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 08/02/2024 MGI 6.24 |
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