ProfileGDS1065 / 217971_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 71% 73% 83% 80% 79% 72% 72% 65% 72% 66% 60% 73% 83% 82% 82% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1111.371
GSM24653Normal subject 2116.673
GSM24654Normal subject 3275.783
GSM24655A3243G-MELAS subject 1115.680
GSM24656A3243G-MELAS subject 2170.279
GSM24657A3243G-MELAS subject 3184.372
GSM24658A3243G-MELAS subject 4105.772
GSM24659A3243G-PEO subject 16565
GSM24660A3243G-PEO subject 2102.272
GSM24661A3243G-PEO subject 359.966
GSM24662A3243G-PEO subject 456.860
GSM24663mtDNA "Common"-deletion subject 1127.873
GSM24664mtDNA "Common"-deletion subject 238783
GSM24665mtDNA "Common"-deletion subject 3313.782
GSM24666mtDNA "Common"-deletion subject 4371.582