ProfileGDS1065 / 217748_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 85% 80% 90% 89% 88% 81% 84% 86% 85% 82% 76% 84% 86% 89% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1262.285
GSM24653Normal subject 2172.280
GSM24654Normal subject 3562.290
GSM24655A3243G-MELAS subject 1215.489
GSM24656A3243G-MELAS subject 2308.288
GSM24657A3243G-MELAS subject 3314.681
GSM24658A3243G-MELAS subject 4229.284
GSM24659A3243G-PEO subject 1193.586
GSM24660A3243G-PEO subject 222685
GSM24661A3243G-PEO subject 3144.382
GSM24662A3243G-PEO subject 4116.376
GSM24663mtDNA "Common"-deletion subject 1241.184
GSM24664mtDNA "Common"-deletion subject 2502.686
GSM24665mtDNA "Common"-deletion subject 3613.589
GSM24666mtDNA "Common"-deletion subject 4412.984