About Help FAQ

Symbol
Name
ID

Cox10
heme A:farnesyltransferase cytochrome c oxidase assembly factor 10
MGI:1917633

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Increased serum pyruvate	Hyperprolinemia	Hyperalaninemia	Increased CSF lactate	Neonatal hypoglycemia	Increased circulating lactate concentration	Lactic acidosis	Metabolic acidosis
Disease(s) Associated with COX10
mitochondrial complex IV deficiency nuclear type 3

Mouse Phenotypes		decreased dopamine level	abnormal enzyme/coenzyme activity
Availability	Mouse Genotype	decreased dopamine level	abnormal enzyme/coenzyme activity
	Cox10^tm1Ctm/Cox10^tm1Ctm Tg(Camk2a-cre)#Szi/0 (conditional)
	Cox10^tm1Ctm/Cox10^tm1Ctm Slc6a3^{tm1.1(cre)Bkmn}/? (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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23