Gene
tnnc2.1
- ID
- ZDB-GENE-090312-215
- Name
- troponin C2, fast skeletal type, tandem duplicate 1
- Symbol
- tnnc2.1 Nomenclature History
- Previous Names
-
- si:rp71-17i16.4
- Type
- protein_coding_gene
- Location
- Chr: 23 Mapping Details/Browsers
- Description
- Predicted to enable calcium ion binding activity. Predicted to be involved in skeletal muscle contraction. Predicted to be part of troponin complex. Human ortholog(s) of this gene implicated in congenital myopathy 15. Orthologous to human TNNC2 (troponin C2, fast skeletal type).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| congenital myopathy 15 | Alliance | Congenital myopathy 15 | 620161 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Calmodulin/Myosin light chain/Troponin C-like | EF-Hand 1, calcium-binding site | EF-hand domain | EF-hand domain pair |
|---|---|---|---|---|---|
|
UniProtKB:A0A8M9Q7U4
|
161 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
si:rp71-17i16.4-201
(1)
|
Ensembl | 580 nt |
Interactions and Pathways
No data available
Plasmids
No data available