ProfileGDS1065 / 210498_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 19% 0% 3% 1% 2% 1% 23% 9% 1% 23% 2% 14% 26% 5% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.719
GSM24653Normal subject 20.40
GSM24654Normal subject 323
GSM24655A3243G-MELAS subject 111
GSM24656A3243G-MELAS subject 222
GSM24657A3243G-MELAS subject 31.31
GSM24658A3243G-MELAS subject 49.623
GSM24659A3243G-PEO subject 14.29
GSM24660A3243G-PEO subject 20.71
GSM24661A3243G-PEO subject 37.623
GSM24662A3243G-PEO subject 41.32
GSM24663mtDNA "Common"-deletion subject 16.114
GSM24664mtDNA "Common"-deletion subject 223.926
GSM24665mtDNA "Common"-deletion subject 33.75
GSM24666mtDNA "Common"-deletion subject 414.622