ProfileGDS1065 / 217697_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 39% 16% 29% 32% 28% 40% 35% 26% 27% 37% 14% 20% 30% 22% 24% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 128.539
GSM24653Normal subject 26.716
GSM24654Normal subject 318.529
GSM24655A3243G-MELAS subject 115.432
GSM24656A3243G-MELAS subject 217.628
GSM24657A3243G-MELAS subject 340.940
GSM24658A3243G-MELAS subject 42035
GSM24659A3243G-PEO subject 112.426
GSM24660A3243G-PEO subject 213.827
GSM24661A3243G-PEO subject 317.237
GSM24662A3243G-PEO subject 45.114
GSM24663mtDNA "Common"-deletion subject 18.920
GSM24664mtDNA "Common"-deletion subject 23130
GSM24665mtDNA "Common"-deletion subject 31522
GSM24666mtDNA "Common"-deletion subject 417.324