ProfileGDS1065 / 201067_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 88% 87% 91% 82% 90% 89% 92% 82% 82% 84% 87% 86% 88% 92% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1350.488
GSM24653Normal subject 2295.687
GSM24654Normal subject 3626.591
GSM24655A3243G-MELAS subject 1129.182
GSM24656A3243G-MELAS subject 240290
GSM24657A3243G-MELAS subject 3599.389
GSM24658A3243G-MELAS subject 447892
GSM24659A3243G-PEO subject 1145.782
GSM24660A3243G-PEO subject 2176.182
GSM24661A3243G-PEO subject 3160.384
GSM24662A3243G-PEO subject 4234.787
GSM24663mtDNA "Common"-deletion subject 1286.286
GSM24664mtDNA "Common"-deletion subject 2589.288
GSM24665mtDNA "Common"-deletion subject 3891.792
GSM24666mtDNA "Common"-deletion subject 4895.191