ProfileGDS1065 / 208694_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 75% 64% 68% 67% 78% 77% 73% 70% 71% 72% 72% 75% 76% 75% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1136.875
GSM24653Normal subject 274.864
GSM24654Normal subject 3115.968
GSM24655A3243G-MELAS subject 160.967
GSM24656A3243G-MELAS subject 2161.778
GSM24657A3243G-MELAS subject 3233.677
GSM24658A3243G-MELAS subject 4113.173
GSM24659A3243G-PEO subject 178.570
GSM24660A3243G-PEO subject 29771
GSM24661A3243G-PEO subject 379.172
GSM24662A3243G-PEO subject 496.272
GSM24663mtDNA "Common"-deletion subject 1136.775
GSM24664mtDNA "Common"-deletion subject 2254.876
GSM24665mtDNA "Common"-deletion subject 3202.775
GSM24666mtDNA "Common"-deletion subject 4262.977