ProfileGDS1065 / 220724_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 1% 0% 3% 2% 1% 1% 1% 1% 1% 28% 0% 1% 2% 8% 15% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111
GSM24653Normal subject 20.20
GSM24654Normal subject 32.23
GSM24655A3243G-MELAS subject 11.12
GSM24656A3243G-MELAS subject 211
GSM24657A3243G-MELAS subject 31.21
GSM24658A3243G-MELAS subject 40.91
GSM24659A3243G-PEO subject 111
GSM24660A3243G-PEO subject 20.81
GSM24661A3243G-PEO subject 310.828
GSM24662A3243G-PEO subject 40.40
GSM24663mtDNA "Common"-deletion subject 10.81
GSM24664mtDNA "Common"-deletion subject 22.92
GSM24665mtDNA "Common"-deletion subject 34.98
GSM24666mtDNA "Common"-deletion subject 48.215