Symbol Name ID |
Pex6
peroxisomal biogenesis factor 6 MGI:2385054 |
Darker colors indicate more annotations |
Human Phenotypes | Global developmental delay |
Seizure |
Disease(s) Associated with PEX6 | ||
Heimler syndrome 2 | ||
peroxisome biogenesis disorder 4A |
Mouse Phenotypes | abnormal optic disk morphology |
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Availability | Mouse Genotype | |
Pex6em1(IMPC)Tcp/Pex6+ |
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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