ProfileGDS1065 / 211402_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 39% 14% 41% 60% 59% 42% 51% 11% 45% 39% 56% 45% 46% 55% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 128.339
GSM24653Normal subject 25.514
GSM24654Normal subject 334.541
GSM24655A3243G-MELAS subject 147.260
GSM24656A3243G-MELAS subject 267.359
GSM24657A3243G-MELAS subject 34442
GSM24658A3243G-MELAS subject 441.651
GSM24659A3243G-PEO subject 14.811
GSM24660A3243G-PEO subject 234.345
GSM24661A3243G-PEO subject 319.339
GSM24662A3243G-PEO subject 44756
GSM24663mtDNA "Common"-deletion subject 136.745
GSM24664mtDNA "Common"-deletion subject 266.146
GSM24665mtDNA "Common"-deletion subject 379.955
GSM24666mtDNA "Common"-deletion subject 458.447