Adult solid tumours for rare disease
Gene: CDK4EnsemblGeneIds (GRCh38): ENSG00000135446
EnsemblGeneIds (GRCh37): ENSG00000135446
OMIM: 123829, Gene2Phenotype
CDK4 is in 7 panels
1 review
Clare Turnbull (Queen Mary University London)
Gain of functionCreated: 5 Jul 2017, 12:19 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Hereditary Melanoma
Mode of pathogenicity
Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Hereditary Melanoma
- OMIM
- 123829
- Clinvar variants
- Variants in CDK4
- Penetrance
- None
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)5th March 2018 - promoted to version 1 after expert review and internal clinical review.
Added New Source
Ellen McDonagh (Genomics England Curator)CDK4 was added to Adult solid tumours for rare disease panel. Sources: Expert list,Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)CDK4 was created by Ellen McDonagh