基因名：
FGG
产品别名：
FGG； fibrinogen gamma chain； fibrinogen gamma chain； fibrinogen gamma chain； fibrinogen, gamma polypeptide； testicular tissue protein Li 70； 纤维蛋白原γ(FGg)； 纤维蛋白原γ(FGg)真核蛋白； 纤维蛋白原γ链；
背景信息：
Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.
Involvement in disease: Defects in FGG are a cause of thrombophilia. Defects in FGG are a cause of congenital afibrinogenemia (CAFBN). It is a rare autosomal recessive disorder characterized by complete absence of detectable fibrinogen.
