Harmonizome 3.0

component of oligomeric golgi complex 5

The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. The encoded protein is organized with conserved oligomeric Golgi complex components 6, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants. Mutations in this gene result in congenital disorder of glycosylation type 2I.[provided by RefSeq, Jan 2011]

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cog5 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From Pathway Commons Protein-Protein Interactions

interacting proteins for COG5 from the Pathway Commons Protein-Protein Interactions dataset.

From CORUM Protein Complexes

proteins in the COG1-COG8-COG5-COG6-COG7 subcomplex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the COG5-COG6-COG7 subcomplex protein complex from the CORUM Protein Complexes dataset.

From DisGeNET Gene-Disease Associations

genes associated with the disease Cog5 Congenital Disorder Of Glycosylation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the COG5-congenital disorder of glycosylation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.