| Human Disease |
Term: Spastic Paraplegia 4, Autosomal Dominant; SPG4
OMIM ID: 182601
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| Synonyms |
Familial Spastic Paraplegia, Autosomal Dominant, 2; FSP2 |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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  ...both mouse and human orthologous genes. |
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Mouse Models
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1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes.
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Analysis Tools