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Gene entry

COG4

component of oligomeric golgi complex 4

Chromosome
16
Cytoband
16q22.1
Variants (rsID)
10

COG4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.1). Its official name is “component of oligomeric golgi complex 4”. The reference table lists 10 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs113455884Benignsingle nucleotide variantCOG4-congenital disorder of glycosylation
  • rs372162273Likely benignsingle nucleotide variantCOG4-congenital disorder of glycosylation
  • rs376663459Likely pathogenicsingle nucleotide variantCOG4-congenital disorder of glycosylation
  • rs267606740Pathogenicsingle nucleotide variantCOG4-congenital disorder of glycosylation|See cases

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.