ProfileGDS1065 / 221525_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 23% 22% 21% 17% 14% 18% 17% 46% 33% 27% 27% 29% 20% 23% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111.123
GSM24653Normal subject 29.722
GSM24654Normal subject 310.421
GSM24655A3243G-MELAS subject 16.117
GSM24656A3243G-MELAS subject 26.714
GSM24657A3243G-MELAS subject 31018
GSM24658A3243G-MELAS subject 45.917
GSM24659A3243G-PEO subject 132.846
GSM24660A3243G-PEO subject 219.433
GSM24661A3243G-PEO subject 39.627
GSM24662A3243G-PEO subject 412.327
GSM24663mtDNA "Common"-deletion subject 115.729
GSM24664mtDNA "Common"-deletion subject 21620
GSM24665mtDNA "Common"-deletion subject 315.623
GSM24666mtDNA "Common"-deletion subject 418.125