ProfileGDS1065 / 209643_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 30% 30% 29% 27% 28% 52% 26% 29% 33% 32% 29% 32% 28% 29% 46% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 117.230
GSM24653Normal subject 216.930
GSM24654Normal subject 318.729
GSM24655A3243G-MELAS subject 111.527
GSM24656A3243G-MELAS subject 216.928
GSM24657A3243G-MELAS subject 369.252
GSM24658A3243G-MELAS subject 411.726
GSM24659A3243G-PEO subject 115.329
GSM24660A3243G-PEO subject 219.833
GSM24661A3243G-PEO subject 313.332
GSM24662A3243G-PEO subject 414.229
GSM24663mtDNA "Common"-deletion subject 118.632
GSM24664mtDNA "Common"-deletion subject 228.328
GSM24665mtDNA "Common"-deletion subject 323.229
GSM24666mtDNA "Common"-deletion subject 45646