ProfileGDS1065 / 218099_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% 88% 89% 88% 89% 85% 86% 86% 87% 89% 84% 87% 87% 88% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1372.489
GSM24653Normal subject 230388
GSM24654Normal subject 3456.789
GSM24655A3243G-MELAS subject 1201.588
GSM24656A3243G-MELAS subject 2353.189
GSM24657A3243G-MELAS subject 343385
GSM24658A3243G-MELAS subject 4269.186
GSM24659A3243G-PEO subject 1189.286
GSM24660A3243G-PEO subject 2265.487
GSM24661A3243G-PEO subject 3237.989
GSM24662A3243G-PEO subject 4199.684
GSM24663mtDNA "Common"-deletion subject 1304.787
GSM24664mtDNA "Common"-deletion subject 2523.387
GSM24665mtDNA "Common"-deletion subject 3564.288
GSM24666mtDNA "Common"-deletion subject 4649.889