ProfileGDS1065 / 213592_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 84% 85% 71% 85% 80% 86% 70% 87% 80% 83% 79% 72% 80% 66% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1247.984
GSM24653Normal subject 2249.285
GSM24654Normal subject 3138.371
GSM24655A3243G-MELAS subject 1153.285
GSM24656A3243G-MELAS subject 2176.580
GSM24657A3243G-MELAS subject 3446.586
GSM24658A3243G-MELAS subject 497.670
GSM24659A3243G-PEO subject 120387
GSM24660A3243G-PEO subject 2152.280
GSM24661A3243G-PEO subject 3148.783
GSM24662A3243G-PEO subject 414179
GSM24663mtDNA "Common"-deletion subject 1119.172
GSM24664mtDNA "Common"-deletion subject 2323.180
GSM24665mtDNA "Common"-deletion subject 312766
GSM24666mtDNA "Common"-deletion subject 4267.178