| Human Disease |
Mitochondrial DNA Depletion Syndrome 1 (mngie Type); MTDPS1 OMIM ID: 603041 |
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| Synonyms | Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Tymp-Related; Mngie, Tymp-Related; Myoneurogastrointestinal Encephalopathy Syndrome; Polip Syndrome; Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudoobstruction | |||||||||||||||||||||
| View all models | View ALL (2) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI. | |||||||||||||||||||||
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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 |
| Tymptm1Akiy/Tymptm1Akiy |
involves: 129X1/SvJ | J:78036 | View |
| Tymptm1Akiy/Tymptm1Akiy Upp1tm1Akiy/Upp1tm1Akiy |
involves: 129X1/SvJ | J:78036 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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