ProfileGDS1065 / 212183_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 81% 80% 55% 91% 82% 89% 75% 85% 88% 81% 87% 85% 85% 83% 89% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1195.781
GSM24653Normal subject 2167.980
GSM24654Normal subject 36655
GSM24655A3243G-MELAS subject 127491
GSM24656A3243G-MELAS subject 2199.982
GSM24657A3243G-MELAS subject 3573.289
GSM24658A3243G-MELAS subject 4127.375
GSM24659A3243G-PEO subject 1172.985
GSM24660A3243G-PEO subject 2299.188
GSM24661A3243G-PEO subject 3129.281
GSM24662A3243G-PEO subject 423487
GSM24663mtDNA "Common"-deletion subject 1265.485
GSM24664mtDNA "Common"-deletion subject 2438.385
GSM24665mtDNA "Common"-deletion subject 3356.583
GSM24666mtDNA "Common"-deletion subject 4661.489