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TNNC1

Gene

troponin C1, slow skeletal and cardiac type

HGNCHGNC:11943EnsemblENSG00000114854NCBI Gene7134
Locus: gene with protein productLocation: 3p21.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asTNNC
View full nomenclature history (2)
Previous symbolsTNNC
Previous namestroponin C type 1 (slow)

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Cardiomyopathy, Hypertrophic
Familial isolated dilated cardiomyopathy
Rare familial disorder with hypertrophic cardiomyopathy
Neurodegenerative Diseases
Cardiomyopathy, Dilated
Heart Failure
Cardiovascular Diseases

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

EF-hand domain containingTroponin complex subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.