Home Details
| Official Symbol of Gene | CD69 |
| Species | Homo sapiens |
| Entrez Gene ID | 969 |
| Official Full Name | CD69 molecule |
| Also known as | AIM; EA1; MLR-3; CLEC2C; GP32/28; BL-AC/P26 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000110848 MIM:107273; AllianceGenome:HGNC:1694 |
| Map Location | 12p13.31 |
| Variation Type | N/A |
| refSNP ID | rs3176798 |
| Detected Sample | Peripheral blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 364 Norwegian MS patients |
| Pubmed ID | 16764945 |
| Year | 2006 |
| Title | Coding region polymorphisms in T cell signal transduction genes.Prevalence and association to development of multiple sclerosis |
| Risk Type | Disease risk |
| Main Result | Typing the 41 SNPs with functioning DCE assay (Fischer and Lerman, 1983) in the pooled Norwegian controls (n= 4000) demonstrated that 16 of these (39%) were heterozygous in the Norwegian population , four of these displaying a minor allele frequency of less than 1% |
| Result | Heterozygosity (HZ) in 4000 controls |
| Mechanism/Pathway | Genes that control T cell activation downstream of the initial presentation of peptide antigen by HLA molecules may be regarded as prime candidate susceptibility genes in T cell mediated autoimmune diseases, such as MS |

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