ProfileGDS1065 / 207071_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 83% 86% 84% 86% 85% 84% 82% 88% 86% 83% 89% 87% 87% 86% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1221.783
GSM24653Normal subject 2271.286
GSM24654Normal subject 3293.184
GSM24655A3243G-MELAS subject 1166.586
GSM24656A3243G-MELAS subject 2248.385
GSM24657A3243G-MELAS subject 3393.684
GSM24658A3243G-MELAS subject 4189.782
GSM24659A3243G-PEO subject 1222.288
GSM24660A3243G-PEO subject 2246.486
GSM24661A3243G-PEO subject 3151.183
GSM24662A3243G-PEO subject 4295.889
GSM24663mtDNA "Common"-deletion subject 1309.687
GSM24664mtDNA "Common"-deletion subject 2513.987
GSM24665mtDNA "Common"-deletion subject 3450.886
GSM24666mtDNA "Common"-deletion subject 4468.685