A synthesized peptide derived from human ATP2A3.
A synthesized peptide derived from human ATP2B1/2/3, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human ATP2B2, corresponding to a region within N-terminal amino acids.
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.
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