Multiple Tumours
Gene: FLCNEnsemblGeneIds (GRCh38): ENSG00000154803
EnsemblGeneIds (GRCh37): ENSG00000154803
OMIM: 607273, Gene2Phenotype
FLCN is in 12 panels
1 review
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Promoted from red to green, as this gene is reported as part of germline findings in the Cancer Programme, for Renal cancer.Created: 18 Apr 2017, 9:38 a.m.
Information from TruSight panel: Pathogenic Mutations are Inactivating.Created: 5 Feb 2016, 11:46 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- Birt-Hogg-Dube Syndrome
- Renal cell cancer, oncocytoma
- OMIM
- 607273
- Clinvar variants
- Variants in FLCN
- Penetrance
- Complete
- Panels with this gene
-
- Renal cancer pertinent cancer susceptibility
- Thoracic aortic aneurysm or dissection (GMS)
- Multiple monogenic benign skin tumours
- Adult solid tumours cancer susceptibility
- Familial pulmonary fibrosis
- Thoracic aortic aneurysm or dissection
- Inherited renal cancer
- Cystic kidney disease
- Ehlers Danlos syndrome with a likely monogenic cause
- Fetal anomalies
- Pneumothorax - familial
- Adult solid tumours for rare disease
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Mode of inheritance for FLCN was changed to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Created
Ellen McDonagh (Genomics England Curator)FLCN was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)FLCN was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)