ProfileGDS1065 / 219030_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 89% 89% 93% 87% 89% 88% 88% 82% 85% 85% 80% 88% 91% 91% 90% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1370.989
GSM24653Normal subject 2356.389
GSM24654Normal subject 3780.293
GSM24655A3243G-MELAS subject 1187.687
GSM24656A3243G-MELAS subject 2362.889
GSM24657A3243G-MELAS subject 3561.488
GSM24658A3243G-MELAS subject 4303.388
GSM24659A3243G-PEO subject 1143.482
GSM24660A3243G-PEO subject 2218.585
GSM24661A3243G-PEO subject 3174.785
GSM24662A3243G-PEO subject 4143.980
GSM24663mtDNA "Common"-deletion subject 135088
GSM24664mtDNA "Common"-deletion subject 2761.591
GSM24665mtDNA "Common"-deletion subject 3718.291
GSM24666mtDNA "Common"-deletion subject 4777.890