Rab39b, member ras oncogene family

Preferred Label : Rab39b, member ras oncogene family;

Symbol : RAB39B;

CISMeF acronym : RAB39B;

Type : Gene;

Alternative titles and symbols : Ras-associated protein rab39b;

Ensembl ID : ENSG00000155961;

Prefixed ID : *300774;

Details

Origin ID

300774;

UMLS CUI

C1424331;

Automatic exact mappings (from CISMeF team)
- RAB39B, member RAS oncogene family [HGNC gene]
- RAB39B, member RAS oncogene family [ORDO Gene]
HGNC gene
- RAB39B, member RAS oncogene family [HGNC gene]
NCIt concept(s)
- RAB39B Gene [NCIt concept]
- RAB39B wt Allele [NCIt concept]
- Ras-Related Protein Rab-39B [NCIt concept]
ORDO concept(s)
- RAB39B, member RAS oncogene family [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder, X-linked 72 [OMIM Phenotype]
- Waisman syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RAB39B, member RAS oncogene family [HGNC gene]

Keyword's position in hierarchy(ies) :

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