Varaico: Literature-Extracted Genetic Variants

Gene:KCNE3
Variant:p.V17M
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KCNE3

NM_005472.5:p.V17M

Associated Papers

Influence of genetic mutations to atria vulnerability to atrial fibrillation: An in-silico 3D human atria study.

Belletti R et al.

Computer Methods and Programs in Biomedicine, 2024

Regulation of cardiac ion channels by transcription factors: Looking for new opportunities of druggable targets for the treatment of arrhythmias.

Crespo-García T et al.

Biochemical Pharmacology, 2022

1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants.

Bajaj A et al.

Human Genomics, 2022

Inherited and Acquired Rhythm Disturbances in Sick Sinus Syndrome, Brugada Syndrome, and Atrial Fibrillation: Lessons from Preclinical Modeling.

Iop L et al.

Cells, 2021

Atrial fibrillation-a complex polygenetic disease.

Andersen JH et al.

European Journal of Human Genetics : Ejhg, 2021

33279945 (PubMed )
Supplement: 41431_2020_784_MOESM1_ESM.docx

Arrhythmogenic Effects of Genetic Mutations Affecting Potassium Channels in Human Atrial Fibrillation: A Simulation Study.

Belletti R et al.

Frontiers in Physiology, 2021

Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance.

van Lint FHM et al.

Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation, 2019

30847666 (PubMed )
Supplement: 12471_2019_1250_MOESM2_ESM.xlsx › Blad1

Novel exon 1 protein-coding regions N-terminally extend human KCNE3 and KCNE4.

Abbott GW

Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2016

Genetics of atrial fibrillation: from families to genomes.

Christophersen IE et al.

Journal of Human Genetics, 2016

Atrial fibrillation: the role of common and rare genetic variants.

Olesen MS et al.

European Journal of Human Genetics : Ejhg, 2014

Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus.

Sand PG et al.

Behavioral and Brain Functions : Bbf, 2011

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation.

Lundby A et al.

Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology, 2008

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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."