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. Is expressed in several structures, including anterior axial hypoblast; mesoderm; nervous system; tail bud; and trunk. Human ortholog(s) of this gene implicated in congenital fiber-type disproportion and rigid spine muscular dystrophy 1. 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