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 have calcium ion binding activity. Is expressed in adaxial cell; fin; musculature system; and somite. Orthologous to human MYL1 (myosin light chain 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 23 figures from 7 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 | EF-hand domain | EF-hand domain pair |
|---|---|---|---|
|
UniProtKB:Q6P0G6
|
190 |
Interactions and Pathways
No data available
Plasmids
No data available