ProfileGDS1065 / 209455_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 80% 81% 89% 86% 90% 85% 85% 82% 86% 83% 81% 84% 88% 89% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1189.280
GSM24653Normal subject 2183.981
GSM24654Normal subject 3461.989
GSM24655A3243G-MELAS subject 1170.286
GSM24656A3243G-MELAS subject 2377.590
GSM24657A3243G-MELAS subject 3414.485
GSM24658A3243G-MELAS subject 423285
GSM24659A3243G-PEO subject 1150.182
GSM24660A3243G-PEO subject 2230.286
GSM24661A3243G-PEO subject 3149.483
GSM24662A3243G-PEO subject 416181
GSM24663mtDNA "Common"-deletion subject 1241.284
GSM24664mtDNA "Common"-deletion subject 2590.288
GSM24665mtDNA "Common"-deletion subject 3574.689
GSM24666mtDNA "Common"-deletion subject 4674.189