Symbol Name ID |
Pex5
peroxisomal biogenesis factor 5 MGI:1098808 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the mitochondrion |
Disease(s) Associated with PEX5 | |
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 |
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Availability | Mouse Genotype | |||||||||
Pex5tm1Pec/Pex5tm1Pec Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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 08/21/2024 MGI 6.24 |
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