ProfileGDS1065 / 202592_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 94% 95% 92% 94% 92% 95% 93% 95% 94% 94% 92% 93% 92% 91% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 177894
GSM24653Normal subject 2762.795
GSM24654Normal subject 3653.692
GSM24655A3243G-MELAS subject 1453.594
GSM24656A3243G-MELAS subject 2543.292
GSM24657A3243G-MELAS subject 31350.895
GSM24658A3243G-MELAS subject 4552.893
GSM24659A3243G-PEO subject 1558.395
GSM24660A3243G-PEO subject 2611.694
GSM24661A3243G-PEO subject 3492.894
GSM24662A3243G-PEO subject 4439.892
GSM24663mtDNA "Common"-deletion subject 1689.893
GSM24664mtDNA "Common"-deletion subject 2852.392
GSM24665mtDNA "Common"-deletion subject 3790.391
GSM24666mtDNA "Common"-deletion subject 41012.492