ProfileGDS1065 / 222372_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 17% 9% 31% 25% 5% 45% 48% 22% 30% 10% 29% 26% 17% 25% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.117
GSM24653Normal subject 23.99
GSM24654Normal subject 321.531
GSM24655A3243G-MELAS subject 110.125
GSM24656A3243G-MELAS subject 22.95
GSM24657A3243G-MELAS subject 350.645
GSM24658A3243G-MELAS subject 436.248
GSM24659A3243G-PEO subject 110.122
GSM24660A3243G-PEO subject 216.430
GSM24661A3243G-PEO subject 33.110
GSM24662A3243G-PEO subject 413.929
GSM24663mtDNA "Common"-deletion subject 113.426
GSM24664mtDNA "Common"-deletion subject 212.817
GSM24665mtDNA "Common"-deletion subject 318.625
GSM24666mtDNA "Common"-deletion subject 440.639