ProfileGDS1065 / 220125_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 39% 43% 21% 45% 51% 27% 45% 26% 41% 19% 39% 24% 35% 38% 16% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.539
GSM24653Normal subject 231.443
GSM24654Normal subject 310.421
GSM24655A3243G-MELAS subject 126.645
GSM24656A3243G-MELAS subject 249.151
GSM24657A3243G-MELAS subject 320.127
GSM24658A3243G-MELAS subject 43245
GSM24659A3243G-PEO subject 112.526
GSM24660A3243G-PEO subject 228.841
GSM24661A3243G-PEO subject 3619
GSM24662A3243G-PEO subject 423.639
GSM24663mtDNA "Common"-deletion subject 111.524
GSM24664mtDNA "Common"-deletion subject 240.635
GSM24665mtDNA "Common"-deletion subject 337.838
GSM24666mtDNA "Common"-deletion subject 48.816