ProfileGDS1065 / 205833_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 6% 29% 9% 7% 8% 24% 5% 19% 12% 20% 43% 23% 27% 5% 34% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.86
GSM24653Normal subject 215.729
GSM24654Normal subject 34.19
GSM24655A3243G-MELAS subject 12.97
GSM24656A3243G-MELAS subject 24.18
GSM24657A3243G-MELAS subject 316.224
GSM24658A3243G-MELAS subject 42.15
GSM24659A3243G-PEO subject 18.219
GSM24660A3243G-PEO subject 25.212
GSM24661A3243G-PEO subject 36.620
GSM24662A3243G-PEO subject 428.443
GSM24663mtDNA "Common"-deletion subject 110.723
GSM24664mtDNA "Common"-deletion subject 226.127
GSM24665mtDNA "Common"-deletion subject 33.55
GSM24666mtDNA "Common"-deletion subject 431.734