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MIR96

Chr 7q32.2

microRNA 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

    0.53
  • deafness

    0.20
  • Non-syndromic genetic deafness

    0.20
  • nonsyndromic genetic hearing loss

    0.18
  • Hearing impairment

    0.12
  • hearing loss, autosomal recessive

    0.08
  • Usher syndrome

    0.08
  • Usher syndrome type 1

    0.08
  • mirror movements 4

    0.07
  • mirror movements 2

    0.07

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.