HGF gene

hepatocyte growth factor

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a protein that binds to the hepatocyte growth factor receptor to regulate cell growth, cell motility and morphogenesis in numerous cell and tissue types. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate alpha and beta chains, which form the mature heterodimer. This protein is secreted by mesenchymal cells and acts as a multi-functional cytokine on cells of mainly epithelial origin. This protein also plays a role in angiogenesis, tumorogenesis, and tissue regeneration. Although the encoded protein is a member of the peptidase S1 family of serine proteases, it lacks peptidase activity. Mutations in this gene are associated with nonsyndromic hearing loss. [provided by RefSeq, Nov 2015]

From UniProt:

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. Activating ligand for the receptor tyrosine kinase MET by binding to it and promoting its dimerization.

Covered on Genetics Home Reference:

From NCBI Gene:

  • Deafness, autosomal recessive 39

From UniProt:

Deafness, autosomal recessive, 39 (DFNB39): A form of profound prelingual sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. [MIM:608265]

Cytogenetic Location: 7q21.1, which is the long (q) arm of chromosome 7 at position 21.1

Molecular Location: base pairs 81,699,006 to 81,770,438 on chromosome 7 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 7q21.1, which is the long (q) arm of chromosome 7 at position 21.1
  • DFNB39
  • F-TCF
  • HGFB
  • HPTA
  • SF