GI tract tumours
Gene: CDKN2AEnsemblGeneIds (GRCh38): ENSG00000147889
EnsemblGeneIds (GRCh37): ENSG00000147889
OMIM: 600160, Gene2Phenotype
CDKN2A is in 12 panels
1 review
Ian Frayling (Cardiff University)
May possibly act as a modifier of colorectal cancer risk, but no evidence that this is a major predisposition locusCreated: 8 Dec 2015, 2:15 p.m.
Details
- Sources
-
- Emory Genetics Laboratory
- Phenotypes
-
- Gastrointestinal and Colorectal Cancer
- OMIM
- 600160
- Clinvar variants
- Variants in CDKN2A
- Penetrance
- Complete
- Panels with this gene
-
- Inherited pancreatic cancer
- Multiple monogenic benign skin tumours
- Adult solid tumours for rare disease
- Adult solid tumours cancer susceptibility
- GI tract tumours
- Bilateral congenital or childhood onset cataracts
- Familial melanoma
- Cytopenias and congenital anaemias
- Melanoma pertinent cancer susceptibility
- Familial tumours of the nervous system
- Childhood solid tumours
- Pigmentary skin disorders
History Filter Activity
panel promoted to version 1
Sarah Leigh (Genomics England Curator)This panel has been formed as a result of merging Familial colon cancer (Version 1.5), Multiple bowel polyps (Version 1.9), Peutz-Jeghers syndrome (Version 0.20) panels and copying the reviews from each panel into this united GI Tract panel
Added New Source
Ellen McDonagh (Genomics England Curator)CDKN2A was added to GI tractpanel. Sources: Emory Genetics Laboratory
Created
Ellen McDonagh (Genomics England Curator)CDKN2A was created by ellenmcdonagh