ProfileGDS1065 / 60084_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 17% 4% 12% 16% 27% 27% 21% 21% 26% 24% 26% 25% 28% 30% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.517
GSM24653Normal subject 22.24
GSM24654Normal subject 35.512
GSM24655A3243G-MELAS subject 15.616
GSM24656A3243G-MELAS subject 215.827
GSM24657A3243G-MELAS subject 319.927
GSM24658A3243G-MELAS subject 47.921
GSM24659A3243G-PEO subject 19.521
GSM24660A3243G-PEO subject 213.426
GSM24661A3243G-PEO subject 38.324
GSM24662A3243G-PEO subject 41226
GSM24663mtDNA "Common"-deletion subject 11225
GSM24664mtDNA "Common"-deletion subject 228.728
GSM24665mtDNA "Common"-deletion subject 326.130
GSM24666mtDNA "Common"-deletion subject 426.631