ProfileGDS1065 / 208115_x_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% 16% 14% 4% 8% 24% 4% 24% 12% 37% 16% 9% 25% 12% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.82
GSM24653Normal subject 26.716
GSM24654Normal subject 36.314
GSM24655A3243G-MELAS subject 11.84
GSM24656A3243G-MELAS subject 24.18
GSM24657A3243G-MELAS subject 315.724
GSM24658A3243G-MELAS subject 41.74
GSM24659A3243G-PEO subject 111.124
GSM24660A3243G-PEO subject 25.112
GSM24661A3243G-PEO subject 317.637
GSM24662A3243G-PEO subject 45.716
GSM24663mtDNA "Common"-deletion subject 13.89
GSM24664mtDNA "Common"-deletion subject 222.925
GSM24665mtDNA "Common"-deletion subject 37.212
GSM24666mtDNA "Common"-deletion subject 45.710