ProfileGDS1065 / 219450_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 38% 40% 40% 36% 32% 40% 38% 37% 46% 30% 45% 43% 39% 31% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.838
GSM24653Normal subject 228.340
GSM24654Normal subject 333.440
GSM24655A3243G-MELAS subject 118.536
GSM24656A3243G-MELAS subject 221.532
GSM24657A3243G-MELAS subject 340.740
GSM24658A3243G-MELAS subject 423.138
GSM24659A3243G-PEO subject 121.837
GSM24660A3243G-PEO subject 235.246
GSM24661A3243G-PEO subject 311.630
GSM24662A3243G-PEO subject 431.245
GSM24663mtDNA "Common"-deletion subject 134.343
GSM24664mtDNA "Common"-deletion subject 250.439
GSM24665mtDNA "Common"-deletion subject 326.831
GSM24666mtDNA "Common"-deletion subject 429.433