ProfileGDS1065 / 212927_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 67% 57% 51% 48% 74% 64% 57% 54% 65% 58% 66% 58% 64% 66% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 191.267
GSM24653Normal subject 256.557
GSM24654Normal subject 354.351
GSM24655A3243G-MELAS subject 129.648
GSM24656A3243G-MELAS subject 2125.174
GSM24657A3243G-MELAS subject 3122.564
GSM24658A3243G-MELAS subject 453.257
GSM24659A3243G-PEO subject 142.754
GSM24660A3243G-PEO subject 274.465
GSM24661A3243G-PEO subject 343.658
GSM24662A3243G-PEO subject 472.466
GSM24663mtDNA "Common"-deletion subject 162.858
GSM24664mtDNA "Common"-deletion subject 214364
GSM24665mtDNA "Common"-deletion subject 3130.266
GSM24666mtDNA "Common"-deletion subject 425677