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NCBI Reference Sequence: NR_172498.1
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LOCUS NR_172498 2970 bp RNA linear PRI 19-APR-2022 DEFINITION Homo sapiens MIR3976 host gene (MIR3976HG), transcript variant 5, long non-coding RNA. ACCESSION NR_172498 VERSION NR_172498.1 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 2970) AUTHORS Comuzzie AG, Cole SA, Laston SL, Voruganti VS, Haack K, Gibbs RA and Butte NF. TITLE Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population JOURNAL PLoS One 7 (12), e51954 (2012) PUBMED 23251661 REFERENCE 2 (bases 1 to 2970) AUTHORS Kutsche K, Glauner E, Knauf S, Pomarino A, Schmidt M, Schroder B, Nothwang H, Schuler H, Goecke T, Kersten A, Althaus C and Gal A. TITLE Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium JOURNAL Cytogenet Cell Genet 91 (1-4), 141-147 (2000) PUBMED 11173847 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AP005231.2, AP005433.3 and AP001021.5. Sequence Note: The RefSeq transcript was derived from the reference genome assembly. The genomic coordinates were determined from alignments. ##Evidence-Data-START## RNAseq introns :: partial sample support SAMEA1968968, SAMEA2148093 [ECO:0000350] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-166 AP005231.2 70389-70554 167-226 AP005231.2 82578-82637 227-402 AP005231.2 83888-84063 403-506 AP005231.2 91353-91456 507-662 AP005433.3 36783-36938 663-868 AP005433.3 110309-110514 869-1000 AP005433.3 119449-119580 1001-1177 AP005433.3 121639-121815 1178-1375 AP005433.3 123767-123964 1376-1577 AP005433.3 130717-130918 1578-1671 AP005433.3 132276-132369 1672-2970 AP001021.5 8595-9893 FEATURES Location/Qualifiers source 1..2970 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="18" /map="18p11.31" gene 1..2970 /gene="MIR3976HG" /gene_synonym="LINC01469" /note="MIR3976 host gene" /db_xref="GeneID:645355" /db_xref="HGNC:HGNC:51104" ncRNA 1..2970 /ncRNA_class="lncRNA" /gene="MIR3976HG" /gene_synonym="LINC01469" /product="MIR3976 host gene, transcript variant 5" /db_xref="GeneID:645355" /db_xref="HGNC:HGNC:51104" ORIGIN 1 aactctctct ctttctgatt gagtgtaagc tgctatatga agggatccac aagacgaata 61 attaaggggg acctctgatc aacagccagc aaggaactga atccctcaga cccacaactc 121 acaagaaact gaagctgaag cagattcttc ctcagtcaag cttcaggacc tgctttgcag 181 aaaggatctc attgagaata gcaaaaggaa gttgggaacc attacagtgc ccagctgtat 241 tggtagagga gaccaaccac accctccaca gcacagcacc tggagaggaa ctgctgccat 301 gaccatagag gacaccctct ggatacaatg ccagacttga tgtgggactg accaacctat 361 ggaccccagg caccaccacc cagacctgct cagcacctga aacattcaca gccgtggaga 421 gagaactgtt cactgctacc atccacactt ctgggcccct tcagcagcag ggtgacaagg 481 aagagggaaa tcgacttgga aaagagggga cctctgaccc aagagttcgg tcaatgcata 541 tgttggcagc cagctgcaca tcgcaccaaa tatgaacttc aaatagaaga aagcctcatt 601 tggaagaaag