ProfileGDS1065 / 216862_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 90% 84% 86% 91% 86% 89% 85% 89% 88% 88% 89% 88% 87% 85% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1423.890
GSM24653Normal subject 2229.184
GSM24654Normal subject 3365.186
GSM24655A3243G-MELAS subject 1267.891
GSM24656A3243G-MELAS subject 2264.286
GSM24657A3243G-MELAS subject 3600.989
GSM24658A3243G-MELAS subject 4244.985
GSM24659A3243G-PEO subject 1244.789
GSM24660A3243G-PEO subject 2285.588
GSM24661A3243G-PEO subject 3211.988
GSM24662A3243G-PEO subject 4297.689
GSM24663mtDNA "Common"-deletion subject 1340.288
GSM24664mtDNA "Common"-deletion subject 2534.287
GSM24665mtDNA "Common"-deletion subject 3401.685
GSM24666mtDNA "Common"-deletion subject 4295.579