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KCNQ2 encodes the Kv7.2 subunit, a pore-forming component of voltage-gated potassium channels crucial for generating the M-current in neurons. The M-current regulates neuronal excitability by stabilizing the resting membrane potential and controlling action potential firing thresholds. Mutations in KCNQ2 are associated with neurological disorders like Benign Familial Neonatal Seizures (BFNS) due to reduced M-current function.
Linopirdine and XE991 block KCNQ2 channels. Retigabine activates KCNQ2 channels.
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