Gene
cog7
- ID
- ZDB-GENE-061013-463
- Name
- component of oligomeric golgi complex 7
- Symbol
- cog7 Nomenclature History
- Previous Names
-
- zgc:152912
- zgc:153470
- Type
- protein_coding_gene
- Location
- Chr: 24 Mapping Details/Browsers
- Description
- Predicted to be involved in Golgi organization and retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum. Predicted to localize to Golgi transport complex. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIe. Is expressed in female organism. Orthologous to human COG7 (component of oligomeric golgi complex 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Newman et al., 2019
- 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 IIe | Alliance | Congenital disorder of glycosylation, type IIe | 608779 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019335 | Conserved oligomeric Golgi complex subunit 7 |
Domain Details Per Protein
| Protein | Length | Conserved oligomeric Golgi complex subunit 7 |
|---|---|---|
|
UniProtKB:Q08BK1
|
767 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available