ATP6V0D2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | ATP6V0D2, ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2, ATP6D2, VMA6, ATPase H+ transporting V0 subunit d2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 618072; MGI: 1924415; HomoloGene: 72090; GeneCards: ATP6V0D2; OMA:ATP6V0D2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2 is a protein in humans that is encoded by the ATP6V0D2 gene. It is part of proton pumps in the plasma membranes of osteoclasts and aids with extracellular acidification in bone resorption.
References
- ^ GRCh38: Ensembl release 89: ENSG00000147614 – Ensembl, May 2017
- ^ GRCm38: Ensembl release 89: ENSMUSG00000028238 – Ensembl, May 2017
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2". Retrieved 2012-11-12.
- 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. doi:10.1359/jbmr.081239. PMC 2672205. PMID 19113919.
External links
- Human ATP6V0D2 genome location and ATP6V0D2 gene details page in the UCSC Genome Browser.
Further reading
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