ProfileGDS1065 / 213604_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% 91% 91% 91% 91% 91% 91% 92% 91% 92% 89% 93% 91% 91% 91% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1464.291
GSM24653Normal subject 242191
GSM24654Normal subject 3600.891
GSM24655A3243G-MELAS subject 125991
GSM24656A3243G-MELAS subject 2461.691
GSM24657A3243G-MELAS subject 3777.991
GSM24658A3243G-MELAS subject 4436.191
GSM24659A3243G-PEO subject 1340.392
GSM24660A3243G-PEO subject 2386.891
GSM24661A3243G-PEO subject 3347.592
GSM24662A3243G-PEO subject 4306.389
GSM24663mtDNA "Common"-deletion subject 1628.493
GSM24664mtDNA "Common"-deletion subject 2827.191
GSM24665mtDNA "Common"-deletion subject 3802.191
GSM24666mtDNA "Common"-deletion subject 4834.491