Entity Details

Primary name MOG_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ16653
EntryNameMOG_HUMAN
FullNameMyelin-oligodendrocyte glycoprotein
TaxID9606
Evidenceevidence at protein level
Length247
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesMOG

GO terms

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GOName
GO:0001618 virus receptor activity
GO:0001817 regulation of cytokine production
GO:0005102 signaling receptor binding
GO:0005886 plasma membrane
GO:0007155 cell adhesion
GO:0007417 central nervous system development
GO:0009897 external side of plasma membrane
GO:0016021 integral component of membrane
GO:0050852 T cell receptor signaling pathway

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR003599 Immunoglobulin subtypeDomainDomain
IPR007110 Immunoglobulin-like domainDomainDomain
IPR013106 Immunoglobulin V-set domainDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR016663 Myelin-oligodendrocyte glycoproteinFamilyFamily
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
614250 OMIMNarcolepsy 7 (NRCLP7)Neurological disabling sleep disorder, characterized by excessive daytime sleepiness, sleep fragmentation, symptoms of abnormal rapid-eye-movement (REM) sleep, cataplexy, hypnagogic hallucinations, and sleep paralysis. Cataplexy is a sudden loss of muscle tone triggered by emotions, which is the most valuable clinical feature used to diagnose narcolepsy. Human narcolepsy is primarily a sporadically occurring disorder but familial clustering has been observed. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions