ProfileGDS1065 / 202340_x_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% 49% 72% 61% 68% 63% 67% 74% 75% 79% 76% 69% 63% 68% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 182.665
GSM24653Normal subject 241.549
GSM24654Normal subject 3147.172
GSM24655A3243G-MELAS subject 148.261
GSM24656A3243G-MELAS subject 296.468
GSM24657A3243G-MELAS subject 311363
GSM24658A3243G-MELAS subject 485.867
GSM24659A3243G-PEO subject 194.374
GSM24660A3243G-PEO subject 2120.375
GSM24661A3243G-PEO subject 3116.679
GSM24662A3243G-PEO subject 4114.876
GSM24663mtDNA "Common"-deletion subject 1101.369
GSM24664mtDNA "Common"-deletion subject 2135.763
GSM24665mtDNA "Common"-deletion subject 3144.268
GSM24666mtDNA "Common"-deletion subject 4179.871