ProfileGDS1065 / 208379_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 51% 33% 39% 49% 40% 41% 48% 56% 45% 48% 44% 33% 29% 46% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 146.551
GSM24653Normal subject 220.233
GSM24654Normal subject 331.939
GSM24655A3243G-MELAS subject 131.249
GSM24656A3243G-MELAS subject 231.640
GSM24657A3243G-MELAS subject 343.241
GSM24658A3243G-MELAS subject 436.748
GSM24659A3243G-PEO subject 147.556
GSM24660A3243G-PEO subject 234.145
GSM24661A3243G-PEO subject 329.348
GSM24662A3243G-PEO subject 42944
GSM24663mtDNA "Common"-deletion subject 119.533
GSM24664mtDNA "Common"-deletion subject 229.429
GSM24665mtDNA "Common"-deletion subject 354.446
GSM24666mtDNA "Common"-deletion subject 452.445