×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
GeneticVariation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
GeneticVariation
CLINVAR
Mechanistic basis of desmosome-targeted diseases.
23911551
2013
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
GeneticVariation
CLINVAR
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy.
23381804
2013
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
CausalMutation
CLINVAR
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy.
23381804
2013
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
CausalMutation
CLINVAR
Mechanistic basis of desmosome-targeted diseases.
23911551
2013
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
CausalMutation
CLINVAR
Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.
21397041
2011
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
CausalMutation
CLINVAR
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
20400443
2010
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
CausalMutation
CLINVAR
Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy.
20864495
2010
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.700
CausalMutation
CLINVAR
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy.
16505173
2006
×
Entrez Id:
100652770
Gene Symbol:
DSG2-AS1
DSG2-AS1
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.100
CausalMutation
CLINVAR
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy.
23381804
2013
×
Entrez Id:
100652770
Gene Symbol:
DSG2-AS1
DSG2-AS1
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.100
CausalMutation
CLINVAR
Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.
21397041
2011
×
Entrez Id:
100652770
Gene Symbol:
DSG2-AS1
DSG2-AS1
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.100
CausalMutation
CLINVAR
Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy.
20864495
2010
×
Entrez Id:
100652770
Gene Symbol:
DSG2-AS1
DSG2-AS1
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.100
GeneticVariation
CLINVAR