ATP2B3 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ATP2B3 wild-type allele is located within Xq28 and is approximately 65 kb in length. This allele, which encodes plasma membrane calcium-transporting ATPase 3 protein, is involved in both cation transport and ATP hydrolysis. Mutation of the gene is associated with spinocerebellar ataxia, X-linked type 1.

**Synonyms:** - ATPase Plasma Membrane Ca2+ Transporting 3 wt Allele - ATPase, Ca(2+)-Transporting, Plasma Membrane, 3 Gene - ATPase, Ca++ Transporting, Plasma Membrane 3 Gene - CLA2 - Cerebellar Ataxia 2 (X-Linked) Gene - OPCA - PMCA3 - PMCA3a - Plasma Membrane Ca(2+)-ATPase, Type 3 Gene - SCAX1 - Spinocerebellar Ataxia, X-Linked 1 Gene