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Basic information of IRF5 :

Official Symbol of Gene IRF5
Species Homo sapiens
Entrez Gene ID 3663
Official Full Name interferon regulatory factor 5
Also known as SLEB10
Gene Type protein coding
dbXrefs Ensembl:ENSG00000128604 MIM:607218; AllianceGenome:HGNC:6120
Map Location 7q32.1
Variation Type Allele
refSNP ID NA

Sample information of multiple sclerosis:

Detected Sample peripheral blood
Sample Detail NA
Detected Method PCR
Disease MS
Disease subtype MS
Population NA
Sample Size 145MS/300Control

Literature information of multiple sclerosis :

Pubmed ID 26112714
Year 2015
Title Variants of Interferon Regulatory Factor 5 are Associated with Neither Neuromyelitis Optica Nor Multiple Sclerosis in the Southeastern Han Chinese Population

Results of multiple sclerosis :

Risk Type Disease risk
Main Result Negative
Result Our preliminary study indicates that genetic variants in IRF5 may affect neither NMO nor MS in the Southeastern Han Chinese population. Further studies with a large sample size and diverse ancestry populations are needed to clarify this issue.
Mechanism/Pathway Neuromyelitis optica (NMO) and multiple sclerosis (MS) are demyelinating disorders of the central nervous system. Interferon regulatory factor 5 (IRF5) is a common susceptibility gene to different autoimmune disorders. However, the association of IRF5 variants with NMO and MS patients has not been well studied. Therefore, we aimed to evaluate whether IRF5 variants were associated with NMO and MS in the Southeastern Han Chinese population.