ProfileGDS1065 / 214032_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 27% 40% 6% 9% 12% 24% 9% 3% 13% 19% 16% 33% 27% 22% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.527
GSM24653Normal subject 227.940
GSM24654Normal subject 336
GSM24655A3243G-MELAS subject 13.29
GSM24656A3243G-MELAS subject 25.712
GSM24657A3243G-MELAS subject 316.624
GSM24658A3243G-MELAS subject 43.19
GSM24659A3243G-PEO subject 11.93
GSM24660A3243G-PEO subject 25.313
GSM24661A3243G-PEO subject 35.919
GSM24662A3243G-PEO subject 4616
GSM24663mtDNA "Common"-deletion subject 119.633
GSM24664mtDNA "Common"-deletion subject 225.627
GSM24665mtDNA "Common"-deletion subject 314.922
GSM24666mtDNA "Common"-deletion subject 414.322