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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