ProfileGDS1065 / 216725_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 10% 10% 13% 8% 8% 6% 3% 7% 4% 13% 11% 5% 5% 7% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.310
GSM24653Normal subject 24.310
GSM24654Normal subject 36.113
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 24.18
GSM24657A3243G-MELAS subject 33.56
GSM24658A3243G-MELAS subject 41.53
GSM24659A3243G-PEO subject 13.37
GSM24660A3243G-PEO subject 22.44
GSM24661A3243G-PEO subject 34.113
GSM24662A3243G-PEO subject 43.811
GSM24663mtDNA "Common"-deletion subject 12.85
GSM24664mtDNA "Common"-deletion subject 24.45
GSM24665mtDNA "Common"-deletion subject 34.67
GSM24666mtDNA "Common"-deletion subject 42.74