ProfileGDS1065 / 217818_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 20% 9% 21% 6% 9% 8% 9% 9% 19% 13% 18% 18% 7% 17% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1920
GSM24653Normal subject 23.99
GSM24654Normal subject 310.721
GSM24655A3243G-MELAS subject 12.56
GSM24656A3243G-MELAS subject 24.59
GSM24657A3243G-MELAS subject 34.48
GSM24658A3243G-MELAS subject 43.19
GSM24659A3243G-PEO subject 13.99
GSM24660A3243G-PEO subject 28.519
GSM24661A3243G-PEO subject 33.913
GSM24662A3243G-PEO subject 46.718
GSM24663mtDNA "Common"-deletion subject 17.918
GSM24664mtDNA "Common"-deletion subject 25.87
GSM24665mtDNA "Common"-deletion subject 31017
GSM24666mtDNA "Common"-deletion subject 45.510