ProfileGDS1065 / 50376_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 78% 82% 70% 77% 76% 79% 70% 82% 81% 81% 85% 84% 69% 69% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1161.778
GSM24653Normal subject 2200.682
GSM24654Normal subject 3131.270
GSM24655A3243G-MELAS subject 193.977
GSM24656A3243G-MELAS subject 2144.376
GSM24657A3243G-MELAS subject 3267.879
GSM24658A3243G-MELAS subject 499.770
GSM24659A3243G-PEO subject 1149.582
GSM24660A3243G-PEO subject 2163.581
GSM24661A3243G-PEO subject 313181
GSM24662A3243G-PEO subject 4214.885
GSM24663mtDNA "Common"-deletion subject 1242.384
GSM24664mtDNA "Common"-deletion subject 2179.969
GSM24665mtDNA "Common"-deletion subject 3153.169
GSM24666mtDNA "Common"-deletion subject 4183.971