ProfileGDS1065 / 220368_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 37% 30% 52% 29% 45% 24% 30% 34% 36% 28% 11% 37% 50% 42% 34% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 12537
GSM24653Normal subject 216.730
GSM24654Normal subject 356.852
GSM24655A3243G-MELAS subject 112.729
GSM24656A3243G-MELAS subject 238.645
GSM24657A3243G-MELAS subject 316.224
GSM24658A3243G-MELAS subject 41530
GSM24659A3243G-PEO subject 119.234
GSM24660A3243G-PEO subject 222.436
GSM24661A3243G-PEO subject 310.628
GSM24662A3243G-PEO subject 43.911
GSM24663mtDNA "Common"-deletion subject 125.537
GSM24664mtDNA "Common"-deletion subject 277.850
GSM24665mtDNA "Common"-deletion subject 347.142
GSM24666mtDNA "Common"-deletion subject 430.834