# Troponin T1, slow skeletal type

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21116980](https://www.wikidata.org/wiki/Q21116980)  
**Source**: https://4ort.xyz/entity/troponin-t1-slow-skeletal-type


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P13805)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13805&geneProductId=UniProtKB:P13805)
5. [Cellular Fate of Truncated Slow Skeletal Muscle Troponin T Produced by Glu180 Nonsense Mutation in Amish Nemaline Myopathy](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13805&geneProductId=UniProtKB:P13805)
6. [A Proteome-Scale Map of the Human Interactome Network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
7. [Next-generation sequencing to generate interactome datasets](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
9. [Cellular Fate of Truncated Slow Skeletal Muscle Troponin T Produced by Glu180 Nonsense Mutation in Amish Nemaline Myopathy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
11. [A Troponin T Mutation That Causes Infantile Restrictive Cardiomyopathy Increases Ca2+ Sensitivity of Force Development and Impairs the Inhibitory Properties of Troponin](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13805&geneProductId=UniProtKB:P13805)
12. [A Troponin T Mutation That Causes Infantile Restrictive Cardiomyopathy Increases Ca2+ Sensitivity of Force Development and Impairs the Inhibitory Properties of Troponin](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
13. [A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13805&geneProductId=UniProtKB:P13805)
14. [A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13805)
15. Ensembl Release 99