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Symbol
Name
ID

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

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties in infancy	Agitation
Disease(s) Associated with COX10	Feeding difficulties in infancy	Agitation
mitochondrial complex IV deficiency nuclear type 3

Mouse Phenotypes		abnormal motor capabilities/coordination/movement	impaired coordination	abnormal locomotor activation	decreased vertical activity	decreased locomotor activity
Availability	Mouse Genotype	abnormal motor capabilities/coordination/movement	impaired coordination	abnormal locomotor activation	decreased vertical activity	decreased locomotor activity
	Cox10^tm1Ctm/Cox10^tm1Ctm Myl1^tm1(cre)Sjb/Myl1⁺ (conditional)
	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)
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