ProfileGDS1065 / 212443_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 31% 17% 27% 33% 11% 36% 38% 16% 13% 27% 41% 26% 35% 31% 17% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 118.731
GSM24653Normal subject 26.817
GSM24654Normal subject 316.527
GSM24655A3243G-MELAS subject 11633
GSM24656A3243G-MELAS subject 25.411
GSM24657A3243G-MELAS subject 333.636
GSM24658A3243G-MELAS subject 423.438
GSM24659A3243G-PEO subject 16.616
GSM24660A3243G-PEO subject 25.313
GSM24661A3243G-PEO subject 39.827
GSM24662A3243G-PEO subject 426.441
GSM24663mtDNA "Common"-deletion subject 113.226
GSM24664mtDNA "Common"-deletion subject 240.635
GSM24665mtDNA "Common"-deletion subject 326.631
GSM24666mtDNA "Common"-deletion subject 49.817