Non-Fanconi anaemia
Gene: CD59EnsemblGeneIds (GRCh38): ENSG00000085063
EnsemblGeneIds (GRCh37): ENSG00000085063
OMIM: 107271, Gene2Phenotype
CD59 is in 6 panels
1 review
Helen Savage (Congenica Ltd)
Reports of mutations causing CD59-mediated haemolytic anaemia in multiple, unrelated families.Created: 27 Jan 2016, 9:28 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CD59-mediated haemolytic anaemia
Publications
Details
- Sources
-
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy, 612300
- OMIM
- 107271
- Clinvar variants
- Variants in CD59
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)CD59 was added to Non-Fanconi anaemiapanel. Source: Radboud University Medical Center, Nijmegen
Added New Source
Ellen McDonagh (Genomics England Curator)CD59 was added to Non-Fanconi anaemiapanel. Source: Radboud University Medical Center, Nijmegen
Added New Source
Ellen McDonagh (Genomics England Curator)CD59 was added to Non-Fanconi anaemiapanel. Sources: Radboud University Medical Center, Nijmegen