XB-FEAT-5796324

fancf

This is the community wiki page for the gene fancf please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase

summary from NCBI

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group F. [provided by RefSeq, Jul 2008]

nomenclature changes

05.14.2018 Human name has changed for Entrez Gene: 2188. From Fanconi anemia complementation group F to FA complementation group F