Human Disease and Mouse Model Detail
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Human Disease
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Spastic Paraplegia 4, Autosomal Dominant; SPG4
OMIM ID: 182601
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Synonyms
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Familial Spastic Paraplegia, Autosomal Dominant, 2; FSP2
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View all models
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View ALL (2) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Spast*
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SPAST*
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View 2 models
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1:1 Homology
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Mouse Models
Human Disease Modeled: Spastic Paraplegia 4, Autosomal Dominant; SPG4
Associated Mouse Gene:
Spast
Analysis Tools