ProfileGDS1065 / 207641_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 65% 65% 60% 52% 58% 38% 42% 63% 59% 25% 54% 57% 58% 57% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 183.965
GSM24653Normal subject 278.765
GSM24654Normal subject 380.160
GSM24655A3243G-MELAS subject 134.752
GSM24656A3243G-MELAS subject 265.658
GSM24657A3243G-MELAS subject 336.738
GSM24658A3243G-MELAS subject 427.642
GSM24659A3243G-PEO subject 161.963
GSM24660A3243G-PEO subject 258.959
GSM24661A3243G-PEO subject 38.925
GSM24662A3243G-PEO subject 444.554
GSM24663mtDNA "Common"-deletion subject 160.857
GSM24664mtDNA "Common"-deletion subject 2108.858
GSM24665mtDNA "Common"-deletion subject 385.957
GSM24666mtDNA "Common"-deletion subject 46148