ProfileGDS1065 / 220850_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 1% 29% 8% 4% 1% 14% 1% 2% 3% 0% 2% 29% 2% 16% 0% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.21
GSM24653Normal subject 215.729
GSM24654Normal subject 33.98
GSM24655A3243G-MELAS subject 11.84
GSM24656A3243G-MELAS subject 21.51
GSM24657A3243G-MELAS subject 37.814
GSM24658A3243G-MELAS subject 411
GSM24659A3243G-PEO subject 11.72
GSM24660A3243G-PEO subject 21.73
GSM24661A3243G-PEO subject 30.30
GSM24662A3243G-PEO subject 41.42
GSM24663mtDNA "Common"-deletion subject 115.829
GSM24664mtDNA "Common"-deletion subject 22.82
GSM24665mtDNA "Common"-deletion subject 39.316
GSM24666mtDNA "Common"-deletion subject 40.60