ProfileGDS1065 / 219392_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 88% 80% 82% 77% 83% 86% 84% 90% 89% 90% 91% 86% 85% 80% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1355.888
GSM24653Normal subject 2166.380
GSM24654Normal subject 3270.582
GSM24655A3243G-MELAS subject 19477
GSM24656A3243G-MELAS subject 2218.783
GSM24657A3243G-MELAS subject 3461.686
GSM24658A3243G-MELAS subject 421584
GSM24659A3243G-PEO subject 1274.490
GSM24660A3243G-PEO subject 2303.189
GSM24661A3243G-PEO subject 3270.490
GSM24662A3243G-PEO subject 4352.891
GSM24663mtDNA "Common"-deletion subject 1282.386
GSM24664mtDNA "Common"-deletion subject 2461.885
GSM24665mtDNA "Common"-deletion subject 3283.180
GSM24666mtDNA "Common"-deletion subject 4540.787