Symbol: Name: ID: |
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1 GFS:2871 |
Gene name: | ATP2C1 |
Chromosome: | 3q21.3 |
Previous Symbols: | BCPM |
Previous Names: | benign chronic pemphigus (Hailey-Hailey disease) |
Aliases: | KIAA1347, ATP2C1A, PMR1, SPCA1 |
Name Aliases: | secretory pathway Ca2+/Mn2+ ATPase 1 |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | MGI:1889008 | Rat Genome Database ID: | RGD:621311 |
HGNC ID: | HGNC:13211 | RefSeq IDs: | NM_001001485 |
Entrez Gene ID: | 27032 | Ensembl Gene ID: | ENSG00000017260 |
VEGA IDs: | OTTHUMG00000136802 | UniProt ID: | P98194 |
UCSC ID: | uc003ens.2 | OMIM ID: | 604384 |
Pubmed: | PMID10615129 PMID 10767338 | ||
CCDS IDs: | CCDSCCDS33856.1 CCDS CCDS46912.1 CCDS CCDS46913.1 CCDS CCDS46914.1 |
Calcium-transporting ATPase type 2C member 1 is an enzyme that in humans is encoded by the ATP2C1 gene.
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. [provided by RefSeq].
Function: This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium.
Products for ATP2C1 gene
Catalog | Product Name | Application | Company |
GFS:E02871 | ATPase, Ca++ transporting, type 2C, member 1; ELISA kit | ELISA | n/a |
GFS:A02871 | ATPase, Ca++ transporting, type 2C, member 1; Anti | ANTIBODIES | n/a |
GFS:P02871 | ATPase, Ca++ transporting, type 2C, member 1; Protien | Protien | n/a |