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MOG

myelin oligodendrocyte glycoprotein

HCNC Approved Symbol
MOG (HGNC:7197)
Genomic Coordinates
6:29,657,092 - 29,672,365 (6p22.1)
Synonyms
BTN6, BTNL11
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Narcolepsy 7
614250AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MOG gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results