HOXA1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HOXA1 wild-type allele is located in the vicinity of 7p15.3 and is approximately 3 kb in length. This allele, which encodes homeobox protein Hox-A1, is involved in the modulation of embryotic segment patterning. Mutation of the gene is associated with Athabaskan brainstem dysgenesis syndrome and Bosley-Salih-Alorainy syndrome.

**Synonyms:** - BSAS - HOX1 - HOX1F - Homeo Box A1 Gene - Homeobox 1F Gene - Homeobox A1 wt Allele - Hox-1.6, Mouse, Homolog of Gene - Lab, Drosophila, Homolog of Gene