ProfileGDS1065 / 202188_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 62% 58% 68% 31% 42% 54% 68% 29% 19% 46% 56% 41% 62% 48% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 173.362
GSM24653Normal subject 259.258
GSM24654Normal subject 3119.268
GSM24655A3243G-MELAS subject 114.531
GSM24656A3243G-MELAS subject 234.142
GSM24657A3243G-MELAS subject 375.554
GSM24658A3243G-MELAS subject 487.468
GSM24659A3243G-PEO subject 11529
GSM24660A3243G-PEO subject 28.419
GSM24661A3243G-PEO subject 32746
GSM24662A3243G-PEO subject 447.956
GSM24663mtDNA "Common"-deletion subject 13041
GSM24664mtDNA "Common"-deletion subject 2129.162
GSM24665mtDNA "Common"-deletion subject 360.148
GSM24666mtDNA "Common"-deletion subject 4129.564