ProfileGDS1065 / 212192_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 90% 91% 92% 89% 91% 92% 90% 86% 89% 89% 85% 88% 90% 90% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1446.190
GSM24653Normal subject 241991
GSM24654Normal subject 3653.392
GSM24655A3243G-MELAS subject 1222.289
GSM24656A3243G-MELAS subject 245291
GSM24657A3243G-MELAS subject 3894.992
GSM24658A3243G-MELAS subject 4370.690
GSM24659A3243G-PEO subject 119786
GSM24660A3243G-PEO subject 2320.289
GSM24661A3243G-PEO subject 3242.289
GSM24662A3243G-PEO subject 4214.285
GSM24663mtDNA "Common"-deletion subject 1340.288
GSM24664mtDNA "Common"-deletion subject 2699.790
GSM24665mtDNA "Common"-deletion subject 3645.790
GSM24666mtDNA "Common"-deletion subject 4809.191