ProfileGDS1065 / 217982_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 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1281598
GSM24653Normal subject 22609.898
GSM24654Normal subject 33034.298
GSM24655A3243G-MELAS subject 11437.598
GSM24656A3243G-MELAS subject 22704.298
GSM24657A3243G-MELAS subject 33969.898
GSM24658A3243G-MELAS subject 42159.498
GSM24659A3243G-PEO subject 12142.798
GSM24660A3243G-PEO subject 22741.398
GSM24661A3243G-PEO subject 32017.798
GSM24662A3243G-PEO subject 42227.698
GSM24663mtDNA "Common"-deletion subject 1254198
GSM24664mtDNA "Common"-deletion subject 23616.498
GSM24665mtDNA "Common"-deletion subject 33805.498
GSM24666mtDNA "Common"-deletion subject 45552.398