ProfileGDS1065 / 207418_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 6% 7% 15% 17% 14% 8% 7% 14% 5% 9% 10% 8% 5% 15% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.96
GSM24653Normal subject 23.37
GSM24654Normal subject 3715
GSM24655A3243G-MELAS subject 1617
GSM24656A3243G-MELAS subject 26.514
GSM24657A3243G-MELAS subject 34.78
GSM24658A3243G-MELAS subject 42.57
GSM24659A3243G-PEO subject 15.814
GSM24660A3243G-PEO subject 22.65
GSM24661A3243G-PEO subject 32.99
GSM24662A3243G-PEO subject 43.710
GSM24663mtDNA "Common"-deletion subject 13.68
GSM24664mtDNA "Common"-deletion subject 24.75
GSM24665mtDNA "Common"-deletion subject 38.615
GSM24666mtDNA "Common"-deletion subject 447