node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
CHRNA7 | GRIN1 | ENSBTAP00000020942 | ENSBTAP00000056506 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | Glutamate ionotropic receptor NMDA type subunit 1. | 0.922 |
CHRNA7 | GRIN2C | ENSBTAP00000020942 | ENSBTAP00000015137 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | Glutamate ionotropic receptor NMDA type subunit 2C. | 0.908 |
CHRNA7 | GRIN2D | ENSBTAP00000020942 | ENSBTAP00000040185 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | Glutamate ionotropic receptor NMDA type subunit 2D. | 0.924 |
CHRNA7 | P2RX1 | ENSBTAP00000020942 | ENSBTAP00000009437 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. | 0.910 |
CHRNA7 | P2RX2 | ENSBTAP00000020942 | ENSBTAP00000009869 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. | 0.902 |
CHRNA7 | P2RX4 | ENSBTAP00000020942 | ENSBTAP00000014321 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | P2X purinoceptor 4; Receptor for ATP that acts as a ligand-gated ion channel. This receptor is insensitive to the antagonists PPADS and suramin (By similarity). | 0.906 |
CHRNA7 | P2RX7 | ENSBTAP00000020942 | ENSBTAP00000011779 | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. Belongs to the P2X receptor family. | 0.906 |
GRIN1 | CHRNA7 | ENSBTAP00000056506 | ENSBTAP00000020942 | Glutamate ionotropic receptor NMDA type subunit 1. | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | 0.922 |
GRIN1 | GRIN2C | ENSBTAP00000056506 | ENSBTAP00000015137 | Glutamate ionotropic receptor NMDA type subunit 1. | Glutamate ionotropic receptor NMDA type subunit 2C. | 0.980 |
GRIN1 | GRIN2D | ENSBTAP00000056506 | ENSBTAP00000040185 | Glutamate ionotropic receptor NMDA type subunit 1. | Glutamate ionotropic receptor NMDA type subunit 2D. | 0.991 |
GRIN1 | P2RX1 | ENSBTAP00000056506 | ENSBTAP00000009437 | Glutamate ionotropic receptor NMDA type subunit 1. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. | 0.905 |
GRIN1 | P2RX2 | ENSBTAP00000056506 | ENSBTAP00000009869 | Glutamate ionotropic receptor NMDA type subunit 1. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. | 0.904 |
GRIN1 | P2RX4 | ENSBTAP00000056506 | ENSBTAP00000014321 | Glutamate ionotropic receptor NMDA type subunit 1. | P2X purinoceptor 4; Receptor for ATP that acts as a ligand-gated ion channel. This receptor is insensitive to the antagonists PPADS and suramin (By similarity). | 0.938 |
GRIN1 | P2RX7 | ENSBTAP00000056506 | ENSBTAP00000011779 | Glutamate ionotropic receptor NMDA type subunit 1. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. Belongs to the P2X receptor family. | 0.932 |
GRIN2C | CHRNA7 | ENSBTAP00000015137 | ENSBTAP00000020942 | Glutamate ionotropic receptor NMDA type subunit 2C. | Neuronal acetylcholine receptor subunit alpha-7; After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. The channel is blocked by alpha-bungarotoxin. | 0.908 |
GRIN2C | GRIN1 | ENSBTAP00000015137 | ENSBTAP00000056506 | Glutamate ionotropic receptor NMDA type subunit 2C. | Glutamate ionotropic receptor NMDA type subunit 1. | 0.980 |
GRIN2C | GRIN2D | ENSBTAP00000015137 | ENSBTAP00000040185 | Glutamate ionotropic receptor NMDA type subunit 2C. | Glutamate ionotropic receptor NMDA type subunit 2D. | 0.962 |
GRIN2C | P2RX1 | ENSBTAP00000015137 | ENSBTAP00000009437 | Glutamate ionotropic receptor NMDA type subunit 2C. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. | 0.920 |
GRIN2C | P2RX2 | ENSBTAP00000015137 | ENSBTAP00000009869 | Glutamate ionotropic receptor NMDA type subunit 2C. | P2X purinoceptor; Receptor for ATP that acts as a ligand-gated ion channel. | 0.927 |
GRIN2C | P2RX4 | ENSBTAP00000015137 | ENSBTAP00000014321 | Glutamate ionotropic receptor NMDA type subunit 2C. | P2X purinoceptor 4; Receptor for ATP that acts as a ligand-gated ion channel. This receptor is insensitive to the antagonists PPADS and suramin (By similarity). | 0.901 |