ProfileGDS1065 / 216207_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 59% 52% 31% 63% 30% 67% 41% 32% 53% 34% 25% 55% 52% 57% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 164.259
GSM24653Normal subject 245.352
GSM24654Normal subject 321.531
GSM24655A3243G-MELAS subject 151.263
GSM24656A3243G-MELAS subject 21930
GSM24657A3243G-MELAS subject 3137.967
GSM24658A3243G-MELAS subject 426.741
GSM24659A3243G-PEO subject 117.232
GSM24660A3243G-PEO subject 24753
GSM24661A3243G-PEO subject 314.934
GSM24662A3243G-PEO subject 410.725
GSM24663mtDNA "Common"-deletion subject 154.955
GSM24664mtDNA "Common"-deletion subject 284.752
GSM24665mtDNA "Common"-deletion subject 386.757
GSM24666mtDNA "Common"-deletion subject 4118.763