ProfileGDS1065 / 218056_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% 82% 75% 83% 84% 85% 71% 81% 81% 76% 81% 86% 84% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126885
GSM24653Normal subject 2204.883
GSM24654Normal subject 3265.882
GSM24655A3243G-MELAS subject 187.775
GSM24656A3243G-MELAS subject 2223.483
GSM24657A3243G-MELAS subject 3387.384
GSM24658A3243G-MELAS subject 4246.285
GSM24659A3243G-PEO subject 184.271
GSM24660A3243G-PEO subject 2164.581
GSM24661A3243G-PEO subject 3133.881
GSM24662A3243G-PEO subject 4118.976
GSM24663mtDNA "Common"-deletion subject 1207.481
GSM24664mtDNA "Common"-deletion subject 2488.886
GSM24665mtDNA "Common"-deletion subject 339384
GSM24666mtDNA "Common"-deletion subject 4369.982