gene_symbol":"MIRLET7D","gene_name":"microRNA let-7d [Source:HGNC Symbol;Acc:HGNC:31481]","synonyms":"MIRNLET7D,hsa-let-7d","biotype":"miRNA","ncbi_id":"406886","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94178834,"end":94178920,"strand":1,"description":"microRNA let-7d [Source:HGNC Symbol;Acc:HGNC:31481]"}, {"versioned_ensembl_gene_id":"ENSG00000200377.1","gene_symbol":"SNORD56","gene_name":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]","synonyms":"U56,RNU56","biotype":"snoRNA","ncbi_id":"26793","summary":null,"start":153446813,"end":153446883,"strand":-1,"description":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]"}, {"versioned_ensembl_gene_id":"ENSG00000283609.1","gene_symbol":"MIR4662A","gene_name":"microRNA 4662a [Source:HGNC Symbol;Acc:HGNC:41826]","synonyms":"hsa-mir-4662a","biotype":"miRNA","ncbi_id":"100616221","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124821985,"end":124822051,"strand":1,"description":"microRNA 4662a [Source:HGNC Symbol;Acc:HGNC:41826]"}, {"versioned_ensembl_gene_id":"ENSG00000253047.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"ACA40,SNORA40A","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":150600539,"end":150600659,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000199360.1","gene_symbol":"RNU6-1115P","gene_name":"RNA, U6 small nuclear 1115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48078]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480639","summary":null,"start":110856417,"end":110856522,"strand":1,"description":"RNA, U6 small nuclear 1115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48078]"}, {"versioned_ensembl_gene_id":"ENSG00000265278.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31653519,"end":31653632,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207053.1","gene_symbol":"RNU6-937P","gene_name":"RNA, U6 small nuclear 937, pseudogene [Source:HGNC Symbol;Acc:HGNC:47900]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479980","summary":null,"start":35928570,"end":35928675,"strand":-1,"description":"RNA, U6 small nuclear 937, pseudogene [Source:HGNC Symbol;Acc:HGNC:47900]"}, {"versioned_ensembl_gene_id":"ENSG00000223131.1","gene_symbol":"RNA5SP304","gene_name":"RNA, 5S ribosomal pseudogene 304 [Source:HGNC Symbol;Acc:HGNC:43204]","synonyms":"RN5S304","biotype":"rRNA","ncbi_id":"100873578","summary":null,"start":22997255,"end":22997358,"strand":1,"description":"RNA, 5S ribosomal pseudogene 304 [Source:HGNC Symbol;Acc:HGNC:43204]"}, {"versioned_ensembl_gene_id":"ENSG00000252157.1","gene_symbol":"RNU6-479P","gene_name":"RNA, U6 small nuclear 479, pseudogene [Source:HGNC Symbol;Acc:HGNC:47442]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481331","summary":null,"start":183653572,"end":183653676,"strand":-1,"description":"RNA, U6 small nuclear 479, pseudogene [Source:HGNC Symbol;Acc:HGNC:47442]"}, {"versioned_ensembl_gene_id":"ENSG00000201954.1","gene_symbol":"RNU6-673P","gene_name":"RNA, U6 small nuclear 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:47636]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481394","summary":null,"start":76260800,"end":76260903,"strand":-1,"description":"RNA, U6 small nuclear 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:47636]"}, {"versioned_ensembl_gene_id":"ENSG00000222413.1","gene_symbol":"RN7SKP125","gene_name":"RNA, 7SK small nuclear pseudogene 125 [Source:HGNC Symbol;Acc:HGNC:45849]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479150","summary":null,"start":117276985,"end":117277286,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 125 [Source:HGNC Symbol;Acc:HGNC:45849]"}, {"versioned_ensembl_gene_id":"ENSG00000252759.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":200863152,"end":200863247,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276275.1","gene_symbol":"SNORD5","gene_name":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]","synonyms":"mgh28S-2410","biotype":"snoRNA","ncbi_id":"692072","summary":null,"start":141453377,"end":141453451,"strand":1,"description":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]"}, {"versioned_ensembl_gene_id":"ENSG00000168350.7","gene_symbol":"DEGS2","gene_name":"delta 4-desaturase, sphingolipid 2 [Source:HGNC Symbol;Acc:HGNC:20113]","synonyms":"FADS8,DES2,C14orf66","biotype":"protein_coding","ncbi_id":"123099","summary":"This gene encodes a bifunctional enzyme that is involved in the biosynthesis of phytosphingolipids in human skin and in other phytosphingolipid-containing tissues. This enzyme can act as a sphingolipid delta(4)-desaturase, and also as a sphingolipid C4-hydroxylase. [provided by RefSeq, Oct 2008]","start":100143957,"end":100160163,"strand":-1,"description":"delta 4-desaturase, sphingolipid 2 [Source:HGNC Symbol;Acc:HGNC:20113]"}, {"versioned_ensembl_gene_id":"ENSG00000272071.1","gene_symbol":"AC122710.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6779458,"end":6779998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185269.11","gene_symbol":"NOTUM","gene_name":"NOTUM, palmitoleoyl-protein carboxylesterase [Source:HGNC Symbol;Acc:HGNC:27106]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147111","summary":null,"start":81952507,"end":81961840,"strand":-1,"description":"NOTUM, palmitoleoyl-protein carboxylesterase [Source:HGNC Symbol;Acc:HGNC:27106]"}, {"versioned_ensembl_gene_id":"ENSG00000284149.1","gene_symbol":"MIR4784","gene_name":"microRNA 4784 [Source:HGNC Symbol;Acc:HGNC:41580]","synonyms":"hsa-mir-4784","biotype":"miRNA","ncbi_id":"100616378","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":131491160,"end":131491236,"strand":-1,"description":"microRNA 4784 [Source:HGNC Symbol;Acc:HGNC:41580]"}, {"versioned_ensembl_gene_id":"ENSG00000264864.1","gene_symbol":"MIR3613","gene_name":"microRNA 3613 [Source:HGNC Symbol;Acc:HGNC:38964]","synonyms":"hsa-mir-3613","biotype":"miRNA","ncbi_id":"100500908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49996415,"end":49996501,"strand":-1,"description":"microRNA 3613 [Source:HGNC Symbol;Acc:HGNC:38964]"}, {"versioned_ensembl_gene_id":"ENSG00000238302.1","gene_symbol":"RNU7-120P","gene_name":"RNA, U7 small nuclear 120 pseudogene [Source:HGNC Symbol;Acc:HGNC:45654]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480817","summary":null,"start":89282223,"end":89282285,"strand":-1,"description":"RNA, U7 small nuclear 120 pseudogene [Source:HGNC Symbol;Acc:HGNC:45654]"}, {"versioned_ensembl_gene_id":"ENSG00000272025.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":65158662,"end":65158860,"strand":1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000200325.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30309015,"end":30309126,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241291.3","gene_symbol":"RN7SL791P","gene_name":"RNA, 7SL, cytoplasmic 791, pseudogene [Source:HGNC Symbol;Acc:HGNC:46807]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481860","summary":null,"start":146656401,"end":146656695,"strand":-1,"description":"RNA, 7SL, cytoplasmic 791, pseudogene [Source:HGNC Symbol;Acc:HGNC:46807]"}, {"versioned_ensembl_gene_id":"ENSG00000206878.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":228652436,"end":228652560,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000206680.1","gene_symbol":"SNORD21","gene_name":"small nucleolar RNA, C/D box 21 [Source:HGNC Symbol;Acc:HGNC:10144]","synonyms":"U21,RNU21","biotype":"snoRNA","ncbi_id":"6083","summary":"This gene encodes a small nucleolar RNA (snoRNA) that may be involved in biogenesis of the large (28S) ribosomal subunit. This gene is found within an intron of the RPL5 gene. [provided by RefSeq, Mar 2009]","start":92837289,"end":92837383,"strand":1,"description":"small nucleolar RNA, C/D box 21 [Source:HGNC Symbol;Acc:HGNC:10144]"}, {"versioned_ensembl_gene_id":"ENSG00000207600.3","gene_symbol":"MIR598","gene_name":"microRNA 598 [Source:HGNC Symbol;Acc:HGNC:32854]","synonyms":"MIRN598,hsa-mir-598","biotype":"miRNA","ncbi_id":"693183","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11035206,"end":11035302,"strand":-1,"description":"microRNA 598 [Source:HGNC Symbol;Acc:HGNC:32854]"}, {"versioned_ensembl_gene_id":"ENSG00000266618.1","gene_symbol":"MIR4742","gene_name":"microRNA 4742 [Source:HGNC Symbol;Acc:HGNC:41565]","synonyms":"hsa-mir-4742","biotype":"miRNA","ncbi_id":"100616468","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":224398227,"end":224398311,"strand":-1,"description":"microRNA 4742 [Source:HGNC Symbol;Acc:HGNC:41565]"}, {"versioned_ensembl_gene_id":"ENSG00000263511.1","gene_symbol":"MIR5699","gene_name":"microRNA 5699 [Source:HGNC Symbol;Acc:HGNC:43456]","synonyms":"hsa-mir-5699","biotype":"miRNA","ncbi_id":"100847086","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":641689,"end":641778,"strand":-1,"description":"microRNA 5699 [Source:HGNC Symbol;Acc:HGNC:43456]"}, {"versioned_ensembl_gene_id":"ENSG00000185105.5","gene_symbol":"MYADML2","gene_name":"myeloid associated differentiation marker like 2 [Source:HGNC Symbol;Acc:HGNC:34548]","synonyms":"LOC255275","biotype":"protein_coding","ncbi_id":"255275","summary":null,"start":81939645,"end":81947233,"strand":-1,"description":"myeloid associated differentiation marker like 2 [Source:HGNC Symbol;Acc:HGNC:34548]"}, {"versioned_ensembl_gene_id":"ENSG00000167842.15","gene_symbol":"MIS12","gene_name":"MIS12, kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24967]","synonyms":"MTW1,MGC2488,KNTC2AP,hMIS12","biotype":"protein_coding","ncbi_id":"79003","summary":null,"start":5486285,"end":5490814,"strand":1,"description":"MIS12, kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24967]"}, {"versioned_ensembl_gene_id":"ENSG00000275091.1","gene_symbol":"AC022098.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14006422,"end":14006773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277817.1","gene_symbol":"MIR6738","gene_name":"microRNA 6738 [Source:HGNC Symbol;Acc:HGNC:49939]","synonyms":"hsa-mir-6738","biotype":"miRNA","ncbi_id":"102465442","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155951273,"end":155951336,"strand":-1,"description":"microRNA 6738 [Source:HGNC Symbol;Acc:HGNC:49939]"}, {"versioned_ensembl_gene_id":"ENSG00000266144.1","gene_symbol":"MIR4654","gene_name":"microRNA 4654 [Source:HGNC Symbol;Acc:HGNC:41643]","synonyms":"hsa-mir-4654","biotype":"miRNA","ncbi_id":"100616386","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":162157107,"end":162157182,"strand":1,"description":"microRNA 4654 [Source:HGNC Symbol;Acc:HGNC:41643]"}, {"versioned_ensembl_gene_id":"ENSG00000284247.1","gene_symbol":"MIR2682","gene_name":"microRNA 2682 [Source:HGNC Symbol;Acc:HGNC:41688]","synonyms":"hsa-mir-2682","biotype":"miRNA","ncbi_id":"100616452","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98045242,"end":98045351,"strand":-1,"description":"microRNA 2682 [Source:HGNC Symbol;Acc:HGNC:41688]"}, {"versioned_ensembl_gene_id":"ENSG00000266110.1","gene_symbol":"MIR4423","gene_name":"microRNA 4423 [Source:HGNC Symbol;Acc:HGNC:41784]","synonyms":"hsa-mir-4423","biotype":"miRNA","ncbi_id":"100616481","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85133794,"end":85133873,"strand":1,"description":"microRNA 4423 [Source:HGNC Symbol;Acc:HGNC:41784]"}, {"versioned_ensembl_gene_id":"ENSG00000222370.1","gene_symbol":"SNORA36B","gene_name":"small nucleolar RNA, H/ACA box 36B [Source:HGNC Symbol;Acc:HGNC:32629]","synonyms":"ACA36b","biotype":"snoRNA","ncbi_id":"677818","summary":null,"start":220200546,"end":220200676,"strand":-1,"description":"small nucleolar RNA, H/ACA box 36B [Source:HGNC Symbol;Acc:HGNC:32629]"}, {"versioned_ensembl_gene_id":"ENSG00000251728.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140094697,"end":140094792,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206603.1","gene_symbol":"SNORA22B","gene_name":"small nucleolar RNA, H/ACA box 22B [Source:HGNC Symbol;Acc:HGNC:52196]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616964","summary":null,"start":56055365,"end":56055502,"strand":1,"description":"small nucleolar RNA, H/ACA box 22B [Source:HGNC Symbol;Acc:HGNC:52196]"}, {"versioned_ensembl_gene_id":"ENSG00000265421.1","gene_symbol":"MIR4459","gene_name":"microRNA 4459 [Source:HGNC Symbol;Acc:HGNC:41551]","synonyms":"hsa-mir-4459","biotype":"miRNA","ncbi_id":"100616233","summary":"This record was withdrawn by miRBase.","start":54075518,"end":54075583,"strand":-1,"description":"microRNA 4459 [Source:HGNC Symbol;Acc:HGNC:41551]"}, {"versioned_ensembl_gene_id":"ENSG00000273839.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28500089,"end":28500346,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252108.1","gene_symbol":"RNU6-1232P","gene_name":"RNA, U6 small nuclear 1232, pseudogene [Source:HGNC Symbol;Acc:HGNC:48195]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480105","summary":null,"start":68159061,"end":68159146,"strand":-1,"description":"RNA, U6 small nuclear 1232, pseudogene [Source:HGNC Symbol;Acc:HGNC:48195]"}, {"versioned_ensembl_gene_id":"ENSG00000275304.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54539846,"end":54539952,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000283950.1","gene_symbol":"MIR6791","gene_name":"microRNA 6791 [Source:HGNC Symbol;Acc:HGNC:50097]","synonyms":"hsa-mir-6791","biotype":"miRNA","ncbi_id":"102465474","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6736712,"end":6736778,"strand":-1,"description":"microRNA 6791 [Source:HGNC Symbol;Acc:HGNC:50097]"}, {"versioned_ensembl_gene_id":"ENSG00000072849.10","gene_symbol":"DERL2","gene_name":"derlin 2 [Source:HGNC Symbol;Acc:HGNC:17943]","synonyms":"FLANa,F-LANa,F-LAN-1,derlin-2,CGI-101","biotype":"protein_coding","ncbi_id":"51009","summary":"Proteins that are unfolded or misfolded in the endoplasmic reticulum (ER) must be refolded or degraded to maintain the homeostasis of the ER. DERL2 is involved in the degradation of misfolded glycoproteins in the ER (Oda et al., 2006 [PubMed 16449189]).[supplied by OMIM, Mar 2008]","start":5471251,"end":5486811,"strand":-1,"description":"derlin 2 [Source:HGNC Symbol;Acc:HGNC:17943]"}, {"versioned_ensembl_gene_id":"ENSG00000202146.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":54099191,"end":54099302,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277533.1","gene_symbol":"MIR8077","gene_name":"microRNA 8077 [Source:HGNC Symbol;Acc:HGNC:50266]","synonyms":"hsa-mir-8077","biotype":"miRNA","ncbi_id":"102465875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42351131,"end":42351205,"strand":1,"description":"microRNA 8077 [Source:HGNC Symbol;Acc:HGNC:50266]"}, {"versioned_ensembl_gene_id":"ENSG00000264468.1","gene_symbol":"MIR4520-1","gene_name":"microRNA 4520-1 [Source:HGNC Symbol;Acc:HGNC:41775]","synonyms":"MIR4520A,hsa-mir-4520a","biotype":"miRNA","ncbi_id":"100616401","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6655440,"end":6655509,"strand":-1,"description":"microRNA 4520-1 [Source:HGNC Symbol;Acc:HGNC:41775]"}, {"versioned_ensembl_gene_id":"ENSG00000208001.1","gene_symbol":"MIR431","gene_name":"microRNA 431 [Source:HGNC Symbol;Acc:HGNC:32027]","synonyms":"MIRN431,hsa-mir-431","biotype":"miRNA","ncbi_id":"574038","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100881007,"end":100881120,"strand":1,"description":"microRNA 431 [Source:HGNC Symbol;Acc:HGNC:32027]"}, {"versioned_ensembl_gene_id":"ENSG00000263643.1","gene_symbol":"MIR4515","gene_name":"microRNA 4515 [Source:HGNC Symbol;Acc:HGNC:41800]","synonyms":"hsa-mir-4515","biotype":"miRNA","ncbi_id":"100616404","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":83067335,"end":83067415,"strand":1,"description":"microRNA 4515 [Source:HGNC Symbol;Acc:HGNC:41800]"}, {"versioned_ensembl_gene_id":"ENSG00000276873.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39171462,"end":39171560,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000278038.1","gene_symbol":"MIR6076","gene_name":"microRNA 6076 [Source:HGNC Symbol;Acc:HGNC:50232]","synonyms":"hsa-mir-6076","biotype":"miRNA","ncbi_id":"102464828","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49966399,"end":49966511,"strand":1,"description":"microRNA 6076 [Source:HGNC Symbol;Acc:HGNC:50232]"}, {"versioned_ensembl_gene_id":"ENSG00000265793.1","gene_symbol":"MIR3118-4","gene_name":"microRNA 3118-4 [Source:HGNC Symbol;Acc:HGNC:38287]","synonyms":"hsa-mir-3118-4","biotype":"miRNA","ncbi_id":"100422935","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21843750,"end":21843824,"strand":1,"description":"microRNA 3118-4 [Source:HGNC Symbol;Acc:HGNC:38287]"}, {"versioned_ensembl_gene_id":"ENSG00000171136.6","gene_symbol":"RLN3","gene_name":"relaxin 3 [Source:HGNC Symbol;Acc:HGNC:17135]","synonyms":"ZINS4,RXN3,H3","biotype":"protein_coding","ncbi_id":"117579","summary":"This gene encodes a member of the relaxin family of insulin-like hormones that is expressed predominantly in the brain and plays a role in physiological processes such as stress, memory and appetite regulation. The encoded protein is a precursor that is proteolytically processed to generate a heterodimeric mature form consisting A and B chains interlinked by disulfide bonds. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2015]","start":14028148,"end":14031042,"strand":1,"description":"relaxin 3 [Source:HGNC Symbol;Acc:HGNC:17135]"}, {"versioned_ensembl_gene_id":"ENSG00000284115.1","gene_symbol":"AC113189.10","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7439506,"end":7445966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266174.1","gene_symbol":"MIR4666A","gene_name":"microRNA 4666a [Source:HGNC Symbol;Acc:HGNC:41750]","synonyms":"MIR4666,hsa-mir-4666","biotype":"miRNA","ncbi_id":"100616308","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":228462074,"end":228462152,"strand":1,"description":"microRNA 4666a [Source:HGNC Symbol;Acc:HGNC:41750]"}, {"versioned_ensembl_gene_id":"ENSG00000275635.1","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":23137805,"end":23137864,"strand":-1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000243103.3","gene_symbol":"RN7SL452P","gene_name":"RNA, 7SL, cytoplasmic 452, pseudogene [Source:HGNC Symbol;Acc:HGNC:46468]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479387","summary":null,"start":50637691,"end":50637981,"strand":-1,"description":"RNA, 7SL, cytoplasmic 452, pseudogene [Source:HGNC Symbol;Acc:HGNC:46468]"}, {"versioned_ensembl_gene_id":"ENSG00000212546.1","gene_symbol":"RNU6-995P","gene_name":"RNA, U6 small nuclear 995, pseudogene [Source:HGNC Symbol;Acc:HGNC:47958]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481494","summary":null,"start":80936434,"end":80936540,"strand":1,"description":"RNA, U6 small nuclear 995, pseudogene [Source:HGNC Symbol;Acc:HGNC:47958]"}, {"versioned_ensembl_gene_id":"ENSG00000201413.1","gene_symbol":"RNA5SP141","gene_name":"RNA, 5S ribosomal pseudogene 141 [Source:HGNC Symbol;Acc:HGNC:43041]","synonyms":"RN5S141","biotype":"rRNA","ncbi_id":"100873408","summary":null,"start":134783436,"end":134783555,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 141 [Source:HGNC Symbol;Acc:HGNC:43041]"}, {"versioned_ensembl_gene_id":"ENSG00000242236.2","gene_symbol":"RN7SL594P","gene_name":"RNA, 7SL, cytoplasmic 594, pseudogene [Source:HGNC Symbol;Acc:HGNC:46610]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479439","summary":null,"start":25654595,"end":25654881,"strand":-1,"description":"RNA, 7SL, cytoplasmic 594, pseudogene [Source:HGNC Symbol;Acc:HGNC:46610]"}, {"versioned_ensembl_gene_id":"ENSG00000207416.