ProfileGDS1065 / 209048_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 76% 78% 72% 76% 73% 77% 72% 80% 70% 78% 75% 71% 72% 72% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1149.876
GSM24653Normal subject 2151.578
GSM24654Normal subject 3143.872
GSM24655A3243G-MELAS subject 192.976
GSM24656A3243G-MELAS subject 2119.873
GSM24657A3243G-MELAS subject 3238.477
GSM24658A3243G-MELAS subject 4105.872
GSM24659A3243G-PEO subject 1132.380
GSM24660A3243G-PEO subject 292.170
GSM24661A3243G-PEO subject 3109.778
GSM24662A3243G-PEO subject 410975
GSM24663mtDNA "Common"-deletion subject 111471
GSM24664mtDNA "Common"-deletion subject 2203.772
GSM24665mtDNA "Common"-deletion subject 3171.172
GSM24666mtDNA "Common"-deletion subject 4163.869