ProfileGDS1065 / 203403_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 85% 83% 90% 86% 89% 84% 85% 75% 81% 78% 65% 82% 87% 90% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1268.685
GSM24653Normal subject 2205.783
GSM24654Normal subject 3533.390
GSM24655A3243G-MELAS subject 1168.186
GSM24656A3243G-MELAS subject 2364.789
GSM24657A3243G-MELAS subject 3378.284
GSM24658A3243G-MELAS subject 4235.985
GSM24659A3243G-PEO subject 1101.275
GSM24660A3243G-PEO subject 2168.381
GSM24661A3243G-PEO subject 3111.978
GSM24662A3243G-PEO subject 467.765
GSM24663mtDNA "Common"-deletion subject 1216.682
GSM24664mtDNA "Common"-deletion subject 2535.987
GSM24665mtDNA "Common"-deletion subject 3675.290
GSM24666mtDNA "Common"-deletion subject 4682.289