ProfileGDS1065 / 214555_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 13% 12% 9% 9% 4% 25% 6% 35% 25% 13% 26% 7% 4% 5% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.413
GSM24653Normal subject 2512
GSM24654Normal subject 34.29
GSM24655A3243G-MELAS subject 13.49
GSM24656A3243G-MELAS subject 22.84
GSM24657A3243G-MELAS subject 317.425
GSM24658A3243G-MELAS subject 42.36
GSM24659A3243G-PEO subject 12035
GSM24660A3243G-PEO subject 21225
GSM24661A3243G-PEO subject 33.913
GSM24662A3243G-PEO subject 411.926
GSM24663mtDNA "Common"-deletion subject 13.37
GSM24664mtDNA "Common"-deletion subject 24.14
GSM24665mtDNA "Common"-deletion subject 33.75
GSM24666mtDNA "Common"-deletion subject 47.614