IUGR and IGF abnormalities
Gene: FANCFEnsemblGeneIds (GRCh38): ENSG00000183161
EnsemblGeneIds (GRCh37): ENSG00000183161
OMIM: 613897, Gene2Phenotype
FANCF is in 20 panels
1 review
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Is on the non-fanconi gene panel, and should be included as green on this panel.Created: 7 Jun 2016, 12:38 p.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert review
- Phenotypes
-
- Fanconi Anemia
- Fanconi anemia, complementation group F, 603467
- Fanconi anemia
- OMIM
- 613897
- Clinvar variants
- Variants in FANCF
- Penetrance
- Complete
- Panels with this gene
-
- Adult solid tumours cancer susceptibility
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Haematological malignancies cancer susceptibility
- Severe microcephaly
- Monogenic short stature
- Cytopenias and congenital anaemias
- COVID-19 research
- Fanconi anaemia or Bloom syndrome
- Neurofibromatosis Type 1
- Haematological malignancies for rare disease
- Intellectual disability
- Fetal anomalies
- Limb disorders
- Head and neck cancer pertinent cancer susceptibility
- IUGR and IGF abnormalities
- Childhood solid tumours
- DDG2P
- Pigmentary skin disorders
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)FANCF was added to IUGR and IGF abnormalitiespanel. Sources: Expert review
Created
Ellen McDonagh (Genomics England Curator)FANCF was created by ellenmcdonagh