2025-05-09 19:34:18, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_006896 2018 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens homeobox A7 (HOXA7), mRNA. ACCESSION NM_006896 VERSION NM_006896.3 GI:84105267 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 2018) AUTHORS Li,Z., Huang,H., Li,Y., Jiang,X., Chen,P., Arnovitz,S., Radmacher,M.D., Maharry,K., Elkahloun,A., Yang,X., He,C., He,M., Zhang,Z., Dohner,K., Neilly,M.B., Price,C., Lussier,Y.A., Zhang,Y., Larson,R.A., Le Beau,M.M., Caligiuri,M.A., Bullinger,L., Valk,P.J., Delwel,R., Lowenberg,B., Liu,P.P., Marcucci,G., Bloomfield,C.D., Rowley,J.D. and Chen,J. TITLE Up-regulation of a HOXA-PBX3 homeobox-gene signature following down-regulation of miR-181 is associated with adverse prognosis in patients with cytogenetically abnormal AML JOURNAL Blood 119 (10), 2314-2324 (2012) PUBMED 22251480 REMARK GeneRIF: Data show that up-regulation of the HOXA7, HOXA9, HOXA11, and PBX3 resulting from the down-regulation of miR-181 family members probably contribute to the poor prognosis of patients with nonfavorable cytogenetically abnormal AML (CA-AML). REFERENCE 2 (bases 1 to 2018) AUTHORS Jo,S., Lee,H., Kim,S., Hwang,E.M., Park,J.Y., Kang,S.S. and Chung,H. TITLE Inhibition of PCGF2 enhances granulocytic differentiation of acute promyelocytic leukemia cell line HL-60 via induction of HOXA7 JOURNAL Biochem. Biophys. Res. Commun. 416 (1-2), 86-91 (2011) PUBMED 22085718 REMARK GeneRIF: Taken together, these results support the notion that down-regulation of PCGF2 is sufficient to induce granulocytic differentiation of HL-60 cells via de-repression of HOXA7 gene expression. REFERENCE 3 (bases 1 to 2018) AUTHORS Orlovsky,K., Kalinkovich,A., Rozovskaia,T., Shezen,E., Itkin,T., Alder,H., Ozer,H.G., Carramusa,L., Avigdor,A., Volinia,S., Buchberg,A., Mazo,A., Kollet,O., Largman,C., Croce,C.M., Nakamura,T., Lapidot,T. and Canaani,E. TITLE Down-regulation of homeobox genes MEIS1 and HOXA in MLL-rearranged acute leukemia impairs engraftment and reduces proliferation JOURNAL Proc. Natl. Acad. Sci. U.S.A. 108 (19), 7956-7961 (2011) PUBMED 21518888 REMARK GeneRIF: Several targets of MLL fusions, MEIS1, HOXA7, HOXA9, and HOXA10 are functionally related and have been implicated in leukemias. Each of the four genes was knocked down separately in the precursor B-cell leukemic line RS4;11 expressing MLL-AF4. REFERENCE 4 (bases 1 to 2018) AUTHORS Liborio,T.N., Acquafreda,T., Matizonkas-Antonio,L.F., Silva-Valenzuela,M.G., Ferraz,A.R. and Nunes,F.D. TITLE In situ hybridization detection of homeobox genes reveals distinct expression patterns in oral squamous cell carcinomas JOURNAL Histopathology 58 (2), 225-233 (2011) PUBMED 21323949 REMARK GeneRIF: HOXA7, PIXT1 and PRRX1 homeobox genes have different patterns of expression in oral squamous cell carcinomas depending on its histological features. REFERENCE 5 (bases 1 to 2018) AUTHORS Jugessur,A., Shi,M., Gjessing,H.K., Lie,R.T., Wilcox,A.J., Weinberg,C.R., Christensen,K., Boyles,A.L., Daack-Hirsch,S., Nguyen,T.T., Christiansen,L., Lidral,A.C. and Murray,J.C. TITLE Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia JOURNAL PLoS ONE 5 (7), E11493 (2010) PUBMED 20634891 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) Publication Status: Online-Only REFERENCE 6 (bases 1 to 2018) AUTHORS Scott,M.P. TITLE Vertebrate homeobox gene nomenclature JOURNAL Cell 71 (4), 551-553 (1992) PUBMED 1358459 REFERENCE 7 (bases 1 to 2018) AUTHORS McAlpine,P.J. and Shows,T.B. TITLE Nomenclature for human homeobox genes JOURNAL Genomics 7 (3), 460 (1990) PUBMED 1973146 REFERENCE 8 (bases 1 to 2018) 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 9 (bases 1 to 2018) AUTHORS Balling,R., Mutter,G., Gruss,P. and Kessel,M. TITLE Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice JOURNAL Cell 58 (2), 337-347 (1989) PUBMED 2568891 REFERENCE 10 (bases 1 to 2018) AUTHORS Boncinelli,E., Acampora,D., Pannese,M., D'Esposito,M., Somma,R., Gaudino,G., Stornaiuolo,A., Cafiero,M., Faiella,A. and Simeone,A. TITLE Organization of human class I homeobox genes JOURNAL Genome 31 (2), 745-756 (1989) PUBMED 2576652 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC004080.2 and AF026397.1. On Dec 30, 2005 this sequence version replaced gi:24497555. 