ProfileGDS1065 / 208076_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 52% 46% 44% 56% 45% 41% 42% 50% 51% 44% 32% 49% 48% 50% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 148.452
GSM24653Normal subject 236.746
GSM24654Normal subject 340.344
GSM24655A3243G-MELAS subject 140.656
GSM24656A3243G-MELAS subject 238.845
GSM24657A3243G-MELAS subject 34241
GSM24658A3243G-MELAS subject 428.142
GSM24659A3243G-PEO subject 137.350
GSM24660A3243G-PEO subject 243.251
GSM24661A3243G-PEO subject 324.344
GSM24662A3243G-PEO subject 417.332
GSM24663mtDNA "Common"-deletion subject 144.649
GSM24664mtDNA "Common"-deletion subject 272.448
GSM24665mtDNA "Common"-deletion subject 363.750
GSM24666mtDNA "Common"-deletion subject 44742