ProfileGDS1065 / 217959_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 76% 74% 82% 82% 70% 79% 81% 69% 75% 71% 76% 74% 83% 80% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1141.876
GSM24653Normal subject 2120.574
GSM24654Normal subject 3269.582
GSM24655A3243G-MELAS subject 1125.682
GSM24656A3243G-MELAS subject 2105.970
GSM24657A3243G-MELAS subject 3275.679
GSM24658A3243G-MELAS subject 4182.881
GSM24659A3243G-PEO subject 175.269
GSM24660A3243G-PEO subject 2118.475
GSM24661A3243G-PEO subject 375.871
GSM24662A3243G-PEO subject 4118.776
GSM24663mtDNA "Common"-deletion subject 1132.574
GSM24664mtDNA "Common"-deletion subject 2380.383
GSM24665mtDNA "Common"-deletion subject 327280
GSM24666mtDNA "Common"-deletion subject 4294.579