ProfileGDS1065 / 209763_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% 90% 80% 79% 77% 82% 77% 88% 70% 88% 76% 80% 78% 79% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1178.779
GSM24653Normal subject 2365.790
GSM24654Normal subject 3227.380
GSM24655A3243G-MELAS subject 1110.179
GSM24656A3243G-MELAS subject 2153.977
GSM24657A3243G-MELAS subject 332782
GSM24658A3243G-MELAS subject 414077
GSM24659A3243G-PEO subject 1230.488
GSM24660A3243G-PEO subject 292.270
GSM24661A3243G-PEO subject 3224.188
GSM24662A3243G-PEO subject 4119.876
GSM24663mtDNA "Common"-deletion subject 1188.680
GSM24664mtDNA "Common"-deletion subject 2282.778
GSM24665mtDNA "Common"-deletion subject 3257.579
GSM24666mtDNA "Common"-deletion subject 4404.384