ProfileGDS1065 / 206370_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 0% 1% 2% 1% 1% 2% 3% 0% 0% 1% 1% 1% 0% 1% 1% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 10.40
GSM24653Normal subject 211
GSM24654Normal subject 31.62
GSM24655A3243G-MELAS subject 10.91
GSM24656A3243G-MELAS subject 20.81
GSM24657A3243G-MELAS subject 32.12
GSM24658A3243G-MELAS subject 41.43
GSM24659A3243G-PEO subject 10.50
GSM24660A3243G-PEO subject 20.50
GSM24661A3243G-PEO subject 30.71
GSM24662A3243G-PEO subject 411
GSM24663mtDNA "Common"-deletion subject 10.71
GSM24664mtDNA "Common"-deletion subject 20.60
GSM24665mtDNA "Common"-deletion subject 31.91
GSM24666mtDNA "Common"-deletion subject 41.21