ProfileGDS1065 / 221471_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 86% 87% 90% 90% 89% 88% 85% 79% 85% 82% 83% 88% 90% 87% 88% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1298.786
GSM24653Normal subject 2293.787
GSM24654Normal subject 3510.390
GSM24655A3243G-MELAS subject 123490
GSM24656A3243G-MELAS subject 2359.689
GSM24657A3243G-MELAS subject 3550.388
GSM24658A3243G-MELAS subject 4237.285
GSM24659A3243G-PEO subject 112079
GSM24660A3243G-PEO subject 2222.385
GSM24661A3243G-PEO subject 3142.182
GSM24662A3243G-PEO subject 418483
GSM24663mtDNA "Common"-deletion subject 1365.488
GSM24664mtDNA "Common"-deletion subject 2707.490
GSM24665mtDNA "Common"-deletion subject 3512.187
GSM24666mtDNA "Common"-deletion subject 4604.188