ProfileGDS1065 / 214833_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 12% 20% 31% 32% 22% 16% 30% 14% 25% 15% 9% 23% 19% 39% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1512
GSM24653Normal subject 28.920
GSM24654Normal subject 321.531
GSM24655A3243G-MELAS subject 114.632
GSM24656A3243G-MELAS subject 211.622
GSM24657A3243G-MELAS subject 3916
GSM24658A3243G-MELAS subject 414.630
GSM24659A3243G-PEO subject 15.814
GSM24660A3243G-PEO subject 212.525
GSM24661A3243G-PEO subject 34.715
GSM24662A3243G-PEO subject 43.49
GSM24663mtDNA "Common"-deletion subject 110.823
GSM24664mtDNA "Common"-deletion subject 215.619
GSM24665mtDNA "Common"-deletion subject 340.439
GSM24666mtDNA "Common"-deletion subject 413.621