ProfileGDS1065 / 218366_x_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% 87% 82% 73% 82% 79% 85% 80% 76% 79% 77% 87% 84% 83% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1260.985
GSM24653Normal subject 2282.987
GSM24654Normal subject 3253.582
GSM24655A3243G-MELAS subject 177.973
GSM24656A3243G-MELAS subject 2195.482
GSM24657A3243G-MELAS subject 3278.179
GSM24658A3243G-MELAS subject 4248.785
GSM24659A3243G-PEO subject 1131.580
GSM24660A3243G-PEO subject 2126.876
GSM24661A3243G-PEO subject 3119.179
GSM24662A3243G-PEO subject 412377
GSM24663mtDNA "Common"-deletion subject 1315.787
GSM24664mtDNA "Common"-deletion subject 2433.384
GSM24665mtDNA "Common"-deletion subject 3339.783
GSM24666mtDNA "Common"-deletion subject 4497.186