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Symbol
Name
ID

Cox15
cytochrome c oxidase assembly protein 15
MGI:1920112

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties	Emotional lability
Disease(s) Associated with COX15	Decreased fetal movement	Feeding difficulties	Emotional lability
Leigh disease
mitochondrial complex IV deficiency nuclear type 6

Mouse Phenotypes		abnormal motor capabilities/coordination/movement
Availability	Mouse Genotype	abnormal motor capabilities/coordination/movement
	Cox15^tm1.1Zev/Cox15^tm1.1Zev Tg(ACTA1-cre)79Jme/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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