ProfileGDS1065 / 213149_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 88% 86% 90% 90% 91% 89% 89% 90% 89% 89% 87% 87% 89% 87% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1350.188
GSM24653Normal subject 2269.286
GSM24654Normal subject 355290
GSM24655A3243G-MELAS subject 1237.690
GSM24656A3243G-MELAS subject 2444.991
GSM24657A3243G-MELAS subject 3614.189
GSM24658A3243G-MELAS subject 4339.589
GSM24659A3243G-PEO subject 128590
GSM24660A3243G-PEO subject 2321.289
GSM24661A3243G-PEO subject 3237.389
GSM24662A3243G-PEO subject 4240.887
GSM24663mtDNA "Common"-deletion subject 133087
GSM24664mtDNA "Common"-deletion subject 2619.289
GSM24665mtDNA "Common"-deletion subject 3491.987
GSM24666mtDNA "Common"-deletion subject 4530.287