| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| F3 | PLAT | ENSCAFP00000063299 | ENSCAFP00000060201 | Coagulation factor III, tissue factor. | Uncharacterized protein. | 0.442 |
| F3 | PLG | ENSCAFP00000063299 | ENSCAFP00000001078 | Coagulation factor III, tissue factor. | Plasmin heavy chain A; Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation. In ovulation, weakens the walls of the Graafian follicle. It activates the urokinase-type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. Cleavage of fibronectin and laminin leads to cell detachment and apoptosis. Also cleaves fibrin, thrombospondin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be m [...] | 0.481 |
| F3 | TFPI2 | ENSCAFP00000063299 | ENSCAFP00000003004 | Coagulation factor III, tissue factor. | Tissue factor pathway inhibitor. | 0.615 |
| F3 | THBD | ENSCAFP00000063299 | ENSCAFP00000007702 | Coagulation factor III, tissue factor. | Thrombomodulin; Thrombomodulin is a specific endothelial cell receptor that forms a 1:1 stoichiometric complex with thrombin. This complex is responsible for the conversion of protein C to the activated protein C (protein Ca). Once evolved, protein Ca scissions the activated cofactors of the coagulation mechanism, factor Va and factor VIIIa, and thereby reduces the amount of thrombin generated (By similarity). | 0.584 |
| F3 | VWF | ENSCAFP00000063299 | ENSCAFP00000053390 | Coagulation factor III, tissue factor. | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.559 |
| F7 | PLG | ENSCAFP00000055494 | ENSCAFP00000001078 | Coagulation factor X. | Plasmin heavy chain A; Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation. In ovulation, weakens the walls of the Graafian follicle. It activates the urokinase-type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. Cleavage of fibronectin and laminin leads to cell detachment and apoptosis. Also cleaves fibrin, thrombospondin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be m [...] | 0.506 |
| F7 | PROCR | ENSCAFP00000055494 | ENSCAFP00000052069 | Coagulation factor X. | MHC_I-like_Ag-recog domain-containing protein. | 0.584 |
| F7 | SERPINC1 | ENSCAFP00000055494 | ENSCAFP00000021382 | Coagulation factor X. | Serpin family C member 1; Belongs to the serpin family. | 0.960 |
| F7 | SERPIND1 | ENSCAFP00000055494 | ENSCAFP00000022517 | Coagulation factor X. | Serpin family D member 1; Belongs to the serpin family. | 0.732 |
| F7 | TFPI2 | ENSCAFP00000055494 | ENSCAFP00000003004 | Coagulation factor X. | Tissue factor pathway inhibitor. | 0.641 |
| F7 | THBD | ENSCAFP00000055494 | ENSCAFP00000007702 | Coagulation factor X. | Thrombomodulin; Thrombomodulin is a specific endothelial cell receptor that forms a 1:1 stoichiometric complex with thrombin. This complex is responsible for the conversion of protein C to the activated protein C (protein Ca). Once evolved, protein Ca scissions the activated cofactors of the coagulation mechanism, factor Va and factor VIIIa, and thereby reduces the amount of thrombin generated (By similarity). | 0.449 |
| F7 | VWF | ENSCAFP00000055494 | ENSCAFP00000053390 | Coagulation factor X. | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.430 |
| PLAT | F3 | ENSCAFP00000060201 | ENSCAFP00000063299 | Uncharacterized protein. | Coagulation factor III, tissue factor. | 0.442 |
| PLAT | PLG | ENSCAFP00000060201 | ENSCAFP00000001078 | Uncharacterized protein. | Plasmin heavy chain A; Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation. In ovulation, weakens the walls of the Graafian follicle. It activates the urokinase-type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. Cleavage of fibronectin and laminin leads to cell detachment and apoptosis. Also cleaves fibrin, thrombospondin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be m [...] | 0.937 |
| PLAT | SERPINC1 | ENSCAFP00000060201 | ENSCAFP00000021382 | Uncharacterized protein. | Serpin family C member 1; Belongs to the serpin family. | 0.705 |
| PLAT | SERPIND1 | ENSCAFP00000060201 | ENSCAFP00000022517 | Uncharacterized protein. | Serpin family D member 1; Belongs to the serpin family. | 0.403 |
| PLAT | TFPI2 | ENSCAFP00000060201 | ENSCAFP00000003004 | Uncharacterized protein. | Tissue factor pathway inhibitor. | 0.696 |
| PLAT | THBD | ENSCAFP00000060201 | ENSCAFP00000007702 | Uncharacterized protein. | Thrombomodulin; Thrombomodulin is a specific endothelial cell receptor that forms a 1:1 stoichiometric complex with thrombin. This complex is responsible for the conversion of protein C to the activated protein C (protein Ca). Once evolved, protein Ca scissions the activated cofactors of the coagulation mechanism, factor Va and factor VIIIa, and thereby reduces the amount of thrombin generated (By similarity). | 0.779 |
| PLAT | VWF | ENSCAFP00000060201 | ENSCAFP00000053390 | Uncharacterized protein. | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.700 |
| PLG | F3 | ENSCAFP00000001078 | ENSCAFP00000063299 | Plasmin heavy chain A; Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation. In ovulation, weakens the walls of the Graafian follicle. It activates the urokinase-type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. Cleavage of fibronectin and laminin leads to cell detachment and apoptosis. Also cleaves fibrin, thrombospondin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be m [...] | Coagulation factor III, tissue factor. | 0.481 |