ProfileGDS1065 / 206280_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% 45% 35% 37% 45% 27% 18% 55% 49% 45% 45% 47% 40% 43% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137.846
GSM24653Normal subject 235.245
GSM24654Normal subject 326.335
GSM24655A3243G-MELAS subject 119.637
GSM24656A3243G-MELAS subject 238.445
GSM24657A3243G-MELAS subject 319.527
GSM24658A3243G-MELAS subject 46.618
GSM24659A3243G-PEO subject 145.555
GSM24660A3243G-PEO subject 240.649
GSM24661A3243G-PEO subject 325.645
GSM24662A3243G-PEO subject 430.545
GSM24663mtDNA "Common"-deletion subject 14147
GSM24664mtDNA "Common"-deletion subject 252.640
GSM24665mtDNA "Common"-deletion subject 349.143
GSM24666mtDNA "Common"-deletion subject 457.547