ProfileGDS1065 / 211501_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 85% 83% 83% 80% 82% 85% 89% 79% 84% 84% 87% 85% 86% 86% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1266.185
GSM24653Normal subject 2214.883
GSM24654Normal subject 3288.383
GSM24655A3243G-MELAS subject 1115.480
GSM24656A3243G-MELAS subject 2205.782
GSM24657A3243G-MELAS subject 3416.285
GSM24658A3243G-MELAS subject 4327.889
GSM24659A3243G-PEO subject 1121.279
GSM24660A3243G-PEO subject 2207.284
GSM24661A3243G-PEO subject 3157.384
GSM24662A3243G-PEO subject 4239.787
GSM24663mtDNA "Common"-deletion subject 1273.585
GSM24664mtDNA "Common"-deletion subject 2507.386
GSM24665mtDNA "Common"-deletion subject 346686
GSM24666mtDNA "Common"-deletion subject 4426.584