Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 Biomarker phenotype CTD_human [Pulmonary arterial thromboembolism and thrombophilias: optimization of diagnostics and treatment]. 16875063 2006
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 GeneticVariation phenotype LHGDN Influence of factor V HR2 on thrombin generation and clinical manifestation in rare bleeding disorders. 16772740 2005
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 GeneticVariation phenotype LHGDN HR2 haplotype in Arab population and patients with venous thrombosis in Kuwait. 15978104 2005
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 Biomarker phenotype CTD_human Factor V Leiden and G20210A prothrombin mutation and the risk of subclavian vein thrombosis in patients with breast cancer and a central venous catheter. 15033664 2004
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 GeneticVariation phenotype LHGDN Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis. 15077257 2004
Entrez Id: 2155
Gene Symbol: F7
F7
0.500 Biomarker phenotype CTD_human Administration of a small molecule tissue factor/factor VIIa inhibitor in a non-human primate thrombosis model of venous thrombosis: effects on thrombus formation and bleeding time. 14967414 2003
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 Biomarker phenotype CTD_human DVT: Factor V Leiden, a case report. 12827938 2003
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 Biomarker phenotype CTD_human Recurrent episodes of deep vein thrombosis in a young man. 12865888 2003
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 Biomarker phenotype LHGDN The relationship between FV Leiden and pulmonary embolism. 11806843 2002
Entrez Id: 2153
Gene Symbol: F5
F5
0.500 Biomarker phenotype CTD_human Detection of factor V leiden and prothrombin gene mutations in patients who died with thrombotic events. 12296757 2002
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 Biomarker phenotype CTD_human JAK2 V617F mutation, mesenteric vein thrombosis, and myeloproliferative disorders. 20434300 2010
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 GeneticVariation phenotype LHGDN Absence of the JAK2 exon 12 mutations in patients with splanchnic venous thrombosis and without overt myeloproliferative neoplasms. 19105231 2009
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 GeneticVariation phenotype LHGDN The V617F JAK 2 mutation is not a frequent event in patients with cerebral venous thrombosis without overt chronic myeloproliferative disorder. 18521518 2008
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 GeneticVariation phenotype LHGDN JAK2V617F mutation screening as part of the hypercoagulable work-up in the absence of splanchnic venous thrombosis or overt myeloproliferative neoplasm: assessment of value in a series of 664 consecutive patients. 18380991 2008
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 GeneticVariation phenotype LHGDN Venous thrombosis in oral contraceptive users and the presence of the JAK2 V617F mutation. 18327418 2008
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 GeneticVariation phenotype LHGDN A substantial proportion of patients with splanchnic venous thrombosis and a small, but significant, number of patients with CVT can be recognized as carriers of the JAK2 V617F mutation in the absence of overt signs of CMD. 17263783 2007
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 GeneticVariation phenotype LHGDN JAK2V617F prevalence and allele burden in non-splanchnic venous thrombosis in the absence of overt myeloproliferative disorder. 17460706 2007
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.460 Biomarker phenotype HPO
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.430 Biomarker phenotype CTD_human Compound heterozygous protein C deficiency in a family with venous thrombosis: Identification and in vitro study of p.Asp297His and p.Val420Leu mutations. 25748729 2015
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.430 GeneticVariation phenotype LHGDN Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients. 18160601 2008
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.430 Biomarker phenotype LHGDN Four cases of venous thrombosis in athletes with silent hereditary defects of the protein C system. 16113841 2005
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.430 Biomarker phenotype LHGDN Regulation of blood coagulation by the protein C anticoagulant pathway: novel insights into structure-function relationships and molecular recognition. 15860736 2005
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.430 Biomarker phenotype CTD_human The increase in resistance to APC was not explained by changes in protein S, protein C, or prothrombin and may contribute to the increased incidence of venous thrombosis in users of hormone replacement therapy. 12730085 2003
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.430 Biomarker phenotype HPO
Entrez Id: 93183
Gene Symbol: PIGM
PIGM
0.400 Biomarker phenotype CTD_human Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency. 16767100 2006