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Descriptor English: KCNQ Potassium Channels
Descriptor Spanish: Canales de Potasio KCNQ
Descriptor canales del potasio KCNQ
Scope note: Familia de canales de potasio rectificadores tardíos activados por voltaje que comparten homología con su miembro fundador, la PROTEÍNA KCNQ1. Los canales de potasio KCNQ han sido implicados en diversas enfermedades, como el SÍNDROME DE QT PROLONGADO, SORDERA Y EPILEPSIA.
Descriptor Portuguese: Canais de Potássio KCNQ
Descriptor French: Canaux potassiques KNCQ
Entry term(s): KvLQT Potassium Channels
Potassium Channels, KCNQ
Potassium Channels, KvLQT
Tree number(s): D12.776.157.530.400.600.900.124.249
D12.776.543.550.450.750.900.124.249
D12.776.543.585.400.750.900.124.249
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D051656
Scope note: 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.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Public MeSH Note: 2006; KCNQ POTASSIUM CHANNELS was indexed under POTASSIUM CHANNELS, VOLTAGE-GATED 2005 & under POTASSIUM CHANNELS 1996-2004
History Note: 2006(1996)
DeCS ID: 50869
Unique ID: D051656
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2006/01/01
Date of Entry: 2005/06/30
Revision Date: 2016/07/01
KCNQ Potassium Channels - Preferred
Concept UI M0481301
Scope note 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.
Preferred term KCNQ Potassium Channels
Entry term(s) KvLQT Potassium Channels
Potassium Channels, KCNQ
Potassium Channels, KvLQT



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