ProfileGDS1065 / 206316_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 37% 22% 23% 32% 6% 29% 38% 25% 37% 41% 32% 13% 31% 40% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 125.637
GSM24653Normal subject 21022
GSM24654Normal subject 312.623
GSM24655A3243G-MELAS subject 114.632
GSM24656A3243G-MELAS subject 23.66
GSM24657A3243G-MELAS subject 323.229
GSM24658A3243G-MELAS subject 422.838
GSM24659A3243G-PEO subject 111.925
GSM24660A3243G-PEO subject 224.337
GSM24661A3243G-PEO subject 32141
GSM24662A3243G-PEO subject 416.632
GSM24663mtDNA "Common"-deletion subject 15.713
GSM24664mtDNA "Common"-deletion subject 23331
GSM24665mtDNA "Common"-deletion subject 342.940
GSM24666mtDNA "Common"-deletion subject 438.738