ProfileGDS1065 / 209047_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 95% 95% 95% 94% 95% 96% 96% 93% 93% 95% 95% 95% 95% 94% 95% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1985.295
GSM24653Normal subject 2837.995
GSM24654Normal subject 31176.995
GSM24655A3243G-MELAS subject 1422.394
GSM24656A3243G-MELAS subject 2813.795
GSM24657A3243G-MELAS subject 31635.796
GSM24658A3243G-MELAS subject 41016.696
GSM24659A3243G-PEO subject 1385.693
GSM24660A3243G-PEO subject 2538.293
GSM24661A3243G-PEO subject 362995
GSM24662A3243G-PEO subject 4723.195
GSM24663mtDNA "Common"-deletion subject 1942.195
GSM24664mtDNA "Common"-deletion subject 21531.495
GSM24665mtDNA "Common"-deletion subject 31141.294
GSM24666mtDNA "Common"-deletion subject 41773.995