ProfileGDS1065 / 212137_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 93% 94% 91% 94% 95% 93% 92% 93% 93% 94% 94% 94% 92% 92% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1664.693
GSM24653Normal subject 2709.594
GSM24654Normal subject 3587.391
GSM24655A3243G-MELAS subject 1402.294
GSM24656A3243G-MELAS subject 2798.995
GSM24657A3243G-MELAS subject 3962.193
GSM24658A3243G-MELAS subject 4496.892
GSM24659A3243G-PEO subject 1418.693
GSM24660A3243G-PEO subject 2512.293
GSM24661A3243G-PEO subject 3465.394
GSM24662A3243G-PEO subject 4660.594
GSM24663mtDNA "Common"-deletion subject 1738.794
GSM24664mtDNA "Common"-deletion subject 2939.792
GSM24665mtDNA "Common"-deletion subject 3936.492
GSM24666mtDNA "Common"-deletion subject 41385.894