Varaico: Literature-Extracted Genetic Variants

Gene:HCN4
Variant:p.S672R
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HCN4

NM_005477.3:p.S672R

Associated Papers

A rare HCN4 variant combined with sick sinus syndrome, left ventricular noncompaction, and complex congenital heart disease.

Zhang F et al.

Channels (austin, Tex.), 2025

Computational analysis of congenital heart disease associated SNPs: unveiling their impact on the gene regulatory system.

Vashisht S et al.

Bmc Genomics, 2025

39838281 (PubMed )
Supplement: 12864_2025_11232_MOESM4_ESM.xlsx › ClinVar_CHD-SNPs_uniq

The Action Potential Clamp Technique as a Tool for Risk Stratification of Sinus Bradycardia Due to Loss-of-Function Mutations in HCN4: An In Silico Exploration Based on In Vitro and In Vivo Data.

Verkerk AO et al.

Biomedicines, 2023

Channel HCN4 mutation R666Q associated with sporadic arrhythmia decreases channel electrophysiological function and increases protein degradation.

Wang H et al.

The Journal of Biological Chemistry, 2022

Altered cyclic nucleotide binding and pore opening in a diseased human HCN4 channel.

Ng LCT et al.

Biophysical Journal, 2022

Fetal Arrhythmias: Genetic Background and Clinical Implications.

Yuan SM

Pediatric Cardiology, 2019

NMR methods to dissect the molecular mechanisms of disease-related mutations (DRMs): Understanding how DRMs remodel functional free energy landscapes.

Byun JA et al.

Methods (san Diego, Calif.), 2018

Genetic Determinants of Hereditary Bradyarrhythmias: A Contemporary Review of a Diverse Group of Disorders.

Rezazadeh S et al.

The Canadian Journal of Cardiology, 2017

Free energy landscape remodeling of the cardiac pacemaker channel explains the molecular basis of familial sinus bradycardia.

Boulton S et al.

The Journal of Biological Chemistry, 2017

A gain-of-function mutation in the cardiac pacemaker HCN4 channel increasing cAMP sensitivity is associated with familial Inappropriate Sinus Tachycardia.

Baruscotti M et al.

European Heart Journal, 2017

Current understanding of the pathophysiological mechanisms responsible for inappropriate sinus tachycardia: role of the If "funny" current.

Baruscotti M et al.

Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing, 2016

The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction.

Milanesi R et al.

Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing, 2015

HCN4, Sinus Bradycardia and Atrial Fibrillation.

DiFrancesco D

Arrhythmia & Electrophysiology Review, 2015

HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy.

Milano A et al.

Journal of the American College of Cardiology, 2014

Pacemaker activity of the human sinoatrial node: effects of HCN4 mutations on the hyperpolarization-activated current.

Verkerk AO et al.

Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology, 2014

A novel HCN4 mutation, G1097W, is associated with atrioventricular block.

Zhou J et al.

Circulation Journal : Official Journal of the Japanese Circulation Society, 2014

Local and global interpretations of a disease-causing mutation near the ligand entry path in hyperpolarization-activated cAMP-gated channel.

Xu X et al.

Structure (london, England : 1993), 2012

Not very funny: how a single mutation causes heritable bradycardia.

Buraei Z et al.

Structure (london, England : 1993), 2012

Evolutionary genomics reveals the premetazoan origin of opposite gating polarity in animal-type voltage-gated ion channels.

Cai X

Genomics, 2012

The HCN4 channel mutation D553N associated with bradycardia has a C-linker mediated gating defect.

Netter MF et al.

Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology, 2012

Genetic analysis of hyperpolarization-activated cyclic nucleotide-gated cation channels in sudden unexpected death in epilepsy cases.

Tu E et al.

Brain Pathology (zurich, Switzerland), 2011

A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.

Laish-Farkash A et al.

Journal of Cardiovascular Electrophysiology, 2010

Structural basis for the cAMP-dependent gating in the human HCN4 channel.

Xu X et al.

The Journal of Biological Chemistry, 2010

PhenoHM: human-mouse comparative phenome-genome server.

Sardana D et al.

Nucleic Acids Research, 2010

20507906 (PubMed )
Supplement: gkq472_nar-00429-web-b-2010-File006.xls › MPO_to_OMIM_allelic_Variants

The Contribution of HCN4 to normal sinus node function in humans and animal models.

Nof E et al.

Pacing and Clinical Electrophysiology : Pace, 2010

Pacemaker activity of the human sinoatrial node: role of the hyperpolarization-activated current, I(f).

Verkerk AO et al.

International Journal of Cardiology, 2009

Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Ryu GM et al.

Nucleic Acids Research, 2009

19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File006.xls › TypeI-_

Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel.

Milanesi R et al.

The New England Journal of Medicine, 2006

HCN4 and arrhythmias: Insights into base mutations.

Fan W et al.

Mutation Research. Reviews in Mutation Research, 0

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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."