ProfileGDS1065 / 218259_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 93% 91% 88% 89% 91% 91% 91% 89% 91% 91% 90% 90% 89% 92% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1610.193
GSM24653Normal subject 2417.391
GSM24654Normal subject 341688
GSM24655A3243G-MELAS subject 1213.889
GSM24656A3243G-MELAS subject 2426.691
GSM24657A3243G-MELAS subject 3776.791
GSM24658A3243G-MELAS subject 4418.291
GSM24659A3243G-PEO subject 1251.589
GSM24660A3243G-PEO subject 2385.391
GSM24661A3243G-PEO subject 3305.191
GSM24662A3243G-PEO subject 431790
GSM24663mtDNA "Common"-deletion subject 1431.290
GSM24664mtDNA "Common"-deletion subject 2644.189
GSM24665mtDNA "Common"-deletion subject 3873.292
GSM24666mtDNA "Common"-deletion subject 4896.191