cereblon - CISMeF

Preferred Label : cereblon;

Approved symbol HGNC : CRBN;

Alias symbols HGNC : MRT2;

Chromosome HGNC : 3p26.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000113851;

Details

Origin ID

HGNC:30185;

UMLS CUI

C1539136;

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

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