ProfileGDS1065 / 204122_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 67% 67% 56% 69% 59% 71% 71% 70% 62% 66% 70% 55% 64% 67% 60% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 190.767
GSM24653Normal subject 284.167
GSM24654Normal subject 369.656
GSM24655A3243G-MELAS subject 167.769
GSM24656A3243G-MELAS subject 267.659
GSM24657A3243G-MELAS subject 3169.871
GSM24658A3243G-MELAS subject 4104.571
GSM24659A3243G-PEO subject 179.770
GSM24660A3243G-PEO subject 265.462
GSM24661A3243G-PEO subject 359.266
GSM24662A3243G-PEO subject 485.970
GSM24663mtDNA "Common"-deletion subject 156.255
GSM24664mtDNA "Common"-deletion subject 2138.464
GSM24665mtDNA "Common"-deletion subject 313467
GSM24666mtDNA "Common"-deletion subject 4106.460