ProfileGDS1065 / 208650_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 2% 25% 29% 26% 19% 8% 28% 26% 15% 19% 19% 0% 23% 27% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.72
GSM24653Normal subject 212.525
GSM24654Normal subject 318.629
GSM24655A3243G-MELAS subject 110.426
GSM24656A3243G-MELAS subject 29.119
GSM24657A3243G-MELAS subject 34.68
GSM24658A3243G-MELAS subject 41328
GSM24659A3243G-PEO subject 112.126
GSM24660A3243G-PEO subject 26.515
GSM24661A3243G-PEO subject 35.919
GSM24662A3243G-PEO subject 47.219
GSM24663mtDNA "Common"-deletion subject 10.50
GSM24664mtDNA "Common"-deletion subject 22023
GSM24665mtDNA "Common"-deletion subject 320.627
GSM24666mtDNA "Common"-deletion subject 46.612