57 phenotypes from 4 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf23tm1.1Kew/Fgf23+ B6.129-Fgf23tm1.1Kew	decreased circulating phosphate level	J:180061
	increased circulating alkaline phosphatase level	J:180061
Fgf23tm1.1Kew/Fgf23tm1.1Kew B6.129-Fgf23tm1.1Kew	abnormal compact bone morphology	J:180061
	abnormal osteoid morphology	J:180061
	abnormal vitamin D level	J:180061
	decreased circulating phosphate level	J:180061
	increased circulating alkaline phosphatase level	J:180061
	increased osteoid thickness	J:180061
	osteomalacia	J:180061
Fgf23tm1Blan/Fgf23tm1Blan involves: 129 * C57BL/6	decreased body size	J:173962
	increased circulating phosphate level	J:173962
	premature death	J:173962
Fgf23tm1Blan/Fgf23tm1Blan involves: 129/Sv * C57BL/6	abnormal bone mineralization	J:121006
	abnormal bronchus morphology	J:121006
	decreased body weight	J:121006
	decreased circulating insulin level	J:121006
	decreased circulating serum albumin level	J:121006
	decreased compact bone thickness	J:121006
	decreased volumetric bone mineral density	J:121006
	hypoglycemia	J:121006
	improved glucose tolerance	J:121006
	increased blood urea nitrogen level	J:121006
	increased circulating alkaline phosphatase level	J:121006
	increased circulating calcium level	J:121006
	increased circulating phosphate level	J:121006
	small spleen	J:121006
	thin skin	J:121006
Fgf23tm1Blan/Fgf23tm1Blan Not Specified	abnormal axial skeleton morphology	J:94041
	abnormal bone mineralization	J:94041
	abnormal femur morphology	J:94041
	abnormal mineral homeostasis	J:94041
	abnormal rib morphology	J:94041
	abnormal vertebrae morphology	J:94041
	decreased body weight	J:94041
	decreased bone mineral density	J:94041
	decreased chondrocyte number	J:94041
	decreased long bone epiphyseal plate size	J:94041
	decreased volumetric bone mineral density	J:94041
	fragile skeleton	J:94041
	increased bone mineral content	J:94041
	increased circulating alkaline phosphatase level	J:94041
	increased circulating phosphate level	J:94041
	postnatal growth retardation	J:94041
	premature death	J:94041
	thickened long bone epiphysis	J:94041
Fgf23tm1Sliu/Fgf23tm1Sliu involves: 129S/SvEv * C57BL/6	abnormal bone mineralization	J:110579
	abnormal bone structure	J:110579
	abnormal circulating calcium level	J:110579
	abnormal circulating phosphate level	J:110579
	abnormal long bone hypertrophic chondrocyte zone	J:110579
	abnormal long bone metaphysis morphology	J:110579
	abnormal long bone morphology	J:110579
	abnormal trabecular bone morphology	J:110579
	abnormal vitamin D level	J:110579
	decreased body length	J:110579
	decreased body weight	J:110579
	decreased bone mineral density	J:110579
	decreased circulating parathyroid hormone level	J:110579
	premature death	J:110579
	short femur	J:110579
Fgf23tm1Tyam/Fgf23tm1Tyam involves: C57BL/6 * CBA	abnormal blood urea nitrogen level	J:88172
	abnormal kidney morphology	J:88172
	abnormal renal glomerulus morphology	J:88172
	abnormal renal phosphate reabsorption	J:88172
	abnormal reproductive system morphology	J:88172
	abnormal skeleton development	J:88172
	abnormal vitamin D level	J:88172
	decreased body size	J:88172
	decreased body weight	J:88172
	decreased bone mineral density	J:88172
	decreased chondrocyte number	J:88172
	decreased circulating parathyroid hormone level	J:88172
	decreased circulating triglyceride level	J:88172
	decreased lymphocyte cell number	J:88172
	hypoglycemia	J:88172
	increased circulating calcium level	J:88172
	increased circulating cholesterol level	J:88172
	increased circulating phosphate level	J:88172
	infertility	J:88172
	postnatal growth retardation	J:88172
	premature death	J:88172
	short femur	J:88172
	spleen hypoplasia	J:88172
	thymus atrophy	J:88172