Gene
myl9b
- ID
- ZDB-GENE-040426-2296
- Name
- myosin, light chain 9b, regulatory
- Symbol
- myl9b Nomenclature History
- Previous Names
-
- myl9
- myl9l
- zgc:77916
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to enable calcium ion binding activity. Predicted to be involved in myofibril assembly. Predicted to be active in myofibril and stress fiber. Is expressed in smooth muscle cell. Human ortholog(s) of this gene implicated in familial hypertrophic cardiomyopathy and megacystis-microcolon-intestinal hypoperistalsis syndrome. Orthologous to human MYL9 (myosin light chain 9).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- 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 |
|---|---|---|---|
| ?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 | Myosin regulatory light chain |
|---|---|---|---|---|---|
|
UniProtKB:Q6NVA6
|
173 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available