node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
ADAMTS13 | DGKE | ENSCAFP00000029268 | ENSCAFP00000025617 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | Diacylglycerol kinase. | 0.811 |
ADAMTS13 | TFPI | ENSCAFP00000029268 | ENSCAFP00000021748 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | Tissue factor pathway inhibitor. | 0.564 |
ADAMTS13 | TFPI2 | ENSCAFP00000029268 | ENSCAFP00000003004 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | Tissue factor pathway inhibitor. | 0.491 |
ADAMTS13 | THBD | ENSCAFP00000029268 | ENSCAFP00000007702 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | 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). | 0.808 |
ADAMTS13 | VWF | ENSCAFP00000029268 | ENSCAFP00000053390 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | 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). | 0.928 |
DGKE | ADAMTS13 | ENSCAFP00000025617 | ENSCAFP00000029268 | Diacylglycerol kinase. | ADAM metallopeptidase with thrombospondin type 1 motif 13. | 0.811 |
DGKE | PROCR | ENSCAFP00000025617 | ENSCAFP00000052069 | Diacylglycerol kinase. | MHC_I-like_Ag-recog domain-containing protein. | 0.561 |
DGKE | THBD | ENSCAFP00000025617 | ENSCAFP00000007702 | Diacylglycerol kinase. | 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). | 0.833 |
F2 | PROC | ENSCAFP00000037638 | ENSCAFP00000064602 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | Vitamin K-dependent protein C heavy chain; Protein C is a vitamin K-dependent serine protease that regulates blood coagulation by inactivating factors Va and VIIIa in the presence of calcium ions and phospholipids. Exerts a protective effect on the endothelial cell barrier function. Belongs to the peptidase S1 family. | 0.953 |
F2 | PROCR | ENSCAFP00000037638 | ENSCAFP00000052069 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | MHC_I-like_Ag-recog domain-containing protein. | 0.738 |
F2 | SERPINC1 | ENSCAFP00000037638 | ENSCAFP00000021382 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | Serpin family C member 1; Belongs to the serpin family. | 0.998 |
F2 | TFPI | ENSCAFP00000037638 | ENSCAFP00000021748 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | Tissue factor pathway inhibitor. | 0.631 |
F2 | TFPI2 | ENSCAFP00000037638 | ENSCAFP00000003004 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | Tissue factor pathway inhibitor. | 0.440 |
F2 | THBD | ENSCAFP00000037638 | ENSCAFP00000007702 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | 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). | 0.978 |
F2 | VWF | ENSCAFP00000037638 | ENSCAFP00000053390 | Coagulation factor II, thrombin; Belongs to the peptidase S1 family. | 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). | 0.637 |
PLAT | SERPINC1 | ENSCAFP00000060201 | ENSCAFP00000021382 | Uncharacterized protein. | Serpin family C member 1; Belongs to the serpin family. | 0.635 |
PLAT | TFPI | ENSCAFP00000060201 | ENSCAFP00000021748 | Uncharacterized protein. | Tissue factor pathway inhibitor. | 0.784 |
PLAT | TFPI2 | ENSCAFP00000060201 | ENSCAFP00000003004 | Uncharacterized protein. | Tissue factor pathway inhibitor. | 0.748 |
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). | 0.794 |
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). | 0.728 |