ATP6V1C2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

V-type proton ATPase subunit C 2 is an enzyme that in humans is encoded by the ATP6V1C2 gene.[5][6]

AliasesATP6V1C2, ATP6C2, VMA5, ATPase H+ transporting V1 subunit C2
End10,785,110 bp[1]
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ATP6V1C2
Identifiers
AliasesATP6V1C2, ATP6C2, VMA5, ATPase H+ transporting V1 subunit C2
External IDsOMIM: 618070; MGI: 1916025; HomoloGene: 15866; GeneCards: ATP6V1C2; OMA:ATP6V1C2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001039362
NM_144583

NM_001159632
NM_133699

RefSeq (protein)

NP_001034451
NP_653184

NP_001153104
NP_598460

Location (UCSC)Chr 2: 10.72 – 10.79 MbChr 12: 17.33 – 17.38 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle 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, three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. This gene encodes alternate transcriptional splice variants, encoding different V1 domain C subunit isoforms.[6]

References

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