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Basic information of IFNG :

Official Symbol of Gene IFNG
Species Homo sapiens
Entrez Gene ID 3458
Official Full Name interferon gamma
Also known as IFG; IFI; IMD69
Gene Type protein coding
dbXrefs Ensembl:ENSG00000111537 MIM:147570; AllianceGenome:HGNC:5438
Map Location 12q15
Variation Type SNP
refSNP ID IFN-γ intron III (+2118 site A/G and +3586 site G/ACT).

Sample information of multiple sclerosis:

Detected Sample venous blood
Sample Detail N/A
Detected Method PCR-RFL
Disease MS
Disease subtype N/A
Population N/A
Sample Size 58 patients/40 healthy controls

Literature information of multiple sclerosis :

Pubmed ID 28218775
Year 2017
Title Polymorphism in the third intron of the interferonγ gene is associated with susceptibility to multiple sclerosis

Results of multiple sclerosis :

Risk Type Disease risk
Main Result Positive
Result The frequency of the A allele at the IFN-γ +2118 site was increased in the MS group as compared with the control group.However, no significant difference was observed between the MS and control groups in genotype distribution and allele frequency at the IFN-γ +3586 site.Thus, polymorphisms at the +2118 A/G site in the IFN-γ intron III gene may be associated with susceptibility to multiple sclerosis.
Mechanism/Pathway Interferon-gamma (IFN-γ), which is a pro-inflammatory cytokine secreted by Th1 cells, can regulate the activity of immune cells and induce general inflammation. Studies have shown that level of IFN-γ increases in the acute phase of MS. IFN-γ may therefore act as a direct inducer of demyelination in the central nervous system.