ProfileGDS1065 / 203035_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 65% 59% 48% 66% 58% 55% 59% 59% 55% 62% 62% 55% 60% 57% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 182.965
GSM24653Normal subject 260.459
GSM24654Normal subject 347.648
GSM24655A3243G-MELAS subject 158.166
GSM24656A3243G-MELAS subject 264.358
GSM24657A3243G-MELAS subject 380.755
GSM24658A3243G-MELAS subject 457.859
GSM24659A3243G-PEO subject 152.459
GSM24660A3243G-PEO subject 251.155
GSM24661A3243G-PEO subject 350.262
GSM24662A3243G-PEO subject 459.762
GSM24663mtDNA "Common"-deletion subject 155.655
GSM24664mtDNA "Common"-deletion subject 2117.360
GSM24665mtDNA "Common"-deletion subject 387.557
GSM24666mtDNA "Common"-deletion subject 498.259