ProfileGDS1065 / 219005_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 26% 26% 29% 29% 26% 23% 18% 30% 30% 28% 25% 29% 25% 15% 14% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 11426
GSM24653Normal subject 213.226
GSM24654Normal subject 31829
GSM24655A3243G-MELAS subject 112.529
GSM24656A3243G-MELAS subject 215.626
GSM24657A3243G-MELAS subject 314.723
GSM24658A3243G-MELAS subject 46.618
GSM24659A3243G-PEO subject 115.830
GSM24660A3243G-PEO subject 216.230
GSM24661A3243G-PEO subject 310.228
GSM24662A3243G-PEO subject 410.925
GSM24663mtDNA "Common"-deletion subject 11629
GSM24664mtDNA "Common"-deletion subject 222.325
GSM24665mtDNA "Common"-deletion subject 38.915
GSM24666mtDNA "Common"-deletion subject 47.914