ProfileGDS1065 / 219451_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% 88% 87% 73% 86% 90% 85% 88% 89% 87% 88% 84% 78% 84% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1346.388
GSM24653Normal subject 2299.688
GSM24654Normal subject 3376.287
GSM24655A3243G-MELAS subject 180.473
GSM24656A3243G-MELAS subject 2271.986
GSM24657A3243G-MELAS subject 3660.190
GSM24658A3243G-MELAS subject 4247.285
GSM24659A3243G-PEO subject 1215.888
GSM24660A3243G-PEO subject 2321.789
GSM24661A3243G-PEO subject 3210.787
GSM24662A3243G-PEO subject 4276.188
GSM24663mtDNA "Common"-deletion subject 1250.784
GSM24664mtDNA "Common"-deletion subject 2287.578
GSM24665mtDNA "Common"-deletion subject 3368.984
GSM24666mtDNA "Common"-deletion subject 4670.389