Fanconi Anemia Mutation Database

* Mutation in RAD51C is associated with a Fanconi anemia-like syndrome (OMIM: 613390)
**specific mutations in ERCC4 (XPF) are associated with xeroderma pigmentosum (OMIM: 278760) and XFE progeroid syndrome (OMIM: 610965)
***A dominant mutation in RAD51 is associated with a Fanconi anemia-like syndrome