Gene
reep2
- ID
- ZDB-GENE-050706-125
- Name
- receptor accessory protein 2
- Symbol
- reep2 Nomenclature History
- Previous Names
-
- zgc:110128
- Type
- protein_coding_gene
- Location
- Chr: 14 Mapping Details/Browsers
- Description
- Predicted to localize to cytoplasmic microtubule. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 72. Orthologous to human REEP2 (receptor accessory protein 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- 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 |
|---|---|---|---|
| hereditary spastic paraplegia 72A | Alliance | Spastic paraplegia 72A, autosomal dominant | 615625 |
| ?Spastic paraplegia 72B, autosomal recessive | 620606 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
| Protein | Length |
|---|---|
|
UniProtKB:A0A8M2BKF7
|
267 |
|
UniProtKB:Q4KMI4
|
268 |
Interactions and Pathways
No data available
Plasmids
No data available