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| Official Symbol of Gene | LILRA3 |
| Species | Homo sapiens |
| Entrez Gene ID | 11026 |
| Official Full Name | leukocyte immunoglobulin like receptor A3 |
| Also known as | HM31; HM43; ILT6; LIR4; CD85E; ILT-6; LIR-4 |
| Gene Type | protein coding |
| dbXrefs | MIM:604818 |
| Map Location | 19q13.4 |
| Detected Sample | peripheral blood |
| Sample Detail | NA |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | RRMS/PPMS/SPMS |
| Population | Caucasian German and French MS patients |
| Sample Size | 723 cases and 751 controls |
| Pubmed ID | 15815690 |
| Year | 2005 |
| Title | Association of multiple sclerosis with ILT6 deficiency |
| Expression | down-regulation |
| Risk type | Disease risk |
| Result | ILT6 deficiency is associated with MS in the German population and hence a likely risk factor for autoimmune disorders |
| Mechanism/Pathway | Family studies have shown strong genetic contributions. Linkage analyses have revealed several regions harboring risk genes including chromosome region 19q13. |

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