FGF22
Description
The FGF22 (fibroblast growth factor 22) is a protein-coding gene located on chromosome 19.
Fibroblast growth factor 22 (FGF22) is a protein encoded by the FGF22 gene. It belongs to the fibroblast growth factor (FGF) family, known for their diverse roles in cell growth, development, and repair. Like other FGFs, FGF22 is involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. While its specific function in humans is still being studied, research in mice suggests a role in hair development. This information comes from the U.S. National Library of Medicine, which is in the public domain.
FGF22 plays a role in the body's response to fasting, regulating glucose levels, breaking down and building fats (lipolysis and lipogenesis). It can also stimulate cell growth in laboratory settings. Additionally, it may be involved in hair development.
FGF22 is also known as -.
Associated Diseases
- cancer
- isolated asymptomatic elevation of creatine phosphokinase
- distal myopathy with anterior tibial onset
- pentosuria
- papilloma
- spinal cord injury
