×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
Biomarker
group
HPO
×
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
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy.
11684629
2001
×
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
GeneticVariation
group
BEFREE
TNNT2 mutations can also lead to dilated cardiomyopathy , a leading cause of heart failure.
11967535
2002
×
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
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
CausalMutation
group
CLINVAR
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
15542288
2004
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
15542288
2004
×
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
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
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
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
Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.
15464434
2005
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
Biomarker
group
CTD_human
Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation.
17556660
2007
×
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
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
Biomarker
group
MGD
Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation.
17556660
2007
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
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
×
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
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Mutations in sarcomere protein genes in left ventricular noncompaction.
18506004
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
GeneticVariation
group
CLINVAR
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
19412328
2008
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.630
CausalMutation
group
CLINVAR
Mutations in sarcomere protein genes in left ventricular noncompaction.
18506004
2008
×
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