|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome.
|
27677334 |
2016 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?
|
24529773 |
2014 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.
|
23257389 |
2013 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.
|
21051419 |
2011 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.
|
20226894 |
2010 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype.
|
20031595 |
2009 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
MGD |
Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties.
|
19351516 |
2009 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties.
|
19351516 |
2009 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Modulation of Na(v)1.5 by beta1-- and beta3-subunit co-expression in mammalian cells.
|
15455233 |
2005 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
Distinct subcellular localization of different sodium channel alpha and beta subunits in single ventricular myocytes from mouse heart.
|
15007009 |
2004 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.500 |
Biomarker
|
phenotype |
CLINGEN |
The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart.
|
11744748 |
2001 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation.
|
28217227 |
2017 |
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
|
27272739 |
2017 |
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Novel SCN10A variants associated with Brugada syndrome.
|
25842276 |
2016 |
|
| Entrez Id: |
6327 |
| Gene Symbol: |
SCN2B |
SCN2B
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Contrasting Nav1.8 Activity in Scn10a-/- Ventricular Myocytes and the Intact Heart.
|
27806966 |
2016 |
|
| Entrez Id: |
10021 |
| Gene Symbol: |
HCN4 |
HCN4
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function.
|
27553229 |
2016 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
|
| Entrez Id: |
5318 |
| Gene Symbol: |
PKP2 |
PKP2
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
|
25998140 |
2015 |
|
| Entrez Id: |
6327 |
| Gene Symbol: |
SCN2B |
SCN2B
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Scn1b deletion leads to increased tetrodotoxin-sensitive sodium current, altered intracellular calcium homeostasis and arrhythmias in murine hearts.
|
25772295 |
2015 |
|
| Entrez Id: |
3752 |
| Gene Symbol: |
KCND3 |
KCND3
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function.
|
26016905 |
2015 |
|
| Entrez Id: |
6327 |
| Gene Symbol: |
SCN2B |
SCN2B
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
|
| Entrez Id: |
5318 |
| Gene Symbol: |
PKP2 |
PKP2
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Epicardial Ventricular Tachycardia Ablation in a Patient With Brugada ECG Pattern and Mutation of PKP2 and DSP Genes.
|
25900994 |
2015 |