ProfileGDS1065 / 201158_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 12% 28% 52% 33% 6% 59% 47% 41% 32% 29% 33% 33% 18% 44% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.212
GSM24653Normal subject 214.628
GSM24654Normal subject 358.452
GSM24655A3243G-MELAS subject 115.833
GSM24656A3243G-MELAS subject 23.36
GSM24657A3243G-MELAS subject 396.959
GSM24658A3243G-MELAS subject 433.947
GSM24659A3243G-PEO subject 12641
GSM24660A3243G-PEO subject 218.932
GSM24661A3243G-PEO subject 311.129
GSM24662A3243G-PEO subject 417.933
GSM24663mtDNA "Common"-deletion subject 120.533
GSM24664mtDNA "Common"-deletion subject 213.818
GSM24665mtDNA "Common"-deletion subject 350.244
GSM24666mtDNA "Common"-deletion subject 448.943