ProfileGDS1065 / 211964_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% 89% 85% 91% 85% 93% 93% 92% 86% 91% 91% 88% 85% 83% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1385.689
GSM24653Normal subject 2337.989
GSM24654Normal subject 3315.885
GSM24655A3243G-MELAS subject 1285.791
GSM24656A3243G-MELAS subject 2243.785
GSM24657A3243G-MELAS subject 31021.293
GSM24658A3243G-MELAS subject 4562.193
GSM24659A3243G-PEO subject 1366.492
GSM24660A3243G-PEO subject 2243.686
GSM24661A3243G-PEO subject 3326.491
GSM24662A3243G-PEO subject 4360.291
GSM24663mtDNA "Common"-deletion subject 1340.688
GSM24664mtDNA "Common"-deletion subject 2458.885
GSM24665mtDNA "Common"-deletion subject 335283
GSM24666mtDNA "Common"-deletion subject 4359.882