RAB27A, member RAS oncogene family

Preferred Label : RAB27A, member RAS oncogene family;

Approved symbol HGNC : RAB27A;

Alias symbols HGNC : HsT18676; GS2; RAB27; RAM;

Chromosome HGNC : 15q21.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000069974;

Details

Origin ID

HGNC:9766;

UMLS CUI

C1419195;

Automatic exact mappings (from CISMeF team)
- Griscelli syndrome, type 2 [OMIM Phenotype]
- RAB27A, member RAS oncogene family [ORDO Gene]
- Ras-associated protein rab27a [OMIM gene]
NCIt concept
- RAB27A Gene [NCIt concept]
OMIM gene
- Ras-associated protein rab27a [OMIM gene]
Orphanet gene
- RAB27A, member RAS oncogene family [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RAB27A Gene [NCIt concept]
- Ras-associated protein rab27a [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients