ProfileGDS1065 / 212495_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 79% 75% 79% 74% 80% 79% 75% 78% 82% 77% 80% 77% 74% 81% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1169.879
GSM24653Normal subject 2123.675
GSM24654Normal subject 3218.379
GSM24655A3243G-MELAS subject 183.474
GSM24656A3243G-MELAS subject 2174.380
GSM24657A3243G-MELAS subject 3271.379
GSM24658A3243G-MELAS subject 4124.875
GSM24659A3243G-PEO subject 111778
GSM24660A3243G-PEO subject 2175.182
GSM24661A3243G-PEO subject 3104.477
GSM24662A3243G-PEO subject 4147.380
GSM24663mtDNA "Common"-deletion subject 1159.277
GSM24664mtDNA "Common"-deletion subject 2226.274
GSM24665mtDNA "Common"-deletion subject 3295.981
GSM24666mtDNA "Common"-deletion subject 4324.480