ProfileGDS1065 / 211208_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 73% 73% 69% 73% 72% 73% 70% 78% 74% 72% 71% 75% 70% 68% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1122.873
GSM24653Normal subject 2112.973
GSM24654Normal subject 3127.769
GSM24655A3243G-MELAS subject 180.473
GSM24656A3243G-MELAS subject 2117.272
GSM24657A3243G-MELAS subject 3186.173
GSM24658A3243G-MELAS subject 496.870
GSM24659A3243G-PEO subject 1113.378
GSM24660A3243G-PEO subject 211374
GSM24661A3243G-PEO subject 378.772
GSM24662A3243G-PEO subject 491.871
GSM24663mtDNA "Common"-deletion subject 113675
GSM24664mtDNA "Common"-deletion subject 2185.870
GSM24665mtDNA "Common"-deletion subject 3144.768
GSM24666mtDNA "Common"-deletion subject 4201.973