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36986739,"end":36986851,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284363.1","gene_symbol":"MIR224","gene_name":"microRNA 224 [Source:HGNC Symbol;Acc:HGNC:31604]","synonyms":"MIRN224,hsa-mir-224","biotype":"miRNA","ncbi_id":"407009","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151958578,"end":151958658,"strand":-1,"description":"microRNA 224 [Source:HGNC Symbol;Acc:HGNC:31604]"}, {"versioned_ensembl_gene_id":"ENSG00000278527.1","gene_symbol":"SNORD22","gene_name":"Small nucleolar RNA SNORD22 [Source:RFAM;Acc:RF00099]","synonyms":"RNU22,U22","biotype":"snoRNA","ncbi_id":"9304","summary":null,"start":62854161,"end":62854285,"strand":-1,"description":"Small nucleolar RNA SNORD22 [Source:RFAM;Acc:RF00099]"}, {"versioned_ensembl_gene_id":"ENSG00000284157.1","gene_symbol":"MIR106A","gene_name":"microRNA 106a [Source:HGNC Symbol;Acc:HGNC:31494]","synonyms":"MIRN106A,hsa-mir-106a","biotype":"miRNA","ncbi_id":"406899","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134170198,"end":134170278,"strand":-1,"description":"microRNA 106a [Source:HGNC Symbol;Acc:HGNC:31494]"}, {"versioned_ensembl_gene_id":"ENSG00000275335.1","gene_symbol":"MIR8088","gene_name":"microRNA 8088 [Source:HGNC Symbol;Acc:HGNC:50167]","synonyms":"hsa-mir-8088","biotype":"miRNA","ncbi_id":"102466880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52336557,"end":52336642,"strand":-1,"description":"microRNA 8088 [Source:HGNC Symbol;Acc:HGNC:50167]"}, {"versioned_ensembl_gene_id":"ENSG00000207587.1","gene_symbol":"MIR544A","gene_name":"microRNA 544a [Source:HGNC Symbol;Acc:HGNC:32530]","synonyms":"MIRN544,MIR544,hsa-mir-544","biotype":"miRNA","ncbi_id":"664613","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101048658,"end":101048748,"strand":1,"description":"microRNA 544a [Source:HGNC Symbol;Acc:HGNC:32530]"}, {"versioned_ensembl_gene_id":"ENSG00000276421.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"PRP31,hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000266016.3","gene_symbol":"MIR548Z","gene_name":"microRNA 548z [Source:HGNC Symbol;Acc:HGNC:38929]","synonyms":"hsa-mir-548z","biotype":"miRNA","ncbi_id":"100500856","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64622509,"end":64622605,"strand":-1,"description":"microRNA 548z [Source:HGNC Symbol;Acc:HGNC:38929]"}, {"versioned_ensembl_gene_id":"ENSG00000279724.1","gene_symbol":"AC005086.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":102188599,"end":102188828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146250.6","gene_symbol":"PRSS35","gene_name":"protease, serine 35 [Source:HGNC Symbol;Acc:HGNC:21387]","synonyms":"MGC46520,dJ223E3.1,C6orf158","biotype":"protein_coding","ncbi_id":"167681","summary":null,"start":83512538,"end":83525704,"strand":1,"description":"protease, serine 35 [Source:HGNC Symbol;Acc:HGNC:21387]"}, {"versioned_ensembl_gene_id":"ENSG00000173156.6","gene_symbol":"RHOD","gene_name":"ras homolog family member D [Source:HGNC Symbol;Acc:HGNC:670]","synonyms":"RhoHP1,RhoD,Rho,ARHD","biotype":"protein_coding","ncbi_id":"29984","summary":"Ras homolog, or Rho, proteins interact with protein kinases and may serve as targets for activated GTPase. They play a critical role in muscle differentiation. The protein encoded by this gene binds GTP and is a member of the small GTPase superfamily. It is involved in endosome dynamics and reorganization of the actin cytoskeleton, and it may coordinate membrane transport with the function of the cytoskeleton. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":67056818,"end":67072013,"strand":1,"description":"ras homolog family member D [Source:HGNC Symbol;Acc:HGNC:670]"}, {"versioned_ensembl_gene_id":"ENSG00000124279.11","gene_symbol":"FASTKD3","gene_name":"FAST kinase domains 3 [Source:HGNC Symbol;Acc:HGNC:28758]","synonyms":"MGC5297,FLJ23274","biotype":"protein_coding","ncbi_id":"79072","summary":"This gene encodes a member of a small family of Fas-activated serine/threonine kinase domain (FASTKD) containing proteins that share an amino terminal mitochondrial targeting domain and multiple carboxy terminal FAST domains as well as a putative RNA-binding RAP domain. The members of this family are ubiquitously expressed and are generally most abundant in mitochondria-enriched tissues such as heart, skeletal muscle and brown-adipose tissue. Some members of this protein family may play a role in apoptosis. The protein encoded by this gene interacts with components of the mitochondrial respiratory and translation networks. A pseudogene of this gene is also present on chromosome 5. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":7859159,"end":7869037,"strand":-1,"description":"FAST kinase domains 3 [Source:HGNC Symbol;Acc:HGNC:28758]"}, {"versioned_ensembl_gene_id":"ENSG00000223783.1","gene_symbol":"LINC01983","gene_name":"long intergenic non-protein coding RNA 1983 [Source:HGNC Symbol;Acc:HGNC:52813]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929697","summary":null,"start":195836193,"end":195860404,"strand":-1,"description":"long intergenic non-protein coding RNA 1983 [Source:HGNC Symbol;Acc:HGNC:52813]"}, {"versioned_ensembl_gene_id":"ENSG00000124275.14","gene_symbol":"MTRR","gene_name":"5-methyltetrahydrofolate-homocysteine methyltransferase reductase [Source:HGNC Symbol;Acc:HGNC:7473]","synonyms":"cblE","biotype":"protein_coding","ncbi_id":"4552","summary":"This gene encodes a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. This protein functions in the synthesis of methionine by regenerating methionine synthase to a functional state. Because methionine synthesis requires methyl-group transfer by a folate donor, activity of the encoded enzyme is important for folate metabolism and cellular methylation. Mutations in this gene can cause homocystinuria-megaloblastic anemia, cbl E type. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":7851186,"end":7906025,"strand":1,"description":"5-methyltetrahydrofolate-homocysteine methyltransferase reductase [Source:HGNC Symbol;Acc:HGNC:7473]"}, {"versioned_ensembl_gene_id":"ENSG00000282980.1","gene_symbol":"AC055839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5512040,"end":5512537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091592.15","gene_symbol":"NLRP1","gene_name":"NLR family pyrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14374]","synonyms":"NALP1,NAC,KIAA0926,DKFZp586O1822,DEFCAP,CLR17.1,CARD7,VAMAS1,SLEV1","biotype":"protein_coding","ncbi_id":"22861","summary":"This gene encodes a member of the Ced-4 family of apoptosis proteins. Ced-family members contain a caspase recruitment domain (CARD) and are known to be key mediators of programmed cell death. The encoded protein contains a distinct N-terminal pyrin-like motif, which is possibly involved in protein-protein interactions. This protein interacts strongly with caspase 2 and weakly with caspase 9. Overexpression of this gene was demonstrated to induce apoptosis in cells. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":5499427,"end":5619424,"strand":-1,"description":"NLR family pyrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14374]"}, {"versioned_ensembl_gene_id":"ENSG00000198625.12","gene_symbol":"MDM4","gene_name":"MDM4, p53 regulator [Source:HGNC Symbol;Acc:HGNC:6974]","synonyms":"MDMX,HDMX","biotype":"protein_coding","ncbi_id":"4194","summary":"This gene encodes a nuclear protein that contains a p53 binding domain at the N-terminus and a RING finger domain at the C-terminus, and shows structural similarity to p53-binding protein MDM2. Both proteins bind the p53 tumor suppressor protein and inhibit its activity, and have been shown to be overexpressed in a variety of human cancers. However, unlike MDM2 which degrades p53, this protein inhibits p53 by binding its transcriptional activation domain. This protein also interacts with MDM2 protein via the RING finger domain, and inhibits the latter's degradation. So this protein can reverse MDM2-targeted degradation of p53, while maintaining suppression of p53 transactivation and apoptotic functions. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2011]","start":204516379,"end":204558120,"strand":1,"description":"MDM4, p53 regulator [Source:HGNC Symbol;Acc:HGNC:6974]"}, {"versioned_ensembl_gene_id":"ENSG00000264811.1","gene_symbol":"AC138761.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22299134,"end":22299467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257101.1","gene_symbol":"LRRC37A13P","gene_name":"leucine rich repeat containing 37 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:43817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479024","summary":null,"start":113791466,"end":113791752,"strand":1,"description":"leucine rich repeat containing 37 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:43817]"}, {"versioned_ensembl_gene_id":"ENSG00000126457.21","gene_symbol":"PRMT1","gene_name":"protein arginine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:5187]","synonyms":"HRMT1L2,HCP1,ANM1","biotype":"protein_coding","ncbi_id":"3276","summary":"This gene encodes a member of the protein arginine N-methyltransferase (PRMT) family. Post-translational modification of target proteins by PRMTs plays an important regulatory role in many biological processes, whereby PRMTs methylate arginine residues by transferring methyl groups from S-adenosyl-L-methionine to terminal guanidino nitrogen atoms. The encoded protein is a type I PRMT and is responsible for the majority of cellular arginine methylation activity. Increased expression of this gene may play a role in many types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Dec 2011]","start":49675786,"end":49689029,"strand":1,"description":"protein arginine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:5187]"}, {"versioned_ensembl_gene_id":"ENSG00000265043.1","gene_symbol":"AC068418.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21456513,"end":21460215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183010.16","gene_symbol":"PYCR1","gene_name":"pyrroline-5-carboxylate reductase 1 [Source:HGNC Symbol;Acc:HGNC:9721]","synonyms":"P5C","biotype":"protein_coding","ncbi_id":"5831","summary":"This gene encodes an enzyme that catalyzes the NAD(P)H-dependent conversion of pyrroline-5-carboxylate to proline. This enzyme may also play a physiologic role in the generation of NADP(+) in some cell types. The protein forms a homopolymer and localizes to the mitochondrion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":81932384,"end":81942412,"strand":-1,"description":"pyrroline-5-carboxylate reductase 1 [Source:HGNC Symbol;Acc:HGNC:9721]"}, {"versioned_ensembl_gene_id":"ENSG00000197063.10","gene_symbol":"MAFG","gene_name":"MAF bZIP transcription factor G [Source:HGNC Symbol;Acc:HGNC:6781]","synonyms":"MGC20149,MGC13090","biotype":"protein_coding","ncbi_id":"4097","summary":"Globin gene expression is regulated through nuclear factor erythroid-2 (NFE2) elements located in enhancer-like locus control regions positioned many kb upstream of alpha- and beta-gene clusters (summarized by Blank et al., 1997 [PubMed 9166829]). NFE2 DNA-binding activity consists of a heterodimer containing a ubiquitous small Maf protein (MafF, MIM 604877; MafG; or MafK, MIM 600197) and the tissue-restricted protein p45 NFE2 (MIM 601490). Both subunits are members of the activator protein-1-like superfamily of basic leucine zipper (bZIP) proteins (see MIM 165160).[supplied by OMIM, Mar 2010]","start":81918270,"end":81927714,"strand":-1,"description":"MAF bZIP transcription factor G [Source:HGNC Symbol;Acc:HGNC:6781]"}, {"versioned_ensembl_gene_id":"ENSG00000004939.13","gene_symbol":"SLC4A1","gene_name":"solute carrier family 4 member 1 (Diego blood group) [Source:HGNC Symbol;Acc:HGNC:11027]","synonyms":"FR,EPB3,DI,CD233,AE1,WR,WD,SW,RTA1A","biotype":"protein_coding","ncbi_id":"6521","summary":"The protein encoded by this gene is part of the anion exchanger (AE) family and is expressed in the erythrocyte plasma membrane, where it functions as a chloride/bicarbonate exchanger involved in carbon dioxide transport from tissues to lungs. The protein comprises two domains that are structurally and functionally distinct. The N-terminal 40kDa domain is located in the cytoplasm and acts as an attachment site for the red cell skeleton by binding ankyrin. The glycosylated C-terminal membrane-associated domain contains 12-14 membrane spanning segments and carries out the stilbene disulphonate-sensitive exchange transport of anions. The cytoplasmic tail at the extreme C-terminus of the membrane domain binds carbonic anhydrase II. The encoded protein associates with the red cell membrane protein glycophorin A and this association promotes the correct folding and translocation of the exchanger. This protein is predominantly dimeric but forms tetramers in the presence of ankyrin. Many mutations in this gene are known in man, and these mutations can lead to two types of disease: destabilization of red cell membrane leading to hereditary spherocytosis, and defective kidney acid secretion leading to distal renal tubular acidosis. Other mutations that do not give rise to disease result in novel blood group antigens, which form the Diego blood group system. Southeast Asian ovalocytosis (SAO, Melanesian ovalocytosis) results from the heterozygous presence of a deletion in the encoded protein and is common in areas where Plasmodium falciparum malaria is endemic. One null mutation in this gene is known, resulting in very severe anemia and nephrocalcinosis. [provided by RefSeq, Jul 2008]","start":44248385,"end":44268141,"strand":-1,"description":"solute carrier family 4 member 1 (Diego blood group) [Source:HGNC Symbol;Acc:HGNC:11027]"}, {"versioned_ensembl_gene_id":"ENSG00000267691.1","gene_symbol":"AC003102.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44228760,"end":44230228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258400.1","gene_symbol":"AL591767.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49707667,"end":49708792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197776.7","gene_symbol":"KLHDC1","gene_name":"kelch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19836]","synonyms":"MST025","biotype":"protein_coding","ncbi_id":"122773","summary":null,"start":49693105,"end":49753152,"strand":1,"description":"kelch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19836]"}, {"versioned_ensembl_gene_id":"ENSG00000104870.12","gene_symbol":"FCGRT","gene_name":"Fc fragment of IgG receptor and transporter [Source:HGNC Symbol;Acc:HGNC:3621]","synonyms":"alpha-chain,FCRN","biotype":"protein_coding","ncbi_id":"2217","summary":"This gene encodes a receptor that binds the Fc region of monomeric immunoglobulin G. The encoded protein transfers immunoglobulin G antibodies from mother to fetus across the placenta. This protein also binds immunoglobulin G to protect the antibody from degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":49506816,"end":49526333,"strand":1,"description":"Fc fragment of IgG receptor and transporter [Source:HGNC Symbol;Acc:HGNC:3621]"}, {"versioned_ensembl_gene_id":"ENSG00000224797.1","gene_symbol":"AL359092.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130724786,"end":130725050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249605.1","gene_symbol":"AC008652.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":144369334,"end":144385310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266074.8","gene_symbol":"BAHCC1","gene_name":"BAH domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:29279]","synonyms":"KIAA1447,BAHD2","biotype":"protein_coding","ncbi_id":"57597","summary":null,"start":81395475,"end":81466332,"strand":1,"description":"BAH domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:29279]"}, {"versioned_ensembl_gene_id":"ENSG00000274833.1","gene_symbol":"AC110285.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81387415,"end":81387766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258462.2","gene_symbol":"AL591767.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49681302,"end":49681886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249637.1","gene_symbol":"AC008438.