KCNQ4
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 4 |
| Gene ID | Human: 9132 Mouse: 60613 Rat: 298496 Monkey: 100426025 |
| UniProt ID | Human: P56696 Mouse: Q9JK97 Rat: Q9JK96 Monkey: F7CRG2 |
| Alternative Names | DFNA2; KV7.4; DFNA2A; potassium voltage-gated channel subfamily KQT member 4; potassium channel KQT-like 4; potassium channel subunit alpha KvLQT4; potassium channel, voltage gated KQT-like subfamily Q, member 4; potassium voltage-gated channel, KQT-like subfamily, member 4; KCNQ4; Potassium voltage-gated channel subfamily Q member 4 |
Product List
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Magic™ mPro Human KCNQ4 Cell Line
[CAT#: S01YF-1122-KX109]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNQ4 Target Family: Voltage Gated Potassium Channel Target Protein Species: Human
mProX™ Human KCNQ4 Stable Cell Line
[CAT#: S01YF-1123-KX33]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNQ4 Target Family: Kv7 Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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