Cullin 4b - CISMeF

Preferred Label : Cullin 4b;

Symbol : CUL4B;

CISMeF acronym : CUL4B;

Type : Gene;

Alternative titles and symbols : KIAA0695;

Ensembl ID : ENSG00000158290;

Prefixed ID : *300304;

Details

Origin ID

300304;

UMLS CUI

C1413826;

Automatic exact mappings (from CISMeF team)
- CUL4B Gene [NCIt concept]
- CUL4B wt Allele [NCIt concept]
- Cullin-4B [NCIt concept]
- cullin 4B [ORDO Gene]
- cullin 4B [HGNC gene]
HGNC gene
- cullin 4B [HGNC gene]
NCIt concept(s)
- CUL4B Gene [NCIt concept]
- CUL4B wt Allele [NCIt concept]
- Cullin-4B [NCIt concept]
ORDO concept(s)
- cullin 4B [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder, X-linked, syndromic, cabezas type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CUL4B Gene [NCIt concept]
- cullin 4B [HGNC gene]

Keyword's position in hierarchy(ies) :

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