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Human Disease and Mouse Model Detail
Human Disease Kearns-Sayre Syndrome; KSS
OMIM ID: 530000
Synonyms Chronic Progressive External Ophthalmoplegia with Myopathy; CPEO with Myopathy; CPEO with Ragged-Red Fibers; Mitochondrial Cytopathy; Oculocraniosomatic Syndrome; Ophthalmoplegia, Pigmentary Degeneration of Retina, and Cardiomyopathy; Ophthalmoplegia, Progressive External, with Ragged-Red Fibers; Ophthalmoplegia-Plus Syndrome
View all models View ALL (2) mouse models for this human 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
     Tfam* TFAM View 2 models 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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Funding Information
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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory