Cyclin k - CISMeF

Preferred Label : Cyclin k;

Symbol : CCNK;

CISMeF acronym : CCNK;

Type : Gene;

Alternative titles and symbols : CYCK;

Ensembl ID : ENSG00000090061;

Prefixed ID : *603544;

Details

Origin ID

603544;

UMLS CUI

C1413183;

Automatic exact mappings (from CISMeF team)
- CCNK Gene [NCIt concept]
- CCNK wt Allele [NCIt concept]
- Cyclin-K [NCIt concept]
- cyclin K [HGNC gene]
HGNC gene
- cyclin K [HGNC gene]
NCIt concept(s)
- CCNK Gene [NCIt concept]
- CCNK wt Allele [NCIt concept]
- Cyclin-K [NCIt concept]
ORDO concept(s)
- cyclin K [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder with hypertelorism and distinctive facies [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CCNK Gene [NCIt concept]
- cyclin K [HGNC gene]

Keyword's position in hierarchy(ies) :

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