2025-05-09 20:34:15, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_037939 2276 bp RNA linear PRI 16-JUL-2013 DEFINITION Homo sapiens homeobox A10 (HOXA10), transcript variant 2, non-coding RNA. ACCESSION NR_037939 VERSION NR_037939.1 GI:325652049 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 2276) AUTHORS Ekici,A.B., Strissel,P.L., Oppelt,P.G., Renner,S.P., Brucker,S., Beckmann,M.W. and Strick,R. TITLE HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina JOURNAL Gene 518 (2), 267-272 (2013) PUBMED 23376215 REMARK GeneRIF: Rare DNA sequence variations in the HOXA10 gene could contribute to the misdevelopment of female internal genitalia. REFERENCE 2 (bases 1 to 2276) AUTHORS Gallo,M., Ho,J., Coutinho,F.J., Vanner,R., Lee,L., Head,R., Ling,E.K., Clarke,I.D. and Dirks,P.B. TITLE A tumorigenic MLL-homeobox network in human glioblastoma stem cells JOURNAL Cancer Res. 73 (1), 417-427 (2013) PUBMED 23108137 REMARK GeneRIF: We found that MLL directly activates the Homeobox gene HOXA10 in human glioblastoma REFERENCE 3 (bases 1 to 2276) AUTHORS Bei,L., Shah,C., Wang,H., Huang,W., Roy,R. and Eklund,E.A. TITLE beta-Catenin activates the HOXA10 and CDX4 genes in myeloid progenitor cells JOURNAL J. Biol. Chem. 287 (47), 39589-39601 (2012) PUBMED 23038246 REMARK GeneRIF: a molecular mechanisms through which increased expression of HoxA10 increases Cdx4 expression by direct CDX4 activation and by Fgf2-induced beta-catenin activity. This results in Cdx4-induced HoxA10-expression, creating a positive feedback mechanism REFERENCE 4 (bases 1 to 2276) AUTHORS Zhang,Y.J., Jia,X.H., Li,J.C. and Xu,Y.H. TITLE [Effect of HOXA10 gene silenced by shRNA on proliferation and apoptosis of U937cell line] JOURNAL Zhongguo Dang Dai Er Ke Za Zhi 14 (10), 785-791 (2012) PUBMED 23092574 REMARK GeneRIF: Compared with the negative control and untreated groups, mRNA level of HOXA10 decreased by (92.3+/-1.3)%, protein levels decreased by 91.1%, and the inhibition rate of U937 cells [(43.9+/-0.7)%] increased in the interference group REFERENCE 5 (bases 1 to 2276) AUTHORS Wang,X., Shaffer,J.R., Zeng,Z., Begum,F., Vieira,A.R., Noel,J., Anjomshoaa,I., Cuenco,K.T., Lee,M.K., Beck,J., Boerwinkle,E., Cornelis,M.C., Hu,F.B., Crosslin,D.R., Laurie,C.C., Nelson,S.C., Doheny,K.F., Pugh,E.W., Polk,D.E., Weyant,R.J., Crout,R., McNeil,D.W., Weeks,D.E., Feingold,E. and Marazita,M.L. TITLE Genome-wide association scan of dental caries in the permanent dentition JOURNAL BMC Oral Health 12, 57 (2012) PUBMED 23259602 REMARK Publication Status: Online-Only REFERENCE 6 (bases 1 to 2276) AUTHORS Scott,M.P. TITLE Vertebrate homeobox gene nomenclature JOURNAL Cell 71 (4), 551-553 (1992) PUBMED 1358459 REFERENCE 7 (bases 1 to 2276) AUTHORS Lowney,P., Corral,J., Detmer,K., LeBeau,M.M., Deaven,L., Lawrence,H.J. and Largman,C. TITLE A human Hox 1 homeobox gene exhibits myeloid-specific expression of alternative transcripts in human hematopoietic cells JOURNAL Nucleic Acids Res. 19 (12), 3443-3449 (1991) PUBMED 1676505 REFERENCE 8 (bases 1 to 2276) AUTHORS McAlpine,P.J. and Shows,T.B. TITLE Nomenclature for human homeobox genes JOURNAL Genomics 7 (3), 460 (1990) PUBMED 1973146 REFERENCE 9 (bases 1 to 2276) AUTHORS Acampora,D., D'Esposito,M., Faiella,A., Pannese,M., Migliaccio,E., Morelli,F., Stornaiuolo,A., Nigro,V., Simeone,A. and Boncinelli,E. TITLE The human HOX gene family JOURNAL Nucleic Acids Res. 17 (24), 10385-10402 (1989) PUBMED 2574852 REFERENCE 10 (bases 1 to 2276) AUTHORS Shen,W.F., Largman,C., Lowney,P., Corral,J.C., Detmer,K., Hauser,C.A., Simonitch,T.A., Hack,F.M. and Lawrence,H.J. TITLE Lineage-restricted expression of homeobox-containing genes in human hematopoietic cell lines JOURNAL Proc. Natl. Acad. Sci. U.S.A. 86 (21), 8536-8540 (1989) PUBMED 2573064 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AL710880.1, DB267919.1, BC071843.1, BC013971.2 and BF196481.1. 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]. Transcript Variant: This variant (2) contains an alternate 5' exon, compared to variant 1. It is represented as non-coding due to the presence of an upstream ORF that is predicted to interfere with translation of the longest ORF; translation of the upstream ORF renders the transcript a candidate for nonsense-mediated mRNA decay (NMD). