ProfileGDS1065 / 217988_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 85% 84% 86% 80% 84% 80% 83% 83% 83% 87% 77% 89% 85% 84% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1261.885
GSM24653Normal subject 2223.384
GSM24654Normal subject 3355.286
GSM24655A3243G-MELAS subject 1114.380
GSM24656A3243G-MELAS subject 2238.484
GSM24657A3243G-MELAS subject 3280.580
GSM24658A3243G-MELAS subject 4203.283
GSM24659A3243G-PEO subject 1159.983
GSM24660A3243G-PEO subject 2187.683
GSM24661A3243G-PEO subject 3198.487
GSM24662A3243G-PEO subject 4122.677
GSM24663mtDNA "Common"-deletion subject 1374.689
GSM24664mtDNA "Common"-deletion subject 2468.285
GSM24665mtDNA "Common"-deletion subject 338584
GSM24666mtDNA "Common"-deletion subject 4467.585