Potassium voltage-gated channel subfamily KQT member 4, also known as voltage-gated potassium channel subunit Kv7.4, is a protein that in humans is encoded by the KCNQ4 gene.
Function The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene.
Clinical significance The current generated by this channel is inhibited by muscarinic acetylcholine receptor M1 and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene.
Ligands ML213: KCNQ2/Q4 channel opener.
See also Voltage-gated potassium channel
References
Further reading
External links GeneReviews/NCBI/NIH/UW entry on Deafness and Hereditary Hearing Loss Overview KCNQ4+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) GeneReviews/NCBI/NIH/UW entry on DFNA2 Nonsyndromic Hearing Loss
This article incorporates text from the United States National Library of Medicine, which is in the public domain.






