ProfileGDS1065 / 218724_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 37% 34% 24% 31% 21% 24% 16% 27% 26% 34% 12% 17% 38% 28% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 125.837
GSM24653Normal subject 221.434
GSM24654Normal subject 313.124
GSM24655A3243G-MELAS subject 114.331
GSM24656A3243G-MELAS subject 210.721
GSM24657A3243G-MELAS subject 315.824
GSM24658A3243G-MELAS subject 45.416
GSM24659A3243G-PEO subject 113.327
GSM24660A3243G-PEO subject 213.126
GSM24661A3243G-PEO subject 31534
GSM24662A3243G-PEO subject 44.212
GSM24663mtDNA "Common"-deletion subject 17.217
GSM24664mtDNA "Common"-deletion subject 24738
GSM24665mtDNA "Common"-deletion subject 322.328
GSM24666mtDNA "Common"-deletion subject 442.740