Gene
selenon
- ID
- ZDB-GENE-030327-7
- Name
- selenoprotein N
- Symbol
- selenon Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 17 Mapping Details/Browsers
- Description
- Predicted to enable oxidoreductase activity. Involved in muscle cell development; muscle tissue development; and regulation of ryanodine-sensitive calcium-release channel activity. Acts upstream of or within regulation of locomotion; skeletal muscle fiber development; and swimming behavior. Predicted to be located in endoplasmic reticulum and membrane. Predicted to be active in endoplasmic reticulum membrane. Is expressed in several structures, including anterior axial hypoblast; mesoderm; nervous system; tail bud; and trunk. Human ortholog(s) of this gene implicated in rigid spine muscular dystrophy 1. Orthologous to human SELENON (selenoprotein N).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 12 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb686 (26 images)
Wild Type Expression Summary
- All Phenotype Data
- 12 figures from 3 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| rigid spine muscular dystrophy 1 | Alliance | Congenital myopathy 3 with rigid spine | 602771 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
| Protein | Additional Resources | Length |
|---|---|---|
| UniProtKB:Q3Y4E2 | InterPro | 557 |
Interactions and Pathways
No data available
Plasmids
No data available