ProfileGDS1065 / 208259_x_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% 46% 41% 48% 45% 34% 9% 55% 44% 38% 41% 45% 51% 31% 38% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 126.438
GSM24653Normal subject 236.246
GSM24654Normal subject 335.541
GSM24655A3243G-MELAS subject 130.348
GSM24656A3243G-MELAS subject 239.745
GSM24657A3243G-MELAS subject 331.134
GSM24658A3243G-MELAS subject 43.19
GSM24659A3243G-PEO subject 145.355
GSM24660A3243G-PEO subject 233.144
GSM24661A3243G-PEO subject 318.938
GSM24662A3243G-PEO subject 425.641
GSM24663mtDNA "Common"-deletion subject 136.545
GSM24664mtDNA "Common"-deletion subject 281.151
GSM24665mtDNA "Common"-deletion subject 327.431
GSM24666mtDNA "Common"-deletion subject 438.138