ProfileGDS1065 / 201260_s_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% 93% 93% 93% 95% 92% 93% 93% 94% 93% 93% 92% 94% 95% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1694.193
GSM24653Normal subject 2543.293
GSM24654Normal subject 3768.893
GSM24655A3243G-MELAS subject 1364.693
GSM24656A3243G-MELAS subject 2898.695
GSM24657A3243G-MELAS subject 386792
GSM24658A3243G-MELAS subject 4561.393
GSM24659A3243G-PEO subject 1394.793
GSM24660A3243G-PEO subject 2627.394
GSM24661A3243G-PEO subject 339093
GSM24662A3243G-PEO subject 4500.793
GSM24663mtDNA "Common"-deletion subject 1528.892
GSM24664mtDNA "Common"-deletion subject 21161.394
GSM24665mtDNA "Common"-deletion subject 31333.495
GSM24666mtDNA "Common"-deletion subject 41513.495