| Details |
| Disease Name | Hearing Loss, Central |
| Nocoding RNA Name | hsa-miR-96 |
| Expression Pattern | mutated |
| Species | Homo sapiens |
| Detection Methods | Mutational screening etc. |
| Target | MYRIP |
| Tissue | blood |
| Treatment | N/A |
| PubMed ID | 22038834 |
| Year | 2012 |
| Detail Description | five heterozygous nt variations were identified in NSHL cases: two of them, miR-96(+42C>T) and miR-182(+106G>A), were previously reported as single nt polymorphisms (SNPs rs73159662 and rs76481776, respectively), and were found also in controls. Two novelMIR183variants,miR-183(+3G>T) and miR-183(-27C>T), were detected,The last variant identified, miR-96(+57T>C) is located in the stem region of the pre-miRNA and replaces a residue that is fully conserved throughout vertebrate evolution,from fish to primates. |
NSDNA: The Nervous System Disease NcRNAome Atlas
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