| Human Disease |
Dystonia, Dopa-Responsive; DRD OMIM ID: 128230 |
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| Synonyms | Dopa-Responsive Dystonia, Autosomal Dominant; Dystonia 5; DYT5; Dystonia, Dopa-Responsive, Autosomal Dominant; Dystonia, Progressive, with Diurnal Variation; Dystonia-Parkinsonism with Diurnal Fluctuation; Segawa Syndrome, Autosomal Dominant | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Ptstm1Ich/Ptstm1Ich Tg(DBH-PTS)6Csic/0 |
involves: 129X1/SvJ * C57BL/6J | J:138968 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ptstm1Ich/Ptstm1Ich Tg(DBH-PTS)6Csic/0 |
B6.Cg-Ptstm1Ich Tg(DBH-PTS)6Csic | J:102278 | 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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