ProfileGDS1065 / 204963_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 78% 78% 77% 80% 80% 75% 72% 72% 73% 74% 73% 74% 78% 83% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1162.378
GSM24653Normal subject 2150.578
GSM24654Normal subject 3190.177
GSM24655A3243G-MELAS subject 1114.280
GSM24656A3243G-MELAS subject 2179.880
GSM24657A3243G-MELAS subject 3212.575
GSM24658A3243G-MELAS subject 4105.472
GSM24659A3243G-PEO subject 186.372
GSM24660A3243G-PEO subject 2107.573
GSM24661A3243G-PEO subject 386.174
GSM24662A3243G-PEO subject 4101.173
GSM24663mtDNA "Common"-deletion subject 1129.974
GSM24664mtDNA "Common"-deletion subject 2283.678
GSM24665mtDNA "Common"-deletion subject 3344.983
GSM24666mtDNA "Common"-deletion subject 4379.983