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 have oxidoreductase activity. Involved in calcium-mediated signaling; regulation of ryanodine-sensitive calcium-release channel activity; and skeletal muscle fiber development. Predicted to localize to endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in rigid spine muscular dystrophy 1. Is expressed in several structures, including anterior axial hypoblast; mesoderm; nervous system; tail bud; and trunk. Orthologous to human SELENON (selenoprotein N).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 11 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb686 (26 images)
Wild Type Expression Summary
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 | Length |
|---|---|
|
UniProtKB:Q3Y4E2
|
557 |
Interactions and Pathways
No data available
Plasmids
No data available