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Summary Expression Phenotypes Gene Literature (2) GO Terms (33) Nucleotides (351) Proteins (48) Interactants (47) Wiki
XB-GENEPAGE-941730
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 atp6v1b2

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ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2

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LOC108711609 ( Nomenclature history )

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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...[+]



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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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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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