ProfileGDS1065 / 214974_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 21% 23% 21% 23% 26% 14% 12% 29% 19% 14% 23% 14% 20% 14% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.721
GSM24653Normal subject 210.923
GSM24654Normal subject 310.621
GSM24655A3243G-MELAS subject 18.723
GSM24656A3243G-MELAS subject 215.126
GSM24657A3243G-MELAS subject 37.614
GSM24658A3243G-MELAS subject 44.112
GSM24659A3243G-PEO subject 11529
GSM24660A3243G-PEO subject 28.519
GSM24661A3243G-PEO subject 34.414
GSM24662A3243G-PEO subject 49.623
GSM24663mtDNA "Common"-deletion subject 15.814
GSM24664mtDNA "Common"-deletion subject 216.720
GSM24665mtDNA "Common"-deletion subject 38.214
GSM24666mtDNA "Common"-deletion subject 47.814