ProfileGDS1065 / 219079_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 56% 46% 67% 59% 59% 36% 52% 39% 51% 54% 45% 51% 54% 64% 60% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 156.956
GSM24653Normal subject 236.946
GSM24654Normal subject 3113.167
GSM24655A3243G-MELAS subject 144.859
GSM24656A3243G-MELAS subject 267.759
GSM24657A3243G-MELAS subject 333.936
GSM24658A3243G-MELAS subject 443.152
GSM24659A3243G-PEO subject 123.939
GSM24660A3243G-PEO subject 242.951
GSM24661A3243G-PEO subject 337.254
GSM24662A3243G-PEO subject 431.445
GSM24663mtDNA "Common"-deletion subject 14751
GSM24664mtDNA "Common"-deletion subject 293.254
GSM24665mtDNA "Common"-deletion subject 311964
GSM24666mtDNA "Common"-deletion subject 4102.260