ProfileGDS1065 / 211180_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 43% 21% 17% 49% 45% 35% 49% 50% 12% 14% 52% 51% 35% 35% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 133.843
GSM24653Normal subject 29.621
GSM24654Normal subject 37.917
GSM24655A3243G-MELAS subject 131.449
GSM24656A3243G-MELAS subject 239.245
GSM24657A3243G-MELAS subject 331.935
GSM24658A3243G-MELAS subject 437.949
GSM24659A3243G-PEO subject 137.650
GSM24660A3243G-PEO subject 25.112
GSM24661A3243G-PEO subject 34.514
GSM24662A3243G-PEO subject 441.152
GSM24663mtDNA "Common"-deletion subject 14851
GSM24664mtDNA "Common"-deletion subject 240.635
GSM24665mtDNA "Common"-deletion subject 333.835
GSM24666mtDNA "Common"-deletion subject 46.813