ProfileGDS1065 / 208455_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 38% 18% 8% 25% 30% 33% 34% 43% 35% 13% 37% 38% 28% 25% 29% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 126.738
GSM24653Normal subject 27.618
GSM24654Normal subject 33.88
GSM24655A3243G-MELAS subject 11025
GSM24656A3243G-MELAS subject 219.730
GSM24657A3243G-MELAS subject 329.633
GSM24658A3243G-MELAS subject 418.734
GSM24659A3243G-PEO subject 128.643
GSM24660A3243G-PEO subject 221.535
GSM24661A3243G-PEO subject 34.113
GSM24662A3243G-PEO subject 421.537
GSM24663mtDNA "Common"-deletion subject 125.938
GSM24664mtDNA "Common"-deletion subject 228.828
GSM24665mtDNA "Common"-deletion subject 317.925
GSM24666mtDNA "Common"-deletion subject 423.929