ProfileGDS1065 / 214849_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 66% 62% 64% 68% 73% 62% 67% 71% 74% 72% 77% 74% 66% 63% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 187.266
GSM24653Normal subject 268.362
GSM24654Normal subject 397.464
GSM24655A3243G-MELAS subject 163.368
GSM24656A3243G-MELAS subject 2120.373
GSM24657A3243G-MELAS subject 3112.162
GSM24658A3243G-MELAS subject 484.467
GSM24659A3243G-PEO subject 183.571
GSM24660A3243G-PEO subject 210974
GSM24661A3243G-PEO subject 378.772
GSM24662A3243G-PEO subject 412277
GSM24663mtDNA "Common"-deletion subject 1130.974
GSM24664mtDNA "Common"-deletion subject 2156.466
GSM24665mtDNA "Common"-deletion subject 3112.663
GSM24666mtDNA "Common"-deletion subject 4112.462