| Human Disease |
Spastic Paraplegia 20, Autosomal Recessive; SPG20 OMIM ID: 275900 |
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| Synonyms | Spastic Paraparesis, Childhood-Onset, with Distal Muscle Wasting; Spastic Paraplegia, Autosomal Recessive, Troyer Type; Troyer Syndrome | |||||||||||||||||||||
| 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 |
| Spg20tm1.1Xen/Spg20tm1.1Xen |
involves: C57BL/6J | J:185987 | 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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