ProfileGDS1065 / 206898_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 38% 55% 49% 27% 30% 41% 37% 35% 25% 23% 27% 18% 27% 34% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.138
GSM24653Normal subject 251.655
GSM24654Normal subject 350.949
GSM24655A3243G-MELAS subject 111.527
GSM24656A3243G-MELAS subject 21930
GSM24657A3243G-MELAS subject 343.541
GSM24658A3243G-MELAS subject 422.537
GSM24659A3243G-PEO subject 120.135
GSM24660A3243G-PEO subject 21225
GSM24661A3243G-PEO subject 37.923
GSM24662A3243G-PEO subject 412.127
GSM24663mtDNA "Common"-deletion subject 17.618
GSM24664mtDNA "Common"-deletion subject 227.327
GSM24665mtDNA "Common"-deletion subject 33134
GSM24666mtDNA "Common"-deletion subject 414.522