ProfileGDS1065 / 221269_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 22% 16% 54% 18% 16% 51% 68% 49% 46% 39% 46% 17% 30% 48% 32% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.122
GSM24653Normal subject 26.716
GSM24654Normal subject 362.754
GSM24655A3243G-MELAS subject 16.418
GSM24656A3243G-MELAS subject 27.516
GSM24657A3243G-MELAS subject 366.551
GSM24658A3243G-MELAS subject 488.468
GSM24659A3243G-PEO subject 136.249
GSM24660A3243G-PEO subject 235.946
GSM24661A3243G-PEO subject 319.639
GSM24662A3243G-PEO subject 432.346
GSM24663mtDNA "Common"-deletion subject 17.317
GSM24664mtDNA "Common"-deletion subject 231.630
GSM24665mtDNA "Common"-deletion subject 358.548
GSM24666mtDNA "Common"-deletion subject 427.732