Skip to content
GenoLensGenoLens

VCAN

Chr 5q14.2-q14.3

versican

Aliases:
PG-M
MANE:
ENST00000265077.8

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Retinal disorders

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Stickler syndrome

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Glaucoma (developmental)

  • Structural eye disease

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Disease associations (Open Targets)

  • Wagner disease

    0.75
  • Abnormality of the skeletal system

    0.57
  • diverticular disease

    0.51
  • Retinal dystrophy

    0.45
  • hereditary disease

    0.42
  • eye disorder

    0.37
  • abdominal aortic aneurysm

    0.36
  • aortic aneurysm

    0.36
  • carpal tunnel syndrome

    0.36
  • Stickler syndrome

    0.34

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

Protein function (UniProt)

Versican core protein

May play a role in intercellular signaling and in connecting cells with the extracellular matrix. May take part in the regulation of cell motility, growth and differentiation. Binds hyaluronic acid

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.