ProfileGDS1065 / 209774_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 50% 45% 28% 7% 66% 16% 26% 14% 5% 8% 11% 21% 74% 5% 52% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 144.250
GSM24653Normal subject 234.645
GSM24654Normal subject 317.428
GSM24655A3243G-MELAS subject 12.87
GSM24656A3243G-MELAS subject 286.666
GSM24657A3243G-MELAS subject 38.916
GSM24658A3243G-MELAS subject 411.126
GSM24659A3243G-PEO subject 15.914
GSM24660A3243G-PEO subject 22.65
GSM24661A3243G-PEO subject 32.78
GSM24662A3243G-PEO subject 43.911
GSM24663mtDNA "Common"-deletion subject 19.521
GSM24664mtDNA "Common"-deletion subject 2223.574
GSM24665mtDNA "Common"-deletion subject 33.65
GSM24666mtDNA "Common"-deletion subject 471.652