ProfileGDS1065 / 217602_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 3% 9% 13% 1% 0% 1% 2% 1% 1% 2% 1% 0% 0% 0% 1% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123
GSM24653Normal subject 23.99
GSM24654Normal subject 35.913
GSM24655A3243G-MELAS subject 10.61
GSM24656A3243G-MELAS subject 20.50
GSM24657A3243G-MELAS subject 30.91
GSM24658A3243G-MELAS subject 41.12
GSM24659A3243G-PEO subject 10.61
GSM24660A3243G-PEO subject 20.81
GSM24661A3243G-PEO subject 312
GSM24662A3243G-PEO subject 40.61
GSM24663mtDNA "Common"-deletion subject 10.50
GSM24664mtDNA "Common"-deletion subject 20.90
GSM24665mtDNA "Common"-deletion subject 30.80
GSM24666mtDNA "Common"-deletion subject 41.41