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
- Predicted to enable calcium ion binding activity. 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; 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 | Length | Calmodulin/Myosin light chain/Troponin C-like | EF-hand domain | EF-hand domain pair |
|---|---|---|---|---|
|
UniProtKB:Q6P0G6
|
190 |
Interactions and Pathways
No data available
Plasmids
No data available