ProfileGDS1065 / 205786_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 54% 60% 48% 61% 43% 66% 71% 51% 54% 56% 64% 49% 65% 58% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 151.954
GSM24653Normal subject 262.860
GSM24654Normal subject 347.548
GSM24655A3243G-MELAS subject 147.961
GSM24656A3243G-MELAS subject 235.243
GSM24657A3243G-MELAS subject 3132.966
GSM24658A3243G-MELAS subject 4102.871
GSM24659A3243G-PEO subject 138.951
GSM24660A3243G-PEO subject 248.754
GSM24661A3243G-PEO subject 340.656
GSM24662A3243G-PEO subject 465.764
GSM24663mtDNA "Common"-deletion subject 144.249
GSM24664mtDNA "Common"-deletion subject 2149.365
GSM24665mtDNA "Common"-deletion subject 39258
GSM24666mtDNA "Common"-deletion subject 4124.864