ProfileGDS1065 / 212983_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 94% 91% 87% 89% 88% 92% 91% 94% 91% 94% 93% 90% 85% 89% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1765.494
GSM24653Normal subject 2416.491
GSM24654Normal subject 3389.687
GSM24655A3243G-MELAS subject 1227.889
GSM24656A3243G-MELAS subject 2313.388
GSM24657A3243G-MELAS subject 3875.792
GSM24658A3243G-MELAS subject 4441.391
GSM24659A3243G-PEO subject 1501.994
GSM24660A3243G-PEO subject 2402.491
GSM24661A3243G-PEO subject 347994
GSM24662A3243G-PEO subject 4480.393
GSM24663mtDNA "Common"-deletion subject 1452.190
GSM24664mtDNA "Common"-deletion subject 2448.585
GSM24665mtDNA "Common"-deletion subject 3577.689
GSM24666mtDNA "Common"-deletion subject 4544.187