ProfileGDS1065 / 209429_x_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 86% 85% 88% 91% 88% 90% 88% 91% 89% 90% 88% 90% 88% 85% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1299.886
GSM24653Normal subject 2247.185
GSM24654Normal subject 342388
GSM24655A3243G-MELAS subject 1258.891
GSM24656A3243G-MELAS subject 2307.488
GSM24657A3243G-MELAS subject 3664.690
GSM24658A3243G-MELAS subject 4300.388
GSM24659A3243G-PEO subject 1324.291
GSM24660A3243G-PEO subject 2300.689
GSM24661A3243G-PEO subject 3264.590
GSM24662A3243G-PEO subject 426088
GSM24663mtDNA "Common"-deletion subject 1410.490
GSM24664mtDNA "Common"-deletion subject 2561.488
GSM24665mtDNA "Common"-deletion subject 3404.485
GSM24666mtDNA "Common"-deletion subject 4483.986