ProfileGDS1065 / 217675_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 11% 3% 5% 2% 5% 7% 7% 1% 5% 24% 5% 7% 4% 2% 3% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.711
GSM24653Normal subject 22.13
GSM24654Normal subject 32.75
GSM24655A3243G-MELAS subject 11.12
GSM24656A3243G-MELAS subject 22.95
GSM24657A3243G-MELAS subject 347
GSM24658A3243G-MELAS subject 42.47
GSM24659A3243G-PEO subject 111
GSM24660A3243G-PEO subject 22.55
GSM24661A3243G-PEO subject 38.424
GSM24662A3243G-PEO subject 42.35
GSM24663mtDNA "Common"-deletion subject 13.27
GSM24664mtDNA "Common"-deletion subject 23.94
GSM24665mtDNA "Common"-deletion subject 322
GSM24666mtDNA "Common"-deletion subject 42.33