×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
22675533
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
11106718
2000
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.
11862580
2002
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
20031601
2009
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
15923195
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
18612386
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
15923195
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
[Association of TNNT2 gene mutations with idiopathic dilated cardiomyopathy in a Chengdu population].
19253838
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
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
0.630
CausalMutation
group
CLINVAR
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity.
23539503
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform.
15623536
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.
22517884
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
15769782
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395
2016
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
24503780
2014
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
21551322
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.
29367539
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.
11773635
2002
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
19324435
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM).
24992688
2014
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
22675533
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Cardiomyopathy-causing deletion K210 in cardiac troponin T alters phosphorylation propensity of sarcomeric proteins.
20079745
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization.
14654368
2003
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Different functional properties of troponin T mutants that cause dilated cardiomyopathy.
12923187
2003
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
17932326
2007