About   Help   FAQ
Symbol
Name
ID
Mto1
mitochondrial tRNA translation optimization 1
MGI:1915541
Phenotype annotations related to cellular
Darker colors indicate more annotations
Human Phenotypes
Decreased activity of mitochondrial complex III
Disease(s) Associated with MTO1
combined oxidative phosphorylation deficiency 10

Mouse Phenotypes
decreased myocardial fiber mitochondrial DNA content
cardiac muscle necrosis
abnormal mitochondrial inner membrane morphology
abnormal mitochondrial physiology
Availability Mouse Genotype
Mto1Gt(G019A03)Wrst/Mto1Gt(G019A03)Wrst

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
The Jackson Laboratory