ProfileGDS1065 / 212686_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 45% 41% 28% 49% 23% 36% 33% 58% 39% 5% 50% 22% 39% 31% 29% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 136.245
GSM24653Normal subject 22941
GSM24654Normal subject 317.428
GSM24655A3243G-MELAS subject 13149
GSM24656A3243G-MELAS subject 212.623
GSM24657A3243G-MELAS subject 333.436
GSM24658A3243G-MELAS subject 417.833
GSM24659A3243G-PEO subject 149.658
GSM24660A3243G-PEO subject 226.139
GSM24661A3243G-PEO subject 31.95
GSM24662A3243G-PEO subject 436.750
GSM24663mtDNA "Common"-deletion subject 110.222
GSM24664mtDNA "Common"-deletion subject 249.239
GSM24665mtDNA "Common"-deletion subject 327.331
GSM24666mtDNA "Common"-deletion subject 424.529