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Symbol
Name
ID
Sco2
SCO2 cytochrome c oxidase assembly protein
MGI:3818630
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Death in infancy
Disease(s) Associated with SCO2
mitochondrial complex IV deficiency nuclear type 2

Mouse Phenotypes
embryonic lethality between implantation and placentation, complete penetrance
Availability Mouse Genotype
Sco2tm1.1Easc/Sco2tm1.1Easc

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
04/16/2024
MGI 6.23
The Jackson Laboratory