ProfileGDS1065 / 218743_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 79% 78% 74% 79% 77% 80% 75% 84% 82% 85% 88% 82% 74% 75% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1172.779
GSM24653Normal subject 214878
GSM24654Normal subject 3160.774
GSM24655A3243G-MELAS subject 1107.279
GSM24656A3243G-MELAS subject 2150.877
GSM24657A3243G-MELAS subject 3286.680
GSM24658A3243G-MELAS subject 4124.275
GSM24659A3243G-PEO subject 116284
GSM24660A3243G-PEO subject 2185.682
GSM24661A3243G-PEO subject 3174.785
GSM24662A3243G-PEO subject 4270.488
GSM24663mtDNA "Common"-deletion subject 1221.182
GSM24664mtDNA "Common"-deletion subject 2232.474
GSM24665mtDNA "Common"-deletion subject 3200.675
GSM24666mtDNA "Common"-deletion subject 4268.778