|Homo sapiens Gene: HOXA13|
|Last Modified||2014-10-13 [Report errors or provide feedback]|
|Gene Name||homeobox A13|
|Useful resources||Stemformatics EHFPI ImmGen|
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]
|Genomic Location||Chromosome 7:27193503-27200106|
|Number of Interactions||
This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
Not yet available
|UniProt Splice Variant|
|RNA Seq Atlas|