Cereblon - CISMeF

Preferred Label : Cereblon;

Symbol : CRBN;

CISMeF acronym : CRBN;

Type : Gene;

Ensembl ID : ENSG00000113851;

Prefixed ID : *609262;

Details

Origin ID

609262;

UMLS CUI

C1539136;

Automatic exact mappings (from CISMeF team)
- CRBN Gene [NCIt concept]
- Protein Cereblon [NCIt concept]
- cereblon [ORDO Gene]
- cereblon [HGNC gene]
HGNC gene
- cereblon [HGNC gene]
NCIt concept(s)
- CRBN Gene [NCIt concept]
- CRBN wt Allele [NCIt concept]
- Protein Cereblon [NCIt concept]
ORDO concept(s)
- cereblon [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder, autosomal recessive 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CRBN Gene [NCIt concept]
- cereblon [HGNC gene]

Keyword's position in hierarchy(ies) :

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