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-4 AL710880.1 1-4 5-577 DB267919.1 2-574 578-1557 BC071843.1 213-1192 1558-1827 BC013971.2 1898-2167 1828-2191 BF196481.1 10-373 c 2192-2276 BC013971.2 2534-2618 FEATURES Location/Qualifiers source 1..2276 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="7" /map="7p15.2" gene 1..2276 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /note="homeobox A10" /db_xref="GeneID:3206" /db_xref="HGNC:5100" /db_xref="MIM:142957" misc_RNA 1..2276 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /product="homeobox A10, transcript variant 2" /db_xref="GeneID:3206" /db_xref="HGNC:5100" /db_xref="MIM:142957" exon 1..616 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /inference="alignment:Splign:1.39.8" misc_feature 352..513 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /inference="COORDINATES: ab initio prediction:ORF Finder" /note="long (>35aa) upstream ORF has strong Kozak sequence; nonsense-mediated decay (NMD) candidate" misc_feature 607..891 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /inference="COORDINATES: alignment:Blast2seq::RefSeq|NM_018951.3" /note="primary ORF" exon 617..2199 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /inference="alignment:Splign:1.39.8" variation 861 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" /replace="a" /replace="g" /db_xref="dbSNP:34957925" polyA_signal 2166..2171 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" polyA_site 2199 /gene="HOXA10" /gene_synonym="HOX1; HOX1.8; HOX1H; PL" ORIGIN
aaccaaagtctctcaagttgctagagagagtctagccaggaggactgctcgcgggcgggcggcgggcgggcgcgggtttgatttctgagccctataaaagcccatcctccgatggctgtgacaatgtggtcgtaaacccgtccggggccggccaatttgcatatttggaatgcgccgctataaacccggctggggttttgcagcgatttcttagatgtaaaaatgagatctcaatagcagcgggctgggcacatcctctcctctctccttctctctctgcccggagctggtttccgtctctcggctcggggctggaactccggcccaacctaggcgcgcagccgccacgagatggcgcacttccgatcaatgtcaaagccgccggggagccgggaaccccagcatgattcttggcctttgttcgcttctgatactaagagcagcacggtacattatttcacttgtcccgctccccttcataacagaaaaaggggactcaccctcaagaagtgattggtatggtaatttaaagcaacgcgcattcgctaggcctcgcgagcgtcgccgcgcggagaagccagctgtcccttggcagtgatttcggaaatgtgtcaaggcaattccaaaggtgaaaacgcagccaactggctcacggcaaagagtggtcggaagaagcgctgcccctacacgaagcaccagacactggagctggagaaggagtttctgttcaatatgtaccttactcgagagcggcgcctagagattagccgcagcgtccacctcacggacagacaagtgaaaatctggtttcagaaccgcaggatgaaactgaagaaaatgaatcgagaaaaccggatccgggagctcacagccaactttaatttttcctgatgaatctccaggcgacgcggttttttcacttcccgagcgctggtcccctccctctgtcttcaggctctgcccaggaactcgcacctgtgctggagccctgttcctccctcccacactcgccatctcctgggccgttacatctgtgcagggctggtttgttctgactttttgtttctttgtgtttgcttggtgctggtttatttgttgttttctgggggaaaaagccatatcatgctaaaattctatagagatagatattgtcctaagtgtcaagtcctgactgggctgggtttgctgtcttggggtcccactgctcgaaatggcccctgtcttcggccgagctggtttcctgcccagcctggggcaaacctagccggaaggccgaggtcccattgttggcgctgaggtgtctggcctgaggtcaatggtgcaaaggagccgccaccgggcatgtctgcctggagtgctgtgctgtgtttaatcaggggatacaggcccctgggtttcttttttctttcttcctttcttccttggccaagagaagggcttacaggcatggacatgcaggttggcaaacgggcttgactttggctgatttaaaaagtgagaaagaaagtaaaaaaggttaatttttccttcctctgtaagatatcccagctttaaaaagaaaaaaaaagaattaccaagagaaggggacttctcttccagtttctgtaaggtcttacattgcctgactaaaatgtttcatttacctctaaatttccatatccttctggctgtagataaataatgtagttttgtttatgcatttggaattagtggatttttttgtcattaaaattgttaccactggtaacatgtgacaagcacaccacaattctccctatcttgtgaagttgtttttttaaatcgccttgaacaaaaagttttttttttgtttgtttttgctttctgaaattcacagaagcctaggaggactggggtaagcggaataaactagagaagggagacattgtttggatttcctttatactgtgaagttacatgcataaaagggtcaaacctgtagatgcagaaaaagaaaaaaactataaatacaaatctgtataaatgtctattattatgaagaattgccaatcttgttttaagcaaatgcattctatcgttattataaatgttagttctagctctatttacttctaatcttaaatcagaataaattaatattgtattgctgctgtgcgtggaaaaagacgatgtttatgttcttatagaataaaagctgtggaatgaagctttttaattttaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:3206 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:3206 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:3206 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:3206 -> Biological process: GO:0001501 [skeletal system development] evidence: IEA GeneID:3206 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:3206 -> Biological process: GO:0007275 [multicellular organismal development] evidence: TAS GeneID:3206 -> Biological process: GO:0007283 [spermatogenesis] evidence: TAS GeneID:3206 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: IEA GeneID:3206 -> Biological process: GO:0009954 [proximal/distal pattern formation] evidence: IEA GeneID:3206 -> Biological process: GO:0030326 [embryonic limb morphogenesis] evidence: IEA GeneID:3206 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IEA
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