ProfileGDS1065 / 206226_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 58% 45% 52% 26% 46% 49% 50% 49% 64% 43% 56% 53% 38% 42% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 160.558
GSM24653Normal subject 235.145
GSM24654Normal subject 358.452
GSM24655A3243G-MELAS subject 110.926
GSM24656A3243G-MELAS subject 241.346
GSM24657A3243G-MELAS subject 361.149
GSM24658A3243G-MELAS subject 44050
GSM24659A3243G-PEO subject 136.649
GSM24660A3243G-PEO subject 27064
GSM24661A3243G-PEO subject 322.843
GSM24662A3243G-PEO subject 447.456
GSM24663mtDNA "Common"-deletion subject 151.853
GSM24664mtDNA "Common"-deletion subject 247.738
GSM24665mtDNA "Common"-deletion subject 346.142
GSM24666mtDNA "Common"-deletion subject 459.247