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Human Disease and Mouse Model Detail
Human Disease Spastic Paraplegia 11, Autosomal Recessive; SPG11
OMIM ID: 604360
Human Phenotype Ontology associations
Synonyms HSP-TCC; Spastic Paraplegia; Spastic Paraplegia, Autosomal Recessive, Complicated, with Thin Corpus Callosum; Spastic Paraplegia, Autosomal Recessive, with Mental Impairment and Thin Corpus Callosum
View all models View ALL (1) mouse models for this human disease.
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
     SPG11* Spg11* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (1)

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 6.07
The Jackson Laboratory