ProfileGDS1065 / 215354_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 68% 68% 49% 70% 71% 72% 76% 72% 62% 74% 72% 73% 66% 59% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 195.268
GSM24653Normal subject 290.468
GSM24654Normal subject 349.949
GSM24655A3243G-MELAS subject 16870
GSM24656A3243G-MELAS subject 2107.771
GSM24657A3243G-MELAS subject 3184.372
GSM24658A3243G-MELAS subject 4134.576
GSM24659A3243G-PEO subject 18772
GSM24660A3243G-PEO subject 26762
GSM24661A3243G-PEO subject 386.874
GSM24662A3243G-PEO subject 495.172
GSM24663mtDNA "Common"-deletion subject 112773
GSM24664mtDNA "Common"-deletion subject 2151.666
GSM24665mtDNA "Common"-deletion subject 396.459
GSM24666mtDNA "Common"-deletion subject 4159.868