FGF23 wt Allele

Human FGF23 wild-type allele is located in the vicinity of 12p13.3 and is approximately 12 kb in length. This allele, which encodes fibroblast growth factor 23 protein, plays a role in regulation of phosphate homeostasis. Mutations in this gene are associated with autosomal dominant hypophosphatemic rickets (ADHR) and familial tumoral calcinosis with hyperphosphatemia. It is overexpressed in oncogenic hypophosphatemic osteomalacia (OHO). (NCI Thesaurus)

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FGF23 Gene

This gene is involved in phosphate homeostasis.

FGF21 wt Allele

Human FGF21 wild-type allele is located within 19q13.1-qter and is approximately 3 kb in length. This allele, which encodes fibroblast growth factor…

FGF21 Gene

This gene plays a role in signal transduction.

FGF20 wt Allele

Human FGF20 wild-type allele is located within 8p22-p21.3 and is approximately 9 kb in length. This allele, which encodes fibroblast growth factor…

FGF20 Gene

This gene plays a role in development, cell growth, morphogenesis and tissue repair.

FGF2 wt Allele

Human FGF2 wild-type allele is located within 4q26-q27 and is approximately 72 kb in length. This allele, which encodes heparin-binding growth factor…