Symbol Name ID |
Pex5
peroxisomal biogenesis factor 5 MGI:1098808 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Intrahepatic biliary dysgenesis |
Jaundice |
Disease(s) Associated with PEX5 | |||
peroxisome biogenesis disorder 2A |
Mouse Phenotypes | liver/biliary system phenotype |
enlarged liver |
liver hyperplasia |
abnormal liver morphology |
increased liver tumor incidence |
|
Availability | Mouse Genotype | |||||
Pex5tm1Baes/Pex5tm1Baes | ||||||
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 04/16/2024 MGI 6.23 |
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