| ncRNA name | hsa-miR-184 |
| ncRNA Category | miRNA |
| Disease name | keratoconus |
| Species | Homo sapiens |
| Tissues/Cell_line | corneas, ciliary bodies, retinas and trabecular meshwork |
| Methods | DNA-seq, RNA-seq |
| Expression pattern | up-regulated |
| Functional description | Mutation in MIR184 is a rare cause of KC alone and may be more relevant to cases of KC associated with other ocular abnormalities. The increased expression of miR-184 versus miR-205 in normal cornea samples implies a possible role of miR184 in cornea development and/or corneal diseases. |
| PubMed ID | 26380287 |
| Year | 2015 |
| Title | Screening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia. |
| Drug-related ncRNA | NO |
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