×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3.
31568572
2019
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy.
31333075
2019
×
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
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
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
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
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
Usefulness of running wheel for detection of congestive heart failure in dilated cardiomyopathy mouse model.
23383212
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.
24205113
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.
24367593
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
24119082
2013
×
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
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.
22517884
2012
×
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
Cardiac structural and sarcomere genes associated with cardiomyopathy exhibit marked intolerance of genetic variation.
23074333
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Genetic testing for dilated cardiomyopathy in clinical practice.
22464770
2012
×
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
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
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
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy.
20978592
2010
×
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
GeneticVariation
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
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
CausalMutation
group
CLINVAR
[Association of TNNT2 gene mutations with idiopathic dilated cardiomyopathy in a Chengdu population].
19253838
2008