ProfileGDS1065 / 204332_s_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 77% 55% 74% 65% 70% 65% 68% 69% 73% 76% 68% 71% 65% 72% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1154.277
GSM24653Normal subject 251.855
GSM24654Normal subject 3163.474
GSM24655A3243G-MELAS subject 157.365
GSM24656A3243G-MELAS subject 2104.670
GSM24657A3243G-MELAS subject 3125.965
GSM24658A3243G-MELAS subject 488.368
GSM24659A3243G-PEO subject 175.869
GSM24660A3243G-PEO subject 2108.173
GSM24661A3243G-PEO subject 395.776
GSM24662A3243G-PEO subject 476.668
GSM24663mtDNA "Common"-deletion subject 1114.171
GSM24664mtDNA "Common"-deletion subject 2149.565
GSM24665mtDNA "Common"-deletion subject 3177.572
GSM24666mtDNA "Common"-deletion subject 4128.664