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Li, V. F9 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5506 (accessed on 21 September 2026).
Li V. F9 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5506. Accessed September 21, 2026.
Li, Vivi. "F9 Gene" Encyclopedia, https://encyclopedia.pub/entry/5506 (accessed September 21, 2026).
Li, V. (2020, December 25). F9 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5506
Li, Vivi. "F9 Gene." Encyclopedia. Web. 25 December, 2020.
F9 Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/f9

Coagulation Factor IX: The F9 gene provides instructions for making a protein called coagulation factor IX. 

genes

References

  1. Bolton-Maggs PH, Pasi KJ. Haemophilias A and B. Lancet. 2003 May24;361(9371):1801-9. Review.
  2. Bowen DJ. Haemophilia A and haemophilia B: molecular insights. Mol Pathol.2002 Apr;55(2):127-44. Review. Erratum in: Mol Pathol 2002 Jun;55(3):208.
  3. Chu K, Wu SM, Stanley T, Stafford DW, High KA. A mutation in the propeptide ofFactor IX leads to warfarin sensitivity by a novel mechanism. J Clin Invest. 1996Oct 1;98(7):1619-25.
  4. Giangrande P. Haemophilia B: Christmas disease. Expert Opin Pharmacother. 2005Aug;6(9):1517-24. Review.
  5. Kristensen SR. Warfarin treatment of a patient with coagulation factor IXpropeptide mutation causing warfarin hypersensitivity. Blood. 2002 Oct1;100(7):2676-7.
  6. Lillicrap D. The molecular basis of haemophilia B. Haemophilia. 1998Jul;4(4):350-7. Review.
  7. Oldenburg J, Kriz K, Wuillemin WA, Maly FE, von Felten A, Siegemund A, KeelingDM, Baker P, Chu K, Konkle BA, Lämmle B, Albert T; Study Group on HereditaryWarfarin Sensitivity. Genetic predisposition to bleeding during oralanticoagulant therapy: evidence for common founder mutations (FIXVal-10 andFIXThr-10) and an independent CpG hotspot mutation (FIXThr-10). Thromb Haemost.2001 Mar;85(3):454-7.
  8. Oldenburg J, Quenzel EM, Harbrecht U, Fregin A, Kress W, Müller CR, HertfelderHJ, Schwaab R, Brackmann HH, Hanfland P. Missense mutations at ALA-10 in thefactor IX propeptide: an insignificant variant in normal life but a decisivecause of bleeding during oral anticoagulant therapy. Br J Haematol. 1997Jul;98(1):240-4.
  9. Ulrich S, Brand B, Speich R, Oldenburg J, Asmis L. Congenital hypersensitivityto vitamin K antagonists due to FIX propeptide mutation at locus -10: a (not so) rare cause of bleeding under oral anticoagulant therapy in Switzerland. Swiss MedWkly. 2008 Feb 23;138(7-8):100-7. doi: 2008/07/smw-12022.
  10. Zögg T, Brandstetter H. Activation mechanisms of coagulation factor IX. BiolChem. 2009 May-Jun;390(5-6):391-400. doi: 10.1515/BC.2009.057. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
View Times: 765
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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