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| Official Symbol of Gene | USP18 |
| Species | Homo sapiens |
| Entrez Gene ID | 11274 |
| Official Full Name | ubiquitin specific peptidase 18 |
| Also known as | ISG43; UBP43; PTORCH2 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000184979 MIM:607057; AllianceGenome:HGNC:12616 |
| Map Location | 22q11.21 |
| Variation Type | SNP |
| refSNP ID | rs9618216 |
| Detected Sample | Peripheral blood |
| Sample Detail | N/A |
| Detected Method | real-time PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | Spanish |
| Sample Size | 691 unrelated relapseonset MS patients/The healthy control population comprised 1028 |
| Pubmed ID | 23700969 |
| Year | 2013 |
| Title | Roles of the ubiquitin peptidase USP18 in multiple sclerosis and the response to interferon-b treatment |
| Risk Type | Disease risk |
| Main Result | Altogether, these results point to a role of USP18 in MS pathogenesis and the therapeutic response to IFNb. |
| Result | Two USP18 haplotypes were significantly associated with MS, TG and CG. Additional experiments revealed that CG carriers were characterized by lower USP18 gene expression levels in peripheral blood mononuclear cells and higher clinical disease activity. Finally, AA homozygosis for the intronic polymorphism rs2542109 was associated with the responder phenotype; however, USP18 expression levels induced by IFNb did not differ amongst MS patients carrying different rs2542109 genotypes |
| Mechanism/Pathway | Ubiquitin specific peptidase 18 (USP18) is a deubiquitinating enzyme that functions as a negative regulator of the type I interferon (IFN) signalling pathway and is specifically induced by type I IFNs. In the present study, previous observations by our group were expanded suggesting an implication of USP18 in multiple sclerosis (MS) based on the finding of a deficient expression of the gene in peripheral blood mononuclear cells from MS patients compared with healthy controls |

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