ProfileGDS1065 / 201511_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 83% 82% 75% 77% 82% 81% 85% 81% 84% 81% 80% 81% 73% 82% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 122883
GSM24653Normal subject 219182
GSM24654Normal subject 3167.675
GSM24655A3243G-MELAS subject 194.777
GSM24656A3243G-MELAS subject 2201.182
GSM24657A3243G-MELAS subject 330681
GSM24658A3243G-MELAS subject 4237.685
GSM24659A3243G-PEO subject 1139.981
GSM24660A3243G-PEO subject 221384
GSM24661A3243G-PEO subject 3130.381
GSM24662A3243G-PEO subject 4148.980
GSM24663mtDNA "Common"-deletion subject 1206.681
GSM24664mtDNA "Common"-deletion subject 2217.873
GSM24665mtDNA "Common"-deletion subject 3324.782
GSM24666mtDNA "Common"-deletion subject 4289.179