Cog4 - component of oligomeric golgi complex 4 Gene

Mus musculus

Also known as D8Ertd515e

Gene ID: 102339 | Gene type: protein coding

About Cog4

Summary

Predicted to enable identical protein binding activity. Predicted to be involved in Golgi organization; Golgi vesicle prefusion complex stabilization; and retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum. Predicted to act upstream of or within protein transport. Predicted to be located in Golgi apparatus and membrane. Predicted to be part of Golgi transport complex. Human ortholog(s) of this gene implicated in Saul-Wilson syndrome and congenital disorder of glycosylation type IIj. Orthologous to human COG4 (component of oligomeric golgi complex 4). [provided by Alliance of Genome Resources, Apr 2022]

Cog4 Products(2)

mRNA	Protein	Name
NM_001310607.1	NP_001297536.1	conserved oligomeric Golgi complex subunit 4 isoform 2
NM_133973.2	NP_598734.1	conserved oligomeric Golgi complex subunit 4 isoform 1

Protein Preferred Names

Protein Names

conserved oligomeric Golgi complex subunit 4

COG complex subunit 4

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02953	COG4 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Cog4	NCBI	NCBI:25839

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