ProfileGDS1065 / 219699_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 14% 18% 17% 21% 15% 19% 13% 18% 13% 19% 17% 14% 13% 17% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.714
GSM24653Normal subject 27.718
GSM24654Normal subject 38.317
GSM24655A3243G-MELAS subject 17.421
GSM24656A3243G-MELAS subject 2715
GSM24657A3243G-MELAS subject 311.319
GSM24658A3243G-MELAS subject 44.413
GSM24659A3243G-PEO subject 17.418
GSM24660A3243G-PEO subject 25.713
GSM24661A3243G-PEO subject 35.919
GSM24662A3243G-PEO subject 46.317
GSM24663mtDNA "Common"-deletion subject 1614
GSM24664mtDNA "Common"-deletion subject 29.413
GSM24665mtDNA "Common"-deletion subject 310.517
GSM24666mtDNA "Common"-deletion subject 410.418