ProfileGDS1065 / 202854_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% 78% 83% 87% 80% 81% 85% 79% 81% 69% 78% 86% 88% 85% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1175.279
GSM24653Normal subject 2150.978
GSM24654Normal subject 3285.583
GSM24655A3243G-MELAS subject 1188.887
GSM24656A3243G-MELAS subject 218180
GSM24657A3243G-MELAS subject 3299.381
GSM24658A3243G-MELAS subject 4243.385
GSM24659A3243G-PEO subject 1125.979
GSM24660A3243G-PEO subject 2167.881
GSM24661A3243G-PEO subject 368.669
GSM24662A3243G-PEO subject 4129.978
GSM24663mtDNA "Common"-deletion subject 1281.186
GSM24664mtDNA "Common"-deletion subject 2604.188
GSM24665mtDNA "Common"-deletion subject 3414.785
GSM24666mtDNA "Common"-deletion subject 4427.884