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]. 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. ##Evidence-Data-START## Transcript exon combination :: AF026397.1, BC061916.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025084 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-232 AC004080.2 29816-30047 c 233-953 AF026397.1 233-953 954-2018 AC004080.2 27086-28150 c FEATURES Location/Qualifiers source 1..2018 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7p15.2" gene 1..2018 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /note="homeobox A7" /db_xref="GeneID:3204" /db_xref="HGNC:5108" /db_xref="MIM:142950" exon 1..511 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /inference="alignment:Splign:1.39.8" STS 11..235 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100580" /db_xref="UniSTS:425377" STS 15..970 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /db_xref="UniSTS:489818" misc_feature 97..99 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /note="upstream in-frame stop codon" CDS 133..825 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /note="homeo box A7; homeobox protein HOX-1A; homeobox protein Hox 1.1" /codon_start=1 /product="homeobox protein Hox-A7" /protein_id="NP_008827.2" /db_xref="GI:24497556" /db_xref="CCDS:CCDS5408.1" /db_xref="GeneID:3204" /db_xref="HGNC:5108" /db_xref="MIM:142950" /translation="
MSSSYYVNALFSKYTAGASLFQNAEPTSCSFAPNSQRSGYGAGAGAFASTVPGLYNVNSPLYQSPFASGYGLGADAYGNLPCASYDQNIPGLCSDLAKGACDKTDEGALHGAAEANFRIYPWMRSSGPDRKRGRQTYTRYQTLELEKEFHFNRYLTRRRRIEIAHALCLTERQIKIWFQNRRMKWKKEHKDEGPTAAAAPEGAVPSAAATAAADKADEEDDDEEEEDEEE
" misc_feature 487..504 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P31268.3); Region: Antp-type hexapeptide" misc_feature 523..699 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /note="Homeodomain; DNA binding domains involved in the transcriptional regulation of key eukaryotic developmental processes; may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner; Region: homeodomain; cd00086" /db_xref="CDD:28970" misc_feature order(523..537,541..543,592..594,610..612,649..651, 655..660,667..672,676..684,688..693) /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(529..531,538..540,658..660,667..672,679..681) /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" STS 155..231 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="Hoxa7" /db_xref="UniSTS:536645" STS 196..497 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="Hoxa7" /db_xref="UniSTS:143372" STS 222..496 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100579" /db_xref="UniSTS:425376" exon 512..2018 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /inference="alignment:Splign:1.39.8" STS 642..807 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="RH48711" /db_xref="UniSTS:37664" STS 659..807 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="RH47950" /db_xref="UniSTS:37665" STS 698..968 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100573" /db_xref="UniSTS:425370" STS 958..1185 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100572" /db_xref="UniSTS:425369" STS 959..1500 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="ECD12537" /db_xref="UniSTS:293570" STS 1164..1428 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100571" /db_xref="UniSTS:425368" STS 1423..1672 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100570" /db_xref="UniSTS:425367" STS 1653..1911 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /standard_name="REN100569" /db_xref="UniSTS:425366" variation 1750 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" /replace="a" /replace="t" /db_xref="dbSNP:1057512" polyA_signal 1991..1996 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" polyA_site 2018 /gene="HOXA7" /gene_synonym="ANTP; HOX1; HOX1.1; HOX1A" ORIGIN
