ProfileGDS1065 / 48106_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 82% 80% 78% 77% 79% 85% 78% 87% 84% 85% 85% 86% 82% 79% 80% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1207.482
GSM24653Normal subject 2171.580
GSM24654Normal subject 3203.678
GSM24655A3243G-MELAS subject 19877
GSM24656A3243G-MELAS subject 2167.479
GSM24657A3243G-MELAS subject 3399.285
GSM24658A3243G-MELAS subject 4154.578
GSM24659A3243G-PEO subject 1214.887
GSM24660A3243G-PEO subject 2204.184
GSM24661A3243G-PEO subject 3175.385
GSM24662A3243G-PEO subject 4212.285
GSM24663mtDNA "Common"-deletion subject 1290.786
GSM24664mtDNA "Common"-deletion subject 2366.782
GSM24665mtDNA "Common"-deletion subject 3262.379
GSM24666mtDNA "Common"-deletion subject 4316.780