ProfileGDS1065 / 215481_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% 10% 45% 31% 39% 29% 38% 39% 43% 41% 49% 28% 14% 44% 30% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12032
GSM24653Normal subject 24.310
GSM24654Normal subject 343.345
GSM24655A3243G-MELAS subject 114.431
GSM24656A3243G-MELAS subject 229.539
GSM24657A3243G-MELAS subject 323.129
GSM24658A3243G-MELAS subject 422.838
GSM24659A3243G-PEO subject 124.639
GSM24660A3243G-PEO subject 231.843
GSM24661A3243G-PEO subject 321.241
GSM24662A3243G-PEO subject 436.649
GSM24663mtDNA "Common"-deletion subject 114.728
GSM24664mtDNA "Common"-deletion subject 210.114
GSM24665mtDNA "Common"-deletion subject 351.544
GSM24666mtDNA "Common"-deletion subject 425.630