ProfileGDS1065 / 211340_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 78% 87% 75% 89% 82% 87% 84% 84% 79% 85% 81% 83% 83% 76% 80% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1167.878
GSM24653Normal subject 2287.787
GSM24654Normal subject 3171.375
GSM24655A3243G-MELAS subject 1226.789
GSM24656A3243G-MELAS subject 2201.382
GSM24657A3243G-MELAS subject 3496.187
GSM24658A3243G-MELAS subject 4225.784
GSM24659A3243G-PEO subject 1165.484
GSM24660A3243G-PEO subject 2150.779
GSM24661A3243G-PEO subject 3173.785
GSM24662A3243G-PEO subject 4160.981
GSM24663mtDNA "Common"-deletion subject 1231.883
GSM24664mtDNA "Common"-deletion subject 2397.583
GSM24665mtDNA "Common"-deletion subject 3222.376
GSM24666mtDNA "Common"-deletion subject 4317.980