ProfileGDS1065 / 221031_s_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 72% 69% 73% 57% 90% 73% 77% 79% 69% 73% 75% 73% 78% 60% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1119.272
GSM24653Normal subject 292.869
GSM24654Normal subject 3149.773
GSM24655A3243G-MELAS subject 142.357
GSM24656A3243G-MELAS subject 2383.590
GSM24657A3243G-MELAS subject 3194.773
GSM24658A3243G-MELAS subject 4141.677
GSM24659A3243G-PEO subject 1121.779
GSM24660A3243G-PEO subject 286.869
GSM24661A3243G-PEO subject 38473
GSM24662A3243G-PEO subject 4108.675
GSM24663mtDNA "Common"-deletion subject 1124.773
GSM24664mtDNA "Common"-deletion subject 2282.578
GSM24665mtDNA "Common"-deletion subject 397.760
GSM24666mtDNA "Common"-deletion subject 4158.568