Home Details
| Official Symbol of Gene | DHX58 |
| Species | Homo sapiens |
| Entrez Gene ID | 79132 |
| Official Full Name | DExH-box helicase 58 |
| Also known as | LGP2; RLR-3; D11LGP2; D11lgp2e |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000108771 MIM:608588; AllianceGenome:HGNC:29517 |
| Map Location | 17q21.2 |
| Variation Type | SNP |
| refSNP ID | rs2074158 |
| Detected Sample | blood |
| Sample Detail | N/A |
| Detected Method | RFLP |
| Disease | MS |
| Disease subtype | RRMS, PPMS, SPMS, CIS |
| Population | Germany |
| Sample Size | 716 MS patients / 706 healthy controls |
| Pubmed ID | 25288302 |
| Year | 2014 |
| Title | Analysis of polymorphisms in RIG-I-like receptor genes in German multiple sclerosis patients |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | Evaluation of single nucleotide polymorphisms (SNPs) in the gene did not reveal significant single-SNP associations with MS risk. |
| Mechanism/Pathway | Increased activation of RLR genes has been demonstrated in peripheral blood cells of MS patients.It was speculated that genetic alterations in the RIG-I-like receptor signaling pathway may lead to inadequate immune responses and increase the susceptibility for autoimmune disorders. |

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