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Symbol
Name
ID

Pex7
peroxisomal biogenesis factor 7
MGI:1321392

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Spasticity	Delayed CNS myelination	Cerebral cortical atrophy	Intellectual disability	Seizure
Disease(s) Associated with PEX7
rhizomelic chondrodysplasia punctata type 1

Mouse Phenotypes		abnormal neuronal migration	abnormal hippocampus morphology	abnormal cerebral cortex morphology	abnormal spinal cord morphology	demyelination
Availability	Mouse Genotype	abnormal neuronal migration	abnormal hippocampus morphology	abnormal cerebral cortex morphology	abnormal spinal cord morphology	demyelination
	Pex7^tm1Nbra/Pex7^tm1Nbra
	Pex7^tm1Rjaw/Pex7^tm1Rjaw

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