Atpase, h transporting, lysosomal, 56/58-kd, v1 subunit b, isoform 2

Preferred Label : Atpase, h transporting, lysosomal, 56/58-kd, v1 subunit b, isoform 2;

Symbol : ATP6V1B2;

CISMeF acronym : ATP6V1B2;

Type : Gene;

Alternative titles and symbols : Vacuolar proton pump b isoform 2; ATP6B2;

Ensembl ID : ENSG00000147416;

Prefixed ID : *606939;

Détails

Origin ID

606939;

UMLS CUI

C1412674;

Automatic exact mappings (from CISMeF team)
- ATPase H+ transporting V1 subunit B2 [HGNC gene]
- ATPase H+ transporting V1 subunit B2 [ORDO Gene]
HGNC gene
- ATPase H+ transporting V1 subunit B2 [HGNC gene]
NCIt concept(s)
- ATP6V1B2 Gene [NCIt concept]
- ATP6V1B2 wt Allele [NCIt concept]
- V-Type Proton ATPase Subunit B, Brain Isoform [NCIt concept]
ORDO concept(s)
- ATPase H+ transporting V1 subunit B2 [ORDO Gene]
Phenotypes related
- Deafness, congenital, with onychodystrophy, autosomal dominant [OMIM Phenotype]
- Zimmermann-laband syndrome 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ATP6V1B2 Gene [NCIt concept]
- ATPase H+ transporting V1 subunit B2 [HGNC gene]

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