|
| Entrez Id: |
10060 |
| Gene Symbol: |
ABCC9 |
ABCC9
|
0.300 |
GeneticVariation
|
disease |
ORPHANET |
KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation.
|
17245405 |
2007 |
|
| Entrez Id: |
2626 |
| Gene Symbol: |
GATA4 |
GATA4
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation.
|
22552926 |
2012 |
|
| Entrez Id: |
2626 |
| Gene Symbol: |
GATA4 |
GATA4
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
GATA4 loss-of-function mutations in familial atrial fibrillation.
|
21708142 |
2011 |
|
| Entrez Id: |
2626 |
| Gene Symbol: |
GATA4 |
GATA4
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Novel GATA4 mutations in lone atrial fibrillation.
|
21874226 |
2011 |
|
| Entrez Id: |
140628 |
| Gene Symbol: |
GATA5 |
GATA5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.
|
23295592 |
2012 |
|
| Entrez Id: |
140628 |
| Gene Symbol: |
GATA5 |
GATA5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.
|
23175127 |
2013 |
|
| Entrez Id: |
140628 |
| Gene Symbol: |
GATA5 |
GATA5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation.
|
22483626 |
2012 |
|
| Entrez Id: |
2627 |
| Gene Symbol: |
GATA6 |
GATA6
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation.
|
22257684 |
2012 |
|
| Entrez Id: |
2627 |
| Gene Symbol: |
GATA6 |
GATA6
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation.
|
22824924 |
2012 |
|
| Entrez Id: |
2627 |
| Gene Symbol: |
GATA6 |
GATA6
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
GATA6 loss-of-function mutation in atrial fibrillation.
|
22750565 |
2012 |
|
| Entrez Id: |
2702 |
| Gene Symbol: |
GJA5 |
GJA5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
|
20650941 |
2010 |
|
| Entrez Id: |
3741 |
| Gene Symbol: |
KCNA5 |
KCNA5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.
|
19343045 |
2009 |
|
| Entrez Id: |
3741 |
| Gene Symbol: |
KCNA5 |
KCNA5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.
|
16772329 |
2006 |
|
| Entrez Id: |
3753 |
| Gene Symbol: |
KCNE1 |
KCNE1
|
0.300 |
GeneticVariation
|
disease |
ORPHANET |
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.
|
22471742 |
2012 |
|
| Entrez Id: |
9992 |
| Gene Symbol: |
KCNE2 |
KCNE2
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.
|
15368194 |
2004 |
|
| Entrez Id: |
3759 |
| Gene Symbol: |
KCNJ2 |
KCNJ2
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
|
15922306 |
2005 |
|
| Entrez Id: |
3784 |
| Gene Symbol: |
KCNQ1 |
KCNQ1
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
KCNQ1 gain-of-function mutation in familial atrial fibrillation.
|
12522251 |
2003 |
|
| Entrez Id: |
3784 |
| Gene Symbol: |
KCNQ1 |
KCNQ1
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.
|
22471742 |
2012 |
|
| Entrez Id: |
4635 |
| Gene Symbol: |
MYL4 |
MYL4
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.
|
27066836 |
2016 |
|
| Entrez Id: |
1482 |
| Gene Symbol: |
NKX2-5 |
NKX2-5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.
|
22818067 |
2012 |
|
| Entrez Id: |
1482 |
| Gene Symbol: |
NKX2-5 |
NKX2-5
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
|
23525379 |
2013 |
|
| Entrez Id: |
137814 |
| Gene Symbol: |
NKX2-6 |
NKX2-6
|
0.300 |
SusceptibilityMutation
|
disease |
ORPHANET |
NKX2-6 mutation predisposes to familial atrial fibrillation.
|
25319568 |
2014 |
|
| Entrez Id: |
4878 |
| Gene Symbol: |
NPPA |
NPPA
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.
|
18614783 |
2008 |
|
| Entrez Id: |
9631 |
| Gene Symbol: |
NUP155 |
NUP155
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.
|
19070573 |
2008 |
|
| Entrez Id: |
5308 |
| Gene Symbol: |
PITX2 |
PITX2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|