ATP13A2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ATP13A2 wild-type allele is located in the vicinity of 1p36.13 and is approximately 26 kb in length. This allele, which encodes polyamine-transporting ATPase 13A2 protein, is involved in cation transport, including lysosomal export of spermine. Mutation of the gene is associated with both Parkinson disease 9 and autosomal recessive spastic paraplegia 78.

**Synonyms:** - ATPase 13A2 Gene - ATPase Cation Transporting 13A2 wt Allele - ATPase Type 13A2 Gene - CLN12 - Cation-Transporting ATPase 13A2 Gene - HSA9947 - KRPPD - PARK9 - Parkinson Disease (Autosomal Recessive) 9 (Kufor-Rakeb Syndrome) Gene - Probable Cation-Transporting ATPase 13A2 Gene - SPG78