Atpase, h transporting, lysosomal, v0 subunit a1

Preferred Label : Atpase, h transporting, lysosomal, v0 subunit a1;

Symbol : ATP6V0A1;

CISMeF acronym : ATP6V0A1;

Type : Gene;

Alternative titles and symbols : Atpase, h transporting, lysosomal, noncatalytic accessory protein 1a; Vacuolar proton pump, subunit 1; ATP6N1A; ATP6N1; VPP1;

Ensembl ID : ENSG00000033627;

Prefixed ID : *192130;

Details

Origin ID

192130;

UMLS CUI

C1412685;

Automatic exact mappings (from CISMeF team)
- ATP6V0A1 Gene [NCIt concept]
- ATP6V0A1 wt Allele [NCIt concept]
- ATPase H+ transporting V0 subunit a1 [HGNC gene]
- V-Type Proton ATPase 116 kDa Subunit A 1 [NCIt concept]
HGNC gene
- ATPase H+ transporting V0 subunit a1 [HGNC gene]
NCIt concept(s)
- ATP6V0A1 Gene [NCIt concept]
- ATP6V0A1 wt Allele [NCIt concept]
- V-Type Proton ATPase 116 kDa Subunit A 1 [NCIt concept]
Phenotypes related
- Developmental and epileptic encephalopathy 104 [OMIM Phenotype]
- Neurodevelopmental disorder with epilepsy and brain atrophy [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ATP6V0A1 Gene [NCIt concept]
- ATPase H+ transporting V0 subunit a1 [HGNC gene]

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