Dec 25, 2024 · KCNQ1 (Potassium Voltage-Gated Channel Subfamily Q Member 1) is a Protein Coding gene. Diseases associated with KCNQ1 include Long Qt Syndrome 1 and Jervell And …

The KCNQ1 gene belongs to a large family of genes that provide instructions for making potassium channels. These channels, which transport positively charged atoms (ions) of …

Gene ID: 3784, updated on 8-Feb-2025. This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form …

Apr 30, 2007 · Background— Type-1 long-QT syndrome (LQTS) is caused by loss-of-function mutations in the KCNQ1-encoded I Ks cardiac potassium channel. We evaluated the effect of …

Oct 11, 2017 · In this study, we curated from the literature a high-quality set of 107 functionally characterized KCNQ1 variants. Based on this data set, we completed a detailed quantitative …

Jan 23, 2020 · KCNQ1, also known as Kv7.1, is a voltage-dependent K + channel that regulates gastric acid secretion, salt and glucose homeostasis, and heart rhythm. Its functional …

Feb 8, 2025 · Title: Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients. A mutation in the cardiac KV7.1 channel possibly disrupts …

Oct 10, 2024 · Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. Identification of KvLQT1 K+ channels as new regulators of non-small cell lung cancer cell …

Jan 23, 2020 · KCNQ1, also known as Kv7.1, is a voltage-dependent K + channel that regulates gastric acid secretion, salt and glucose homeostasis, and heart rhythm. Its functional …

KCNQ1 (KvLTQ1) is co-assembled with the product of the KCNE1 (minimal K(+)-channel protein) gene in the heart to form a cardiac-delayed rectifier-like K(+) current. Mutations in this channel …