ProfileGDS1065 / 200986_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 87% 86% 86% 88% 81% 88% 92% 88% 88% 87% 87% 85% 83% 85% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1316.487
GSM24653Normal subject 2263.886
GSM24654Normal subject 3355.486
GSM24655A3243G-MELAS subject 1198.188
GSM24656A3243G-MELAS subject 2189.681
GSM24657A3243G-MELAS subject 3565.488
GSM24658A3243G-MELAS subject 4501.992
GSM24659A3243G-PEO subject 1222.988
GSM24660A3243G-PEO subject 2280.188
GSM24661A3243G-PEO subject 3209.287
GSM24662A3243G-PEO subject 424787
GSM24663mtDNA "Common"-deletion subject 1269.985
GSM24664mtDNA "Common"-deletion subject 2385.183
GSM24665mtDNA "Common"-deletion subject 341485
GSM24666mtDNA "Common"-deletion subject 4478.186