Your search for "atp6v0a2" returned 197 TaqMan® SNP Genotyping Assays
ATPase H+ transporting V0 subunit a2
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]
8430408C20RIK, A2, AI385560, ARCL, ARCL2A, ATP6A2, ATP6N1D, ATP6N2, ATP6V0A2, AW489264, C76904, CC1-3, ISF, J6B7, RTF, SHIF, STV1, TJ6, TJ6M, TJ6S, V-ATPASE 116 KDA, V-ATPASE A2, VPH1, WSS
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