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Symbol Name ID |
Pex2
peroxisomal biogenesis factor 2 MGI:107486 |
| Darker colors indicate more annotations |
| Human Phenotypes | Splenomegaly |
Hepatosplenomegaly |
Hepatomegaly |
Failure to thrive |
Small for gestational age |
Intrauterine growth retardation |
| Disease(s) Associated with PEX2 | ||||||
| peroxisome biogenesis disorder 5A |
| Mouse Phenotypes | decreased embryo weight |
microcephaly |
postnatal growth retardation |
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| Availability | Mouse Genotype | |||
| Pex2tm1Plf/Pex2tm1Plf | ||||
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 04/30/2024 MGI 6.23 |
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