ProfileGDS1065 / 216913_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 25% 64% 80% 9% 26% 29% 69% 28% 10% 88% 29% 65% 9% 19% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11325
GSM24653Normal subject 275.764
GSM24654Normal subject 3233.680
GSM24655A3243G-MELAS subject 13.39
GSM24656A3243G-MELAS subject 215.126
GSM24657A3243G-MELAS subject 322.429
GSM24658A3243G-MELAS subject 494.269
GSM24659A3243G-PEO subject 114.428
GSM24660A3243G-PEO subject 24.310
GSM24661A3243G-PEO subject 3212.488
GSM24662A3243G-PEO subject 413.929
GSM24663mtDNA "Common"-deletion subject 187.365
GSM24664mtDNA "Common"-deletion subject 27.29
GSM24665mtDNA "Common"-deletion subject 312.219
GSM24666mtDNA "Common"-deletion subject 482.255