ProfileGDS1065 / 207793_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 4% 0% 1% 1% 1% 1% 3% 2% 6% 10% 13% 0% 8% 0% 0% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.24
GSM24653Normal subject 20.40
GSM24654Normal subject 30.81
GSM24655A3243G-MELAS subject 10.81
GSM24656A3243G-MELAS subject 211
GSM24657A3243G-MELAS subject 311
GSM24658A3243G-MELAS subject 41.43
GSM24659A3243G-PEO subject 11.62
GSM24660A3243G-PEO subject 22.86
GSM24661A3243G-PEO subject 33.210
GSM24662A3243G-PEO subject 44.513
GSM24663mtDNA "Common"-deletion subject 10.40
GSM24664mtDNA "Common"-deletion subject 268
GSM24665mtDNA "Common"-deletion subject 30.80
GSM24666mtDNA "Common"-deletion subject 40.20