ProfileGDS1065 / 203089_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 69% 65% 70% 74% 58% 77% 75% 59% 60% 72% 67% 64% 78% 77% 68% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1102.269
GSM24653Normal subject 277.865
GSM24654Normal subject 3131.470
GSM24655A3243G-MELAS subject 183.774
GSM24656A3243G-MELAS subject 26558
GSM24657A3243G-MELAS subject 3235.677
GSM24658A3243G-MELAS subject 4127.475
GSM24659A3243G-PEO subject 151.759
GSM24660A3243G-PEO subject 260.260
GSM24661A3243G-PEO subject 379.572
GSM24662A3243G-PEO subject 474.867
GSM24663mtDNA "Common"-deletion subject 181.664
GSM24664mtDNA "Common"-deletion subject 2283.678
GSM24665mtDNA "Common"-deletion subject 3227.677
GSM24666mtDNA "Common"-deletion subject 4153.268