|
| 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 |
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.
|
24205113 |
2013 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
CausalMutation
|
disease |
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
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Ubiquitin proteasome dysfunction in human hypertrophic and dilated cardiomyopathies.
|
20159828 |
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 |
CausalMutation
|
disease |
CLINVAR |
The chromosome, its anatomy, and its aberrations.
|
2003160 |
1991 |
|
| 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 |
GeneticVariation
|
disease |
UNIPROT |
Sudden death due to troponin T mutations.
|
9060892 |
1997 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
Sudden death due to troponin T mutations.
|
9060892 |
1997 |
|
| 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 |
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
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
Sarcomeric hypertrophic cardiomyopathy: genetic profile in a Portuguese population.
|
22857948 |
2012 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Sarcomeric hypertrophic cardiomyopathy: genetic profile in a Portuguese population.
|
22857948 |
2012 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Sarcomere mutation-specific expression patterns in human hypertrophic cardiomyopathy.
|
25031304 |
2014 |
|
| 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 |
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 |
CausalMutation
|
disease |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.
|
12860912 |
2003 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy.
|
20624503 |
2011 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany.
|
14636924 |
2003 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
|
24119082 |
2013 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.
|
22517884 |
2012 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy.
|
9140840 |
1997 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy.
|
9140840 |
1997 |