Gene
myl1
- ID
- ZDB-GENE-030131-8109
- Name
- myosin, light chain 1, alkali; skeletal, fast
- Symbol
- myl1 Nomenclature History
- Previous Names
-
- fj53a11
- wu:fj53a11
- zgc:77231 (1)
- Type
- protein_coding_gene
- Location
- Chr: 9 Mapping Details/Browsers
- Description
- Acts upstream of or within skeletal muscle tissue development. Predicted to be part of myosin II complex. Predicted to be active in contractile muscle fiber. Is expressed in adaxial cell; fin; head; musculature system; and somite. Human ortholog(s) of this gene implicated in congenital myopathy 14. Orthologous to human MYL1 (myosin light chain 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 25 figures from 9 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:65785 (12 images)
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Ravenscroft et al., 2018
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| congenital myopathy 14 | Alliance | Congenital myopathy 14 | 618414 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Additional Resources | Length | Calmodulin/Myosin light chain/Troponin C-like | EF-hand domain | EF-hand domain pair |
|---|---|---|---|---|---|
| UniProtKB:Q6P0G6 | InterPro | 190 |
Interactions and Pathways
No data available
Plasmids
No data available