ProfileGDS1065 / 220779_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% 24% 25% 26% 19% 24% 17% 25% 18% 29% 22% 29% 22% 18% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.925
GSM24653Normal subject 211.524
GSM24654Normal subject 313.625
GSM24655A3243G-MELAS subject 110.526
GSM24656A3243G-MELAS subject 29.619
GSM24657A3243G-MELAS subject 316.624
GSM24658A3243G-MELAS subject 4617
GSM24659A3243G-PEO subject 11225
GSM24660A3243G-PEO subject 27.818
GSM24661A3243G-PEO subject 31129
GSM24662A3243G-PEO subject 48.722
GSM24663mtDNA "Common"-deletion subject 116.129
GSM24664mtDNA "Common"-deletion subject 219.222
GSM24665mtDNA "Common"-deletion subject 310.718
GSM24666mtDNA "Common"-deletion subject 413.921