ProfileGDS1065 / 219974_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 44% 53% 70% 45% 50% 45% 53% 44% 50% 58% 54% 52% 52% 66% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 134.344
GSM24653Normal subject 247.553
GSM24654Normal subject 3130.570
GSM24655A3243G-MELAS subject 126.545
GSM24656A3243G-MELAS subject 247.550
GSM24657A3243G-MELAS subject 351.345
GSM24658A3243G-MELAS subject 444.953
GSM24659A3243G-PEO subject 130.544
GSM24660A3243G-PEO subject 241.450
GSM24661A3243G-PEO subject 343.458
GSM24662A3243G-PEO subject 443.354
GSM24663mtDNA "Common"-deletion subject 148.552
GSM24664mtDNA "Common"-deletion subject 284.152
GSM24665mtDNA "Common"-deletion subject 3130.766
GSM24666mtDNA "Common"-deletion subject 496.859