ProfileGDS1065 / 206357_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 23% 4% 25% 14% 17% 22% 24% 15% 15% 25% 15% 4% 8% 4% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111.323
GSM24653Normal subject 22.44
GSM24654Normal subject 314.225
GSM24655A3243G-MELAS subject 1514
GSM24656A3243G-MELAS subject 2817
GSM24657A3243G-MELAS subject 314.122
GSM24658A3243G-MELAS subject 49.824
GSM24659A3243G-PEO subject 16.415
GSM24660A3243G-PEO subject 26.315
GSM24661A3243G-PEO subject 38.825
GSM24662A3243G-PEO subject 45.515
GSM24663mtDNA "Common"-deletion subject 12.44
GSM24664mtDNA "Common"-deletion subject 26.18
GSM24665mtDNA "Common"-deletion subject 33.14
GSM24666mtDNA "Common"-deletion subject 410.418