ProfileGDS1065 / 212925_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 43% 40% 55% 26% 23% 30% 41% 70% 41% 22% 19% 43% 30% 46% 40% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 133.343
GSM24653Normal subject 228.340
GSM24654Normal subject 364.855
GSM24655A3243G-MELAS subject 110.526
GSM24656A3243G-MELAS subject 212.323
GSM24657A3243G-MELAS subject 323.830
GSM24658A3243G-MELAS subject 426.141
GSM24659A3243G-PEO subject 178.370
GSM24660A3243G-PEO subject 228.741
GSM24661A3243G-PEO subject 37.322
GSM24662A3243G-PEO subject 47.119
GSM24663mtDNA "Common"-deletion subject 134.343
GSM24664mtDNA "Common"-deletion subject 232.630
GSM24665mtDNA "Common"-deletion subject 356.146
GSM24666mtDNA "Common"-deletion subject 442.440