Multiple Tumours
Gene: FANCFEnsemblGeneIds (GRCh38): ENSG00000183161
EnsemblGeneIds (GRCh37): ENSG00000183161
OMIM: 613897, Gene2Phenotype
FANCF is in 20 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
-
- Fanconi Anemia (F)
- Myeloid hematological malignancy (leukemia, myelodysplastic syndrome)
- Squamous cell carcinoma (head and neck, esophagus, genital tract)
- Paediatric congenital malformation-dysmorphism-tumour syndromes
- OMIM
- 613897
- Clinvar variants
- Variants in FANCF
- Penetrance
- Complete
- Panels with this gene
-
- Fetal anomalies
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
- Haematological malignancies cancer susceptibility
- Cytopenias and congenital anaemias
- Intellectual disability
- Severe microcephaly
- COVID-19 research
- Limb disorders
- Monogenic short stature
- Neurofibromatosis Type 1
- Childhood solid tumours
- Haematological malignancies for rare disease
- Confirmed Fanconi anaemia or Bloom syndrome
- Pigmentary skin disorders
- Head and neck cancer pertinent cancer susceptibility
- Adult solid tumours cancer susceptibility
- IUGR and IGF abnormalities
- Primary immunodeficiency or monogenic inflammatory bowel disease
- DDG2P
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)FANCF was added to Multiple Tumourspanel. Source: Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)FANCF was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)FANCF was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)