Skip to content
GenoLensGenoLens

VEGFC

Chr 4q34.3

vascular endothelial growth factor C

Aliases:
VRP, VEGF-C
MANE:
ENST00000618562.2

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Fetal anomalies

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Primary lymphoedema

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Disease associations (Open Targets)

  • Milroy disease

    0.62
  • hypothyroidism

    0.53
  • Abnormality of the skeletal system

    0.48
  • thyroid gland disorder

    0.41
  • neurodegenerative disease

    0.37
  • diabetic macular edema

    0.34
  • Alzheimer disease

    0.33
  • macular retinal edema

    0.33
  • retinal vein occlusion

    0.32
  • choroidal neovascularization

    0.28

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

Protein function (UniProt)

Vascular endothelial growth factor C

Growth factor active in angiogenesis, and endothelial cell growth, stimulating their proliferation and migration and also has effects on the permeability of blood vessels. May function in angiogenesis of the venous and lymphatic vascular systems during embryogenesis, and also in the maintenance of differentiated lymphatic endothelium in adults. Binds and activates KDR/VEGFR2 and FLT4/VEGFR3 receptors

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.