ProfileGDS1065 / 215178_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 69% 75% 62% 72% 77% 60% 73% 79% 74% 66% 69% 70% 66% 71% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 198.469
GSM24653Normal subject 2123.675
GSM24654Normal subject 390.362
GSM24655A3243G-MELAS subject 175.172
GSM24656A3243G-MELAS subject 214977
GSM24657A3243G-MELAS subject 3100.360
GSM24658A3243G-MELAS subject 4112.873
GSM24659A3243G-PEO subject 1119.879
GSM24660A3243G-PEO subject 2112.874
GSM24661A3243G-PEO subject 359.166
GSM24662A3243G-PEO subject 480.669
GSM24663mtDNA "Common"-deletion subject 1107.470
GSM24664mtDNA "Common"-deletion subject 2153.466
GSM24665mtDNA "Common"-deletion subject 3166.771
GSM24666mtDNA "Common"-deletion subject 4160.268