Skip to content
GenoLensGenoLens

RDX

Chr 11q22.3

radixin

MANE:
ENST00000645495.2

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Monogenic hearing loss

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • hearing loss, autosomal recessive

    0.70
  • nonsyndromic genetic hearing loss

    0.44
  • deafness

    0.38
  • Non-syndromic genetic deafness

    0.38
  • hearing loss disorder

    0.37
  • Rare genetic deafness

    0.34
  • cervical carcinoma

    0.32
  • myocardial infarction

    0.31
  • abdominal aortic aneurysm

    0.29
  • coronary artery disorder

    0.24

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

Protein function (UniProt)

Radixin

Probably plays a crucial role in the binding of the barbed end of actin filaments to the plasma membrane

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.