ProfileGDS1065 / 200933_x_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11009599
GSM24653Normal subject 29115.199
GSM24654Normal subject 38860.299
GSM24655A3243G-MELAS subject 15238.599
GSM24656A3243G-MELAS subject 27122.399
GSM24657A3243G-MELAS subject 311218.399
GSM24658A3243G-MELAS subject 48789.799
GSM24659A3243G-PEO subject 17500.699
GSM24660A3243G-PEO subject 27477.699
GSM24661A3243G-PEO subject 37206.499
GSM24662A3243G-PEO subject 4963799
GSM24663mtDNA "Common"-deletion subject 19726.799
GSM24664mtDNA "Common"-deletion subject 211633.999
GSM24665mtDNA "Common"-deletion subject 311242.499
GSM24666mtDNA "Common"-deletion subject 412858.599