ProfileGDS1065 / 217045_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 71% 75% 69% 77% 74% 70% 72% 82% 75% 76% 74% 71% 72% 68% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1111.271
GSM24653Normal subject 2130.375
GSM24654Normal subject 3126.769
GSM24655A3243G-MELAS subject 197.377
GSM24656A3243G-MELAS subject 2130.274
GSM24657A3243G-MELAS subject 3160.470
GSM24658A3243G-MELAS subject 411072
GSM24659A3243G-PEO subject 114482
GSM24660A3243G-PEO subject 2114.775
GSM24661A3243G-PEO subject 395.676
GSM24662A3243G-PEO subject 4104.874
GSM24663mtDNA "Common"-deletion subject 1116.171
GSM24664mtDNA "Common"-deletion subject 2207.572
GSM24665mtDNA "Common"-deletion subject 3145.468
GSM24666mtDNA "Common"-deletion subject 4155.568