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Symbol Name ID |
Pex2
peroxisomal biogenesis factor 2 MGI:107486 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Persistent open anterior fontanelle |
Wide anterior fontanel |
Large fontanelles |
Metatarsus adductus |
Cubitus valgus |
Camptodactyly |
Epiphyseal stippling |
Stippled chondral calcification |
| Disease(s) Associated with PEX2 | |||||||||
| peroxisome biogenesis disorder 5A |
| Mouse Phenotypes | abnormal neurocranium morphology |
abnormal frontal bone morphology |
abnormal interparietal bone morphology |
decreased bone mineral density |
decreased bone mineralization |
delayed intramembranous bone ossification |
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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 04/16/2024 MGI 6.23 |
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