ProfileGDS1065 / 210976_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% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17272.999
GSM24653Normal subject 24481.899
GSM24654Normal subject 38859.599
GSM24655A3243G-MELAS subject 12970.599
GSM24656A3243G-MELAS subject 25223.499
GSM24657A3243G-MELAS subject 37639.599
GSM24658A3243G-MELAS subject 46458.199
GSM24659A3243G-PEO subject 14829.399
GSM24660A3243G-PEO subject 2583199
GSM24661A3243G-PEO subject 33964.299
GSM24662A3243G-PEO subject 43845.999
GSM24663mtDNA "Common"-deletion subject 1804699
GSM24664mtDNA "Common"-deletion subject 29981.699
GSM24665mtDNA "Common"-deletion subject 38913.999
GSM24666mtDNA "Common"-deletion subject 49771.199