ProfileGDS1065 / 213079_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% 73% 73% 75% 78% 74% 76% 70% 80% 68% 77% 74% 72% 74% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 196.468
GSM24653Normal subject 2114.973
GSM24654Normal subject 3155.973
GSM24655A3243G-MELAS subject 186.475
GSM24656A3243G-MELAS subject 2160.778
GSM24657A3243G-MELAS subject 320674
GSM24658A3243G-MELAS subject 4131.676
GSM24659A3243G-PEO subject 178.870
GSM24660A3243G-PEO subject 2154.580
GSM24661A3243G-PEO subject 365.668
GSM24662A3243G-PEO subject 4122.977
GSM24663mtDNA "Common"-deletion subject 1128.774
GSM24664mtDNA "Common"-deletion subject 2200.572
GSM24665mtDNA "Common"-deletion subject 3191.774
GSM24666mtDNA "Common"-deletion subject 4172.170