ProfileGDS1065 / 33768_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 74% 81% 76% 81% 81% 71% 74% 82% 79% 83% 81% 78% 79% 79% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1129.774
GSM24653Normal subject 2178.881
GSM24654Normal subject 3174.676
GSM24655A3243G-MELAS subject 1118.581
GSM24656A3243G-MELAS subject 219581
GSM24657A3243G-MELAS subject 3171.471
GSM24658A3243G-MELAS subject 4121.174
GSM24659A3243G-PEO subject 1144.482
GSM24660A3243G-PEO subject 2150.279
GSM24661A3243G-PEO subject 3150.883
GSM24662A3243G-PEO subject 4152.881
GSM24663mtDNA "Common"-deletion subject 1165.578
GSM24664mtDNA "Common"-deletion subject 2310.279
GSM24665mtDNA "Common"-deletion subject 3267.279
GSM24666mtDNA "Common"-deletion subject 4171.270