Gene

cog6

ID

ZDB-GENE-040426-909

Name

component of oligomeric golgi complex 6

Symbol

cog6 Nomenclature History

Previous Names

si:ch211-203f4.1 (1)
zgc:56117

Type

protein_coding_gene

Location

Chr: 15 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 IIl. Orthologous to human COG6 (component of oligomeric golgi complex 6).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

No data available

Cross-Species Comparison

High Throughput Data

GEO (1)

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

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 cog6 Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
congenital disorder of glycosylation type IIl	Alliance	Congenital disorder of glycosylation, type IIl	614576
		Shaheen syndrome	615328

Associated With cog6 Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Domain	IPR048368	Conserved oligomeric complex COG6, N-terminal
Domain	IPR048369	Conserved Oligomeric Golgi complex subunit 6, C-terminal
Family	IPR010490	Conserved oligomeric Golgi complex subunit 6