FANCF wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human FANCF wild-type allele is located in the vicinity of 11p15 and is approximately 3 kb in length. This allele, which encodes Fanconi anemia group F protein, may play a role in the modulation of both cell cycle progression and DNA repair. Mutation of the gene is associated with Fanconi anemia.

**Synonyms:** - FA Complementation Group F wt Allele - FAF - Fanconi Anemia Complementation Group F Gene - Fanconi Anemia, Complementation Group F Gene - MGC126856