ProfileGDS1065 / 208868_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 27% 31% 52% 51% 54% 43% 34% 13% 36% 26% 42% 21% 40% 47% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.527
GSM24653Normal subject 21831
GSM24654Normal subject 356.552
GSM24655A3243G-MELAS subject 133.351
GSM24656A3243G-MELAS subject 254.754
GSM24657A3243G-MELAS subject 34843
GSM24658A3243G-MELAS subject 418.434
GSM24659A3243G-PEO subject 15.413
GSM24660A3243G-PEO subject 222.836
GSM24661A3243G-PEO subject 39.126
GSM24662A3243G-PEO subject 426.842
GSM24663mtDNA "Common"-deletion subject 19.621
GSM24664mtDNA "Common"-deletion subject 252.840
GSM24665mtDNA "Common"-deletion subject 356.547
GSM24666mtDNA "Common"-deletion subject 449.243