SATB2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SATB2 wild-type allele is located in the vicinity of 2q33 and is approximately 191 kb in length. This allele, which encodes DNA binding protein SATB2, plays roles in craniofacial development and inhibition of apoptosis. Mutations in this gene are associated with Cleft Palate.

**Synonyms:** - SATB Homeobox 2 wt Allele