ProfileGDS1065 / 221585_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 10% 8% 20% 8% 12% 16% 8% 17% 13% 13% 17% 8% 8% 7% 14% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 14.310
GSM24653Normal subject 23.48
GSM24654Normal subject 39.920
GSM24655A3243G-MELAS subject 13.18
GSM24656A3243G-MELAS subject 25.812
GSM24657A3243G-MELAS subject 38.616
GSM24658A3243G-MELAS subject 42.98
GSM24659A3243G-PEO subject 17.117
GSM24660A3243G-PEO subject 25.313
GSM24661A3243G-PEO subject 34.113
GSM24662A3243G-PEO subject 46.317
GSM24663mtDNA "Common"-deletion subject 13.68
GSM24664mtDNA "Common"-deletion subject 26.48
GSM24665mtDNA "Common"-deletion subject 34.47
GSM24666mtDNA "Common"-deletion subject 47.914