Gene: F5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 AlteredExpression phenotype LHGDN Factor V Leiden causing activated protein C resistance is the most common inherited form of thrombophilia leading to thrombosis. 17456626 2007
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 Biomarker phenotype LHGDN The roles of factor V Hong Kong (FV Hong Kong), factor V Leiden (FV Leiden), factor II G20210A (FII G20210A), methylenetetrahydrofolate reductase (MTHFR) C677T, and MTHFR A1298C mutations in Turkish patients with thrombosis (270 patients) compared with healthy controls (114 subjects) were evaluated. 17911197 2007
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 Biomarker phenotype LHGDN ABO blood group genotypes and the risk of venous thrombosis: effect of factor V Leiden. 15634288 2005
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 GeneticVariation phenotype LHGDN The G20210A prothrombin gene, factor V Leiden, and MTHFR C677T mutations have been identified as predisposing genetic factors for thrombosis. 15958894 2005
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 GeneticVariation phenotype LHGDN Absence of factor V Arg306--Thr and low factor V Arg306->Gly mutation prevalence in Thai blood donors. 15691154 2004
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 GeneticVariation phenotype LHGDN Functional characterization of factor V-Ile359Thr: a novel mutation associated with thrombosis. 14695241 2004
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 GeneticVariation phenotype LHGDN These data suggested that the factor V Leiden mutation might be a risk factor for the development of thrombosis in Behcet's disease patients. 12632020 2003
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 GeneticVariation phenotype LHGDN Factor V(LEIDEN) and cardiopulmonary bypass: investigation of haemostatic parameters and the effect of aprotinin using an ex vivo model. 11761087 2001
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 Biomarker phenotype CTD_human Although larger studies are required, this case report suggests that thrombomodulin gene mutations could be an additional genetic risk factor for thrombosis in carriers of the factor V Leiden mutation. 11132655 2000
Entrez Id: 2153
Gene Symbol: F5
F5 		0.380 Biomarker phenotype CTD_human Lipoprotein (a): its role in childhood thromboembolism. 9164807 1997