ProfileGDS1065 / 208517_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% 99% 98% 98% 98% 99% 98% 98% 98% 98% 99% 98% 99% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13540.198
GSM24653Normal subject 23196.998
GSM24654Normal subject 35435.699
GSM24655A3243G-MELAS subject 11927.598
GSM24656A3243G-MELAS subject 22587.798
GSM24657A3243G-MELAS subject 34548.698
GSM24658A3243G-MELAS subject 4381699
GSM24659A3243G-PEO subject 11814.898
GSM24660A3243G-PEO subject 23006.698
GSM24661A3243G-PEO subject 31889.398
GSM24662A3243G-PEO subject 42237.298
GSM24663mtDNA "Common"-deletion subject 1432299
GSM24664mtDNA "Common"-deletion subject 25425.298
GSM24665mtDNA "Common"-deletion subject 36520.899
GSM24666mtDNA "Common"-deletion subject 45357.198