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Human Disease and Mouse Model Detail
Human Disease Charcot-Marie-Tooth Disease, X-Linked Recessive, 5; CMTX5
OMIM ID: 311070
Synonyms Charcot-Marie-Tooth Disease; Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 5; Optic Atrophy, Polyneuropathy, and Deafness; Rosenberg-Chutorian Syndrome
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
     Prps1 PRPS1*   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
12/09/2014
MGI 5.20
The Jackson Laboratory