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140370891,"end":140401367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113580.14","gene_symbol":"NR3C1","gene_name":"nuclear receptor subfamily 3 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7978]","synonyms":"GRL,GR","biotype":"protein_coding","ncbi_id":"2908","summary":"This gene encodes glucocorticoid receptor, which can function both as a transcription factor that binds to glucocorticoid response elements in the promoters of glucocorticoid responsive genes to activate their transcription, and as a regulator of other transcription factors. This receptor is typically found in the cytoplasm, but upon ligand binding, is transported into the nucleus. It is involved in inflammatory responses, cellular proliferation, and differentiation in target tissues. Mutations in this gene are associated with generalized glucocorticoid resistance. Alternative splicing of this gene results in transcript variants encoding either the same or different isoforms. Additional isoforms resulting from the use of alternate in-frame translation initiation sites have also been described, and shown to be functional, displaying diverse cytoplasm-to-nucleus trafficking patterns and distinct transcriptional activities (PMID:15866175). [provided by RefSeq, Feb 2011]","start":143277931,"end":143435512,"strand":-1,"description":"nuclear receptor subfamily 3 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7978]"}, {"versioned_ensembl_gene_id":"ENSG00000148357.16","gene_symbol":"HMCN2","gene_name":"hemicentin 2 [Source:HGNC Symbol;Acc:HGNC:21293]","synonyms":"FLJ23816,DKFZp434P0216","biotype":"protein_coding","ncbi_id":"256158","summary":null,"start":130265882,"end":130434123,"strand":1,"description":"hemicentin 2 [Source:HGNC Symbol;Acc:HGNC:21293]"}, {"versioned_ensembl_gene_id":"ENSG00000131023.12","gene_symbol":"LATS1","gene_name":"large tumor suppressor kinase 1 [Source:HGNC Symbol;Acc:HGNC:6514]","synonyms":"WARTS","biotype":"protein_coding","ncbi_id":"9113","summary":"The protein encoded by this gene is a putative serine/threonine kinase that localizes to the mitotic apparatus and complexes with cell cycle controller CDC2 kinase in early mitosis. The protein is phosphorylated in a cell-cycle dependent manner, with late prophase phosphorylation remaining through metaphase. The N-terminal region of the protein binds CDC2 to form a complex showing reduced H1 histone kinase activity, indicating a role as a negative regulator of CDC2/cyclin A. In addition, the C-terminal kinase domain binds to its own N-terminal region, suggesting potential negative regulation through interference with complex formation via intramolecular binding. Biochemical and genetic data suggest a role as a tumor suppressor. This is supported by studies in knockout mice showing development of soft-tissue sarcomas, ovarian stromal cell tumors and a high sensitivity to carcinogenic treatments. [provided by RefSeq, Apr 2017]","start":149658153,"end":149718256,"strand":-1,"description":"large tumor suppressor kinase 1 [Source:HGNC Symbol;Acc:HGNC:6514]"}, {"versioned_ensembl_gene_id":"ENSG00000106771.12","gene_symbol":"TMEM245","gene_name":"transmembrane protein 245 [Source:HGNC Symbol;Acc:HGNC:1363]","synonyms":"CG-2,C9orf5","biotype":"protein_coding","ncbi_id":"23731","summary":null,"start":109015152,"end":109119945,"strand":-1,"description":"transmembrane protein 245 [Source:HGNC Symbol;Acc:HGNC:1363]"}, {"versioned_ensembl_gene_id":"ENSG00000113068.9","gene_symbol":"PFDN1","gene_name":"prefoldin subunit 1 [Source:HGNC Symbol;Acc:HGNC:8866]","synonyms":"PFD1","biotype":"protein_coding","ncbi_id":"5201","summary":"This gene encodes a member of the prefoldin beta subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The complex, consisting of two alpha and four beta subunits, forms a double beta barrel assembly with six protruding coiled-coils. [provided by RefSeq, Jul 2008]","start":140245039,"end":140303121,"strand":-1,"description":"prefoldin subunit 1 [Source:HGNC Symbol;Acc:HGNC:8866]"}, {"versioned_ensembl_gene_id":"ENSG00000230339.2","gene_symbol":"AC015818.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20554137,"end":20554380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188770.9","gene_symbol":"OPTC","gene_name":"opticin [Source:HGNC Symbol;Acc:HGNC:8158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26254","summary":"Opticin belongs to class III of the small leucine-rich repeat protein (SLRP) family. Members of this family are typically associated with the extracellular matrix. Opticin is present in significant quantities in the vitreous of the eye and also localizes to the cornea, iris, ciliary body, optic nerve, choroid, retina, and fetal liver. Opticin may noncovalently bind collagen fibrils and regulate fibril morphology, spacing, and organization. The opticin gene is mapped to a region of chromosome 1 that is associated with the inherited eye diseases age-related macular degeneration (AMD) and posterior column ataxia with retinosa pigmentosa (AXPC1). [provided by RefSeq, Jul 2008]","start":203494143,"end":203508864,"strand":1,"description":"opticin [Source:HGNC Symbol;Acc:HGNC:8158]"}, {"versioned_ensembl_gene_id":"ENSG00000250069.1","gene_symbol":"AC011379.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":140200163,"end":140203187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254363.6","gene_symbol":"AC011379.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":140157319,"end":140173051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272081.1","gene_symbol":"AC008972.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72955206,"end":72955699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269469.1","gene_symbol":"AC010619.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49462752,"end":49486231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229983.1","gene_symbol":"AL606468.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212168207,"end":212190259,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187866.8","gene_symbol":"FAM122A","gene_name":"family with sequence similarity 122A [Source:HGNC Symbol;Acc:HGNC:23490]","synonyms":"MGC17347,C9orf42","biotype":"protein_coding","ncbi_id":"116224","summary":null,"start":68780034,"end":68784608,"strand":1,"description":"family with sequence similarity 122A [Source:HGNC Symbol;Acc:HGNC:23490]"}, {"versioned_ensembl_gene_id":"ENSG00000013392.7","gene_symbol":"RWDD2A","gene_name":"RWD domain containing 2A [Source:HGNC Symbol;Acc:HGNC:21385]","synonyms":"RWDD2,MGC13523,dJ747H23.2","biotype":"protein_coding","ncbi_id":"112611","summary":null,"start":83193379,"end":83198932,"strand":1,"description":"RWD domain containing 2A [Source:HGNC Symbol;Acc:HGNC:21385]"}, {"versioned_ensembl_gene_id":"ENSG00000262313.1","gene_symbol":"AC127496.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80940418,"end":80942033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104872.10","gene_symbol":"PIH1D1","gene_name":"PIH1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26075]","synonyms":"NOP17,FLJ20643","biotype":"protein_coding","ncbi_id":"55011","summary":null,"start":49446298,"end":49453497,"strand":-1,"description":"PIH1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26075]"}, {"versioned_ensembl_gene_id":"ENSG00000259586.1","gene_symbol":"AC015712.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100846604,"end":100846767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213741.9","gene_symbol":"RPS29","gene_name":"ribosomal protein S29 [Source:HGNC Symbol;Acc:HGNC:10419]","synonyms":"S29","biotype":"protein_coding","ncbi_id":"6235","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit and a member of the S14P family of ribosomal proteins. The protein, which contains a C2-C2 zinc finger-like domain that can bind to zinc, can enhance the tumor suppressor activity of Ras-related protein 1A (KREV1). It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2013]","start":49570984,"end":49599164,"strand":-1,"description":"ribosomal protein S29 [Source:HGNC Symbol;Acc:HGNC:10419]"}, {"versioned_ensembl_gene_id":"ENSG00000278009.1","gene_symbol":"AL139099.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49601011,"end":49601124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114491.13","gene_symbol":"UMPS","gene_name":"uridine monophosphate synthetase [Source:HGNC Symbol;Acc:HGNC:12563]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7372","summary":"This gene encodes a uridine 5'-monophosphate synthase. The encoded protein is a bifunctional enzyme that catalyzes the final two steps of the de novo pyrimidine biosynthetic pathway. The first reaction is carried out by the N-terminal enzyme orotate phosphoribosyltransferase which converts orotic acid to orotidine-5'-monophosphate. The terminal reaction is carried out by the C-terminal enzyme OMP decarboxylase which converts orotidine-5'-monophosphate to uridine monophosphate. Defects in this gene are the cause of hereditary orotic aciduria. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":124730366,"end":124749273,"strand":1,"description":"uridine monophosphate synthetase [Source:HGNC Symbol;Acc:HGNC:12563]"}, {"versioned_ensembl_gene_id":"ENSG00000145819.15","gene_symbol":"ARHGAP26","gene_name":"Rho GTPase activating protein 26 [Source:HGNC Symbol;Acc:HGNC:17073]","synonyms":"OPHN1L1,OPHN1L,KIAA0621,GRAF","biotype":"protein_coding","ncbi_id":"23092","summary":"Interaction of a cell with the extracellular matrix triggers integrin cell surface receptors to begin signaling cascades that regulate the organization of the actin-cytoskeleton. One of the proteins involved in these cascades is focal adhesion kinase. The protein encoded by this gene is a GTPase activating protein that binds to focal adhesion kinase and mediates the activity of the GTP binding proteins RhoA and Cdc42. Defects in this gene are a cause of juvenile myelomonocytic leukemia (JMML). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2017]","start":142770384,"end":143229011,"strand":1,"description":"Rho GTPase activating protein 26 [Source:HGNC Symbol;Acc:HGNC:17073]"}, {"versioned_ensembl_gene_id":"ENSG00000250056.5","gene_symbol":"LINC01018","gene_name":"long intergenic non-protein coding RNA 1018 [Source:HGNC Symbol;Acc:HGNC:27394]","synonyms":null,"biotype":"lincRNA","ncbi_id":"255167","summary":null,"start":6582136,"end":6588499,"strand":1,"description":"long intergenic non-protein coding RNA 1018 [Source:HGNC Symbol;Acc:HGNC:27394]"}, {"versioned_ensembl_gene_id":"ENSG00000262580.5","gene_symbol":"AC087741.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80200673,"end":80205949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271230.1","gene_symbol":"AC027334.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6532891,"end":6533200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225864.1","gene_symbol":"AL645939.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29722981,"end":29723971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141570.10","gene_symbol":"CBX8","gene_name":"chromobox 8 [Source:HGNC Symbol;Acc:HGNC:15962]","synonyms":"RC1,PC3,HPC3","biotype":"protein_coding","ncbi_id":"57332","summary":null,"start":79792132,"end":79801683,"strand":-1,"description":"chromobox 8 [Source:HGNC Symbol;Acc:HGNC:15962]"}, {"versioned_ensembl_gene_id":"ENSG00000250347.1","gene_symbol":"AC005740.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142036707,"end":142037125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231534.1","gene_symbol":"FBXO36-IT1","gene_name":"FBXO36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41489]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874344","summary":null,"start":229942728,"end":229945137,"strand":1,"description":"FBXO36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41489]"}, {"versioned_ensembl_gene_id":"ENSG00000227638.2","gene_symbol":"HNRNPA1P14","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39132]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421351","summary":null,"start":88410529,"end":88411463,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39132]"}, {"versioned_ensembl_gene_id":"ENSG00000152253.8","gene_symbol":"SPC25","gene_name":"SPC25, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24031]","synonyms":"AD024,SPBC25,MGC22228","biotype":"protein_coding","ncbi_id":"57405","summary":"This gene encodes a protein that may be involved in kinetochore-microtubule interaction and spindle checkpoint activity. [provided by RefSeq, Jul 2008]","start":168834132,"end":168913371,"strand":-1,"description":"SPC25, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24031]"}, {"versioned_ensembl_gene_id":"ENSG00000276182.1","gene_symbol":"AL163051.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":96537170,"end":96537904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258601.1","gene_symbol":"AL162464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36808871,"end":36828729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116977.18","gene_symbol":"LGALS8","gene_name":"galectin 8 [Source:HGNC Symbol;Acc:HGNC:6569]","synonyms":"PCTA-1","biotype":"protein_coding","ncbi_id":"3964","summary":"This gene encodes a member of the galectin family. Galectins are beta-galactoside-binding animal lectins with conserved carbohydrate recognition domains. The galectins have been implicated in many essential functions including development, differentiation, cell-cell adhesion, cell-matrix interaction, growth regulation, apoptosis, and RNA splicing. This gene is widely expressed in tumoral tissues and seems to be involved in integrin-like cell interactions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":236518000,"end":236552981,"strand":1,"description":"galectin 8 [Source:HGNC Symbol;Acc:HGNC:6569]"}, {"versioned_ensembl_gene_id":"ENSG00000261266.2","gene_symbol":"AC008870.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23687049,"end":23687689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228485.1","gene_symbol":"GRK5-IT1","gene_name":"GRK5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49478]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"101927868","summary":null,"start":119208531,"end":119211760,"strand":1,"description":"GRK5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49478]"}, {"versioned_ensembl_gene_id":"ENSG00000248385.7","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069895,"end":54081365,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000167123.18","gene_symbol":"CERCAM","gene_name":"cerebral endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:23723]","synonyms":"GLT25D3,CerCAM,CEECAM1","biotype":"protein_coding","ncbi_id":"51148","summary":null,"start":128411751,"end":128437351,"strand":1,"description":"cerebral endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:23723]"}, {"versioned_ensembl_gene_id":"ENSG00000258301.3","gene_symbol":"VASH1-AS1","gene_name":"VASH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53215]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506603","summary":null,"start":76781733,"end":76786724,"strand":-1,"description":"VASH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53215]"}, {"versioned_ensembl_gene_id":"ENSG00000254997.3","gene_symbol":"KRTAP5-9","gene_name":"keratin associated protein 5-9 [Source:HGNC Symbol;Acc:HGNC:23604]","synonyms":"KRTAP5.9,KRTAP5-1,KRN1","biotype":"protein_coding","ncbi_id":"3846","summary":null,"start":71548418,"end":71549553,"strand":1,"description":"keratin associated protein 5-9 [Source:HGNC Symbol;Acc:HGNC:23604]"}, {"versioned_ensembl_gene_id":"ENSG00000186567.12","gene_symbol":"CEACAM19","gene_name":"carcinoembryonic antigen related cell adhesion molecule 19 [Source:HGNC Symbol;Acc:HGNC:31951]","synonyms":"CEAL1","biotype":"protein_coding","ncbi_id":"56971","summary":null,"start":44662278,"end":44684359,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 19 [Source:HGNC Symbol;Acc:HGNC:31951]"}, {"versioned_ensembl_gene_id":"ENSG00000272367.1","gene_symbol":"AC018754.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87376256,"end":87377180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100592.15","gene_symbol":"DAAM1","gene_name":"dishevelled associated activator of morphogenesis 1 [Source:HGNC Symbol;Acc:HGNC:18142]","synonyms":"KIAA0666","biotype":"protein_coding","ncbi_id":"23002","summary":"Cell motility, adhesion, cytokinesis, and other functions of the cell cortex are mediated by reorganization of the actin cytoskeleton and several formin homology (FH) proteins have been associated with these processes. The protein encoded by this gene contains two FH domains and belongs to a novel FH protein subfamily implicated in cell polarity. A key regulator of cytoskeletal architecture, the small GTPase Rho, is activated during development by Wnt/Fz signaling to control cell polarity and movement. The protein encoded by this gene is thought to function as a scaffolding protein for the Wnt-induced assembly of a disheveled (Dvl)-Rho complex. This protein also promotes the nucleation and elongation of new actin filaments and regulates cell growth through the stabilization of microtubules. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2012]","start":59188646,"end":59371405,"strand":1,"description":"dishevelled associated activator of morphogenesis 1 [Source:HGNC Symbol;Acc:HGNC:18142]"}, {"versioned_ensembl_gene_id":"ENSG00000184640.17","gene_symbol":"SEPT9","gene_name":"septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]","synonyms":"MSF1,MSF,KIAA0991,AF17q25,SeptD1,PNUTL4","biotype":"protein_coding","ncbi_id":"10801","summary":"This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]","start":77280569,"end":77500596,"strand":1,"description":"septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]"}, {"versioned_ensembl_gene_id":"ENSG00000108852.14","gene_symbol":"MPP2","gene_name":"membrane palmitoylated protein 2 [Source:HGNC Symbol;Acc:HGNC:7220]","synonyms":"DLG2,DKFZp761D0712","biotype":"protein_coding","ncbi_id":"4355","summary":" Palmitoylated membrane protein 2 is a member of a family of membrane-associated proteins termed MAGUKs (membrane-associated guanylate kinase homologs). MAGUKs interact with the cytoskeleton and regulate cell proliferation, signaling pathways, and intracellular junctions. Palmitoylated membrane protein 2 contains a conserved sequence, called the SH3 (src homology 3) motif, found in several other proteins that associate with the cytoskeleton and are suspected to play important roles in signal transduction. [provided by RefSeq, Jul 2008]","start":43875357,"end":43909711,"strand":-1,"description":"membrane palmitoylated protein 2 [Source:HGNC Symbol;Acc:HGNC:7220]"}, {"versioned_ensembl_gene_id":"ENSG00000262881.1","gene_symbol":"CR936218.