ProfileGDS1065 / 218790_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 18% 24% 22% 53% 24% 40% 16% 29% 33% 19% 27% 33% 32% 23% 17% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.718
GSM24653Normal subject 211.424
GSM24654Normal subject 311.722
GSM24655A3243G-MELAS subject 135.653
GSM24656A3243G-MELAS subject 213.224
GSM24657A3243G-MELAS subject 340.440
GSM24658A3243G-MELAS subject 45.616
GSM24659A3243G-PEO subject 114.629
GSM24660A3243G-PEO subject 219.233
GSM24661A3243G-PEO subject 36.219
GSM24662A3243G-PEO subject 412.727
GSM24663mtDNA "Common"-deletion subject 119.633
GSM24664mtDNA "Common"-deletion subject 234.632
GSM24665mtDNA "Common"-deletion subject 315.823
GSM24666mtDNA "Common"-deletion subject 49.617