HAP1 knockout cell lines

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HAP1 Parental Cell Lines available

ATP6V0A2 ( Human )

Entrez Gene 23545 entrezgene 23545
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ATPase H+ transporting V0 subunit a2

Alias

ARCL | ARCL2A | ATP6A2 | ATP6N1D | J6B7 | RTF | STV1 | TJ6 | TJ6M | TJ6S | VPH1 | WSS

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].