About   Help   FAQ
Symbol
Name
ID
Cox15
cytochrome c oxidase assembly protein 15
MGI:1920112
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Spasticity
Progressive spastic paraplegia
Muscular hypotonia
Generalized hypotonia
Disease(s) Associated with COX15
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2
Leigh disease

Mouse Phenotypes
increased variability of skeletal muscle fiber size
centrally nucleated skeletal muscle fibers
myopathy
Availability Mouse Genotype
Cox15tm1.1Zev/Cox15tm1.1Zev
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 & Copyright Notice
Send questions and comments to User Support.
last database update
02/11/2020
MGI 6.14
The Jackson Laboratory