ProfileGDS1065 / 203755_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 23% 16% 26% 29% 22% 29% 36% 43% 26% 17% 12% 40% 38% 18% 28% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 111.123
GSM24653Normal subject 26.316
GSM24654Normal subject 314.726
GSM24655A3243G-MELAS subject 112.429
GSM24656A3243G-MELAS subject 21222
GSM24657A3243G-MELAS subject 322.429
GSM24658A3243G-MELAS subject 420.536
GSM24659A3243G-PEO subject 129.243
GSM24660A3243G-PEO subject 212.926
GSM24661A3243G-PEO subject 35.317
GSM24662A3243G-PEO subject 44.312
GSM24663mtDNA "Common"-deletion subject 129.740
GSM24664mtDNA "Common"-deletion subject 247.138
GSM24665mtDNA "Common"-deletion subject 31118
GSM24666mtDNA "Common"-deletion subject 422.928