Gene
cog1
- ID
- ZDB-GENE-050302-128
- Name
- component of oligomeric golgi complex 1
- Symbol
- cog1 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 3 Mapping Details/Browsers
- Description
- Predicted to be involved in intra-Golgi vesicle-mediated transport. Predicted to localize to Golgi apparatus. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIg. Orthologous to human COG1 (component of oligomeric golgi complex 1).
- 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 |
|---|---|---|---|
| congenital disorder of glycosylation type IIg | Alliance | Congenital disorder of glycosylation, type IIg | 611209 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR033370 | Conserved oligomeric Golgi complex subunit 1 |
Domain Details Per Protein
| Protein | Length | Conserved oligomeric Golgi complex subunit 1 |
|---|---|---|
|
UniProtKB:A0A8M1RH56
|
937 |
Interactions and Pathways
No data available
Plasmids
No data available