| GENE NAME | TNNI3 |
| CHROMOSOME | 19 |
| ENSEMBL ID | ENSG00000129991 |
| ENTREZ ID | 7137 |
| UNIPROT ACCESSION NUMBER | P19429 |
| GO MOLECULAR FUNCTION | metal ion binding; protein binding; actin binding |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa04024; hsa04261; hsa05414; R-HSA-390522; hsa04261; hsa05414; hsa04024; hsa05410; R-HSA-5576891; R-HSA-5578775; hsa04260; R-HSA-397014; hsa05410; hsa04260 |
| 1 combination linked to TNNI3 | OLI451 |
| 1 variant linked to TNNI3 | Copy Number Variant deletion on chromosome 19 of the whole gene in the gene TNNI3 |
| 1 disease linked to TNNI3 | Hypertrophic cardiomyopathy |