TNNI3 - Gene browser

TNNI3

troponin I3, cardiac type

HCNC Approved Symbol: TNNI3 (HGNC:11947)
Genomic Coordinates: 19:55,151,767 - 55,157,732 (19q13.42)
Synonyms: TNNC1, CMH7, cTNI, CMD2A
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

Diagnosed Cases

114Patients

In total, 114 patients were diagnosed with a variant in the TNNI3 gene.

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

0114
Patient count

Left ventricular hypertrophy: 86 (75.4%)
Patient Count: 86 (75.4%)
% of total patients presenting each phenotype is shown in parentheses.
86 (75.4%)
Heart failure: 22 (19.3%)
Patient Count: 22 (19.3%)
% of total patients presenting each phenotype is shown in parentheses.
22 (19.3%)
Hypertrophic cardiomyopathy: 15 (13.2%)
Patient Count: 15 (13.2%)
% of total patients presenting each phenotype is shown in parentheses.
15 (13.2%)
Arrhythmias: 13 (11.4%)
Patient Count: 13 (11.4%)
% of total patients presenting each phenotype is shown in parentheses.
13 (11.4%)
Syncope: 9 (7.9%)
Patient Count: 9 (7.9%)
% of total patients presenting each phenotype is shown in parentheses.
9 (7.9%)