ProfileGDS1065 / 219631_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 40% 24% 44% 38% 34% 30% 44% 12% 30% 28% 23% 32% 33% 41% 41% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 129.840
GSM24653Normal subject 211.424
GSM24654Normal subject 339.944
GSM24655A3243G-MELAS subject 119.938
GSM24656A3243G-MELAS subject 224.334
GSM24657A3243G-MELAS subject 323.930
GSM24658A3243G-MELAS subject 430.644
GSM24659A3243G-PEO subject 15.212
GSM24660A3243G-PEO subject 216.830
GSM24661A3243G-PEO subject 310.628
GSM24662A3243G-PEO subject 49.323
GSM24663mtDNA "Common"-deletion subject 118.732
GSM24664mtDNA "Common"-deletion subject 238.133
GSM24665mtDNA "Common"-deletion subject 344.941
GSM24666mtDNA "Common"-deletion subject 443.841