ProfileGDS1065 / 214726_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 77% 76% 78% 64% 81% 73% 79% 86% 78% 85% 76% 79% 79% 68% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1155.477
GSM24653Normal subject 2134.576
GSM24654Normal subject 3208.278
GSM24655A3243G-MELAS subject 15464
GSM24656A3243G-MELAS subject 2194.481
GSM24657A3243G-MELAS subject 3191.173
GSM24658A3243G-MELAS subject 4157.379
GSM24659A3243G-PEO subject 1191.386
GSM24660A3243G-PEO subject 2139.378
GSM24661A3243G-PEO subject 3167.585
GSM24662A3243G-PEO subject 4116.576
GSM24663mtDNA "Common"-deletion subject 1178.679
GSM24664mtDNA "Common"-deletion subject 2295.279
GSM24665mtDNA "Common"-deletion subject 3138.968
GSM24666mtDNA "Common"-deletion subject 4149.867