ProfileGDS1065 / 206896_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% 39% 48% 38% 50% 59% 51% 51% 46% 56% 67% 54% 52% 46% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 175.563
GSM24653Normal subject 226.639
GSM24654Normal subject 348.448
GSM24655A3243G-MELAS subject 12038
GSM24656A3243G-MELAS subject 247.650
GSM24657A3243G-MELAS subject 397.159
GSM24658A3243G-MELAS subject 44151
GSM24659A3243G-PEO subject 138.751
GSM24660A3243G-PEO subject 235.446
GSM24661A3243G-PEO subject 339.756
GSM24662A3243G-PEO subject 474.867
GSM24663mtDNA "Common"-deletion subject 154.154
GSM24664mtDNA "Common"-deletion subject 284.252
GSM24665mtDNA "Common"-deletion subject 354.846
GSM24666mtDNA "Common"-deletion subject 454.345