| Human Disease |
Dentatorubral-Pallidoluysian Atrophy; DRPLA OMIM ID: 125370 |
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| Synonyms | Ataxia, Chorea, Seizures, and Dementia; Haw River Syndrome; HRS; Myoclonic Epilepsy with Choreoathetosis; Naito-Oyanagi Disease; NOD | |||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Tg(ATN1*)Q129Stsu/0 |
involves: 129S/SvEv * C57BL/6J | J:144379 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Eno2-ATN1)3Tx/Tg(Eno2-ATN1)3Tx |
B6.Cg-Tg(Eno2-ATN1)3Tx | J:112706 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Eno2-ATN1)14Tx/0 |
B6.Cg-Tg(Eno2-ATN1)14Tx | J:112706 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Prnp-ATN1)124Dbo/? |
involves: C3H * C57BL/6 | J:70362 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Prnp-ATN1)150Dbo/? |
involves: C3H * C57BL/6 | J:70362 | 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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