Gene
spg21
- ID
- ZDB-GENE-040426-2722
- Name
- SPG21 abhydrolase domain containing, maspardin
- Symbol
- spg21 Nomenclature History
- Previous Names
-
- wu:fd07h02
- zgc:73091 (1)
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Predicted to have CD4 receptor binding activity. Predicted to localize to cytosol and trans-Golgi network transport vesicle. Human ortholog(s) of this gene implicated in Mast syndrome and hereditary spastic paraplegia. Orthologous to human SPG21 (SPG21 abhydrolase domain containing, maspardin).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:73091 (1 image)
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 |
|---|---|---|---|
| Mast syndrome | Alliance | Mast syndrome | 248900 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Alpha/Beta hydrolase fold | Alpha/beta hydrolase fold-1 | Maspardin |
|---|---|---|---|---|
|
UniProtKB:Q6PC62
|
311 |
Interactions and Pathways
No data available
Plasmids
No data available