ProfileGDS1065 / 211904_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 40% 30% 29% 38% 47% 30% 40% 34% 38% 42% 45% 18% 41% 39% 36% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 129.440
GSM24653Normal subject 217.630
GSM24654Normal subject 31829
GSM24655A3243G-MELAS subject 120.438
GSM24656A3243G-MELAS subject 242.647
GSM24657A3243G-MELAS subject 324.530
GSM24658A3243G-MELAS subject 425.340
GSM24659A3243G-PEO subject 119.234
GSM24660A3243G-PEO subject 224.838
GSM24661A3243G-PEO subject 322.642
GSM24662A3243G-PEO subject 430.845
GSM24663mtDNA "Common"-deletion subject 17.518
GSM24664mtDNA "Common"-deletion subject 255.241
GSM24665mtDNA "Common"-deletion subject 341.139
GSM24666mtDNA "Common"-deletion subject 43536