The F11 gene provides instructions for making a protein called factor XI. This protein plays a role in the coagulation cascade, which is a series of chemical reactions that forms blood clots in response to injury. After an injury, clots seal off blood vessels to stop bleeding and trigger blood vessel repair.
Factor XI is made primarily by cells in the liver. The protein circulates in the bloodstream and is normally turned off (inactive) until the coagulation cascade is turned on (activated) by an injury that damages blood vessels. When factor XI is activated, it interacts with other coagulation factors, resulting in conversion of an important coagulation protein called prothrombin to its active form, thrombin. Thrombin then converts a protein called fibrinogen into fibrin, which is the material that forms blood clots.
Health Conditions Related to Genetic Changes
Factor XI deficiency
About 250 mutations in the F11 gene have been found to cause a rare bleeding disorder called factor XI deficiency. This disorder, while usually mild, can cause nosebleeds, easy bruising, bleeding under the skin, bleeding of the gums, and prolonged or excessive bleeding following surgery, dental procedures, or trauma. The F11 gene mutations that cause factor XI deficiency reduce the amount of factor XI in the bloodstream or result in the production of a factor XI protein with impaired function. A deficiency of functional factor XI slows blood clotting, causing episodes of abnormal bleeding.
The amount of functional factor XI remaining varies depending on the particular mutation and whether one or both copies of the F11 gene in each cell have mutations. However, the severity of the bleeding problems in affected individuals does not necessarily correspond to the amount of factor XI in the bloodstream, and can vary even within the same family. Other genetic and environmental factors likely play a role in determining the severity of this condition.More About This Health Condition
Other Names for This Gene
- coagulation factor XI preproprotein
- plasma thromboplastin antecedent
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
- Duga S, Salomon O. Congenital factor XI deficiency: an update. Semin Thromb Hemost. 2013 Sep;39(6):621-31. doi: 10.1055/s-0033-1353420. Epub 2013 Aug 8. Citation on PubMed
- Duga S, Salomon O. Factor XI Deficiency. Semin Thromb Hemost. 2009 Jun;35(4):416-25. doi: 10.1055/s-0029-1225764. Epub 2009 Jul 13. Citation on PubMed
- Emsley J, McEwan PA, Gailani D. Structure and function of factor XI. Blood. 2010 Apr 1;115(13):2569-77. doi: 10.1182/blood-2009-09-199182. Epub 2010 Jan 28. Citation on PubMed or Free article on PubMed Central
- Gomez K, Bolton-Maggs P. Factor XI deficiency. Haemophilia. 2008 Nov;14(6):1183-9. doi: 10.1111/j.1365-2516.2008.01667.x. Epub 2008 Feb 27. Citation on PubMed
- He R, Chen D, He S. Factor XI: hemostasis, thrombosis, and antithrombosis. Thromb Res. 2012 May;129(5):541-50. doi: 10.1016/j.thromres.2011.11.051. Epub 2011 Dec 22. Citation on PubMed
- Peretz H, Salomon O, Mor-Cohen R, Usher S, Zucker M, Zivelin A, Seligsohn U. Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews. J Thromb Haemost. 2013 Apr;11(4):724-30. doi: 10.1111/jth.12137. Citation on PubMed
- Puy C, Rigg RA, McCarty OJ. The hemostatic role of factor XI. Thromb Res. 2016 May;141 Suppl 2(Suppl 2):S8-S11. doi: 10.1016/S0049-3848(16)30354-1. Citation on PubMed
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