Gene
aga
- ID
- ZDB-GENE-040426-2311
- Name
- aspartylglucosaminidase
- Symbol
- aga Nomenclature History
- Previous Names
-
- zgc:77327
- Type
- protein_coding_gene
- Location
- Chr: 14 Mapping Details/Browsers
- Description
- Predicted to have N4-(beta-N-acetylglucosaminyl)-L-asparaginase activity. Predicted to be involved in protein deglycosylation. Predicted to localize to lysosome. Human ortholog(s) of this gene implicated in aspartylglucosaminuria and lysosomal storage disease. Orthologous to human AGA (aspartylglucosaminidase).
- 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:77327 (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 |
|---|---|---|---|
| aspartylglucosaminuria | Alliance | Aspartylglucosaminuria | 208400 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Nucleophile aminohydrolases, N-terminal | Peptidase T2, asparaginase 2 |
|---|---|---|---|
|
UniProtKB:A0A8M9PZ91
|
215 | ||
|
UniProtKB:A8KC00
|
337 |
Interactions and Pathways
No data available
Plasmids
No data available