ProfileGDS1065 / 212456_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% 93% 88% 95% 95% 93% 93% 94% 93% 96% 96% 95% 94% 90% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1740.894
GSM24653Normal subject 2570.793
GSM24654Normal subject 3414.188
GSM24655A3243G-MELAS subject 1473.195
GSM24656A3243G-MELAS subject 2790.695
GSM24657A3243G-MELAS subject 31048.793
GSM24658A3243G-MELAS subject 4605.893
GSM24659A3243G-PEO subject 1480.694
GSM24660A3243G-PEO subject 2520.493
GSM24661A3243G-PEO subject 3791.396
GSM24662A3243G-PEO subject 4863.196
GSM24663mtDNA "Common"-deletion subject 195395
GSM24664mtDNA "Common"-deletion subject 21323.494
GSM24665mtDNA "Common"-deletion subject 3646.190
GSM24666mtDNA "Common"-deletion subject 4802.891