ProfileGDS1065 / 214297_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 16% 47% 30% 40% 27% 50% 47% 43% 22% 33% 54% 45% 15% 23% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.816
GSM24653Normal subject 237.847
GSM24654Normal subject 319.430
GSM24655A3243G-MELAS subject 122.140
GSM24656A3243G-MELAS subject 216.627
GSM24657A3243G-MELAS subject 364.950
GSM24658A3243G-MELAS subject 434.747
GSM24659A3243G-PEO subject 128.643
GSM24660A3243G-PEO subject 29.922
GSM24661A3243G-PEO subject 31433
GSM24662A3243G-PEO subject 444.854
GSM24663mtDNA "Common"-deletion subject 136.945
GSM24664mtDNA "Common"-deletion subject 210.815
GSM24665mtDNA "Common"-deletion subject 316.323
GSM24666mtDNA "Common"-deletion subject 433.235