ProfileGDS1065 / 214259_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 96% 95% 91% 94% 94% 97% 95% 97% 95% 96% 97% 95% 95% 94% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11220.796
GSM24653Normal subject 2859.695
GSM24654Normal subject 3573.391
GSM24655A3243G-MELAS subject 1463.394
GSM24656A3243G-MELAS subject 2742.394
GSM24657A3243G-MELAS subject 32144.297
GSM24658A3243G-MELAS subject 4787.595
GSM24659A3243G-PEO subject 11002.197
GSM24660A3243G-PEO subject 2785.995
GSM24661A3243G-PEO subject 3729.396
GSM24662A3243G-PEO subject 41230.697
GSM24663mtDNA "Common"-deletion subject 11032.295
GSM24664mtDNA "Common"-deletion subject 2138195
GSM24665mtDNA "Common"-deletion subject 31195.494
GSM24666mtDNA "Common"-deletion subject 41301.394