ProfileGDS1065 / 215224_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% 25% 31% 5% 9% 17% 24% 28% 11% 14% 6% 2% 11% 19% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.16
GSM24653Normal subject 212.225
GSM24654Normal subject 320.931
GSM24655A3243G-MELAS subject 12.35
GSM24656A3243G-MELAS subject 24.79
GSM24657A3243G-MELAS subject 39.417
GSM24658A3243G-MELAS subject 410.124
GSM24659A3243G-PEO subject 113.828
GSM24660A3243G-PEO subject 24.711
GSM24661A3243G-PEO subject 34.314
GSM24662A3243G-PEO subject 42.56
GSM24663mtDNA "Common"-deletion subject 11.72
GSM24664mtDNA "Common"-deletion subject 2811
GSM24665mtDNA "Common"-deletion subject 311.619
GSM24666mtDNA "Common"-deletion subject 4611