ProfileGDS1065 / 207454_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 2% 11% 11% 7% 5% 8% 3% 4% 4% 8% 10% 14% 6% 18% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.72
GSM24653Normal subject 24.611
GSM24654Normal subject 34.811
GSM24655A3243G-MELAS subject 12.97
GSM24656A3243G-MELAS subject 23.25
GSM24657A3243G-MELAS subject 34.48
GSM24658A3243G-MELAS subject 41.53
GSM24659A3243G-PEO subject 12.54
GSM24660A3243G-PEO subject 22.24
GSM24661A3243G-PEO subject 32.78
GSM24662A3243G-PEO subject 43.510
GSM24663mtDNA "Common"-deletion subject 16.114
GSM24664mtDNA "Common"-deletion subject 25.26
GSM24665mtDNA "Common"-deletion subject 310.718
GSM24666mtDNA "Common"-deletion subject 45.410