coagulation factor V
Sign in to saveAlso known as Proaccelerin, labile factor, coagulation factor V jinjiang A2 domain, F5, factor V Leiden, activated protein c cofactor, coagulation factor V (proaccelerin, labile factor), Factor V
mammalian protein found in Homo sapiens
Protein · UniProt
Coagulation factor V
- Gene
- F5
- Organism
- Homo sapiens (Human)
- Length
- 2,224 aa
- Molecular mass
- 251,703 Da
- Evidence
- 1: Evidence at protein level
Central regulator of hemostasis. It serves as a critical cofactor for the prothrombinase activity of factor Xa that results in the activation of prothrombin to thrombin
3D-structureBlood coagulationCalciumCopperDisease variantDisulfide bondGlycoproteinHemostasis
View on UniProt →
Swiss-Prot (reviewed) · via UniProt
Research
11,437 papers- Congenital coagulation factor V deficiency with intracranial hemorrhage.Journal of clinical laboratory analysis · 2022
- Coagulation factor V.The international journal of biochemistry & cell biology · 2004
- Coagulation factor V and thrombophilia: background and mechanisms.Thrombosis and haemostasis · 2007
- Coagulation factor V: an old star shines again.Thrombosis and haemostasis · 1997
- Cryo-EM structure of coagulation factor V short.Blood · 2023
via PubMed
Clinical Trials
15 registered- TERMINATEDIdentify Genetic Variations That Affect The Ability of Patients To Metabolize Drugs Through Metabolic PathwaysBracane Company · NCT02525887
- COMPLETEDPrediction of Outcome in Severe PreeclampsiaCairo University · NCT03871764
- COMPLETEDStudy of Abnormal Blood Clotting in Children With StrokeNational Institute of Neurological Disorders and Stroke (NINDS) · NCT00001927
- COMPLETEDDetection of Factor V Leiden G1691A and Factor II (Prothrombin) G20210A Point Mutations in DNAIllumina, Inc. · NCT00959504
- RECRUITINGEngagement Study for Participants With Factor V Leiden and Prothrombin G20210A MutationsRichmond Research Institute · NCT07584265
- COMPLETEDAssessment of the Prevalence of Major Psychiatric Disorders in a Cohort of Women With Clinical Criteria Corresponding to Pure, Abortive-form, Obstetrical, Antiphospholipid SyndromeCentre Hospitalier Universitaire de Nīmes · NCT02833194
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protein
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chromosome
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