ProfileGDS1065 / 218243_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 87% 88% 86% 84% 87% 85% 85% 88% 87% 90% 89% 88% 88% 86% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1329.287
GSM24653Normal subject 2309.488
GSM24654Normal subject 3366.786
GSM24655A3243G-MELAS subject 1140.184
GSM24656A3243G-MELAS subject 2300.787
GSM24657A3243G-MELAS subject 3433.385
GSM24658A3243G-MELAS subject 4242.885
GSM24659A3243G-PEO subject 1220.188
GSM24660A3243G-PEO subject 2259.387
GSM24661A3243G-PEO subject 3263.490
GSM24662A3243G-PEO subject 4295.989
GSM24663mtDNA "Common"-deletion subject 1360.188
GSM24664mtDNA "Common"-deletion subject 2574.288
GSM24665mtDNA "Common"-deletion subject 3439.186
GSM24666mtDNA "Common"-deletion subject 4542.787