ProfileGDS1065 / 203706_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 87% 86% 86% 91% 85% 86% 86% 88% 87% 85% 83% 85% 88% 91% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1319.887
GSM24653Normal subject 2269.286
GSM24654Normal subject 3374.786
GSM24655A3243G-MELAS subject 1274.291
GSM24656A3243G-MELAS subject 225385
GSM24657A3243G-MELAS subject 3461.786
GSM24658A3243G-MELAS subject 4261.486
GSM24659A3243G-PEO subject 1232.388
GSM24660A3243G-PEO subject 2256.787
GSM24661A3243G-PEO subject 3175.785
GSM24662A3243G-PEO subject 4177.283
GSM24663mtDNA "Common"-deletion subject 1273.885
GSM24664mtDNA "Common"-deletion subject 2598.688
GSM24665mtDNA "Common"-deletion subject 373491
GSM24666mtDNA "Common"-deletion subject 4902.792