| ncRNA name | hsa-miR-182 |
| ncRNA Category | miRNA |
| Disease name | Vogt-Koyanagi-Harada disease |
| Species | Homo sapiens |
| Tissues/Cell_line | blood |
| Methods | genotyping, qPCR |
| Expression pattern | associated |
| Functional description | The results showed significantly decreased frequencies of the miR-182/rs76481776 CC genotype and C allele in BD (P = 3.36 × 10(-4), OR = 0.55; P = 4.74 × 10(-4), OR = 0.59) and VKH patients (P = 1.11 × 10(-4), OR = 0.53; P = 1.26 × 10(-4), OR = 0.56). |
| PubMed ID | 24801147 |
| Year | 2014 |
| Title | Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182. |
| Drug-related ncRNA | NO |
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