TNNT1 - Gene browser

TNNT1

troponin T1, slow skeletal type

HCNC Approved Symbol: TNNT1 (HGNC:11948)
Genomic Coordinates: 19:55,132,698 - 55,149,206 (19q13.42)
Synonyms: ANM, STNT, TNT, TNTS, FLJ98147, MGC104241, NEM5
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the TNNT1 gene.

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

03
Patient count

Myopathy: 3 (100.0%)
Patient Count: 3 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (100.0%)
Distal muscular weakness: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Muscular dystrophy, congenital: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Congenital muscular dystrophy: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)