ProfileGDS1065 / 200829_x_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 91% 89% 91% 89% 88% 92% 88% 90% 90% 91% 90% 92% 89% 89% 90% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1474.291
GSM24653Normal subject 2332.689
GSM24654Normal subject 3624.591
GSM24655A3243G-MELAS subject 1222.689
GSM24656A3243G-MELAS subject 2333.488
GSM24657A3243G-MELAS subject 3816.192
GSM24658A3243G-MELAS subject 4311.188
GSM24659A3243G-PEO subject 1282.490
GSM24660A3243G-PEO subject 2361.290
GSM24661A3243G-PEO subject 3325.991
GSM24662A3243G-PEO subject 4335.990
GSM24663mtDNA "Common"-deletion subject 1539.192
GSM24664mtDNA "Common"-deletion subject 2624.489
GSM24665mtDNA "Common"-deletion subject 3607.689
GSM24666mtDNA "Common"-deletion subject 4743.790