conserved oligomeric Golgi complex component 1 (COG1, low density lipoprotein receptor defect B-complementing protein, LDLB, KIAA1381)
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Function
- required for normal Golgi function (putative)
- component of the conserved oligomeric Golgi complex
Structure
belongs to the COG1 family
Compartment
- Golgi membrane, cytoplasmic side
Pathology
- defects in COG1 are the cause of congenital disorder of glycosylation type 2G