Multiple Tumours
Gene: MUTYHEnsemblGeneIds (GRCh38): ENSG00000132781
EnsemblGeneIds (GRCh37): ENSG00000132781
OMIM: 604933, Gene2Phenotype
MUTYH is in 10 panels
1 review
Ellen McDonagh (Genomics England Curator)
Information from TruSight panel: Pathogenic Mutations are Inactivating.Created: 5 Feb 2016, 11:46 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- Colorectal cancer, adenoma
- Familial colon cancer
- Multiple bowel polyps
- OMIM
- 604933
- Clinvar variants
- Variants in MUTYH
- Penetrance
- Complete
- Panels with this gene
-
- Colorectal cancer pertinent cancer susceptibility
- Adult solid tumours for rare disease
- Familial breast cancer
- Additional findings health related - CNV analysis adult specific
- GI tract tumours
- Additional findings health related - adult specific
- Adult solid tumours cancer susceptibility
- Inherited ovarian cancer (without breast cancer)
- Additional findings health related
- Inherited polyposis and early onset colorectal cancer - germline testing
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)MUTYH was added to Multiple Tumourspanel. Source: Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)MUTYH was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)MUTYH was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)