ProfileGDS1065 / 219454_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 37% 32% 43% 44% 41% 15% 29% 35% 36% 36% 28% 34% 33% 38% 22% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 125.537
GSM24653Normal subject 21932
GSM24654Normal subject 338.543
GSM24655A3243G-MELAS subject 125.544
GSM24656A3243G-MELAS subject 233.441
GSM24657A3243G-MELAS subject 38.415
GSM24658A3243G-MELAS subject 413.629
GSM24659A3243G-PEO subject 120.235
GSM24660A3243G-PEO subject 222.736
GSM24661A3243G-PEO subject 316.636
GSM24662A3243G-PEO subject 413.528
GSM24663mtDNA "Common"-deletion subject 121.434
GSM24664mtDNA "Common"-deletion subject 236.833
GSM24665mtDNA "Common"-deletion subject 338.138
GSM24666mtDNA "Common"-deletion subject 414.222