| ncRNA name | hsa-miR-184 |
| ncRNA Category | miRNA |
| Disease name | keratoconus |
| Species | Homo sapiens |
| Tissues/Cell_line | peripheral blood leukocytes; human embryonic kidney cell line HEK293T |
| Methods | DNA sequencing, transfection, qRT-PCR |
| Expression pattern | associated |
| Functional description | Two novel heterozygous substitution mutations in MIR184 were identified in two patients with isolated keratoconus: miR-184(+8C>A) and miR-184(+3A>G). Mutations in MIR184 are a rare cause of keratoconus and were found in 2 of 780 (0.25%) cases. |
| PubMed ID | 23833072 |
| Year | 2013 |
| Title | Mutational analysis of MIR184 in sporadic keratoconus and myopia. |
| Drug-related ncRNA | NO |
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