ProfileGDS1065 / 215799_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 13% 12% 10% 14% 9% 9% 5% 12% 7% 9% 6% 9% 7% 5% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.513
GSM24653Normal subject 24.912
GSM24654Normal subject 34.610
GSM24655A3243G-MELAS subject 14.814
GSM24656A3243G-MELAS subject 24.79
GSM24657A3243G-MELAS subject 359
GSM24658A3243G-MELAS subject 42.15
GSM24659A3243G-PEO subject 15.112
GSM24660A3243G-PEO subject 23.17
GSM24661A3243G-PEO subject 32.89
GSM24662A3243G-PEO subject 42.56
GSM24663mtDNA "Common"-deletion subject 13.99
GSM24664mtDNA "Common"-deletion subject 25.77
GSM24665mtDNA "Common"-deletion subject 33.55
GSM24666mtDNA "Common"-deletion subject 44.68