ProfileGDS1065 / 218621_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 53% 45% 17% 48% 22% 45% 40% 45% 17% 39% 54% 47% 45% 16% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149.653
GSM24653Normal subject 234.645
GSM24654Normal subject 38.317
GSM24655A3243G-MELAS subject 130.548
GSM24656A3243G-MELAS subject 211.322
GSM24657A3243G-MELAS subject 350.545
GSM24658A3243G-MELAS subject 425.740
GSM24659A3243G-PEO subject 131.245
GSM24660A3243G-PEO subject 27.417
GSM24661A3243G-PEO subject 319.339
GSM24662A3243G-PEO subject 444.354
GSM24663mtDNA "Common"-deletion subject 139.647
GSM24664mtDNA "Common"-deletion subject 263.245
GSM24665mtDNA "Common"-deletion subject 39.316
GSM24666mtDNA "Common"-deletion subject 417.625