ProfileGDS1065 / 53968_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 82% 83% 70% 82% 81% 84% 77% 86% 83% 87% 88% 85% 79% 75% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 121582
GSM24653Normal subject 2202.683
GSM24654Normal subject 313470
GSM24655A3243G-MELAS subject 1130.482
GSM24656A3243G-MELAS subject 2189.581
GSM24657A3243G-MELAS subject 3382.584
GSM24658A3243G-MELAS subject 4146.677
GSM24659A3243G-PEO subject 1189.386
GSM24660A3243G-PEO subject 2188.383
GSM24661A3243G-PEO subject 3209.187
GSM24662A3243G-PEO subject 425788
GSM24663mtDNA "Common"-deletion subject 1266.585
GSM24664mtDNA "Common"-deletion subject 2296.979
GSM24665mtDNA "Common"-deletion subject 3202.375
GSM24666mtDNA "Common"-deletion subject 4276.678