Home Details
| 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 |
| Variation Type | deletion |
| refSNP ID | N/A |
| Detected Sample | Blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | RRMS |
| Population | Spanish |
| Sample Size | 126 R-MS patients and 174 healthy |
| Pubmed ID | 19421224 |
| Year | 2009 |
| Title | Multiple sclerosis associates with LILRA3 deletion in Spanish patients |
| Risk Type | Disease risk |
| Main Result | positive |
| Result | We analyse here two series of Spanish patients and healthy controls and show that relapsing MS (R-MS) is associated with a gene deletion affecting the hypothetically soluble leukocyte immunoglobulin (Ig)-like receptor A3 (LILRA3, 19q13.4), in agreement with an earlier finding in German patients. |
| Mechanism/Pathway | N/A |

2023,CopyRight © HMU. College of Bioinformatics Science and Technology, Harbin, China.