HOXA11

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Homeobox protein Hox-A11 is a protein that in humans is encoded by the HOXA11 gene.[5][6][7]

AliasesHOXA11, HOX1, HOX1I, RUSAT1, homeobox A11
End27,185,232 bp[1]
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HOXA11
Identifiers
AliasesHOXA11, HOX1, HOX1I, RUSAT1, homeobox A11
External IDsOMIM: 142958; MGI: 96172; HomoloGene: 4033; GeneCards: HOXA11; OMA:HOXA11 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005523

NM_010450

RefSeq (protein)

NP_005514

NP_034580

Location (UCSC)Chr 7: 27.18 – 27.19 MbChr 6: 52.22 – 52.22 Mb
PubMed search[3][4]
Wikidata
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Function

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 involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radioulnar synostosis with amegakaryocytic thrombocytopenia.[7]

See also

References

Further reading

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