HOXA13 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HOXA13 wild-type allele is located in the vicinity of 7p15.2 and is approximately 7 kb in length. This allele, which encodes homeobox protein Hox-A13, is involved in transcriptional regulation during skeletal development. Mutation of the gene is associated with hand-foot-genital syndrome and Guttmacher syndrome.

**Synonyms:** - HOX1 - HOX1J - Homeo Box 1J Gene - Homeo Box A13 Gene - Homeobox A13 wt Allele