ProfileGDS1065 / 211514_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% 38% 27% 22% 27% 24% 39% 2% 31% 3% 8% 28% 11% 11% 6% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 136
GSM24653Normal subject 225.638
GSM24654Normal subject 315.927
GSM24655A3243G-MELAS subject 18.122
GSM24656A3243G-MELAS subject 215.827
GSM24657A3243G-MELAS subject 316.624
GSM24658A3243G-MELAS subject 424.439
GSM24659A3243G-PEO subject 11.82
GSM24660A3243G-PEO subject 216.931
GSM24661A3243G-PEO subject 31.53
GSM24662A3243G-PEO subject 43.18
GSM24663mtDNA "Common"-deletion subject 115.328
GSM24664mtDNA "Common"-deletion subject 28.111
GSM24665mtDNA "Common"-deletion subject 36.411
GSM24666mtDNA "Common"-deletion subject 43.86