ProfileGDS1065 / 217885_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 66% 74% 76% 71% 73% 77% 76% 79% 75% 71% 77% 77% 76% 70% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18666
GSM24653Normal subject 2121.974
GSM24654Normal subject 3177.676
GSM24655A3243G-MELAS subject 173.471
GSM24656A3243G-MELAS subject 2121.573
GSM24657A3243G-MELAS subject 323477
GSM24658A3243G-MELAS subject 413776
GSM24659A3243G-PEO subject 1120.779
GSM24660A3243G-PEO subject 2117.175
GSM24661A3243G-PEO subject 37771
GSM24662A3243G-PEO subject 4126.277
GSM24663mtDNA "Common"-deletion subject 1153.177
GSM24664mtDNA "Common"-deletion subject 2257.876
GSM24665mtDNA "Common"-deletion subject 3158.970
GSM24666mtDNA "Common"-deletion subject 4236.576