ProfileGDS1065 / 205699_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 29% 2% 27% 22% 37% 30% 27% 33% 34% 31% 37% 29% 25% 29% 27% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 116.329
GSM24653Normal subject 21.42
GSM24654Normal subject 315.727
GSM24655A3243G-MELAS subject 1822
GSM24656A3243G-MELAS subject 227.837
GSM24657A3243G-MELAS subject 323.530
GSM24658A3243G-MELAS subject 412.427
GSM24659A3243G-PEO subject 118.133
GSM24660A3243G-PEO subject 22034
GSM24661A3243G-PEO subject 312.631
GSM24662A3243G-PEO subject 421.737
GSM24663mtDNA "Common"-deletion subject 115.829
GSM24664mtDNA "Common"-deletion subject 22325
GSM24665mtDNA "Common"-deletion subject 323.729
GSM24666mtDNA "Common"-deletion subject 420.427