ProfileGDS1065 / 221249_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 70% 79% 70% 74% 70% 77% 78% 76% 71% 73% 66% 68% 73% 69% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1106.570
GSM24653Normal subject 2158.679
GSM24654Normal subject 3133.970
GSM24655A3243G-MELAS subject 18274
GSM24656A3243G-MELAS subject 2104.570
GSM24657A3243G-MELAS subject 3244.977
GSM24658A3243G-MELAS subject 4147.678
GSM24659A3243G-PEO subject 110776
GSM24660A3243G-PEO subject 295.771
GSM24661A3243G-PEO subject 380.973
GSM24662A3243G-PEO subject 471.766
GSM24663mtDNA "Common"-deletion subject 199.368
GSM24664mtDNA "Common"-deletion subject 2217.773
GSM24665mtDNA "Common"-deletion subject 314769
GSM24666mtDNA "Common"-deletion subject 4204.273