ProfileGDS1065 / 218618_s_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 66% 73% 77% 70% 70% 70% 75% 71% 62% 66% 60% 70% 61% 73% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18966
GSM24653Normal subject 2113.673
GSM24654Normal subject 3194.577
GSM24655A3243G-MELAS subject 169.870
GSM24656A3243G-MELAS subject 2105.870
GSM24657A3243G-MELAS subject 3160.870
GSM24658A3243G-MELAS subject 412875
GSM24659A3243G-PEO subject 182.771
GSM24660A3243G-PEO subject 266.262
GSM24661A3243G-PEO subject 360.666
GSM24662A3243G-PEO subject 455.560
GSM24663mtDNA "Common"-deletion subject 1108.170
GSM24664mtDNA "Common"-deletion subject 2122.161
GSM24665mtDNA "Common"-deletion subject 3179.673
GSM24666mtDNA "Common"-deletion subject 4202.273