| Human Disease |
Mitochondrial DNA Depletion Syndrome 2 (myopathic Type); MTDPS2 OMIM ID: 609560 |
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| Synonyms | Mitochondrial DNA Depletion Myopathy, Tk2-Related | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tk2tm1Mihi/Tk2tm1Mihi |
involves: 129X1/SvJ * C57BL/6J | J:139195, J:166725 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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