MIR96
Chr 7q32.2microRNA 96
- Aliases:
- hsa-mir-96
Annotations refreshed 9 hours ago.
Predicted protein structure
No predicted 3D structure for MIR96. Non-coding genes and pseudogenes typically have no protein product.
Clinical relevance (Genomics England PanelApp)
Moderate Evidence (Amber)
Monogenic hearing loss
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Disease associations (Open Targets)
autosomal dominant nonsyndromic hearing loss
0.53deafness
0.20Non-syndromic genetic deafness
0.20nonsyndromic genetic hearing loss
0.18Hearing impairment
0.12hearing loss, autosomal recessive
0.08Usher syndrome
0.08Usher syndrome type 1
0.08mirror movements 4
0.07mirror movements 2
0.07
Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.