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Human Disease and Mouse Model Detail
Human Disease Spastic Paraplegia 3, Autosomal Dominant; SPG3A
OMIM ID: 182600
Synonyms Familial Spastic Paraplegia, Autosomal Dominant, 1; FSP1; Spastic Paraplegia; SPG3; Strumpell Disease
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Atl1 ATL1*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/11/2014
MGI 5.20
The Jackson Laboratory