node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
ADAMTS18 | B3GLCT | ENSCAFP00000029691 | ENSCAFP00000046538 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | Beta 3-glucosyltransferase. | 0.561 |
ADAMTS18 | CCDC51 | ENSCAFP00000029691 | ENSCAFP00000018464 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | Coiled-coil domain containing 51. | 0.558 |
ADAMTS18 | CDKN1B | ENSCAFP00000029691 | ENSCAFP00000019502 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | Cyclin-dependent kinase inhibitor 1B; Important regulator of cell cycle progression. Inhibits the kinase activity of CDK2 bound to cyclin A, but has little inhibitory activity on CDK2 bound to SPDYA. Involved in G1 arrest. Potent inhibitor of cyclin E- and cyclin A-CDK2 complexes. Forms a complex with cyclin type D-CDK4 complexes and is involved in the assembly, stability, and modulation of CCND1-CDK4 complex activation. Acts either as an inhibitor or an activator of cyclin type D-CDK4 complexes depending on its phosphorylation state and/or stoichometry. | 0.559 |
ADAMTS18 | GPR84 | ENSCAFP00000029691 | ENSCAFP00000009750 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | G protein-coupled receptor 84. | 0.637 |
ADAMTS18 | HIVEP3 | ENSCAFP00000029691 | ENSCAFP00000003747 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | Human immunodeficiency virus type I enhancer binding protein 3. | 0.664 |
ADAMTS18 | MORF4L2 | ENSCAFP00000029691 | ENSCAFP00000020825 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | Mortality factor 4 like 2. | 0.701 |
ADAMTS18 | RAB3GAP2 | ENSCAFP00000029691 | ENSCAFP00000016399 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | RAB3 GTPase activating non-catalytic protein subunit 2. | 0.591 |
ADAMTS18 | REL | ENSCAFP00000029691 | ENSCAFP00000004425 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | REL proto-oncogene, NF-kB subunit. | 0.528 |
ADAMTS18 | TBC1D20 | ENSCAFP00000029691 | ENSCAFP00000040784 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | TBC1 domain family member 20. | 0.607 |
ADAMTS18 | TET2 | ENSCAFP00000029691 | ENSCAFP00000015986 | ADAM metallopeptidase with thrombospondin type 1 motif 18. | Tet methylcytosine dioxygenase 2. | 0.531 |
B3GLCT | ADAMTS18 | ENSCAFP00000046538 | ENSCAFP00000029691 | Beta 3-glucosyltransferase. | ADAM metallopeptidase with thrombospondin type 1 motif 18. | 0.561 |
CCDC51 | ADAMTS18 | ENSCAFP00000018464 | ENSCAFP00000029691 | Coiled-coil domain containing 51. | ADAM metallopeptidase with thrombospondin type 1 motif 18. | 0.558 |
CDKN1B | ADAMTS18 | ENSCAFP00000019502 | ENSCAFP00000029691 | Cyclin-dependent kinase inhibitor 1B; Important regulator of cell cycle progression. Inhibits the kinase activity of CDK2 bound to cyclin A, but has little inhibitory activity on CDK2 bound to SPDYA. Involved in G1 arrest. Potent inhibitor of cyclin E- and cyclin A-CDK2 complexes. Forms a complex with cyclin type D-CDK4 complexes and is involved in the assembly, stability, and modulation of CCND1-CDK4 complex activation. Acts either as an inhibitor or an activator of cyclin type D-CDK4 complexes depending on its phosphorylation state and/or stoichometry. | ADAM metallopeptidase with thrombospondin type 1 motif 18. | 0.559 |
CDKN1B | MORF4L2 | ENSCAFP00000019502 | ENSCAFP00000020825 | Cyclin-dependent kinase inhibitor 1B; Important regulator of cell cycle progression. Inhibits the kinase activity of CDK2 bound to cyclin A, but has little inhibitory activity on CDK2 bound to SPDYA. Involved in G1 arrest. Potent inhibitor of cyclin E- and cyclin A-CDK2 complexes. Forms a complex with cyclin type D-CDK4 complexes and is involved in the assembly, stability, and modulation of CCND1-CDK4 complex activation. Acts either as an inhibitor or an activator of cyclin type D-CDK4 complexes depending on its phosphorylation state and/or stoichometry. | Mortality factor 4 like 2. | 0.636 |
CDKN1B | REL | ENSCAFP00000019502 | ENSCAFP00000004425 | Cyclin-dependent kinase inhibitor 1B; Important regulator of cell cycle progression. Inhibits the kinase activity of CDK2 bound to cyclin A, but has little inhibitory activity on CDK2 bound to SPDYA. Involved in G1 arrest. Potent inhibitor of cyclin E- and cyclin A-CDK2 complexes. Forms a complex with cyclin type D-CDK4 complexes and is involved in the assembly, stability, and modulation of CCND1-CDK4 complex activation. Acts either as an inhibitor or an activator of cyclin type D-CDK4 complexes depending on its phosphorylation state and/or stoichometry. | REL proto-oncogene, NF-kB subunit. | 0.545 |
GPR84 | ADAMTS18 | ENSCAFP00000009750 | ENSCAFP00000029691 | G protein-coupled receptor 84. | ADAM metallopeptidase with thrombospondin type 1 motif 18. | 0.637 |
GPR84 | HIVEP3 | ENSCAFP00000009750 | ENSCAFP00000003747 | G protein-coupled receptor 84. | Human immunodeficiency virus type I enhancer binding protein 3. | 0.582 |
GPR84 | TET2 | ENSCAFP00000009750 | ENSCAFP00000015986 | G protein-coupled receptor 84. | Tet methylcytosine dioxygenase 2. | 0.556 |
HIVEP3 | ADAMTS18 | ENSCAFP00000003747 | ENSCAFP00000029691 | Human immunodeficiency virus type I enhancer binding protein 3. | ADAM metallopeptidase with thrombospondin type 1 motif 18. | 0.664 |
HIVEP3 | GPR84 | ENSCAFP00000003747 | ENSCAFP00000009750 | Human immunodeficiency virus type I enhancer binding protein 3. | G protein-coupled receptor 84. | 0.582 |