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Symbol
Name
ID
Pepd
peptidase D
MGI:97542
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Abnormality of retinal pigmentation
Hypertelorism
Proptosis
Visual impairment
Ptosis
Disease(s) Associated with PEPD
prolidase deficiency

Mouse Phenotypes
abnormal optic disk morphology
abnormal cornea 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