Gene
rtn2b
- ID
- ZDB-GENE-060331-95
- Name
- reticulon 2b
- Symbol
- rtn2b Nomenclature History
- Previous Names
-
- rtn8 (1)
- zgc:136618
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Predicted to localize to endoplasmic reticulum membrane and integral component of membrane. Is expressed in skeletal muscle. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 12. Orthologous to human RTN2 (reticulon 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Housley et al., 2014
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
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 |
|---|---|---|---|
| hereditary spastic paraplegia 12 | Alliance | Spastic paraplegia 12, autosomal dominant | 604805 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Domain | IPR003388 | Reticulon |
Domain Details Per Protein
| Protein | Length | Reticulon |
|---|---|---|
|
UniProtKB:A9JRN7
|
208 | |
|
UniProtKB:Q4G5T7
|
208 |
Interactions and Pathways
No data available
Plasmids
No data available