Home Details
| Official Symbol of Gene | CD226 |
| Species | Homo sapiens |
| Entrez Gene ID | 10666 |
| Official Full Name | CD226 molecule |
| Also known as | PTA1; DNAM1; DNAM-1; TLiSA1 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000150637 MIM:605397; AllianceGenome:HGNC:16961 |
| Map Location | 18q22.2 |
| Variation Type | SNP |
| refSNP ID | rs1788229 |
| Detected Sample | Blood |
| Sample Detail | N/A |
| Detected Method | TaqMan |
| Disease | MS |
| Disease subtype | N/A |
| Population | Korean |
| Sample Size | 80 MS patients, and 237 controls |
| Pubmed ID | 23922043 |
| Year | 2013 |
| Title | Lack of association between CD226 genetic variants and inflammatory demyelinating diseases in Korean population |
| Risk Type | N/A |
| Main Result | negative |
| Result | However, the significance of rs1788229 disappeared after a multiple testing correction of the data (p>0.05). |
| Mechanism/Pathway | However, our results suggest that the causal genes for inflammatory demyelinating diseases may vary depending on the population. |

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