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Symbol
Name
ID
Cox10
heme A:farnesyltransferase cytochrome c oxidase assembly factor 10
MGI:1917633
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Death in infancy
Disease(s) Associated with COX10
mitochondrial complex IV deficiency nuclear type 3

Mouse Phenotypes
premature death
Availability Mouse Genotype
Cox10tm1Ctm/Cox10tm1Ctm
Myl1tm1(cre)Sjb/Myl1+  (conditional)
Cox10tm1Ctm/Cox10tm1Ctm
Tg(Camk2a-cre)#Szi/0  (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
04/16/2024
MGI 6.23
The Jackson Laboratory