ProfileGDS1065 / 215879_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 1% 25% 15% 26% 5% 22% 25% 29% 14% 19% 10% 19% 17% 17% 2% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.31
GSM24653Normal subject 212.325
GSM24654Normal subject 37.215
GSM24655A3243G-MELAS subject 110.526
GSM24656A3243G-MELAS subject 23.25
GSM24657A3243G-MELAS subject 314.322
GSM24658A3243G-MELAS subject 410.625
GSM24659A3243G-PEO subject 114.829
GSM24660A3243G-PEO subject 25.814
GSM24661A3243G-PEO subject 36.219
GSM24662A3243G-PEO subject 43.710
GSM24663mtDNA "Common"-deletion subject 18.219
GSM24664mtDNA "Common"-deletion subject 213.117
GSM24665mtDNA "Common"-deletion subject 310.417
GSM24666mtDNA "Common"-deletion subject 42.12