ProfileGDS1065 / 216990_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 0% 1% 3% 2% 1% 7% 2% 2% 1% 2% 1% 7% 1% 0% 2% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 10.40
GSM24653Normal subject 21.11
GSM24654Normal subject 323
GSM24655A3243G-MELAS subject 11.42
GSM24656A3243G-MELAS subject 21.11
GSM24657A3243G-MELAS subject 33.97
GSM24658A3243G-MELAS subject 41.12
GSM24659A3243G-PEO subject 11.62
GSM24660A3243G-PEO subject 21.31
GSM24661A3243G-PEO subject 31.12
GSM24662A3243G-PEO subject 40.71
GSM24663mtDNA "Common"-deletion subject 13.37
GSM24664mtDNA "Common"-deletion subject 21.61
GSM24665mtDNA "Common"-deletion subject 30.80
GSM24666mtDNA "Common"-deletion subject 41.72