Also known as FAF, Fanconi anemia complementation group F, FA complementation group F
Fanconi anemia group F protein is a protein that in humans is encoded by the FANCF gene.
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].
via MyGene.info
Fanconi anemia group F protein is a protein that in humans is encoded by the FANCF gene.
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).