ProfileGDS1065 / 216457_s_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% 85% 76% 79% 86% 84% 76% 83% 87% 86% 85% 79% 71% 85% 82% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1201.481
GSM24653Normal subject 2249.485
GSM24654Normal subject 3173.876
GSM24655A3243G-MELAS subject 1107.579
GSM24656A3243G-MELAS subject 2268.386
GSM24657A3243G-MELAS subject 338984
GSM24658A3243G-MELAS subject 413776
GSM24659A3243G-PEO subject 1156.683
GSM24660A3243G-PEO subject 2257.487
GSM24661A3243G-PEO subject 3189.486
GSM24662A3243G-PEO subject 4214.185
GSM24663mtDNA "Common"-deletion subject 1183.579
GSM24664mtDNA "Common"-deletion subject 2192.471
GSM24665mtDNA "Common"-deletion subject 3407.985
GSM24666mtDNA "Common"-deletion subject 4352.182