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2025-10-28 01:55:30, 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
//
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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