ProfileGDS1065 / 203550_s_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 88% 82% 74% 81% 81% 84% 82% 84% 87% 85% 85% 78% 78% 76% 81% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1333.988
GSM24653Normal subject 2199.182
GSM24654Normal subject 3160.374
GSM24655A3243G-MELAS subject 1117.581
GSM24656A3243G-MELAS subject 2191.981
GSM24657A3243G-MELAS subject 3395.484
GSM24658A3243G-MELAS subject 4189.582
GSM24659A3243G-PEO subject 1163.484
GSM24660A3243G-PEO subject 2258.387
GSM24661A3243G-PEO subject 3165.885
GSM24662A3243G-PEO subject 4205.385
GSM24663mtDNA "Common"-deletion subject 1171.878
GSM24664mtDNA "Common"-deletion subject 2279.778
GSM24665mtDNA "Common"-deletion subject 3214.576
GSM24666mtDNA "Common"-deletion subject 4344.881