ProfileGDS1065 / 204804_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 63% 75% 62% 76% 70% 74% 72% 79% 75% 73% 72% 71% 70% 65% 67% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 175.563
GSM24653Normal subject 2128.375
GSM24654Normal subject 39062
GSM24655A3243G-MELAS subject 189.276
GSM24656A3243G-MELAS subject 2103.270
GSM24657A3243G-MELAS subject 3197.474
GSM24658A3243G-MELAS subject 4108.472
GSM24659A3243G-PEO subject 1120.779
GSM24660A3243G-PEO subject 2114.975
GSM24661A3243G-PEO subject 38473
GSM24662A3243G-PEO subject 494.672
GSM24663mtDNA "Common"-deletion subject 1111.771
GSM24664mtDNA "Common"-deletion subject 2186.570
GSM24665mtDNA "Common"-deletion subject 3125.265
GSM24666mtDNA "Common"-deletion subject 4148.367