Symbol Name ID |
Pex10
peroxisomal biogenesis factor 10 MGI:2684988 |
Darker colors indicate more annotations |
Human Phenotypes | Colpocephaly |
Pachygyria |
Severe global developmental delay |
Seizure |
Disease(s) Associated with PEX10 | ||||
peroxisome biogenesis disorder 6A |
Mouse Phenotypes | abnormal axon extension |
abnormal axon fasciculation |
decreased Schwann cell number |
abnormal axon morphology |
abnormal neuromuscular synapse morphology |
abnormal endplate potential |
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Availability | Mouse Genotype | ||||||
Pex10m1Nisw/Pex10m1Nisw |
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 08/02/2024 MGI 6.24 |
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