Symbol Name ID |
Pex5
peroxisomal biogenesis factor 5 MGI:1098808 |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Short stature |
Failure to thrive |
Growth delay |
Intrauterine growth retardation |
Disease(s) Associated with PEX5 | |||||
peroxisome biogenesis disorder 2A | |||||
rhizomelic chondrodysplasia punctata type 5 |
Mouse Phenotypes | embryonic growth retardation |
decreased body weight |
slow postnatal weight gain |
abnormal postnatal growth |
enlarged liver |
liver hyperplasia |
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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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