ProfileGDS1065 / 208735_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 89% 86% 85% 72% 82% 84% 84% 84% 86% 87% 85% 80% 76% 84% 81% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1367.189
GSM24653Normal subject 225886
GSM24654Normal subject 3332.385
GSM24655A3243G-MELAS subject 176.372
GSM24656A3243G-MELAS subject 2198.182
GSM24657A3243G-MELAS subject 3391.784
GSM24658A3243G-MELAS subject 4220.584
GSM24659A3243G-PEO subject 1168.584
GSM24660A3243G-PEO subject 2239.786
GSM24661A3243G-PEO subject 321087
GSM24662A3243G-PEO subject 4202.685
GSM24663mtDNA "Common"-deletion subject 1188.680
GSM24664mtDNA "Common"-deletion subject 2248.576
GSM24665mtDNA "Common"-deletion subject 3376.584
GSM24666mtDNA "Common"-deletion subject 4346.881