ProfileGDS1065 / 209110_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 90% 86% 84% 87% 87% 85% 86% 89% 90% 94% 89% 89% 87% 82% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1420.990
GSM24653Normal subject 2271.886
GSM24654Normal subject 3300.884
GSM24655A3243G-MELAS subject 1183.387
GSM24656A3243G-MELAS subject 2292.687
GSM24657A3243G-MELAS subject 3420.185
GSM24658A3243G-MELAS subject 4270.486
GSM24659A3243G-PEO subject 1240.489
GSM24660A3243G-PEO subject 233990
GSM24661A3243G-PEO subject 3535.594
GSM24662A3243G-PEO subject 4286.789
GSM24663mtDNA "Common"-deletion subject 1391.489
GSM24664mtDNA "Common"-deletion subject 2513.587
GSM24665mtDNA "Common"-deletion subject 3318.382
GSM24666mtDNA "Common"-deletion subject 4390.283