ProfileGDS1065 / 217773_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16189.999
GSM24653Normal subject 25395.399
GSM24654Normal subject 36356.199
GSM24655A3243G-MELAS subject 12591.899
GSM24656A3243G-MELAS subject 23734.799
GSM24657A3243G-MELAS subject 3732899
GSM24658A3243G-MELAS subject 44321.399
GSM24659A3243G-PEO subject 14087.599
GSM24660A3243G-PEO subject 23950.599
GSM24661A3243G-PEO subject 34175.799
GSM24662A3243G-PEO subject 44910.299
GSM24663mtDNA "Common"-deletion subject 1622999
GSM24664mtDNA "Common"-deletion subject 26997.499
GSM24665mtDNA "Common"-deletion subject 37140.399
GSM24666mtDNA "Common"-deletion subject 48436.899