ProfileGDS1065 / 215252_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 41% 42% 20% 26% 14% 27% 23% 33% 21% 15% 24% 26% 36% 23% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.641
GSM24653Normal subject 230.942
GSM24654Normal subject 310.120
GSM24655A3243G-MELAS subject 110.626
GSM24656A3243G-MELAS subject 26.514
GSM24657A3243G-MELAS subject 32027
GSM24658A3243G-MELAS subject 49.623
GSM24659A3243G-PEO subject 118.633
GSM24660A3243G-PEO subject 29.421
GSM24661A3243G-PEO subject 34.615
GSM24662A3243G-PEO subject 41024
GSM24663mtDNA "Common"-deletion subject 113.126
GSM24664mtDNA "Common"-deletion subject 243.536
GSM24665mtDNA "Common"-deletion subject 315.723
GSM24666mtDNA "Common"-deletion subject 423.229