ProfileGDS1065 / 215026_x_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 24% 57% 45% 58% 50% 60% 57% 57% 60% 48% 67% 43% 48% 25% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.124
GSM24653Normal subject 255.857
GSM24654Normal subject 341.745
GSM24655A3243G-MELAS subject 142.858
GSM24656A3243G-MELAS subject 24850
GSM24657A3243G-MELAS subject 3101.260
GSM24658A3243G-MELAS subject 451.757
GSM24659A3243G-PEO subject 148.357
GSM24660A3243G-PEO subject 261.660
GSM24661A3243G-PEO subject 329.648
GSM24662A3243G-PEO subject 475.867
GSM24663mtDNA "Common"-deletion subject 134.143
GSM24664mtDNA "Common"-deletion subject 272.648
GSM24665mtDNA "Common"-deletion subject 31825
GSM24666mtDNA "Common"-deletion subject 430.333