| Human Disease |
Spastic Paraplegia 7, Autosomal Recessive; SPG7 OMIM ID: 607259 |
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| 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 |
| Spg7tm1Eir/Spg7tm1Eir |
either: 129/Sv-Spg7tm1Eir or (involves: 129/Sv * C57BL/6) | J:87616 | 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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