About   Help   FAQ
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     TFAM Tfam* View 2 models HomoloGene and HGNC
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
05/20/2015
MGI 5.22
The Jackson Laboratory