ProfileGDS1065 / 215495_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 97% 90% 96% 91% 95% 97% 91% 95% 94% 95% 95% 94% 89% 97% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11671.897
GSM24653Normal subject 2392.690
GSM24654Normal subject 31456.896
GSM24655A3243G-MELAS subject 1272.291
GSM24656A3243G-MELAS subject 2920.195
GSM24657A3243G-MELAS subject 32445.797
GSM24658A3243G-MELAS subject 4426.291
GSM24659A3243G-PEO subject 1583.795
GSM24660A3243G-PEO subject 2641.994
GSM24661A3243G-PEO subject 3604.895
GSM24662A3243G-PEO subject 4728.895
GSM24663mtDNA "Common"-deletion subject 1709.794
GSM24664mtDNA "Common"-deletion subject 2662.289
GSM24665mtDNA "Common"-deletion subject 33032.897
GSM24666mtDNA "Common"-deletion subject 41544.695