ProfileGDS1065 / 212754_s_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 68% 70% 66% 71% 63% 67% 63% 67% 59% 65% 60% 67% 75% 69% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 195.168
GSM24653Normal subject 298.670
GSM24654Normal subject 3105.566
GSM24655A3243G-MELAS subject 17271
GSM24656A3243G-MELAS subject 277.563
GSM24657A3243G-MELAS subject 3136.667
GSM24658A3243G-MELAS subject 468.663
GSM24659A3243G-PEO subject 170.667
GSM24660A3243G-PEO subject 258.359
GSM24661A3243G-PEO subject 357.665
GSM24662A3243G-PEO subject 455.560
GSM24663mtDNA "Common"-deletion subject 192.467
GSM24664mtDNA "Common"-deletion subject 2243.975
GSM24665mtDNA "Common"-deletion subject 3150.569
GSM24666mtDNA "Common"-deletion subject 4148.867