ProfileGDS1065 / 221654_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% 69% 67% 66% 69% 71% 71% 70% 70% 73% 70% 70% 70% 64% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1146.776
GSM24653Normal subject 293.969
GSM24654Normal subject 3111.867
GSM24655A3243G-MELAS subject 159.266
GSM24656A3243G-MELAS subject 2101.869
GSM24657A3243G-MELAS subject 3167.271
GSM24658A3243G-MELAS subject 4100.971
GSM24659A3243G-PEO subject 180.670
GSM24660A3243G-PEO subject 293.670
GSM24661A3243G-PEO subject 381.273
GSM24662A3243G-PEO subject 487.270
GSM24663mtDNA "Common"-deletion subject 1108.870
GSM24664mtDNA "Common"-deletion subject 2187.470
GSM24665mtDNA "Common"-deletion subject 3116.964
GSM24666mtDNA "Common"-deletion subject 4219.874