ProfileGDS1065 / 218068_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 90% 89% 85% 88% 88% 86% 88% 88% 89% 87% 91% 89% 85% 84% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1426.990
GSM24653Normal subject 2350.589
GSM24654Normal subject 3329.385
GSM24655A3243G-MELAS subject 1191.688
GSM24656A3243G-MELAS subject 2322.988
GSM24657A3243G-MELAS subject 3462.186
GSM24658A3243G-MELAS subject 430488
GSM24659A3243G-PEO subject 1232.388
GSM24660A3243G-PEO subject 2310.989
GSM24661A3243G-PEO subject 3199.387
GSM24662A3243G-PEO subject 4349.591
GSM24663mtDNA "Common"-deletion subject 1388.389
GSM24664mtDNA "Common"-deletion subject 2459.785
GSM24665mtDNA "Common"-deletion subject 3377.184
GSM24666mtDNA "Common"-deletion subject 4432.184