ProfileGDS1065 / 214768_x_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 17% 28% 11% 19% 15% 18% 16% 21% 13% 15% 7% 15% 16% 7% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.217
GSM24653Normal subject 214.628
GSM24654Normal subject 34.911
GSM24655A3243G-MELAS subject 16.819
GSM24656A3243G-MELAS subject 27.115
GSM24657A3243G-MELAS subject 310.718
GSM24658A3243G-MELAS subject 45.316
GSM24659A3243G-PEO subject 19.521
GSM24660A3243G-PEO subject 25.613
GSM24661A3243G-PEO subject 34.615
GSM24662A3243G-PEO subject 42.87
GSM24663mtDNA "Common"-deletion subject 16.515
GSM24664mtDNA "Common"-deletion subject 21216
GSM24665mtDNA "Common"-deletion subject 34.77
GSM24666mtDNA "Common"-deletion subject 46.913