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| Official Symbol of Gene | HLA-DRB1 |
| Species | Homo sapiens |
| Entrez Gene ID | 3123 |
| Official Full Name | major histocompatibility complex, class II, DR beta 1 |
| Also known as | SS1; DRB1; HLA-DRB; HLA-DR1B |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000196126 MIM:142857; AllianceGenome:HGNC:4948 |
| Map Location | 6p21.32 |
| Variation Type | polymorphism |
| refSNP ID | HLA-DRB1*15:01 |
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | N/A |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 652 patients with MS |
| Pubmed ID | 27244296 |
| Year | 2016 |
| Title | Association of HLA Genetic Risk Burden With Disease Phenotypes in Multiple Sclerosis |
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | A higher HLAGB was associated with younger age at onset and the atrophy of subcortical gray matter fraction in women with relapsing-onset MS (standard β = 1.20 × 101; P = 1.7 × 102 and standard β = 1.67 × 101; P = 2.3 × 104, respectively), which were driven mainly by the HLA-DRB1*15:01 haplotype. |
| Mechanism/Pathway | N/A |

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