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Gene entry

MOG

myelin oligodendrocyte glycoprotein

Chromosome
6
Cytoband
6p22.1
Variants (rsID)
30

MOG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p22.1). Its official name is “myelin oligodendrocyte glycoprotein”. The reference table lists 30 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs3130250Not classifiedsynonymous_variantSynonymous_S5S|Synonymous_S5S|Synonymous_S5S|Synonymous_S5S|Synonymous_S5S
  • rs3130253Not classifiedmissense_variantAutoimmune Disease|Multiple Sclerosis|Missense_I174V|Missense_I174V|Missense_I58V

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.