ProfileGDS1065 / 218277_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 69% 73% 77% 70% 72% 74% 72% 68% 70% 69% 66% 74% 79% 80% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1101.169
GSM24653Normal subject 211373
GSM24654Normal subject 319177
GSM24655A3243G-MELAS subject 168.970
GSM24656A3243G-MELAS subject 2112.872
GSM24657A3243G-MELAS subject 3199.674
GSM24658A3243G-MELAS subject 4108.472
GSM24659A3243G-PEO subject 172.868
GSM24660A3243G-PEO subject 292.170
GSM24661A3243G-PEO subject 370.369
GSM24662A3243G-PEO subject 470.666
GSM24663mtDNA "Common"-deletion subject 1130.574
GSM24664mtDNA "Common"-deletion subject 2297.679
GSM24665mtDNA "Common"-deletion subject 327480
GSM24666mtDNA "Common"-deletion subject 4260.577