ProfileGDS1065 / 207316_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 27% 32% 14% 18% 33% 27% 45% 22% 27% 33% 34% 33% 33% 36% 36% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 114.627
GSM24653Normal subject 219.532
GSM24654Normal subject 36.314
GSM24655A3243G-MELAS subject 16.518
GSM24656A3243G-MELAS subject 223.133
GSM24657A3243G-MELAS subject 319.327
GSM24658A3243G-MELAS subject 431.745
GSM24659A3243G-PEO subject 110.122
GSM24660A3243G-PEO subject 214.227
GSM24661A3243G-PEO subject 314.333
GSM24662A3243G-PEO subject 419.234
GSM24663mtDNA "Common"-deletion subject 120.633
GSM24664mtDNA "Common"-deletion subject 236.633
GSM24665mtDNA "Common"-deletion subject 335.136
GSM24666mtDNA "Common"-deletion subject 434.536