ProfileGDS1065 / 213534_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 53% 56% 50% 28% 43% 29% 27% 35% 20% 27% 45% 38% 46% 36% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 150.353
GSM24653Normal subject 254.956
GSM24654Normal subject 353.550
GSM24655A3243G-MELAS subject 111.628
GSM24656A3243G-MELAS subject 235.643
GSM24657A3243G-MELAS subject 322.929
GSM24658A3243G-MELAS subject 41227
GSM24659A3243G-PEO subject 120.535
GSM24660A3243G-PEO subject 28.720
GSM24661A3243G-PEO subject 39.627
GSM24662A3243G-PEO subject 430.545
GSM24663mtDNA "Common"-deletion subject 126.238
GSM24664mtDNA "Common"-deletion subject 267.746
GSM24665mtDNA "Common"-deletion subject 334.836
GSM24666mtDNA "Common"-deletion subject 449.543