KCNQ5
This gene encodes a potassium channel that is thought to be extremely important for controlling neuronal excitability, especially in the sensory cells of the cochlea. M1 muscarinic acetylcholine receptors inhibit the current produced by this channel, which is then triggered by the novel anti-convulsant medication retigabine. When combined with the protein produced by the KCNQ3 gene, the encoded protein can either form a homomultimeric potassium channel or, less often, a heteromultimeric channel.
| Full Name | Potassium voltage-gated channel subfamily Q member 5 |
| Gene ID | Human: 56479 Mouse: 226922 Rat: 259273 Monkey: 715426 |
| UniProt ID | Human: Q9NR82 Mouse: Q9JK45 Rat: O88944 Monkey: F6Q5P1 |
| Alternative Names | Kv7.5; MRD46; potassium voltage-gated channel subfamily KQT member 5; KQT-like 5; potassium channel protein; potassium channel subunit alpha KvLQT5; potassium channel, voltage gated KQT-like subfamily Q, member 5; voltage-gated potassium channel subunit Kv7.5 |
Product List
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mProX™ Human KCNQ5 Stable Cell Line
[CAT#: S01YF-1123-KX34]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNQ5 Target Family: Kv7 Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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