ProfileGDS1065 / 207313_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 44% 43% 30% 42% 40% 43% 41% 57% 48% 50% 58% 44% 24% 32% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 134.844
GSM24653Normal subject 231.443
GSM24654Normal subject 319.230
GSM24655A3243G-MELAS subject 123.842
GSM24656A3243G-MELAS subject 230.940
GSM24657A3243G-MELAS subject 347.943
GSM24658A3243G-MELAS subject 426.741
GSM24659A3243G-PEO subject 148.857
GSM24660A3243G-PEO subject 23948
GSM24661A3243G-PEO subject 331.450
GSM24662A3243G-PEO subject 450.758
GSM24663mtDNA "Common"-deletion subject 135.444
GSM24664mtDNA "Common"-deletion subject 22224
GSM24665mtDNA "Common"-deletion subject 328.732
GSM24666mtDNA "Common"-deletion subject 438.538