Fanconi Anemia, Group G (FANCG)

Fanconi anemia, group G is an autosomal recessive disease caused by pathogenic variants in the gene FANCG. While it has been detected in multiple ethnicities, it is most prevalent in black individuals from South Africa due to the presence of a founder mutation. Clinical features include bone marrow failure and anemia due to a lack of neutrophils, platelets, and red and white blood cells. Some patients also have developmental problems of the kidneys, including missing or malformed kidneys, and/or skeletal abnormalities of the thumbs and radius. Patients also have an increased incidence of cancer. Due to bone marrow failure and the increased risk of malignancy, the life expectancy for a patient with Fanconi anemia is 29 years old, although some patients survive longer. Patients with two null variants are likely to have more severe disease than patients carrying at least one allele with residual protein function.

For information about carrier frequency and residual risk, please see the residual risk table.

This gene is included on the following panel(s):