ProfileGDS1065 / 34764_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 70% 71% 73% 67% 65% 72% 65% 73% 70% 75% 69% 73% 68% 68% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1106.170
GSM24653Normal subject 2101.571
GSM24654Normal subject 3149.973
GSM24655A3243G-MELAS subject 159.967
GSM24656A3243G-MELAS subject 283.365
GSM24657A3243G-MELAS subject 3176.572
GSM24658A3243G-MELAS subject 477.265
GSM24659A3243G-PEO subject 189.473
GSM24660A3243G-PEO subject 292.870
GSM24661A3243G-PEO subject 392.875
GSM24662A3243G-PEO subject 48269
GSM24663mtDNA "Common"-deletion subject 1126.273
GSM24664mtDNA "Common"-deletion subject 2172.668
GSM24665mtDNA "Common"-deletion subject 3144.668
GSM24666mtDNA "Common"-deletion subject 4170.770