ProfileGDS1065 / 203323_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 84% 88% 83% 89% 88% 85% 87% 85% 83% 86% 81% 80% 88% 84% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1239.584
GSM24653Normal subject 2300.288
GSM24654Normal subject 3278.483
GSM24655A3243G-MELAS subject 1209.789
GSM24656A3243G-MELAS subject 2306.688
GSM24657A3243G-MELAS subject 3408.585
GSM24658A3243G-MELAS subject 4281.687
GSM24659A3243G-PEO subject 1179.885
GSM24660A3243G-PEO subject 2190.583
GSM24661A3243G-PEO subject 3181.886
GSM24662A3243G-PEO subject 4156.981
GSM24663mtDNA "Common"-deletion subject 119180
GSM24664mtDNA "Common"-deletion subject 2557.888
GSM24665mtDNA "Common"-deletion subject 3365.984
GSM24666mtDNA "Common"-deletion subject 4542.387