About   Help   FAQ
Symbol
Name
ID
Ppib
peptidylprolyl isomerase B
MGI:97750
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Decreased calvarial ossification
Wormian bones
Dentinogenesis imperfecta
Disease(s) Associated with PPIB
osteogenesis imperfecta type 9

Mouse Phenotypes
abnormal neurocranium morphology
Availability Mouse Genotype
PpibGt(RST139)Byg/PpibGt(RST139)Byg

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/09/2024
MGI 6.23
The Jackson Laboratory