FGF20 Chromosome 8

Fibroblast growth factor 20
2 variants 2 Health Risk

Upload your DNA to see your personal genotypes for variants in FGF20.

What This Gene Does
The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene product is a secreted neurotrophic factor but lacks a typical signal peptide. It is expressed in normal brain, particularly the cerebellum, and may regulate central nervous system development and function. Homodimerization of this protein was shown to regulate its receptor binding activity and concentration gradient in the extracellular matrix. Genetic variations of this gene have been associated with Parkinson disease susceptibility. [provided by RefSeq, Oct 2009]
Gene Info
Gene Group
Fibroblast growth factor family
Locus Type
gene with protein product
Location
8p22
Ensembl
ENSG00000078579
Associated Conditions (1)
Renal hypodysplasia/aplasia 2
Key Variants
All Variants (2)
RSID Category Clinical Significance Conditions
RS1585100306 Health Risk Likely pathogenic Renal hypodysplasia/aplasia 2, Renal hypodysplasia/aplasia 2
RS587777282 Health Risk Pathogenic Renal hypodysplasia/aplasia 2, Renal hypodysplasia/aplasia 2
Sign Up to Analyze Your DNA Log In