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Symbol Name ID |
Pex13
peroxisomal biogenesis factor 13 MGI:1919379 |
| Darker colors indicate more annotations |
| Human Phenotypes | CNS hypomyelination |
Lissencephaly |
Polymicrogyria |
Global developmental delay |
Seizure |
| Disease(s) Associated with PEX13 | |||||
| peroxisome biogenesis disorder 11A |
| Mouse Phenotypes | abnormal Purkinje cell differentiation |
abnormal cerebellar granule cell migration |
decreased brain plasmalogen level |
abnormal cerebellum development |
reduced cerebellar foliation |
abnormal cerebellum external granule cell layer morphology |
abnormal cerebral cortex morphology |
thin cerebral cortex |
abnormal cerebellar Purkinje cell layer |
abnormal Purkinje cell morphology |
abnormal Purkinje cell dendrite morphology |
thin cerebellar molecular layer |
abnormal cerebellum fissure morphology |
astrocytosis |
gliosis |
neuron degeneration |
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| Availability | Mouse Genotype | ||||||||||||||||
| Pex13tm1.1Crne/Pex13tm1.1Crne | |||||||||||||||||
| Pex13tm1Crne/Pex13tm1.1Crne Tg(Nes-cre)1Kln/0 (conditional) |
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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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