gtgctgcggcgagctccgtccaaaagaaaatggggtttggtgtaaatctgggggtgtaatgttatcatatatcactctacctcgtaaaaccgacactgaaagctgccggacaacaaatcacaggtcaaaattatgagttcttcgtattatgtgaacgcgctttttagcaaatatacggcgggggcttctctgttccaaaatgccgagccgacttcttgctcctttgctcccaactcacagagaagcggctacggggcgggcgccggcgccttcgcctcgaccgttccgggcttatacaatgtcaacagccccctttatcagagcccctttgcgtccggctacggcctgggcgccgacgcctacggcaacctgccctgcgcctcctacgaccaaaacatccccgggctctgcagtgacctcgccaaaggcgcctgcgacaagacggacgagggcgcgctgcatggcgcggctgaggccaatttccgcatctacccctggatgcggtcttcaggacctgacaggaagcggggccgccagacctacacgcgctaccagacgctggagctggagaaggagttccacttcaaccgctacctgacgcggcgccgccgcattgaaatcgcccacgcgctctgcctcaccgagcgccagattaagatctggttccagaaccgccgcatgaagtggaagaaagagcataaggacgaaggtccgactgccgccgcagctcccgagggcgccgtgccctctgccgccgccactgctgccgcggacaaggccgacgaggaggacgatgatgaagaagaggaagacgaggaggaatgaggggccgatccggggccctctctgcaccggacagtcggaaaagcgtctttaagagactcactggttttacttacaaaaatgggaaaaataaaagaaaatgtaaaaaacaaaaacaaaaacaaaaaagcaacccagtccccaacctgcactctacccacccccatcacctactccagctcccaacttttgtggactgagcggccgcagagactgggtcgccttggattccctctgcctccgaggaccccaaaagacacccccaaccccaggccagccggccctgctctggcgcgtccaaaatactacctagcacaggcctctgctcgaggcacccccaaactacctatgtatccagccccagagggcctccattcccaggaagtccctatgtatcccaacactggcagacacccagcaccaccctcccagacccgcaagaaagtgaatctcactactacctactcccctaaaactacctattttgtgctggctggcttgcctgctacctagtgccgactgctcccaggcaagtcccctgctgcttacagcccgcagcttttggggtccctgaggctgccctgagaatgtgctgaggtccaggatcagggtattggcatctatttaaatcgaaaaataatatatttattccaaaaagcatcctaagtgcttgcaccctagaatcaatccctccttctctggcttggcacccacagctcaggcccatcaacccccacttctggaggggaatgttcctgagctggctgcagatctgtgggttagcttctgcttagcaggactgtggagatgcttccagcttcgctgtcctttcctctggctcctgtatcttactgttcagctgtgttaaatatgtacgccctgatgtttcctataatagcagatactgtatatttgaacaagatttttttttatcatttctatagtcttggagttcatttgtaaggcagtgtcttgacttggaaaggatgtgttaatggggtgactttgtagcatggtatgttgtcttgagttaactgtagtgggtggggaggtccaatgccctccgcaatgcccttcatctcctgtgttgtcctgtaccctgctcagctccatcctggggttcagggaaggcacacttcccagcccagctgtgttttatgtaaccgaaaataaagatgcgtggtgacaaagaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:3204 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:3204 -> Molecular function: GO:0008134 [transcription factor binding] evidence: IPI GeneID:3204 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IDA GeneID:3204 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:3204 -> Biological process: GO:0001525 [angiogenesis] evidence: IEP GeneID:3204 -> Biological process: GO:0001953 [negative regulation of cell-matrix adhesion] evidence: IDA GeneID:3204 -> Biological process: GO:0002686 [negative regulation of leukocyte migration] evidence: IDA GeneID:3204 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:3204 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: IEA GeneID:3204 -> Biological process: GO:0045617 [negative regulation of keratinocyte differentiation] evidence: IDA GeneID:3204 -> Biological process: GO:0045656 [negative regulation of monocyte differentiation] evidence: IDA GeneID:3204 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA GeneID:3204 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA GeneID:3204 -> Biological process: GO:0048704 [embryonic skeletal system morphogenesis] evidence: IEA GeneID:3204 -> Biological process: GO:0048863 [stem cell differentiation] evidence: IEA GeneID:3204 -> Cellular component: GO:0005634 [nucleus] evidence: IC
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