ProfileGDS1065 / 221156_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 42% 44% 46% 43% 48% 47% 40% 35% 39% 37% 36% 45% 40% 46% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.442
GSM24653Normal subject 233.444
GSM24654Normal subject 344.546
GSM24655A3243G-MELAS subject 124.443
GSM24656A3243G-MELAS subject 243.548
GSM24657A3243G-MELAS subject 355.547
GSM24658A3243G-MELAS subject 425.740
GSM24659A3243G-PEO subject 119.935
GSM24660A3243G-PEO subject 22639
GSM24661A3243G-PEO subject 31837
GSM24662A3243G-PEO subject 421.336
GSM24663mtDNA "Common"-deletion subject 13745
GSM24664mtDNA "Common"-deletion subject 252.340
GSM24665mtDNA "Common"-deletion subject 355.846
GSM24666mtDNA "Common"-deletion subject 450.144