ProfileGDS1065 / 201249_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 44% 43% 34% 63% 40% 35% 38% 59% 44% 44% 49% 37% 40% 50% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.344
GSM24653Normal subject 231.843
GSM24654Normal subject 325.334
GSM24655A3243G-MELAS subject 152.963
GSM24656A3243G-MELAS subject 232.140
GSM24657A3243G-MELAS subject 332.835
GSM24658A3243G-MELAS subject 423.138
GSM24659A3243G-PEO subject 152.859
GSM24660A3243G-PEO subject 233.244
GSM24661A3243G-PEO subject 324.744
GSM24662A3243G-PEO subject 435.549
GSM24663mtDNA "Common"-deletion subject 125.337
GSM24664mtDNA "Common"-deletion subject 251.740
GSM24665mtDNA "Common"-deletion subject 366.250
GSM24666mtDNA "Common"-deletion subject 447.742