ProfileGDS1065 / 219214_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 56% 43% 63% 39% 60% 61% 57% 60% 54% 63% 57% 63% 59% 60% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 157.256
GSM24653Normal subject 231.343
GSM24654Normal subject 391.963
GSM24655A3243G-MELAS subject 120.739
GSM24656A3243G-MELAS subject 269.160
GSM24657A3243G-MELAS subject 3104.561
GSM24658A3243G-MELAS subject 453.357
GSM24659A3243G-PEO subject 154.460
GSM24660A3243G-PEO subject 247.854
GSM24661A3243G-PEO subject 351.963
GSM24662A3243G-PEO subject 449.857
GSM24663mtDNA "Common"-deletion subject 178.763
GSM24664mtDNA "Common"-deletion subject 2115.859
GSM24665mtDNA "Common"-deletion subject 398.760
GSM24666mtDNA "Common"-deletion subject 484.456