×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
UNIPROT
Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.
16199542
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Low prevalence of cardiac troponin T mutations in a Greek hypertrophic cardiomyopathy cohort.
15958377
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
15769782
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
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
0.900
CausalMutation
disease
CLINVAR
[Family hypertrophic cardiomyopathy caused by a 14035c > t mutation in cardiac troponin T gene].
17456375
2007
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
17932326
2007
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
The changes of the cardiac structure and function in cTnTR141W transgenic mice.
18606313
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.
18651846
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Differential interactions of thin filament proteins in two cardiac troponin T mouse models of hypertrophic and dilated cardiomyopathies.
18349139
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Late gadolinium enhancement cardiovascular magnetic resonance in genotyped hypertrophic cardiomyopathy with normal phenotype.
19087273
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Shared genetic causes of cardiac hypertrophy in children and adults.
18403758
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Mutations in sarcomere protein genes in left ventricular noncompaction.
18506004
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
IMAGE CARDIO MED: Inducible malignant ventricular tachyarrhythmia in a patient with genotyped hypertrophic cardiomyopathy in absence of left ventricular hypertrophy or enlargement.
19487599
2009
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
Biomarker
disease
GENOMICS_ENGLAND
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
20031601
2009
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
CLINVAR
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
20031601
2009
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
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
0.900
Biomarker
disease
GENOMICS_ENGLAND
The genetics of dilated cardiomyopathy.
20186049
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
CLINVAR
Ubiquitin proteasome dysfunction in human hypertrophic and dilated cardiomyopathies.
20159828
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Cardiomyopathy-causing deletion K210 in cardiac troponin T alters phosphorylation propensity of sarcomeric proteins.
20079745
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
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
0.900
CausalMutation
disease
CLINVAR
Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging.
20439259
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
CLINVAR
Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging.
20439259
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Defective dynamic properties of human cardiac troponin mutations.
20057144
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
21551322
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
21310275
2011