ProfileGDS1065 / 215024_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 24% 34% 42% 45% 35% 30% 4% 47% 25% 41% 29% 39% 27% 26% 37% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 111.724
GSM24653Normal subject 221.334
GSM24654Normal subject 337.442
GSM24655A3243G-MELAS subject 127.245
GSM24656A3243G-MELAS subject 22535
GSM24657A3243G-MELAS subject 324.430
GSM24658A3243G-MELAS subject 41.84
GSM24659A3243G-PEO subject 134.247
GSM24660A3243G-PEO subject 212.325
GSM24661A3243G-PEO subject 321.341
GSM24662A3243G-PEO subject 41429
GSM24663mtDNA "Common"-deletion subject 127.939
GSM24664mtDNA "Common"-deletion subject 227.327
GSM24665mtDNA "Common"-deletion subject 319.426
GSM24666mtDNA "Common"-deletion subject 436.937