Gene
alg9
- ID
- ZDB-GENE-040426-1270
- Name
- ALG9 alpha-1,2-mannosyltransferase
- Symbol
- alg9 Nomenclature History
- Previous Names
-
- zgc:63820
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to have mannosyltransferase activity. Predicted to localize to endoplasmic reticulum. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation Il. Is expressed in central nervous system; epiphysis; polster; and retina. Orthologous to human ALG9 (ALG9 alpha-1,2-mannosyltransferase).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 8 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:63820 (9 images)
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 |
|---|---|---|---|
| congenital disorder of glycosylation Il | Alliance | Congenital disorder of glycosylation, type Il | 608776 |
| Gillessen-Kaesbach-Nishimura syndrome | 263210 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR005599 | GPI mannosyltransferase |
Domain Details Per Protein
| Protein | Length | GPI mannosyltransferase |
|---|---|---|
|
UniProtKB:A5PMV6
|
615 | |
|
UniProtKB:A0A8M3AZY9
|
641 |
Interactions and Pathways
No data available
Plasmids
No data available