ProfileGDS1065 / 210115_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 32% 40% 35% 17% 40% 31% 30% 36% 27% 33% 31% 46% 29% 38% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 119.432
GSM24653Normal subject 228.240
GSM24654Normal subject 326.535
GSM24655A3243G-MELAS subject 15.917
GSM24656A3243G-MELAS subject 23240
GSM24657A3243G-MELAS subject 325.631
GSM24658A3243G-MELAS subject 414.530
GSM24659A3243G-PEO subject 120.936
GSM24660A3243G-PEO subject 213.527
GSM24661A3243G-PEO subject 313.933
GSM24662A3243G-PEO subject 416.131
GSM24663mtDNA "Common"-deletion subject 138.846
GSM24664mtDNA "Common"-deletion subject 230.729
GSM24665mtDNA "Common"-deletion subject 338.638
GSM24666mtDNA "Common"-deletion subject 42731