ProfileGDS1065 / 221504_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 88% 88% 85% 85% 87% 86% 87% 81% 85% 82% 84% 86% 86% 88% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1343.488
GSM24653Normal subject 2323.888
GSM24654Normal subject 333185
GSM24655A3243G-MELAS subject 115385
GSM24656A3243G-MELAS subject 2283.187
GSM24657A3243G-MELAS subject 3447.586
GSM24658A3243G-MELAS subject 4283.887
GSM24659A3243G-PEO subject 1136.781
GSM24660A3243G-PEO subject 2219.585
GSM24661A3243G-PEO subject 3138.782
GSM24662A3243G-PEO subject 4193.184
GSM24663mtDNA "Common"-deletion subject 1299.786
GSM24664mtDNA "Common"-deletion subject 2500.886
GSM24665mtDNA "Common"-deletion subject 3555.688
GSM24666mtDNA "Common"-deletion subject 4576.988