ProfileGDS1065 / 213108_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 60% 44% 55% 81% 80% 52% 85% 63% 77% 68% 61% 62% 55% 45% 46% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 166.260
GSM24653Normal subject 233.744
GSM24654Normal subject 364.655
GSM24655A3243G-MELAS subject 1116.781
GSM24656A3243G-MELAS subject 2183.580
GSM24657A3243G-MELAS subject 370.452
GSM24658A3243G-MELAS subject 4249.985
GSM24659A3243G-PEO subject 161.863
GSM24660A3243G-PEO subject 2130.977
GSM24661A3243G-PEO subject 366.268
GSM24662A3243G-PEO subject 457.361
GSM24663mtDNA "Common"-deletion subject 177.362
GSM24664mtDNA "Common"-deletion subject 296.755
GSM24665mtDNA "Common"-deletion subject 353.745
GSM24666mtDNA "Common"-deletion subject 455.346