ProfileGDS1065 / 213421_x_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 21% 52% 46% 62% 8% 55% 62% 66% 42% 62% 61% 61% 59% 54% 51% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 19.521
GSM24653Normal subject 246.152
GSM24654Normal subject 344.546
GSM24655A3243G-MELAS subject 15062
GSM24656A3243G-MELAS subject 24.18
GSM24657A3243G-MELAS subject 381.455
GSM24658A3243G-MELAS subject 465.762
GSM24659A3243G-PEO subject 16766
GSM24660A3243G-PEO subject 229.642
GSM24661A3243G-PEO subject 351.762
GSM24662A3243G-PEO subject 458.461
GSM24663mtDNA "Common"-deletion subject 173.361
GSM24664mtDNA "Common"-deletion subject 2112.459
GSM24665mtDNA "Common"-deletion subject 378.554
GSM24666mtDNA "Common"-deletion subject 470.351