ProfileGDS1065 / 218518_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 58% 69% 70% 61% 49% 54% 60% 62% 45% 59% 56% 73% 65% 58% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 160.558
GSM24653Normal subject 292.569
GSM24654Normal subject 312970
GSM24655A3243G-MELAS subject 148.761
GSM24656A3243G-MELAS subject 244.749
GSM24657A3243G-MELAS subject 378.154
GSM24658A3243G-MELAS subject 459.960
GSM24659A3243G-PEO subject 158.562
GSM24660A3243G-PEO subject 233.545
GSM24661A3243G-PEO subject 34659
GSM24662A3243G-PEO subject 447.656
GSM24663mtDNA "Common"-deletion subject 1125.973
GSM24664mtDNA "Common"-deletion subject 2150.265
GSM24665mtDNA "Common"-deletion subject 390.758
GSM24666mtDNA "Common"-deletion subject 4162.469