Lentiviral human ATP2C1 sgRNA gene knockout kit

Human ATP2C1

Gene symbol: ATP2C1
Synonyms: ATP2C1A BCPM HHD hSPCA1 PMR1 SPCA1
Species: HUMAN
Gene ID: 27032
Summary: 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].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_014382:8:8 NM_001001487:8:8 NM_001001485:9:8 NM_001001486:8:8 NM_001199179:9:8 NM_001199180:8:8 NM_001199181:8:8 NM_001199182:7:7 NM_001199183:8:7 NM_001199184:8:7 NM_001199185:8:8