Symbol Name ID |
Pepd
peptidase D MGI:97542 |
Darker colors indicate more annotations |
Human Phenotypes | Micrognathia |
Hypoplasia of the zygomatic bone |
Genu valgum |
Arachnodactyly |
Abnormal hip bone morphology |
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 |
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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 04/16/2024 MGI 6.23 |
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