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Symbol
Name
ID

Pex5
peroxisomal biogenesis factor 5
MGI:1098808

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Abnormality of the mitochondrion	Palpebral edema	Elevated circulating long chain fatty acid concentration	Aminoaciduria	Stippled chondral calcification
Disease(s) Associated with PEX5	Abnormality of the mitochondrion	Palpebral edema	Elevated circulating long chain fatty acid concentration	Aminoaciduria	Stippled chondral calcification
peroxisome biogenesis disorder 2A
peroxisome biogenesis disorder 2B

Mouse Phenotypes		abnormal fatty acid beta-oxidation	abnormal blood homeostasis	increased circulating lactate level	abnormal glucose homeostasis	abnormal bile salt homeostasis
Availability	Mouse Genotype
	Pex5^tm1Pec/Pex5^tm1Pec Speer6-ps1^{Tg(Alb-cre)21Mgn}/Speer6-ps1⁺ (conditional)

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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