27032235574ENSG00000017260ENSMUSG00000032570P98194Q80XR2NM_001199181NM_001199182NM_001199183NM_001199184NM_001199185NM_014382NM_001378511NM_001378512NM_001378513NM_001378514NM_001378687NM_001359823NP_001186110NP_001186111NP_001186112NP_001186113NP_001186114NP_055197NP_001365440NP_001365441NP_001365442NP_001365443NP_001365616NP_001346752Calcium-transporting ATPase type 2C member 1 is an enzyme that in humans is encoded by the ATP2C1 gene.

[5][6][7] This gene encodes one of the SPCA proteins, a Ca2+ ion-transporting P-type ATPase.

This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium.

Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder.

Alternatively spliced transcript variants encoding different isoforms have been identified.