Haematological malignancies for rare disease
Gene: FANCD2EnsemblGeneIds (GRCh38): ENSG00000144554
EnsemblGeneIds (GRCh37): ENSG00000144554
OMIM: 613984, Gene2Phenotype
FANCD2 is in 21 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
-
- Expert Review Green
- Curated sources
- Phenotypes
-
- Class: BM failure FA, (typ AR)
- AML
- leukaemia
- Fanconi anaemia D2
- MDS
- AML, Acute myeloid leukaemia (AML)
- Bone marrow failure
- Head and neck and anogenital squamous cell cancers, liver cancer, esophageal cancer, Squamous cell carcinoma: oral, GI, vulvar
- OMIM
- 613984
- Clinvar variants
- Variants in FANCD2
- Penetrance
- None
- Publications
- Panels with this gene
-
- Monogenic short stature
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
- Intellectual disability
- Adult solid tumours cancer susceptibility
- Haematological malignancies cancer susceptibility
- Pigmentary skin disorders
- Cytopenias and congenital anaemias
- COVID-19 research
- Limb disorders
- Severe microcephaly
- Fanconi anaemia or Bloom syndrome
- Fetal anomalies
- Neurofibromatosis Type 1
- Haematological malignancies for rare disease
- Ductal plate malformation
- Head and neck cancer pertinent cancer susceptibility
- Structural eye disease
- 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)FANCD2 was added to Haematological malignancies for rare disease panel. Sources: Curated sources,Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)FANCD2 was created by Ellen McDonagh