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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
Human Phenotype Ontology associations
Synonyms Melas Syndrome
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
     COX1* mt-Co1   HomoloGene and HGNC
COX2* mt-Co2   HomoloGene and HGNC
COX3* mt-Co3   HomoloGene and HGNC
CYTB* mt-Cytb   HomoloGene and HGNC
ND1* mt-Nd1   HomoloGene and HGNC
ND5* mt-Nd5   HomoloGene and HGNC
ND6* mt-Nd6   HomoloGene and HGNC
TRNC* mt-Tc   HGNC
TRNF* mt-Tf   HGNC
TRNK* mt-Tk   HGNC
TRNL1* mt-Tl1   HGNC
TRNQ* mt-Tq   HGNC
TRNS1* mt-Ts1   HGNC
TRNS2* mt-Ts2   HGNC
TRNV* mt-Tv   HGNC
TRNW* mt-Tw   HGNC

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 6.07
The Jackson Laboratory