ProfileGDS1065 / 212392_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 30% 26% 32% 31% 49% 34% 31% 20% 20% 16% 5% 14% 37% 25% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11730
GSM24653Normal subject 212.726
GSM24654Normal subject 321.832
GSM24655A3243G-MELAS subject 114.331
GSM24656A3243G-MELAS subject 244.849
GSM24657A3243G-MELAS subject 330.234
GSM24658A3243G-MELAS subject 415.631
GSM24659A3243G-PEO subject 18.820
GSM24660A3243G-PEO subject 28.720
GSM24661A3243G-PEO subject 3516
GSM24662A3243G-PEO subject 42.15
GSM24663mtDNA "Common"-deletion subject 1614
GSM24664mtDNA "Common"-deletion subject 245.137
GSM24665mtDNA "Common"-deletion subject 318.625
GSM24666mtDNA "Common"-deletion subject 414.122