ProfileGDS1065 / 206869_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 15% 14% 12% 13% 10% 21% 21% 12% 9% 14% 13% 13% 12% 12% 18% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 16.315
GSM24653Normal subject 25.614
GSM24654Normal subject 35.612
GSM24655A3243G-MELAS subject 14.613
GSM24656A3243G-MELAS subject 24.810
GSM24657A3243G-MELAS subject 312.521
GSM24658A3243G-MELAS subject 48.421
GSM24659A3243G-PEO subject 1512
GSM24660A3243G-PEO subject 23.99
GSM24661A3243G-PEO subject 34.314
GSM24662A3243G-PEO subject 44.713
GSM24663mtDNA "Common"-deletion subject 15.513
GSM24664mtDNA "Common"-deletion subject 28.812
GSM24665mtDNA "Common"-deletion subject 37.212
GSM24666mtDNA "Common"-deletion subject 410.418