ProfileGDS1065 / 217600_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 5% 38% 35% 16% 40% 33% 7% 13% 9% 13% 31% 13% 30% 25% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.65
GSM24653Normal subject 225.238
GSM24654Normal subject 326.235
GSM24655A3243G-MELAS subject 15.716
GSM24656A3243G-MELAS subject 232.240
GSM24657A3243G-MELAS subject 329.433
GSM24658A3243G-MELAS subject 42.57
GSM24659A3243G-PEO subject 15.313
GSM24660A3243G-PEO subject 24.19
GSM24661A3243G-PEO subject 33.913
GSM24662A3243G-PEO subject 416.231
GSM24663mtDNA "Common"-deletion subject 15.413
GSM24664mtDNA "Common"-deletion subject 231.230
GSM24665mtDNA "Common"-deletion subject 318.725
GSM24666mtDNA "Common"-deletion subject 439.939