ProfileGDS1065 / 203009_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 25% 15% 15% 29% 22% 51% 36% 33% 19% 24% 48% 35% 36% 32% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.125
GSM24653Normal subject 26.215
GSM24654Normal subject 37.215
GSM24655A3243G-MELAS subject 112.729
GSM24656A3243G-MELAS subject 211.822
GSM24657A3243G-MELAS subject 366.451
GSM24658A3243G-MELAS subject 42136
GSM24659A3243G-PEO subject 118.333
GSM24660A3243G-PEO subject 28.319
GSM24661A3243G-PEO subject 38.224
GSM24662A3243G-PEO subject 434.748
GSM24663mtDNA "Common"-deletion subject 122.535
GSM24664mtDNA "Common"-deletion subject 242.736
GSM24665mtDNA "Common"-deletion subject 329.232
GSM24666mtDNA "Common"-deletion subject 460.848