Varaico: Literature-Extracted Genetic Variants

Gene:KCNE5
Variant:p.P33S
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KCNE5

NM_012282.4:p.P33S

Associated Papers

Genetic Variants in Potassium Channel Genes and Their Clinical Implications in Kazakhstani Patients with Cardiac Arrhythmias.

Chamoieva A et al.

Journal of Personalized Medicine, 2026

41745353 (PubMed )
Supplement: jpm-16-00060-s001.zip › jpm-4035150-supplementary.xlsx › Table_S2

Currently favored sampling practices for tumor sequencing can produce optimal results in the clinical setting.

Pongor LS et al.

Scientific Reports, 2020

32873813 (PubMed )
Supplement: 41598_2020_71382_MOESM6_ESM.xlsx › Hypermutating

Deletion in mice of X-linked, Brugada syndrome- and atrial fibrillation-associated Kcne5 augments ventricular KV currents and predisposes to ventricular arrhythmia.

David JP et al.

Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2019

KCNE4 and KCNE5: K(+) channel regulation and cardiac arrhythmogenesis.

Abbott GW

Gene, 2016

Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder family.

Kanters JK et al.

Scandinavian Journal of Clinical and Laboratory Investigation, 2015

Arrhythmogenic KCNE gene variants: current knowledge and future challenges.

Crump SM et al.

Frontiers in Genetics, 2014

Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk.

Mann SA et al.

Journal of the American College of Cardiology, 2012

KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients.

Palmer BR et al.

Journal of Cardiovascular Electrophysiology, 2012

The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.

Hedley PL et al.

Journal of Negative Results in Biomedicine, 2011

Potassium channel gene mutations rarely cause atrial fibrillation.

Ellinor PT et al.

Bmc Medical Genetics, 2006

[Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?].

Sinner MF et al.

Herzschrittmachertherapie & Elektrophysiologie, 2006

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation.

Ravn LS et al.

The American Journal of Cardiology, 2005

Does KCNE5 play a role in long QT syndrome?

Hofman-Bang J et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2004

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."