ProfileGDS1065 / 212697_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 94% 94% 86% 92% 94% 94% 93% 94% 94% 95% 96% 93% 92% 91% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1712.494
GSM24653Normal subject 2703.494
GSM24654Normal subject 3356.986
GSM24655A3243G-MELAS subject 1316.492
GSM24656A3243G-MELAS subject 2650.194
GSM24657A3243G-MELAS subject 31085.594
GSM24658A3243G-MELAS subject 458793
GSM24659A3243G-PEO subject 1508.694
GSM24660A3243G-PEO subject 2593.994
GSM24661A3243G-PEO subject 3622.595
GSM24662A3243G-PEO subject 4854.996
GSM24663mtDNA "Common"-deletion subject 1619.693
GSM24664mtDNA "Common"-deletion subject 2916.292
GSM24665mtDNA "Common"-deletion subject 3808.491
GSM24666mtDNA "Common"-deletion subject 4881.591