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Symbol
Name
ID
Pepd
peptidase D
MGI:97542
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Hypoplasia of the zygomatic bone
Genu valgum
Arachnodactyly
Abnormality of the hip bone
Reduced bone mineral density
Disease(s) Associated with PEPD
prolidase deficiency

Mouse Phenotypes
short tibia
abnormal bone structure
decreased bone mineral content
decreased bone mineral density
abnormal joint morphology
Availability Mouse Genotype
Pepdtm1a(KOMP)Wtsi/Pepdtm1a(KOMP)Wtsi
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
06/23/2020
MGI 6.15
The Jackson Laboratory