ProfileGDS1065 / 222047_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 92% 91% 88% 90% 90% 92% 91% 92% 91% 92% 93% 94% 92% 88% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1555.192
GSM24653Normal subject 2457.291
GSM24654Normal subject 3441.488
GSM24655A3243G-MELAS subject 1249.990
GSM24656A3243G-MELAS subject 2397.190
GSM24657A3243G-MELAS subject 3817.392
GSM24658A3243G-MELAS subject 4448.291
GSM24659A3243G-PEO subject 1372.592
GSM24660A3243G-PEO subject 2407.491
GSM24661A3243G-PEO subject 3364.792
GSM24662A3243G-PEO subject 4529.993
GSM24663mtDNA "Common"-deletion subject 1704.894
GSM24664mtDNA "Common"-deletion subject 288192
GSM24665mtDNA "Common"-deletion subject 3522.388
GSM24666mtDNA "Common"-deletion subject 4833.991