ProfileGDS1065 / 217549_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 31% 24% 27% 27% 28% 13% 24% 31% 30% 29% 22% 15% 24% 21% 36% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 118.131
GSM24653Normal subject 211.824
GSM24654Normal subject 316.127
GSM24655A3243G-MELAS subject 111.427
GSM24656A3243G-MELAS subject 216.828
GSM24657A3243G-MELAS subject 37.213
GSM24658A3243G-MELAS subject 49.724
GSM24659A3243G-PEO subject 116.831
GSM24660A3243G-PEO subject 216.330
GSM24661A3243G-PEO subject 311.129
GSM24662A3243G-PEO subject 48.822
GSM24663mtDNA "Common"-deletion subject 16.515
GSM24664mtDNA "Common"-deletion subject 220.924
GSM24665mtDNA "Common"-deletion subject 313.621
GSM24666mtDNA "Common"-deletion subject 435.936