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Symbol
Name
ID
Sco1
SCO1 cytochrome c oxidase assembly protein
MGI:106362
Phenotype annotations related to cellular
Darker colors indicate more annotations
Human Phenotypes
Decreased plasma free carnitine
Disease(s) Associated with SCO1
mitochondrial complex IV deficiency nuclear type 4

Mouse Phenotypes
increased mitochondrial number
abnormal mitochondrial physiology
Availability Mouse Genotype
Sco1tm1c(KOMP)Wtsi/Sco1tm1c(KOMP)Wtsi
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+  (conditional)

Contributing Projects:
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
04/23/2024
MGI 6.23
The Jackson Laboratory