ProfileGDS1065 / 214786_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 11% 2% 8% 8% 10% 17% 16% 0% 6% 25% 8% 13% 6% 3% 1% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.611
GSM24653Normal subject 21.52
GSM24654Normal subject 33.88
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 24.810
GSM24657A3243G-MELAS subject 39.917
GSM24658A3243G-MELAS subject 45.316
GSM24659A3243G-PEO subject 10.30
GSM24660A3243G-PEO subject 22.86
GSM24661A3243G-PEO subject 38.525
GSM24662A3243G-PEO subject 438
GSM24663mtDNA "Common"-deletion subject 15.313
GSM24664mtDNA "Common"-deletion subject 24.86
GSM24665mtDNA "Common"-deletion subject 32.73
GSM24666mtDNA "Common"-deletion subject 411