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XB-GENEPAGE-941730
???displayGene.symbol???:
atp6v1b2
???displayGene.name???:
ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2
???displayGene.synonyms???
LOC108711609
(
Nomenclature history )
???displayGene.geneFunction???
Vacuolar H+-ATPase V1 sector, subunit B
AI Protein Function
:
The atp6v1b2 gene encodes the b2 subunit of vacuolar-type H+-ATPase (V-ATPase), a multi-subunit proton pump. This protein is an integral membrane component of the V-ATPase complex, localizing to intrac...[+]
InterPro
:
???displayGene.geneInteractants???
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Diseases:
Disease Ontology:
autosomal dominant congenital deafness with onychodystrophy
MIM:
DEAFNESS, CONGENITAL, WITH ONYCHODYSTROPHY, AUTOSOMAL DOMINANT; DDOD
External Links:
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