ProfileGDS1065 / 208348_s_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 27% 35% 18% 21% 32% 13% 4% 8% 34% 24% 11% 11% 25% 7% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.527
GSM24653Normal subject 222.535
GSM24654Normal subject 38.718
GSM24655A3243G-MELAS subject 17.521
GSM24656A3243G-MELAS subject 221.432
GSM24657A3243G-MELAS subject 37.113
GSM24658A3243G-MELAS subject 41.84
GSM24659A3243G-PEO subject 13.78
GSM24660A3243G-PEO subject 220.334
GSM24661A3243G-PEO subject 38.424
GSM24662A3243G-PEO subject 44.111
GSM24663mtDNA "Common"-deletion subject 14.511
GSM24664mtDNA "Common"-deletion subject 22325
GSM24665mtDNA "Common"-deletion subject 34.47
GSM24666mtDNA "Common"-deletion subject 45.811