Atpase, h transporting, lysosomal, v0 subunit a2

Preferred Label : Atpase, h transporting, lysosomal, v0 subunit a2;

Symbol : ATP6V0A2;

CISMeF acronym : ATP6V0A2;

Type : Gene;

Alternative titles and symbols : A2V-ATPase;

Ensembl ID : ENSG00000185344;

Prefixed ID : *611716;

Details

Origin ID

611716;

UMLS CUI

C1425544;

Automatic exact mappings (from CISMeF team)
- ATPase H+ transporting V0 subunit a2 [ORDO Gene]
- ATPase H+ transporting V0 subunit a2 [HGNC gene]
HGNC gene
- ATPase H+ transporting V0 subunit a2 [HGNC gene]
ORDO concept(s)
- ATPase H+ transporting V0 subunit a2 [ORDO Gene]
Phenotypes related
- Cutis laxa, autosomal recessive, type iia [OMIM Phenotype]
- Wrinkly skin syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ATPase H+ transporting V0 subunit a2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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