ProfileGDS1065 / 218357_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% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13037.998
GSM24653Normal subject 22163.998
GSM24654Normal subject 33143.298
GSM24655A3243G-MELAS subject 1156698
GSM24656A3243G-MELAS subject 21950.998
GSM24657A3243G-MELAS subject 33574.698
GSM24658A3243G-MELAS subject 42164.798
GSM24659A3243G-PEO subject 1180998
GSM24660A3243G-PEO subject 22086.398
GSM24661A3243G-PEO subject 32028.898
GSM24662A3243G-PEO subject 4229898
GSM24663mtDNA "Common"-deletion subject 12414.898
GSM24664mtDNA "Common"-deletion subject 23229.798
GSM24665mtDNA "Common"-deletion subject 33642.698
GSM24666mtDNA "Common"-deletion subject 43100.697