ProfileGDS1065 / 219053_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 89% 86% 85% 88% 87% 88% 84% 87% 87% 87% 90% 89% 86% 85% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1380.789
GSM24653Normal subject 2266.186
GSM24654Normal subject 3317.485
GSM24655A3243G-MELAS subject 1202.788
GSM24656A3243G-MELAS subject 2295.587
GSM24657A3243G-MELAS subject 355488
GSM24658A3243G-MELAS subject 4225.484
GSM24659A3243G-PEO subject 1203.687
GSM24660A3243G-PEO subject 2270.287
GSM24661A3243G-PEO subject 3210.387
GSM24662A3243G-PEO subject 4340.890
GSM24663mtDNA "Common"-deletion subject 1400.789
GSM24664mtDNA "Common"-deletion subject 2485.286
GSM24665mtDNA "Common"-deletion subject 3422.785
GSM24666mtDNA "Common"-deletion subject 4399.783