STK32B wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human STK32B wild-type allele is located in the vicinity of 4p16.2 and is approximately 450 kb in length. This allele, which encodes serine/threonine-protein kinase 32B protein, plays a role in limb development. Deletion of the gene is associated with the autosomal recessive skeletal dysplasia, Ellis-van Creveld syndrome.

**Synonyms:** - HSA250839 - STK32 - STKG6 - Serine/Threonine Kinase 32B wt Allele - UNQ3003/PRO9744 - YANK2