ATP6V0D2

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

ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2 is a protein in humans that is encoded by the ATP6V0D2 gene. [5] It is part of proton pumps in the plasma membranes of osteoclasts and aids with extracellular acidification in bone resorption. [6]

AliasesATP6V0D2, ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2, ATP6D2, VMA6, ATPase H+ transporting V0 subunit d2
End86,154,225 bp[1]
Quick facts Identifiers, Aliases ...
ATP6V0D2
Identifiers
AliasesATP6V0D2, ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2, ATP6D2, VMA6, ATPase H+ transporting V0 subunit d2
External IDsOMIM: 618072; MGI: 1924415; HomoloGene: 72090; GeneCards: ATP6V0D2; OMA:ATP6V0D2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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[3][4]
Wikidata
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