ProfileGDS1065 / 213747_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 22% 21% 5% 22% 2% 19% 22% 29% 9% 29% 20% 46% 8% 10% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11022
GSM24653Normal subject 29.521
GSM24654Normal subject 32.85
GSM24655A3243G-MELAS subject 18.222
GSM24656A3243G-MELAS subject 21.62
GSM24657A3243G-MELAS subject 311.419
GSM24658A3243G-MELAS subject 48.922
GSM24659A3243G-PEO subject 115.329
GSM24660A3243G-PEO subject 23.89
GSM24661A3243G-PEO subject 31129
GSM24662A3243G-PEO subject 47.620
GSM24663mtDNA "Common"-deletion subject 138.546
GSM24664mtDNA "Common"-deletion subject 26.28
GSM24665mtDNA "Common"-deletion subject 35.810
GSM24666mtDNA "Common"-deletion subject 410.718