×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
Cardiomyopathy, Dilated
0.900
GeneticVariation
CLINVAR
Neuromuscular transmission defects in myopathies: Rare but worth searching for.
30536954
2019
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Cardiomyopathy, Dilated
0.630
GeneticVariation
CLINVAR
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3.
31568572
2019
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Cardiomyopathy, Dilated
0.630
GeneticVariation
CLINVAR
RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy.
31333075
2019
×
Entrez Id:
100506866
Gene Symbol:
TTN-AS1
TTN-AS1
Cardiomyopathy, Dilated
0.100
GeneticVariation
CLINVAR
Neuromuscular transmission defects in myopathies: Rare but worth searching for.
30536954
2019
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope.
29943882
2018
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Next-Generation Sequencing to Diagnose Muscular Dystrophy, Rhabdomyolysis, and HyperCKemia.
29382405
2018
×
Entrez Id:
513
Gene Symbol:
ATP5F1D
ATP5F1D
Cardiomyopathy, Dilated
0.100
CausalMutation
CLINVAR
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
29478781
2018
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
Cardiomyopathy, Dilated
0.900
GeneticVariation
CLINVAR
Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes.
28941705
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Cardiomyopathy, Dilated
0.630
GeneticVariation
CLINVAR
Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
28669108
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Cardiomyopathy, Dilated
0.630
GeneticVariation
CLINVAR
Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.
29367539
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
28679633
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
28679633
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Limb-girdle muscular dystrophy with severe heart failure overlapping with lipodystrophy in a patient with LMNA mutation p.Ser334del.
27585670
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Lamin A/C -Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation.
28790152
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.
29237675
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.
29149195
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Massive parallel sequencing questions the pathogenic role of missense variants in dilated cardiomyopathy.
27886618
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.
28798025
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly.
27723096
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Genetic Testing in Pediatric Left Ventricular Noncompaction.
29212898
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
Cardiomyopathy, Dilated
0.430
CausalMutation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
9531
Gene Symbol:
BAG3
BAG3
Cardiomyopathy, Dilated
0.400
CausalMutation
CLINVAR
Loss-of-function mutations in co-chaperone BAG3 destabilize small HSPs and cause cardiomyopathy.
28737513
2017