ProfileGDS1065 / 218389_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 66% 65% 66% 90% 79% 71% 90% 58% 78% 77% 76% 64% 62% 62% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 187.266
GSM24653Normal subject 278.365
GSM24654Normal subject 3108.466
GSM24655A3243G-MELAS subject 125090
GSM24656A3243G-MELAS subject 2165.979
GSM24657A3243G-MELAS subject 3170.171
GSM24658A3243G-MELAS subject 4362.790
GSM24659A3243G-PEO subject 150.858
GSM24660A3243G-PEO subject 213878
GSM24661A3243G-PEO subject 3102.477
GSM24662A3243G-PEO subject 4118.276
GSM24663mtDNA "Common"-deletion subject 182.864
GSM24664mtDNA "Common"-deletion subject 2128.862
GSM24665mtDNA "Common"-deletion subject 3105.262
GSM24666mtDNA "Common"-deletion subject 4101.359