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 act upstream of or within intracellular protein transport. Predicted to be located in Golgi membrane. Predicted to be part of Golgi transport complex. Is expressed in female organism. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIe. Orthologous to human COG7 (component of oligomeric golgi complex 7).
Genome Resources
Note
None
Comparative Information
Expression
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
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With cog7 Human Ortholog
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
Associated With cog7 Via Experimental Models
No data available
Gene Ontology
Protein Domains
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:F1RBH5 733
UniProtKB:Q08BK1 767
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations