ProfileGDS1065 / 218581_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% 85% 80% 85% 83% 77% 83% 86% 83% 83% 84% 87% 84% 82% 80% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1216.982
GSM24653Normal subject 2241.685
GSM24654Normal subject 3223.380
GSM24655A3243G-MELAS subject 1157.485
GSM24656A3243G-MELAS subject 2220.683
GSM24657A3243G-MELAS subject 3241.977
GSM24658A3243G-MELAS subject 4203.483
GSM24659A3243G-PEO subject 1193.786
GSM24660A3243G-PEO subject 2196.483
GSM24661A3243G-PEO subject 3149.983
GSM24662A3243G-PEO subject 4187.284
GSM24663mtDNA "Common"-deletion subject 1329.587
GSM24664mtDNA "Common"-deletion subject 2403.884
GSM24665mtDNA "Common"-deletion subject 3324.482
GSM24666mtDNA "Common"-deletion subject 4312.380