| ncRNA name | LOC399959 |
| ncRNA Category | lncRNA |
| ID | 399959 |
| Ensembl | ENSG00000255248 |
| Synonyms | MIR100HG; AGD1; lncRNA-N2; linc-NeD125 |
| Disease name | myopia |
| Species | Homo sapiens |
| Tissues/Cell_line | peripheral blood leukocytes |
| Methods | genotyping |
| Expression pattern | associated |
| Functional description | The meta-analysis combining the first and second stages identified an SNP, rs577948, at chromosome 11q24.1, which was associated with pathological myopia (P = 2.22x10(-7) and OR of 1.37 with 95% confidence interval: 1.21-1.54). Two genes, BLID and LOC399959, were identified within a 200-kb DNA encompassing rs577948. |
| PubMed ID | 19779542 |
| Year | 2009 |
| Title | A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1. |
| Drug-related ncRNA | NO |
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