ProfileGDS1065 / 209360_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 28% 20% 26% 23% 19% 34% 26% 28% 24% 31% 27% 32% 30% 23% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.428
GSM24653Normal subject 28.620
GSM24654Normal subject 314.926
GSM24655A3243G-MELAS subject 18.723
GSM24656A3243G-MELAS subject 29.519
GSM24657A3243G-MELAS subject 330.734
GSM24658A3243G-MELAS subject 411.226
GSM24659A3243G-PEO subject 114.228
GSM24660A3243G-PEO subject 211.824
GSM24661A3243G-PEO subject 312.731
GSM24662A3243G-PEO subject 412.427
GSM24663mtDNA "Common"-deletion subject 119.332
GSM24664mtDNA "Common"-deletion subject 231.230
GSM24665mtDNA "Common"-deletion subject 315.323
GSM24666mtDNA "Common"-deletion subject 414.422