ATP6V0D2

ATP6V0D2
Identifiers
AliasesATP6V0D2, ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2, ATP6D2, VMA6, ATPase H+ transporting V0 subunit d2
External IDsMGI: 1924415 HomoloGene: 72090 GeneCards: ATP6V0D2
Orthologs
SpeciesHumanMouse
Entrez

245972

242341

Ensembl

ENSG00000147614

ENSMUSG00000028238

UniProt

Q8N8Y2

Q80SY3

RefSeq (mRNA)

NM_152565

NM_175406

RefSeq (protein)

NP_689778

NP_780615

Location (UCSC)Chr 8: 85.99 – 86.15 MbChr 4: 19.88 – 19.92 Mb
PubMed search[1][2]
Wikidata
View/Edit HumanView/Edit Mouse

ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2 is a protein in humans that is encoded by the ATP6V0D2 gene. [3] It is part of proton pumps in the plasma membranes of osteoclasts and aids with extracellular acidification in bone resorption. [4]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Mouse PubMed Reference:".
  3. ↑ "Entrez Gene: ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2". Retrieved 2012-11-12.
  4. ↑ Wu H, Xu G, Li YP (May 2009). "Atp6v0d2 is an essential component of the osteoclast-specific proton pump that mediates extracellular acidification in bone resorption". Journal of Bone and Mineral Research. 24 (5): 871–85. PMID 19113919. doi:10.1359/jbmr.081239.

Further reading

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