Undiagnosed neurocutaneous disorders
Gene: FANCAEnsemblGeneIds (GRCh38): ENSG00000187741
EnsemblGeneIds (GRCh37): ENSG00000187741
OMIM: 607139, Gene2Phenotype
FANCA is in 21 panels
0 reviews
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- UKGTN
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Fanconi anemia, complementation group A, 227650
- Fanconi Anemia
- Fanconi Anaemia
- OMIM
- 607139
- Clinvar variants
- Variants in FANCA
- Penetrance
- Complete
- Panels with this gene
-
- Adult solid tumours cancer susceptibility
- Severe microcephaly
- Haematological malignancies cancer susceptibility
- Monogenic short stature
- Cytopenias and congenital anaemias
- Primary ovarian insufficiency
- COVID-19 research
- Fanconi anaemia or Bloom syndrome
- DDG2P
- Neurofibromatosis Type 1
- Fetal anomalies
- Haematological malignancies for rare disease
- Intellectual disability
- Limb disorders
- Head and neck cancer pertinent cancer susceptibility
- Structural eye disease
- IUGR and IGF abnormalities
- Childhood solid tumours
- Pigmentary skin disorders
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)FANCA was added to Undiagnosed neurocutaneous disorderspanel. Source: UKGTN
Set Mode of Inheritance, Added New Source
Ellen McDonagh (Genomics England Curator)FANCA was added to Undiagnosed neurocutaneous disorderspanel. Source: Illumina TruGenome Clinical Sequencing Services Model of inheritance for gene FANCA was set to BIALLELIC, autosomal or pseudoautosomal
Added New Source
Ellen McDonagh (Genomics England Curator)FANCA was added to Undiagnosed neurocutaneous disorderspanel. Sources: Radboud University Medical Center, Nijmegen
Created
Ellen McDonagh (Genomics England Curator)FANCA was created by ellenmcdonagh