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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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     COX1* mt-Co1   HomoloGene
COX2* mt-Co2   HomoloGene
COX3* mt-Co3   HomoloGene
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*   HGNC
TRNF*   HGNC
TRNK*   HGNC
TRNL1*   HGNC
TRNQ*   HGNC
TRNS1*   HGNC
TRNS2*   HGNC
TRNV*   HGNC
TRNW*   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
06/23/2015
MGI 5.22
The Jackson Laboratory