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ATP6V0A2, ATPase H+ transporting V0 subunit a2

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ATP6V0A2, 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]

  • Gene Synonyms (V-type proton ATPase 116 kDa subunit a2, V-type proton ATPase 116 kDa subunit a, A2V-ATPase, ATPase, H+ transporting, lysosomal V0 subunit a2, V-ATPase 116 kDa subunit a2, lysosomal H(+)-transporting ATPase V0 subunit a2, regeneration and tolerance factor, v-ATPase 116 kDa, v-type proton ATPase 116 kDa subunit a, vacuolar proton translocating ATPase 116 kDa subunit a, A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS,)
  • NCBI Gene ID: 23545
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9Y487
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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