TNNT2 - Gene browser

TNNT2

troponin T2, cardiac type

HCNC Approved Symbol: TNNT2 (HGNC:11949)
Genomic Coordinates: 1:201,359,014 - 201,377,680 (1q32.1)
Synonyms: CMPD2, CMH2, CMD1D
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

Diagnosed Cases

39Patients

In total, 39 patients were diagnosed with a variant in the TNNT2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

039
Patient count

Left ventricular hypertrophy: 19 (48.7%)
Patient Count: 19 (48.7%)
% of total patients presenting each phenotype is shown in parentheses.
19 (48.7%)
Heart failure: 6 (15.4%)
Patient Count: 6 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
6 (15.4%)
Dilated cardiomyopathy: 4 (10.3%)
Patient Count: 4 (10.3%)
% of total patients presenting each phenotype is shown in parentheses.
4 (10.3%)
Hypertrophic cardiomyopathy: 4 (10.3%)
Patient Count: 4 (10.3%)
% of total patients presenting each phenotype is shown in parentheses.
4 (10.3%)
Hypertension: 3 (7.7%)
Patient Count: 3 (7.7%)
% of total patients presenting each phenotype is shown in parentheses.
3 (7.7%)