Haematological malignancies for rare disease
Gene: FANCGEnsemblGeneIds (GRCh38): ENSG00000221829
EnsemblGeneIds (GRCh37): ENSG00000221829
OMIM: 602956, Gene2Phenotype
FANCG is in 20 panels
1 review
Clare Turnbull (Queen Mary University London)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Curated sources
- Expert Review Green
- Phenotypes
-
- Class: BM failure FA, (typ AR)
- AML
- leukaemia
- Fanconi anaemia G
- MDS
- AML, Leukaemia
- Bone marrow failure
- Head and neck and anogenital squamous cell cancers, liver cancer, esophageal cancer, Squamous cell carcinoma: oral, GI, vulvar
- OMIM
- 602956
- Clinvar variants
- Variants in FANCG
- Penetrance
- None
- Publications
- Panels with this gene
-
- Monogenic short stature
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
- Fetal anomalies
- Adult solid tumours cancer susceptibility
- Haematological malignancies cancer susceptibility
- Pigmentary skin disorders
- Cytopenias and congenital anaemias
- Primary ovarian insufficiency
- COVID-19 research
- Limb disorders
- Severe microcephaly
- Fanconi anaemia or Bloom syndrome
- Intellectual disability
- Neurofibromatosis Type 1
- Haematological malignancies for rare disease
- Head and neck cancer pertinent cancer susceptibility
- IUGR and IGF abnormalities
- Childhood solid tumours
- DDG2P
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)22nd August 2018: Reviewed by Helen Brittain, and suggested changes approved by Clare Turnbull. Changes made prior to promoting to version 1.
Added New Source
Ellen McDonagh (Genomics England Curator)FANCG was added to Haematological malignancies for rare disease panel. Sources: Expert Review Green,Curated sources
Created
Ellen McDonagh (Genomics England Curator)FANCG was created by Ellen McDonagh