ProfileGDS1065 / 201435_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 73% 69% 86% 76% 80% 71% 71% 65% 78% 70% 63% 66% 81% 81% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112373
GSM24653Normal subject 29569
GSM24654Normal subject 335686
GSM24655A3243G-MELAS subject 19176
GSM24656A3243G-MELAS subject 2183.580
GSM24657A3243G-MELAS subject 317171
GSM24658A3243G-MELAS subject 4102.571
GSM24659A3243G-PEO subject 165.365
GSM24660A3243G-PEO subject 2135.478
GSM24661A3243G-PEO subject 372.270
GSM24662A3243G-PEO subject 463.363
GSM24663mtDNA "Common"-deletion subject 191.166
GSM24664mtDNA "Common"-deletion subject 2335.481
GSM24665mtDNA "Common"-deletion subject 3294.281
GSM24666mtDNA "Common"-deletion subject 4283.278