ProfileGDS1065 / 209593_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 63% 70% 72% 65% 68% 67% 69% 57% 64% 59% 63% 70% 69% 71% 69% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 177.363
GSM24653Normal subject 299.870
GSM24654Normal subject 3145.172
GSM24655A3243G-MELAS subject 157.165
GSM24656A3243G-MELAS subject 296.168
GSM24657A3243G-MELAS subject 3137.167
GSM24658A3243G-MELAS subject 491.869
GSM24659A3243G-PEO subject 147.957
GSM24660A3243G-PEO subject 270.664
GSM24661A3243G-PEO subject 345.459
GSM24662A3243G-PEO subject 462.763
GSM24663mtDNA "Common"-deletion subject 1106.270
GSM24664mtDNA "Common"-deletion subject 2180.569
GSM24665mtDNA "Common"-deletion subject 3163.771
GSM24666mtDNA "Common"-deletion subject 4162.669