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Symbol
Name
ID

Pex5
peroxisomal biogenesis factor 5
MGI:1098808

Phenotype annotations related to cellular

Darker colors indicate more annotations

Human Phenotypes	Abnormality of the mitochondrion
Disease(s) Associated with PEX5	Abnormality of the mitochondrion
peroxisome biogenesis disorder 2A

Mouse Phenotypes		abnormal cell morphology	abnormal endoplasmic reticulum morphology	abnormal mitochondrial inner membrane morphology	abnormal mitochondrial crista morphology	abnormal mitochondrial shape	abnormal lysosome morphology	abnormal respiratory electron transport chain	abnormal mitochondrial ATP synthesis coupled electron transport	abnormal fatty acid beta-oxidation
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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