ProfileGDS1065 / 201518_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 87% 89% 89% 89% 89% 89% 88% 85% 87% 87% 83% 87% 89% 90% 90% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1310.187
GSM24653Normal subject 2327.789
GSM24654Normal subject 3484.189
GSM24655A3243G-MELAS subject 1217.689
GSM24656A3243G-MELAS subject 2359.389
GSM24657A3243G-MELAS subject 3586.889
GSM24658A3243G-MELAS subject 4309.888
GSM24659A3243G-PEO subject 1173.685
GSM24660A3243G-PEO subject 2269.787
GSM24661A3243G-PEO subject 3194.787
GSM24662A3243G-PEO subject 418383
GSM24663mtDNA "Common"-deletion subject 1320.287
GSM24664mtDNA "Common"-deletion subject 2665.989
GSM24665mtDNA "Common"-deletion subject 3640.290
GSM24666mtDNA "Common"-deletion subject 4755.390