ProfileGDS1065 / 43544_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 82% 82% 77% 82% 81% 88% 82% 91% 86% 88% 88% 86% 84% 81% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1217.782
GSM24653Normal subject 2198.982
GSM24654Normal subject 3192.677
GSM24655A3243G-MELAS subject 1130.582
GSM24656A3243G-MELAS subject 2192.881
GSM24657A3243G-MELAS subject 3562.888
GSM24658A3243G-MELAS subject 4197.982
GSM24659A3243G-PEO subject 1294.891
GSM24660A3243G-PEO subject 2246.186
GSM24661A3243G-PEO subject 3219.388
GSM24662A3243G-PEO subject 4274.488
GSM24663mtDNA "Common"-deletion subject 1295.186
GSM24664mtDNA "Common"-deletion subject 2407.284
GSM24665mtDNA "Common"-deletion subject 3295.281
GSM24666mtDNA "Common"-deletion subject 4279.878