ProfileGDS1065 / 216981_x_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 22% 15% 19% 23% 14% 16% 38% 21% 11% 28% 24% 19% 24% 23% 20% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.222
GSM24653Normal subject 2615
GSM24654Normal subject 3919
GSM24655A3243G-MELAS subject 1923
GSM24656A3243G-MELAS subject 26.514
GSM24657A3243G-MELAS subject 38.616
GSM24658A3243G-MELAS subject 423.138
GSM24659A3243G-PEO subject 19.421
GSM24660A3243G-PEO subject 24.811
GSM24661A3243G-PEO subject 310.228
GSM24662A3243G-PEO subject 49.824
GSM24663mtDNA "Common"-deletion subject 18.519
GSM24664mtDNA "Common"-deletion subject 221.524
GSM24665mtDNA "Common"-deletion subject 315.823
GSM24666mtDNA "Common"-deletion subject 412.320