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Symbol
Name
ID
Ppib
peptidylprolyl isomerase B
MGI:97750
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Decreased calvarial ossification
Wormian bones
Dentinogenesis imperfecta
Short lower limbs
Bowing of limbs due to multiple fractures
Multiple prenatal fractures
Recurrent fractures
Multiple rib fractures
Pectus carinatum
Pectus excavatum
Kyphosis
Scoliosis
Platyspondyly
Disease(s) Associated with PPIB
osteogenesis imperfecta type 9

Mouse Phenotypes
abnormal neurocranium morphology
abnormal femur morphology
decreased femur compact bone thickness
decreased femoral compact bone area
short femur
increased internal diameter of femur
short tibia
abnormal thoracic cage morphology
kyphosis
decreased bone mineral density of vertebrae
decreased areal bone mineral density
decreased bone mineral density of femur
decreased bone mineral density
decreased trabecular bone volume
decreased bone trabecula number
increased bone trabecular spacing
decreased trabecular bone thickness
osteoporosis
decreased bone mineralization
decreased femur stiffness
decreased bone strength
decreased femur maximal load
decreased femur yield load
fragile skeleton
Availability Mouse Genotype
PpibGt(RST139)Byg/PpibGt(RST139)Byg
Ppibtm1.1Rjb/Ppibtm1.1Rjb

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory