ProfileGDS1065 / 220783_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 48% 57% 43% 59% 47% 41% 51% 56% 50% 40% 50% 49% 48% 50% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 140.848
GSM24653Normal subject 255.557
GSM24654Normal subject 339.143
GSM24655A3243G-MELAS subject 144.159
GSM24656A3243G-MELAS subject 242.147
GSM24657A3243G-MELAS subject 342.841
GSM24658A3243G-MELAS subject 441.151
GSM24659A3243G-PEO subject 147.356
GSM24660A3243G-PEO subject 24150
GSM24661A3243G-PEO subject 320.740
GSM24662A3243G-PEO subject 43850
GSM24663mtDNA "Common"-deletion subject 143.449
GSM24664mtDNA "Common"-deletion subject 273.648
GSM24665mtDNA "Common"-deletion subject 364.950
GSM24666mtDNA "Common"-deletion subject 482.455