Cyclin d1 - CISMeF

Preferred Label : Cyclin d1;

Symbol : CCND1;

CISMeF acronym : CCND1;

Type : Gene;

Alternative titles and symbols : Parathyroid adenomatosis 1; B-cell cll/lymphoma 1; B-cell leukemia 1; PRAD1; BCL1;

Included titles and symbols : Ccnd1/ighg1 fusion gene; Ccnd1/pth fusion gene; Ccnd1/iglc1 fusion gene; Ccnd1/fstl3 fusion gene;

Ensembl ID : ENSG00000110092;

Prefixed ID : *168461;

Details

Origin ID

168461;

UMLS CUI

C1413172;

Automatic exact mappings (from CISMeF team)
- BCL1 [LOINC component]
- CCND1 Gene [NCIt concept]
- CCND1 gene [LOINC component]
- CCND1 wt Allele [NCIt concept]
- CCND1/FSTL3 Fusion Gene [NCIt concept]
- CCND1/IGHG1 Fusion Gene [NCIt concept]
- CCND1/IGLC1 Fusion Gene [NCIt concept]
- CCND1/PTH Fusion Gene [NCIt concept]
- G1/S-Specific Cyclin-D1 [NCIt concept]
- cyclin D1 [ORDO Gene]
- cyclin D1 [MeSH Descriptor]
- cyclin D1 [MeSH concept]
- cyclin D1 [HGNC gene]
- genes, bcl-1 [MeSH Descriptor]
- genes, bcl-1 [MeSH concept]
HGNC gene
- cyclin D1 [HGNC gene]
NCIt concept(s)
- BCL1 Oncogene [NCIt concept]
- CCND1 Gene [NCIt concept]
- CCND1 wt Allele [NCIt concept]
- G1/S-Specific Cyclin-D1 [NCIt concept]
- G1/S-Specific Cyclin-D1b [NCIt concept]
ORDO concept(s)
- cyclin D1 [ORDO Gene]
Phenotypes related
- Colorectal cancer [OMIM Phenotype]
- Myeloma, multiple [OMIM Phenotype]
- Von hippel-lindau syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CCND1 Gene [NCIt concept]
- CCND1 gene [LOINC component]
- CCND1/FSTL3 Fusion Gene [NCIt concept]
- CCND1/IGLC1 Fusion Gene [NCIt concept]
- CCND1/PTH Fusion Gene [NCIt concept]
- cyclin D1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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