Gene
cog5
- ID
- ZDB-GENE-041210-47
- Name
- component of oligomeric golgi complex 5
- Symbol
- cog5 Nomenclature History
- Previous Names
-
- si:dkey-217k21.3
- Type
- protein_coding_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Predicted to be involved in 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 IIi. Orthologous to human COG5 (component of oligomeric golgi complex 5).
- 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 IIi | Alliance | Congenital disorder of glycosylation, type IIi | 613612 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Conserved oligomeric Golgi complex subunit 5 | Conserved oligomeric Golgi complex subunit 5, helical domain | Conserved oligomeric Golgi complex subunit 5, N-terminal |
|---|---|---|---|---|
|
UniProtKB:A0A2R8RQB0
|
810 | |||
|
UniProtKB:F6NMG5
|
809 |
Interactions and Pathways
No data available
Plasmids
No data available