Symbol Name ID |
Pepd
peptidase D MGI:97542 |
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 |
abnormal retina morphology |
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Availability | Mouse Genotype | |||
Pepdtm1a(KOMP)Wtsi/Pepdtm1a(KOMP)Wtsi | ||||
Pepdtm1b(KOMP)Wtsi/Pepdtm1b(KOMP)Wtsi |
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 09/03/2024 MGI 6.24 |
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