ProfileGDS1065 / 216984_x_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 24% 20% 26% 16% 20% 24% 16% 26% 26% 30% 21% 18% 16% 38% 17% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 111.724
GSM24653Normal subject 28.720
GSM24654Normal subject 314.626
GSM24655A3243G-MELAS subject 15.616
GSM24656A3243G-MELAS subject 29.920
GSM24657A3243G-MELAS subject 316.224
GSM24658A3243G-MELAS subject 45.516
GSM24659A3243G-PEO subject 112.726
GSM24660A3243G-PEO subject 212.926
GSM24661A3243G-PEO subject 311.830
GSM24662A3243G-PEO subject 48.321
GSM24663mtDNA "Common"-deletion subject 17.718
GSM24664mtDNA "Common"-deletion subject 211.716
GSM24665mtDNA "Common"-deletion subject 338.238
GSM24666mtDNA "Common"-deletion subject 49.917