ProfileGDS1065 / 217450_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 33% 16% 43% 39% 31% 45% 26% 49% 41% 59% 28% 54% 41% 61% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.833
GSM24653Normal subject 26.616
GSM24654Normal subject 339.543
GSM24655A3243G-MELAS subject 121.139
GSM24656A3243G-MELAS subject 220.631
GSM24657A3243G-MELAS subject 351.545
GSM24658A3243G-MELAS subject 411.726
GSM24659A3243G-PEO subject 135.749
GSM24660A3243G-PEO subject 228.541
GSM24661A3243G-PEO subject 344.859
GSM24662A3243G-PEO subject 413.528
GSM24663mtDNA "Common"-deletion subject 153.354
GSM24664mtDNA "Common"-deletion subject 253.241
GSM24665mtDNA "Common"-deletion subject 3102.661
GSM24666mtDNA "Common"-deletion subject 445.341