Details

Home Details


Basic information of MOG :

Official Symbol of Gene MOG
Species Homo sapiens
Entrez Gene ID 4340
Official Full Name myelin oligodendrocyte glycoprotein
Also known as BTN6; BTNL11; MOGIG2; NRCLP7
Gene Type protein coding
dbXrefs Ensembl:ENSG00000204655 MIM:159465; AllianceGenome:HGNC:7197
Map Location 6p22.1
Variation Type restriction fragment length polymorphism (RFLP)
refSNP ID 1.9 kb Taq 1

Sample information of multiple sclerosis:

Detected Sample venous blood
Sample Detail N/A
Detected Method Southern blotting
Disease MS
Disease subtype N/A
Population Southampton area
Sample Size 40 patients with MS / 80 age and sex matched controls

Literature information of multiple sclerosis :

Pubmed ID 9436746
Year 1998
Title Lack of association of a Taq 1 polymorphism of the human myelin oligodendrocyte glycoprotein gene with multiple sclerosis in a population of patients from the Southampton area

Results of multiple sclerosis :

Risk Type Disease risk
Main Result Negative
Result None of these distribution of the Taq1 digest polymorphic bands between patients with multiple sclerosis and controls in the present study differences were statistically significant.The incidence in the two sets of patients with multiple sclerosis is very similar.
Mechanism/Pathway The lesions of multiple sclerosis are most often held to be caused by an immune attack on CNS myelin.The nature of the antigens involved remains obscure, but peptides from at least two major myelin proteins—myelin basic protein and proteolipid protein—are known to cause cell mediated demyelination in animals (experimental allergic encephalomyelitis) which in some ways resembles human multiple sclerosis.Minor myelin components may presumably also act as autoantigens.Myelin oligodendrocyte glycoprotein (MOG) is a quantitatively minor myelin protein localised to oligodendrocyte cell bodies and processes and to the outer layer of CNS myelin sheaths.In common with several other members of this family, MOG has a membrane spanning domain and an extracellular glycosylated N-terminus and its presence on the outermost surface of myelin and the oligodendrocyte plasma membrane may make MOG accessible to the immune system.