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TNNT2

—Troponin T2 Cardiac Type

Chromosome: 1

Location: 1:201359002-201379773

OMIM: 191045

Ensembl: ENSG00000118194

Official·OMIM:191045 Official·ENSG00000118194

Encodes cardiac troponin T. Mutations cause hypertrophic cardiomyopathy.

Treatment Roadmap — TNNT2

Preclinical

Phase 1

Phase 2

1 trial

Phase 3

1 trial

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Hypertrophic Cardiomyopathy

Autosomal DominantPrevalence: ~20Mcardiac

Official·OMIM:192600 Official·ORPHA217569

Summary

Clinical Trial

Approved Therapy

Registered Variant