ATP2C1 Polyclonal Antibody

The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

1700121J11Rik; AT2C1; ATP dependent Ca (2+) pump PMR1; ATP-dependent Ca (2+) pump PMR1; ATP2C1; ATP2C1A; ATPase 2C1; ATPase Ca (2+) sequestering; ATPase Ca++ transporting type 2C member 1; AW061228; BCPM; Calcium transporting ATPase type 2C member 1; Calcium-transporting ATPase type 2C member 1; D930003G21Rik; HHD; hSPCA1; HUSSY 28; KIAA1347; MGC58010; MGC93231; OTTHUMP00000216066; OTTHUMP00000216068; OTTHUMP00000216069; OTTHUMP00000216071; OTTHUMP00000216072; OTTHUMP00000216073; OTTHUMP00000216074; OTTHUMP00000216075; PMR1; PMR1; rat; homolog of; PMR1L; Secretory pathway Ca (2+) ATPase 1; Secretory pathway Ca (2+) -transporting ATPase; Secretory pathway Ca2+/Mn2+ ATPase 1; SPCA; SPCA1