This gene encodes a member of the fibroblast growth factor family of proteins, which possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. The product of this gene regulates phosphate homeostasis and transport in the kidney. The full-length, functional protein may be deactivated via cleavage into N-terminal and C-terminal chains. Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR). Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC). [provided by RefSeq, Feb 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FGF23-20-RE | 20 (40 μL) | 200 μL |  |
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| FGF23-20-OR | 20 (40 μL) | 200 μL |  |
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| FGF23-20-GO | 20 (40 μL) | 200 μL |  |
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| FGF23-20-GR | 20 (40 μL) | 200 μL |  |
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| FGF23-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the fibroblast growth factor family of proteins, which possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. The product of this gene regulates phosphate homeostasis and transport in the kidney. The full-length, functional protein may be deactivated via cleavage into N-terminal and C-terminal chains. Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR). Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC). [provided by RefSeq, Feb 2013]
Gene Symbol : FGF23
Gene Name : Fibroblast growth factor 23
Chromosome : CHR 12: 437,972,7-436,822,6
Locus : 12p13.32
Alt. Genes : OPTN
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