ProfileGDS1065 / 213684_s_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 99% 98% 99% 99% 99% 98% 99% 98% 99% 99% 98% 98% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15465.499
GSM24653Normal subject 23723.498
GSM24654Normal subject 36709.199
GSM24655A3243G-MELAS subject 12254.499
GSM24656A3243G-MELAS subject 24451.999
GSM24657A3243G-MELAS subject 35283.298
GSM24658A3243G-MELAS subject 45143.599
GSM24659A3243G-PEO subject 1209698
GSM24660A3243G-PEO subject 24475.399
GSM24661A3243G-PEO subject 3341499
GSM24662A3243G-PEO subject 42847.498
GSM24663mtDNA "Common"-deletion subject 13524.498
GSM24664mtDNA "Common"-deletion subject 26483.499
GSM24665mtDNA "Common"-deletion subject 37294.199
GSM24666mtDNA "Common"-deletion subject 48107.899