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Symbol Name ID |
Sco2
SCO2 cytochrome c oxidase assembly protein MGI:3818630 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hepatomegaly |
| Disease(s) Associated with SCO2 | |
| mitochondrial complex IV deficiency nuclear type 2 |
| Mouse Phenotypes | increased liver copper level |
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| Availability | Mouse Genotype | |
| Sco2tm1.1Easc/Sco2tm2.1Easc | ||
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 05/14/2024 MGI 6.23 |
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