Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2147
Gene Symbol: F2
F2
0.580 Biomarker phenotype CTD_human Pharmacological effects of a novel recombinant hirudin, CX-397, in vivo and in vitro: comparison with recombinant hirudin variant-1, heparin, and argatroban. 10064001 1999
Entrez Id: 6403
Gene Symbol: SELP
SELP
0.320 Biomarker phenotype CTD_human A flow cytometric assay of platelet activation marker P-selectin (CD62P) distinguishes heparin-induced thrombocytopenia (HIT) from HIT with thrombosis (HITT). 10544909 1999
Entrez Id: 2147
Gene Symbol: F2
F2
0.580 Biomarker phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.510 Biomarker phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.510 Therapeutic phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
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: 5624
Gene Symbol: PROC
PROC
0.340 Biomarker phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
Entrez Id: 5627
Gene Symbol: PROS1
PROS1
0.320 Biomarker phenotype CTD_human First-degree relatives with a PROS1 gene defect had a 5.0-fold higher risk of thrombosis (95% confidence interval, 1. 10706858 2000
Entrez Id: 5627
Gene Symbol: PROS1
PROS1
0.320 Biomarker phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
Entrez Id: 7056
Gene Symbol: THBD
THBD
0.310 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: 183
Gene Symbol: AGT
AGT
0.300 Biomarker phenotype CTD_human The antithrombotic effect of angiotensin-(1-7) closely resembles that of losartan. 11881036 2000
Entrez Id: 183
Gene Symbol: AGT
AGT
0.300 Therapeutic phenotype CTD_human The antithrombotic effect of angiotensin-(1-7) closely resembles that of losartan. 11881036 2000
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: 5624
Gene Symbol: PROC
PROC
0.340 GeneticVariation phenotype LHGDN The data from this model predict an increased risk of perioperative thrombosis due to inhibition of APC function in cardiac surgical patients heterozygous for the F5L mutation. 11761087 2001
Entrez Id: 2621
Gene Symbol: GAS6
GAS6
0.310 Biomarker phenotype CTD_human These findings warrant further evaluation of the possible therapeutic use of Gas6 inhibition for prevention of thrombosis. 11175853 2001
Entrez Id: 7056
Gene Symbol: THBD
THBD
0.310 Biomarker phenotype CTD_human Endothelium-specific loss of murine thrombomodulin disrupts the protein C anticoagulant pathway and causes juvenile-onset thrombosis. 11518727 2001
Entrez Id: 2212
Gene Symbol: FCGR2A
FCGR2A
0.310 Biomarker phenotype CTD_human Heparin-induced thrombocytopenia/thrombosis in a transgenic mouse model requires human platelet factor 4 and platelet activation through FcgammaRIIA. 11588041 2001
Entrez Id: 5196
Gene Symbol: PF4
PF4
0.310 Biomarker phenotype CTD_human Heparin-induced thrombocytopenia/thrombosis in a transgenic mouse model requires human platelet factor 4 and platelet activation through FcgammaRIIA. 11588041 2001
Entrez Id: 2621
Gene Symbol: GAS6
GAS6
0.310 Biomarker phenotype LHGDN These findings warrant further evaluation of the possible therapeutic use of Gas6 inhibition for prevention of thrombosis. 11175853 2001
Entrez Id: 728
Gene Symbol: C5AR1
C5AR1
0.200 Biomarker phenotype RGD The role of C5a in the development of thrombotic glomerulonephritis in rats. 11422211 2001
Entrez Id: 7450
Gene Symbol: VWF
VWF
0.340 Biomarker phenotype LHGDN Control of von Willebrand factor multimer size and implications for disease. 12163004 2002
Entrez Id: 2152
Gene Symbol: F3
F3
0.340 Biomarker phenotype CTD_human Mechanism of resveratrol-mediated suppression of tissue factor gene expression. 11858183 2002
Entrez Id: 7450
Gene Symbol: VWF
VWF
0.340 Biomarker phenotype LHGDN Functional property of von Willebrand factor under flowing blood. 11843285 2002
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1
0.340 GeneticVariation phenotype LHGDN PAI-1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs. 12353306 2002
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1
0.340 Biomarker phenotype CTD_human Well characterized atheroprotective mechanisms include inhibition of thrombosis (increased tissue-type plasminogen activator and decreased plasminogen activator inhibitor-1), inhibition of endothelial cell apoptosis, limitation of permeability (uptake of low-density lipoprotein), prevention of white blood cell binding and transmigration (no expression of adhesion molecules such as intercellular adhesion molecule-1 [ICAM-1] and vascular cell adhesion molecule-1 [VCAM-1] and no release of monocyte chemotactic protein-1) and increased bioavailability of nitric oxide (because of increased expression of endothelial nitric oxide synthase and manganese superoxide dismutase). 12677255 2002