ProfileGDS1065 / 206250_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 36% 4% 19% 14% 9% 18% 25% 21% 18% 22% 22% 17% 16% 19% 17% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 124.136
GSM24653Normal subject 22.44
GSM24654Normal subject 39.119
GSM24655A3243G-MELAS subject 14.814
GSM24656A3243G-MELAS subject 24.49
GSM24657A3243G-MELAS subject 310.718
GSM24658A3243G-MELAS subject 410.825
GSM24659A3243G-PEO subject 19.421
GSM24660A3243G-PEO subject 27.918
GSM24661A3243G-PEO subject 37.122
GSM24662A3243G-PEO subject 48.922
GSM24663mtDNA "Common"-deletion subject 17.217
GSM24664mtDNA "Common"-deletion subject 212.316
GSM24665mtDNA "Common"-deletion subject 311.819
GSM24666mtDNA "Common"-deletion subject 49.717