ProfileGDS1065 / 203894_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 41% 48% 46% 49% 42% 46% 46% 45% 48% 29% 45% 55% 50% 47% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.741
GSM24653Normal subject 239.548
GSM24654Normal subject 344.546
GSM24655A3243G-MELAS subject 130.749
GSM24656A3243G-MELAS subject 23542
GSM24657A3243G-MELAS subject 353.946
GSM24658A3243G-MELAS subject 432.546
GSM24659A3243G-PEO subject 130.845
GSM24660A3243G-PEO subject 237.948
GSM24661A3243G-PEO subject 311.429
GSM24662A3243G-PEO subject 430.245
GSM24663mtDNA "Common"-deletion subject 15655
GSM24664mtDNA "Common"-deletion subject 279.750
GSM24665mtDNA "Common"-deletion subject 356.547
GSM24666mtDNA "Common"-deletion subject 452.345