ProfileGDS1065 / 204115_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% 88% 80% 88% 81% 90% 85% 86% 81% 85% 87% 83% 81% 78% 85% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1197.681
GSM24653Normal subject 2303.888
GSM24654Normal subject 3224.280
GSM24655A3243G-MELAS subject 1195.888
GSM24656A3243G-MELAS subject 2183.881
GSM24657A3243G-MELAS subject 3686.290
GSM24658A3243G-MELAS subject 4242.485
GSM24659A3243G-PEO subject 1198.286
GSM24660A3243G-PEO subject 2172.681
GSM24661A3243G-PEO subject 3169.885
GSM24662A3243G-PEO subject 4251.487
GSM24663mtDNA "Common"-deletion subject 123383
GSM24664mtDNA "Common"-deletion subject 2340.481
GSM24665mtDNA "Common"-deletion subject 3243.478
GSM24666mtDNA "Common"-deletion subject 4434.585