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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 04/30/2024 MGI 6.23 |
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