ProfileGDS1065 / 221887_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 34% 24% 25% 13% 25% 39% 20% 23% 32% 22% 25% 21% 20% 25% 25% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 121.234
GSM24653Normal subject 211.624
GSM24654Normal subject 313.725
GSM24655A3243G-MELAS subject 14.513
GSM24656A3243G-MELAS subject 214.325
GSM24657A3243G-MELAS subject 338.739
GSM24658A3243G-MELAS subject 47.320
GSM24659A3243G-PEO subject 110.623
GSM24660A3243G-PEO subject 217.932
GSM24661A3243G-PEO subject 37.322
GSM24662A3243G-PEO subject 410.825
GSM24663mtDNA "Common"-deletion subject 19.621
GSM24664mtDNA "Common"-deletion subject 216.120
GSM24665mtDNA "Common"-deletion subject 317.925
GSM24666mtDNA "Common"-deletion subject 418.325