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Symbol
Name
ID
Mto1
mitochondrial tRNA translation optimization 1
MGI:1915541
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Spasticity
Hypotonia
Disease(s) Associated with MTO1
combined oxidative phosphorylation deficiency 10

Mouse Phenotypes
decreased myocardial fiber mitochondrial DNA content
myocardial fiber degeneration
cardiac muscle necrosis
cardiomyopathy
dilated sarcoplasmic reticulum
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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory