ProfileGDS1065 / 200832_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 2% 82% 7% 49% 19% 8% 16% 7% 3% 25% 18% 8% 4% 5% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.72
GSM24653Normal subject 2189.282
GSM24654Normal subject 33.57
GSM24655A3243G-MELAS subject 13149
GSM24656A3243G-MELAS subject 29.719
GSM24657A3243G-MELAS subject 34.58
GSM24658A3243G-MELAS subject 45.516
GSM24659A3243G-PEO subject 13.37
GSM24660A3243G-PEO subject 21.93
GSM24661A3243G-PEO subject 38.525
GSM24662A3243G-PEO subject 46.718
GSM24663mtDNA "Common"-deletion subject 13.78
GSM24664mtDNA "Common"-deletion subject 244
GSM24665mtDNA "Common"-deletion subject 33.75
GSM24666mtDNA "Common"-deletion subject 44.17