Skip to content
GenoLensGenoLens

MOG

Chr 6p22.1

myelin oligodendrocyte glycoprotein

Aliases:
BTN6, BTNL11
MANE:
ENST00000376917.8

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Moderate Evidence (Amber)

  • Kleine-Levin syndrome

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Paroxysmal central nervous system disorders

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Disease associations (Open Targets)

  • transient neonatal diabetes mellitus

    0.54
  • narcolepsy-cataplexy syndrome

    0.51
  • hereditary disease

    0.19
  • monogenic diabetes

    0.17
  • myeloid sarcoma

    0.12
  • Alzheimer disease

    0.12
  • acute disseminated encephalomyelitis

    0.11
  • myelitis

    0.11
  • neuromyelitis optica

    0.11
  • optic neuritis

    0.10

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Myelin-oligodendrocyte glycoprotein

Mediates homophilic cell-cell adhesion (By similarity). Minor component of the myelin sheath. May be involved in completion and/or maintenance of the myelin sheath and in cell-cell communication

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.