ProfileGDS1065 / 213047_x_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 91% 90% 95% 92% 93% 91% 92% 86% 91% 85% 83% 91% 93% 95% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1484.691
GSM24653Normal subject 2366.490
GSM24654Normal subject 31194.295
GSM24655A3243G-MELAS subject 1320.892
GSM24656A3243G-MELAS subject 2561.293
GSM24657A3243G-MELAS subject 3726.391
GSM24658A3243G-MELAS subject 4525.492
GSM24659A3243G-PEO subject 1198.186
GSM24660A3243G-PEO subject 2413.791
GSM24661A3243G-PEO subject 3173.185
GSM24662A3243G-PEO subject 4183.983
GSM24663mtDNA "Common"-deletion subject 1506.991
GSM24664mtDNA "Common"-deletion subject 21087.593
GSM24665mtDNA "Common"-deletion subject 31485.195
GSM24666mtDNA "Common"-deletion subject 41056.693