ProfileGDS1065 / 202618_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 79% 73% 72% 77% 76% 71% 64% 79% 74% 79% 74% 78% 76% 70% 66% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1175.379
GSM24653Normal subject 2111.473
GSM24654Normal subject 3143.272
GSM24655A3243G-MELAS subject 195.777
GSM24656A3243G-MELAS subject 2139.576
GSM24657A3243G-MELAS subject 3171.371
GSM24658A3243G-MELAS subject 473.664
GSM24659A3243G-PEO subject 1123.479
GSM24660A3243G-PEO subject 2111.474
GSM24661A3243G-PEO subject 3116.779
GSM24662A3243G-PEO subject 4107.374
GSM24663mtDNA "Common"-deletion subject 117278
GSM24664mtDNA "Common"-deletion subject 2254.476
GSM24665mtDNA "Common"-deletion subject 3156.970
GSM24666mtDNA "Common"-deletion subject 4141.266