Is a Gene or Genome.
"Human FANCM wild-type allele is located in the vicinity of 14q21.3 and is approximately 65 kb in length. This allele, which encodes Fanconi anemia group M protein, is involved in a specific protein ubiquination that is necessary for DNA repair. Cytogenetic aberrations in the FANCM gene are both a cause of Fanconi anemia and a predisposing factor in the development of malignancies."
FANCMA is related to the following diseases/condition. Listed after each condition are other genes/proteins which are also associated with it (Learn more about these by double clicking on them):