Preferred Label : ATP13A2 wt Allele;
NCIt synonyms : PARK9; Parkinson Disease (Autosomal Recessive) 9 (Kufor-Rakeb Syndrome) Gene; Probable Cation-Transporting ATPase 13A2 Gene; ATPase Cation Transporting 13A2 wt Allele; ATPase 13A2 Gene; HSA9947; KRPPD; Cation-Transporting ATPase 13A2 Gene; ATPase Type 13A2 Gene; CLN12; SPG78;
NCIt 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.;
GenBank Accession Number : AL354615;
Origin ID : C215313;
OMIM relation
- gene_found_in_organism
- gene_plays_role_in_process
