ProfileGDS1065 / 204308_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% 76% 74% 77% 73% 77% 77% 75% 75% 71% 81% 80% 74% 72% 74% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1166.878
GSM24653Normal subject 2133.376
GSM24654Normal subject 3161.474
GSM24655A3243G-MELAS subject 193.677
GSM24656A3243G-MELAS subject 2122.673
GSM24657A3243G-MELAS subject 3239.177
GSM24658A3243G-MELAS subject 4142.477
GSM24659A3243G-PEO subject 1100.675
GSM24660A3243G-PEO subject 2115.775
GSM24661A3243G-PEO subject 374.671
GSM24662A3243G-PEO subject 4161.481
GSM24663mtDNA "Common"-deletion subject 1191.480
GSM24664mtDNA "Common"-deletion subject 2222.174
GSM24665mtDNA "Common"-deletion subject 3171.872
GSM24666mtDNA "Common"-deletion subject 4212.774