ProfileGDS1065 / 201882_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 11% 18% 17% 34% 23% 18% 22% 13% 13% 25% 22% 40% 22% 19% 18% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 14.511
GSM24653Normal subject 27.418
GSM24654Normal subject 37.917
GSM24655A3243G-MELAS subject 116.734
GSM24656A3243G-MELAS subject 212.223
GSM24657A3243G-MELAS subject 310.518
GSM24658A3243G-MELAS subject 48.822
GSM24659A3243G-PEO subject 15.413
GSM24660A3243G-PEO subject 25.513
GSM24661A3243G-PEO subject 38.625
GSM24662A3243G-PEO subject 48.622
GSM24663mtDNA "Common"-deletion subject 129.240
GSM24664mtDNA "Common"-deletion subject 219.322
GSM24665mtDNA "Common"-deletion subject 31219
GSM24666mtDNA "Common"-deletion subject 410.818