ProfileGDS1065 / 217437_s_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 46% 41% 49% 31% 39% 55% 41% 24% 25% 36% 40% 51% 42% 53% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137.746
GSM24653Normal subject 228.841
GSM24654Normal subject 351.649
GSM24655A3243G-MELAS subject 11431
GSM24656A3243G-MELAS subject 229.639
GSM24657A3243G-MELAS subject 378.655
GSM24658A3243G-MELAS subject 426.141
GSM24659A3243G-PEO subject 11124
GSM24660A3243G-PEO subject 212.625
GSM24661A3243G-PEO subject 316.536
GSM24662A3243G-PEO subject 424.940
GSM24663mtDNA "Common"-deletion subject 146.851
GSM24664mtDNA "Common"-deletion subject 256.842
GSM24665mtDNA "Common"-deletion subject 373.853
GSM24666mtDNA "Common"-deletion subject 468.751