ProfileGDS1065 / 212319_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 74% 74% 71% 79% 73% 69% 73% 81% 80% 76% 76% 77% 75% 72% 70% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1130.174
GSM24653Normal subject 2121.274
GSM24654Normal subject 3140.671
GSM24655A3243G-MELAS subject 1108.179
GSM24656A3243G-MELAS subject 2121.673
GSM24657A3243G-MELAS subject 3157.169
GSM24658A3243G-MELAS subject 4111.873
GSM24659A3243G-PEO subject 113481
GSM24660A3243G-PEO subject 2154.680
GSM24661A3243G-PEO subject 397.376
GSM24662A3243G-PEO subject 4116.876
GSM24663mtDNA "Common"-deletion subject 1153.177
GSM24664mtDNA "Common"-deletion subject 2237.475
GSM24665mtDNA "Common"-deletion subject 3169.472
GSM24666mtDNA "Common"-deletion subject 4177.470