ProfileGDS1065 / 206912_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 20% 5% 4% 28% 24% 21% 2% 1% 19% 4% 2% 11% 2% 31% 7% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 19.120
GSM24653Normal subject 22.55
GSM24654Normal subject 32.64
GSM24655A3243G-MELAS subject 111.928
GSM24656A3243G-MELAS subject 213.224
GSM24657A3243G-MELAS subject 312.721
GSM24658A3243G-MELAS subject 41.32
GSM24659A3243G-PEO subject 11.21
GSM24660A3243G-PEO subject 28.419
GSM24661A3243G-PEO subject 31.74
GSM24662A3243G-PEO subject 41.42
GSM24663mtDNA "Common"-deletion subject 14.611
GSM24664mtDNA "Common"-deletion subject 22.52
GSM24665mtDNA "Common"-deletion subject 327.831
GSM24666mtDNA "Common"-deletion subject 43.97