MIR96 is a microRNA that has been found to be associated with progressive hearing loss [PMC3259013]. Understanding the pathogenic mechanisms that connect MIR96 mutations to this condition is crucial for the development of personalized therapeutic approaches for individuals carrying these mutations [PMC3259013]. However, there is insufficient coverage of MIR96, which may limit our current knowledge about its role in hearing loss [PMC8738750]. Further research is needed to fully comprehend the impact of MIR96 mutations and to explore potential therapeutic interventions for affected individuals.
ugg g U A UU --- uc cc au UUGGCACU GCACAU UUGCUu gug u || || |||||||| |||||| |||||| ||| gg UA AACCGUGA CGUGUA AAcgag cgc c aaa G U - CU ucu cu
Name | Accession | Chromosome | Start | End | Strand | Confidence |
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Disease | Description | Category | PubMed ID |
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Accession | MIMAT0000095 |
Description | Homo sapiens hsa-miR-96-5p mature miRNA |
Sequence | 9 - UUUGGCACUAGCACAUUUUUGCU - 31 |
Evidence |
experimental
cloned [1-3] |
Database links |
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Predicted targets |
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Accession | MIMAT0004510 |
Description | Homo sapiens hsa-miR-96-3p mature miRNA |
Sequence | 52 - AAUCAUGUGCAGUGCCAAUAUG - 73 |
Evidence |
experimental
cloned [2] |
Database links |
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Predicted targets |
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