Symbol Name ID |
Pex1
peroxisomal biogenesis factor 1 MGI:1918632 |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Cirrhosis |
Hepatic fibrosis |
Intrahepatic biliary dysgenesis |
Prolonged neonatal jaundice |
Disease(s) Associated with PEX1 | |||||
peroxisome biogenesis disorder 1A | |||||
peroxisome biogenesis disorder 1B |
Mouse Phenotypes | bile duct proliferation |
enlarged liver |
decreased liver glycogen level |
increased liver cholesterol level |
increased liver triglyceride level |
liver inflammation |
abnormal liver morphology |
hepatic necrosis |
microvesicular hepatic steatosis |
liver fibrosis |
increased liver adenoma incidence |
cholestasis |
|
Availability | Mouse Genotype | ||||||||||||
Pex1tm1.1Hrw/Pex1tm1.1Hrw | |||||||||||||
Pex1tm1.1Sjms/Pex1tm1.1Sjms |
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 08/02/2024 MGI 6.24 |
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