ProfileGDS1065 / 203443_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 51% 63% 52% 60% 44% 46% 52% 63% 38% 46% 65% 53% 59% 39% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 145.551
GSM24653Normal subject 273.163
GSM24654Normal subject 356.752
GSM24655A3243G-MELAS subject 147.360
GSM24656A3243G-MELAS subject 237.944
GSM24657A3243G-MELAS subject 352.846
GSM24658A3243G-MELAS subject 443.552
GSM24659A3243G-PEO subject 159.763
GSM24660A3243G-PEO subject 225.338
GSM24661A3243G-PEO subject 326.546
GSM24662A3243G-PEO subject 468.365
GSM24663mtDNA "Common"-deletion subject 151.853
GSM24664mtDNA "Common"-deletion subject 2115.959
GSM24665mtDNA "Common"-deletion subject 34039
GSM24666mtDNA "Common"-deletion subject 439.638