ProfileGDS1065 / 210107_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 42% 34% 46% 42% 60% 30% 45% 65% 54% 55% 45% 38% 41% 30% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13242
GSM24653Normal subject 220.934
GSM24654Normal subject 345.246
GSM24655A3243G-MELAS subject 123.542
GSM24656A3243G-MELAS subject 269.960
GSM24657A3243G-MELAS subject 323.530
GSM24658A3243G-MELAS subject 431.745
GSM24659A3243G-PEO subject 165.565
GSM24660A3243G-PEO subject 249.254
GSM24661A3243G-PEO subject 338.455
GSM24662A3243G-PEO subject 431.145
GSM24663mtDNA "Common"-deletion subject 126.938
GSM24664mtDNA "Common"-deletion subject 254.341
GSM24665mtDNA "Common"-deletion subject 325.230
GSM24666mtDNA "Common"-deletion subject 447.142