ProfileGDS1065 / 214607_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 61% 66% 54% 59% 59% 48% 48% 58% 52% 56% 50% 63% 57% 46% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 170.661
GSM24653Normal subject 281.366
GSM24654Normal subject 362.254
GSM24655A3243G-MELAS subject 144.559
GSM24656A3243G-MELAS subject 266.459
GSM24657A3243G-MELAS subject 358.548
GSM24658A3243G-MELAS subject 436.648
GSM24659A3243G-PEO subject 151.158
GSM24660A3243G-PEO subject 24552
GSM24661A3243G-PEO subject 340.356
GSM24662A3243G-PEO subject 437.550
GSM24663mtDNA "Common"-deletion subject 178.263
GSM24664mtDNA "Common"-deletion subject 2106.657
GSM24665mtDNA "Common"-deletion subject 356.146
GSM24666mtDNA "Common"-deletion subject 46850