ProfileGDS1065 / 210234_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 62% 55% 61% 68% 69% 58% 59% 69% 68% 68% 57% 56% 63% 63% 60% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 172.962
GSM24653Normal subject 251.955
GSM24654Normal subject 386.661
GSM24655A3243G-MELAS subject 164.468
GSM24656A3243G-MELAS subject 29869
GSM24657A3243G-MELAS subject 389.558
GSM24658A3243G-MELAS subject 45859
GSM24659A3243G-PEO subject 177.669
GSM24660A3243G-PEO subject 282.968
GSM24661A3243G-PEO subject 366.868
GSM24662A3243G-PEO subject 450.457
GSM24663mtDNA "Common"-deletion subject 157.956
GSM24664mtDNA "Common"-deletion subject 2132.363
GSM24665mtDNA "Common"-deletion subject 3112.963
GSM24666mtDNA "Common"-deletion subject 4105.560