ProfileGDS1065 / 220110_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% 5% 9% 9% 10% 5% 9% 4% 10% 6% 8% 8% 5% 5% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.96
GSM24653Normal subject 22.75
GSM24654Normal subject 34.19
GSM24655A3243G-MELAS subject 13.29
GSM24656A3243G-MELAS subject 24.910
GSM24657A3243G-MELAS subject 33.35
GSM24658A3243G-MELAS subject 439
GSM24659A3243G-PEO subject 12.54
GSM24660A3243G-PEO subject 24.210
GSM24661A3243G-PEO subject 32.26
GSM24662A3243G-PEO subject 43.18
GSM24663mtDNA "Common"-deletion subject 13.58
GSM24664mtDNA "Common"-deletion subject 24.35
GSM24665mtDNA "Common"-deletion subject 33.55
GSM24666mtDNA "Common"-deletion subject 44.48