ProfileGDS1065 / 220680_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 25% 22% 23% 12% 28% 3% 24% 4% 13% 14% 19% 5% 15% 14% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.625
GSM24653Normal subject 210.322
GSM24654Normal subject 312.423
GSM24655A3243G-MELAS subject 14.212
GSM24656A3243G-MELAS subject 217.528
GSM24657A3243G-MELAS subject 32.33
GSM24658A3243G-MELAS subject 410.324
GSM24659A3243G-PEO subject 12.54
GSM24660A3243G-PEO subject 25.513
GSM24661A3243G-PEO subject 34.314
GSM24662A3243G-PEO subject 4719
GSM24663mtDNA "Common"-deletion subject 12.65
GSM24664mtDNA "Common"-deletion subject 210.815
GSM24665mtDNA "Common"-deletion subject 38.314
GSM24666mtDNA "Common"-deletion subject 45.410