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Symbol Name ID |
Pex2
peroxisomal biogenesis factor 2 MGI:107486 |
| Darker colors indicate more annotations |
| Human Phenotypes | Oculomotor apraxia |
Colpocephaly |
Pachygyria |
Polymicrogyria |
Agenesis of corpus callosum |
Cerebellar vermis atrophy |
Cerebellar hypoplasia |
Cerebellar atrophy |
Ataxia |
Dysmetria |
Athetosis |
Tremor |
Lethargy |
Dysarthria |
Intellectual disability |
Vegetative state |
Areflexia |
Hyporeflexia |
Unsteady gait |
Global developmental delay |
Seizure |
Generalized-onset seizure |
| Disease(s) Associated with PEX2 | ||||||||||||||||||||||
| peroxisome biogenesis disorder 5A | ||||||||||||||||||||||
| Peroxisome biogenesis disorder 5B |
| Mouse Phenotypes | abnormal cerebellar foliation |
abnormal cerebellum external granule cell layer morphology |
decreased brain size |
abnormal brain white matter morphology |
abnormal cerebral cortex lamination |
abnormal cerebellum morphology |
abnormal Purkinje cell morphology |
abnormal cerebellar granule layer morphology |
small cerebellum |
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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 07/08/2026 MGI 6.24 |
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