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Symbol
Name
ID
Pex1
peroxisomal biogenesis factor 1
MGI:1918632
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Elevated circulating long chain fatty acid concentration
Albuminuria
Aminoaciduria
Hyperoxaluria
Epiphyseal stippling
Disease(s) Associated with PEX1
peroxisome biogenesis disorder 1A
peroxisome biogenesis disorder 1B

Mouse Phenotypes
abnormal intestinal lipid absorption
hyperglycemia
abnormal circulating phospholipid level
abnormal venous thrombosis
decreased liver glycogen level
abnormal bile salt homeostasis
increased liver cholesterol level
abnormal fatty acids level
decreased fatty acids level
increased fatty acids level
increased saturated fatty acids level
abnormal phospholipid level
increased liver triglyceride level
Availability Mouse Genotype
Pex1tm1.1Hrw/Pex1tm1.1Hrw
Pex1tm1.1Sjms/Pex1tm1.1Sjms

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory