ProfileGDS1065 / 201217_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 98% 98% 98% 99% 97% 98% 98% 98% 98% 98% 99% 98% 98% 98% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13216.798
GSM24653Normal subject 23251.998
GSM24654Normal subject 32951.598
GSM24655A3243G-MELAS subject 12601.199
GSM24656A3243G-MELAS subject 21652.597
GSM24657A3243G-MELAS subject 35036.698
GSM24658A3243G-MELAS subject 4342398
GSM24659A3243G-PEO subject 12514.698
GSM24660A3243G-PEO subject 21992.898
GSM24661A3243G-PEO subject 32122.898
GSM24662A3243G-PEO subject 44171.999
GSM24663mtDNA "Common"-deletion subject 13674.798
GSM24664mtDNA "Common"-deletion subject 23864.298
GSM24665mtDNA "Common"-deletion subject 33684.698
GSM24666mtDNA "Common"-deletion subject 43866.898