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45907670,"end":45910779,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124920.13","gene_symbol":"MYRF","gene_name":"myelin regulatory factor [Source:HGNC Symbol;Acc:HGNC:1181]","synonyms":"pqn-47,Ndt80,MRF,C11orf9","biotype":"protein_coding","ncbi_id":"745","summary":"This gene encodes a transcription factor that is required for central nervous system myelination and may regulate oligodendrocyte differentiation. It is thought to act by increasing the expression of genes that effect myelin production but may also directly promote myelin gene expression. Loss of a similar gene in mouse models results in severe demyelination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":61752642,"end":61788518,"strand":1,"description":"myelin regulatory factor [Source:HGNC Symbol;Acc:HGNC:1181]"}, {"versioned_ensembl_gene_id":"ENSG00000164761.8","gene_symbol":"TNFRSF11B","gene_name":"TNF receptor superfamily member 11b [Source:HGNC Symbol;Acc:HGNC:11909]","synonyms":"TR1,OPG,OCIF","biotype":"protein_coding","ncbi_id":"4982","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This protein is an osteoblast-secreted decoy receptor that functions as a negative regulator of bone resorption. This protein specifically binds to its ligand, osteoprotegerin ligand, both of which are key extracellular regulators of osteoclast development. Studies of the mouse counterpart also suggest that this protein and its ligand play a role in lymph-node organogenesis and vascular calcification. Alternatively spliced transcript variants of this gene have been reported, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":118923557,"end":118952200,"strand":-1,"description":"TNF receptor superfamily member 11b [Source:HGNC Symbol;Acc:HGNC:11909]"}, {"versioned_ensembl_gene_id":"ENSG00000232514.1","gene_symbol":"AL356968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48497263,"end":48497736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254979.5","gene_symbol":"AP000781.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57387365,"end":57424059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205835.8","gene_symbol":"GMNC","gene_name":"geminin coiled-coil domain containing [Source:HGNC Symbol;Acc:HGNC:40049]","synonyms":"GEMC1","biotype":"protein_coding","ncbi_id":"647309","summary":null,"start":190852877,"end":190892429,"strand":-1,"description":"geminin coiled-coil domain containing [Source:HGNC Symbol;Acc:HGNC:40049]"}, {"versioned_ensembl_gene_id":"ENSG00000234848.1","gene_symbol":"AC008758.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12450935,"end":12460705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236483.1","gene_symbol":"MTND2P40","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52084]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075280","summary":null,"start":12502675,"end":12504106,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52084]"}, {"versioned_ensembl_gene_id":"ENSG00000214147.2","gene_symbol":"AC092952.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190830965,"end":190832173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235401.1","gene_symbol":"AL935156.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215267,"end":29216210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218297.2","gene_symbol":"AL935156.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181515,"end":29182450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227334.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30341216,"end":30341350,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000255289.1","gene_symbol":"AC068389.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60660820,"end":60664530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229267.2","gene_symbol":"AC016708.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":214810229,"end":214963274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107581.12","gene_symbol":"EIF3A","gene_name":"eukaryotic translation initiation factor 3 subunit A [Source:HGNC Symbol;Acc:HGNC:3271]","synonyms":"TIF32,KIAA0139,EIF3S10,eIF3a,eIF3-theta,eIF3-p170,EIF3","biotype":"protein_coding","ncbi_id":"8661","summary":null,"start":119033670,"end":119080823,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit A [Source:HGNC Symbol;Acc:HGNC:3271]"}, {"versioned_ensembl_gene_id":"ENSG00000167642.12","gene_symbol":"SPINT2","gene_name":"serine peptidase inhibitor, Kunitz type 2 [Source:HGNC Symbol;Acc:HGNC:11247]","synonyms":"Kop,HAI-2","biotype":"protein_coding","ncbi_id":"10653","summary":"This gene encodes a transmembrane protein with two extracellular Kunitz domains that inhibits a variety of serine proteases. The protein inhibits HGF activator which prevents the formation of active hepatocyte growth factor. This gene is a putative tumor suppressor, and mutations in this gene result in congenital sodium diarrhea. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":38244035,"end":38292614,"strand":1,"description":"serine peptidase inhibitor, Kunitz type 2 [Source:HGNC Symbol;Acc:HGNC:11247]"}, {"versioned_ensembl_gene_id":"ENSG00000149136.8","gene_symbol":"SSRP1","gene_name":"structure specific recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:11327]","synonyms":"FACT80","biotype":"protein_coding","ncbi_id":"6749","summary":"The protein encoded by this gene is a subunit of a heterodimer that, along with SUPT16H, forms chromatin transcriptional elongation factor FACT. FACT interacts specifically with histones H2A/H2B to effect nucleosome disassembly and transcription elongation. FACT and cisplatin-damaged DNA may be crucial to the anticancer mechanism of cisplatin. This encoded protein contains a high mobility group box which most likely constitutes the structure recognition element for cisplatin-modified DNA. This protein also functions as a co-activator of the transcriptional activator p63. An alternatively spliced transcript variant of this gene has been described, but its full-length nature is not known. [provided by RefSeq, Jul 2008]","start":57325985,"end":57335877,"strand":-1,"description":"structure specific recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:11327]"}, {"versioned_ensembl_gene_id":"ENSG00000128563.13","gene_symbol":"PRKRIP1","gene_name":"PRKR interacting protein 1 (IL11 inducible) [Source:HGNC Symbol;Acc:HGNC:21894]","synonyms":"KRBOX3,FLJ13902,C114","biotype":"protein_coding","ncbi_id":"79706","summary":null,"start":102363872,"end":102426676,"strand":1,"description":"PRKR interacting protein 1 (IL11 inducible) [Source:HGNC Symbol;Acc:HGNC:21894]"}, {"versioned_ensembl_gene_id":"ENSG00000247077.6","gene_symbol":"PGAM5","gene_name":"PGAM family member 5, mitochondrial serine/threonine protein phosphatase [Source:HGNC Symbol;Acc:HGNC:28763]","synonyms":"MGC5352,BXLBv68","biotype":"protein_coding","ncbi_id":"192111","summary":null,"start":132710819,"end":132722734,"strand":1,"description":"PGAM family member 5, mitochondrial serine/threonine protein phosphatase [Source:HGNC Symbol;Acc:HGNC:28763]"}, {"versioned_ensembl_gene_id":"ENSG00000167139.8","gene_symbol":"TBC1D21","gene_name":"TBC1 domain family member 21 [Source:HGNC Symbol;Acc:HGNC:28536]","synonyms":"MgcRabGAP,MGC34741","biotype":"protein_coding","ncbi_id":"161514","summary":null,"start":73873608,"end":73889214,"strand":1,"description":"TBC1 domain family member 21 [Source:HGNC Symbol;Acc:HGNC:28536]"}, {"versioned_ensembl_gene_id":"ENSG00000211964.3","gene_symbol":"IGHV3-48","gene_name":"immunoglobulin heavy variable 3-48 [Source:HGNC Symbol;Acc:HGNC:5606]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28424","summary":null,"start":106537810,"end":106538344,"strand":-1,"description":"immunoglobulin heavy variable 3-48 [Source:HGNC Symbol;Acc:HGNC:5606]"}, {"versioned_ensembl_gene_id":"ENSG00000211965.4","gene_symbol":"IGHV3-49","gene_name":"immunoglobulin heavy variable 3-49 [Source:HGNC Symbol;Acc:HGNC:5607]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28423","summary":null,"start":106556936,"end":106557477,"strand":-1,"description":"immunoglobulin heavy variable 3-49 [Source:HGNC Symbol;Acc:HGNC:5607]"}, {"versioned_ensembl_gene_id":"ENSG00000145348.16","gene_symbol":"TBCK","gene_name":"TBC1 domain containing kinase [Source:HGNC Symbol;Acc:HGNC:28261]","synonyms":"MGC16169,HSPC302","biotype":"protein_coding","ncbi_id":"93627","summary":"This gene encodes a protein that contains a protein kinase domain, a Rhodanase-like domain and the Tre-2/Bub2/Cdc16 (TBC) domain. The encoded protein is thought to play a role in actin organization, cell growth and cell proliferation by regulating the mammalian target of the rapamycin (mTOR) signaling pathway. This protein may also be involved in the transcriptional regulation of the components of the mTOR complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":106041599,"end":106321495,"strand":-1,"description":"TBC1 domain containing kinase [Source:HGNC Symbol;Acc:HGNC:28261]"}, {"versioned_ensembl_gene_id":"ENSG00000253509.1","gene_symbol":"AC104393.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41275115,"end":41277003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105352.10","gene_symbol":"CEACAM4","gene_name":"carcinoembryonic antigen related cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:1816]","synonyms":"CGM7","biotype":"protein_coding","ncbi_id":"1089","summary":null,"start":41618971,"end":41627074,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:1816]"}, {"versioned_ensembl_gene_id":"ENSG00000171720.9","gene_symbol":"HDAC3","gene_name":"histone deacetylase 3 [Source:HGNC Symbol;Acc:HGNC:4854]","synonyms":"RPD3-2,RPD3,HD3","biotype":"protein_coding","ncbi_id":"8841","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to the histone deacetylase/acuc/apha family. It has histone deacetylase activity and represses transcription when tethered to a promoter. It may participate in the regulation of transcription through its binding with the zinc-finger transcription factor YY1. This protein can also down-regulate p53 function and thus modulate cell growth and apoptosis. This gene is regarded as a potential tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":141620876,"end":141636870,"strand":-1,"description":"histone deacetylase 3 [Source:HGNC Symbol;Acc:HGNC:4854]"}, {"versioned_ensembl_gene_id":"ENSG00000229291.1","gene_symbol":"AL139161.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235957879,"end":235971825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272676.1","gene_symbol":"AP001521.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57045091,"end":57045390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225858.1","gene_symbol":"BX295541.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72660470,"end":72660719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279430.1","gene_symbol":"AL590560.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":159910094,"end":159910554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235630.2","gene_symbol":"BX000688.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29573828,"end":29574755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101276.14","gene_symbol":"SLC52A3","gene_name":"solute carrier family 52 member 3 [Source:HGNC Symbol;Acc:HGNC:16187]","synonyms":"RFVT3,hRFT2,C20orf54,bA371L19.1","biotype":"protein_coding","ncbi_id":"113278","summary":"This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]","start":760080,"end":776015,"strand":-1,"description":"solute carrier family 52 member 3 [Source:HGNC Symbol;Acc:HGNC:16187]"}, {"versioned_ensembl_gene_id":"ENSG00000260573.2","gene_symbol":"AC007493.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50407666,"end":50522638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227640.2","gene_symbol":"SOX21-AS1","gene_name":"SOX21 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39807]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507533","summary":null,"start":94712716,"end":94716246,"strand":1,"description":"SOX21 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39807]"}, {"versioned_ensembl_gene_id":"ENSG00000246225.6","gene_symbol":"AC006299.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22829380,"end":22945393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249210.1","gene_symbol":"GAPDHP38","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:37792]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729493","summary":null,"start":46558641,"end":46559642,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:37792]"}, {"versioned_ensembl_gene_id":"ENSG00000211956.2","gene_symbol":"IGHV4-34","gene_name":"immunoglobulin heavy variable 4-34 [Source:HGNC Symbol;Acc:HGNC:5650]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28395","summary":null,"start":106373663,"end":106374145,"strand":-1,"description":"immunoglobulin heavy variable 4-34 [Source:HGNC Symbol;Acc:HGNC:5650]"}, {"versioned_ensembl_gene_id":"ENSG00000248790.1","gene_symbol":"AC097103.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139466430,"end":139466795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255359.2","gene_symbol":"CCDC179","gene_name":"coiled-coil domain containing 179 [Source:HGNC Symbol;Acc:HGNC:44653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100500938","summary":null,"start":22846931,"end":22860426,"strand":-1,"description":"coiled-coil domain containing 179 [Source:HGNC Symbol;Acc:HGNC:44653]"}, {"versioned_ensembl_gene_id":"ENSG00000253440.1","gene_symbol":"IGHV3-33-2","gene_name":"immunoglobulin heavy variable 3-33-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5597]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28433","summary":null,"start":106369107,"end":106369546,"strand":-1,"description":"immunoglobulin heavy variable 3-33-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5597]"}, {"versioned_ensembl_gene_id":"ENSG00000196616.13","gene_symbol":"ADH1B","gene_name":"alcohol dehydrogenase 1B (class I), beta polypeptide [Source:HGNC Symbol;Acc:HGNC:250]","synonyms":"ADH2","biotype":"protein_coding","ncbi_id":"125","summary":"The protein encoded by this gene is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. This encoded protein, consisting of several homo- and heterodimers of alpha, beta, and gamma subunits, exhibits high activity for ethanol oxidation and plays a major role in ethanol catabolism. Three genes encoding alpha, beta and gamma subunits are tandemly organized in a genomic segment as a gene cluster. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":99304964,"end":99352760,"strand":-1,"description":"alcohol dehydrogenase 1B (class I), beta polypeptide [Source:HGNC Symbol;Acc:HGNC:250]"}, {"versioned_ensembl_gene_id":"ENSG00000235734.4","gene_symbol":"HMGN1P36","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728851","summary":null,"start":97827248,"end":97827545,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39380]"}, {"versioned_ensembl_gene_id":"ENSG00000160469.16","gene_symbol":"BRSK1","gene_name":"BR serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:18994]","synonyms":"KIAA1811","biotype":"protein_coding","ncbi_id":"84446","summary":null,"start":55282072,"end":55312533,"strand":1,"description":"BR serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:18994]"}, {"versioned_ensembl_gene_id":"ENSG00000249318.1","gene_symbol":"AC010468.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111265809,"end":111270089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139579.12","gene_symbol":"NABP2","gene_name":"nucleic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:28412]","synonyms":"hSSB1,SSB1,SOSS-B1,OBFC2B,MGC2731","biotype":"protein_coding","ncbi_id":"79035","summary":"Single-stranded DNA (ssDNA)-binding proteins, such as OBFC2B, are ubiquitous and essential for a variety of DNA metabolic processes, including replication, recombination, and detection and repair of damage (Richard et al., 2008 [PubMed 18449195]).[supplied by OMIM, Jun 2008]","start":56222015,"end":56229854,"strand":1,"description":"nucleic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:28412]"}, {"versioned_ensembl_gene_id":"ENSG00000115085.13","gene_symbol":"ZAP70","gene_name":"zeta chain of T-cell receptor associated protein kinase 70 [Source:HGNC Symbol;Acc:HGNC:12858]","synonyms":"ZAP-70,STD,SRK","biotype":"protein_coding","ncbi_id":"7535","summary":"This gene encodes an enzyme belonging to the protein tyrosine kinase family, and it plays a role in T-cell development and lymphocyte activation. This enzyme, which is phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation, functions in the initial step of TCR-mediated signal transduction in combination with the Src family kinases, Lck and Fyn. This enzyme is also essential for thymocyte development. Mutations in this gene cause selective T-cell defect, a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells. Two transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":97713560,"end":97739862,"strand":1,"description":"zeta chain of T-cell receptor associated protein kinase 70 [Source:HGNC Symbol;Acc:HGNC:12858]"}, {"versioned_ensembl_gene_id":"ENSG00000273881.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000115286.19","gene_symbol":"NDUFS7","gene_name":"NADH:ubiquinone oxidoreductase core subunit S7 [Source:HGNC Symbol;Acc:HGNC:7714]","synonyms":"PSST,FLJ46880,FLJ45860,CI-20","biotype":"protein_coding","ncbi_id":"374291","summary":"This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq, Jul 2008]","start":1383527,"end":1395589,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit S7 [Source:HGNC Symbol;Acc:HGNC:7714]"}, {"versioned_ensembl_gene_id":"ENSG00000283948.1","gene_symbol":"AC247036.7","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106170749,"end":106171052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257863.1","gene_symbol":"AC090049.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91901458,"end":91906187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206515.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"MAS-L,dJ994E9.2,MRG","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486639,"end":29487775,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000278345.1","gene_symbol":"GU182343.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54814919,"end":54820584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111231.8","gene_symbol":"GPN3","gene_name":"GPN-loop GTPase 3 [Source:HGNC Symbol;Acc:HGNC:30186]","synonyms":"MGC14560,ATPBD1C","biotype":"protein_coding","ncbi_id":"51184","summary":null,"start":110452484,"end":110469268,"strand":-1,"description":"GPN-loop GTPase 3 [Source:HGNC Symbol;Acc:HGNC:30186]"}, {"versioned_ensembl_gene_id":"ENSG00000198408.13","gene_symbol":"MGEA5","gene_name":"meningioma expressed antigen 5 (hyaluronidase) [Source:HGNC Symbol;Acc:HGNC:7056]","synonyms":"OGA,NCOAT,MEA5","biotype":"protein_coding","ncbi_id":"10724","summary":"The dynamic modification of cytoplasmic and nuclear proteins by O-linked N-acetylglucosamine (O-GlcNAc) addition and removal on serine and threonine residues is catalyzed by OGT (MIM 300255), which adds O-GlcNAc, and MGEA5, a glycosidase that removes O-GlcNAc modifications (Gao et al., 2001 [PubMed 11148210]).