ProfileGDS1065 / 215504_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 76% 70% 79% 77% 71% 73% 59% 86% 82% 80% 80% 82% 79% 80% 73% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1147.976
GSM24653Normal subject 29770
GSM24654Normal subject 3219.679
GSM24655A3243G-MELAS subject 196.177
GSM24656A3243G-MELAS subject 2111.471
GSM24657A3243G-MELAS subject 3188.773
GSM24658A3243G-MELAS subject 45959
GSM24659A3243G-PEO subject 1196.286
GSM24660A3243G-PEO subject 2174.882
GSM24661A3243G-PEO subject 3125.180
GSM24662A3243G-PEO subject 4145.780
GSM24663mtDNA "Common"-deletion subject 1220.582
GSM24664mtDNA "Common"-deletion subject 2293.279
GSM24665mtDNA "Common"-deletion subject 327680
GSM24666mtDNA "Common"-deletion subject 4202.173