ProfileGDS1065 / 202845_s_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 86% 87% 88% 85% 87% 87% 84% 84% 86% 84% 88% 86% 84% 88% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1281.286
GSM24653Normal subject 2290.287
GSM24654Normal subject 3419.788
GSM24655A3243G-MELAS subject 1154.485
GSM24656A3243G-MELAS subject 2300.387
GSM24657A3243G-MELAS subject 3515.187
GSM24658A3243G-MELAS subject 4214.784
GSM24659A3243G-PEO subject 116384
GSM24660A3243G-PEO subject 2239.986
GSM24661A3243G-PEO subject 3155.284
GSM24662A3243G-PEO subject 4260.988
GSM24663mtDNA "Common"-deletion subject 1289.186
GSM24664mtDNA "Common"-deletion subject 242184
GSM24665mtDNA "Common"-deletion subject 3567.588
GSM24666mtDNA "Common"-deletion subject 4483.986