ctcatgcaca gactgtaaat atttcagagc agattgtgtc tctgtagatt 661 aacaccatgt tgctcctcct cggacacagg ctgatcctat ctcagcattc ttggaaggct 721 aagagagagt aatagaagaa caaaactgtg tctgaaaatg tagggctgca tggttgctac 781 acctattgac acaagtgagg gatggacata aaaatgcaaa taattaaaaa ggcctttttg 841 acaggaaaga gtggctccta cagccaagcc ggatacagtg gcttgcacct gtggtctcag 901 cgacttgggc gactgaagca agaagatcac ttgagcctag gagttcgagg ctacagcaag 961 ctatgaccgt gccactgcac tccagcctgg gcgtgacaga ccagctcttc ttctgaagga 1021 tgaccacctg gaataagagc agccctaggc cccccacctc actccaggtg gcagatccac 1081 agagatggta gcgatacaga agcacagctt ccgatggctt ccccgtgtct tcagtttgca 1141 gccttatttc ggtgcttgga cgtgcttaac ttctcaggat tatattctgc tttggagtgc 1201 aaggagaaag tcacagtcta gttttatgaa gaccaaacta gagaaaatcg agttatctta 1261 aagtgtatga catctccaca aatgaatgtt tatggcttta cacttggagt gttcttggaa 1321 cactcttcat agcaaatcct ccctcagaag acccccacct ggcatcagaa caaacgtcta 1381 cctaatcttc caaactctgt gtaaatcctg gatccaccat ttaccagctg tgtaaccctg 1441 gacaacaatt ccatctttct gacctcagtg tctttctctg caaaacagcg gtaagaatga 1501 tcctacttca atagagttgc tgtgaggatt cactgagatc atgtgtacca agctcctaca 1561 atagtactga acccacagcc atggatcaag accattaact tataatcagt gatagccaag 1621 aggatgggaa gagaatatta agcctggtgc tctgcaaatt aatacttgca ggttgggaag 1681 ccagatatcc acattatctc acatcacatc actgagctct gtggcccagt tctgactaca 1741 tgttagaagc agaagtctgc aggggatggc ttctgagaaa acttgtattt attatttaaa 1801 tttaaccttc tagcctggga ataaattcca gcttgcttag aacaatacag cacagaagag 1861 agcctgagtt cctggtgcat ccctgtgcca gtgtctcaat cctgccccac cgatttccaa 1921 tttcttatta tgtgaaaagc aaccctccct tctttgatta agtcattatt gatagggttt 1981 ttttggtgac ttgcatccaa atgcattcct taactcaaac aaaatagaag gggaattcca 2041 cattcacact gttgcatcag acaagctctg gcttctcaga actttagttt tccatttact 2101 agagctcaga atcaaagaga cagtaaagaa acccatttaa aaattgcttg gcatatatat 2161 cttgggtgat gggacttcat gggtaatatt tttaaaattt ctttgtgtat ttttctttta 2221 ttgtcaaacg ttattaaaga gaccatagat accttttgta attataataa aaaacaaaat 2281 gttactaaga acagtgagaa ctcttaagct aactacaaga taattaatat ataactgcaa 2341 aatataaaat accaaagcca ttttcaaata aagaaacaga gccacatgaa actttgcagt 2401 ttagccaaag tcatttcagg attctgaagc tggggaggaa gcaaggctta cttagcccgt 2461 ggctagaatt cacttttgaa aactccattt ttgtccattc cctcttatca ctacttgctt 2521 gcaagttagg aaacaaatta gaacaaaagc attgtttgtc gtcagtggtc aatgttcatt 2581 gctttaccag aggctcggga ttagaagatt ctcagaacca gttagctcct gatacaatcg 2641 ggccttgata tggtttggat ttgtgtcccc acccaaatct catgtcgaat tagaggaggg 2701 gcctggtggg aggtgattgg atcatggggg cagatttccc tcttgctgtt ctcatgatag 2761 tgactgagtt ctcaaagatc ttagggttta aaacttttgt ggcacttcca tcttcgctct 2821 ctcttcctct ctcatgctgc catgtgaaga aggtgcctgc ttcccctttg ctttctgcca 2881 tgattgtacg tttcctgagg cctcccagtt gtgcttcctg ataagcctat ggaactgtga 2941 gtcaattaaa tctcttttct atataaataa //
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