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Disease Info Card
Long Qt Syndrome
Information about Long Qt Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Long Qt Syndrome
Most recent studies have shown that Long Qt Syndrome shares some biological mechanisms with bradycardia, brugada-syndrome-(disorder), cardiac-arrest, cardiac-arrhythmia, cardiac-death, cardiac-fibrillation, cardiomyopathies, heart-diseases, heart-failure, hypertrophy, long-qt-syndrome-congenital, myocardial-infarction, polymorphic-ventricular-tachycardia, sudden-cardiac-death, sudden-death, syncope, tachycardia-ventricular, torsades-de-pointes, ventricular-fibrillation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Long Qt Syndrome, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Proliferation, Cellular Localization, Excretion, Gastric Acid Secretion, Glycosylation, Innervation, Insulin Secretion, Localization, Membrane Depolarization, Pathogenesis, Reflex, Response To Drug, Rna Interference, Secretion, Swimming, Translation, Transport, Transposition
Quite a number of genes have been found to play important roles in Long Qt Syndrome, such as ACE, COL18A1, ERG, KCNA4, KCNA5, KCNE1, KCNE2, KCNH2, KCNH6, KCNJ2, KCNK3, KCNQ1, MINK1, OXSM, PGR, SCN5A. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.