ProfileGDS1065 / 200735_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 98% 98% 98% 98% 98% 99% 99% 98% 98% 98% 98% 98% 98% 98% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13823.198
GSM24653Normal subject 23555.598
GSM24654Normal subject 33646.998
GSM24655A3243G-MELAS subject 11977.498
GSM24656A3243G-MELAS subject 23013.898
GSM24657A3243G-MELAS subject 35758.399
GSM24658A3243G-MELAS subject 44193.499
GSM24659A3243G-PEO subject 12059.198
GSM24660A3243G-PEO subject 22472.498
GSM24661A3243G-PEO subject 31962.198
GSM24662A3243G-PEO subject 42220.198
GSM24663mtDNA "Common"-deletion subject 13818.198
GSM24664mtDNA "Common"-deletion subject 25472.698
GSM24665mtDNA "Common"-deletion subject 34230.298
GSM24666mtDNA "Common"-deletion subject 45672.898