Official Full Name
potassium voltage-gated channel, KQT-like subfamily, member 4
The human KCNQ4 gene encodes the pore-forming subunit of Kv7.4, a voltage-gated potassium channel. KCNQ4 loss-of-function mutations cause hereditary deafness. Kv7.4 channels expressed in neurons are therapeutic targets in seizure.
KCNQ4; potassium voltage-gated channel, KQT-like subfamily, member 4; DFNA2; KV7.4; DFNA2A; potassium voltage-gated channel subfamily KQT member 4; potassium channel KQT-like 4; potassium channel subunit alpha KvLQT4; voltage-gated potassium channel subunit Kv7.4; OTTHUMP00000009219; OTTHUMP00000220901; OTTHUMP00000220902; KQT-like 4; KCNQ4 Potassium Channel