ProfileGDS1065 / 48531_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 90% 86% 82% 81% 80% 88% 84% 88% 89% 90% 88% 90% 86% 85% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1408.590
GSM24653Normal subject 2250.786
GSM24654Normal subject 3259.982
GSM24655A3243G-MELAS subject 1120.581
GSM24656A3243G-MELAS subject 2182.280
GSM24657A3243G-MELAS subject 3547.788
GSM24658A3243G-MELAS subject 4224.684
GSM24659A3243G-PEO subject 1232.888
GSM24660A3243G-PEO subject 2316.789
GSM24661A3243G-PEO subject 3286.690
GSM24662A3243G-PEO subject 4260.688
GSM24663mtDNA "Common"-deletion subject 1426.590
GSM24664mtDNA "Common"-deletion subject 2472.186
GSM24665mtDNA "Common"-deletion subject 339685
GSM24666mtDNA "Common"-deletion subject 4458.985