ProfileGDS1065 / 213671_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 80% 81% 80% 82% 81% 81% 83% 86% 84% 83% 85% 89% 86% 81% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1182.680
GSM24653Normal subject 2177.781
GSM24654Normal subject 3226.380
GSM24655A3243G-MELAS subject 112982
GSM24656A3243G-MELAS subject 2184.681
GSM24657A3243G-MELAS subject 3304.481
GSM24658A3243G-MELAS subject 4201.583
GSM24659A3243G-PEO subject 1196.186
GSM24660A3243G-PEO subject 2202.684
GSM24661A3243G-PEO subject 3149.183
GSM24662A3243G-PEO subject 4208.785
GSM24663mtDNA "Common"-deletion subject 1396.589
GSM24664mtDNA "Common"-deletion subject 2491.186
GSM24665mtDNA "Common"-deletion subject 329281
GSM24666mtDNA "Common"-deletion subject 4287.979