ProfileGDS1065 / 203538_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 91% 90% 90% 86% 90% 92% 91% 91% 90% 91% 90% 90% 90% 90% 92% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1497.991
GSM24653Normal subject 237990
GSM24654Normal subject 3561.990
GSM24655A3243G-MELAS subject 1170.786
GSM24656A3243G-MELAS subject 2393.590
GSM24657A3243G-MELAS subject 3827.492
GSM24658A3243G-MELAS subject 4452.191
GSM24659A3243G-PEO subject 1295.391
GSM24660A3243G-PEO subject 2343.890
GSM24661A3243G-PEO subject 3307.891
GSM24662A3243G-PEO subject 4334.990
GSM24663mtDNA "Common"-deletion subject 1419.890
GSM24664mtDNA "Common"-deletion subject 2748.390
GSM24665mtDNA "Common"-deletion subject 3708.690
GSM24666mtDNA "Common"-deletion subject 4958.992