ProfileGDS1065 / 218784_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 24% 21% 26% 22% 15% 23% 33% 26% 24% 17% 17% 26% 21% 26% 31% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 111.824
GSM24653Normal subject 29.421
GSM24654Normal subject 314.926
GSM24655A3243G-MELAS subject 18.122
GSM24656A3243G-MELAS subject 27.215
GSM24657A3243G-MELAS subject 314.723
GSM24658A3243G-MELAS subject 417.833
GSM24659A3243G-PEO subject 112.626
GSM24660A3243G-PEO subject 211.724
GSM24661A3243G-PEO subject 35.317
GSM24662A3243G-PEO subject 46.217
GSM24663mtDNA "Common"-deletion subject 113.226
GSM24664mtDNA "Common"-deletion subject 217.221
GSM24665mtDNA "Common"-deletion subject 319.126
GSM24666mtDNA "Common"-deletion subject 427.431