ProfileGDS1065 / 219158_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 32% 28% 52% 37% 38% 37% 46% 25% 35% 28% 27% 29% 39% 50% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 119.232
GSM24653Normal subject 215.428
GSM24654Normal subject 358.452
GSM24655A3243G-MELAS subject 119.637
GSM24656A3243G-MELAS subject 228.838
GSM24657A3243G-MELAS subject 335.637
GSM24658A3243G-MELAS subject 433.346
GSM24659A3243G-PEO subject 11225
GSM24660A3243G-PEO subject 221.435
GSM24661A3243G-PEO subject 310.728
GSM24662A3243G-PEO subject 412.327
GSM24663mtDNA "Common"-deletion subject 115.529
GSM24664mtDNA "Common"-deletion subject 250.839
GSM24665mtDNA "Common"-deletion subject 363.650
GSM24666mtDNA "Common"-deletion subject 445.141