ProfileGDS1065 / 206197_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 43% 49% 52% 47% 43% 35% 41% 40% 48% 40% 45% 56% 48% 38% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.843
GSM24653Normal subject 241.549
GSM24654Normal subject 358.752
GSM24655A3243G-MELAS subject 129.547
GSM24656A3243G-MELAS subject 236.143
GSM24657A3243G-MELAS subject 332.735
GSM24658A3243G-MELAS subject 426.341
GSM24659A3243G-PEO subject 125.640
GSM24660A3243G-PEO subject 237.748
GSM24661A3243G-PEO subject 320.540
GSM24662A3243G-PEO subject 430.945
GSM24663mtDNA "Common"-deletion subject 157.856
GSM24664mtDNA "Common"-deletion subject 273.648
GSM24665mtDNA "Common"-deletion subject 338.238
GSM24666mtDNA "Common"-deletion subject 445.141