ProfileGDS1065 / 215028_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 21% 26% 30% 23% 16% 23% 32% 23% 28% 19% 15% 22% 31% 25% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.421
GSM24653Normal subject 21326
GSM24654Normal subject 319.930
GSM24655A3243G-MELAS subject 18.623
GSM24656A3243G-MELAS subject 27.916
GSM24657A3243G-MELAS subject 314.823
GSM24658A3243G-MELAS subject 416.532
GSM24659A3243G-PEO subject 110.723
GSM24660A3243G-PEO subject 21528
GSM24661A3243G-PEO subject 35.919
GSM24662A3243G-PEO subject 45.515
GSM24663mtDNA "Common"-deletion subject 110.322
GSM24664mtDNA "Common"-deletion subject 23431
GSM24665mtDNA "Common"-deletion subject 317.725
GSM24666mtDNA "Common"-deletion subject 418.225