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Symbol
Name
ID

Pex1
peroxisomal biogenesis factor 1
MGI:1918632

Phenotype annotations related to liver/biliary system

Darker colors indicate more annotations

Human Phenotypes	Hepatomegaly	Cirrhosis	Hepatic fibrosis	Intrahepatic biliary dysgenesis	Prolonged neonatal jaundice
Disease(s) Associated with PEX1	Hepatomegaly	Cirrhosis	Hepatic fibrosis	Intrahepatic biliary dysgenesis	Prolonged neonatal jaundice
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

Pex1^tm1.1Hrw/Pex1^tm1.1Hrw

Pex1^tm1.1Sjms/Pex1^tm1.1Sjms

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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