ProfileGDS1065 / 211062_s_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 9% 10% 10% 13% 7% 9% 6% 10% 9% 20% 9% 14% 9% 28% 5% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13.99
GSM24653Normal subject 24.210
GSM24654Normal subject 34.610
GSM24655A3243G-MELAS subject 14.513
GSM24656A3243G-MELAS subject 23.97
GSM24657A3243G-MELAS subject 34.99
GSM24658A3243G-MELAS subject 42.36
GSM24659A3243G-PEO subject 14.510
GSM24660A3243G-PEO subject 249
GSM24661A3243G-PEO subject 36.320
GSM24662A3243G-PEO subject 43.29
GSM24663mtDNA "Common"-deletion subject 15.914
GSM24664mtDNA "Common"-deletion subject 26.79
GSM24665mtDNA "Common"-deletion subject 32328
GSM24666mtDNA "Common"-deletion subject 43.45