Symbol Name ID |
Pex1
peroxisomal biogenesis factor 1 MGI:1918632 |
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 |
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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