ProfileGDS1065 / 204691_x_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 76% 75% 71% 83% 80% 69% 80% 85% 84% 83% 83% 81% 78% 77% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1142.376
GSM24653Normal subject 2124.575
GSM24654Normal subject 3137.171
GSM24655A3243G-MELAS subject 1139.583
GSM24656A3243G-MELAS subject 217980
GSM24657A3243G-MELAS subject 315769
GSM24658A3243G-MELAS subject 4167.680
GSM24659A3243G-PEO subject 1182.485
GSM24660A3243G-PEO subject 2210.284
GSM24661A3243G-PEO subject 3149.183
GSM24662A3243G-PEO subject 418483
GSM24663mtDNA "Common"-deletion subject 1205.381
GSM24664mtDNA "Common"-deletion subject 227678
GSM24665mtDNA "Common"-deletion subject 3228.777
GSM24666mtDNA "Common"-deletion subject 4205.773