ProfileGDS1065 / 217892_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 84% 81% 83% 82% 81% 79% 84% 81% 80% 79% 76% 82% 85% 84% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 125384
GSM24653Normal subject 2185.481
GSM24654Normal subject 328683
GSM24655A3243G-MELAS subject 1127.282
GSM24656A3243G-MELAS subject 2192.581
GSM24657A3243G-MELAS subject 3272.479
GSM24658A3243G-MELAS subject 4224.784
GSM24659A3243G-PEO subject 1138.681
GSM24660A3243G-PEO subject 2152.680
GSM24661A3243G-PEO subject 3113.779
GSM24662A3243G-PEO subject 4118.976
GSM24663mtDNA "Common"-deletion subject 1220.382
GSM24664mtDNA "Common"-deletion subject 2435.785
GSM24665mtDNA "Common"-deletion subject 3378.784
GSM24666mtDNA "Common"-deletion subject 4357.682