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Symbol
Name
ID
Fgf23
fibroblast growth factor 23
MGI:1891427
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Hypoplasia of dental enamel
Hypophosphatemic rickets
Vascular calcification
Osteomalacia
Bone pain
Disease(s) Associated with FGF23
autosomal dominant hypophosphatemic rickets
hyperphosphatemic familial tumoral calcinosis

Mouse Phenotypes
abnormal femur morphology
short femur
abnormal long bone morphology
abnormal long bone hypertrophic chondrocyte zone
decreased long bone epiphyseal plate size
thickened long bone epiphysis
abnormal long bone metaphysis morphology
abnormal axial skeleton morphology
abnormal rib morphology
abnormal vertebrae morphology
abnormal bone structure
increased bone mineral content
decreased volumetric bone mineral density
decreased bone mineral density
abnormal compact bone morphology
decreased compact bone thickness
abnormal trabecular bone morphology
decreased chondrocyte number
abnormal skeleton development
abnormal osteoid morphology
increased osteoid thickness
abnormal bone mineralization
osteomalacia
fragile skeleton
Availability Mouse Genotype
Fgf23tm1.1Kew/Fgf23tm1.1Kew
Fgf23tm1Blan/Fgf23tm1Blan
Fgf23tm1Sliu/Fgf23tm1Sliu
Fgf23tm1Tyam/Fgf23tm1Tyam

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/16/2018
MGI 6.12
The Jackson Laboratory