Gene
cog2
- ID
- ZDB-GENE-040426-2671
- Name
- component of oligomeric golgi complex 2
- Symbol
- cog2 Nomenclature History
- Previous Names
-
- zgc:56436
- Type
- protein_coding_gene
- Location
- Chr: 13 Mapping Details/Browsers
- Description
- Predicted to be involved in Golgi organization and intra-Golgi vesicle-mediated transport. Predicted to localize to Golgi transport complex. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIq. Orthologous to human COG2 (component of oligomeric golgi complex 2).
- 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:56436 (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 |
|---|---|---|---|
| congenital disorder of glycosylation type IIq | Alliance | ?Congenital disorder of glycosylation, type IIq | 617395 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | COG complex component, COG2 | COG complex component, COG2, C-terminal | Conserved oligomeric Golgi complex, subunit 2, N-terminal |
|---|---|---|---|---|
|
UniProtKB:Q7ZUD7
|
730 |
Interactions and Pathways
No data available
Plasmids
No data available