ProfileGDS1065 / 221699_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 86% 84% 87% 84% 80% 85% 88% 80% 78% 72% 74% 82% 87% 89% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1283.386
GSM24653Normal subject 2224.284
GSM24654Normal subject 3385.187
GSM24655A3243G-MELAS subject 1145.284
GSM24656A3243G-MELAS subject 2180.480
GSM24657A3243G-MELAS subject 3406.485
GSM24658A3243G-MELAS subject 4316.788
GSM24659A3243G-PEO subject 1129.480
GSM24660A3243G-PEO subject 2135.978
GSM24661A3243G-PEO subject 378.472
GSM24662A3243G-PEO subject 4102.774
GSM24663mtDNA "Common"-deletion subject 121882
GSM24664mtDNA "Common"-deletion subject 2529.787
GSM24665mtDNA "Common"-deletion subject 3587.389
GSM24666mtDNA "Common"-deletion subject 4578.588