ProfileGDS1065 / 201652_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 93% 92% 95% 91% 92% 94% 94% 90% 92% 91% 88% 91% 94% 93% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1609.493
GSM24653Normal subject 2503.892
GSM24654Normal subject 31251.395
GSM24655A3243G-MELAS subject 127691
GSM24656A3243G-MELAS subject 253892
GSM24657A3243G-MELAS subject 31097.694
GSM24658A3243G-MELAS subject 4654.394
GSM24659A3243G-PEO subject 1273.390
GSM24660A3243G-PEO subject 2471.692
GSM24661A3243G-PEO subject 3301.591
GSM24662A3243G-PEO subject 4279.588
GSM24663mtDNA "Common"-deletion subject 1490.391
GSM24664mtDNA "Common"-deletion subject 21135.594
GSM24665mtDNA "Common"-deletion subject 31044.293
GSM24666mtDNA "Common"-deletion subject 41189.393