ProfileGDS1065 / 217788_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 90% 88% 88% 86% 91% 91% 91% 89% 93% 89% 91% 92% 92% 91% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1422.490
GSM24653Normal subject 2305.988
GSM24654Normal subject 3446.388
GSM24655A3243G-MELAS subject 1173.886
GSM24656A3243G-MELAS subject 2444.691
GSM24657A3243G-MELAS subject 3791.791
GSM24658A3243G-MELAS subject 445791
GSM24659A3243G-PEO subject 1258.489
GSM24660A3243G-PEO subject 2550.493
GSM24661A3243G-PEO subject 3248.189
GSM24662A3243G-PEO subject 435891
GSM24663mtDNA "Common"-deletion subject 1565.292
GSM24664mtDNA "Common"-deletion subject 2919.992
GSM24665mtDNA "Common"-deletion subject 3809.691
GSM24666mtDNA "Common"-deletion subject 4679.489