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KCNQ Potassium Channels

More information in Books or onNLM PubMed
Definition: A family of delayed rectifier voltage-gated potassium channels that share homology with their founding member, KCNQ1 PROTEIN. KCNQ potassium channels have been implicated in a variety of diseases including LONG QT SYNDROME; DEAFNESS; and EPILEPSY.     
Examples KCNQ1 Potassium Channel; KCNQ2 Potassium Channel; KCNQ3 Potassium Channel
Other names Potassium Channels, KvLQT; Potassium Channels, KCNQ; KvLQT Potassium Channels
 
SubstanceCAS Registry & nameCategoriesSourceDrugs*
KCNQ5 channel, mouse  0   *KCNQ Potassium Channels. Brain Res Mol Brain Res 2005 Sep 13;139(1):52-62
Kcnq5 protein, rat  0   *KCNQ Potassium Channels.
Kcnq4 protein, mouse  0   *KCNQ Potassium Channels Hearing Loss, Sensorineural.
Kcnq4 protein, rat  0   *KCNQ Potassium Channels Hearing Loss, Sensorineural.
KCNQ5 protein, human  0   *KCNQ Potassium Channels. J Biol Chem 2000 Jul 21;275(29):22395-400
KCNQ4 protein, human  0   *KCNQ Potassium Channels Hearing Loss, Sensorineural. Cell 1999 Feb 5;96(3):437-46

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
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