[supplied by OMIM, Mar 2008]","start":101784443,"end":101818465,"strand":-1,"description":"meningioma expressed antigen 5 (hyaluronidase) [Source:HGNC Symbol;Acc:HGNC:7056]"}, {"versioned_ensembl_gene_id":"ENSG00000160584.15","gene_symbol":"SIK3","gene_name":"SIK family kinase 3 [Source:HGNC Symbol;Acc:HGNC:29165]","synonyms":"QSK,L19,KIAA0999,FLJ12240","biotype":"protein_coding","ncbi_id":"23387","summary":null,"start":116843402,"end":117098437,"strand":-1,"description":"SIK family kinase 3 [Source:HGNC Symbol;Acc:HGNC:29165]"}, {"versioned_ensembl_gene_id":"ENSG00000276775.1","gene_symbol":"IGHV4-4","gene_name":"immunoglobulin heavy variable 4-4 [Source:HGNC Symbol;Acc:HGNC:5652]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28401","summary":null,"start":106011922,"end":106012420,"strand":-1,"description":"immunoglobulin heavy variable 4-4 [Source:HGNC Symbol;Acc:HGNC:5652]"}, {"versioned_ensembl_gene_id":"ENSG00000185834.10","gene_symbol":"RPL12P4","gene_name":"ribosomal protein L12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16587]","synonyms":"dJ800C24.1","biotype":"processed_pseudogene","ncbi_id":"116149","summary":null,"start":55074644,"end":55075140,"strand":1,"description":"ribosomal protein L12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16587]"}, {"versioned_ensembl_gene_id":"ENSG00000235038.1","gene_symbol":"AL445193.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58060139,"end":58080274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159176.13","gene_symbol":"CSRP1","gene_name":"cysteine and glycine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:2469]","synonyms":"D1S181E,CYRP,CSRP","biotype":"protein_coding","ncbi_id":"1465","summary":"This gene encodes a member of the cysteine-rich protein (CSRP) family. This gene family includes a group of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this gene product occurs in proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2010]","start":201483530,"end":201509456,"strand":-1,"description":"cysteine and glycine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:2469]"}, {"versioned_ensembl_gene_id":"ENSG00000230030.1","gene_symbol":"AL353742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108252154,"end":108254820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206646.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68361075,"end":68361187,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211928.1","gene_symbol":"IGHD5-5","gene_name":"immunoglobulin heavy diversity 5-5 [Source:HGNC Symbol;Acc:HGNC:5511]","synonyms":"IGHD55,DK4","biotype":"IG_D_gene","ncbi_id":"28492","summary":null,"start":105912257,"end":105912276,"strand":-1,"description":"immunoglobulin heavy diversity 5-5 [Source:HGNC Symbol;Acc:HGNC:5511]"}, {"versioned_ensembl_gene_id":"ENSG00000211925.1","gene_symbol":"IGHD2-8","gene_name":"immunoglobulin heavy diversity 2-8 [Source:HGNC Symbol;Acc:HGNC:5492]","synonyms":"IGHD28,DLR1","biotype":"IG_D_gene","ncbi_id":"28504","summary":null,"start":105907211,"end":105907241,"strand":-1,"description":"immunoglobulin heavy diversity 2-8 [Source:HGNC Symbol;Acc:HGNC:5492]"}, {"versioned_ensembl_gene_id":"ENSG00000272663.1","gene_symbol":"AC093635.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48440043,"end":48440597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165669.13","gene_symbol":"FAM204A","gene_name":"family with sequence similarity 204 member A [Source:HGNC Symbol;Acc:HGNC:25794]","synonyms":"FLJ13188,C10orf84,bA319I23.1","biotype":"protein_coding","ncbi_id":"63877","summary":null,"start":118297930,"end":118342328,"strand":-1,"description":"family with sequence similarity 204 member A [Source:HGNC Symbol;Acc:HGNC:25794]"}, {"versioned_ensembl_gene_id":"ENSG00000187772.7","gene_symbol":"LIN28B","gene_name":"lin-28 homolog B [Source:HGNC Symbol;Acc:HGNC:32207]","synonyms":"FLJ16517,CSDD2","biotype":"protein_coding","ncbi_id":"389421","summary":"The protein encoded by this gene belongs to the lin-28 family, which is characterized by the presence of a cold-shock domain and a pair of CCHC zinc finger domains. This gene is highly expressed in testis, fetal liver, placenta, and in primary human tumors and cancer cell lines. It is negatively regulated by microRNAs that target sites in the 3' UTR, and overexpression of this gene in primary tumors is linked to the repression of let-7 family of microRNAs and derepression of let-7 targets, which facilitates cellular transformation. [provided by RefSeq, Jun 2012]","start":104936616,"end":105083332,"strand":1,"description":"lin-28 homolog B [Source:HGNC Symbol;Acc:HGNC:32207]"}, {"versioned_ensembl_gene_id":"ENSG00000180089.5","gene_symbol":"TMEM86B","gene_name":"transmembrane protein 86B [Source:HGNC Symbol;Acc:HGNC:28448]","synonyms":"MGC30208","biotype":"protein_coding","ncbi_id":"255043","summary":null,"start":55226639,"end":55229264,"strand":-1,"description":"transmembrane protein 86B [Source:HGNC Symbol;Acc:HGNC:28448]"}, {"versioned_ensembl_gene_id":"ENSG00000253613.2","gene_symbol":"AC008572.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111076921,"end":111092115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145777.14","gene_symbol":"TSLP","gene_name":"thymic stromal lymphopoietin [Source:HGNC Symbol;Acc:HGNC:30743]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85480","summary":"This gene encodes a hemopoietic cytokine proposed to signal through a heterodimeric receptor complex composed of the thymic stromal lymphopoietin receptor and the IL-7R alpha chain. It mainly impacts myeloid cells and induces the release of T cell-attracting chemokines from monocytes and enhances the maturation of CD11c(+) dendritic cells. The protein promotes T helper type 2 (TH2) cell responses that are associated with immunity in various inflammatory diseases, including asthma, allergic inflammation and chronic obstructive pulmonary disease. The protein is therefore considered a potential therapeutic target for the treatment of such diseases. In addition, the shorter (predominant) isoform is an antimicrobial protein, displaying antibacterial and antifungal activity against B. cereus, E. coli, E. faecalis, S. mitis, S. epidermidis, and C. albicans. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":111070062,"end":111078024,"strand":1,"description":"thymic stromal lymphopoietin [Source:HGNC Symbol;Acc:HGNC:30743]"}, {"versioned_ensembl_gene_id":"ENSG00000197345.12","gene_symbol":"MRPL21","gene_name":"mitochondrial ribosomal protein L21 [Source:HGNC Symbol;Acc:HGNC:14479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219927","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Multiple transcript variants encoding different isoforms were identified through sequence analysis although some may be subject to nonsense-mediated decay (NMD). [provided by RefSeq, Jul 2008]","start":68891276,"end":68903835,"strand":-1,"description":"mitochondrial ribosomal protein L21 [Source:HGNC Symbol;Acc:HGNC:14479]"}, {"versioned_ensembl_gene_id":"ENSG00000211904.2","gene_symbol":"IGHJ2","gene_name":"immunoglobulin heavy joining 2 [Source:HGNC Symbol;Acc:HGNC:5534]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28481","summary":null,"start":105865199,"end":105865250,"strand":-1,"description":"immunoglobulin heavy joining 2 [Source:HGNC Symbol;Acc:HGNC:5534]"}, {"versioned_ensembl_gene_id":"ENSG00000211905.1","gene_symbol":"IGHJ1","gene_name":"immunoglobulin heavy joining 1 [Source:HGNC Symbol;Acc:HGNC:5532]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28483","summary":null,"start":105865407,"end":105865458,"strand":-1,"description":"immunoglobulin heavy joining 1 [Source:HGNC Symbol;Acc:HGNC:5532]"}, {"versioned_ensembl_gene_id":"ENSG00000280776.1","gene_symbol":"AC021079.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161910252,"end":162001196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272195.1","gene_symbol":"AL356512.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":244969350,"end":244971088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189129.13","gene_symbol":"PLAC9","gene_name":"placenta specific 9 [Source:HGNC Symbol;Acc:HGNC:19255]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219348","summary":null,"start":80131682,"end":80145359,"strand":1,"description":"placenta specific 9 [Source:HGNC Symbol;Acc:HGNC:19255]"}, {"versioned_ensembl_gene_id":"ENSG00000254647.6","gene_symbol":"INS","gene_name":"insulin [Source:HGNC Symbol;Acc:HGNC:6081]","synonyms":"IDDM2,IDDM1","biotype":"protein_coding","ncbi_id":"3630","summary":"This gene encodes insulin, a peptide hormone that plays a vital role in the regulation of carbohydrate and lipid metabolism. After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form insulin, and C-peptide. Binding of insulin to the insulin receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified, including insulin-dependent diabetes mellitus, permanent neonatal diabetes diabetes mellitus, maturity-onset diabetes of the young type 10 and hyperproinsulinemia. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region. [provided by RefSeq, May 2020]","start":2159779,"end":2161341,"strand":-1,"description":"insulin [Source:HGNC Symbol;Acc:HGNC:6081]"}, {"versioned_ensembl_gene_id":"ENSG00000229961.2","gene_symbol":"AL357143.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":157171116,"end":157191963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092094.10","gene_symbol":"OSGEP","gene_name":"O-sialoglycoprotein endopeptidase [Source:HGNC Symbol;Acc:HGNC:18028]","synonyms":"TCS3,PRSMG1,OSGEP1,KAE1,GCPL1","biotype":"protein_coding","ncbi_id":"55644","summary":null,"start":20446411,"end":20455105,"strand":-1,"description":"O-sialoglycoprotein endopeptidase [Source:HGNC Symbol;Acc:HGNC:18028]"}, {"versioned_ensembl_gene_id":"ENSG00000273841.4","gene_symbol":"TAF9","gene_name":"TATA-box binding protein associated factor 9 [Source:HGNC Symbol;Acc:HGNC:11542]","synonyms":"MGC5067,MGC3647,MGC1603,CGI-137,TAFIID32,AD-004,TAFII32,TAFII31,TAF2G","biotype":"protein_coding","ncbi_id":"6880","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the smaller subunits of TFIID that binds to the basal transcription factor GTF2B as well as to several transcriptional activators such as p53 and VP16. In human, TAF9 and AK6 (GeneID: 102157402) are two distinct genes that share 5' exons. A similar but distinct gene (TAF9L) has been found on the X chromosome and a pseudogene has been identified on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":69364743,"end":69370013,"strand":-1,"description":"TATA-box binding protein associated factor 9 [Source:HGNC Symbol;Acc:HGNC:11542]"}, {"versioned_ensembl_gene_id":"ENSG00000231582.2","gene_symbol":"MTND4LP21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42255]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075306","summary":null,"start":235541412,"end":235541706,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42255]"}, {"versioned_ensembl_gene_id":"ENSG00000267144.1","gene_symbol":"AC067968.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44023604,"end":44025262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010319.6","gene_symbol":"SEMA3G","gene_name":"semaphorin 3G [Source:HGNC Symbol;Acc:HGNC:30400]","synonyms":"sem2,FLJ00014","biotype":"protein_coding","ncbi_id":"56920","summary":"The transcription of this gene is activated by PPAR-gamma, and the resulting protein product plays a role in endothelial cell migration. Expression of this gene also inhibits tumor cell migration and invasion. [provided by RefSeq, Jul 2016]","start":52433053,"end":52445085,"strand":-1,"description":"semaphorin 3G [Source:HGNC Symbol;Acc:HGNC:30400]"}, {"versioned_ensembl_gene_id":"ENSG00000229644.6","gene_symbol":"NAMPTP1","gene_name":"nicotinamide phosphoribosyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17633]","synonyms":"PBEF2,NAMPTL,bA92J19.4","biotype":"processed_pseudogene","ncbi_id":"646309","summary":null,"start":36521721,"end":36524234,"strand":-1,"description":"nicotinamide phosphoribosyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17633]"}, {"versioned_ensembl_gene_id":"ENSG00000260740.2","gene_symbol":"AC026471.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31487370,"end":31488492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110852.4","gene_symbol":"CLEC2B","gene_name":"C-type lectin domain family 2 member B [Source:HGNC Symbol;Acc:HGNC:2053]","synonyms":"HP10085,CLECSF2,AICL","biotype":"protein_coding","ncbi_id":"9976","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may function as a cell activation antigen. An alternative splice variant has been described but its full-length sequence has not been determined. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]","start":9852984,"end":9870136,"strand":-1,"description":"C-type lectin domain family 2 member B [Source:HGNC Symbol;Acc:HGNC:2053]"}, {"versioned_ensembl_gene_id":"ENSG00000271420.1","gene_symbol":"AL109936.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23378380,"end":23379029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253537.2","gene_symbol":"PCDHGA7","gene_name":"protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:HGNC:8705]","synonyms":"PCDH-GAMMA-A7","biotype":"protein_coding","ncbi_id":"56108","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141382739,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:HGNC:8705]"}, {"versioned_ensembl_gene_id":"ENSG00000226473.2","gene_symbol":"AC079807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47939738,"end":47940218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272456.1","gene_symbol":"AC087045.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134722947,"end":134723949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220556.4","gene_symbol":"AL035690.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39039603,"end":39039985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167612.12","gene_symbol":"ANKRD33","gene_name":"ankyrin repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:13788]","synonyms":"PANKY,DKFZp686O1689,C12orf7","biotype":"protein_coding","ncbi_id":"341405","summary":null,"start":51887960,"end":51891664,"strand":1,"description":"ankyrin repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:13788]"}, {"versioned_ensembl_gene_id":"ENSG00000173868.11","gene_symbol":"PHOSPHO1","gene_name":"phosphoethanolamine/phosphocholine phosphatase [Source:HGNC Symbol;Acc:HGNC:16815]","synonyms":null,"biotype":"protein_coding","ncbi_id":"162466","summary":null,"start":49223362,"end":49230766,"strand":-1,"description":"phosphoethanolamine/phosphocholine phosphatase [Source:HGNC Symbol;Acc:HGNC:16815]"}, {"versioned_ensembl_gene_id":"ENSG00000227475.1","gene_symbol":"AL355300.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36089086,"end":36089389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235195.1","gene_symbol":"AL929561.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29071811,"end":29072586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275545.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54746462,"end":54760779,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000211891.6","gene_symbol":"IGHE","gene_name":"immunoglobulin heavy constant epsilon [Source:HGNC Symbol;Acc:HGNC:5522]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3497","summary":null,"start":105597691,"end":105601728,"strand":-1,"description":"immunoglobulin heavy constant epsilon [Source:HGNC Symbol;Acc:HGNC:5522]"}, {"versioned_ensembl_gene_id":"ENSG00000233527.8","gene_symbol":"ZNF529-AS1","gene_name":"ZNF529 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51275]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927599","summary":null,"start":36573070,"end":36594708,"strand":1,"description":"ZNF529 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51275]"}, {"versioned_ensembl_gene_id":"ENSG00000161298.17","gene_symbol":"ZNF382","gene_name":"zinc finger protein 382 [Source:HGNC Symbol;Acc:HGNC:17409]","synonyms":"KS1,FLJ14686","biotype":"protein_coding","ncbi_id":"84911","summary":"This gene encodes a KRAB domain zinc finger transcription factor (KZNF). KZNFs play critical roles in the regulation of many cellular processes including differentiation, proliferation and apoptosis. The encoded protein inhibits activating protein 1 (AP-1) and nuclear factor kappa-B (NF-kB) signaling and may function as a tumor suppressor in multiple carcinomas. This gene is found in a cluster with other zinc finger protein genes on the long arm of chromosome 19, and alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":36604817,"end":36634113,"strand":1,"description":"zinc finger protein 382 [Source:HGNC Symbol;Acc:HGNC:17409]"}, {"versioned_ensembl_gene_id":"ENSG00000240724.2","gene_symbol":"AP002852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102503753,"end":102504137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271612.1","gene_symbol":"HSPE1P14","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49333]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481674","summary":null,"start":102451763,"end":102452483,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49333]"}, {"versioned_ensembl_gene_id":"ENSG00000207403.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":121378797,"end":121378898,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000259004.1","gene_symbol":"LINC02285","gene_name":"long intergenic non-protein coding RNA 2285 [Source:HGNC Symbol;Acc:HGNC:53202]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929422","summary":null,"start":101120856,"end":101123542,"strand":1,"description":"long intergenic non-protein coding RNA 2285 [Source:HGNC Symbol;Acc:HGNC:53202]"}, {"versioned_ensembl_gene_id":"ENSG00000223547.9","gene_symbol":"ZNF844","gene_name":"zinc finger protein 844 [Source:HGNC Symbol;Acc:HGNC:25932]","synonyms":"FLJ14959","biotype":"protein_coding","ncbi_id":"284391","summary":null,"start":12064699,"end":12081565,"strand":1,"description":"zinc finger protein 844 [Source:HGNC Symbol;Acc:HGNC:25932]"}, {"versioned_ensembl_gene_id":"ENSG00000204920.10","gene_symbol":"ZNF155","gene_name":"zinc finger protein 155 [Source:HGNC Symbol;Acc:HGNC:12940]","synonyms":"pHZ-96","biotype":"protein_coding","ncbi_id":"7711","summary":null,"start":43967862,"end":43998325,"strand":1,"description":"zinc finger protein 155 [Source:HGNC Symbol;Acc:HGNC:12940]"}, {"versioned_ensembl_gene_id":"ENSG00000277560.