Gene
myl9a
- ID
- ZDB-GENE-041010-120
- Name
- myosin, light chain 9a, regulatory
- Symbol
- myl9a Nomenclature History
- Previous Names
-
- mlc9a (1)
- myl9
- zgc:103467
- Type
- protein_coding_gene
- Location
- Chr: 23 Mapping Details/Browsers
- Description
- Predicted to have calcium ion binding activity. Human ortholog(s) of this gene implicated in familial hypertrophic cardiomyopathy. Is expressed in several structures, including cardiovascular system; hypochord; intestinal bulb; nervous system; and thyroid follicle. Orthologous to human MYL9 (myosin light chain 9).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 10 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:103467 (17 images)
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 |
|---|---|---|---|
| ?Megacystis-microcolon-intestinal hypoperistalsis syndrome 4 | 619365 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | EF-Hand 1, calcium-binding site | EF-hand domain | EF-hand domain pair |
|---|---|---|---|---|
|
UniProtKB:Q5XJB0
|
174 | |||
|
UniProtKB:F1QYK9
|
174 |
Interactions and Pathways
No data available
Plasmids
No data available