ProfileGDS1065 / 210585_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 47% 56% 33% 12% 32% 42% 21% 17% 33% 25% 45% 50% 46% 29% 26% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13947
GSM24653Normal subject 253.956
GSM24654Normal subject 323.533
GSM24655A3243G-MELAS subject 14.212
GSM24656A3243G-MELAS subject 221.732
GSM24657A3243G-MELAS subject 345.242
GSM24658A3243G-MELAS subject 48.121
GSM24659A3243G-PEO subject 17.317
GSM24660A3243G-PEO subject 219.233
GSM24661A3243G-PEO subject 38.525
GSM24662A3243G-PEO subject 431.245
GSM24663mtDNA "Common"-deletion subject 144.750
GSM24664mtDNA "Common"-deletion subject 267.246
GSM24665mtDNA "Common"-deletion subject 323.629
GSM24666mtDNA "Common"-deletion subject 419.326