ProfileGDS1065 / 215803_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 15% 14% 1% 2% 6% 3% 22% 0% 1% 0% 0% 2% 14% 14% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.415
GSM24653Normal subject 25.514
GSM24654Normal subject 31.21
GSM24655A3243G-MELAS subject 11.32
GSM24656A3243G-MELAS subject 23.36
GSM24657A3243G-MELAS subject 32.23
GSM24658A3243G-MELAS subject 48.522
GSM24659A3243G-PEO subject 10.10
GSM24660A3243G-PEO subject 20.81
GSM24661A3243G-PEO subject 30.20
GSM24662A3243G-PEO subject 40.20
GSM24663mtDNA "Common"-deletion subject 11.52
GSM24664mtDNA "Common"-deletion subject 210.214
GSM24665mtDNA "Common"-deletion subject 38.114
GSM24666mtDNA "Common"-deletion subject 46.512