ProfileGDS1065 / 212214_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 83% 81% 86% 85% 89% 85% 85% 87% 84% 82% 76% 85% 87% 86% 85% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1221.383
GSM24653Normal subject 218781
GSM24654Normal subject 3369.486
GSM24655A3243G-MELAS subject 1160.885
GSM24656A3243G-MELAS subject 235489
GSM24657A3243G-MELAS subject 341885
GSM24658A3243G-MELAS subject 4249.785
GSM24659A3243G-PEO subject 1204.987
GSM24660A3243G-PEO subject 2206.984
GSM24661A3243G-PEO subject 3136.882
GSM24662A3243G-PEO subject 4119.176
GSM24663mtDNA "Common"-deletion subject 1267.985
GSM24664mtDNA "Common"-deletion subject 253687
GSM24665mtDNA "Common"-deletion subject 3433.786
GSM24666mtDNA "Common"-deletion subject 4471.785