ProfileGDS1065 / 200892_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 78% 75% 84% 79% 84% 76% 79% 72% 78% 76% 79% 82% 80% 85% 85% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1161.878
GSM24653Normal subject 2126.575
GSM24654Normal subject 3305.184
GSM24655A3243G-MELAS subject 1105.979
GSM24656A3243G-MELAS subject 2225.984
GSM24657A3243G-MELAS subject 3230.276
GSM24658A3243G-MELAS subject 4161.779
GSM24659A3243G-PEO subject 188.372
GSM24660A3243G-PEO subject 2140.978
GSM24661A3243G-PEO subject 397.376
GSM24662A3243G-PEO subject 4141.579
GSM24663mtDNA "Common"-deletion subject 1210.182
GSM24664mtDNA "Common"-deletion subject 2330.380
GSM24665mtDNA "Common"-deletion subject 3420.185
GSM24666mtDNA "Common"-deletion subject 4447.585