ProfileGDS1065 / 213720_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 80% 81% 75% 82% 79% 80% 83% 85% 82% 83% 87% 84% 77% 70% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1181.480
GSM24653Normal subject 2179.681
GSM24654Normal subject 3167.775
GSM24655A3243G-MELAS subject 112882
GSM24656A3243G-MELAS subject 2165.579
GSM24657A3243G-MELAS subject 3284.580
GSM24658A3243G-MELAS subject 4203.883
GSM24659A3243G-PEO subject 1177.985
GSM24660A3243G-PEO subject 2179.582
GSM24661A3243G-PEO subject 3146.183
GSM24662A3243G-PEO subject 425087
GSM24663mtDNA "Common"-deletion subject 1255.584
GSM24664mtDNA "Common"-deletion subject 2261.377
GSM24665mtDNA "Common"-deletion subject 3156.970
GSM24666mtDNA "Common"-deletion subject 4302.479