ProfileGDS1065 / 211789_s_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 2% 4% 2% 9% 9% 5% 8% 3% 5% 1% 3% 2% 9% 10% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.42
GSM24653Normal subject 22.44
GSM24654Normal subject 31.42
GSM24655A3243G-MELAS subject 13.29
GSM24656A3243G-MELAS subject 24.59
GSM24657A3243G-MELAS subject 33.25
GSM24658A3243G-MELAS subject 42.98
GSM24659A3243G-PEO subject 123
GSM24660A3243G-PEO subject 22.75
GSM24661A3243G-PEO subject 30.81
GSM24662A3243G-PEO subject 41.63
GSM24663mtDNA "Common"-deletion subject 11.52
GSM24664mtDNA "Common"-deletion subject 26.89
GSM24665mtDNA "Common"-deletion subject 36.110
GSM24666mtDNA "Common"-deletion subject 45.19