ProfileGDS1065 / 218448_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% 87% 81% 86% 85% 88% 85% 87% 85% 89% 88% 89% 87% 84% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1350.988
GSM24653Normal subject 2276.487
GSM24654Normal subject 3243.481
GSM24655A3243G-MELAS subject 1173.886
GSM24656A3243G-MELAS subject 2248.885
GSM24657A3243G-MELAS subject 3558.588
GSM24658A3243G-MELAS subject 4242.985
GSM24659A3243G-PEO subject 1214.187
GSM24660A3243G-PEO subject 2223.985
GSM24661A3243G-PEO subject 3240.389
GSM24662A3243G-PEO subject 4271.988
GSM24663mtDNA "Common"-deletion subject 1378.989
GSM24664mtDNA "Common"-deletion subject 2533.987
GSM24665mtDNA "Common"-deletion subject 337584
GSM24666mtDNA "Common"-deletion subject 4388.683