Lentiviral human ATP6V0A2 sgRNA gene knockout kit

Human ATP6V0A2

Gene symbol: ATP6V0A2
Synonyms: A2 ARCL ARCL2A ATP6A2 ATP6N1D J6B7 RTF STV1 TJ6 TJ6M TJ6S VPH1 WSS
Species: HUMAN
Gene ID: 23545
Summary: The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_012463:12:12