ProfileGDS1065 / 206183_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 34% 41% 58% 43% 56% 40% 32% 36% 46% 30% 28% 49% 45% 48% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 121.834
GSM24653Normal subject 229.341
GSM24654Normal subject 374.558
GSM24655A3243G-MELAS subject 124.643
GSM24656A3243G-MELAS subject 260.656
GSM24657A3243G-MELAS subject 340.540
GSM24658A3243G-MELAS subject 416.732
GSM24659A3243G-PEO subject 121.636
GSM24660A3243G-PEO subject 234.946
GSM24661A3243G-PEO subject 312.130
GSM24662A3243G-PEO subject 413.628
GSM24663mtDNA "Common"-deletion subject 14449
GSM24664mtDNA "Common"-deletion subject 265.245
GSM24665mtDNA "Common"-deletion subject 359.648
GSM24666mtDNA "Common"-deletion subject 477.654