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Symbol Name ID |
Sco1
SCO1 cytochrome c oxidase assembly protein MGI:106362 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hepatomegaly |
Failure to thrive |
Intrauterine growth retardation |
| Disease(s) Associated with SCO1 | |||
| mitochondrial complex IV deficiency nuclear type 4 |
| Mouse Phenotypes | weight loss |
decreased body size |
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| Availability | Mouse Genotype | ||
| Sco1tm1c(KOMP)Wtsi/Sco1tm1c(KOMP)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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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 05/21/2024 MGI 6.23 |
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