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786463,"end":54790318,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000223358.5","gene_symbol":"EHHADH-AS1","gene_name":"EHHADH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44133]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"339926","summary":null,"start":185162871,"end":185191955,"strand":1,"description":"EHHADH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44133]"}, {"versioned_ensembl_gene_id":"ENSG00000183251.4","gene_symbol":"OR51B4","gene_name":"olfactory receptor family 51 subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:14708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79339","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5301014,"end":5301946,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:14708]"}, {"versioned_ensembl_gene_id":"ENSG00000251173.1","gene_symbol":"UCHL1-AS1","gene_name":"UCHL1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40600]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410542","summary":null,"start":41220074,"end":41256727,"strand":-1,"description":"UCHL1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40600]"}, {"versioned_ensembl_gene_id":"ENSG00000154134.14","gene_symbol":"ROBO3","gene_name":"roundabout guidance receptor 3 [Source:HGNC Symbol;Acc:HGNC:13433]","synonyms":"RBIG1,HGPS,HGPPS,FLJ21044","biotype":"protein_coding","ncbi_id":"64221","summary":"This gene is a member of the Roundabout (ROBO) gene family that controls neurite outgrowth, growth cone guidance, and axon fasciculation. ROBO proteins are a subfamily of the immunoglobulin transmembrane receptor superfamily. SLIT proteins 1-3, a family of secreted chemorepellants, are ligands for ROBO proteins and SLIT/ROBO interactions regulate myogenesis, leukocyte migration, kidney morphogenesis, angiogenesis, and vasculogenesis in addition to neurogenesis. This gene, ROBO3, has a putative extracellular domain with five immunoglobulin (Ig)-like loops and three fibronectin (Fn) type III motifs, a transmembrane segment, and a cytoplasmic tail with three conserved signaling motifs: CC0, CC2, and CC3 (CC for conserved cytoplasmic). Unlike other ROBO family members, ROBO3 lacks motif CC1. The ROBO3 gene regulates axonal navigation at the ventral midline of the neural tube. In mouse, loss of Robo3 results in a complete failure of commissural axons to cross the midline throughout the spinal cord and the hindbrain. Mutations ROBO3 result in horizontal gaze palsy with progressive scoliosis (HGPPS); an autosomal recessive disorder characterized by congenital absence of horizontal gaze, progressive scoliosis, and failure of the corticospinal and somatosensory axon tracts to cross the midline in the medulla. [provided by RefSeq, May 2019]","start":124865386,"end":124881470,"strand":1,"description":"roundabout guidance receptor 3 [Source:HGNC Symbol;Acc:HGNC:13433]"}, {"versioned_ensembl_gene_id":"ENSG00000218459.1","gene_symbol":"AL121972.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73618346,"end":73618597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137710.14","gene_symbol":"RDX","gene_name":"radixin [Source:HGNC Symbol;Acc:HGNC:9944]","synonyms":"DFNB24","biotype":"protein_coding","ncbi_id":"5962","summary":"Radixin is a cytoskeletal protein that may be important in linking actin to the plasma membrane. It is highly similar in sequence to both ezrin and moesin. The radixin gene has been localized by fluorescence in situ hybridization to 11q23. A truncated version representing a pseudogene (RDXP2) was assigned to Xp21.3. Another pseudogene that seemed to lack introns (RDXP1) was mapped to 11p by Southern and PCR analyses. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":110174880,"end":110296722,"strand":-1,"description":"radixin [Source:HGNC Symbol;Acc:HGNC:9944]"}, {"versioned_ensembl_gene_id":"ENSG00000270780.1","gene_symbol":"AL591742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114001433,"end":114002235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185515.14","gene_symbol":"BRCC3","gene_name":"BRCA1/BRCA2-containing complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:24185]","synonyms":"CXorf53,C6.1A,BRCC36","biotype":"protein_coding","ncbi_id":"79184","summary":"This gene encodes a subunit of the BRCA1-BRCA2-containing complex (BRCC), which is an E3 ubiquitin ligase. This complex plays a role in the DNA damage response, where it is responsible for the stable accumulation of BRCA1 at DNA break sites. The component encoded by this gene can specifically cleave Lys 63-linked polyubiquitin chains, and it regulates the abundance of these polyubiquitin chains in chromatin. The loss of this gene results in abnormal angiogenesis and is associated with syndromic moyamoya, a cerebrovascular angiopathy. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jun 2011]","start":155071420,"end":155123074,"strand":1,"description":"BRCA1/BRCA2-containing complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:24185]"}, {"versioned_ensembl_gene_id":"ENSG00000235572.1","gene_symbol":"AL353615.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135352684,"end":135354220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279771.1","gene_symbol":"AP000997.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":115659168,"end":115661417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227958.1","gene_symbol":"AL390778.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135204722,"end":135237597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225100.2","gene_symbol":"DPY19L2P5","gene_name":"DPY19L2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480421","summary":null,"start":79982910,"end":79983240,"strand":-1,"description":"DPY19L2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51620]"}, {"versioned_ensembl_gene_id":"ENSG00000188486.3","gene_symbol":"H2AFX","gene_name":"H2A histone family member X [Source:HGNC Symbol;Acc:HGNC:4739]","synonyms":"H2AX","biotype":"protein_coding","ncbi_id":"3014","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the histone H2A family, and generates two transcripts through the use of the conserved stem-loop termination motif, and the polyA addition motif. [provided by RefSeq, Oct 2015]","start":119093854,"end":119095467,"strand":-1,"description":"H2A histone family member X [Source:HGNC Symbol;Acc:HGNC:4739]"}, {"versioned_ensembl_gene_id":"ENSG00000187609.15","gene_symbol":"EXD3","gene_name":"exonuclease 3'-5' domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26023]","synonyms":"FLJ20433,mut-7,LOC54932","biotype":"protein_coding","ncbi_id":"54932","summary":null,"start":137306896,"end":137423262,"strand":-1,"description":"exonuclease 3'-5' domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26023]"}, {"versioned_ensembl_gene_id":"ENSG00000267019.1","gene_symbol":"NTF6A","gene_name":"neurotrophin 6 alpha (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8025]","synonyms":"PSI-NT4,NTF6,NTF5P","biotype":"unprocessed_pseudogene","ncbi_id":"4910","summary":null,"start":49025461,"end":49026020,"strand":-1,"description":"neurotrophin 6 alpha (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8025]"}, {"versioned_ensembl_gene_id":"ENSG00000163121.9","gene_symbol":"NEURL3","gene_name":"neuralized E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:25162]","synonyms":"LOC93082,Lincr","biotype":"protein_coding","ncbi_id":"93082","summary":null,"start":96497643,"end":96508109,"strand":-1,"description":"neuralized E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:25162]"}, {"versioned_ensembl_gene_id":"ENSG00000160117.14","gene_symbol":"ANKLE1","gene_name":"ankyrin repeat and LEM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26812]","synonyms":"LEMD6,FLJ39369,ANKRD41","biotype":"protein_coding","ncbi_id":"126549","summary":null,"start":17281645,"end":17287646,"strand":1,"description":"ankyrin repeat and LEM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26812]"}, {"versioned_ensembl_gene_id":"ENSG00000267335.2","gene_symbol":"AC008687.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49022953,"end":49036895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280029.3","gene_symbol":"AC244517.11","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141136683,"end":141245380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272108.1","gene_symbol":"AC244517.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141118680,"end":141120765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280336.1","gene_symbol":"AC244517.12","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141168231,"end":141168893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187372.11","gene_symbol":"PCDHB13","gene_name":"protocadherin beta 13 [Source:HGNC Symbol;Acc:HGNC:8684]","synonyms":"PCDH-BETA13","biotype":"protein_coding","ncbi_id":"56123","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141213919,"end":141218979,"strand":1,"description":"protocadherin beta 13 [Source:HGNC Symbol;Acc:HGNC:8684]"}, {"versioned_ensembl_gene_id":"ENSG00000196136.17","gene_symbol":"SERPINA3","gene_name":"serpin family A member 3 [Source:HGNC Symbol;Acc:HGNC:16]","synonyms":"ACT,AACT","biotype":"protein_coding","ncbi_id":"12","summary":"The protein encoded by this gene is a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. This gene is one in a cluster of serpin genes located on the q arm of chromosome 14. Polymorphisms in this protein appear to be tissue specific and influence protease targeting. Variations in this protein's sequence have been implicated in Alzheimer's disease, and deficiency of this protein has been associated with liver disease. Mutations have been identified in patients with Parkinson disease and chronic obstructive pulmonary disease. [provided by RefSeq, Jun 2020]","start":94612377,"end":94624055,"strand":1,"description":"serpin family A member 3 [Source:HGNC Symbol;Acc:HGNC:16]"}, {"versioned_ensembl_gene_id":"ENSG00000168434.12","gene_symbol":"COG7","gene_name":"component of oligomeric golgi complex 7 [Source:HGNC Symbol;Acc:HGNC:18622]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91949","summary":"The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]","start":23388493,"end":23453180,"strand":-1,"description":"component of oligomeric golgi complex 7 [Source:HGNC Symbol;Acc:HGNC:18622]"}, {"versioned_ensembl_gene_id":"ENSG00000276447.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54626866,"end":54631219,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000236403.1","gene_symbol":"AL353611.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134937151,"end":134943195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257286.1","gene_symbol":"AC089999.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113185624,"end":113192161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241721.1","gene_symbol":"SUMO1P1","gene_name":"SUMO1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33148]","synonyms":"UBL6,UBL2,PIC1L","biotype":"processed_pseudogene","ncbi_id":"391257","summary":null,"start":53875252,"end":53875557,"strand":-1,"description":"SUMO1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33148]"}, {"versioned_ensembl_gene_id":"ENSG00000171403.9","gene_symbol":"KRT9","gene_name":"keratin 9 [Source:HGNC Symbol;Acc:HGNC:6447]","synonyms":"K9,EPPK,CK-9","biotype":"protein_coding","ncbi_id":"3857","summary":"This gene encodes the type I keratin 9, an intermediate filament chain expressed only in the terminally differentiated epidermis of palms and soles. Mutations in this gene cause epidermolytic palmoplantar keratoderma. [provided by RefSeq, Jul 2008]","start":41565841,"end":41572058,"strand":-1,"description":"keratin 9 [Source:HGNC Symbol;Acc:HGNC:6447]"}, {"versioned_ensembl_gene_id":"ENSG00000276960.1","gene_symbol":"AL109933.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160755398,"end":160757518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206476.13","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"G7a,VARS2L,DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30897815,"end":30916043,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000114861.18","gene_symbol":"FOXP1","gene_name":"forkhead box P1 [Source:HGNC Symbol;Acc:HGNC:3823]","synonyms":"hFKH1B,12CC4,QRF1,HSPC215","biotype":"protein_coding","ncbi_id":"27086","summary":"This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":70954693,"end":71583989,"strand":-1,"description":"forkhead box P1 [Source:HGNC Symbol;Acc:HGNC:3823]"}, {"versioned_ensembl_gene_id":"ENSG00000254713.2","gene_symbol":"HNRNPA1P72","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:48802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480236","summary":null,"start":84545131,"end":84546846,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:48802]"}, {"versioned_ensembl_gene_id":"ENSG00000224980.1","gene_symbol":"RPL23AP85","gene_name":"ribosomal protein L23a pseudogene 85 [Source:HGNC Symbol;Acc:HGNC:51576]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419650","summary":null,"start":56585612,"end":56586242,"strand":-1,"description":"ribosomal protein L23a pseudogene 85 [Source:HGNC Symbol;Acc:HGNC:51576]"}, {"versioned_ensembl_gene_id":"ENSG00000229297.1","gene_symbol":"AL451140.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106584142,"end":106591952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125450.10","gene_symbol":"NUP85","gene_name":"nucleoporin 85 [Source:HGNC Symbol;Acc:HGNC:8734]","synonyms":"NUP75,FLJ12549","biotype":"protein_coding","ncbi_id":"79902","summary":"This gene encodes a protein component of the Nup107-160 subunit of the nuclear pore complex. Nuclear pore complexes are embedded in the nuclear envelope and promote bidirectional transport of macromolecules between the cytoplasm and nucleus. The encoded protein can also bind to the C-terminus of chemokine (C-C motif) receptor 2 (CCR2) and promote chemotaxis of monocytes, thereby participating in the inflammatory response. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":75205659,"end":75235758,"strand":1,"description":"nucleoporin 85 [Source:HGNC Symbol;Acc:HGNC:8734]"}, {"versioned_ensembl_gene_id":"ENSG00000254798.1","gene_symbol":"AP001981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109907004,"end":109907741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226857.1","gene_symbol":"DUTP3","gene_name":"deoxyuridine triphosphatase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39516]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100861485","summary":null,"start":147146342,"end":147146756,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39516]"}, {"versioned_ensembl_gene_id":"ENSG00000205683.11","gene_symbol":"DPF3","gene_name":"double PHD fingers 3 [Source:HGNC Symbol;Acc:HGNC:17427]","synonyms":"FLJ14079,Cerd4,cer-d4,BAF45c","biotype":"protein_coding","ncbi_id":"8110","summary":"This gene encodes a member of the D4 protein family. The encoded protein is a transcription regulator that binds acetylated histones and is a component of the BAF chromatin remodeling complex. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":72619296,"end":72894116,"strand":-1,"description":"double PHD fingers 3 [Source:HGNC Symbol;Acc:HGNC:17427]"}, {"versioned_ensembl_gene_id":"ENSG00000279342.2","gene_symbol":"AP000866.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":124789240,"end":124792818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232391.1","gene_symbol":"RANP2","gene_name":"RAN, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39857]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874191","summary":null,"start":147167344,"end":147167572,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39857]"}, {"versioned_ensembl_gene_id":"ENSG00000254941.1","gene_symbol":"AP000866.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124807822,"end":124808269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230190.1","gene_symbol":"AC005518.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":147671711,"end":147673143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224699.8","gene_symbol":"LAMTOR5-AS1","gene_name":"LAMTOR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40823]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101410535","summary":null,"start":110347116,"end":110443817,"strand":1,"description":"LAMTOR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40823]"}, {"versioned_ensembl_gene_id":"ENSG00000228102.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29748203,"end":29748623,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000260686.1","gene_symbol":"AC008669.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":122832356,"end":122834533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280077.1","gene_symbol":"AL353763.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41012231,"end":41014133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274427.1","gene_symbol":"AC145423.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123515275,"end":123515513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227150.1","gene_symbol":"AL669970.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134552738,"end":134553897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184209.14","gene_symbol":"SNRNP35","gene_name":"small nuclear ribonucleoprotein U11/U12 subunit 35 [Source:HGNC Symbol;Acc:HGNC:30852]","synonyms":"U1SNRNPBP","biotype":"protein_coding","ncbi_id":"11066","summary":"The protein encoded by this gene is a homolog of the U1-snRNP binding protein. The N-terminal half contains a RNA recognition motif and the C-terminal half is rich in Arg/Asp and Arg/Glu dipeptides, which is a characteristic of a variety of splicing factors. This protein is a component of the U11/U12 small nuclear ribonucleoproteins (snRNP) that form part of the U12-type spliceosome. Alternative splicing results in multiple transcript variants encoding two distinct isoforms and representing a non-protein coding variant. [provided by RefSeq, Aug 2013]","start":123457641,"end":123473154,"strand":1,"description":"small nuclear ribonucleoprotein U11/U12 subunit 35 [Source:HGNC Symbol;Acc:HGNC:30852]"}, {"versioned_ensembl_gene_id":"ENSG00000188986.6","gene_symbol":"NELFB","gene_name":"negative elongation factor complex member B [Source:HGNC Symbol;Acc:HGNC:24324]","synonyms":"NELF-B,KIAA1182,COBRA1","biotype":"protein_coding","ncbi_id":"25920","summary":"NELFB is a subunit of negative elongation factor (NELF), which also includes NELFA (WHSC2; MIM 606026), either NELFC or NELFD (TH1L; MIM 605297), and NELFE (RDBP; MIM 154040). NELF acts with DRB sensitivity-inducing factor (DSIF), a heterodimer of SPT4 (SUPT4H1; MIM 603555) and SPT5 (SUPT5H; MIM 602102), to cause transcriptional pausing of RNA polymerase II (see MIM 180660) (Narita et al., 2003 [PubMed 12612062]).