ProfileGDS1065 / 44120_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 79% 77% 73% 66% 68% 75% 75% 80% 77% 76% 74% 84% 73% 73% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1169.279
GSM24653Normal subject 2139.977
GSM24654Normal subject 3149.773
GSM24655A3243G-MELAS subject 157.466
GSM24656A3243G-MELAS subject 294.968
GSM24657A3243G-MELAS subject 3210.775
GSM24658A3243G-MELAS subject 4128.875
GSM24659A3243G-PEO subject 1126.980
GSM24660A3243G-PEO subject 2131.377
GSM24661A3243G-PEO subject 399.876
GSM24662A3243G-PEO subject 4102.474
GSM24663mtDNA "Common"-deletion subject 1249.484
GSM24664mtDNA "Common"-deletion subject 2220.173
GSM24665mtDNA "Common"-deletion subject 3179.373
GSM24666mtDNA "Common"-deletion subject 4160.669