miRNA Gene
dre-mir-96
- ID
- ZDB-MIRNAG-070111-4
- Name
- microRNA 96
- Symbol
- dre-mir-96 Nomenclature History
- Previous Names
- Type
- miRNA_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Involved in otic vesicle development. Human ortholog(s) of this gene implicated in attention deficit hyperactivity disorder and autosomal dominant nonsyndromic deafness 50. Is expressed in brain; gill; hair cell; head; and sensory system. Orthologous to human MIR96 (microRNA 96).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 9 figures from 7 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Fogerty et al., 2019
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal dominant nonsyndromic deafness 50 | Alliance | Deafness, autosomal dominant 50 | 613074 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
- Genome Browsers
- No data available
Interactions and Pathways
No data available
Plasmids
No data available