HOXA13
Sign in to saveAlso known as HOX1, HOX1J, homeobox A13
Homeobox protein Hox-A13 is a protein that in humans is encoded by the HOXA13 gene.
Gene data
HOXA13- Name
- homeobox A13
- Type
- protein-coding
- Position
- 27,193,503–27,200,091 (−)
- Aliases
- HOX1, HOX1J
- Ensembl
- ENSG00000106031
- RefSeq RNA
- NM_000522.5
- RefSeq protein
- NP_000513.2
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. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Cellular component
via MyGene.info
Gene · Ensembl
homeobox A13
- Symbol
- HOXA13
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 7:27,193,503-27,200,091
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 73882
- exact match
- identifiers.org/ncbigene/3209
- genomic start
- 27233122
- genomic end
- 27200091
- cytogenetic location
- 7p15.2
Sources (4)
via Wikidata · CC0
~1 min read
Article
6 sectionsContents
- Function
- Clinical significance
- See also
- References
- Further reading
- External links
Homeobox protein Hox-A13 is a protein that in humans is encoded by the HOXA13 gene.
== Function ==