ProfileGDS1065 / 213662_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 4% 20% 4% 18% 4% 17% 16% 19% 4% 10% 3% 24% 3% 4% 2% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.34
GSM24653Normal subject 28.620
GSM24654Normal subject 32.34
GSM24655A3243G-MELAS subject 16.518
GSM24656A3243G-MELAS subject 22.74
GSM24657A3243G-MELAS subject 39.517
GSM24658A3243G-MELAS subject 45.316
GSM24659A3243G-PEO subject 17.919
GSM24660A3243G-PEO subject 22.44
GSM24661A3243G-PEO subject 33.310
GSM24662A3243G-PEO subject 41.53
GSM24663mtDNA "Common"-deletion subject 111.324
GSM24664mtDNA "Common"-deletion subject 23.23
GSM24665mtDNA "Common"-deletion subject 33.34
GSM24666mtDNA "Common"-deletion subject 422