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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
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   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 6.05
The Jackson Laboratory