ProfileGDS1065 / 206494_s_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 11% 14% 6% 10% 9% 13% 7% 8% 7% 9% 5% 1% 9% 9% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.411
GSM24653Normal subject 25.514
GSM24654Normal subject 33.36
GSM24655A3243G-MELAS subject 13.610
GSM24656A3243G-MELAS subject 24.69
GSM24657A3243G-MELAS subject 36.913
GSM24658A3243G-MELAS subject 42.67
GSM24659A3243G-PEO subject 13.68
GSM24660A3243G-PEO subject 23.27
GSM24661A3243G-PEO subject 32.89
GSM24662A3243G-PEO subject 42.25
GSM24663mtDNA "Common"-deletion subject 111
GSM24664mtDNA "Common"-deletion subject 279
GSM24665mtDNA "Common"-deletion subject 35.69
GSM24666mtDNA "Common"-deletion subject 45.410