ProfileGDS1065 / 209803_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 29% 45% 35% 40% 32% 34% 28% 37% 21% 34% 32% 29% 28% 30% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 116.829
GSM24653Normal subject 234.245
GSM24654Normal subject 32735
GSM24655A3243G-MELAS subject 122.340
GSM24656A3243G-MELAS subject 221.532
GSM24657A3243G-MELAS subject 330.434
GSM24658A3243G-MELAS subject 413.228
GSM24659A3243G-PEO subject 122.737
GSM24660A3243G-PEO subject 29.521
GSM24661A3243G-PEO subject 314.834
GSM24662A3243G-PEO subject 416.832
GSM24663mtDNA "Common"-deletion subject 115.929
GSM24664mtDNA "Common"-deletion subject 22828
GSM24665mtDNA "Common"-deletion subject 325.330
GSM24666mtDNA "Common"-deletion subject 424.329