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Symbol
Name
ID

Pex5
peroxisomal biogenesis factor 5
MGI:1098808

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Intellectual disability	Intellectual disability, severe	Areflexia	Hyporeflexia	Broad-based gait	Global developmental delay	Peripheral neuropathy	Seizure	Convulsive status epilepticus
Disease(s) Associated with PEX5	Microcephaly	Intellectual disability	Intellectual disability, severe	Areflexia	Hyporeflexia	Broad-based gait	Global developmental delay	Peripheral neuropathy	Seizure	Convulsive status epilepticus
peroxisome biogenesis disorder 2A
peroxisome biogenesis disorder 2B
rhizomelic chondrodysplasia punctata type 5

Mouse Phenotypes		microgliosis	delayed brain development	abnormal brain white matter morphology	abnormal cerebral cortex morphology	abnormal glial cell morphology	abnormal oligodendrocyte morphology	gliosis	abnormal axon morphology	abnormal myelination
Availability	Mouse Genotype	microgliosis	delayed brain development	abnormal brain white matter morphology	abnormal cerebral cortex morphology	abnormal glial cell morphology	abnormal oligodendrocyte morphology	gliosis	abnormal axon morphology	abnormal myelination
	Pex5^tm1Baes/Pex5^tm1Baes
	Pex5^tm1Pec/Pex5^tm1Pec Cnp^tm1(cre)Kan/Cnp⁺ (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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23