ProfileGDS1065 / 207612_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 8% 6% 3% 10% 3% 7% 10% 4% 6% 6% 7% 5% 6% 7% 18% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13.68
GSM24653Normal subject 22.86
GSM24654Normal subject 32.13
GSM24655A3243G-MELAS subject 13.710
GSM24656A3243G-MELAS subject 22.23
GSM24657A3243G-MELAS subject 34.27
GSM24658A3243G-MELAS subject 43.210
GSM24659A3243G-PEO subject 12.44
GSM24660A3243G-PEO subject 22.86
GSM24661A3243G-PEO subject 32.26
GSM24662A3243G-PEO subject 42.77
GSM24663mtDNA "Common"-deletion subject 12.75
GSM24664mtDNA "Common"-deletion subject 24.96
GSM24665mtDNA "Common"-deletion subject 34.37
GSM24666mtDNA "Common"-deletion subject 410.518