ProfileGDS1065 / 206550_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 63% 52% 56% 56% 42% 52% 61% 51% 46% 41% 56% 55% 56% 39% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 177.963
GSM24653Normal subject 24752
GSM24654Normal subject 369.156
GSM24655A3243G-MELAS subject 140.356
GSM24656A3243G-MELAS subject 234.742
GSM24657A3243G-MELAS subject 36952
GSM24658A3243G-MELAS subject 46461
GSM24659A3243G-PEO subject 138.651
GSM24660A3243G-PEO subject 234.846
GSM24661A3243G-PEO subject 321.341
GSM24662A3243G-PEO subject 446.956
GSM24663mtDNA "Common"-deletion subject 15555
GSM24664mtDNA "Common"-deletion subject 2101.856
GSM24665mtDNA "Common"-deletion subject 340.339
GSM24666mtDNA "Common"-deletion subject 496.859