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, Aug 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ATP2C1-20-RE | 20 (40 μL) | 200 μL |  |
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| ATP2C1-20-OR | 20 (40 μL) | 200 μL |  |
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| ATP2C1-20-GO | 20 (40 μL) | 200 μL |  |
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| ATP2C1-20-GR | 20 (40 μL) | 200 μL |  |
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| ATP2C1-20-AQ | 20 (40 μL) | 200 μL |  |
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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, Aug 2011]
Gene Symbol : ATP2C1
Gene Name : ATPase secretory pathway Ca2+ transporting 1
Chromosome : CHR 3: 130,850,499-131,016,711
Locus : 3q22.1
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