Atpase, h transporting, lysosomal, accessory protein 2

Preferred Label : Atpase, h transporting, lysosomal, accessory protein 2;

Symbol : ATP6AP2;

CISMeF acronym : ATP6AP2;

Type : Gene;

Alternative titles and symbols : M8-9, bovine, homolog of; Renin receptor; ATP6M8-9;

Ensembl ID : ENSG00000182220;

Prefixed ID : *300556;

Details

Origin ID

300556;

UMLS CUI

C1425435;

Automatic exact mappings (from CISMeF team)
- ATP6AP2 wt Allele [NCIt concept]
- ATPase H+ transporting accessory protein 2 [ORDO Gene]
- ATPase H+ transporting accessory protein 2 [HGNC gene]
- Prorenin Receptor [MeSH Descriptor]
- Renin Receptor [NCIt concept]
HGNC gene
- ATPase H+ transporting accessory protein 2 [HGNC gene]
NCIt concept(s)
- ATP6AP2 Gene [NCIt concept]
- ATP6AP2 wt Allele [NCIt concept]
- Renin Receptor [NCIt concept]
ORDO concept(s)
- ATPase H+ transporting accessory protein 2 [ORDO Gene]
Phenotypes related
- Congenital disorder of glycosylation, type iir [OMIM Phenotype]
- Intellectual developmental disorder, X-linked, syndromic, hedera type [OMIM Phenotype]
- Parkinsonism with spasticity, X-linked [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ATP6AP2 Gene [NCIt concept]
- ATPase H+ transporting accessory protein 2 [HGNC gene]

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