ProfileGDS1065 / 52159_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 71% 68% 55% 72% 66% 77% 67% 57% 69% 70% 77% 69% 70% 66% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1108.171
GSM24653Normal subject 289.668
GSM24654Normal subject 366.655
GSM24655A3243G-MELAS subject 175.472
GSM24656A3243G-MELAS subject 288.966
GSM24657A3243G-MELAS subject 3245.577
GSM24658A3243G-MELAS subject 482.667
GSM24659A3243G-PEO subject 148.457
GSM24660A3243G-PEO subject 288.469
GSM24661A3243G-PEO subject 372.570
GSM24662A3243G-PEO subject 4122.177
GSM24663mtDNA "Common"-deletion subject 1103.669
GSM24664mtDNA "Common"-deletion subject 2187.170
GSM24665mtDNA "Common"-deletion subject 3128.666
GSM24666mtDNA "Common"-deletion subject 4135.365