Gene

cog8

ID
ZDB-GENE-050320-74
Name
component of oligomeric golgi complex 8
Symbol
cog8 Nomenclature History
Previous Names
  • zgc:110765
Type
protein_coding_gene
Location
Chr: 18 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 IIh. Orthologous to human COG8 (component of oligomeric golgi complex 8).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
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 cog8 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
congenital disorder of glycosylation type IIh Alliance Congenital disorder of glycosylation, type IIh 611182
Associated With cog8 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR007255 Conserved oligomeric Golgi complex subunit 8
Family IPR016632 Conserved oligomeric Golgi complex subunit 8, Metazoal and Viridiplantae
Homologous_superfamily IPR016159 Cullin repeat-like-containing domain superfamily
Domain Details Per Protein
Protein Length Conserved oligomeric Golgi complex subunit 8 Conserved oligomeric Golgi complex subunit 8, Metazoal and Viridiplantae Cullin repeat-like-containing domain superfamily
UniProtKB:Q5BLI1 634
Transcripts
Genome Browsers
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