ProfileGDS1065 / 216188_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 23% 23% 28% 24% 26% 22% 4% 24% 26% 19% 21% 12% 24% 25% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11123
GSM24653Normal subject 210.623
GSM24654Normal subject 317.228
GSM24655A3243G-MELAS subject 19.624
GSM24656A3243G-MELAS subject 215.226
GSM24657A3243G-MELAS subject 313.922
GSM24658A3243G-MELAS subject 41.84
GSM24659A3243G-PEO subject 111.324
GSM24660A3243G-PEO subject 212.826
GSM24661A3243G-PEO subject 3619
GSM24662A3243G-PEO subject 4821
GSM24663mtDNA "Common"-deletion subject 1512
GSM24664mtDNA "Common"-deletion subject 221.324
GSM24665mtDNA "Common"-deletion subject 318.925
GSM24666mtDNA "Common"-deletion subject 41724