ProfileGDS1065 / 208713_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 85% 83% 78% 84% 84% 86% 83% 87% 88% 89% 88% 87% 78% 80% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1267.585
GSM24653Normal subject 2208.683
GSM24654Normal subject 320278
GSM24655A3243G-MELAS subject 1140.484
GSM24656A3243G-MELAS subject 2236.984
GSM24657A3243G-MELAS subject 3448.986
GSM24658A3243G-MELAS subject 4209.983
GSM24659A3243G-PEO subject 1208.487
GSM24660A3243G-PEO subject 2277.988
GSM24661A3243G-PEO subject 3256.789
GSM24662A3243G-PEO subject 4279.188
GSM24663mtDNA "Common"-deletion subject 1314.687
GSM24664mtDNA "Common"-deletion subject 2285.978
GSM24665mtDNA "Common"-deletion subject 3275.380
GSM24666mtDNA "Common"-deletion subject 4380.583