ProfileGDS1065 / 214326_x_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 15% 13% 62% 16% 51% 39% 43% 49% 60% 37% 50% 11% 38% 58% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.315
GSM24653Normal subject 25.313
GSM24654Normal subject 387.962
GSM24655A3243G-MELAS subject 15.416
GSM24656A3243G-MELAS subject 249.251
GSM24657A3243G-MELAS subject 33939
GSM24658A3243G-MELAS subject 429.843
GSM24659A3243G-PEO subject 136.249
GSM24660A3243G-PEO subject 259.960
GSM24661A3243G-PEO subject 31837
GSM24662A3243G-PEO subject 437.150
GSM24663mtDNA "Common"-deletion subject 14.711
GSM24664mtDNA "Common"-deletion subject 247.738
GSM24665mtDNA "Common"-deletion subject 391.658
GSM24666mtDNA "Common"-deletion subject 426.131