ProfileGDS1065 / 208043_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 5% 7% 5% 10% 19% 8% 8% 14% 5% 25% 15% 12% 30% 12% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.55
GSM24653Normal subject 23.27
GSM24654Normal subject 32.75
GSM24655A3243G-MELAS subject 13.810
GSM24656A3243G-MELAS subject 29.419
GSM24657A3243G-MELAS subject 34.48
GSM24658A3243G-MELAS subject 42.78
GSM24659A3243G-PEO subject 1614
GSM24660A3243G-PEO subject 22.75
GSM24661A3243G-PEO subject 38.825
GSM24662A3243G-PEO subject 45.515
GSM24663mtDNA "Common"-deletion subject 15.112
GSM24664mtDNA "Common"-deletion subject 232.230
GSM24665mtDNA "Common"-deletion subject 37.212
GSM24666mtDNA "Common"-deletion subject 41522