ProfileGDS1065 / 207392_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 39% 33% 43% 41% 47% 41% 40% 26% 29% 12% 32% 34% 48% 41% 36% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.439
GSM24653Normal subject 220.533
GSM24654Normal subject 339.143
GSM24655A3243G-MELAS subject 123.341
GSM24656A3243G-MELAS subject 242.447
GSM24657A3243G-MELAS subject 342.141
GSM24658A3243G-MELAS subject 425.640
GSM24659A3243G-PEO subject 112.526
GSM24660A3243G-PEO subject 215.829
GSM24661A3243G-PEO subject 33.812
GSM24662A3243G-PEO subject 416.532
GSM24663mtDNA "Common"-deletion subject 121.334
GSM24664mtDNA "Common"-deletion subject 272.348
GSM24665mtDNA "Common"-deletion subject 345.341
GSM24666mtDNA "Common"-deletion subject 435.836