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Symbol
Name
ID
Tk2
thymidine kinase 2, mitochondrial
MGI:1913266
Phenotype annotations related to cellular
Darker colors indicate more annotations
Human Phenotypes
Decreased activity of mitochondrial respiratory chain
Disease(s) Associated with TK2
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
mitochondrial DNA depletion syndrome 2

Mouse Phenotypes
decreased mitochondrial DNA content
abnormal mitochondrial crista morphology
abnormal mitochondrial ATP synthesis coupled electron transport
Availability Mouse Genotype
Tk2tm1Anka/Tk2tm1Anka
Tk2tm1Mihi/Tk2tm1Mihi

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
05/26/2020
MGI 6.15
The Jackson Laboratory