ProfileGDS1065 / 210406_s_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 87% 89% 92% 90% 91% 87% 88% 86% 88% 86% 86% 90% 91% 92% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132087
GSM24653Normal subject 2343.789
GSM24654Normal subject 3654.492
GSM24655A3243G-MELAS subject 1252.290
GSM24656A3243G-MELAS subject 2447.691
GSM24657A3243G-MELAS subject 3495.687
GSM24658A3243G-MELAS subject 4323.288
GSM24659A3243G-PEO subject 1190.686
GSM24660A3243G-PEO subject 2290.588
GSM24661A3243G-PEO subject 3189.386
GSM24662A3243G-PEO subject 4232.486
GSM24663mtDNA "Common"-deletion subject 1423.390
GSM24664mtDNA "Common"-deletion subject 2805.991
GSM24665mtDNA "Common"-deletion subject 3903.492
GSM24666mtDNA "Common"-deletion subject 4890.391