| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| LOC100125495 | nthl1 | ENSORLP00000008514 | ENSORLP00000014640 | Beta-carotene oxygenase 1. | Endonuclease III-like protein 1; Bifunctional DNA N-glycosylase with associated apurinic/apyrimidinic (AP) lyase function that catalyzes the first step in base excision repair (BER), the primary repair pathway for the repair of oxidative DNA damage. The DNA N-glycosylase activity releases the damaged DNA base from DNA by cleaving the N-glycosidic bond, leaving an AP site. The AP lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination. Primarily recognizes and repairs oxidative base damage of pyrimidines; Belongs to the Nth/MutY family. | 0.602 |
| LOC100125495 | pkd1l2 | ENSORLP00000008514 | ENSORLP00000009492 | Beta-carotene oxygenase 1. | Polycystic kidney disease 1 like 2a. | 0.685 |
| LOC101173336 | pkd1l2 | ENSORLP00000020021 | ENSORLP00000009492 | Glypican 1b; Cell surface proteoglycan that bears heparan sulfate. Belongs to the glypican family. | Polycystic kidney disease 1 like 2a. | 0.610 |
| LOC101173336 | ttc17 | ENSORLP00000020021 | ENSORLP00000044907 | Glypican 1b; Cell surface proteoglycan that bears heparan sulfate. Belongs to the glypican family. | Tetratricopeptide repeat domain 17. | 0.519 |
| dhodh | pkd1l2 | ENSORLP00000007295 | ENSORLP00000009492 | Dihydroorotate dehydrogenase (quinone), mitochondrial; Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily. | Polycystic kidney disease 1 like 2a. | 0.639 |
| dhodh | pkd2l1 | ENSORLP00000007295 | ENSORLP00000017222 | Dihydroorotate dehydrogenase (quinone), mitochondrial; Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily. | EF-hand domain-containing protein. | 0.524 |
| dhodh | slc9a3r2 | ENSORLP00000007295 | ENSORLP00000014675 | Dihydroorotate dehydrogenase (quinone), mitochondrial; Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily. | Uncharacterized protein. | 0.503 |
| nthl1 | LOC100125495 | ENSORLP00000014640 | ENSORLP00000008514 | Endonuclease III-like protein 1; Bifunctional DNA N-glycosylase with associated apurinic/apyrimidinic (AP) lyase function that catalyzes the first step in base excision repair (BER), the primary repair pathway for the repair of oxidative DNA damage. The DNA N-glycosylase activity releases the damaged DNA base from DNA by cleaving the N-glycosidic bond, leaving an AP site. The AP lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination. Primarily recognizes and repairs oxidative base damage of pyrimidines; Belongs to the Nth/MutY family. | Beta-carotene oxygenase 1. | 0.602 |
| nthl1 | pkd1l2 | ENSORLP00000014640 | ENSORLP00000009492 | Endonuclease III-like protein 1; Bifunctional DNA N-glycosylase with associated apurinic/apyrimidinic (AP) lyase function that catalyzes the first step in base excision repair (BER), the primary repair pathway for the repair of oxidative DNA damage. The DNA N-glycosylase activity releases the damaged DNA base from DNA by cleaving the N-glycosidic bond, leaving an AP site. The AP lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination. Primarily recognizes and repairs oxidative base damage of pyrimidines; Belongs to the Nth/MutY family. | Polycystic kidney disease 1 like 2a. | 0.598 |
| pkd1l2 | LOC100125495 | ENSORLP00000009492 | ENSORLP00000008514 | Polycystic kidney disease 1 like 2a. | Beta-carotene oxygenase 1. | 0.685 |
| pkd1l2 | LOC101173336 | ENSORLP00000009492 | ENSORLP00000020021 | Polycystic kidney disease 1 like 2a. | Glypican 1b; Cell surface proteoglycan that bears heparan sulfate. Belongs to the glypican family. | 0.610 |
| pkd1l2 | dhodh | ENSORLP00000009492 | ENSORLP00000007295 | Polycystic kidney disease 1 like 2a. | Dihydroorotate dehydrogenase (quinone), mitochondrial; Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily. | 0.639 |
| pkd1l2 | nthl1 | ENSORLP00000009492 | ENSORLP00000014640 | Polycystic kidney disease 1 like 2a. | Endonuclease III-like protein 1; Bifunctional DNA N-glycosylase with associated apurinic/apyrimidinic (AP) lyase function that catalyzes the first step in base excision repair (BER), the primary repair pathway for the repair of oxidative DNA damage. The DNA N-glycosylase activity releases the damaged DNA base from DNA by cleaving the N-glycosidic bond, leaving an AP site. The AP lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination. Primarily recognizes and repairs oxidative base damage of pyrimidines; Belongs to the Nth/MutY family. | 0.598 |
| pkd1l2 | pkd2 | ENSORLP00000009492 | ENSORLP00000031188 | Polycystic kidney disease 1 like 2a. | Polycystin-2; Component of a heteromeric calcium-permeable ion channel formed by PKD1 and PKD2 that is activated by interaction between PKD1 and a Wnt family member, such as WNT3A and WNT9B. Can also form a functional, homotetrameric ion channel (By similarity). Functions as non-selective, voltage-gated cation channel. Required for normal oscillation of Ca(2+) levels within cilia; these oscillations of the intraciliary Ca(2+) levels can trigger cytoplasmic Ca(2+) signaling cascades (By similarity). May contribute to the release of Ca(2+) stores from the endoplasmic reticulum (By simila [...] | 0.762 |
| pkd1l2 | pkd2l1 | ENSORLP00000009492 | ENSORLP00000017222 | Polycystic kidney disease 1 like 2a. | EF-hand domain-containing protein. | 0.807 |
| pkd1l2 | slc9a3r2 | ENSORLP00000009492 | ENSORLP00000014675 | Polycystic kidney disease 1 like 2a. | Uncharacterized protein. | 0.611 |
| pkd1l2 | ttc17 | ENSORLP00000009492 | ENSORLP00000044907 | Polycystic kidney disease 1 like 2a. | Tetratricopeptide repeat domain 17. | 0.856 |
| pkd1l2 | ttc19 | ENSORLP00000009492 | ENSORLP00000008680 | Polycystic kidney disease 1 like 2a. | Tetratricopeptide repeat domain 19. | 0.613 |
| pkd1l2 | zc3h14 | ENSORLP00000009492 | ENSORLP00000011350 | Polycystic kidney disease 1 like 2a. | Zinc finger CCCH-type containing 14. | 0.599 |
| pkd2 | pkd1l2 | ENSORLP00000031188 | ENSORLP00000009492 | Polycystin-2; Component of a heteromeric calcium-permeable ion channel formed by PKD1 and PKD2 that is activated by interaction between PKD1 and a Wnt family member, such as WNT3A and WNT9B. Can also form a functional, homotetrameric ion channel (By similarity). Functions as non-selective, voltage-gated cation channel. Required for normal oscillation of Ca(2+) levels within cilia; these oscillations of the intraciliary Ca(2+) levels can trigger cytoplasmic Ca(2+) signaling cascades (By similarity). May contribute to the release of Ca(2+) stores from the endoplasmic reticulum (By simila [...] | Polycystic kidney disease 1 like 2a. | 0.762 |