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HGF

Chr 7q21.11

hepatocyte growth factor

Aliases:
SF, F-TCF, HGFB, HPTA
MANE:
ENST00000222390.11

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Monogenic hearing loss

    BIALLELIC, autosomal or pseudoautosomal
  • Primary lymphoedema

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Disease associations (Open Targets)

  • hearing loss, autosomal recessive

    0.61
  • gastric adenocarcinoma

    0.41
  • gastroesophageal junction adenocarcinoma

    0.40
  • prostate carcinoma

    0.40
  • melanoma

    0.40
  • lung carcinoma

    0.40
  • cancer

    0.40
  • deafness

    0.39
  • esophageal adenocarcinoma

    0.39
  • lung adenocarcinoma

    0.39

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

Protein function (UniProt)

Hepatocyte growth factor

Potent mitogen for mature parenchymal hepatocyte cells, seems to be a hepatotrophic factor, and acts as a growth factor for a broad spectrum of tissues and cell types (PubMed:20624990). Activating ligand for the receptor tyrosine kinase MET by binding to it and promoting its dimerization (PubMed:15167892, PubMed:20977675). Activates MAPK signaling following TMPRSS13 cleavage and activation (PubMed:20977675)

Curated MONDO disease pages that list HGF among their top associated genes.

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.