ProfileGDS1065 / 213704_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 84% 87% 84% 87% 87% 86% 86% 86% 88% 81% 90% 90% 88% 89% 87% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1239.184
GSM24653Normal subject 2275.887
GSM24654Normal subject 3311.284
GSM24655A3243G-MELAS subject 1186.987
GSM24656A3243G-MELAS subject 2284.187
GSM24657A3243G-MELAS subject 3454.486
GSM24658A3243G-MELAS subject 425186
GSM24659A3243G-PEO subject 1190.286
GSM24660A3243G-PEO subject 2282.688
GSM24661A3243G-PEO subject 3134.181
GSM24662A3243G-PEO subject 4329.790
GSM24663mtDNA "Common"-deletion subject 1446.390
GSM24664mtDNA "Common"-deletion subject 2563.288
GSM24665mtDNA "Common"-deletion subject 3600.789
GSM24666mtDNA "Common"-deletion subject 4550.287