ProfileGDS1065 / 203822_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 86% 87% 86% 89% 89% 87% 83% 84% 87% 84% 82% 83% 83% 86% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1290.386
GSM24653Normal subject 2277.187
GSM24654Normal subject 3347.886
GSM24655A3243G-MELAS subject 1216.889
GSM24656A3243G-MELAS subject 2352.489
GSM24657A3243G-MELAS subject 3515.187
GSM24658A3243G-MELAS subject 4202.683
GSM24659A3243G-PEO subject 116584
GSM24660A3243G-PEO subject 225687
GSM24661A3243G-PEO subject 3159.384
GSM24662A3243G-PEO subject 4168.382
GSM24663mtDNA "Common"-deletion subject 1233.783
GSM24664mtDNA "Common"-deletion subject 2396.583
GSM24665mtDNA "Common"-deletion subject 344286
GSM24666mtDNA "Common"-deletion subject 4823.991