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| Official Symbol of Gene | IRF1 |
| Species | Homo sapiens |
| Entrez Gene ID | 3659 |
| Official Full Name | interferon regulatory factor 1 |
| Also known as | MAR; IRF-1 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000125347 MIM:147575; AllianceGenome:HGNC:6116 |
| Map Location | 5q31.1 |
| Variation Type | allele |
| refSNP ID | GT repeat alleles |
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | automated fluorescence sequencing system |
| Disease | MS |
| Disease subtype | RRMS,PPMS,SPMS |
| Population | European populations (Germany, Sweden and Northern Italy) |
| Sample Size | 574 MS patients / 527 healthy control |
| Pubmed ID | 11196707 |
| Year | 2000 |
| Title | Lack of association between the interferon regulatory factor-1 (IRF1) locus at 5q31.1 and multiple sclerosis in Germany, northern Italy, Sardinia and Sweden |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | In none of these populations, did we find any significant allelic association with disease. |
| Mechanism/Pathway | Because of their complex effects on the induction and maintenance of inflammatory reactions, cytokines and interferons are considered as an important class of disease-promoting or limiting effector molecules. While administration of IFN-g leads to exacerbation of the disease, recombinant IFN-b reduces exacerbation rates and destruction of the central nervous system (CNS) components. Interferon regulatory factor-1 (IRF-1) is a transcriptional activator of the IFN-b gene, and is itself induced by cytokines such as IFN-g and IL-12. |

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