| Human Disease |
Dystonia 1, Torsion, Autosomal Dominant; DYT1 OMIM ID: 128100 |
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| Synonyms | Dystonia Musculorum Deformans 1; Early-Onset Torsion Dystonia; EOTD | |||||||||||||||||||||
| View all models | View ALL (4) 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tor1atm1Yql/Tor1a+ |
involves: 129S2/SvPas * C57BL/6 | J:104513 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(CMV-TOR1A*)1Nush/0 |
involves: C3H * C57BL/6 | J:98716 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(CMV-TOR1A*)2Nush/0 |
involves: C3H * C57BL/6 | J:98716 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Eno2-TOR1A*)13Shas/0 |
involves: C3H * C57BL/6J | J:95447 | 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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