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Symbol
Name
ID
Pepd
peptidase D
MGI:97542
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Intellectual disability
Global developmental delay
Mild global developmental delay
Febrile seizure (within the age range of 3 months to 6 years)
Disease(s) Associated with PEPD
prolidase deficiency

Mouse Phenotypes
brain vacuoles
abnormal optic disk morphology
Availability Mouse Genotype
Pepddal/Pepddal
Pepdtm1b(KOMP)Wtsi/Pepdtm1b(KOMP)Wtsi

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
11/10/2020
MGI 6.16
The Jackson Laboratory