ProfileGDS1065 / 208181_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 21% 28% 18% 23% 21% 18% 17% 22% 4% 12% 24% 18% 20% 19% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.621
GSM24653Normal subject 214.628
GSM24654Normal subject 38.518
GSM24655A3243G-MELAS subject 18.823
GSM24656A3243G-MELAS subject 210.521
GSM24657A3243G-MELAS subject 310.618
GSM24658A3243G-MELAS subject 45.817
GSM24659A3243G-PEO subject 110.122
GSM24660A3243G-PEO subject 22.24
GSM24661A3243G-PEO subject 33.812
GSM24662A3243G-PEO subject 410.124
GSM24663mtDNA "Common"-deletion subject 17.518
GSM24664mtDNA "Common"-deletion subject 216.520
GSM24665mtDNA "Common"-deletion subject 311.619
GSM24666mtDNA "Common"-deletion subject 45.410