| Human Disease |
Myelopathy, Htlv-1-Associated; HAM OMIM ID: 159580 |
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| Synonyms | Familial Spastic Paraparesis, HTLV-1-Associated | |||||||||||||||||||||
| 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 |
| Zeb1tm1Yhi/Zeb1tm1Yhi |
either: (involves: 129 * C3H * C57BL/6) or (involves: 129 * C57BL/6 * ICR) | J:139194 | 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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