ProfileGDS1065 / 213711_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 18% 13% 15% 13% 10% 10% 24% 19% 19% 12% 18% 14% 9% 16% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1818
GSM24653Normal subject 25.213
GSM24654Normal subject 36.915
GSM24655A3243G-MELAS subject 14.413
GSM24656A3243G-MELAS subject 24.810
GSM24657A3243G-MELAS subject 35.410
GSM24658A3243G-MELAS subject 410.324
GSM24659A3243G-PEO subject 17.919
GSM24660A3243G-PEO subject 28.119
GSM24661A3243G-PEO subject 33.812
GSM24662A3243G-PEO subject 46.518
GSM24663mtDNA "Common"-deletion subject 1614
GSM24664mtDNA "Common"-deletion subject 279
GSM24665mtDNA "Common"-deletion subject 39.516
GSM24666mtDNA "Common"-deletion subject 46.512