ProfileGDS1065 / 216916_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 21% 16% 27% 17% 23% 21% 21% 19% 22% 22% 24% 24% 25% 21% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.821
GSM24653Normal subject 26.316
GSM24654Normal subject 315.627
GSM24655A3243G-MELAS subject 15.917
GSM24656A3243G-MELAS subject 212.123
GSM24657A3243G-MELAS subject 312.521
GSM24658A3243G-MELAS subject 48.421
GSM24659A3243G-PEO subject 18.419
GSM24660A3243G-PEO subject 21022
GSM24661A3243G-PEO subject 37.422
GSM24662A3243G-PEO subject 410.124
GSM24663mtDNA "Common"-deletion subject 111.324
GSM24664mtDNA "Common"-deletion subject 223.725
GSM24665mtDNA "Common"-deletion subject 313.921
GSM24666mtDNA "Common"-deletion subject 45.811