ProfileGDS1065 / 214767_s_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 84% 89% 93% 92% 91% 83% 91% 86% 90% 82% 89% 85% 86% 89% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1237.384
GSM24653Normal subject 2357.289
GSM24654Normal subject 3827.493
GSM24655A3243G-MELAS subject 133092
GSM24656A3243G-MELAS subject 2475.891
GSM24657A3243G-MELAS subject 3348.183
GSM24658A3243G-MELAS subject 4420.691
GSM24659A3243G-PEO subject 1186.886
GSM24660A3243G-PEO subject 2362.790
GSM24661A3243G-PEO subject 3142.382
GSM24662A3243G-PEO subject 4302.689
GSM24663mtDNA "Common"-deletion subject 1269.685
GSM24664mtDNA "Common"-deletion subject 2505.686
GSM24665mtDNA "Common"-deletion subject 3582.289
GSM24666mtDNA "Common"-deletion subject 4458.285