基因名：
FANCG
产品别名：
FAG； XRCC9； FANCG； FA complementation group G； FA complementation group G； Fanconi anemia group G protein； DNA repair protein XRCC9； Fanconi anemia complementation group G； X-ray repair complementing defective repair in Chinese hamster cells 9； X-ray repair, complementing defective, in Chinese hamster, 9； DNA损伤修复基因XRCC9； 磷酸化DNA损伤修复基因XRCC9；
背景信息：
FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
