ProfileGDS1065 / 203149_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 71% 72% 70% 75% 79% 76% 71% 83% 78% 79% 80% 77% 71% 72% 72% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1108.671
GSM24653Normal subject 2110.772
GSM24654Normal subject 3131.670
GSM24655A3243G-MELAS subject 185.575
GSM24656A3243G-MELAS subject 2163.379
GSM24657A3243G-MELAS subject 323076
GSM24658A3243G-MELAS subject 4103.671
GSM24659A3243G-PEO subject 1157.883
GSM24660A3243G-PEO subject 2137.778
GSM24661A3243G-PEO subject 3114.779
GSM24662A3243G-PEO subject 4145.980
GSM24663mtDNA "Common"-deletion subject 1160.577
GSM24664mtDNA "Common"-deletion subject 2196.271
GSM24665mtDNA "Common"-deletion subject 3173.172
GSM24666mtDNA "Common"-deletion subject 4192.872