ProfileGDS1065 / 215603_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 68% 74% 65% 74% 65% 64% 67% 78% 64% 74% 71% 68% 66% 62% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 195.968
GSM24653Normal subject 2121.974
GSM24654Normal subject 3100.465
GSM24655A3243G-MELAS subject 182.574
GSM24656A3243G-MELAS subject 283.965
GSM24657A3243G-MELAS subject 3122.464
GSM24658A3243G-MELAS subject 482.167
GSM24659A3243G-PEO subject 1113.578
GSM24660A3243G-PEO subject 271.264
GSM24661A3243G-PEO subject 387.974
GSM24662A3243G-PEO subject 488.771
GSM24663mtDNA "Common"-deletion subject 197.968
GSM24664mtDNA "Common"-deletion subject 2152.566
GSM24665mtDNA "Common"-deletion subject 310662
GSM24666mtDNA "Common"-deletion subject 496.358