ProfileGDS1065 / 219266_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 27% 32% 43% 43% 47% 42% 47% 37% 37% 44% 41% 48% 40% 43% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.627
GSM24653Normal subject 219.332
GSM24654Normal subject 339.643
GSM24655A3243G-MELAS subject 12543
GSM24656A3243G-MELAS subject 241.547
GSM24657A3243G-MELAS subject 345.942
GSM24658A3243G-MELAS subject 435.347
GSM24659A3243G-PEO subject 121.837
GSM24660A3243G-PEO subject 22437
GSM24661A3243G-PEO subject 323.944
GSM24662A3243G-PEO subject 426.241
GSM24663mtDNA "Common"-deletion subject 141.648
GSM24664mtDNA "Common"-deletion subject 252.840
GSM24665mtDNA "Common"-deletion subject 349.343
GSM24666mtDNA "Common"-deletion subject 450.444