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Symbol
Name
ID

Cox15
cytochrome c oxidase assembly protein 15
MGI:1920112

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Multiple joint contractures	Spasticity	Lower limb spasticity	Spastic diplegia	Hypotonia	Generalized hypotonia	Infantile muscular hypotonia	Muscle weakness	Distal muscle weakness	Skeletal muscle atrophy	Myopathy
Disease(s) Associated with COX15	Multiple joint contractures	Spasticity	Lower limb spasticity	Spastic diplegia	Hypotonia	Generalized hypotonia	Infantile muscular hypotonia	Muscle weakness	Distal muscle weakness	Skeletal muscle atrophy	Myopathy
Leigh disease
mitochondrial complex IV deficiency nuclear type 6

Mouse Phenotypes		abnormal muscle fiber mitochondrial morphology	increased variability of skeletal muscle fiber size	centrally nucleated skeletal muscle fibers	myopathy
Availability	Mouse Genotype
	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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23