ProfileGDS1065 / 217297_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% 8% 7% 9% 4% 7% 15% 23% 13% 22% 21% 16% 11% 33% 17% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.511
GSM24653Normal subject 23.68
GSM24654Normal subject 33.57
GSM24655A3243G-MELAS subject 13.59
GSM24656A3243G-MELAS subject 22.64
GSM24657A3243G-MELAS subject 34.17
GSM24658A3243G-MELAS subject 44.915
GSM24659A3243G-PEO subject 110.223
GSM24660A3243G-PEO subject 25.713
GSM24661A3243G-PEO subject 37.422
GSM24662A3243G-PEO subject 48.421
GSM24663mtDNA "Common"-deletion subject 16.716
GSM24664mtDNA "Common"-deletion subject 27.911
GSM24665mtDNA "Common"-deletion subject 329.533
GSM24666mtDNA "Common"-deletion subject 49.917