ProfileGDS1065 / 217509_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 81% 86% 77% 77% 79% 77% 73% 89% 85% 88% 83% 84% 79% 79% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1195.681
GSM24653Normal subject 2253.386
GSM24654Normal subject 3185.477
GSM24655A3243G-MELAS subject 194.777
GSM24656A3243G-MELAS subject 2166.579
GSM24657A3243G-MELAS subject 3234.377
GSM24658A3243G-MELAS subject 411473
GSM24659A3243G-PEO subject 123989
GSM24660A3243G-PEO subject 2218.285
GSM24661A3243G-PEO subject 3228.788
GSM24662A3243G-PEO subject 4179.583
GSM24663mtDNA "Common"-deletion subject 125784
GSM24664mtDNA "Common"-deletion subject 2309.579
GSM24665mtDNA "Common"-deletion subject 3261.479
GSM24666mtDNA "Common"-deletion subject 4174.670