ATP6V0A4 (Gene)

Synonyms:A4, ATP6N1B, ATP6N2, ATP6V0A4, ATPase H+ transporting V0 subunit a4, DRTA3, ENTREZ:50617, HGNC:866, MIM:605239, NM_020632, NM_130840, NM_130841, NP_065683, NP_570855, NP_570856, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2, XM_005250393, XM_005250394, XP_005250450, XP_005250451
Omim:OMIM:605239
Id:ENSG00000105929
Hgnc:HGNC:866
Entrez:50617
Description:ATPase H+ transporting V0 subunit a4
This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. This gene is one of four genes in man and mouse that encode different isoforms of the a subunit. Alternatively spliced transcript variants encoding the same protein have been described. Mutations in this gene are associated with renal tubular acidosis associated with preserved hearing. [provided by RefSeq, Jul 2008]

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