Species: Hu, Mu, Rt
Applications: WB, ICC/IF, IHC, IP, MA
Host: Mouse Monoclonal
Species: Hu, Mu
Applications: WB, ELISA
Host: Mouse Monoclonal
Species: Hu, Ha
Applications: WB
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Description
KCNQ4 (Potassium voltage-gated channel, KQT-like subfamily, member 4) forms a potassium channel that functions in the regulation of neuronal excitability. It may be responsible for the potassium current involved in regulating the excitability of sensory cells of the cochlea. Mutations in KCNQ4 are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss.
Bioinformatics
| Entrez |
Human
Mouse
Rat
|
| Product By Gene ID |
9132 |
| Alternate Names |
- DFNA2
- DFNA2A
- KCNQ4
- KQT-like 4
- Kv7.4
- potassium channel KQT-like 4
- Potassium channel subunit alpha KvLQT4
- potassium voltage-gated channel subfamily KQT member 4
- potassium voltage-gated channel, KQT-like subfamily, member 4
- Voltage-gated potassium channel subunit Kv7.4
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