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FGF20

Chr 8p22

fibroblast growth factor 20

MANE:
ENST00000180166.6

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Moderate Evidence (Amber)

  • CAKUT

    BIALLELIC, autosomal or pseudoautosomal
  • Fetal anomalies

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • cancer

    0.60
  • bone development disease

    0.60
  • renal hypodysplasia/aplasia 2

    0.40
  • bilateral renal agenesis

    0.38
  • craniosynostosis

    0.38
  • renal agenesis

    0.37
  • ovarian carcinoma

    0.37
  • female reproductive endometrioid cancer

    0.37
  • acrocephalosyndactyly

    0.37
  • Parkinson disease

    0.34

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

Protein function (UniProt)

Fibroblast growth factor 20

Neurotrophic factor that regulates central nervous development and function

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.