[supplied by OMIM, Mar 2008]","start":137255173,"end":137273546,"strand":1,"description":"negative elongation factor complex member B [Source:HGNC Symbol;Acc:HGNC:24324]"}, {"versioned_ensembl_gene_id":"ENSG00000162148.10","gene_symbol":"PPP1R32","gene_name":"protein phosphatase 1 regulatory subunit 32 [Source:HGNC Symbol;Acc:HGNC:28869]","synonyms":"IIIG9,FLJ32771,C11orf66","biotype":"protein_coding","ncbi_id":"220004","summary":null,"start":61481120,"end":61490931,"strand":1,"description":"protein phosphatase 1 regulatory subunit 32 [Source:HGNC Symbol;Acc:HGNC:28869]"}, {"versioned_ensembl_gene_id":"ENSG00000250073.2","gene_symbol":"AP000866.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124759129,"end":124765936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277778.2","gene_symbol":"PGM5P2","gene_name":"phosphoglucomutase 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18965]","synonyms":"AK096159","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"595135","summary":null,"start":41006999,"end":41074617,"strand":-1,"description":"phosphoglucomutase 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18965]"}, {"versioned_ensembl_gene_id":"ENSG00000152256.13","gene_symbol":"PDK1","gene_name":"pyruvate dehydrogenase kinase 1 [Source:HGNC Symbol;Acc:HGNC:8809]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5163","summary":"Pyruvate dehydrogenase (PDH) is a mitochondrial multienzyme complex that catalyzes the oxidative decarboxylation of pyruvate and is one of the major enzymes responsible for the regulation of homeostasis of carbohydrate fuels in mammals. The enzymatic activity is regulated by a phosphorylation/dephosphorylation cycle. Phosphorylation of PDH by a specific pyruvate dehydrogenase kinase (PDK) results in inactivation. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2013]","start":172555373,"end":172608669,"strand":1,"description":"pyruvate dehydrogenase kinase 1 [Source:HGNC Symbol;Acc:HGNC:8809]"}, {"versioned_ensembl_gene_id":"ENSG00000273301.1","gene_symbol":"AC016717.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":225698514,"end":225703654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230667.5","gene_symbol":"SETSIP","gene_name":"SET-like protein [Source:HGNC Symbol;Acc:HGNC:42937]","synonyms":"SETP18","biotype":"protein_coding","ncbi_id":"646817","summary":null,"start":92074533,"end":92075441,"strand":-1,"description":"SET-like protein [Source:HGNC Symbol;Acc:HGNC:42937]"}, {"versioned_ensembl_gene_id":"ENSG00000215833.3","gene_symbol":"QRSL1P1","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43667]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730016","summary":null,"start":168449672,"end":168451211,"strand":-1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43667]"}, {"versioned_ensembl_gene_id":"ENSG00000126216.13","gene_symbol":"TUBGCP3","gene_name":"tubulin gamma complex associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18598]","synonyms":"GCP3,Spc98p,SPBC98","biotype":"protein_coding","ncbi_id":"10426","summary":null,"start":112485005,"end":112588167,"strand":-1,"description":"tubulin gamma complex associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18598]"}, {"versioned_ensembl_gene_id":"ENSG00000256683.6","gene_symbol":"ZNF350","gene_name":"zinc finger protein 350 [Source:HGNC Symbol;Acc:HGNC:16656]","synonyms":"ZFQR,ZBRK1","biotype":"protein_coding","ncbi_id":"59348","summary":null,"start":51964343,"end":51986856,"strand":-1,"description":"zinc finger protein 350 [Source:HGNC Symbol;Acc:HGNC:16656]"}, {"versioned_ensembl_gene_id":"ENSG00000259021.2","gene_symbol":"TPRX1P1","gene_name":"tetrapeptide repeat homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503628","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the TPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":79499666,"end":79499984,"strand":-1,"description":"tetrapeptide repeat homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32176]"}, {"versioned_ensembl_gene_id":"ENSG00000159166.13","gene_symbol":"LAD1","gene_name":"ladinin 1 [Source:HGNC Symbol;Acc:HGNC:6472]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3898","summary":"The protein encoded by this gene may be an anchoring filament that is a component of basement membranes. It may contribute to the stability of the association of the epithelial layers with the underlying mesenchyme. [provided by RefSeq, Jul 2008]","start":201373244,"end":201399915,"strand":-1,"description":"ladinin 1 [Source:HGNC Symbol;Acc:HGNC:6472]"}, {"versioned_ensembl_gene_id":"ENSG00000227722.2","gene_symbol":"AL022100.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":168317497,"end":168376876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276092.1","gene_symbol":"AC040896.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68721082,"end":68721560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165424.6","gene_symbol":"ZCCHC24","gene_name":"zinc finger CCHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:26911]","synonyms":"Z3CXXC8,FLJ90798,C10orf56","biotype":"protein_coding","ncbi_id":"219654","summary":null,"start":79382325,"end":79445627,"strand":-1,"description":"zinc finger CCHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:26911]"}, {"versioned_ensembl_gene_id":"ENSG00000235426.2","gene_symbol":"AL133481.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79382328,"end":79409274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182645.5","gene_symbol":"CCDC172","gene_name":"coiled-coil domain containing 172 [Source:HGNC Symbol;Acc:HGNC:30524]","synonyms":"MGC35062,C10orf96","biotype":"protein_coding","ncbi_id":"374355","summary":null,"start":116324428,"end":116380029,"strand":1,"description":"coiled-coil domain containing 172 [Source:HGNC Symbol;Acc:HGNC:30524]"}, {"versioned_ensembl_gene_id":"ENSG00000235213.1","gene_symbol":"OR6E1P","gene_name":"olfactory receptor family 6 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14739]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79323","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22702143,"end":22703065,"strand":1,"description":"olfactory receptor family 6 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14739]"}, {"versioned_ensembl_gene_id":"ENSG00000107954.10","gene_symbol":"NEURL1","gene_name":"neuralized E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:7761]","synonyms":"h-neu,RNF67,NEURL,neu-1","biotype":"protein_coding","ncbi_id":"9148","summary":null,"start":103493979,"end":103592552,"strand":1,"description":"neuralized E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:7761]"}, {"versioned_ensembl_gene_id":"ENSG00000163933.9","gene_symbol":"RFT1","gene_name":"RFT1 homolog [Source:HGNC Symbol;Acc:HGNC:30220]","synonyms":"CDG1N","biotype":"protein_coding","ncbi_id":"91869","summary":"This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008]","start":53088483,"end":53130462,"strand":-1,"description":"RFT1 homolog [Source:HGNC Symbol;Acc:HGNC:30220]"}, {"versioned_ensembl_gene_id":"ENSG00000159202.17","gene_symbol":"UBE2Z","gene_name":"ubiquitin conjugating enzyme E2 Z [Source:HGNC Symbol;Acc:HGNC:25847]","synonyms":"USE1,FLJ13855","biotype":"protein_coding","ncbi_id":"65264","summary":"This gene encodes an enzyme which ubiquitinates proteins which participate in signaling pathways and apoptosis. [provided by RefSeq, Feb 2012]","start":48908369,"end":48929056,"strand":1,"description":"ubiquitin conjugating enzyme E2 Z [Source:HGNC Symbol;Acc:HGNC:25847]"}, {"versioned_ensembl_gene_id":"ENSG00000196704.11","gene_symbol":"AMZ2","gene_name":"archaelysin family metallopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:28041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51321","summary":"The protein encoded by this gene is a zinc metalloprotease that displays some activity against angiotensin-3. The encoded protein is inhibited by the aminopeptidase inhibitor amastatin, as well as by the general inhibitors o-phenanthroline and batimastat. Defects in this gene may be associated with lung tumorigenesis. [provided by RefSeq, Oct 2016]","start":68247574,"end":68257164,"strand":1,"description":"archaelysin family metallopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:28041]"}, {"versioned_ensembl_gene_id":"ENSG00000183128.7","gene_symbol":"CALHM3","gene_name":"calcium homeostasis modulator 3 [Source:HGNC Symbol;Acc:HGNC:23458]","synonyms":"FAM26A,bA225H22.7","biotype":"protein_coding","ncbi_id":"119395","summary":null,"start":103472804,"end":103479240,"strand":-1,"description":"calcium homeostasis modulator 3 [Source:HGNC Symbol;Acc:HGNC:23458]"}, {"versioned_ensembl_gene_id":"ENSG00000131095.12","gene_symbol":"GFAP","gene_name":"glial fibrillary acidic protein [Source:HGNC Symbol;Acc:HGNC:4235]","synonyms":"FLJ45472","biotype":"protein_coding","ncbi_id":"2670","summary":"This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":44903161,"end":44916937,"strand":-1,"description":"glial fibrillary acidic protein [Source:HGNC Symbol;Acc:HGNC:4235]"}, {"versioned_ensembl_gene_id":"ENSG00000185933.6","gene_symbol":"CALHM1","gene_name":"calcium homeostasis modulator 1 [Source:HGNC Symbol;Acc:HGNC:23494]","synonyms":"FAM26C","biotype":"protein_coding","ncbi_id":"255022","summary":"This gene encodes a calcium channel that plays a role in processing of amyloid-beta precursor protein. A polymorphism at this locus has been reported to be associated with susceptibility to late-onset Alzheimer's disease in some populations, but the pathogenicity of this polymorphism is unclear.[provided by RefSeq, Mar 2010]","start":103453387,"end":103458888,"strand":-1,"description":"calcium homeostasis modulator 1 [Source:HGNC Symbol;Acc:HGNC:23494]"}, {"versioned_ensembl_gene_id":"ENSG00000214447.4","gene_symbol":"FAM187A","gene_name":"family with sequence similarity 187 member A [Source:HGNC Symbol;Acc:HGNC:35153]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528020","summary":null,"start":44899712,"end":44905390,"strand":1,"description":"family with sequence similarity 187 member A [Source:HGNC Symbol;Acc:HGNC:35153]"}, {"versioned_ensembl_gene_id":"ENSG00000274712.1","gene_symbol":"AC005332.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68205489,"end":68207493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267731.1","gene_symbol":"AC005332.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68189884,"end":68192802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120733.13","gene_symbol":"KDM3B","gene_name":"lysine demethylase 3B [Source:HGNC Symbol;Acc:HGNC:1337]","synonyms":"NET22,KIAA1082,JMJD1B,C5orf7","biotype":"protein_coding","ncbi_id":"51780","summary":null,"start":138352596,"end":138437028,"strand":1,"description":"lysine demethylase 3B [Source:HGNC Symbol;Acc:HGNC:1337]"}, {"versioned_ensembl_gene_id":"ENSG00000267708.1","gene_symbol":"AC005332.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68152776,"end":68159043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163935.13","gene_symbol":"SFMBT1","gene_name":"Scm-like with four mbt domains 1 [Source:HGNC Symbol;Acc:HGNC:20255]","synonyms":"SFMBT,RU1,DKFZp434L243","biotype":"protein_coding","ncbi_id":"51460","summary":"This gene shares high similarity with the Drosophila Scm (sex comb on midleg) gene. It encodes a protein which contains four malignant brain tumor repeat (mbt) domains and may be involved in antigen recognition. [provided by RefSeq, Jun 2012]","start":52903572,"end":53046750,"strand":-1,"description":"Scm-like with four mbt domains 1 [Source:HGNC Symbol;Acc:HGNC:20255]"}, {"versioned_ensembl_gene_id":"ENSG00000267352.1","gene_symbol":"AC005332.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68134675,"end":68135604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174576.9","gene_symbol":"NPAS4","gene_name":"neuronal PAS domain protein 4 [Source:HGNC Symbol;Acc:HGNC:18983]","synonyms":"PASD10,NXF,Le-PAS,bHLHe79","biotype":"protein_coding","ncbi_id":"266743","summary":"NXF is a member of the basic helix-loop-helix-PER (MIM 602260)-ARNT (MIM 126110)-SIM (see SIM2; MIM 600892) (bHLH-PAS) class of transcriptional regulators, which are involved in a wide range of physiologic and developmental events (Ooe et al., 2004 [PubMed 14701734]).[supplied by OMIM, Mar 2008]","start":66421004,"end":66426707,"strand":1,"description":"neuronal PAS domain protein 4 [Source:HGNC Symbol;Acc:HGNC:18983]"}, {"versioned_ensembl_gene_id":"ENSG00000277476.1","gene_symbol":"AC005332.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68133201,"end":68135935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242142.1","gene_symbol":"SERBP1P3","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"553148","summary":null,"start":53064283,"end":53065091,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44630]"}, {"versioned_ensembl_gene_id":"ENSG00000280417.1","gene_symbol":"AC096887.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53046166,"end":53048122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238797.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39441665,"end":39441764,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280721.1","gene_symbol":"LINC01943","gene_name":"long intergenic non-protein coding RNA 1943 [Source:HGNC Symbol;Acc:HGNC:52767]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928173","summary":null,"start":87439523,"end":87459044,"strand":-1,"description":"long intergenic non-protein coding RNA 1943 [Source:HGNC Symbol;Acc:HGNC:52767]"}, {"versioned_ensembl_gene_id":"ENSG00000138777.19","gene_symbol":"PPA2","gene_name":"pyrophosphatase (inorganic) 2 [Source:HGNC Symbol;Acc:HGNC:28883]","synonyms":"FLJ20459","biotype":"protein_coding","ncbi_id":"27068","summary":"The protein encoded by this gene is localized to the mitochondrion, is highly similar to members of the inorganic pyrophosphatase (PPase) family, and contains the signature sequence essential for the catalytic activity of PPase. PPases catalyze the hydrolysis of pyrophosphate to inorganic phosphate, which is important for the phosphate metabolism of cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":105369077,"end":105474081,"strand":-1,"description":"pyrophosphatase (inorganic) 2 [Source:HGNC Symbol;Acc:HGNC:28883]"}, {"versioned_ensembl_gene_id":"ENSG00000272305.5","gene_symbol":"AC096887.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52969119,"end":53099453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276348.1","gene_symbol":"AL353770.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66979132,"end":66988373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267023.5","gene_symbol":"LRRC37A16P","gene_name":"leucine rich repeat containing 37 member A16, pseudogene [Source:HGNC Symbol;Acc:HGNC:43820]","synonyms":"LRRC37C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"651250","summary":null,"start":68125777,"end":68152468,"strand":-1,"description":"leucine rich repeat containing 37 member A16, pseudogene [Source:HGNC Symbol;Acc:HGNC:43820]"}, {"versioned_ensembl_gene_id":"ENSG00000264012.1","gene_symbol":"AC091588.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22175465,"end":22176662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224881.1","gene_symbol":"AC068279.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87379880,"end":87380767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165480.15","gene_symbol":"SKA3","gene_name":"spindle and kinetochore associated complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:20262]","synonyms":"RAMA1,MGC4832,C13orf3","biotype":"protein_coding","ncbi_id":"221150","summary":"This gene encodes a component of the spindle and kinetochore-associated protein complex that regulates microtubule attachment to the kinetochores during mitosis. The encoded protein localizes to the outer kinetechore and may be required for normal chromosome segregation and cell division. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":21153595,"end":21176602,"strand":-1,"description":"spindle and kinetochore associated complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:20262]"}, {"versioned_ensembl_gene_id":"ENSG00000213385.3","gene_symbol":"AC105052.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102755146,"end":102755939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173141.4","gene_symbol":"MRPL57","gene_name":"mitochondrial ribosomal protein L57 [Source:HGNC Symbol;Acc:HGNC:14514]","synonyms":"MRP63","biotype":"protein_coding","ncbi_id":"78988","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a protein which belongs to an undetermined ribosomal subunit and which seems to be specific to animal mitoribosomes. Pseudogenes corresponding to this gene are found on chromosomes 1p, 1q, 3p, 5q, 8q, 14q, and Y. [provided by RefSeq, Jul 2008]","start":21176645,"end":21179084,"strand":1,"description":"mitochondrial ribosomal protein L57 [Source:HGNC Symbol;Acc:HGNC:14514]"}, {"versioned_ensembl_gene_id":"ENSG00000265055.1","gene_symbol":"AC145343.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68096046,"end":68101474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275969.2","gene_symbol":"SPATA31A3","gene_name":"SPATA31 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:32003]","synonyms":"DKFZp434B204,OTTHUMG00000013164,FAM75A3","biotype":"protein_coding","ncbi_id":"727830","summary":null,"start":66986304,"end":66992583,"strand":-1,"description":"SPATA31 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:32003]"}, {"versioned_ensembl_gene_id":"ENSG00000244640.1","gene_symbol":"AC096922.