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Human Disease and Mouse Model Detail
Human Disease Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes; MELAS
OMIM ID: 540000
Synonyms Melas 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
     mt-Co1 COX1*   1:1 Homology
mt-Co2 COX2*   1:1 Homology
mt-Co3 COX3*   1:1 Homology
mt-Cytb CYTB*   1:1 Homology
mt-Nd1 ND1*   1:1 Homology
mt-Nd5 ND5*   1:1 Homology
mt-Nd6 ND6*   1:1 Homology
RNR1*  
TRNC*  
TRNF*  
TRNK*  
TRNL1*  
TRNQ*  
TRNS1*  
TRNS2*  
TRNV*  
TRNW*  

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
09/16/2014
MGI 5.19
The Jackson Laboratory