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MIR140

Chr 16q22.1

microRNA 140

Aliases:
hsa-mir-140, MIR-140

Annotations refreshed 1 month ago.

Predicted protein structure

No predicted 3D structure for MIR140. Non-coding genes and pseudogenes typically have no protein product.

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • DDG2P

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Disease associations (Open Targets)

  • Spondyloepiphyseal dysplasia, Nishimura type

    0.39
  • autosomal dominant brachyolmia

    0.08
  • autosomal recessive spondylocostal dysostosis

    0.08
  • osteogenesis imperfecta

    0.07
  • osteomesopyknosis

    0.07
  • spondyloepiphyseal dysplasia tarda, autosomal dominant

    0.07
  • metaphyseal anadysplasia

    0.07
  • Acromesomelic dysplasia, Maroteaux type

    0.07
  • Greenberg dysplasia

    0.07
  • spondylometaphyseal dysplasia, 'corner fracture' type

    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.