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68633706,"end":68634356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131381.12","gene_symbol":"RBSN","gene_name":"rabenosyn, RAB effector [Source:HGNC Symbol;Acc:HGNC:20759]","synonyms":"ZFYVE20","biotype":"protein_coding","ncbi_id":"64145","summary":"This gene encodes a protein that belongs to the FYVE zinc finger family of proteins. The encoded protein interacts with Ras-related proteins that regulate membrane trafficking. A missense mutation in this gene is associated with a defect in the early endocytic pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":15070073,"end":15099163,"strand":-1,"description":"rabenosyn, RAB effector [Source:HGNC Symbol;Acc:HGNC:20759]"}, {"versioned_ensembl_gene_id":"ENSG00000274355.1","gene_symbol":"FAM74A3","gene_name":"family with sequence similarity 74 member A3 [Source:HGNC Symbol;Acc:HGNC:32031]","synonyms":"OTTHUMG00000067149","biotype":"transcribed_processed_pseudogene","ncbi_id":"728495","summary":null,"start":66976520,"end":66976991,"strand":-1,"description":"family with sequence similarity 74 member A3 [Source:HGNC Symbol;Acc:HGNC:32031]"}, {"versioned_ensembl_gene_id":"ENSG00000110975.8","gene_symbol":"SYT10","gene_name":"synaptotagmin 10 [Source:HGNC Symbol;Acc:HGNC:19266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341359","summary":null,"start":33374238,"end":33439819,"strand":-1,"description":"synaptotagmin 10 [Source:HGNC Symbol;Acc:HGNC:19266]"}, {"versioned_ensembl_gene_id":"ENSG00000255794.7","gene_symbol":"RMST","gene_name":"rhabdomyosarcoma 2 associated transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:29893]","synonyms":"NCRNA00054,NCRMS,LINC00054","biotype":"processed_transcript","ncbi_id":"196475","summary":"This gene produces a long non-coding RNA that functions in neurogenesis by aiding in the association of Sox2 transcription factor to its target promoters. [provided by RefSeq, Dec 2017]","start":97430884,"end":97598415,"strand":1,"description":"rhabdomyosarcoma 2 associated transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:29893]"}, {"versioned_ensembl_gene_id":"ENSG00000007520.3","gene_symbol":"TSR3","gene_name":"TSR3, acp transferase ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:14175]","synonyms":"MGC24381,C16orf42","biotype":"protein_coding","ncbi_id":"115939","summary":null,"start":1349240,"end":1351911,"strand":-1,"description":"TSR3, acp transferase ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:14175]"}, {"versioned_ensembl_gene_id":"ENSG00000177189.12","gene_symbol":"RPS6KA3","gene_name":"ribosomal protein S6 kinase A3 [Source:HGNC Symbol;Acc:HGNC:10432]","synonyms":"RSK2,RSK,MRX19,HU-3,CLS","biotype":"protein_coding","ncbi_id":"6197","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 non-identical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Mutations in this gene have been associated with Coffin-Lowry syndrome (CLS). [provided by RefSeq, Jul 2008]","start":20149911,"end":20267100,"strand":-1,"description":"ribosomal protein S6 kinase A3 [Source:HGNC Symbol;Acc:HGNC:10432]"}, {"versioned_ensembl_gene_id":"ENSG00000273584.1","gene_symbol":"AC096708.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68908048,"end":68908599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204849.7","gene_symbol":"SPATA31A1","gene_name":"SPATA31 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:23394]","synonyms":"SPATA31A2,FAM75A2,FAM75A1,DKFZP434B204,C9orf36A,C9orf36","biotype":"protein_coding","ncbi_id":"647060","summary":null,"start":39355669,"end":39361959,"strand":1,"description":"SPATA31 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:23394]"}, {"versioned_ensembl_gene_id":"ENSG00000223730.1","gene_symbol":"Z83838.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":44901547,"end":44902471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233228.1","gene_symbol":"LPCAT2BP","gene_name":"lysophosphatidylcholine acyltransferase 2b, pseudogene [Source:HGNC Symbol;Acc:HGNC:38003]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100128094","summary":null,"start":92066306,"end":92067839,"strand":1,"description":"lysophosphatidylcholine acyltransferase 2b, pseudogene [Source:HGNC Symbol;Acc:HGNC:38003]"}, {"versioned_ensembl_gene_id":"ENSG00000277350.1","gene_symbol":"AL353770.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66942703,"end":66952344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227054.1","gene_symbol":"FDX1P2","gene_name":"ferredoxin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3641]","synonyms":"FDXP2","biotype":"processed_pseudogene","ncbi_id":"2216","summary":null,"start":25692180,"end":25692554,"strand":1,"description":"ferredoxin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3641]"}, {"versioned_ensembl_gene_id":"ENSG00000188186.10","gene_symbol":"LAMTOR4","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 [Source:HGNC Symbol;Acc:HGNC:33772]","synonyms":"C7orf59","biotype":"protein_coding","ncbi_id":"389541","summary":null,"start":100148907,"end":100155944,"strand":1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 [Source:HGNC Symbol;Acc:HGNC:33772]"}, {"versioned_ensembl_gene_id":"ENSG00000143178.12","gene_symbol":"TBX19","gene_name":"T-box 19 [Source:HGNC Symbol;Acc:HGNC:11596]","synonyms":"TPIT,dj747L4.1","biotype":"protein_coding","ncbi_id":"9095","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [provided by RefSeq, Jul 2008]","start":168281040,"end":168314426,"strand":1,"description":"T-box 19 [Source:HGNC Symbol;Acc:HGNC:11596]"}, {"versioned_ensembl_gene_id":"ENSG00000269066.1","gene_symbol":"AC020908.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17095418,"end":17099307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138172.10","gene_symbol":"CALHM2","gene_name":"calcium homeostasis modulator 2 [Source:HGNC Symbol;Acc:HGNC:23493]","synonyms":"FAM26B","biotype":"protein_coding","ncbi_id":"51063","summary":null,"start":103446786,"end":103452402,"strand":-1,"description":"calcium homeostasis modulator 2 [Source:HGNC Symbol;Acc:HGNC:23493]"}, {"versioned_ensembl_gene_id":"ENSG00000249829.2","gene_symbol":"AC016559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79191549,"end":79191747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163312.10","gene_symbol":"HELQ","gene_name":"helicase, POLQ like [Source:HGNC Symbol;Acc:HGNC:18536]","synonyms":"Hel308","biotype":"protein_coding","ncbi_id":"113510","summary":"HEL308 is a single-stranded DNA-dependent ATPase and DNA helicase (Marini and Wood, 2002 [PubMed 11751861]).[supplied by OMIM, Mar 2008]","start":83407343,"end":83455856,"strand":-1,"description":"helicase, POLQ like [Source:HGNC Symbol;Acc:HGNC:18536]"}, {"versioned_ensembl_gene_id":"ENSG00000254736.1","gene_symbol":"BRD9P1","gene_name":"bromodomain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51445]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481721","summary":null,"start":66389609,"end":66390168,"strand":1,"description":"bromodomain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51445]"}, {"versioned_ensembl_gene_id":"ENSG00000255305.1","gene_symbol":"AP004607.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89978540,"end":89980661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230985.9","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"VARS2L,DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL,G7a","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30898953,"end":30917183,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000232406.6","gene_symbol":"AL121895.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36148726,"end":36155760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227591.5","gene_symbol":"AL031316.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":209661364,"end":209724125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105559.11","gene_symbol":"PLEKHA4","gene_name":"pleckstrin homology domain containing A4 [Source:HGNC Symbol;Acc:HGNC:14339]","synonyms":"PEPP1","biotype":"protein_coding","ncbi_id":"57664","summary":"This gene encodes a pleckstrin homology (PH) domain-containing protein. The PH domain is found near the N-terminus and contains a putative phosphatidylinositol 3, 4, 5-triphosphate-binding motif (PPBM). Elevated expression of this gene has been observed in some melanomas. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017]","start":48837097,"end":48868632,"strand":-1,"description":"pleckstrin homology domain containing A4 [Source:HGNC Symbol;Acc:HGNC:14339]"}, {"versioned_ensembl_gene_id":"ENSG00000254655.1","gene_symbol":"AP004607.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89960422,"end":89960624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237524.8","gene_symbol":"TEX51","gene_name":"testis expressed 51 [Source:HGNC Symbol;Acc:HGNC:52387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101929926","summary":null,"start":126898882,"end":126902097,"strand":1,"description":"testis expressed 51 [Source:HGNC Symbol;Acc:HGNC:52387]"}, {"versioned_ensembl_gene_id":"ENSG00000172031.6","gene_symbol":"EPHX4","gene_name":"epoxide hydrolase 4 [Source:HGNC Symbol;Acc:HGNC:23758]","synonyms":"FLJ90341,EPHXRP,ABHD7","biotype":"protein_coding","ncbi_id":"253152","summary":null,"start":92029982,"end":92063536,"strand":1,"description":"epoxide hydrolase 4 [Source:HGNC Symbol;Acc:HGNC:23758]"}, {"versioned_ensembl_gene_id":"ENSG00000265758.1","gene_symbol":"LINC01900","gene_name":"long intergenic non-protein coding RNA 1900 [Source:HGNC Symbol;Acc:HGNC:52719]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724208","summary":null,"start":21981121,"end":22051159,"strand":1,"description":"long intergenic non-protein coding RNA 1900 [Source:HGNC Symbol;Acc:HGNC:52719]"}, {"versioned_ensembl_gene_id":"ENSG00000264289.1","gene_symbol":"AC103987.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21914369,"end":21914660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117594.9","gene_symbol":"HSD11B1","gene_name":"hydroxysteroid 11-beta dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:5208]","synonyms":"SDR26C1,HSD11B,HSD11","biotype":"protein_coding","ncbi_id":"3290","summary":"The protein encoded by this gene is a microsomal enzyme that catalyzes the conversion of the stress hormone cortisol to the inactive metabolite cortisone. In addition, the encoded protein can catalyze the reverse reaction, the conversion of cortisone to cortisol. Too much cortisol can lead to central obesity, and a particular variation in this gene has been associated with obesity and insulin resistance in children. Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency. Alternate splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, May 2011]","start":209686178,"end":209734950,"strand":1,"description":"hydroxysteroid 11-beta dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:5208]"}, {"versioned_ensembl_gene_id":"ENSG00000273123.1","gene_symbol":"AC020634.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123715851,"end":123716399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184887.13","gene_symbol":"BTBD6","gene_name":"BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19897]","synonyms":"BDPL","biotype":"protein_coding","ncbi_id":"90135","summary":null,"start":105248490,"end":105251093,"strand":1,"description":"BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19897]"}, {"versioned_ensembl_gene_id":"ENSG00000250174.5","gene_symbol":"MYLK-AS2","gene_name":"MYLK antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40387]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873940","summary":null,"start":123689644,"end":123692407,"strand":1,"description":"MYLK antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40387]"}, {"versioned_ensembl_gene_id":"ENSG00000242085.1","gene_symbol":"AL928654.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105374618,"end":105374971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078399.17","gene_symbol":"HOXA9","gene_name":"homeobox A9 [Source:HGNC Symbol;Acc:HGNC:5109]","synonyms":"HOX1G,HOX1","biotype":"protein_coding","ncbi_id":"3205","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is highly similar to the abdominal-B (Abd-B) gene of Drosophila. A specific translocation event which causes a fusion between this gene and the NUP98 gene has been associated with myeloid leukemogenesis. Read-through transcription exists between this gene and the upstream homeobox A10 (HOXA10) gene.[provided by RefSeq, Mar 2011]","start":27162435,"end":27175180,"strand":-1,"description":"homeobox A9 [Source:HGNC Symbol;Acc:HGNC:5109]"}, {"versioned_ensembl_gene_id":"ENSG00000261202.1","gene_symbol":"Z83847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40043068,"end":40044530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175699.14","gene_symbol":"CCDC197","gene_name":"coiled-coil domain containing 197 [Source:HGNC Symbol;Acc:HGNC:19860]","synonyms":"c14_5713,C14orf48,LINC00521,C14orf48,LINC00521","biotype":"protein_coding","ncbi_id":"256369","summary":null,"start":93987225,"end":94008863,"strand":1,"description":"coiled-coil domain containing 197 [Source:HGNC Symbol;Acc:HGNC:19860]"}, {"versioned_ensembl_gene_id":"ENSG00000214681.3","gene_symbol":"IQCF5","gene_name":"IQ motif containing F5 [Source:HGNC Symbol;Acc:HGNC:35159]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389124","summary":null,"start":51873721,"end":51875584,"strand":-1,"description":"IQ motif containing F5 [Source:HGNC Symbol;Acc:HGNC:35159]"}, {"versioned_ensembl_gene_id":"ENSG00000184345.4","gene_symbol":"IQCF2","gene_name":"IQ motif containing F2 [Source:HGNC Symbol;Acc:HGNC:31815]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389123","summary":null,"start":51861629,"end":51863424,"strand":1,"description":"IQ motif containing F2 [Source:HGNC Symbol;Acc:HGNC:31815]"}, {"versioned_ensembl_gene_id":"ENSG00000214686.4","gene_symbol":"IQCF6","gene_name":"IQ motif containing F6 [Source:HGNC Symbol;Acc:HGNC:35158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440956","summary":null,"start":51778561,"end":51779187,"strand":-1,"description":"IQ motif containing F6 [Source:HGNC Symbol;Acc:HGNC:35158]"}, {"versioned_ensembl_gene_id":"ENSG00000241534.9","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31927837,"end":31934271,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000278011.1","gene_symbol":"AC024941.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88601862,"end":88602195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233767.1","gene_symbol":"PSMA6P3","gene_name":"proteasome subunit alpha 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39608]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874510","summary":null,"start":46072085,"end":46072248,"strand":-1,"description":"proteasome subunit alpha 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39608]"}, {"versioned_ensembl_gene_id":"ENSG00000088782.4","gene_symbol":"DEFB127","gene_name":"defensin beta 127 [Source:HGNC Symbol;Acc:HGNC:16206]","synonyms":"DEF-27,C20orf73,bA530N10.2","biotype":"protein_coding","ncbi_id":"140850","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":157470,"end":159163,"strand":1,"description":"defensin beta 127 [Source:HGNC Symbol;Acc:HGNC:16206]"}, {"versioned_ensembl_gene_id":"ENSG00000228235.1","gene_symbol":"AP001476.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46052596,"end":46053105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227165.7","gene_symbol":"WDR11-AS1","gene_name":"WDR11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27437]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283089","summary":null,"start":120761812,"end":120851345,"strand":-1,"description":"WDR11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27437]"}, {"versioned_ensembl_gene_id":"ENSG00000224413.1","gene_symbol":"AP001476.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46037052,"end":46039807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253293.4","gene_symbol":"HOXA10","gene_name":"homeobox A10 [Source:HGNC Symbol;Acc:HGNC:5100]","synonyms":"HOX1H,HOX1","biotype":"protein_coding","ncbi_id":"3206","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor that may regulate gene expression, morphogenesis, and differentiation. More specifically, it may function in fertility, embryo viability, and regulation of hematopoietic lineage commitment. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the downstream homeobox A9 (HOXA9) gene. [provided by RefSeq, Mar 2011]","start":27170591,"end":27180261,"strand":-1,"description":"homeobox A10 [Source:HGNC Symbol;Acc:HGNC:5100]"}, {"versioned_ensembl_gene_id":"ENSG00000253322.1","gene_symbol":"AC104051.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57594166,"end":57805029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253821.1","gene_symbol":"AC090796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57492884,"end":57591559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169710.8","gene_symbol":"FASN","gene_name":"fatty acid synthase [Source:HGNC Symbol;Acc:HGNC:3594]","synonyms":"SDR27X1,FAS","biotype":"protein_coding","ncbi_id":"2194","summary":"The enzyme encoded by this gene is a multifunctional protein. Its main function is to catalyze the synthesis of palmitate from acetyl-CoA and malonyl-CoA, in the presence of NADPH, into long-chain saturated fatty acids. In some cancer cell lines, this protein has been found to be fused with estrogen receptor-alpha (ER-alpha), in which the N-terminus of FAS is fused in-frame with the C-terminus of ER-alpha. [provided by RefSeq, Jul 2008]","start":82078333,"end":82098332,"strand":-1,"description":"fatty acid synthase [Source:HGNC Symbol;Acc:HGNC:3594]"}, {"versioned_ensembl_gene_id":"ENSG00000056487.15","gene_symbol":"PHF21B","gene_name":"PHD finger protein 21B [Source:HGNC Symbol;Acc:HGNC:25161]","synonyms":"PHF4,FLJ34161,BHC80L","biotype":"protein_coding","ncbi_id":"112885","summary":null,"start":44881162,"end":45009999,"strand":-1,"description":"PHD finger protein 21B [Source:HGNC Symbol;Acc:HGNC:25161]"}, {"versioned_ensembl_gene_id":"ENSG00000215480.4","gene_symbol":"OR7E37P","gene_name":"olfactory receptor family 7 subfamily E member 37 pseudogene [Source:HGNC Symbol;Acc:HGNC:8410]","synonyms":"hg533","biotype":"unprocessed_pseudogene","ncbi_id":"100506759","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Mar 2011]","start":41442770,"end":41443666,"strand":1,"description":"olfactory receptor family 7 subfamily E member 37 pseudogene [Source:HGNC Symbol;Acc:HGNC:8410]"}, {"versioned_ensembl_gene_id":"ENSG00000227211.2","gene_symbol":"AL035551.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102615473,"end":102615820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261143.1","gene_symbol":"ADAMTS7P3","gene_name":"ADAMTS7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49409]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400406","summary":null,"start":77976042,"end":77993057,"strand":1,"description":"ADAMTS7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49409]"}, {"versioned_ensembl_gene_id":"ENSG00000235005.1","gene_symbol":"AL450468.1","gene_name":null,"synonyms":null,"biot