ProfileGDS1065 / 210372_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 72% 72% 89% 85% 80% 68% 83% 66% 72% 70% 66% 72% 85% 86% 75% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111972
GSM24653Normal subject 2109.472
GSM24654Normal subject 3463.789
GSM24655A3243G-MELAS subject 1151.985
GSM24656A3243G-MELAS subject 2180.280
GSM24657A3243G-MELAS subject 3148.968
GSM24658A3243G-MELAS subject 4212.483
GSM24659A3243G-PEO subject 16966
GSM24660A3243G-PEO subject 2100.572
GSM24661A3243G-PEO subject 373.470
GSM24662A3243G-PEO subject 472.966
GSM24663mtDNA "Common"-deletion subject 1118.572
GSM24664mtDNA "Common"-deletion subject 2457.485
GSM24665mtDNA "Common"-deletion subject 3442.986
GSM24666mtDNA "Common"-deletion subject 4226.675