FANCB wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human FANCB wild-type allele is located in the vicinity of Xp22.2 and is approximately 30 kb in length. This allele, which encodes Fanconi anemia group B protein, may be involved in the modulation of both protein ubiquitination and DNA repair. Mutation of the gene is associated with Fanconi anemia.

**Synonyms:** - FA Complementation Group B wt Allele - FA2 - FAAP90 - FAAP95 - FAB - FACB - FLJ34064 - Fanconi Anemia Complementation Group B Gene - Fanconi Anemia, Complementation Group B Gene - Fanconi Anemia-Associated Polypeptide, 95-kD Gene