ProfileGDS1065 / 220840_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 2% 5% 1% 3% 4% 13% 31% 1% 5% 29% 6% 2% 8% 25% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.72
GSM24653Normal subject 22.75
GSM24654Normal subject 31.11
GSM24655A3243G-MELAS subject 11.53
GSM24656A3243G-MELAS subject 22.74
GSM24657A3243G-MELAS subject 37.213
GSM24658A3243G-MELAS subject 415.431
GSM24659A3243G-PEO subject 11.21
GSM24660A3243G-PEO subject 22.65
GSM24661A3243G-PEO subject 311.329
GSM24662A3243G-PEO subject 42.66
GSM24663mtDNA "Common"-deletion subject 11.42
GSM24664mtDNA "Common"-deletion subject 25.98
GSM24665mtDNA "Common"-deletion subject 317.925
GSM24666mtDNA "Common"-deletion subject 46.913