ProfileGDS1065 / 209668_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 83% 88% 81% 90% 86% 88% 88% 84% 86% 81% 89% 81% 78% 81% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1223.783
GSM24653Normal subject 2311.388
GSM24654Normal subject 3252.981
GSM24655A3243G-MELAS subject 1246.490
GSM24656A3243G-MELAS subject 2278.686
GSM24657A3243G-MELAS subject 3539.488
GSM24658A3243G-MELAS subject 4322.388
GSM24659A3243G-PEO subject 1165.584
GSM24660A3243G-PEO subject 2236.686
GSM24661A3243G-PEO subject 3135.181
GSM24662A3243G-PEO subject 4291.689
GSM24663mtDNA "Common"-deletion subject 1197.581
GSM24664mtDNA "Common"-deletion subject 2284.678
GSM24665mtDNA "Common"-deletion subject 329381
GSM24666mtDNA "Common"-deletion subject 4304.679