ProfileGDS1065 / 205119_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 59% 50% 51% 65% 40% 50% 56% 72% 64% 50% 69% 49% 70% 67% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 165.459
GSM24653Normal subject 243.150
GSM24654Normal subject 355.251
GSM24655A3243G-MELAS subject 156.965
GSM24656A3243G-MELAS subject 231.940
GSM24657A3243G-MELAS subject 364.550
GSM24658A3243G-MELAS subject 450.756
GSM24659A3243G-PEO subject 187.272
GSM24660A3243G-PEO subject 272.564
GSM24661A3243G-PEO subject 331.950
GSM24662A3243G-PEO subject 481.569
GSM24663mtDNA "Common"-deletion subject 143.449
GSM24664mtDNA "Common"-deletion subject 2188.470
GSM24665mtDNA "Common"-deletion subject 3136.967
GSM24666mtDNA "Common"-deletion subject 495.858