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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Bglap2-Phex)1Ldq
transgene insertion 1, L Darryl Quarles
MGI:4431210
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
PhexHyp/Phex+
Tg(Bglap2-Phex)1Ldq/?
involves: C57BL/6J MGI:4431220
tg2
Tg(Bglap2-Phex)1Ldq/? involves: C57BL/6J MGI:4431215


Genotype
MGI:4431220
cx1
Allelic
Composition
PhexHyp/Phex+
Tg(Bglap2-Phex)1Ldq/?
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
PhexHyp mutation (2 available); any Phex mutation (21 available)
Tg(Bglap2-Phex)1Ldq mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• despite increased Phex expression in osteoblasts these mice still have the diminished serum phosphate of hypophosphatemia mutants

skeleton
• despite increased Phex expression in osteoblasts these mice have the same skeletal defects of hypophosphatemia mice including reduced bone mineral density, smaller than normal caudal vertebrae, increased widening and irregularity of growth plates, rickets and osteomalacia




Genotype
MGI:4431215
tg2
Allelic
Composition
Tg(Bglap2-Phex)1Ldq/?
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• despite bone-specific over-expression of Phex shown to cause increased endopeptidase activity, these mice are indistinguishabe from non-transgenic controls including normal serum phosphate levels and normal bone mineralization, osteoid thickness, and bone mass





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory