ProfileGDS1065 / 201388_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 89% 85% 86% 83% 89% 91% 88% 86% 89% 82% 84% 85% 87% 89% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 138889
GSM24653Normal subject 2235.585
GSM24654Normal subject 335186
GSM24655A3243G-MELAS subject 1132.183
GSM24656A3243G-MELAS subject 2342.289
GSM24657A3243G-MELAS subject 3718.291
GSM24658A3243G-MELAS subject 4321.888
GSM24659A3243G-PEO subject 1186.286
GSM24660A3243G-PEO subject 2325.689
GSM24661A3243G-PEO subject 3140.582
GSM24662A3243G-PEO subject 4191.984
GSM24663mtDNA "Common"-deletion subject 1268.985
GSM24664mtDNA "Common"-deletion subject 2537.987
GSM24665mtDNA "Common"-deletion subject 3591.289
GSM24666mtDNA "Common"-deletion subject 4589.488