ProfileGDS1065 / 220858_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 9% 17% 21% 10% 9% 5% 15% 5% 9% 27% 6% 20% 5% 9% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149
GSM24653Normal subject 26.817
GSM24654Normal subject 310.421
GSM24655A3243G-MELAS subject 13.710
GSM24656A3243G-MELAS subject 24.69
GSM24657A3243G-MELAS subject 33.35
GSM24658A3243G-MELAS subject 44.915
GSM24659A3243G-PEO subject 12.65
GSM24660A3243G-PEO subject 23.99
GSM24661A3243G-PEO subject 39.627
GSM24662A3243G-PEO subject 42.56
GSM24663mtDNA "Common"-deletion subject 18.620
GSM24664mtDNA "Common"-deletion subject 24.75
GSM24665mtDNA "Common"-deletion subject 35.29
GSM24666mtDNA "Common"-deletion subject 42.94