Cullin 3 - CISMeF

Preferred Label : Cullin 3;

Symbol : CUL3;

CISMeF acronym : CUL3;

Type : Gene;

Ensembl ID : ENSG00000036257;

Prefixed ID : *603136;

Details

Origin ID

603136;

UMLS CUI

C1332811;

Automatic exact mappings (from CISMeF team)
- CUL3 Gene [NCIt concept]
- Cullin-3 [NCIt concept]
- cullin 3 [ORDO Gene]
- cullin 3 [HGNC gene]
HGNC gene
- cullin 3 [HGNC gene]
NCIt concept(s)
- CUL3 Gene [NCIt concept]
- CUL3 wt Allele [NCIt concept]
- Cullin-3 [NCIt concept]
ORDO concept(s)
- cullin 3 [ORDO Gene]
Phenotypes related
- Neurodevelopmental disorder with or without autism or seizures [OMIM Phenotype]
- Pseudohypoaldosteronism, type iie [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CUL3 Gene [NCIt concept]
- cullin 3 [HGNC gene]

Keyword's position in hierarchy(ies) :

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