ProfileGDS1065 / 65635_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 89% 87% 85% 88% 87% 83% 85% 89% 88% 89% 87% 89% 85% 84% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1367.989
GSM24653Normal subject 2294.187
GSM24654Normal subject 3323.185
GSM24655A3243G-MELAS subject 119488
GSM24656A3243G-MELAS subject 2300.387
GSM24657A3243G-MELAS subject 3356.583
GSM24658A3243G-MELAS subject 4247.685
GSM24659A3243G-PEO subject 1251.189
GSM24660A3243G-PEO subject 2284.188
GSM24661A3243G-PEO subject 3232.889
GSM24662A3243G-PEO subject 424887
GSM24663mtDNA "Common"-deletion subject 1383.889
GSM24664mtDNA "Common"-deletion subject 2442.585
GSM24665mtDNA "Common"-deletion subject 3365.284
GSM24666mtDNA "Common"-deletion subject 4451.985