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Human Disease and Mouse Model Detail
Human Disease Spastic Paraplegia 9a, Autosomal Dominant; SPG9A
OMIM ID: 601162
Synonyms Cataracts with Motor Neuronopathy, Short Stature, and Skeletal Abnormalities; Spastic Paraparesis with Amyopathy, Cataracts, and Gastroesophageal Reflux; Spastic Paraplegia
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ALDH18A1* Aldh18a1   HomoloGene

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
MGI 6.01
The Jackson Laboratory