ProfileGDS1065 / 213788_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 51% 48% 33% 31% 58% 22% 45% 19% 19% 18% 18% 24% 39% 52% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 146.451
GSM24653Normal subject 23948
GSM24654Normal subject 324.533
GSM24655A3243G-MELAS subject 113.931
GSM24656A3243G-MELAS subject 264.458
GSM24657A3243G-MELAS subject 313.922
GSM24658A3243G-MELAS subject 431.345
GSM24659A3243G-PEO subject 1819
GSM24660A3243G-PEO subject 28.119
GSM24661A3243G-PEO subject 35.718
GSM24662A3243G-PEO subject 46.718
GSM24663mtDNA "Common"-deletion subject 111.824
GSM24664mtDNA "Common"-deletion subject 250.139
GSM24665mtDNA "Common"-deletion subject 370.552
GSM24666mtDNA "Common"-deletion subject 44441