ProfileGDS1065 / 219690_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 64% 64% 53% 58% 56% 58% 59% 64% 62% 62% 71% 59% 53% 46% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 180.964
GSM24653Normal subject 275.364
GSM24654Normal subject 359.853
GSM24655A3243G-MELAS subject 142.558
GSM24656A3243G-MELAS subject 25956
GSM24657A3243G-MELAS subject 392.158
GSM24658A3243G-MELAS subject 458.959
GSM24659A3243G-PEO subject 163.764
GSM24660A3243G-PEO subject 26762
GSM24661A3243G-PEO subject 350.362
GSM24662A3243G-PEO subject 49071
GSM24663mtDNA "Common"-deletion subject 165.159
GSM24664mtDNA "Common"-deletion subject 288.353
GSM24665mtDNA "Common"-deletion subject 354.746
GSM24666mtDNA "Common"-deletion subject 475.553