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Human FGF-23 quantitates human FGF-23 in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human FGF-23.
The protein encoded by this gene is a member of the fibroblast growth factor family. FGF family members 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. The product of this gene inhibits renal tubular phosphate transport. This gene was identified by its mutations associated with autosomal dominant hypophosphatemic rickets, an inherited phosphate wasting disorder. Abnormally high level expression of this gene was found in oncogenic hypophosphatemic osteomalacia, a phenotypically similar disease caused by abnormal phosphate metabolism. Mutations in this gene have also been shown to cause familial tumoral calcinosis with hyperphosphatemia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Gene aliases : ADHR, FGF23, FGFN, HPDR2, HYPF, PHPTC, UNQ3027/PRO9828
Gene ID : (Human) 8074
Gene symbol : FGF23
Protein Aliases : FGF-23, Fibroblast growth factor 23, Phosphatonin, tumor-derived hypophosphatemia inducing factor, Tumor-derived hypophosphatemia-inducing factor
UniProt ID (Human) Q9GZV9
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