ProfileGDS1065 / 220302_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 7% 8% 2% 5% 2% 3% 7% 5% 7% 4% 6% 5% 11% 6% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.47
GSM24653Normal subject 23.68
GSM24654Normal subject 31.72
GSM24655A3243G-MELAS subject 12.25
GSM24656A3243G-MELAS subject 21.72
GSM24657A3243G-MELAS subject 32.33
GSM24658A3243G-MELAS subject 42.47
GSM24659A3243G-PEO subject 12.65
GSM24660A3243G-PEO subject 23.27
GSM24661A3243G-PEO subject 31.74
GSM24662A3243G-PEO subject 42.56
GSM24663mtDNA "Common"-deletion subject 12.75
GSM24664mtDNA "Common"-deletion subject 28.411
GSM24665mtDNA "Common"-deletion subject 33.96
GSM24666mtDNA "Common"-deletion subject 42.94