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FGG gene

fibrinogen gamma chain

Key facts

Official symbol
FGG
Full name
FGG
Chromosome
4
Map location
4q32.1
Organism
Homo sapiens
NCBI Gene ID
2266

Function summary

The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing results in transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015].

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Data source: NCBI Gene · alsesAI Gene Library