ProfileGDS1065 / 211890_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 96% 93% 97% 93% 95% 94% 96% 92% 96% 92% 87% 91% 95% 97% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11299.296
GSM24653Normal subject 2572.893
GSM24654Normal subject 32656.797
GSM24655A3243G-MELAS subject 1356.693
GSM24656A3243G-MELAS subject 291095
GSM24657A3243G-MELAS subject 31224.694
GSM24658A3243G-MELAS subject 41186.196
GSM24659A3243G-PEO subject 133492
GSM24660A3243G-PEO subject 299096
GSM24661A3243G-PEO subject 3367.392
GSM24662A3243G-PEO subject 4239.887
GSM24663mtDNA "Common"-deletion subject 1492.291
GSM24664mtDNA "Common"-deletion subject 21560.795
GSM24665mtDNA "Common"-deletion subject 32716.697
GSM24666mtDNA "Common"-deletion subject 4126694