ProfileGDS1065 / 215349_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 22% 23% 11% 31% 22% 24% 38% 27% 39% 13% 48% 9% 25% 24% 32% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.222
GSM24653Normal subject 21123
GSM24654Normal subject 34.911
GSM24655A3243G-MELAS subject 113.931
GSM24656A3243G-MELAS subject 211.322
GSM24657A3243G-MELAS subject 315.924
GSM24658A3243G-MELAS subject 423.338
GSM24659A3243G-PEO subject 113.227
GSM24660A3243G-PEO subject 226.339
GSM24661A3243G-PEO subject 33.913
GSM24662A3243G-PEO subject 434.448
GSM24663mtDNA "Common"-deletion subject 13.89
GSM24664mtDNA "Common"-deletion subject 222.325
GSM24665mtDNA "Common"-deletion subject 316.724
GSM24666mtDNA "Common"-deletion subject 42832