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Symbol
Name
ID
Pex13
peroxisomal biogenesis factor 13
MGI:1919379
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
CNS hypomyelination
Lissencephaly
Polymicrogyria
Global developmental delay
Seizures
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
Availability Mouse Genotype
Pex13tm1.1Crne/Pex13tm1.1Crne
Pex13tm1Crne/Pex13tm1.1Crne
Tg(Nes-cre)1Kln/0  (conditional)

Contributing Projects:
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
12/03/2019
MGI 6.14
The Jackson Laboratory