ProfileGDS1065 / 214313_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 9% 11% 2% 18% 37% 53% 2% 25% 28% 49% 55% 5% 10% 19% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.99
GSM24653Normal subject 24.511
GSM24654Normal subject 31.62
GSM24655A3243G-MELAS subject 16.418
GSM24656A3243G-MELAS subject 227.137
GSM24657A3243G-MELAS subject 373.553
GSM24658A3243G-MELAS subject 41.32
GSM24659A3243G-PEO subject 111.625
GSM24660A3243G-PEO subject 214.628
GSM24661A3243G-PEO subject 33049
GSM24662A3243G-PEO subject 445.655
GSM24663mtDNA "Common"-deletion subject 12.75
GSM24664mtDNA "Common"-deletion subject 27.510
GSM24665mtDNA "Common"-deletion subject 311.919
GSM24666mtDNA "Common"-deletion subject 47.914