Symbol Name ID |
Pepd
peptidase D MGI:97542 |
Darker colors indicate more annotations |
Human Phenotypes | Petechiae |
Splenomegaly |
Erythema |
Diffuse telangiectasia |
Disease(s) Associated with PEPD | ||||
prolidase deficiency |
Mouse Phenotypes | abnormal aorta collagen fibril morphology |
abnormal cardiac muscle tissue morphology |
abnormal myocardial fiber morphology |
myocardium hypertrophy |
increased atrioventricular cushion size |
increased fetal cardiomyocyte size |
abnormal heart morphology |
abnormal heart septum morphology |
atrioventricular septal defect |
thick interventricular septum |
ventricular septal defect |
thick ventricular wall |
decreased heart rate |
prolonged RR interval |
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Availability | Mouse Genotype | ||||||||||||||
Pepddal/Pepddal | |||||||||||||||
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 05/28/2024 MGI 6.13 |
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