ProfileGDS1065 / 215911_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 23% 3% 11% 20% 5% 18% 21% 26% 5% 24% 31% 10% 8% 11% 19% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.723
GSM24653Normal subject 22.13
GSM24654Normal subject 3511
GSM24655A3243G-MELAS subject 17.220
GSM24656A3243G-MELAS subject 23.25
GSM24657A3243G-MELAS subject 310.518
GSM24658A3243G-MELAS subject 48.421
GSM24659A3243G-PEO subject 112.726
GSM24660A3243G-PEO subject 22.65
GSM24661A3243G-PEO subject 38.324
GSM24662A3243G-PEO subject 415.631
GSM24663mtDNA "Common"-deletion subject 14.410
GSM24664mtDNA "Common"-deletion subject 26.38
GSM24665mtDNA "Common"-deletion subject 36.511
GSM24666mtDNA "Common"-deletion subject 411.419