ProfileGDS1065 / 217123_x_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 8% 2% 22% 25% 17% 6% 13% 1% 5% 8% 3% 18% 8% 3% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.78
GSM24653Normal subject 21.52
GSM24654Normal subject 311.522
GSM24655A3243G-MELAS subject 110.125
GSM24656A3243G-MELAS subject 28.317
GSM24657A3243G-MELAS subject 33.86
GSM24658A3243G-MELAS subject 44.413
GSM24659A3243G-PEO subject 11.31
GSM24660A3243G-PEO subject 22.55
GSM24661A3243G-PEO subject 32.68
GSM24662A3243G-PEO subject 41.73
GSM24663mtDNA "Common"-deletion subject 17.618
GSM24664mtDNA "Common"-deletion subject 26.58
GSM24665mtDNA "Common"-deletion subject 32.53
GSM24666mtDNA "Common"-deletion subject 44.17