ProfileGDS1065 / 203437_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 93% 90% 92% 88% 91% 91% 92% 93% 93% 93% 92% 92% 90% 91% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 165693
GSM24653Normal subject 2399.790
GSM24654Normal subject 3714.692
GSM24655A3243G-MELAS subject 1202.588
GSM24656A3243G-MELAS subject 247391
GSM24657A3243G-MELAS subject 3792.491
GSM24658A3243G-MELAS subject 447192
GSM24659A3243G-PEO subject 1414.193
GSM24660A3243G-PEO subject 2544.193
GSM24661A3243G-PEO subject 3442.693
GSM24662A3243G-PEO subject 4456.292
GSM24663mtDNA "Common"-deletion subject 1585.792
GSM24664mtDNA "Common"-deletion subject 2724.690
GSM24665mtDNA "Common"-deletion subject 3796.891
GSM24666mtDNA "Common"-deletion subject 4874.291