ProfileGDS1065 / 216088_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% 90% 91% 88% 89% 91% 91% 86% 88% 87% 88% 89% 90% 92% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1428.290
GSM24653Normal subject 2403.590
GSM24654Normal subject 3597.891
GSM24655A3243G-MELAS subject 1190.788
GSM24656A3243G-MELAS subject 2362.489
GSM24657A3243G-MELAS subject 3753.191
GSM24658A3243G-MELAS subject 4429.891
GSM24659A3243G-PEO subject 1188.586
GSM24660A3243G-PEO subject 2290.488
GSM24661A3243G-PEO subject 319387
GSM24662A3243G-PEO subject 4278.188
GSM24663mtDNA "Common"-deletion subject 1378.689
GSM24664mtDNA "Common"-deletion subject 2705.790
GSM24665mtDNA "Common"-deletion subject 3848.892
GSM24666mtDNA "Common"-deletion subject 4947.392