Home Details
| Official Symbol of Gene | IRF8 |
| Species | Homo sapiens |
| Entrez Gene ID | 3394 |
| Official Full Name | interferon regulatory factor 8 |
| Also known as | ICSBP; IRF-8; ICSBP1; IMD32A; IMD32B; H-ICSBP |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000140968 MIM:601565; AllianceGenome:HGNC:5358 |
| Map Location | 16q24.1 |
| Variation Type | SNP |
| refSNP ID | rs17445836 |
| Detected Sample | peripheral blood |
| Sample Detail | NA |
| Detected Method | Real-Time PCR |
| Disease | MS |
| Disease subtype | MS |
| Population | Poland |
| Sample Size | 174MS |
| Pubmed ID | 30818222 |
| Year | 2019 |
| Title | Analysis of chosen SNVs in GPC5, CD58 and IRF8 genes in multiple sclerosis patients |
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | The study suggests that genetic variants inGPC5, CD58 and IRF8 genes may be of clinical interest in MS as predictors of age of onset and response to therapy. |
| Mechanism/Pathway | Multiple sclerosis (MS) is an autoimmune disease of the central nervous system with a neurodegen-erative compound. Heterogenetic background of autoimmunity pathway components has been suggested in the MS pathogenesis |

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