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Cytopenias and congenital anaemias v1.111 | RAD51 |
Øystein Holla gene: RAD51 was added gene: RAD51 was added to Cytopenias and congenital anaemias. Sources: Literature Mode of inheritance for gene: RAD51 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: RAD51 were set to 26681308; 30907510; 26253028 Phenotypes for gene: RAD51 were set to Fanconi anemia, atypical Penetrance for gene: RAD51 were set to unknown Review for gene: RAD51 was set to GREEN Added comment: Three cases published, all with de novo variants and atypical Fanconi phenotype. Dominant negative effect. RAD51 haploinsufficiency cause mirror movements. Sources: Literature |
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Cytopenias and congenital anaemias | RAD51C | Louise Daugherty commented on RAD51C | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cytopenias and congenital anaemias | RAD51C | Helen Brittain marked RAD51C as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cytopenias and congenital anaemias | RAD51C | Helen Brittain reviewed RAD51C |