ProfileGDS1065 / 211356_x_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% 33% 36% 59% 39% 28% 36% 55% 34% 37% 40% 32% 37% 34% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1818
GSM24653Normal subject 220.133
GSM24654Normal subject 328.436
GSM24655A3243G-MELAS subject 144.959
GSM24656A3243G-MELAS subject 229.739
GSM24657A3243G-MELAS subject 32128
GSM24658A3243G-MELAS subject 421.336
GSM24659A3243G-PEO subject 144.455
GSM24660A3243G-PEO subject 220.734
GSM24661A3243G-PEO subject 31837
GSM24662A3243G-PEO subject 424.740
GSM24663mtDNA "Common"-deletion subject 118.932
GSM24664mtDNA "Common"-deletion subject 245.137
GSM24665mtDNA "Common"-deletion subject 331.634
GSM24666mtDNA "Common"-deletion subject 423.229